BioMedLib Search Engine
[ goto HOMEPAGE ]
Search the biomedical literature, for the most relevant articles.
Skip to content
Advanced Search
Search History
MeSH Query
Page Format
Query is expanded
Login
Skip to content
Export Citations
Search Results
RSS
Email
Articles' Details
Start new query
Reset All
Refine your query
(more in Advanced-Search):
Search all of MEDLINE
Focus on the recent 5 years
Focus on the current year
Focus on the last 30 days
More choices ...
Focus on articles with free fulltexts
More choices ...
Do simple 'keyword' search (no query expansion)
[X] Close
You are about to erase all the values you have customized, search history, page format, etc.
Click
here to
RESET
all values
Click
here to
GO BACK
without resetting any value
Advanced Search
Submit one or more of the following items, and they will be searched along with your query in the search box above.
Any submit button will submit all of the items you have changed.
+
Publication-Date
Published in the last:
30 days
60 days
90 days
6 months
12 months
this year
2 years
3 years
5 years
10 years
Or published in the following date range: From (yyyy/mm/dd - month and day are optional)
to ('to' is optional)
+
Full Text
Retrieve articles with hyperlinks to:
full text (either free or subscription)
free full text
subscription full text
no full text link
+
Sort-Order
Sort the retrieved articles by:
relevance
publication date
+
Language
And with languages:
English
French
German
Italian
Japanese
Russian
Spanish
More languages:
Afrikaans
Albanian
Amharic
Arabic
Armenian
Azerbaijani
Bengali
Bosnian
Bulgarian
Catalan
Chinese
Czech
Danish
Dutch
Esperanto
Estonian
Finnish
Georgian
Scottish Gaelic
Greek, Modern
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Kinyarwanda
Korean
Latin
Latvian
Lithuanian
Macedonian
Malayalam
Maori
Malay
Multiple languages
Norwegian
Persian
Polish
Portuguese
Pushto
Romanian
Sanskrit
Serbian
Croatian
Slovak
Slovenian
Swedish
Thai
Turkish
Ukrainian
Undetermined
Urdu
Vietnamese
Welsh
+
Publication-Type
And with publication types:
Clinical Trial
Editorial
Letter
Meta-Analysis
Practice Guideline
Randomized Controlled Trial
Review
More publication types:
Addresses
Bibliography
Biography
Case Reports
Classical Article
Clinical Conference
Clinical Trial, Phase I
Clinical Trial, Phase II
Clinical Trial, Phase III
Clinical Trial, Phase IV
Comment
Comparative Study
Congresses
Consensus Development Conference
Consensus Development Conference, NIH
Controlled Clinical Trial
Corrected and Republished Article
Dictionary
Directory
Duplicate Publication
English Abstract
Evaluation Studies
Festschrift
Government Publications
Guideline
Historical Article
Interactive Tutorial
Interview
Introductory Journal Article
In Vitro
Journal Article
Lectures
Legal Cases
Legislation
Multicenter Study
News
Newspaper Article
Overall
Patient Education Handout
Periodical Index
Portraits
Published Erratum
Retracted Publication
Research Support, N.I.H., Extramural
Research Support, N.I.H., Intramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.
Retraction of Publication
Scientific Integrity Review
Technical Report
Twin Study
Validation Studies
+
Species
And for:
Humans
Animals
+
Gender
And for:
Male
Female
+
Age
And for these age groups:
Newborn: birth to 1 month
Infant: 1 to 23 months
Preschool child: 2 to 5 years
Child: 6 to 12 years
Adolescent: 13 to 18 years
Adult: 19 to 44 years
Middle aged: 45 to 64 years
Aged: 65+ years
80 and over: 80+ years
+
Title
And for this query matching the titles:
+
Transliterated-Title
And for this query matching the title in original language:
+
Abstract
And for this query matching the abstratcs:
+
Major-Mesh
And for this query matching the MeSH-Major terms:
+
Mesh
And for this query matching any MeSH terms:
+
Journal
And for one or more of these journal abbreviated names:
OR
OR
(see
title abbreviations
)
+
Volume
And with journal volume number:
+
Issue
And with journal issue number:
+
Page
And with page number:
+
ISSN
And with ISSN:
+
Publication-Place
And with journal's country of publication:
+
Author
And for...
all these author names:
AND
AND
(see
help
)
one or more of these author names:
OR
OR
but not having any of these unwanted author names:
NOT
NOT
+
Affiliation
And with affiliation to:
+
Has-Abstract
Find MEDLINE records with the abstract status:
has abstract
does not have abstract
include both record types
include both record types but rank higher the records having abstract (the default BML behavior)
+
PMID
Show me only articles for these PMIDs (PubMed IDs):
+
Semantic-Type
And with semantic types:
A. Entity
A1. Physical Object
A1.1. Organism
A1.1.1. Archaeon
A1.1.2. Bacterium
A1.1.3. Eukaryote
A1.1.3.1. Animal
A1.1.3.1.1. Vertebrate
A1.1.3.1.1.1. Amphibian
A1.1.3.1.1.2. Bird
A1.1.3.1.1.3. Fish
A1.1.3.1.1.4. Mammal
A1.1.3.1.1.4.1. Human
A1.1.3.1.1.5. Reptile
A1.1.3.2. Fungus
A1.1.3.3. Plant
A1.1.4. Virus
A1.2. Anatomical Structure
A1.2.1. Embryonic Structure
A1.2.2. Anatomical Abnormality
A1.2.2.1. Congenital Abnormality
A1.2.2.2. Acquired Abnormality
A1.2.3. Fully Formed Anatomical Structure
A1.2.3.1. Body Part, Organ, or Organ Component
A1.2.3.2. Tissue
A1.2.3.3. Cell
A1.2.3.4. Cell Component
A1.2.3.5. Gene or Genome
A1.3. Manufactured Object
A1.3.1. Medical Device
A1.3.1.1. Drug Delivery Device
A1.3.2. Research Device
A1.3.3. Clinical Drug
A1.4. Substance
A1.4.1. Chemical
A1.4.1.1. Chemical Viewed Functionally
A1.4.1.1.1. Pharmacologic Substance
A1.4.1.1.1.1. Antibiotic
A1.4.1.1.2. Biomedical or Dental Material
A1.4.1.1.3. Biologically Active Substance
A1.4.1.1.3.1. Neuroreactive Substance or Biogenic Amine
A1.4.1.1.3.2. Hormone
A1.4.1.1.3.3. Enzyme
A1.4.1.1.3.4. Vitamin
A1.4.1.1.3.5. Immunologic Factor
A1.4.1.1.3.6. Receptor
A1.4.1.1.4. Indicator, Reagent, or Diagnostic Aid
A1.4.1.1.5. Hazardous or Poisonous Substance
A1.4.1.2. Chemical Viewed Structurally
A1.4.1.2.1. Organic Chemical
A1.4.1.2.1.5. Nucleic Acid, Nucleoside, or Nucleotide
A1.4.1.2.1.6. Organophosphorus Compound
A1.4.1.2.1.7. Amino Acid, Peptide, or Protein
A1.4.1.2.1.8. Carbohydrate
A1.4.1.2.1.9. Lipid
A1.4.1.2.1.9.1. Steroid
A1.4.1.2.1.9.2. Eicosanoid
A1.4.1.2.2. Inorganic Chemical
A1.4.1.2.3. Element, Ion, or Isotope
A1.4.2. Body Substance
A1.4.3. Food
A2. Conceptual Entity
A2.1. Idea or Concept
A2.1.1. Temporal Concept
A2.1.2. Qualitative Concept
A2.1.3. Quantitative Concept
A2.1.4. Functional Concept
A2.1.4.1. Body System
A2.1.5. Spatial Concept
A2.1.5.1. Body Space or Junction
A2.1.5.2. Body Location or Region
A2.1.5.3. Molecular Sequence
A2.1.5.3.1. Nucleotide Sequence
A2.1.5.3.2. Amino Acid Sequence
A2.1.5.3.3. Carbohydrate Sequence
A2.1.5.4. Geographic Area
A2.2. Finding
A2.2.1. Laboratory or Test Result
A2.2.2. Sign or Symptom
A2.3. Organism Attribute
A2.3.1. Clinical Attribute
A2.4. Intellectual Product
A2.4.1. Classification
A2.4.2. Regulation or Law
A2.5. Language
A2.6. Occupation or Discipline
A2.6.1. Biomedical Occupation or Discipline
A2.7. Organization
A2.7.1. Health Care Related Organization
A2.7.2. Professional Society
A2.7.3. Self-help or Relief Organization
A2.8. Group Attribute
A2.9. Group
A2.9.1. Professional or Occupational Group
A2.9.2. Population Group
A2.9.3. Family Group
A2.9.4. Age Group
A2.9.5. Patient or Disabled Group
B. Event
B1. Activity
B1.1. Behavior
B1.1.1. Social Behavior
B1.1.2. Individual Behavior
B1.2. Daily or Recreational Activity
B1.3. Occupational Activity
B1.3.1. Health Care Activity
B1.3.1.1. Laboratory Procedure
B1.3.1.2. Diagnostic Procedure
B1.3.1.3. Therapeutic or Preventive Procedure
B1.3.2. Research Activity
B1.3.2.1. Molecular Biology Research Technique
B1.3.3. Governmental or Regulatory Activity
B1.3.4. Educational Activity
B1.4. Machine Activity
B2. Phenomenon or Process
B2.1. Human-caused Phenomenon or Process
B2.1.1. Environmental Effect of Humans
B2.2. Natural Phenomenon or Process
B2.2.1. Biologic Function
B2.2.1.1. Physiologic Function
B2.2.1.1.1. Organism Function
B2.2.1.1.1.1. Mental Process
B2.2.1.1.2. Organ or Tissue Function
B2.2.1.1.3. Cell Function
B2.2.1.1.4. Molecular Function
B2.2.1.1.4.1. Genetic Function
B2.2.1.2. Pathologic Function
B2.2.1.2.1. Disease or Syndrome
B2.2.1.2.1.1. Mental or Behavioral Dysfunction
B2.2.1.2.1.2. Neoplastic Process
B2.2.1.2.2. Cell or Molecular Dysfunction
B2.2.1.2.3. Experimental Model of Disease
B2.3. Injury or Poisoning
Page Format
Any submit button will submit all of the items you have changed.
[theme]
Use this page design theme:
original
twenty ten
[shown]
Results per page:
5
10
20
50
100
200
500
[expand/collapse]
show these sections expanded by default:
Advanced search
MeSH query
Search history
Page format
Query expansion
Articles details
Export citations
Email
[text size]
use this font size for text:
25%
50%
75%
100%
125%
150%
200%
or enter your choice of font size:
[page width]
use this page width (relative to the default initial value):
25%
50%
75%
100%
125%
150%
200%
or enter your choice of page width:
[highlight color]
use this color to highlight query words in the articles:
red
green
blue
black
purple
yellow
orange
navy
olive
maroon
none
[query history]
maximum number of queries shown in the history section:
[annotate]
Annotate these parts of each article:
title
abstract
both
none
Reset all values
Find best MeSH terms for
Search History
1
adenocarcinomas bronchiolo alveolar 2005:2010[pubdate] *count=100
3729 results
Searchbox
Export
PDF
RSS
Email
Delete
Email this search result to the following email address:
[X] Close
Expand the query
'
adenocarcinomas bronchiolo alveolar
' expanded to all its synonyms;
details
Email the results to the following email address:
Export the checked citations in RIS format (RIS format is used by RefWorks, Endnote, among others).
Items 1 to 100 of about 3729
1.
Inamura K, Togashi Y, Nomura K, Ninomiya H, Hiramatsu M, Satoh Y, Okumura S, Nakagawa K, Ishikawa Y:
let-7 microRNA expression is reduced in bronchioloalveolar carcinoma, a non-invasive carcinoma, and is not correlated with prognosis.
Lung Cancer
; 2007 Dec;58(3):392-6
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
let-7 microRNA expression is reduced in
bronchioloalveolar carcinoma
, a non-invasive
carcinoma
, and is not correlated with prognosis.
It has been proposed that reduced let-7 expression causes RAS expression and correlates with poor survival
of lung cancer
cases, but little is known about correlations with clinicopathologic features.
In this study, we examined 15 early
bronchioloalveolar carcinomas
(
BACs
), usually considered as
adenocarcinomas
in situ, as well as 26 well-differentiated and 25 less-differentiated invasive
adenocarcinomas
, to assess the association between tumor progression and let-7 expression levels.
Additionally, we investigated 47 invasive
lung
adenocarcinomas
for EGFR and KRAS mutations and correlations with let-7 levels.
Relative to the corresponding normal
lung
tissue, reduced let-7 expression was observed in 13 of 15
BACs
(87%) and totally in 52 of the 66
adenocarcinomas
(79%), suggesting a link with early occurrence in carcinogenesis.
On classification of
adenocarcinomas
into two groups according to let-7 expression, no prognostic or genetic differences were observed.
Interestingly, some differences between histological subtypes were observed, such as lower let-7 expression levels in acinar
adenocarcinomas
and mucinous
BACs
.
[MeSH-major]
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ genetics.
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ pathology. Gene Expression Regulation, Neoplastic / genetics. MicroRNAs / genetics
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[CommentIn]
Lung Cancer. 2008 May;60(2):307
[
18395292.001
]
(PMID = 17728006.001).
[ISSN]
0169-5002
[Journal-full-title]
Lung cancer (Amsterdam, Netherlands)
[ISO-abbreviation]
Lung Cancer
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Ireland
[Chemical-registry-number]
0 / MicroRNAs; 0 / mirnlet7 microRNA, human
2.
Khan S, Ng ML, Tan YJ:
Expression of the severe acute respiratory syndrome coronavirus 3a protein and the assembly of coronavirus-like particles in the baculovirus expression system.
Methods Mol Biol
; 2007;379:35-50
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The Bac
-to-
Bac
Baculovirus expression system was used to generate a recombinant baculovirus capable of expressing the severe acute respiratory syndrome (SARS)-coronavirus (CoV) 3a protein.
Using the same expression system, two structural proteins, membrane (M) and envelope (E), were co-expressed to form SARS-CoV virus-like particles (VLPs) within an insect
cell
.
[MeSH-minor]
Animals. Baculoviridae.
Cell
Line. Gene Expression. Humans. Spodoptera / cytology
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17502669.001).
[ISSN]
1064-3745
[Journal-full-title]
Methods in molecular biology (Clifton, N.J.)
[ISO-abbreviation]
Methods Mol. Biol.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Review
[Publication-country]
United States
[Chemical-registry-number]
0 / 3a protein, severe acute respiratory syndrome coronavirus; 0 / Recombinant Proteins; 0 / Viral Proteins
[Number-of-references]
38
3.
Bubeck SS, Cantwell AM, Dube PH:
Delayed inflammatory response to primary pneumonic plague occurs in both outbred and inbred mice.
Infect Immun
; 2007 Feb;75(2):697-705
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Yersinia pestis is the causative agent of plague,
a disease
that can manifest as either bubonic or pneumonic plague.
An interesting feature of plague is that it is a rapidly progressive
disease
, suggesting that Y. pestis either evades and/or suppresses the innate immune response to infection.
A comparative analysis of the course
of disease
in these two strains of mice indicated that they are susceptible to intranasal Y. pestis CO92 infection and have similar 50% lethal doses and kinetics of infection with respect to colonization of the
lung
, liver, and spleen.
Significantly, in both strains of mice, robust neutrophil recruitment to the lungs was not observed until 48 h after infection, suggesting that there was a delay in inflammatory
cell
recruitment to the site of infection.
In addition, proinflammatory cytokines (interleukin-6 [IL-6], tumor necrosis factor alpha, gamma interferon, IL-12p70, monocyte chemoattractant protein 1) and chemokines (KC, MIP-2) in
the bronchoalveolar
lavage fluids were not readily detected until 48 h after infection, which coincided with the increase in polymorphonuclear leukocyte (PMN) recruitment to the lungs.
In comparison, CD1 mice with gram-negative pneumonia caused by Klebsiella pneumoniae exhibited strong inflammatory responses early in infection, with PMNs comprising the majority of the cells in
the bronchoalveolar
lavage fluid 24 h postinfection, indicating that PMN recruitment to the lungs could occur earlier in this infection than in Y. pestis infection.
[MeSH-major]
Cytokines / metabolism.
Lung
/ immunology. Neutrophil Infiltration. Neutrophils / immunology. Plague / immunology. Yersinia pestis / immunology
[MeSH-minor]
Animals.
Bronchoalveolar
Lavage Fluid / cytology.
Bronchoalveolar
Lavage Fluid / immunology. Chemokines / metabolism.
Disease
Models, Animal. Female. Histocytochemistry. Klebsiella Infections / immunology. Klebsiella pneumoniae / immunology. Lethal Dose 50. Liver / microbiology. Mice. Mice, Inbred C57BL. Spleen / microbiology. Time Factors
MedlinePlus Health Information.
consumer health - Plague
.
COS Scholar Universe.
author profiles
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Vaccine. 2000 Oct 15;19(4-5):566-71
[
11027822.001
]
[Cites]
Am J Pathol. 1968 Jul;53(1):99-114
[
4968324.001
]
[Cites]
J Infect Dis. 1974 May;129:Suppl:S53-61
[
4207626.001
]
[Cites]
JAMA. 1984 Feb 17;251(7):929-31
[
6694294.001
]
[Cites]
Infect Immun. 1993 Jan;61(1):23-31
[
8418045.001
]
[Cites]
Infect Immun. 1994 Jun;62(6):2590-9
[
8188382.001
]
[Cites]
Am J Trop Med Hyg. 1994 Jul;51(1):109-14
[
8059908.001
]
[Cites]
J Immunol. 1995 Jan 1;154(1):335-44
[
7995953.001
]
[Cites]
Infect Immun. 1995 Aug;63(8):3021-9
[
7622225.001
]
[Cites]
J Leukoc Biol. 1996 Jan;59(1):24-8
[
8558063.001
]
[Cites]
J Immunol. 1996 Mar 1;156(5):1963-72
[
8596051.001
]
[Cites]
Infect Immun. 1996 Sep;64(9):3609-13
[
8751906.001
]
[Cites]
Infect Immun. 1996 Nov;64(11):4580-5
[
8890210.001
]
[Cites]
Infect Immun. 1997 Aug;65(8):3065-73
[
9234755.001
]
[Cites]
Vaccine. 1998 Apr;16(7):698-707
[
9562689.001
]
[Cites]
Microb Pathog. 1999 Mar;26(3):159-69
[
10089156.001
]
[Cites]
J Infect Dis. 1959 Jan-Feb;104(1):78-84
[
13631290.001
]
[Cites]
J Infect Dis. 1959 Jan-Feb;104(1):85-91
[
13631291.001
]
[Cites]
Am J Pathol. 2005 May;166(5):1427-39
[
15855643.001
]
[Cites]
Infect Immun. 2005 Nov;73(11):7142-50
[
16239508.001
]
[Cites]
Mol Microbiol. 2005 Nov;58(4):1054-73
[
16262790.001
]
[Cites]
Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17786-91
[
16306265.001
]
[Cites]
Infect Immun. 2006 Sep;74(9):5402-7
[
16926436.001
]
[Cites]
Nat Immunol. 2006 Oct;7(10):1066-73
[
16980981.001
]
[Cites]
Infect Immun. 1998 May;66(5):2213-20
[
9573110.001
]
[Cites]
Vet Pathol. 2001 Mar;38(2):165-72
[
11280372.001
]
[Cites]
Infect Immun. 2001 Dec;69(12):7419-24
[
11705916.001
]
[Cites]
J Cell Biol. 2002 Aug 5;158(3):401-8
[
12163464.001
]
[Cites]
Vaccine. 2003 Jun 20;21(21-22):3051-7
[
12798649.001
]
[Cites]
Infect Immun. 2004 Mar;72(3):1645-56
[
14977972.001
]
[Cites]
Infect Immun. 2004 Apr;72(4):2052-6
[
15039326.001
]
[Cites]
Infect Immun. 2004 Jun;72(6):3561-70
[
15155665.001
]
[Cites]
Vaccine. 2004 Jun 30;22(20):2524-32
[
15193377.001
]
[Cites]
Vaccine. 2004 Sep 3;22(25-26):3348-57
[
15308359.001
]
[Cites]
Microb Pathog. 2004 Oct;37(4):177-84
[
15458778.001
]
[Cites]
J Infect Dis. 1965 Dec;115(5):456-64
[
4954349.001
]
[Cites]
Am J Pathol. 1969 Feb;54(2):167-85
[
4974722.001
]
(PMID = 17101642.001).
[ISSN]
0019-9567
[Journal-full-title]
Infection and immunity
[ISO-abbreviation]
Infect. Immun.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article
[Publication-country]
United States
[Chemical-registry-number]
0 / Chemokines; 0 / Cytokines
[Other-IDs]
NLM/ PMC1828510
Advertisement
4.
Slaney JM, Curtis MA:
Mechanisms of evasion of complement by Porphyromonas gingivalis.
Front Biosci
; 2008 Jan 01;13:188-96
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Activation leads to deposition on
the bacterial
surface of C3b and its' inactivation products and phagocytosis of the opsonised bacteria by host cells.
Alternatively the entire complement pathway including
terminal
components C5b-9 may be activated on
the cell
surface which gives rise to generation and insertion of the membrane attack
complex
into
the bacterial
membrane and
cell
lysis.
Bacterial
resistance to complement may be by enzyme digestion of complement components or by the generation or acquisition from the host
of cell
surface molecules which allow the organism to adopt host complement control proteins.
The proteases of Porphyromonas gingivalis breakdown C3 and C5 and prevent the deposition of C3b on
the bacterial cell
surface.
Instead, complement resistance in P. gingivalis is associated with the presence on
the cell
surface of an anionic branched mannan and appears independent of capsule serotype.
[MeSH-major]
Cell
Membrane / metabolism. Complement System Proteins / physiology. Polysaccharides / metabolism. Porphyromonas gingivalis / metabolism
[MeSH-minor]
Bacterial
Outer Membrane Proteins / metabolism. Complement Activation. Humans. Lipopolysaccharides / chemistry. Models, Biological. O Antigens / chemistry. Phagocytosis. Pseudomonas aeruginosa / metabolism
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17981537.001).
[ISSN]
1093-9946
[Journal-full-title]
Frontiers in bioscience : a journal and virtual library
[ISO-abbreviation]
Front. Biosci.
[Language]
eng
[Grant]
United Kingdom / Medical Research Council / / G0501478
[Publication-type]
Journal Article; Review
[Publication-country]
United States
[Chemical-registry-number]
0 / Bacterial Outer Membrane Proteins; 0 / Lipopolysaccharides; 0 / O Antigens; 0 / Polysaccharides; 9007-36-7 / Complement System Proteins
[Number-of-references]
66
5.
Brachtel EF, Iafrate AJ, Mark EJ, Deshpande V:
Cytomorphological correlates of epidermal growth factor receptor mutations in lung carcinoma.
Diagn Cytopathol
; 2007 May;35(5):257-62
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Cytomorphological correlates of epidermal growth factor receptor mutations in
lung carcinoma
.
The initial
diagnosis of lung carcinoma
is frequently made by fine-needle aspiration biopsy.
Novel therapeutic strategies of this
disease
include tyrosine kinase inhibitors (TKI), such as gefitinib (Iressa) or erlotinib (Tarceva), which target the kinase domain of epidermal growth factor receptor (EGFR).
Somatic mutations of this region have been shown to predict a therapeutic response
of lung carcinomas
to TKI.
EGFR mutations have been described in
adenocarcinomas
of the
lung
, especially
the bronchioloalveolar
subtype, which has both cytopathologic and histopathologic definitions.
We identified 37 fine-needle aspiration biopsy
of lung
masses on which molecular analysis for EGFR mutations was available.
Molecular analysis was performed on DNA isolated from formalin-fixed, paraffin-embedded, or frozen tissue from the corresponding core biopsies/
cell
blocks or resection specimens followed by PCR with primers for the tyrosine kinase region exons 18-24 and nucleotide sequence analysis by gel electrophoresis.
All cases were
adenocarcinomas
primary in
the lung
.
Some of the traditional cytomorphological features
of bronchioloalveolar carcinoma
, i.e., flat monolayers, intranuclear inclusions, and the absence of macronucleoli, statistically correlated with the presence of mutations within the tyrosine kinase region of EGFR.
[MeSH-major]
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ genetics.
Lung
Neoplasms / genetics. Mutation. Receptor, Epidermal Growth Factor / genetics
[MeSH-minor]
Aged. Biopsy, Fine-Needle.
Cell
Nucleolus / pathology. DNA Mutational Analysis. DNA, Neoplasm / analysis. Female. Humans. Intranuclear Inclusion Bodies / pathology. Male. Phenotype. Polymerase Chain Reaction. Predictive Value of Tests. Protein Kinase Inhibitors / therapeutic use. Single-Blind Method. src Homology Domains / genetics
MedlinePlus Health Information.
consumer health - Lung Cancer
.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
(c) 2007 Wiley-Liss, Inc.
(PMID = 17427221.001).
[ISSN]
8755-1039
[Journal-full-title]
Diagnostic cytopathology
[ISO-abbreviation]
Diagn. Cytopathol.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Chemical-registry-number]
0 / DNA, Neoplasm; 0 / Protein Kinase Inhibitors; EC 2.7.10.1 / Receptor, Epidermal Growth Factor
6.
Gundersen H, Grüner R, Specht K, Hugdahl K:
The effects of alcohol intoxication on neuronal activation at different levels of cognitive load.
Open Neuroimag J
; 2008;2:65-72
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The aim of this study was to investigate how alcohol intoxication at two blood alcohol concentrations (
BAC
) affected neuronal activation during increasing levels of cognitive load.
Participants in the control group (N=13) were scanned after drinking a soft-drink at both scanning sessions, while participants in the alcohol group (N=12) were scanned once after drinking an alcoholic beverage resulting in
a BAC
of 0.02%, and once after drinking an alcoholic beverage resulting in
a BAC
of 0.08%.
A decrease in neuronal activation was seen in the dorsal anterior cingulate cortex (dACC) and in the cerebellum in the alcohol group at
the BAC
of 0.08% when the participants performed the most demanding task.
The results have revealed that the effect of alcohol intoxication on brain activity is dependent on
BAC
and of cognitive load.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Inj Prev. 2002 Sep;8 Suppl 3:iii1-iii17
[
12486814.001
]
[Cites]
J Abnorm Psychol. 2003 Aug;112(3):476-87
[
12943026.001
]
[Cites]
Annu Rev Neurosci. 2002;25:563-93
[
12052921.001
]
[Cites]
Neuroimage. 2002 Mar;15(3):523-36
[
11848695.001
]
[Cites]
Am Psychol. 2001 Nov;56(11):851-64
[
11785152.001
]
[Cites]
Neuroreport. 2001 Dec 21;12(18):4047-54
[
11742236.001
]
[Cites]
Behav Brain Sci. 2001 Feb;24(1):87-114; discussion 114-85
[
11515286.001
]
[Cites]
Annu Rev Neurosci. 2001;24:167-202
[
11283309.001
]
[Cites]
Neuroimage. 2000 May;11(5 Pt 1):400-8
[
10806027.001
]
[Cites]
Exp Clin Psychopharmacol. 1999 Nov;7(4):372-8
[
10609972.001
]
[Cites]
Psychopharmacology (Berl). 1999 Oct;146(4):465-72
[
10550497.001
]
[Cites]
Alcohol Clin Exp Res. 2007 Sep;31(9):1490-504
[
17624997.001
]
[Cites]
Neuroreport. 2007 Sep 17;18(14):1511-4
[
17712285.001
]
[Cites]
Neuropsychologia. 2007 May 15;45(9):2016-24
[
17379262.001
]
[Cites]
Scand J Psychol. 2007 Apr;48(2):81-6
[
17430361.001
]
[Cites]
Hum Brain Mapp. 2005 May;25(1):46-59
[
15846822.001
]
[Cites]
J Abnorm Psychol. 2004 Nov;113(4):569-81
[
15535789.001
]
[Cites]
Hum Brain Mapp. 1998;6(4):270-82
[
9704265.001
]
[Cites]
Cogn Psychol. 1997 Jun;33(1):5-42
[
9212720.001
]
[Cites]
Psychol Bull. 1993 Nov;114(3):459-76
[
8272466.001
]
[Cites]
Am Psychol. 1990 Aug;45(8):921-33
[
2221564.001
]
[Cites]
Hum Factors. 1974 Apr;16(2):174-80
[
4844761.001
]
[Cites]
Neuropsychopharmacology. 2004 Nov;29(11):2097-17
[
15316570.001
]
[Cites]
Cogn Affect Behav Neurosci. 2003 Dec;3(4):255-74
[
15040547.001
]
[Cites]
Am J Psychiatry. 2004 Feb;161(2):286-93
[
14754778.001
]
[Cites]
Hum Brain Mapp. 2004 Jan;21(1):15-26
[
14689506.001
]
[Cites]
Science. 2002 Dec 13;298(5601):2209-11
[
12424384.001
]
(PMID = 19018317.001).
[ISSN]
1874-4400
[Journal-full-title]
The open neuroimaging journal
[ISO-abbreviation]
Open Neuroimag J
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Netherlands
[Other-IDs]
NLM/ PMC2577939
[Keywords]
NOTNLM ; Alcohol intoxication / brain function / cognitive load / different blood alcohol concentrations
7.
Rogatcheva MB, Chen K, Larkin DM, Meyers SN, Marron BM, He W, Schook LB, Beever JE:
Piggy-BACing the human genome I: constructing a porcine BAC physical map through comparative genomics.
Anim Biotechnol
; 2008;19(1):28-42
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Piggy-BACing the human genome I: constructing a porcine
BAC
physical map through comparative genomics.
Availability of the human genome sequence and high similarity between humans and pigs at the molecular level provides an opportunity to use a comparative mapping approach to piggy-
BAC the
human genome.
In order to advance the pig genome sequencing initiative, sequence similarity between large-scale porcine
BAC
-end sequences (BESs) and human genome sequence was used to construct a comparatively-anchored porcine physical map that is a first step towards sequencing the pig genome.
A total of 50,300 porcine
BAC
clones were end-sequenced, yielding 76,906 BESs after trimming with an average read length of 538 bp.
To anchor the porcine
BACs
on the human genome, these BESs were subjected to BLAST analysis using the human draft sequence, revealing 31.5% significant hits (E < e(-5)).
The strategy of piggy-BACing the human genome described in this study demonstrates that through a directed, targeted comparative genomics approach construction
of a
high-resolution anchored physical map of the pig genome can be achieved.
This map supports the selection
of BACs
to construct a minimal tiling path for genome sequencing and targeted gap filling.
[MeSH-minor]
Animals. Chromosome Mapping. Chromosomes, Artificial,
Bacterial
/ genetics. DNA / genetics. DNA / isolation & purification. Genome. Genomic Library. Humans. Nucleic Acid Hybridization
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18228174.001).
[ISSN]
1532-2378
[Journal-full-title]
Animal biotechnology
[ISO-abbreviation]
Anim. Biotechnol.
[Language]
eng
[Publication-type]
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
United States
[Chemical-registry-number]
9007-49-2 / DNA
8.
Douglas VC, Tong DC, Gillum LA, Zhao S, Brass LM, Dostal J, Johnston SC:
Do the Brain Attack Coalition's criteria for stroke centers improve care for ischemic stroke?
Neurology
; 2005 Feb 8;64(3):422-7
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
BACKGROUND: In 2000, the Brain Attack Coalition (
BAC
) recommended 11 major criteria for the establishment of primary stroke centers.
The BAC
relied heavily on expert opinion because evidence supporting the criteria was sparse.
OBJECTIVE: To assess primary stroke center elements, based on the criteria proposed by
the BAC
, with a questionnaire at 34 academic medical centers.
CONCLUSIONS: Of the 11 stroke center elements recommended by
the BAC
, 7 were associated with increased tPA use.
Genetic Alliance.
consumer health - Ischemic stroke
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 15699369.001).
[ISSN]
1526-632X
[Journal-full-title]
Neurology
[ISO-abbreviation]
Neurology
[Language]
eng
[Grant]
United States / NINDS NIH HHS / NS / NS02254
[Publication-type]
Evaluation Studies; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
[Publication-country]
United States
[Chemical-registry-number]
EC 3.4.21.68 / Tissue Plasminogen Activator
9.
Nord H, Hartmann C, Andersson R, Menzel U, Pfeifer S, Piotrowski A, Bogdan A, Kloc W, Sandgren J, Olofsson T, Hesselager G, Blomquist E, Komorowski J, von Deimling A, Bruder CE, Dumanski JP, DÃaz de StÃ¥hl T:
Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array.
Neuro Oncol
; 2009 Dec;11(6):803-18
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Characterization of novel and
complex
genomic aberrations in glioblastoma using a 32K
BAC
array.
Glioblastomas (GBs) are
malignant
CNS tumors often associated with devastating symptoms.
Patients with GB have a very poor prognosis, and despite treatment, most of them die within 12 months from
diagnosis
.
Several pathways, such as the RAS, tumor protein 53 (TP53), and phosphoinositide kinase 3 (PIK3) pathways, as well as
the cell
cycle control pathway, have been identified to be disrupted in this tumor.
In this study, we have applied a 32K clone-based genomic array, covering 99% of the current assembly of the human genome, to the detailed genetic profiling
of a
set of 78 GBs.
Complex
patterns of aberrations, including high and narrow copy number amplicons, as well as a number of homozygously deleted loci, were identified.
Many of these genes are already linked to several forms
of cancer
; others represent new candidate genes that may serve as prognostic markers or even as therapeutic targets in the future.
The large individual variation observed between the samples demonstrates the underlying complexity of the
disease
and strengthens the demand for an individualized therapy based on the genetic profile of the patient.
[MeSH-major]
Brain Neoplasms / genetics. Chromosome Aberrations. Chromosomes, Artificial,
Bacterial
. Gene Expression Profiling. Genes, Neoplasm. Glioblastoma / genetics
Genetic Alliance.
consumer health - Glioblastoma
.
MedlinePlus Health Information.
consumer health - Brain Tumors
.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Acta Neuropathol. 2006 May;111(5):465-74
[
16557391.001
]
[Cites]
Mol Cancer Res. 2008 Apr;6(4):576-84
[
18403636.001
]
[Cites]
Cancer Res. 2006 Sep 15;66(18):9074-82
[
16982749.001
]
[Cites]
Trends Genet. 2004 Feb;20(2):87-94
[
14746990.001
]
[Cites]
Nat Genet. 2004 Mar;36(3):299-303
[
14981516.001
]
[Cites]
Cancer Res. 2004 Sep 15;64(18):6503-10
[
15374961.001
]
[Cites]
Cancer Res. 2004 Oct 1;64(19):6892-9
[
15466178.001
]
[Cites]
Genes Chromosomes Cancer. 1997 Dec;20(4):399-407
[
9408757.001
]
[Cites]
Nat Genet. 1998 Oct;20(2):207-11
[
9771718.001
]
[Cites]
Int J Cancer. 1999 Nov 26;83(5):610-4
[
10521795.001
]
[Cites]
Insect Biochem Mol Biol. 1999 Oct;29(10):883-97
[
10528409.001
]
[Cites]
Brain Tumor Pathol. 2004;21(1):27-34
[
15696966.001
]
[Cites]
Cancer Res. 2005 Mar 1;65(5):1678-86
[
15753362.001
]
[Cites]
N Engl J Med. 2005 Mar 10;352(10):987-96
[
15758009.001
]
[Cites]
N Engl J Med. 2005 Mar 10;352(10):997-1003
[
15758010.001
]
[Cites]
Biostatistics. 2005 Apr;6(2):279-91
[
15772106.001
]
[Cites]
Clin Cancer Res. 2005 Apr 15;11(8):2907-18
[
15837741.001
]
[Cites]
Genes Chromosomes Cancer. 2005 Oct;44(2):161-9
[
15945096.001
]
[Cites]
N Engl J Med. 2005 Aug 25;353(8):811-22
[
16120861.001
]
[Cites]
Int J Cancer. 2006 Jan 1;118(1):55-61
[
16003758.001
]
[Cites]
N Engl J Med. 2005 Nov 10;353(19):2012-24
[
16282176.001
]
[Cites]
Int J Cancer. 2006 Feb 1;118(3):583-92
[
16106403.001
]
[Cites]
Nat Rev Cancer. 2006 Apr;6(4):307-20
[
16557282.001
]
[Cites]
Bioinformatics. 2006 Apr 15;22(8):1024-6
[
16455749.001
]
[Cites]
Cell Cycle. 2006 Apr;5(7):783-91
[
16582634.001
]
[Cites]
Cancer Res. 2006 Nov 15;66(22):10815-23
[
17090523.001
]
[Cites]
Cancer Res. 2006 Dec 1;66(23):11502-13
[
17114236.001
]
[Cites]
Cancer Res. 2006 Dec 1;66(23):11172-8
[
17145861.001
]
[Cites]
Acta Neuropathol. 2007 Mar;113(3):325-37
[
17265049.001
]
[Cites]
J Neuropathol Exp Neurol. 2007 May;66(5):405-17
[
17483698.001
]
[Cites]
Genes Chromosomes Cancer. 2007 Oct;46(10):875-94
[
17620294.001
]
[Cites]
Int J Cancer. 2007 Oct 15;121(8):1710-6
[
17597111.001
]
[Cites]
Int J Cancer. 2008 Feb 15;122(4):807-15
[
17960622.001
]
[Cites]
BMC Bioinformatics. 2007;8:426
[
17980028.001
]
[Cites]
Hum Mutat. 2008 Mar;29(3):398-408
[
18058796.001
]
[Cites]
Bioinformatics. 2008 Mar 15;24(6):751-8
[
18204059.001
]
[Cites]
Oncogene. 2008 Mar 27;27(14):2097-108
[
17934521.001
]
[Cites]
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):14888-93
[
10611308.001
]
[Cites]
Nat Genet. 2000 May;25(1):25-9
[
10802651.001
]
[Cites]
J Urol. 2001 Sep;166(3):1088-92
[
11490304.001
]
[Cites]
Nucleic Acids Res. 2002 Feb 15;30(4):e15
[
11842121.001
]
[Cites]
Gene. 2002 May 15;290(1-2):73-94
[
12062803.001
]
[Cites]
Genomics. 2002 Jul;80(1):21-30
[
12079279.001
]
[Cites]
Cancer. 2002 Jun 15;94(12):3210-8
[
12115353.001
]
[Cites]
Scand J Immunol. 2002 Sep;56(3):276-85
[
12193229.001
]
[Cites]
Hum Mol Genet. 2002 Dec 1;11(25):3221-9
[
12444106.001
]
[Cites]
Genes Chromosomes Cancer. 2003 Apr;36(4):361-74
[
12619160.001
]
[Cites]
Cancer Biol Ther. 2003 May-Jun;2(3):242-7
[
12878856.001
]
[Cites]
Cell. 2003 Oct 17;115(2):163-75
[
14567914.001
]
[Cites]
Curr Mol Med. 2003 Nov;3(7):589-96
[
14601634.001
]
[Cites]
Nat Rev Mol Cell Biol. 2004 Jan;5(1):45-54
[
14708009.001
]
[Cites]
Science. 2008 Sep 26;321(5897):1807-12
[
18772396.001
]
[Cites]
Nature. 2008 Oct 23;455(7216):1061-8
[
18772890.001
]
[Cites]
Trends Genet. 2006 Aug;22(8):447-55
[
16787682.001
]
(PMID = 19304958.001).
[ISSN]
1523-5866
[Journal-full-title]
Neuro-oncology
[ISO-abbreviation]
Neuro-oncology
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
United States
[Chemical-registry-number]
0 / RNA, Messenger
[Other-IDs]
NLM/ PMC2802400
10.
Ciesielski S, Cydzik-Kwiatkowska A, Pokoj T, Klimiuk E:
Molecular detection and diversity of medium-chain-length polyhydroxyalkanoates-producing bacteria enriched from activated sludge.
J Appl Microbiol
; 2006 Jul;101(1):190-9
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
AIMS: Knowledge of the species composition
of complex bacterial
communities is still very limited.
The results
of a
16S rDNA sequence analysis revealed that three strains belonged to Pseudomonas species and the fourth one was characterized as Comamonas testosteroni.
The results
of a
comparative phylogenetic analysis revealed that mcl-PHA-synthesizing bacteria can be divided into Pseudomonas fluorescens and Pseudomonas aeruginosa groups.
[MeSH-major]
Bacteria / genetics. DNA,
Bacterial
/ analysis. Ecosystem. Genetic Variation. Water Microbiology
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
METHANOL
.
SILVA.
SILVA SSU Database
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 16834606.001).
[ISSN]
1364-5072
[Journal-full-title]
Journal of applied microbiology
[ISO-abbreviation]
J. Appl. Microbiol.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / DNA, Bacterial; EC 2.3.- / Acyltransferases; EC 2.3.1.- / poly(3-hydroxyalkanoic acid) synthase; Y4S76JWI15 / Methanol
11.
Mömke S, Drögemüller C, Distl O:
A high-resolution radiation hybrid map of bovine chromosome 5q1.3-q2.5 compared with human chromosome 12q.
Anim Genet
; 2005 Jun;36(3):248-53
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
In this study we present a comprehensive 3000-rad radiation hybrid map on bovine chromosome 5 (BTA5)
of a
region between 12.8 and 74.0 cM according to the linkage map, which contains a quantitative trait loci for ovulation rate.
We mapped 28 gene-associated sequence tagged site markers derived from sequences of bovine
BAC
clones and 10 microsatellite markers to the BTA5 region.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 15932408.001).
[ISSN]
0268-9146
[Journal-full-title]
Animal genetics
[ISO-abbreviation]
Anim. Genet.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / DNA Primers
12.
Xia Z, Watanabe S, Chen Q, Sato S, Harada K:
A novel manual pooling system for preparing three-dimensional pools of a deep coverage soybean bacterial artificial chromosome library.
Mol Ecol Resour
; 2009 Mar;9(2):516-24
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
A novel manual pooling system for preparing three-dimensional pools
of a
deep coverage soybean
bacterial
artificial chromosome library.
It is time-consuming and labourious to prepare three-dimensional pools for a deep coverage
bacterial
artificial chromosome (
BAC
) library of soybean (1.12 × 10(9)  bp) in the absence of robotic facility.
In the present study, we describe a novel manual pooling system for preparing three-dimensional pools
of a
soybean
BAC
library.
This simple technique enables a single researcher to construct three-dimensional pools for a deep-coverage (12 haploid genome equivalents)
BAC
library of soybean in less than 2 months without any robotic manipulation.
This efficient pooling system could be applied to any other
BAC
libraries without the need for robotic manipulation.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
© 2009 The Authors. Journal compilation © 2009 Blackwell Publishing Ltd.
(PMID = 21564681.001).
[ISSN]
1755-098X
[Journal-full-title]
Molecular ecology resources
[ISO-abbreviation]
Mol Ecol Resour
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
13.
Hien NT, Ushijima H:
Frequency of prenatal care visits by ethnic minority mothers and association with infant birthweight in Bac Kan Province, Vietnam.
Trop Doct
; 2005 Apr;35(2):103-4
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Frequency of prenatal care visits by ethnic minority mothers and association with infant birthweight in
Bac
Kan Province, Vietnam.
The objective of this cross-sectional study was to evaluate the association between prenatal care visits and infant birthweight among ethnic minority mothers in the mountainous
Bac
Kan province.
The frequency of prenatal care visit are probably associated with a decreased risk of LBW among ethnic minority mothers in
Bac
Kan province.
MedlinePlus Health Information.
consumer health - Birth Weight
.
MedlinePlus Health Information.
consumer health - Prenatal Care
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 15970037.001).
[ISSN]
0049-4755
[Journal-full-title]
Tropical doctor
[ISO-abbreviation]
Trop Doct
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
14.
De Preter K, Menten B, De Brouwer S, Kumps C, Michels E, Van Roy N, Vandesompele J, Speleman F:
Low-cost dedicated mini-arrays for high-throughput analysis of DNA copy-number alterations in neuroblastoma.
Cancer Lett
; 2008 Sep 28;269(1):111-6
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
For this purpose, we have constructed a dedicated mini-array that is enriched for
BAC
/PAC clones in the prognostic important regions for neuroblastoma and that only covers a small area on the slide, allowing down-scaling of the labelling and hybridisation reagents and hence reducing the price.
Genetic Alliance.
consumer health - Neuroblastoma
.
MedlinePlus Health Information.
consumer health - Neuroblastoma
.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18555593.001).
[ISSN]
1872-7980
[Journal-full-title]
Cancer letters
[ISO-abbreviation]
Cancer Lett.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Ireland
15.
McMillan D, Miethke P, Alsop AE, Rens W, O'Brien P, Trifonov V, Veyrunes F, Schatzkamer K, Kremitzki CL, Graves T, Warren W, Grützner F, Ferguson-Smith MA, Graves JA:
Characterizing the chromosomes of the platypus (Ornithorhynchus anatinus).
Chromosome Res
; 2007;15(8):961-74
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Like the unique platypus itself, the platypus genome is extraordinary because of its
complex
sex chromosome system, and is controversial because of difficulties in identification of small autosomes and sex chromosomes.
We have established an agreed nomenclature and identified anchor
BAC
clones for each chromosome that will ensure unambiguous gene localizations.
[MeSH-minor]
Animals. Cells, Cultured. Chromosome Banding. Chromosome Mapping. Chromosome Painting. Chromosomes, Artificial,
Bacterial
. Female. Fibroblasts. Genome. In Situ Hybridization, Fluorescence. Karyotyping. Male. Metaphase
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Chromosoma. 1959;10(1):1-72
[
13629774.001
]
[Cites]
Nat Protoc. 2006;1(2):783-90
[
17406308.001
]
[Cites]
J Hered. 1988 Mar-Apr;79(2):115-8
[
3403957.001
]
[Cites]
Chromosome Res. 2007;15(6):777-85
[
17717721.001
]
[Cites]
Genomics. 2007 Jan;89(1):10-21
[
16962738.001
]
[Cites]
Genes Chromosomes Cancer. 1992 Apr;4(3):257-63
[
1382568.001
]
[Cites]
Curr Opin Genet Dev. 2004 Dec;14(6):642-9
[
15531159.001
]
[Cites]
Chromosoma. 1988;96(3):231-47
[
3359880.001
]
[Cites]
PLoS Genet. 2006 Oct;2(10 ):e182
[
17069464.001
]
[Cites]
Genome Biol. 2007;8(8):R175
[
17727704.001
]
[Cites]
Proc Natl Acad Sci U S A. 1990 Sep;87(18):7125-9
[
2402495.001
]
[Cites]
Proc Natl Acad Sci U S A. 2005 Mar 1;102(9):3354-9
[
15718282.001
]
[Cites]
Chromosome Res. 2005;13(6):627-36
[
16170627.001
]
[Cites]
In Vitro. 1984 Apr;20(4):321-8
[
6715011.001
]
[Cites]
Cytogenet Genome Res. 2002;98(1):96-100
[
12584449.001
]
[Cites]
Cytobios. 1973 Jul-Aug;7(28):233-43
[
4760570.001
]
[Cites]
BMC Evol Biol. 2007 Sep 06;7:157
[
17822525.001
]
[Cites]
Nature. 2004 Dec 16;432(7019):913-7
[
15502814.001
]
[Cites]
Cytogenet Genome Res. 2007;116(3):232-4
[
17317965.001
]
[Cites]
Chromosome Res. 2005;13(4):401-10
[
15973504.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Nov 16;101(46):16257-61
[
15534209.001
]
[Cites]
Genome Biol. 2005;6(5):218
[
15892878.001
]
[Cites]
Lancet. 1971 Oct 30;2(7731):971-2
[
4107917.001
]
[Cites]
Cell. 2006 Mar 10;124(5):901-14
[
16530039.001
]
[Cites]
Nature. 2007 Mar 29;446(7135):507-12
[
17392779.001
]
(PMID = 18185982.001).
[ISSN]
0967-3849
[Journal-full-title]
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
[ISO-abbreviation]
Chromosome Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Netherlands
16.
Kim Y, Kim HS, Cui ZY, Lee HS, Ahn JS, Park CK, Park K, Ahn MJ:
Clinicopathological implications of EpCAM expression in adenocarcinoma of the lung.
Anticancer Res
; 2009 May;29(5):1817-22
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Clinicopathological implications of EpCAM expression in
adenocarcinoma of the lung
.
BACKGROUND: The frequency of epithelial
cell
adhesion molecule (EpCAM) expression was investigated in non-small
cell lung cancer
(NSCLC) cells and human tissues, and its clinicopathological significance in
adenocarcinoma of the lung
was evaluated.
MATERIALS AND METHODS: EpCAM expression was analysed by reverse transcription-polymerase chain reaction (
RT
-PCR) and flow cytometry in human NSCLC cells.
EpCAM protein expression was evaluated in 234
adenocarcinoma
tissues using immunohistochemistry.
RESULTS: A high expression level of EpCAM was observed in human NSCLC cells by flow cytometry and
RT
-PCR.
EpCAM overexpression was detected in 120/234 (51.3%) surgically resected
adenocarcinoma
tissues.
EpCAM overexpression occurred significantly more frequently in
adenocarcinoma
than in
bronchioloalveolar carcinoma
(p=0.02).
CONCLUSION: These findings suggest EpCAM plays a role in the carcinogenesis
of adenocarcinoma
of the
lung
and might provide a promising molecule for targeted therapy in NSCLC.
[MeSH-major]
Adenocarcinoma
/ metabolism. Antigens, Neoplasm / metabolism.
Cell
Adhesion Molecules / metabolism.
Lung
Neoplasms / metabolism
[MeSH-minor]
Base Sequence.
Cell
Line, Tumor. DNA Primers. Flow Cytometry. Humans. Reverse Transcriptase Polymerase Chain Reaction
MedlinePlus Health Information.
consumer health - Lung Cancer
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19443410.001).
[ISSN]
0250-7005
[Journal-full-title]
Anticancer research
[ISO-abbreviation]
Anticancer Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Greece
[Chemical-registry-number]
0 / Antigens, Neoplasm; 0 / Cell Adhesion Molecules; 0 / DNA Primers; 0 / EPCAM protein, human
17.
Buffart TE, Carvalho B, Hopmans E, Brehm V, Kranenbarg EK, Schaaij-Visser TB, Eijk PP, van Grieken NC, Ylstra B, van de Velde CJ, Meijer GA:
Gastric cancers in young and elderly patients show different genomic profiles.
J Pathol
; 2007 Jan;211(1):45-51
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Although most gastric cancers occur in elderly patients, a substantial number of cases of this common
disease
occur in young patients.
Gastric
cancer
is a heterogeneous
disease
at the genomic level and different patterns of DNA copy number alterations are associated with different clinical behaviour.
The aim of the present study was to explore differences in DNA copy number alterations in relation to age of onset of gastric
cancer
.
DNA isolated from 46 paraffin-embedded gastric
cancer
tissue samples from 17 patients less than 50 years of age [median 43 (21-49) years] and 29 patients greater than or equal to 70 years of age [median 75 (70-83) years] was analysed by genome-wide microarray comparative genomic hybridization (array CGH) using an array of 5000
BAC
clones.
Gastric cancers of young and old patients belong to groups with different genomic profiles, which likely reflect different pathogenic mechanisms of the
disease
.
[MeSH-major]
Carcinoma
/ genetics. Gene Expression Profiling. Genes, Neoplasm. Oligonucleotide Array Sequence Analysis. Stomach Neoplasms / genetics
MedlinePlus Health Information.
consumer health - Stomach Cancer
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
Copyright (c) 2006 Pathological Society of Great Britain and Ireland.
(PMID = 17117405.001).
[ISSN]
0022-3417
[Journal-full-title]
The Journal of pathology
[ISO-abbreviation]
J. Pathol.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
18.
Stipcevic T, Piljac A, Piljac G:
Enhanced healing of full-thickness burn wounds using di-rhamnolipid.
Burns
; 2006 Feb;32(1):24-34
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The aim of this study was to investigate the properties of di-rhamnolipid [alpha-L-rhamnopyranosyl-(1-2)-alpha-L-rhamnopyranosyl-3-hydroxydecanoyl-3-hydroxydecanoic acid, also referred to as di-rhamnolipid
BAC
-3] relating to the process of cutaneous wound healing.
MedlinePlus Health Information.
consumer health - Burns
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Harefuah. 2002 Nov;141(11):973-8, 1009
[
12476633.001
]
[Cites]
J Dermatol Sci. 2005 Nov;40(2):141-3
[
16199139.001
]
[Cites]
Cell. 1975 Nov;6(3):331-43
[
1052771.001
]
[Cites]
Infect Immun. 1980 Sep;29(3):1028-33
[
6776058.001
]
[Cites]
J Dermatol Surg Oncol. 1985 Jun;11(6):617-22
[
3891806.001
]
[Cites]
J Histochem Cytochem. 1985 Aug;33(8):845-53
[
3894502.001
]
[Cites]
Am J Ophthalmol. 1987 Jun 15;103(6):802-7
[
3496008.001
]
[Cites]
Am Fam Physician. 1992 Mar;45(3):1321-30
[
1543113.001
]
[Cites]
Ann Surg. 1994 Jun;219(6):688-91; discussion 691-2
[
8203978.001
]
[Cites]
Adv Dermatol. 1995;10:77-96; discussion 97
[
7794680.001
]
[Cites]
Br J Plast Surg. 1995 Jun;48(4):189-97
[
7640850.001
]
[Cites]
Science. 1997 Apr 4;276(5309):75-81
[
9082989.001
]
[Cites]
Undersea Hyperb Med. 1997 Sep;24(3):175-9
[
9308140.001
]
[Cites]
Dermatol Surg. 1998 Jun;24(6):661-4
[
9648574.001
]
[Cites]
Ann R Coll Surg Engl. 1998 May;80(3):215-20
[
9682649.001
]
[Cites]
Arch Dermatol Res. 1998 Jul;290 Suppl:S1-11
[
9710378.001
]
[Cites]
J Trauma. 1968 Nov;8(6):1049-51
[
5722120.001
]
(PMID = 16380213.001).
[ISSN]
0305-4179
[Journal-full-title]
Burns : journal of the International Society for Burn Injuries
[ISO-abbreviation]
Burns
[Language]
ENG
[Grant]
United States / NIAMS NIH HHS / AR / A1 R43 AR44443-01A1; United States / NIAMS NIH HHS / AR / R43 AR044443-01A1
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
Netherlands
[Chemical-registry-number]
0 / Glycolipids; 0 / Ointments; 0 / rhamnolipid
[Other-IDs]
NLM/ NIHMS8983; NLM/ PMC1586221
19.
Goidts V, Szamalek JM, de Jong PJ, Cooper DN, Chuzhanova N, Hameister H, Kehrer-Sawatzki H:
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16.
Genome Res
; 2005 Sep;15(9):1232-42
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The p
- and q-arm breakpoints of the inversions in PTR XVI and GGO XVI were found to occur at slightly different locations, consistent with their independent origin.
Further, FISH studies of the homologous chromosomal regions in macaque and orangutan revealed that the region represented by HSA
BAC
RP11-696P19, which spans the inversion breakpoint on HSA 16q11-12, was derived from the ancestral primate chromosome homologous to HSA 1.
[MeSH-minor]
Animals. Base Sequence. Biological Evolution.
Cell
Line. Chromosome Breakage. Chromosomes, Artificial,
Bacterial
/ genetics. DNA / genetics. Humans. In Situ Hybridization, Fluorescence. Models, Genetic. Molecular Sequence Data. Species Specificity
Genetic Alliance.
consumer health - Chromosome 16
.
COS Scholar Universe.
author profiles
.
Coriell Cell Repositories.
culture/stock collections - Coriell Cell Repositories
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Genome Res. 2001 Jul;11(7):1205-10
[
11435402.001
]
[Cites]
Genome Res. 1998 Aug;8(8):758-62
[
9724321.001
]
[Cites]
Hum Mol Genet. 2001 Oct 1;10(20):2215-23
[
11673404.001
]
[Cites]
Cancer Genet Cytogenet. 2001 Nov;131(1):65-8
[
11734321.001
]
[Cites]
Am J Hum Genet. 2002 Jan;70(1):269-78
[
11731935.001
]
[Cites]
Oncogene. 2002 Jan 17;21(3):368-76
[
11821949.001
]
[Cites]
Nat Rev Genet. 2002 Jan;3(1):65-72
[
11823792.001
]
[Cites]
Science. 2002 Apr 12;296(5566):340-3
[
11951044.001
]
[Cites]
Am J Hum Genet. 2002 Aug;71(2):375-88
[
12094327.001
]
[Cites]
Genetics. 1998 Oct;150(2):807-14
[
9755210.001
]
[Cites]
Cytogenet Cell Genet. 1998;82(1-2):71-4
[
9763663.001
]
[Cites]
Cancer Genet Cytogenet. 1999 Aug;113(1):25-8
[
10459342.001
]
[Cites]
Genome Res. 2004 Nov;14(11):2209-20
[
15520286.001
]
[Cites]
J Biol Chem. 2004 Nov 12;279(46):47411-4
[
15326170.001
]
[Cites]
Cytogenet Genome Res. 2005;108(1-3):83-90
[
15545719.001
]
[Cites]
Cytogenet Genome Res. 2005;108(1-3):91-7
[
15545720.001
]
[Cites]
Mol Biol Evol. 2005 Feb;22(2):297-307
[
15483319.001
]
[Cites]
Hum Mutat. 2005 Jan;25(1):45-55
[
15580561.001
]
[Cites]
Nature. 2004 Dec 23;432(7020):988-94
[
15616553.001
]
[Cites]
Genome Res. 2000 May;10(5):597-610
[
10810082.001
]
[Cites]
Hum Mol Genet. 2000 Jan 1;9(1):113-23
[
10587586.001
]
[Cites]
Genome Res. 1999 Dec;9(12):1184-8
[
10613840.001
]
[Cites]
Genome Res. 2000 Mar;10(3):319-29
[
10720573.001
]
[Cites]
Genomics. 2002 Oct;80(4):395-401
[
12376093.001
]
[Cites]
Genome Res. 2002 Nov;12(11):1651-62
[
12421751.001
]
[Cites]
Cytogenet Genome Res. 2002;97(1-2):20-7
[
12438733.001
]
[Cites]
Genome Res. 2003 Jul;13(7):1619-30
[
12840040.001
]
[Cites]
Genetica. 2003 Jul;118(2-3):193-208
[
12868609.001
]
[Cites]
Chromosome Res. 2003;11(4):323-6
[
12906128.001
]
[Cites]
Genome Biol. 2003;4(8):R50
[
12914658.001
]
[Cites]
Hum Mol Genet. 2003 Sep 1;12(17):2201-8
[
12915466.001
]
[Cites]
Bioessays. 2003 Sep;25(9):825-8
[
12938170.001
]
[Cites]
Proc Natl Acad Sci U S A. 2003 Oct 28;100(22):13030-5
[
14557539.001
]
[Cites]
Mol Biol Evol. 2000 Jul;17(7):1081-90
[
10889221.001
]
[Cites]
Am J Hum Genet. 2001 Feb;68(2):444-56
[
11170892.001
]
[Cites]
Trends Genet. 2001 Jun;17(6):299-301
[
11377777.001
]
[Cites]
Curr Opin Genet Dev. 2003 Dec;13(6):629-35
[
14638326.001
]
[Cites]
Nat Rev Genet. 2004 Feb;5(2):114-22
[
14735122.001
]
[Cites]
Genomics. 2004 Mar;83(3):493-501
[
14962675.001
]
[Cites]
Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R57-64
[
14764619.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):2957-62
[
14976249.001
]
[Cites]
Genome Biol. 2004;5(4):R23
[
15059256.001
]
[Cites]
Genome Res. 2004 May;14(5):845-51
[
15123584.001
]
[Cites]
Hum Genet. 2004 Jul;115(2):116-22
[
15133654.001
]
[Cites]
Genomics. 2004 Oct;84(4):757-61
[
15475253.001
]
[Cites]
Trends Genet. 2004 Nov;20(11):524-9
[
15475109.001
]
[Cites]
Nature. 2004 Oct 21;431(7011):927-30
[
15496912.001
]
[Cites]
Cytogenet Cell Genet. 1979;23(1-2):77-83
[
83931.001
]
[Cites]
Science. 1982 Mar 19;215(4539):1525-30
[
7063861.001
]
[Cites]
Genes Chromosomes Cancer. 1994 Dec;11(4):256-62
[
7533529.001
]
[Cites]
Hum Mol Genet. 1996 Jul;5(7):899-912
[
8817324.001
]
[Cites]
Hum Mol Genet. 1997 Jul;6(7):991-1002
[
9215666.001
]
[Cites]
Clin Cancer Res. 1998 Jul;4(7):1779-84
[
9676855.001
]
[Cites]
Genomics. 1998 Jun 15;50(3):368-72
[
9676431.001
]
[Cites]
Nature. 2001 Oct 4;413(6855):514-9
[
11586358.001
]
(PMID = 16140991.001).
[ISSN]
1088-9051
[Journal-full-title]
Genome research
[ISO-abbreviation]
Genome Res.
[Language]
eng
[Databank-accession-numbers]
GENBANK/ AY822675/ AY822676/ AY822677
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
9007-49-2 / DNA
[Other-IDs]
NLM/ PMC1199537
20.
Braun RJ, Kinkl N, Zischka H, Ueffing M:
16-BAC/SDS-PAGE analysis of membrane proteins of yeast mitochondria purified by free flow electrophoresis.
Methods Mol Biol
; 2009;528:83-107
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
16-
BAC
/SDS-PAGE analysis of membrane proteins of yeast mitochondria purified by free flow electrophoresis.
Especially the inner membrane comprises a high content of proteins, for example, the protein
complexes of
the respiratory chain.
High-resolution separation and analysis of such membrane proteins, for example, by two-dimensional gel electrophoresis (2-
DE
), is hampered by their hydrophobicity and tendency for aggregation.
Here, we describe the separation of mitochondrial membrane proteins of Saccharomyces cerevisiae by 16-benzyldimethyl-n-hexadecylammonium chloride/sodium dodecyl sulfate polyacrylamide gel electrophoresis (16-
BAC
/SDS-PAGE).
This method enables the separation of membrane proteins owing to the solubilizing power of the ionic detergents 16-
BAC
and SDS, respectively.
Subsequently, membrane proteins from ZE-FFE-purified mitochondria were enriched by carbonate extraction and subjected to 16-
BAC
/SDS-PAGE.
Hazardous Substances Data Bank.
SODIUM LAURYL SULFATE
.
Hazardous Substances Data Bank.
SODIUM CARBONATE
.
Saccharomyces Genome Database.
Saccharomyces Genome Database
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19153686.001).
[ISSN]
1064-3745
[Journal-full-title]
Methods in molecular biology (Clifton, N.J.)
[ISO-abbreviation]
Methods Mol. Biol.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / Carbonates; 0 / Fatty Alcohols; 0 / Fluorescent Dyes; 0 / Membrane Proteins; 0 / Quaternary Ammonium Compounds; 0 / Saccharomyces cerevisiae Proteins; 368GB5141J / Sodium Dodecyl Sulfate; 45P3261C7T / sodium carbonate; 7UI0TKC3U5 / Ruthenium; 85474O1N9D / cetalkonium chloride
21.
Xiong Z, Kim JS, Pires JC:
Integration of genetic, physical, and cytogenetic maps for Brassica rapa chromosome A7.
Cytogenet Genome Res
; 2010 Jul;129(1-3):190-8
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Bacterial
artificial chromosome (
BAC
) contigs have been genetically mapped to the 10 linkage groups of Brassica rapa by
BAC
end sequences (BES).
To integrate the genetic, physical, and cytogenetic maps, fluorescence in situ hybridization (FISH) was used to anchor the assembly
of BAC
contigs onto Brassica chromosomes using representative
BACs
.
This
BAC
-FISH approach can be used to identify chromosome arms on separate mitotic metaphase chromosomes or to map multiple
BACs
to single long pachytene chromosomes.
As part of an international consortium that is sequencing the B. rapa genome, we integrated the linkage and physical maps with the B. rapa cytogenetic map for chromosome A7 by hybridizing
BACs
to mitotic chromosomes and along the length of pachytene chromosome spreads.
A total of 31
BACs
that were putatively located on A7 were used as probes for FISH analyses; however, only 19
BACs
mapped unambiguously to A7 while the remaining
BACs
either mapped to other chromosomes or hybridized to multiple locations.
We then created a multicolor FISH cocktail of 16
BAC
probes to simultaneously hybridize the entire length of the A7 chromosome.
We successfully applied the 16 A7
BAC
probe mix to B. rapa, B. oleracea, and domesticated and resynthesized genotypes of B. napus to demonstrate that this approach can facilitate studies of genome evolution by integrating the genetic, physical, and cytogenetic maps among closely related species of Brassica.
[MeSH-minor]
Chromosome Mapping. Chromosomes, Artificial,
Bacterial
/ genetics. Contig Mapping. Genetic Markers. In Situ Hybridization, Fluorescence. Physical Chromosome Mapping
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
Copyright 2010 S. Karger AG, Basel.
(PMID = 20628251.001).
[ISSN]
1424-859X
[Journal-full-title]
Cytogenetic and genome research
[ISO-abbreviation]
Cytogenet. Genome Res.
[Language]
eng
[Publication-type]
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
Switzerland
[Chemical-registry-number]
0 / Genetic Markers
22.
Kriegova E, Arakelyan A, Fillerova R, Zatloukal J, Mrazek F, Navratilova Z, Kolek V, du Bois RM, Petrek M:
PSMB2 and RPL32 are suitable denominators to normalize gene expression profiles in bronchoalveolar cells.
BMC Mol Biol
; 2008;9:69
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
PSMB2 and RPL32 are suitable denominators to normalize gene expression profiles in
bronchoalveolar
cells.
To date, no reference genes have been validated for expression studies
of bronchoalveolar
(BAL) cells.
The aims of this study were to identify gene(s) with stable mRNA expression in BAL cells irrespective of gender, smoking, BAL cellular composition,
lung
pathology, treatment; and to assess the influence of reference genes on target gene expression data.
RESULTS: The mRNA expression of ten housekeeping genes (ACTB, ARF1, CANX, G6PD, GAPDH, GPS1, GNB2L1, PSMB2, PSMD2, RPL32) was investigated by qRT-PCR in BAL cells from 71 subjects across a spectrum
of lung
diseases.
CONCLUSION: PSMB2 and RPL32 are, therefore, suitable reference genes to normalize qRT-PCR in BAL cells in sarcoidosis, and other interstitial
lung disease
.
[MeSH-minor]
Adolescent. Adult. Animals. Case-Control Studies. Female. Humans.
Lung
Diseases / genetics. Male. Middle Aged. RNA, Messenger / analysis. Reference Standards. Reverse Transcriptase Polymerase Chain Reaction / standards. Smoking / genetics
MedlinePlus Health Information.
consumer health - Sarcoidosis
.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Eur Respir J. 2006 Feb;27(2):300-6
[
16452584.001
]
[Cites]
J Clin Pathol. 2006 Jan;59(1):28-39
[
16394278.001
]
[Cites]
J Urol. 2006 May;175(5):1915-20
[
16600798.001
]
[Cites]
Am J Physiol Gastrointest Liver Physiol. 2006 May;290(5):G1067-74
[
16399877.001
]
[Cites]
Am J Respir Cell Mol Biol. 2006 Jul;35(1):48-54
[
16484684.001
]
[Cites]
BMC Mol Biol. 2006;7:33
[
17026756.001
]
[Cites]
Vet Immunol Immunopathol. 2007 Jan 15;115(1-2):160-5
[
17074403.001
]
[Cites]
Proc Am Thorac Soc. 2007 Jan;4(1):85-91
[
17202296.001
]
[Cites]
BMC Cancer. 2008;8:20
[
18211679.001
]
[Cites]
BMC Mol Biol. 2008;9:17
[
18226276.001
]
[Cites]
BMC Mol Biol. 2008;9:46
[
18460208.001
]
[Cites]
Biotechniques. 2000 Aug;29(2):332-7
[
10948434.001
]
[Cites]
Sarcoidosis Vasc Diffuse Lung Dis. 2000 Jun;17(2):151-7
[
10957763.001
]
[Cites]
Physiol Genomics. 2000 Apr 27;2(3):143-7
[
11015593.001
]
[Cites]
Am J Respir Crit Care Med. 2001 Jul 15;164(2):265-72
[
11463599.001
]
[Cites]
Physiol Genomics. 2001 Dec 21;7(2):97-104
[
11773596.001
]
[Cites]
Pancreatology. 2002;2(4):421-4
[
12138232.001
]
[Cites]
Genome Biol. 2002 Jun 18;3(7):RESEARCH0034
[
12184808.001
]
[Cites]
Thorax. 2002 Sep;57(9):754-6
[
12200516.001
]
[Cites]
Thorax. 2002 Sep;57(9):765-70
[
12200519.001
]
[Cites]
Nucleic Acids Res. 2001 May 1;29(9):e45
[
11328886.001
]
[Cites]
Eur Respir J. 2002 Nov;20(5):1206-12
[
12449175.001
]
[Cites]
Pediatr Pulmonol. 2004 May;37(5):393-9
[
15095321.001
]
[Cites]
Biotechnol Lett. 2004 Mar;26(6):509-15
[
15127793.001
]
[Cites]
Biotechniques. 2004 Jul;37(1):112-4, 116, 118-9
[
15283208.001
]
[Cites]
Cancer Res. 2004 Aug 1;64(15):5245-50
[
15289330.001
]
[Cites]
J Biomol Tech. 2004 Sep;15(3):155-66
[
15331581.001
]
[Cites]
J Clin Invest. 1985 May;75(5):1488-95
[
3923038.001
]
[Cites]
Am J Physiol. 1993 Mar;264(3 Pt 1):L199-212
[
7681631.001
]
[Cites]
Cas Lek Cesk. 1993 Jun 14;132(12):365-8
[
8343944.001
]
[Cites]
Biotechniques. 1999 Jan;26(1):112-22, 124-5
[
9894600.001
]
[Cites]
Methods Mol Biol. 1998;110:43-61
[
9918038.001
]
[Cites]
Anal Biochem. 2004 Dec 1;335(1):1-9
[
15519565.001
]
[Cites]
Clin Chest Med. 2004 Dec;25(4):637-49, v
[
15564013.001
]
[Cites]
Lab Invest. 2005 Jan;85(1):154-9
[
15543203.001
]
[Cites]
Am J Respir Crit Care Med. 2005 Feb 15;171(4):361-70
[
15579727.001
]
[Cites]
BMC Mol Biol. 2005;6:4
[
15720708.001
]
[Cites]
Obes Res. 2005 Apr;13(4):649-52
[
15897472.001
]
[Cites]
Genes Immun. 2005 Jun;6(4):279-84
[
15815687.001
]
[Cites]
Biotechniques. 2005 May;38(5):785-92
[
15945375.001
]
[Cites]
J Mol Endocrinol. 2005 Jun;34(3):597-601
[
15956331.001
]
[Cites]
Biotechniques. 2005 Jul;39(1):75-85
[
16060372.001
]
[Cites]
Clin Sci (Lond). 2005 Oct;109(4):365-79
[
16171460.001
]
[Cites]
Lab Invest. 2005 Aug;85(8):1040-50
[
15951835.001
]
[Cites]
Eur Respir J. 2005 Dec;26(6):1002-8
[
16319328.001
]
[Cites]
Mol Aspects Med. 2006 Apr-Jun;27(2-3):126-39
[
16469371.001
]
(PMID = 18671841.001).
[ISSN]
1471-2199
[Journal-full-title]
BMC molecular biology
[ISO-abbreviation]
BMC Mol. Biol.
[Language]
eng
[Publication-type]
Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / RNA, Messenger
[Other-IDs]
NLM/ PMC2529339
23.
Zhang J, Liang ZY, Zeng X, Wu SF, Gao J, Liu TH:
[Detection of epidermal growth factor receptor gene mutations in non-small cell lung cancers by real-time polymerase chain reaction using scorpion amplification refractory mutation system].
Zhonghua Bing Li Xue Za Zhi
; 2008 May;37(5):294-9
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
[Detection of epidermal growth factor receptor gene mutations in non-small
cell lung
cancers by real-time polymerase chain reaction using scorpion amplification refractory mutation system].
OBJECTIVE: To investigate mutations of EGFR gene in non-small
cell lung
cancers (NSCLC) using scorpions amplification refractory mutation system (Scorpions ARMS) is in comparing the detection sensitivity with that by PCR-direct sequencing method, and in addition to study the correlation between the mutations and the clinicopathological characteristics of the patients.
METHODS: Tumor cells were collected by microdissection from paraffin embedded tumor specimens and adjacent normal
lung
tissues of 82 NSCLC patients.
Mutations were more common in female, non-smoking patients with
adenocarcinoma
and
bronchioloalveolar carcinoma
histology.
[MeSH-major]
Carcinoma
, Non-Small-
Cell Lung
/ genetics. Codon / genetics. Exons / genetics. Genes, erbB-1 / genetics.
Lung
Neoplasms / genetics. Receptor, Epidermal Growth Factor / genetics. Scorpion Venoms / chemistry
[MeSH-minor]
Adenocarcinoma
/ genetics. Female. Gene Amplification. Humans. Mutation. Point Mutation. Polymerase Chain Reaction / methods. Sensitivity and Specificity. Sequence Deletion
MedlinePlus Health Information.
consumer health - Lung Cancer
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18956645.001).
[ISSN]
0529-5807
[Journal-full-title]
Zhonghua bing li xue za zhi = Chinese journal of pathology
[ISO-abbreviation]
Zhonghua Bing Li Xue Za Zhi
[Language]
chi
[Publication-type]
English Abstract; Journal Article
[Publication-country]
China
[Chemical-registry-number]
0 / Codon; 0 / Scorpion Venoms; EC 2.7.10.1 / Receptor, Epidermal Growth Factor
24.
Shahin H, Gopinath SP, Robertson CS:
Influence of alcohol on early Glasgow Coma Scale in head-injured patients.
J Trauma
; 2010 Nov;69(5):1176-81; discussion 1181
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The remaining 188 patients were further divided into an intoxicated group (blood alcohol concentration [
BAC
] ≥ 0.08%, n = 100 [53%]) and a nonintoxicated group (
BAC
<0.08%, n = 88 [47%]).
To assess whether these results were directly related to
the BAC
%, piecewise regression using a general linear model was used to assess the intercept and slope of alcohol on the changes of GCS with cutting point at
BAC
% = 0.08.
But in the intoxicated range,
BAC
% was significantly positively related to the changes of GCS.
MedlinePlus Health Information.
consumer health - Head Injuries
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
J Int Neuropsychol Soc. 2004 Oct;10(6):807-17
[
15637771.001
]
[Cites]
Arch Surg. 2006 Dec;141(12):1185-91; discussion 1192
[
17178960.001
]
[Cites]
Ann Surg. 2007 Apr;245(4):651-5
[
17414616.001
]
[Cites]
J Trauma. 2007 Aug;63(2):365-9
[
17693837.001
]
[Cites]
Br J Surg. 1976 Feb;63(2):128-30
[
1252711.001
]
[Cites]
Acta Neurochir (Wien). 1976;34(1-4):45-55
[
961490.001
]
[Cites]
J Neurosurg. 1977 Mar;46(3):328-35
[
839257.001
]
[Cites]
Lancet. 1977 Apr 23;1(8017):878-81
[
67287.001
]
[Cites]
Acta Neurol Scand. 1977 Jul;56(1):7-16
[
560096.001
]
[Cites]
Alcohol Clin Exp Res. 1993 Feb;17(1):54-60
[
8383926.001
]
[Cites]
Brain Res. 1993 Oct 8;624(1-2):94-102
[
8252419.001
]
[Cites]
J Neurotrauma. 1992 Mar;9 Suppl 1:S173-87
[
1350312.001
]
[Cites]
J Trauma. 1992 Jan;32(1):60-4
[
1732576.001
]
[Cites]
J Cereb Blood Flow Metab. 1992 Jan;12(1):12-24
[
1345756.001
]
[Cites]
Acta Neurochir Suppl (Wien). 1990;51:277-9
[
1982482.001
]
[Cites]
J Neurotrauma. 1990 Fall;7(3):131-9
[
2258944.001
]
[Cites]
N Engl J Med. 1990 Aug 16;323(7):455-61
[
2197554.001
]
[Cites]
Neuropharmacology. 2000 Jan 28;39(3):515-22
[
10698017.001
]
[Cites]
J Emerg Med. 2000 Jul;19(1):67-71
[
10863122.001
]
[Cites]
J Stud Alcohol. 2002 May;63(3):380-3
[
12086139.001
]
[Cites]
Stroke. 2003 May;34(5):1242-5
[
12690224.001
]
[Cites]
Neurol Res. 2004 Jan;26(1):108-12
[
14977068.001
]
[Cites]
Emerg Med J. 2004 Mar;21(2):185-8
[
14988344.001
]
[Cites]
Am J Med. 1974 Jan;56(1):22-33
[
4358587.001
]
[Cites]
Lancet. 1974 Jul 13;2(7872):81-4
[
4136544.001
]
[Cites]
Br Med J. 1980 Sep 6;281(6241):638-40
[
7437745.001
]
[Cites]
J Trauma. 1981 Feb;21(2):124-9
[
7206001.001
]
[Cites]
Neurosurgery. 1981 Mar;8(3):301-8
[
7242878.001
]
[Cites]
N Engl J Med. 1982 Apr 8;306(14):852-4
[
7062964.001
]
[Cites]
Am J Surg. 1982 Jul;144(1):153-7
[
7091524.001
]
[Cites]
Science. 1983 Apr 15;220(4594):331-3
[
6836278.001
]
[Cites]
J Trauma. 1983 Jun;23(6):494-8
[
6864840.001
]
[Cites]
Haemostasis. 1984;14(2):223-8
[
6735279.001
]
[Cites]
Neurosurgery. 1984 Sep;15(3):303-6
[
6483144.001
]
[Cites]
Crit Care Med. 1986 Oct;14(10):841-6
[
3757524.001
]
[Cites]
Injury. 1986 May;17(3):150-3
[
3818050.001
]
[Cites]
Metabolism. 1987 Jun;36(6):538-43
[
2884551.001
]
[Cites]
J Trauma. 1989 Dec;29(12):1647-53
[
2593195.001
]
[Cites]
J Neurotrauma. 2004 Nov;21(11):1573-83
[
15684650.001
]
[Cites]
J Trauma. 2006 Dec;61(6):1305-11
[
17159670.001
]
[Cites]
Neurosurgery. 1998 Dec;43(6):1369-72; discussion 1372-4
[
9848851.001
]
[Cites]
Pharmacol Biochem Behav. 1998 Apr;59(4):981-91
[
9586859.001
]
[Cites]
J Neurotrauma. 1998 Feb;15(2):105-15
[
9512086.001
]
[Cites]
Brain Inj. 1997 Jun;11(6):391-402
[
9171925.001
]
[Cites]
J Neurosurg. 1997 May;86(5):876-82
[
9126906.001
]
[Cites]
J Neurosurg Anesthesiol. 1997 Apr;9(2):118-27
[
9100180.001
]
[Cites]
Stroke. 1994 Aug;25(8):1637-43
[
8042217.001
]
[Cites]
J Neurosurg. 1995 May;82(5):813-21
[
7714607.001
]
[Cites]
Injury. 1995 Jun;26(5):311-4
[
7649645.001
]
[Cites]
J Neurotrauma. 1995 Oct;12(5):883-90
[
8594215.001
]
[Cites]
Psychosomatics. 1996 May-Jun;37(3):285-8
[
8849505.001
]
(PMID = 21068620.001).
[ISSN]
1529-8809
[Journal-full-title]
The Journal of trauma
[ISO-abbreviation]
J Trauma
[Language]
ENG
[Grant]
United States / NINDS NIH HHS / NS / P01 NS038660; United States / NINDS NIH HHS / NS / P01 NS038660-10S1; United States / NINDS NIH HHS / NS / P01-NS38660
[Publication-type]
Comparative Study; Journal Article; Research Support, N.I.H., Extramural
[Publication-country]
United States
[Other-IDs]
NLM/ NIHMS366060; NLM/ PMC3485579
25.
Stuster J:
Validation of the standardized field sobriety test battery at 0.08% blood alcohol concentration.
Hum Factors
; 2006;48(3):608-14
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
OBJECTIVE: A field study was conducted to evaluate the accuracy of the Standardized Field Sobriety Test (SFST) battery to assist officers in making arrest decisions at blood alcohol concentrations (
BACs
) below 0.10%.
BACKGROUND: The SFST Battery was validated at 0.10%
BAC
in 1981, but since then many states have reduced statutory limits for driving while intoxicated to 0.08%
BAC
.
RESULTS: Overall, officers' decisions were correct in more than 91% of the cases at the 0.08%
BAC
level.
CONCLUSION: The results of this study provide evidence of the validity of the SFST Battery as an accurate and reliable decision aid for discriminating between
BACs
above and below 0.08%.
[MeSH-major]
Alcoholic Intoxication /
diagnosis
. Automobile Driving. Police
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17063973.001).
[ISSN]
0018-7208
[Journal-full-title]
Human factors
[ISO-abbreviation]
Hum Factors
[Language]
eng
[Publication-type]
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Validation Studies
[Publication-country]
United States
26.
Hajirasouliha I, Hormozdiari F, Sahinalp SC, Birol I:
Optimal pooling for genome re-sequencing with ultra-high-throughput short-read technologies.
Bioinformatics
; 2008 Jul 1;24(13):i32-40
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
In this article, we focus on re-sequencing experiments using the Solexa technology, based on
bacterial
artificial chromosome (
BAC
) clones, and address an experimental design problem.
In these specific experiments, approximate coordinates of the
BACs
on a reference genome are known, and fine-scale differences between
the BAC
sequences and the reference are of interest.
The high-throughput characteristics of the sequencing technology makes it possible to multiplex
BAC
sequencing experiments by pooling
BACs
for a cost-effective operation.
However, the way
BACs
are pooled in such re-sequencing experiments has an effect on the downstream analysis of the generated data, mostly due to subsequences common to multiple
BACs
.
[MeSH-major]
Algorithms. Chromosome Mapping / methods. Chromosomes, Artificial,
Bacterial
/ genetics. Sequence Alignment / methods. Sequence Analysis, DNA / methods
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9748-53
[
11504945.001
]
[Cites]
Pharmacogenomics. 2004 Jun;5(4):433-8
[
15165179.001
]
[Cites]
Bioinformatics. 2004 Sep 1;20(13):2067-74
[
15059830.001
]
[Cites]
Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7
[
271968.001
]
[Cites]
J Mol Biol. 1980 Oct 25;143(2):161-78
[
6260957.001
]
[Cites]
J Mol Biol. 1982 Dec 25;162(4):729-73
[
6221115.001
]
[Cites]
Curr Protoc Hum Genet. 2007 Apr;Chapter 5:Unit 5.19
[
18428413.001
]
[Cites]
Nature. 2005 Sep 15;437(7057):376-80
[
16056220.001
]
[Cites]
Bioinformatics. 2007 Feb 15;23(4):500-1
[
17158514.001
]
[Cites]
PLoS One. 2007;2(5):e484
[
17534434.001
]
[Cites]
Genome Res. 2008 Feb;18(2):324-30
[
18083777.001
]
[Cites]
Genome Biol. 2007;8(10):R224
[
17953769.001
]
[Cites]
Genomics. 1995 Mar 20;26(2):345-53
[
7601461.001
]
(PMID = 18586730.001).
[ISSN]
1367-4811
[Journal-full-title]
Bioinformatics (Oxford, England)
[ISO-abbreviation]
Bioinformatics
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
[Other-IDs]
NLM/ PMC2718651
27.
Kramer ML:
A new multiphasic buffer system for benzyldimethyl-n-hexadecylammonium chloride polyacrylamide gel electrophoresis of proteins providing efficient stacking.
Electrophoresis
; 2006 Feb;27(2):347-56
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Acidic PAGE systems using cationic detergents such as benzyldimethyl-n-hexadecylammonium chloride (16-
BAC
) or CTAB have proven useful for the detection of methoxy esters sensitive to alkaline pH, resolving basic proteins such as histones and membrane proteins.
Therefore, a new 16-
BAC
PAGE system based on the theory of moving boundary electrophoresis with properties comparable to the classical SDS-PAGE system was designed.
As a result a new multiphasic analytical 16-
BAC
PAGE system providing efficient stacking and significantly shorter running times is presented here.
Furthermore, the concentration of 16-
BAC
was optimized by determining its previously unknown CMC.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 16331586.001).
[ISSN]
0173-0835
[Journal-full-title]
Electrophoresis
[ISO-abbreviation]
Electrophoresis
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Germany
[Chemical-registry-number]
0 / Buffers; 0 / Coloring Agents; 0 / Detergents; 0 / Fatty Alcohols; 0 / Proteins; 0 / Quaternary Ammonium Compounds; 0 / alpha-Synuclein; 85474O1N9D / cetalkonium chloride
28.
Gunn SR, Bolla AR, Barron LL, Gorre ME, Mohammed MS, Bahler DW, Mellink CH, van Oers MH, Keating MJ, Ferrajoli A, Coombes KR, Abruzzo LV, Robetorye RS:
Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene.
Leuk Res
; 2009 Sep;33(9):1276-81
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
We used
BAC
array-based CGH to detect genomic imbalances in 187 CLL cases.
[MeSH-major]
Alleles. Antigens, Neoplasm / genetics. Chromosome Deletion. Chromosomes, Human, Pair 22. Leukemia, Lymphocytic, Chronic, B-
Cell
/ genetics. Nucleic Acid Hybridization
Genetic Alliance.
consumer health - Chronic Lymphocytic Leukemia
.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19027161.001).
[ISSN]
1873-5835
[Journal-full-title]
Leukemia research
[ISO-abbreviation]
Leuk. Res.
[Language]
eng
[Grant]
United States / NCI NIH HHS / CA / P30 CA016672
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / Antigens, Neoplasm; 0 / PRAME protein, human
29.
Perham N, Moore SC, Shepherd J, Cusens B:
Identifying drunkenness in the night-time economy.
Addiction
; 2007 Mar;102(3):377-80
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
AIMS: To assess the relationship between blood alcohol concentration (
BAC
) and indicators used in field sobriety tests putatively associated with intoxication.
Breath analysis was used to determine respondents'
BAC
.
FINDINGS: Combinations of slurred speech, staggering gait and glazed eyes significantly predicted levels
of BAC
with a staggering gait indicating highest levels of intoxication.
CONCLUSIONS: Subjective ratings of drunkenness by trained observers corresponded with
BAC
.
Transition
BACs
denoting observable behaviour change associated with intoxication have been identified.
[MeSH-major]
Alcoholic Intoxication /
diagnosis
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
ETHANOL
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17298644.001).
[ISSN]
0965-2140
[Journal-full-title]
Addiction (Abingdon, England)
[ISO-abbreviation]
Addiction
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / Biomarkers; 3K9958V90M / Ethanol
30.
Shi G, Wu X, Xiong F, Zhou Y, Liu Z, Deng J, Chen H:
[A successive three-step 'Gap-repair' method to generate the mWAP-hLF hybrid gene locus].
Sheng Wu Gong Cheng Xue Bao
; 2008 Sep;24(9):1538-44
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Then using 'Gap-repair 'method mediated by Red recombination system of lambda-prophage in Escherichia coli, in the first step, the 8 kb 3' flanking region of the mWAP gene was subcloned from
the Bacterial
artificial chromosome which harbors the mWAP gene locus(mWAP
BAC
) into the gap-repair vector; in the second step, the 29 kb hLF genomic sequence from the ATG code to the TAA code was subcloned from the hLF
BAC
; in the third step, the 12 kb 5' flanking region of the mWAP gene was subcloned from the mWAP
BAC
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19160834.001).
[ISSN]
1000-3061
[Journal-full-title]
Sheng wu gong cheng xue bao = Chinese journal of biotechnology
[ISO-abbreviation]
Sheng Wu Gong Cheng Xue Bao
[Language]
chi
[Publication-type]
English Abstract; Journal Article
[Publication-country]
China
[Chemical-registry-number]
0 / Milk Proteins; 0 / whey acidic proteins; EC 3.4.21.- / Lactoferrin
31.
Andrieux J:
[Array-CGH for routine diagnosis of cryptic chromosomal imbalances].
Pathol Biol (Paris)
; 2008 Sep;56(6):368-74
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
[Array-CGH for routine
diagnosis of
cryptic chromosomal imbalances].
[Transliterated title]
Puces à ADN (CGH-array) : application pour le diagnostic
de
déséquilibres cytogénétiques cryptiques.
BAC
/PAC and oligonucleotides array-CGH have transformed the field of genetics and are useful for constitutional, hematological and solid tumors cytogenetics.
[MeSH-major]
Chromosome Disorders /
diagnosis
. Molecular Diagnostic Techniques / methods. Nucleic Acid Hybridization / methods. Oligonucleotide Array Sequence Analysis
[MeSH-minor]
Chromosomes, Artificial,
Bacterial
/ genetics. Gene Dosage. Genetic Testing / methods. Humans. Karyotyping / methods. Molecular Weight. Oligonucleotide Probes
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18514435.001).
[ISSN]
0369-8114
[Journal-full-title]
Pathologie-biologie
[ISO-abbreviation]
Pathol. Biol.
[Language]
fre
[Publication-type]
English Abstract; Journal Article; Review
[Publication-country]
France
[Chemical-registry-number]
0 / Oligonucleotide Probes
[Number-of-references]
82
32.
Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F:
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm.
Mol Hum Reprod
; 2007 Oct;13(10):751-6
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
In order to improve the assessment of meiotic segregation in PAI, we present a new strategy based on the use
of bacterial
artificial chromosome (
BAC
) probes which allow a precise localization of chromosome breakpoints and the identification of all meiotic products in human sperm.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17913851.001).
[ISSN]
1360-9947
[Journal-full-title]
Molecular human reproduction
[ISO-abbreviation]
Mol. Hum. Reprod.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
33.
Pusztaszeri M, Orcurto MV, Schmidt S, Krueger T:
Solitary nodular pure bronchioloalveolar carcinoma.
Respiration
; 2010;79(3):243-4
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Solitary nodular pure
bronchioloalveolar carcinoma
.
[MeSH-major]
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ pathology.
Lung
/ pathology.
Lung
Neoplasms / pathology
MedlinePlus Health Information.
consumer health - Lung Cancer
.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19147987.001).
[ISSN]
1423-0356
[Journal-full-title]
Respiration; international review of thoracic diseases
[ISO-abbreviation]
Respiration
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
Switzerland
34.
Calafat A, Juan M, Duch MA:
Preventive interventions in nightlife: a review.
Adicciones
; 2009;21(4):387-413
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
'Classical' measures (taxation, reduced
BAC
limits, minimum legal purchasing age...) are also evidence-based and effective.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 20011993.001).
[ISSN]
0214-4840
[Journal-full-title]
Adicciones
[ISO-abbreviation]
Adicciones
[Language]
eng; spa
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Review
[Publication-country]
Spain
[Number-of-references]
103
35.
Yin BL, Guo L, Zhang DF, Terzaghi W, Wang XF, Liu TT, He H, Cheng ZK, Deng XW:
Integration of cytological features with molecular and epigenetic properties of rice chromosome 4.
Mol Plant
; 2008 Sep;1(5):816-29
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Fluorescence in-situ hybridization (FISH) experiments using a set
of bacterial
artificial chromosome (
BAC
) clones from chromosome 4 placed all 18 clones in the region predicted by the model.
[MeSH-minor]
Base Sequence. Chromosomes, Artificial,
Bacterial
/ genetics. DNA Methylation / genetics. DNA Transposable Elements / genetics. Euchromatin / genetics. Genes, Plant. Genetic Loci / genetics. Heterochromatin / genetics. Histones / metabolism. In Situ Hybridization, Fluorescence. Oligonucleotide Array Sequence Analysis. Protein Processing, Post-Translational. RNA, Plant / metabolism. Transcription, Genetic
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19825584.001).
[ISSN]
1674-2052
[Journal-full-title]
Molecular plant
[ISO-abbreviation]
Mol Plant
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / DNA Transposable Elements; 0 / Euchromatin; 0 / Heterochromatin; 0 / Histones; 0 / RNA, Plant
36.
Tang LF, Du LZ, Chen ZM, Zou CC:
Levels of matrix metalloproteinase-9 and its inhibitor in bronchoalveolar lavage cells of asthmatic children.
Fetal Pediatr Pathol
; 2006 Jan-Feb;25(1):1-7
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Levels of matrix metalloproteinase-9 and its inhibitor in
bronchoalveolar
lavage cells of asthmatic children.
The levels of MMP-9 and TIMP-1 in
bronchoalveolar
lavage (BAL) cells of asthmatic children were measured immunocytochemically.
The percentages of eosinophils and mast cells in
bronchoalveolar
lavage fluid (BALF) of asthmatic children were increased.
Levels of MMP-9 and TIMP-1 in BAL
cell of
asthmatic children were increased significantly at about 30- and 35-fold relative to the controls, respectively.
[MeSH-minor]
Bronchoalveolar
Lavage. Case-Control Studies.
Cell
Count. Child, Preschool. Eosinophils / chemistry. Eosinophils / pathology. Extracellular Matrix / chemistry. Extracellular Matrix / pathology. Female. Humans. Immunohistochemistry. Infant. Male. Mast Cells / chemistry. Mast Cells / pathology
MedlinePlus Health Information.
consumer health - Asthma
.
MedlinePlus Health Information.
consumer health - Asthma in Children
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 16754484.001).
[ISSN]
1551-3815
[Journal-full-title]
Fetal and pediatric pathology
[ISO-abbreviation]
Fetal Pediatr Pathol
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Chemical-registry-number]
0 / Tissue Inhibitor of Metalloproteinase-1; EC 3.4.24.35 / Matrix Metalloproteinase 9
37.
Bayou N, M'rad R, Belhaj A, Daoud H, Ben Jemaa L, Zemni R, Briault S, Helayem MB, Chaabouni H:
De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.
J Biomed Biotechnol
; 2008;2008:231904
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
De
novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic
disorder
.
The high incidence
of de
novo chromosomal aberrations in a population of persons with autism suggests a causal relationship between certain chromosomal aberrations and the occurrence of isolated idiopathic autism.
We report on the clinical and cytogenetic findings in a male patient with autism, no physical abnormalities and
a de
novo balanced (7;16)(p22.1;p16.2) translocation.
FISH with specific RP11-
BAC
clones mapping near 7p22.1 and 16p11.2 was used to refine the location of the breakpoints.
[MeSH-major]
Abnormalities, Multiple. Autistic
Disorder
/ genetics. Chromosomes, Human, Pair 16 / ultrastructure. Chromosomes, Human, Pair 7 / ultrastructure. Translocation, Genetic
[MeSH-minor]
Arachnoid Cysts. Child. Child Behavior Disorders. Chromosome Banding. Chromosome Disorders / genetics. Chromosome Disorders / pathology. Chromosome Disorders / physiopathology. Chromosomes, Artificial,
Bacterial
. Cisterna Magna / pathology. Humans. In Situ Hybridization, Fluorescence. Karyotyping. Male. Psychomotor Disorders
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Autism. 2004 Jun;8(2):141-61
[
15165431.001
]
[Cites]
J Med Genet. 2003 May;40(5):352-6
[
12746398.001
]
[Cites]
Dev Med Child Neurol. 1985 Jun;27(3):293-304
[
3160621.001
]
[Cites]
Am J Med Genet. 1997 Jan 20;68(2):219-21
[
9028462.001
]
[Cites]
Mutat Res. 1997 Dec 12;396(1-2):129-40
[
9434864.001
]
[Cites]
J Autism Dev Disord. 1998 Oct;28(5):415-25
[
9813777.001
]
[Cites]
Mol Psychiatry. 2006 Jan;11(1):1, 18-28
[
16205736.001
]
[Cites]
Am J Med Genet C Semin Med Genet. 2006 Feb 15;142C(1):13-23
[
16419096.001
]
[Cites]
Eur J Hum Genet. 2006 Jun;14(6):714-20
[
16721407.001
]
[Cites]
J Med Genet. 2006 Nov;43(11):843-9
[
16840569.001
]
[Cites]
Mol Psychiatry. 2007 Jan;12(1):2-22
[
17033636.001
]
[Cites]
Biol Psychiatry. 2007 Feb 15;61(4):429-37
[
16996486.001
]
[Cites]
Nat Genet. 2007 Mar;39(3):319-28
[
17322880.001
]
[Cites]
Neurosci Behav Physiol. 2007 Jul;37(6):553-8
[
17657425.001
]
[Cites]
Psychiatr Genet. 2001 Jun;11(2):57-63
[
11525418.001
]
[Cites]
Am J Med Genet. 2002 Apr 22;109(2):149-53
[
11977164.001
]
[Cites]
Am J Hum Genet. 2002 Jul;71(1):100-15
[
12058345.001
]
[Cites]
Genomics. 2002 Aug;80(2):129-34
[
12160723.001
]
[Cites]
Neuromolecular Med. 2002;2(1):11-28
[
12230302.001
]
[Cites]
Am J Hum Genet. 2002 Oct;71(4):941-6
[
12297988.001
]
[Cites]
JAMA. 2003 Jan 1;289(1):87-9
[
12503982.001
]
[Cites]
J Med Genet. 2004 Jul;41(7):e90
[
15235033.001
]
(PMID = 18475318.001).
[ISSN]
1110-7251
[Journal-full-title]
Journal of biomedicine & biotechnology
[ISO-abbreviation]
J. Biomed. Biotechnol.
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2373955
38.
Courtens W, Wuyts W, Scheers S, Van Luijk R, Reyniers E, Rooms L, Ceulemans B, Kooy F, Wauters J:
A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
Eur J Med Genet
; 2006 Sep-Oct;49(5):402-13
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
A de
novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
We report on a 3-year-old girl with psychomotor retardation, cardiopathy, strabismus, umbilical hernia, and facial dysmorphism in whom
a de
novo unbalanced submicroscopic translocation (10p;18q) was found by MLPA (Multiplex Ligation dependent Probe Amplification) and FISH analyses.
Additional FISH studies with locus specific RP11
BAC
probes and analyses with microsatellites revealed that the translocation resulted in a deletion estimated between 6 and 9 Mb on the maternal chromosome 18 and a subtelomeric 10p duplication of approximately 6.9 Mb.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 16488200.001).
[ISSN]
1769-7212
[Journal-full-title]
European journal of medical genetics
[ISO-abbreviation]
Eur J Med Genet
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Review
[Publication-country]
Netherlands
[Number-of-references]
34
39.
Raz DJ, Odisho AY, Franc BL, Jablons DM:
Tumor fluoro-2-deoxy-D-glucose avidity on positron emission tomographic scan predicts mortality in patients with early-stage pure and mixed bronchioloalveolar carcinoma.
J Thorac Cardiovasc Surg
; 2006 Nov;132(5):1189-95
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Tumor fluoro-2-deoxy-D-glucose avidity on positron emission tomographic scan predicts mortality in patients with early-stage pure and mixed
bronchioloalveolar carcinoma
.
OBJECTIVE:
Bronchioloalveolar carcinoma
is a clinically heterogeneous subtype of non-small
cell lung carcinoma
that frequently has low 2-[18F]fluoro-D-glucose (FDG) uptake on positron emission tomographic scanning.
We investigated whether tumor FDG avidity was associated with worse survival among patients with completely resected node-negative pure and mixed
bronchioloalveolar carcinoma
.
METHODS: We performed a cohort study of 36 patients who had completely resected pure and mixed
bronchioloalveolar carcinoma
between 1998 and 2004, who had no hilar or mediastinal lymph node metastases, and who had undergone a preoperative positron emission tomographic scan.
FDG avidity had a hazard ratio of death of 8.6 (95% confidence interval 1.4-244.7, P = .02) after adjusting for tumor size, the presence of multifocal
bronchioloalveolar carcinoma
, and the presence of histologically mixed
bronchioloalveolar carcinoma
.
CONCLUSIONS: Preoperative tumor FDG standardized uptake value of 2.5 or greater on positron emission tomography is a powerful predictor of long-term mortality in patients with lymph node-negative pure and mixed
bronchioloalveolar carcinoma
who undergo complete surgical resection.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17059942.001).
[ISSN]
1097-685X
[Journal-full-title]
The Journal of thoracic and cardiovascular surgery
[ISO-abbreviation]
J. Thorac. Cardiovasc. Surg.
[Language]
ENG
[Grant]
United States / NCI NIH HHS / CA / CA093708-02; United States / NCI NIH HHS / CA / R01 CA093708; United States / NCRR NIH HHS / RR / M01 RR-00079; United States / NCI NIH HHS / CA / R01 CA093708-02
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18
40.
Augulyte L, Kliaugaite D, Racys V, Jankunaite D, Zaliauskiene A, Bergqvist PA, Andersson PL:
Multivariate analysis of a biologically activated carbon (BAC) system and its efficiency for removing PAHs and aliphatic hydrocarbons from wastewater polluted with petroleum products.
J Hazard Mater
; 2009 Oct 15;170(1):103-10
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Multivariate analysis
of a
biologically activated carbon (
BAC
) system and its efficiency for removing PAHs and aliphatic hydrocarbons from wastewater polluted with petroleum products.
The efficiency
of a
biologically activated carbon system for treating wastewater polluted with petroleum products was examined and the effects of process parameters on its efficacy were evaluated.
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
CARBON
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19482425.001).
[ISSN]
1873-3336
[Journal-full-title]
Journal of hazardous materials
[ISO-abbreviation]
J. Hazard. Mater.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Netherlands
[Chemical-registry-number]
0 / Industrial Waste; 0 / Membranes, Artificial; 0 / Petroleum; 0 / Polycyclic Hydrocarbons, Aromatic; 0 / Water Pollutants, Chemical; 7440-44-0 / Carbon
41.
Grabner B, Blaas L, Musteanu M, Hoffmann T, Birbach A, Eferl R, Casanova E:
A mouse tool for conditional mutagenesis in ovarian granulosa cells.
Genesis
; 2010 Oct 1;48(10):612-7
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
We have expressed the tamoxifen inducible CreER(T)² fusion protein from
a Bacterial
Artificial Chromosome (
BAC
) containing the regulatory elements of the hydroxysteroid (17-beta) dehydrogenase 1 (Hsd17b1) gene.
[MeSH-minor]
Alleles. Animals. Chromosomes, Artificial,
Bacterial
/ genetics. Escherichia coli / genetics. Female. Genes, Reporter. Humans. In Situ Hybridization. Mice. Mice, Transgenic. RNA, Messenger / metabolism. Receptors, Estrogen / genetics. Recombinant Fusion Proteins / biosynthesis. Recombination, Genetic / drug effects. Tamoxifen / pharmacology
Hazardous Substances Data Bank.
TAMOXIFEN
.
Jackson Laboratory JAX®Mice Database.
culture/stock collections - B6N.Cg-Tg(Hsd17b1-icre/ERT2)3Casa/J
(subscription/membership/fee required).
KOMP Repository.
gene/protein/disease-specific - KOMP Repository
(subscription/membership/fee required).
Mouse Genome Informatics (MGI).
Mouse Genome Informatics (MGI)
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
SciCrunch.
Marmoset Gene list: Data: Gene Annotation
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
© 2010 Wiley-Liss, Inc.
(PMID = 20715176.001).
[ISSN]
1526-968X
[Journal-full-title]
Genesis (New York, N.Y. : 2000)
[ISO-abbreviation]
Genesis
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / RNA, Messenger; 0 / Receptors, Estrogen; 0 / Recombinant Fusion Proteins; 094ZI81Y45 / Tamoxifen; EC 2.7.7.- / Cre recombinase; EC 2.7.7.- / Integrases
42.
Datema E, Mueller LA, Buels R, Giovannoni JJ, Visser RG, Stiekema WJ, van Ham RC:
Comparative BAC end sequence analysis of tomato and potato reveals overrepresentation of specific gene families in potato.
BMC Plant Biol
; 2008;8:34
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Comparative
BAC
end sequence analysis of tomato and potato reveals overrepresentation of specific gene families in potato.
This study presents a first genome-wide analysis of these two species, based on two large collections
of BAC
end sequences representing approximately 19% of the tomato genome and 10% of the potato genome.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Genome Res. 2000 Jan;10(1):129-36
[
10645957.001
]
[Cites]
Annu Rev Plant Biol. 2003;54:629-67
[
14503006.001
]
[Cites]
Nature. 2000 Dec 14;408(6814):796-815
[
11130711.001
]
[Cites]
Plant Cell. 2001 Apr;13(4):979-88
[
11283350.001
]
[Cites]
Plant Physiol. 2004 Jun;135(2):756-72
[
15208422.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Oct 5;101(40):14349-54
[
15388850.001
]
[Cites]
Genetics. 1992 Dec;132(4):1141-60
[
1360934.001
]
[Cites]
Science. 1993 Nov 26;262(5138):1432-6
[
7902614.001
]
[Cites]
Nucleic Acids Res. 1997 Sep 1;25(17):3389-402
[
9254694.001
]
[Cites]
Genome. 1999 Jun;42(3):536-44
[
10382301.001
]
[Cites]
Plant Physiol. 2005 Jul;138(3):1310-7
[
16010005.001
]
[Cites]
Cytogenet Genome Res. 2005;110(1-4):462-7
[
16093699.001
]
[Cites]
Nature. 2005 Aug 11;436(7052):793-800
[
16100779.001
]
[Cites]
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D247-51
[
16381856.001
]
[Cites]
Genetics. 2006 Apr;172(4):2541-55
[
16489220.001
]
[Cites]
Theor Appl Genet. 2006 May;112(8):1503-18
[
16575560.001
]
[Cites]
Genetics. 2006 Jun;173(2):1075-87
[
16582432.001
]
[Cites]
Mol Genet Genomics. 2006 Jul;276(1):1-12
[
16703363.001
]
[Cites]
BMC Plant Biol. 2006;6:8
[
16613603.001
]
[Cites]
Plant Cell Rep. 2006 Dec;25(12):1369-79
[
16835751.001
]
[Cites]
Mol Cells. 2006 Dec 31;22(3):300-7
[
17202858.001
]
[Cites]
Nucleic Acids Res. 2007 Jan;35(Database issue):D247-52
[
17130144.001
]
[Cites]
Nucleic Acids Res. 2007 Jan;35(Database issue):D901-5
[
17142232.001
]
[Cites]
Nucleic Acids Res. 2007 Jan;35(Database issue):D224-8
[
17202162.001
]
[Cites]
Theor Appl Genet. 2007 Apr;114(6):1081-90
[
17287974.001
]
[Cites]
BMC Genomics. 2007;8:112
[
17474978.001
]
[Cites]
BMC Plant Biol. 2007;7:29
[
17562019.001
]
[Cites]
Ugeskr Laeger. 2008 Jan 28;170(5):328-30
[
18252159.001
]
[Cites]
Mol Biol Evol. 2001 Jul;18(7):1161-7
[
11420357.001
]
[Cites]
Science. 2002 Apr 5;296(5565):79-92
[
11935017.001
]
[Cites]
Science. 2002 Apr 5;296(5565):92-100
[
11935018.001
]
[Cites]
Plant Cell. 2002 Jul;14(7):1441-56
[
12119366.001
]
[Cites]
Nature. 2003 Mar 27;422(6930):433-8
[
12660784.001
]
[Cites]
Plant J. 2003 May;34(4):529-41
[
12753591.001
]
[Cites]
Proc Natl Acad Sci U S A. 2000 Aug 1;97(16):9121-6
[
10908680.001
]
(PMID = 18405374.001).
[ISSN]
1471-2229
[Journal-full-title]
BMC plant biology
[ISO-abbreviation]
BMC Plant Biol.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / Plant Proteins
[Other-IDs]
NLM/ PMC2324086
43.
Kiss AJ, Cheng CH:
Molecular diversity and genomic organisation of the alpha, beta and gamma eye lens crystallins from the Antarctic toothfish Dissostichus mawsoni.
Comp Biochem Physiol Part D Genomics Proteomics
; 2008 Jun;3(2):155-71
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
A preliminary Fingerprinted Contig analysis of clones containing crystallin genes screened from a toothfish
BAC
library indicated alpha crystallin genes occurred in a single genomic region of ~266 kbp, beta crystallin genes in ~273 kbp, while the gamma crystallin gene family occurred in two separate regions of ~180 and ~296 kbp.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 20483216.001).
[ISSN]
1878-0407
[Journal-full-title]
Comparative biochemistry and physiology. Part D, Genomics & proteomics
[ISO-abbreviation]
Comp. Biochem. Physiol. Part D Genomics Proteomics
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Netherlands
44.
Bentivegna A, Milani D, Gervasini C, Castronovo P, Mottadelli F, Manzini S, Colapietro P, Giordano L, Atzeri F, Divizia MT, Uzielli ML, Neri G, Bedeschi MF, Faravelli F, Selicorni A, Larizza L:
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients.
BMC Med Genet
; 2006;7:77
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
BACKGROUND: Rubinstein-Taybi Syndrome (RSTS, MIM 180849) is a rare congenital
disorder
characterized by mental and growth retardation, broad and duplicated distal phalanges of thumbs and halluces, facial dysmorphisms and increased risk of tumors.
METHODS: Our study is based on the mutation analysis of CREBBP in 31 Italian RSTS patients using segregation analysis of intragenic microsatellites,
BAC
FISH and direct sequencing of PCR and
RT
-PCR fragments.
By direct sequencing a total of 14
de
novo mutations were identified: 10 truncating (5 frameshift and 5 nonsense), one splice site, and three novel missense mutations.
Identification of the p.Asn1978Ser in the healthy mother
of a
patient also carrying
a de
novo frameshift mutation, questions the pathogenetic significance of the missense change reported as recurrent mutation.
Genetic Alliance.
consumer health - Rubinstein-Taybi syndrome
.
Genetics Home Reference.
consumer health - Rubinstein-Taybi syndrome
.
Genetics Home Reference.
consumer health - CREBBP gene
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Eur J Hum Genet. 1999 Oct-Nov;7(7):748-56
[
10573006.001
]
[Cites]
Hum Genet. 2006 Sep;120(2):179-86
[
16783566.001
]
[Cites]
Genes Dev. 2000 Jul 1;14(13):1553-77
[
10887150.001
]
[Cites]
Hum Mol Genet. 2001 May 1;10(10):1071-6
[
11331617.001
]
[Cites]
J Med Genet. 2002 Jun;39(6):415-21
[
12070251.001
]
[Cites]
J Med Genet. 2002 Jul;39(7):496-501
[
12114483.001
]
[Cites]
Hum Mol Genet. 2003 Feb 15;12(4):441-50
[
12566391.001
]
[Cites]
Genes Chromosomes Cancer. 2003 Apr;36(4):402-5
[
12619164.001
]
[Cites]
Hum Mutat. 2004 Mar;23(3):278-84
[
14974086.001
]
[Cites]
Genes Chromosomes Cancer. 2004 Jun;40(2):140-5
[
15101047.001
]
[Cites]
Leukemia. 2004 Jun;18(6):1115-21
[
15085163.001
]
[Cites]
Med Pediatr Oncol. 1989;17(6):485-91
[
2586363.001
]
[Cites]
Genomics. 1992 Dec;14(4):897-911
[
1478671.001
]
[Cites]
Am J Hum Genet. 1993 Feb;52(2):249-54
[
8430691.001
]
[Cites]
Nature. 1995 Mar 2;374(6517):85-8
[
7870179.001
]
[Cites]
Am J Med Genet. 1995 Mar 13;56(1):112-5
[
7747773.001
]
[Cites]
Nature. 1995 Jul 27;376(6538):348-51
[
7630403.001
]
[Cites]
Cell. 1996 May 3;85(3):403-14
[
8616895.001
]
[Cites]
Annu Rev Cell Dev Biol. 1995;11:155-88
[
8689555.001
]
[Cites]
Nature. 1996 Dec 19-26;384(6610):641-3
[
8967953.001
]
[Cites]
Am J Dis Child. 1963 Jun;105:588-608
[
13983033.001
]
[Cites]
Am J Hum Genet. 2005 Apr;76(4):572-80
[
15706485.001
]
[Cites]
J Med Genet. 2005 Jun;42(6):514-8
[
15937088.001
]
[Cites]
Hum Genet. 2005 Sep;117(5):485-93
[
16021471.001
]
[Cites]
J Med Genet. 2000 Mar;37(3):168-76
[
10699051.001
]
(PMID = 17052327.001).
[ISSN]
1471-2350
[Journal-full-title]
BMC medical genetics
[ISO-abbreviation]
BMC Med. Genet.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / CREBBP protein, human; 0 / Nuclear Localization Signals; EC 2.3.1.48 / CREB-Binding Protein
[Other-IDs]
NLM/ PMC1626071
45.
Borg K, Bocian E, Bernaciak J, Nowakowska B, Derwińska K, Obersztyn E, Szczałuba K, Smigiel R, Kostyk E, Mazurczak T:
[Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].
Med Wieku Rozwoj
; 2009 Apr-Jun;13(2):81-93
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The abnormal phenotype might be the result of genomic imbalance or aberrant expression caused by direct breakage
of a
dosage sensitive gene.
Molecular karyotyping was performed in all patients using FISH with region-specific
BAC
clones, high resolution comparative genomic hybridization (HR-CGH) or array CGH (aCGH).
Three rearrangements had more
complex
structure than conventional methods demonstrated.
MedlinePlus Health Information.
consumer health - Developmental Disabilities
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19837989.001).
[Journal-full-title]
Medycyna wieku rozwojowego
[ISO-abbreviation]
Med Wieku Rozwoj
[Language]
pol
[Publication-type]
English Abstract; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Poland
46.
Monnot S, Giuliano F, Massol C, Fossoud C, Cossée M, Lambert JC, Karmous-Benailly H:
Partial Xp11.23-p11.4 duplication with random X inactivation: clinical report and molecular cytogenetic characterization.
Am J Med Genet A
; 2008 May 15;146A(10):1325-9
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The karyotype completed by cytogenetic analysis with the Whole Chromosome Painting probe of chromosome X revealed
a de
novo partial duplication of the short arm of an X chromosome.
In order to further characterize the duplicated segment, we used a series
of BAC
probes extending from band Xp11.22 to Xp22.1.
BACs
from Xp11.23 to Xp11.4 were duplicated.
MedlinePlus Health Information.
consumer health - Craniofacial Abnormalities
.
MedlinePlus Health Information.
consumer health - Developmental Disabilities
.
MedlinePlus Health Information.
consumer health - Facial Injuries and Disorders
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
2008 Wiley-Liss, Inc.
(PMID = 18412111.001).
[ISSN]
1552-4833
[Journal-full-title]
American journal of medical genetics. Part A
[ISO-abbreviation]
Am. J. Med. Genet. A
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
47.
Han HD, Zhou YW, He WJ, Wang DS:
[Comparative study on the organic matter removal in polluted raw water by different techniques at integrated pilot plant].
Huan Jing Ke Xue
; 2006 Nov;27(11):2251-4
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The waterworks that adopted the Grade II source raw water were suggested to use the conventional techniques and seasonal preozonation techniques, while the others were suggested to alternatively select GAC or
BAC
technique to meet the request of new water quality criterion.
Hazardous Substances Data Bank.
OZONE
.
Hazardous Substances Data Bank.
ACTIVATED CHARCOAL
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17326435.001).
[ISSN]
0250-3301
[Journal-full-title]
Huan jing ke xue= Huanjing kexue
[ISO-abbreviation]
Huan Jing Ke Xue
[Language]
CHI
[Publication-type]
Comparative Study; English Abstract; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
China
[Chemical-registry-number]
0 / Organic Chemicals; 0 / Water Pollutants, Chemical; 16291-96-6 / Charcoal; 66H7ZZK23N / Ozone
48.
Frendewey D, Chernomorsky R, Esau L, Om J, Xue Y, Murphy AJ, Yancopoulos GD, Valenzuela DM:
The loss-of-allele assay for ES cell screening and mouse genotyping.
Methods Enzymol
; 2010;476:295-307
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
The loss-of-allele assay for ES
cell
screening and mouse genotyping.
Targeting vectors used to create directed mutations in mouse embryonic stem (ES) cells consist, in their simplest form,
of a
gene for drug selection flanked by mouse genomic sequences, the so-called homology arms that promote site-directed homologous recombination between the vector and the target gene.
The VelociGene method for the creation of targeted mutations in ES cells employs targeting vectors, called BACVecs, that are based on
bacterial
artificial chromosomes.
In a correctly targeted ES
cell
clone, the LOA assay detects one of the two native alleles (for genes not on the X or Y chromosome), the other allele being disrupted by the targeted modification.
We have designed qPCR LOA assays for deletions, insertions, point mutations, domain swaps, conditional, and humanized alleles and have used the insert assays to quantify the copy number of random insertion
BAC
transgenics.
Because of its quantitative precision, specificity, and compatibility with high throughput robotic operations, the LOA assay eliminates bottlenecks in ES
cell
screening and mouse genotyping and facilitates maximal speed and throughput for knockout mouse production.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
Copyright (c) 2010 Elsevier Inc. All rights reserved.
(PMID = 20691873.001).
[ISSN]
1557-7988
[Journal-full-title]
Methods in enzymology
[ISO-abbreviation]
Meth. Enzymol.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
49.
Nagano N, Nagano Y, Nakano R, Okamoto R, Inoue M:
Genetic diversity of the C protein beta-antigen gene and its upstream regions within clonally related groups of type Ia and Ib group B streptococci.
Microbiology
; 2006 Mar;152(Pt 3):771-8
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Genetic diversity of the C protein beta-
antigen
gene and its upstream regions within clonally related groups of type Ia and Ib group B streptococci.
C protein beta
antigen
(
Bac
), a surface protein of group B streptococci (GBS), is known to concurrently bind the Fc portion of IgA and factor H (FH).
The authors' previous work has demonstrated that mRNA expression levels show diversity among clonally related strains containing genes (
bac
) encoding
Bac
, with high expression noted in invasive strains.
In this study,
the bac
gene and upstream regions containing putative promoters, three ORFs and an IS1381 insertion sequence were characterized.
Three invasive strains showed high
bac
expression levels and did not show any notable mutations except one strain producing
Bac
that was able to bind FH but not IgA.
A deletion of 51 amino acid residues, including part of the
Bac
IgA-binding region, was identified and hypothesized to contribute to the loss of the IgA-binding ability of this strain.
A vaginal strain that showed somewhat higher
bac
expression levels and produced
Bac
lacking immunoreactivity contained an 11 bp deletion, which generated a premature termination codon, in the region preceding the IgA-binding region.
In another vaginal strain that did not express
bac
, disruption of the upstream ORFs of the sensor histidine kinase and DNA-binding response regulator, due to frameshift mutations, was noted although it is not known whether these proteins directly affect
bac
expression levels.
An IS1381 insertion into the promoter region was found in another vaginal strain that showed low expression levels and produced
Bac
with a significantly larger proline-rich repeat region.
These results demonstrate considerable genetic diversity of the
bac
and upstream regions of invasive and noninvasive GBS, which may contribute to the variability
of bac
expression levels among those strains.
[MeSH-major]
Antigens,
Bacterial
/ genetics. Antigens, Surface / genetics.
Bacterial
Proteins / genetics. Genetic Variation. Streptococcus agalactiae / classification. Streptococcus agalactiae / genetics
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 16514156.001).
[ISSN]
1350-0872
[Journal-full-title]
Microbiology (Reading, England)
[ISO-abbreviation]
Microbiology (Reading, Engl.)
[Language]
eng
[Databank-accession-numbers]
GENBANK/ AB121739/ AB221536/ X58470/ X59771
[Publication-type]
Journal Article
[Publication-country]
England
[Chemical-registry-number]
0 / Antigens, Bacterial; 0 / Antigens, Surface; 0 / Bacterial Proteins; 0 / Immunoglobulin A; 80295-65-4 / Complement Factor H
50.
Ronen A, Chassidim HS, Gershon P, Parmet Y, Rabinovich A, Bar-Hamburger R, Cassuto Y, Shinar D:
The effect of alcohol, THC and their combination on perceived effects, willingness to drive and performance of driving and non-driving tasks.
Accid Anal Prev
; 2010 Nov;42(6):1855-65
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
1) to investigate the effect of alcohol (
BAC
=0.05%), THC (13 mg) and their combination on driving and non-driving tasks.
Hazardous Substances Data Bank.
delta 9-Tetrahydrocannabinol
.
Hazardous Substances Data Bank.
ETHANOL
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
2010 Elsevier Ltd. All rights reserved.
(PMID = 20728636.001).
[ISSN]
1879-2057
[Journal-full-title]
Accident; analysis and prevention
[ISO-abbreviation]
Accid Anal Prev
[Language]
eng
[Publication-type]
Controlled Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
3K9958V90M / Ethanol; 7J8897W37S / Dronabinol
51.
Massion PP, Zou Y, Chen H, Jiang A, Coulson P, Amos CI, Wu X, Wistuba I, Wei Q, Shyr Y, Spitz MR:
Smoking-related genomic signatures in non-small cell lung cancer.
Am J Respir Crit Care Med
; 2008 Dec 1;178(11):1164-72
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Smoking-related genomic signatures in non-small
cell lung cancer
.
RATIONALE: Tobacco smoking is responsible for 85% of all
lung
cancers.
To further our understanding of the molecular pathogenesis
of lung cancer
, we determined whether smoking history leads to the emergence of specific genomic alterations found in non-small
cell lung cancer
(NSCLC).
Tissue sections were microdissected, and DNA was extracted, purified, and labeled by random priming before hybridization onto
bacterial
artificial chromosome (
BAC
) arrays.
Lung
tumors arising from current-smokers had the greatest number of copy number alterations.
The genomic regions most significantly associated with smoking were located within 60 regions and were functionally associated with genes controlling
the M
phase of the
cell
cycle, the segregation of chromosomes, and the methylation of DNA.
CONCLUSIONS: These findings indicate that smoking history leaves a specific genomic signature in the DNA
of lung
tumors and suggest that these alterations may reflect new molecular pathways to
cancer
development.
Genetic Alliance.
consumer health - Lung Cancer
.
Genetic Alliance.
consumer health - Non-small cell lung cancer
.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
MedlinePlus Health Information.
consumer health - Smoking
.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Cancer Res. 2001 Feb 15;61(4):1309-13
[
11245426.001
]
[Cites]
Genome Biol. 2007;8(10):R224
[
17953769.001
]
[Cites]
Cancer Res. 2001 Jul 1;61(13):5223-30
[
11431363.001
]
[Cites]
Nat Genet. 2001 Nov;29(3):263-4
[
11687795.001
]
[Cites]
Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13790-5
[
11707567.001
]
[Cites]
Ann N Y Acad Sci. 2001 Dec;952:1-12
[
11795428.001
]
[Cites]
Nat Rev Genet. 2002 Jun;3(6):415-28
[
12042769.001
]
[Cites]
Cancer Res. 2002 Jul 1;62(13):3636-40
[
12097266.001
]
[Cites]
Nat Med. 2002 Aug;8(8):816-24
[
12118244.001
]
[Cites]
Carcinogenesis. 2000 Mar;21(3):443-52
[
10688864.001
]
[Cites]
Int J Oncol. 2000 Jul;17(1):67-73
[
10853020.001
]
[Cites]
J Natl Cancer Inst. 2000 Nov 1;92(21):1764-72
[
11058619.001
]
[Cites]
N Engl J Med. 2001 Feb 22;344(8):539-48
[
11207349.001
]
[Cites]
Proc Natl Acad Sci U S A. 2002 Dec 10;99(25):16156-61
[
12461184.001
]
[Cites]
J Natl Cancer Inst. 2003 Jan 1;95(1):14-8
[
12509396.001
]
[Cites]
Bioinformatics. 2003 May 1;19(7):825-33
[
12724292.001
]
[Cites]
Breast Cancer Res Treat. 2003 Apr;78(3):289-98
[
12755488.001
]
[Cites]
Cancer Epidemiol Biomarkers Prev. 2003 Aug;12(8):689-98
[
12917198.001
]
[Cites]
Clin Cancer Res. 2003 Oct 15;9(13):4695-704
[
14581339.001
]
[Cites]
Cancer Res. 2003 Nov 1;63(21):7113-21
[
14612504.001
]
[Cites]
Nucleic Acids Res. 2004 Jan 1;32(Database issue):D258-61
[
14681407.001
]
[Cites]
Nucleic Acids Res. 2004 Jan 1;32(Database issue):D262-6
[
14681408.001
]
[Cites]
Cancer Res. 2004 May 1;64(9):3060-71
[
15126342.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Jul 6;101(27):10143-8
[
15210990.001
]
[Cites]
Int J Cancer. 1989 Mar 15;43(3):403-9
[
2466800.001
]
[Cites]
Cancer Res. 1991 Nov 1;51(21):5786-93
[
1933849.001
]
[Cites]
Cancer Res. 1993 May 15;53(10 Suppl):2279-86
[
8485714.001
]
[Cites]
Control Clin Trials. 1993 Aug;14(4):266-85
[
8365193.001
]
[Cites]
Science. 1996 Oct 18;274(5286):430-2
[
8832894.001
]
[Cites]
Cancer Genet Cytogenet. 1997 May;95(1):20-32
[
9140450.001
]
[Cites]
Nat Genet. 1998 Sep;20(1):19-23
[
9731524.001
]
[Cites]
Nat Genet. 1998 Oct;20(2):207-11
[
9771718.001
]
[Cites]
Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14863-8
[
9843981.001
]
[Cites]
J Natl Cancer Inst. 1999 Apr 7;91(7):614-9
[
10203280.001
]
[Cites]
Mutat Res. 2004 Nov;567(2-3):447-74
[
15572290.001
]
[Cites]
Ann N Y Acad Sci. 2004 Dec;1028:14-27
[
15650228.001
]
[Cites]
BMC Bioinformatics. 2005;6:72
[
15790402.001
]
[Cites]
Clin Cancer Res. 2005 Jun 1;11(11):4128-35
[
15930348.001
]
[Cites]
BMC Bioinformatics. 2005;6:115
[
15890080.001
]
[Cites]
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W741-8
[
15980575.001
]
[Cites]
Cancer Res. 2005 Jul 1;65(13):5561-70
[
15994928.001
]
[Cites]
Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9625-30
[
15983384.001
]
[Cites]
Nature. 2005 Aug 25;436(7054):1103-6
[
16121170.001
]
[Cites]
Int J Cancer. 2006 Mar 15;118(6):1556-64
[
16187286.001
]
[Cites]
N Engl J Med. 2006 Aug 10;355(6):570-80
[
16899777.001
]
[Cites]
J Clin Oncol. 2006 Nov 1;24(31):5079-90
[
17075127.001
]
[Cites]
Nature. 2006 Nov 23;444(7118):444-54
[
17122850.001
]
[Cites]
PLoS Med. 2006 Dec;3(12):e467
[
17194181.001
]
[Cites]
PLoS Med. 2006 Dec;3(12):e486
[
17194187.001
]
[Cites]
CA Cancer J Clin. 2007 Jan-Feb;57(1):43-66
[
17237035.001
]
[Cites]
N Engl J Med. 2007 Feb 15;356(7):731-3
[
17301306.001
]
[Cites]
Nat Med. 2007 Mar;13(3):361-6
[
17334370.001
]
[Cites]
Int J Cancer. 2007 Jun 15;120(12):2687-95
[
17290394.001
]
[Cites]
J Pathol. 2007 May;212(1):91-101
[
17385188.001
]
[Cites]
Am J Respir Crit Care Med. 2007 Sep 1;176(5):505-12
[
17600274.001
]
[Cites]
Nature. 2007 Dec 6;450(7171):893-8
[
17982442.001
]
[Cites]
Proc Natl Acad Sci U S A. 2001 Apr 24;98(9):5116-21
[
11309499.001
]
(PMID = 18776155.001).
[ISSN]
1535-4970
[Journal-full-title]
American journal of respiratory and critical care medicine
[ISO-abbreviation]
Am. J. Respir. Crit. Care Med.
[Language]
ENG
[Grant]
United States / NCI NIH HHS / CA / CA55769; United States / NCI NIH HHS / CA / CA102353; United States / NCI NIH HHS / CA / CA90949; United States / NCI NIH HHS / CA / CA70907; United States / NCI NIH HHS / CA / P50 CA070907
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2720147
52.
Cuzon VC, Yeh PW, Yanagawa Y, Obata K, Yeh HH:
Ethanol consumption during early pregnancy alters the disposition of tangentially migrating GABAergic interneurons in the fetal cortex.
J Neurosci
; 2008 Feb 20;28(8):1854-64
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
This ethanol-induced effect was evident in vivo at embryonic day 14.5 (E14.5) in GAD67 knock-in and
BAC
-Lhx6 embryos, as well as in vitro in isotypic telencephalic slice cocultures obtained from E14.5 embryos exposed to ethanol in utero.
Analysis of heterotypic cocultures indicated that both
cell
-intrinsic and -extrinsic factors contribute to the aberrant migratory profile of MGE-derived cells.
[MeSH-major]
Cell
Movement / drug effects. Cerebral Cortex / drug effects. Cerebral Cortex / embryology. Ethanol / administration & dosage. Interneurons / drug effects. gamma-Aminobutyric Acid / physiology
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
ETHANOL
.
KOMP Repository.
gene/protein/disease-specific - KOMP Repository
(subscription/membership/fee required).
Mouse Genome Informatics (MGI).
Mouse Genome Informatics (MGI)
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18287502.001).
[ISSN]
1529-2401
[Journal-full-title]
The Journal of neuroscience : the official journal of the Society for Neuroscience
[ISO-abbreviation]
J. Neurosci.
[Language]
eng
[Grant]
United States / NIAAA NIH HHS / AA / F31 AA014698; United States / NIMH NIH HHS / MH / R01 MH069826
[Publication-type]
Comparative Study; Journal Article; Research Support, N.I.H., Extramural
[Publication-country]
United States
[Chemical-registry-number]
3K9958V90M / Ethanol; 56-12-2 / gamma-Aminobutyric Acid
53.
Sone S, Matsumoto T, Honda T, Tsushima K, Takayama F, Hanaoka T, Kondo R, Haniuda M:
HRCT features of small peripheral lung carcinomas detected in a low-dose CT screening program.
Acad Radiol
; 2010 Jan;17(1):75-83
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
HRCT features of small peripheral
lung carcinomas
detected in a low-dose CT screening program.
RATIONALE AND OBJECTIVES: To define high-resolution computed tomography (HRCT) features
of lung
cancers detected by computed tomography (CT) screening according to histopathology and prognosis.
METHODS AND MATERIALS: Tumor size, CT value, morphology, and tumor volume doubling time (TVDT) were determined for 10 atypical adenomatous hyperplasias (AAH) and 50
lung
cancers followed between 1996 and 1998 to 2007.
Focal
bronchioloalveolar cell carcinomas
(
BAC
) were denser (mean, -537 HU) than AAH and mostly less dense than -350 HU; all patients remain alive.
All 22
adenocarcinomas
(ADC) were denser than -450 HU (mean, -186 HU); 6 were problematic and measured >-150HU and >10 mm or had >10 mm of central denser zone (CDZ) (partly solid tumors) or tumor size (solid tumor).
Two of four squamous
cell carcinomas
(SCC) measuring 15 and 10 mm, respectively, were problematic.
Two patients with small-
cell lung carcinomas
(SCLC) measuring 15 and 23 mm, respectively, remain alive.
AAH,
BAC
, ADC, and SCC lesions were in general polygonal in shape.
The mean TVDT for AAH,
BAC
, ADC, SCC, and SCLC was 1278, 557, 466, 212, and 103 days, respectively.
[MeSH-major]
Body Burden.
Lung
Neoplasms / radiography. Mass Screening / methods. Radiographic Image Enhancement / methods. Radiography, Thoracic / methods. Tomography, X-Ray Computed / methods
MedlinePlus Health Information.
consumer health - CT Scans
.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19879779.001).
[ISSN]
1878-4046
[Journal-full-title]
Academic radiology
[ISO-abbreviation]
Acad Radiol
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
54.
Murai J, Ikegami D, Okamoto M, Yoshikawa H, Tsumaki N:
Insulation of the ubiquitous Rxrb promoter from the cartilage-specific adjacent gene, Col11a2.
J Biol Chem
; 2008 Oct 10;283(41):27677-87
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
To examine the function of these elements, we prepared
bacterial
artificial chromosome (
BAC
) transgene constructs containing a 142-kb genomic DNA insert with RXRB and COL11A2 sequences in the middle.
In transgenic mouse assays, the wild-type
BAC
transgene partly recapitulated endogenous Rxrb expression patterns.
A 507-bp deletion mutation including 11P enhanced the cartilage-specific activity of the RXRB promoter in
BAC
transgenic mice.
[MeSH-minor]
Animals.
Cell
Line, Tumor. Chromosomes, Artificial,
Bacterial
/ genetics. Enhancer Elements, Genetic / genetics. Introns / genetics. Mice. Mice, Transgenic. Mutation. Rats
KOMP Repository.
gene/protein/disease-specific - KOMP Repository
(subscription/membership/fee required).
Mouse Genome Informatics (MGI).
Mouse Genome Informatics (MGI)
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18682388.001).
[ISSN]
0021-9258
[Journal-full-title]
The Journal of biological chemistry
[ISO-abbreviation]
J. Biol. Chem.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / Col11a2 protein, mouse; 0 / Collagen Type XI; 0 / DNA-Binding Proteins; 0 / Rxrb protein, mouse
55.
González VM, Garcia-Mas J, Arús P, Puigdomènech P:
Generation of a BAC-based physical map of the melon genome.
BMC Genomics
; 2010;11:339
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Generation
of a BAC
-based physical map of the melon genome.
Melon has high intra-specific genetic variation,
morphologic
diversity and a small genome size (450 Mb), which make this species suitable for a great variety of molecular and genetic studies that can lead to the development of tools for breeding varieties of the species.
A number of genetic and genomic resources have already been developed, such as several genetic maps and
BAC
genomic libraries.
These tools are essential for the construction
of a
physical map, a valuable resource for map-based cloning, comparative genomics and assembly of whole genome sequencing data.
A BAC
-based melon physical map will be a useful tool to help assemble and refine the draft genome data that is being produced.
RESULTS: A melon physical map was constructed using a 5.7 x
BAC
library and a genetic map previously developed in our laboratories.
High-information-content fingerprinting (HICF) was carried out on 23,040
BAC
clones, digesting with five restriction enzymes and SNaPshot labeling, followed by contig assembly with FPC software.
The anchoring of 845
BAC
clones to 178 genetic markers (100 RFLPs, 76 SNPs and 2 SSRs) also allowed the genetic positioning of 183 physical map contigs/singletons, representing 55 Mb (12%) of the melon genome, to individual chromosomal loci.
CONCLUSIONS: Here we report the construction of the first physical map
of a
Cucurbitaceae species described so far.
The data presented is already helping to improve the quality of the melon genomic sequence available as a result
of a
project currently being carried out in Spain, adopting a whole genome shotgun approach based on 454 sequencing data.
[MeSH-major]
Chromosomes, Artificial,
Bacterial
/ genetics. Cucumis melo / genetics. Genome, Plant / genetics. Physical Chromosome Mapping / methods
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Genome Res. 2000 Nov;10(11):1772-87
[
11076862.001
]
[Cites]
BMC Bioinformatics. 2009;10:127
[
19405935.001
]
[Cites]
Nature. 2001 Feb 15;409(6822):934-41
[
11237014.001
]
[Cites]
Genome. 2001 Apr;44(2):154-62
[
11341724.001
]
[Cites]
Genomics. 2001 Jun 1;74(2):142-54
[
11386750.001
]
[Cites]
Genome. 2001 Oct;44(5):836-45
[
11681608.001
]
[Cites]
Plant Cell. 2002 Mar;14(3):537-45
[
11910002.001
]
[Cites]
Plant Mol Biol. 2003 Mar;51(5):703-18
[
12678558.001
]
[Cites]
Genomics. 2003 Sep;82(3):378-89
[
12906862.001
]
[Cites]
BMC Plant Biol. 2009;9:90
[
19604363.001
]
[Cites]
BMC Genomics. 2009;10:371
[
19664231.001
]
[Cites]
BMC Genomics. 2009;10:462
[
19814815.001
]
[Cites]
BMC Genomics. 2009;10:467
[
19821986.001
]
[Cites]
BMC Genomics. 2009;10:496
[
19860896.001
]
[Cites]
PLoS Genet. 2009 Nov;5(11):e1000715
[
19936061.001
]
[Cites]
Genome. 2004 Apr;47(2):352-60
[
15060588.001
]
[Cites]
Plant J. 2004 Aug;39(3):283-97
[
15255859.001
]
[Cites]
Nat Genet. 1999 Jul;22(3):271-5
[
10391215.001
]
[Cites]
Nucleic Acids Res. 2005;33(5):e50
[
15767275.001
]
[Cites]
Mol Genet Genomics. 2005 May;273(3):240-51
[
15902490.001
]
[Cites]
Theor Appl Genet. 2005 Sep;111(5):914-22
[
16052354.001
]
[Cites]
Theor Appl Genet. 2005 Dec;112(1):139-48
[
16208502.001
]
[Cites]
Theor Appl Genet. 2006 Jun;113(1):81-9
[
16783592.001
]
[Cites]
Theor Appl Genet. 2006 Jul;113(2):344-56
[
16791700.001
]
[Cites]
Plant J. 2006 Nov;48(3):452-62
[
17026540.001
]
[Cites]
BMC Genomics. 2007;8:40
[
17284319.001
]
[Cites]
BMC Genomics. 2007;8:47
[
17291341.001
]
[Cites]
Genomics. 2007 May;89(5):630-7
[
17270394.001
]
[Cites]
BMC Plant Biol. 2007;7:34
[
17584936.001
]
[Cites]
BMC Genomics. 2007;8:306
[
17767721.001
]
[Cites]
Theor Appl Genet. 2008 Feb;116(4):589-602
[
18094954.001
]
[Cites]
BMC Genomics. 2008;9:28
[
18211698.001
]
[Cites]
BMC Genomics. 2008;9:280
[
18549474.001
]
[Cites]
BMC Plant Biol. 2008;8:66
[
18554400.001
]
[Cites]
Science. 2008 Oct 3;322(5898):101-4
[
18832645.001
]
[Cites]
Theor Appl Genet. 2008 Dec;118(1):139-50
[
18806992.001
]
[Cites]
Theor Appl Genet. 2009 Jan;118(2):275-84
[
18825359.001
]
[Cites]
Nucleic Acids Res. 2009 Apr;37(5):e36
[
19181701.001
]
[Cites]
Genome. 2000 Dec;43(6):963-74
[
11195350.001
]
(PMID = 20509895.001).
[ISSN]
1471-2164
[Journal-full-title]
BMC genomics
[ISO-abbreviation]
BMC Genomics
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Other-IDs]
NLM/ PMC2894041
56.
Ma L, Vu GT, Schubert V, Watanabe K, Stein N, Houben A, Schubert I:
Synteny between Brachypodium distachyon and Hordeum vulgare as revealed by FISH.
Chromosome Res
; 2010 Nov;18(7):841-50
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Of 13
BAC
clones with inserts from different B. distachyon chromosomes, only two belonging to chromosome 1 yielded hybridization signals on a barley metaphase chromosome (on 7HS and 7HL, respectively), confirming synteny between both chromosomes.
Two of four Brachypodium sylvaticum
BACs
spanning a 223-kb interval homologous to the region of barley that harbors a gibberellic-acid-insensitive semi-dwarfing gene, sdw3, hybridized specifically to a central position of B. distachyon chromosome 1 short arm but not to the homologous region of the barley genome.
Repeat-free sequences PCR amplified from four non-overlapping barley
BACs
linked to the core of Sdw3 region yielded signals at distinct positions in the middle of barley chromosome arm 2HS.
[MeSH-minor]
Chromosomes, Artificial,
Bacterial
. Chromosomes, Plant / ultrastructure. Genetic Loci. In Situ Hybridization, Fluorescence
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Funct Integr Genomics. 2004 Mar;4(1):26-33
[
14727148.001
]
[Cites]
Curr Opin Biotechnol. 2010 Apr;21(2):211-7
[
20362425.001
]
[Cites]
Plant Physiol. 2009 Jan;149(1):142-7
[
19126706.001
]
[Cites]
Biotech Histochem. 2006 Mar-Jun;81(2-3):71-8
[
16908431.001
]
[Cites]
Curr Opin Plant Biol. 2010 Apr;13(2):139-45
[
20064738.001
]
[Cites]
Genome. 2006 Sep;49(9):1057-68
[
17110986.001
]
[Cites]
Genetics. 2000 Oct;156(2):833-8
[
11014828.001
]
[Cites]
Genetics. 2006 May;173(1):349-62
[
16489232.001
]
[Cites]
Plant J. 2009 Sep;59(5):712-22
[
19453446.001
]
[Cites]
Plant Physiol. 2001 Dec;127(4):1539-55
[
11743099.001
]
[Cites]
Ann Bot. 2009 Oct;104(5):873-81
[
19633311.001
]
[Cites]
Science. 2009 Nov 20;326(5956):1112-5
[
19965430.001
]
[Cites]
Proc Natl Acad Sci U S A. 2006 Mar 28;103(13):5224-9
[
16549785.001
]
[Cites]
Genome. 1994 Feb;37(1):105-11
[
8181730.001
]
[Cites]
Plant Cell. 2008 Oct;20(10):2559-70
[
18836039.001
]
[Cites]
Nature. 2009 Jan 29;457(7229):551-6
[
19189423.001
]
[Cites]
Chromosome Res. 2004;12(4):397-403
[
15241018.001
]
[Cites]
Chromosome Res. 2007;15(6):711-20
[
17874212.001
]
[Cites]
Cytogenet Genome Res. 2010 Jul;129(1-3):154-61
[
20551612.001
]
[Cites]
Trends Plant Sci. 1999 Jul;4(7):258-263
[
10407441.001
]
[Cites]
Genetics. 2000 Jan;154(1):397-412
[
10628998.001
]
[Cites]
Chromosoma. 2008 Aug;117(4):345-56
[
18317793.001
]
[Cites]
Plant J. 2003 Sep;35(5):647-59
[
12940957.001
]
[Cites]
Genetics. 2007 Jan;175(1):31-9
[
17057234.001
]
[Cites]
Nature. 2010 Feb 11;463(7282):763-8
[
20148030.001
]
[Cites]
Genome Res. 2005 Apr;15(4):516-25
[
15781573.001
]
[Cites]
BMC Genomics. 2008 Oct 31;9:518
[
18976483.001
]
[Cites]
Curr Biol. 1995 Jul 1;5(7):737-9
[
7583118.001
]
[Cites]
Genetics. 2007 Mar;175(3):1047-58
[
17237520.001
]
[Cites]
Funct Integr Genomics. 2010 Nov;10(4):509-21
[
20464438.001
]
(PMID = 21104310.001).
[ISSN]
1573-6849
[Journal-full-title]
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
[ISO-abbreviation]
Chromosome Res.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Netherlands
57.
Kasper K, Kremling C, Geerling G:
[Toxicity of a new moistening agent and preservative in vitro].
Ophthalmologe
; 2008 Jun;105(6):557-62
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
[Toxicity
of a
new moistening agent and preservative in vitro].
PURPOSE: The use of preservatives such as benzalkonium chloride (
BAC
) usually increases the toxicity of pharmaceutical tear substitutes.
We therefore examined the effect of preserved (cetrimide 0.01%) and unpreserved HPMC (hydroxypropylmethyl cellulose) and HP-guar in dose and time-response experiments in a human corneal and conjunctival epithelial
cell
culture model.
The ATP content was quantified by means
of a
luminescence-based ATP assay, intracellular esterase activity by double fluorescent viability staining (calcein AM/ethidium homodimer D-1) and
cell
migration by a colony dispersion assay.
[MeSH-major]
Cell
Movement / drug effects.
Cell
Survival / drug effects. Cetrimonium Compounds / toxicity. Conjunctiva / drug effects. Contact Lens Solutions / toxicity. Epithelial Cells / drug effects. Epithelium, Corneal / drug effects. Methylcellulose / analogs & derivatives. Ophthalmic Solutions / toxicity. Polymers / toxicity. Polysaccharides / toxicity. Preservatives, Pharmaceutical / toxicity
Hazardous Substances Data Bank.
TRIMETHYLHEXADECYLAMMONIUM CHLORIDE
.
Hazardous Substances Data Bank.
METHYL CELLULOSE
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Cornea. 1996 Mar;15(2):120-8
[
8925658.001
]
[Cites]
J Glaucoma. 2005 Aug;14(4):302-4
[
15990612.001
]
[Cites]
Aust N Z J Ophthalmol. 1999 Jun-Aug;27(3-4):214-7
[
10484195.001
]
[Cites]
J Biolumin Chemilumin. 1995 Jan-Feb;10 (1):29-34
[
7762413.001
]
[Cites]
Curr Med Res Opin. 2005 Feb;21(2):255-60
[
15801996.001
]
[Cites]
J Cell Biol. 1997 Jun 16;137(6):1445-57
[
9182674.001
]
[Cites]
Optom Vis Sci. 2002 Dec;79(12):753-61
[
12512683.001
]
[Cites]
Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4309-15
[
17003420.001
]
[Cites]
Cancer Res. 1995 Nov 15;55(22):5276-82
[
7585588.001
]
[Cites]
Adv Ther. 2006 Nov-Dec;23(6):835-41
[
17276951.001
]
[Cites]
Ophthalmologe. 2004 Oct;101(10):998-1005
[
15095107.001
]
[Cites]
J Ocul Pharmacol Ther. 2006 Aug;22(4):267-78
[
16910868.001
]
[Cites]
Invest Ophthalmol Vis Sci. 1995 Mar;36(3):614-21
[
7534282.001
]
[Cites]
Invest Ophthalmol Vis Sci. 2007 Apr;48(4):1559-67
[
17389485.001
]
[Cites]
Br J Ophthalmol. 2006 Feb;90(2):139-41
[
16424520.001
]
[Cites]
Curr Eye Res. 1991 Jul;10(7):645-56
[
1914501.001
]
[Cites]
J Fr Ophtalmol. 1999 Nov;22(9):950-8
[
10609169.001
]
[Cites]
Transfus Med. 2005 Apr;15(2):107-13
[
15859976.001
]
[Cites]
J Antimicrob Chemother. 2003 May;51(5):1153-8
[
12697638.001
]
[Cites]
CLAO J. 1989 Jan-Mar;15(1):57-60
[
2917399.001
]
[Cites]
Ophthalmic Res. 2000 Jan-Feb;32(1):3-8
[
10657748.001
]
[Cites]
Curr Eye Res. 2004 Jun;28(6):437-44
[
15512952.001
]
[Cites]
Invest Ophthalmol Vis Sci. 2006 Jun;47(6):2438-44
[
16723454.001
]
[Cites]
Lens Eye Toxic Res. 1989;6(3):395-403
[
2486935.001
]
[Cites]
Curr Eye Res. 2004 Jan;28(1):55-62
[
14704914.001
]
[Cites]
Invest Ophthalmol Vis Sci. 2001 Apr;42(5):948-56
[
11274071.001
]
[Cites]
Graefes Arch Clin Exp Ophthalmol. 1997 May;235(5):268-76
[
9176674.001
]
[Cites]
Curr Eye Res. 1986 May;5(5):367-72
[
3720343.001
]
[Cites]
J Formos Med Assoc. 2005 Dec;104(12):968-71
[
16607459.001
]
[Cites]
Cont Lens Anterior Eye. 2006 Mar;29(1):31-40
[
16473547.001
]
[Cites]
Lens Eye Toxic Res. 1992;9(3-4):361-75
[
1301792.001
]
(PMID = 18214492.001).
[ISSN]
0941-293X
[Journal-full-title]
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
[ISO-abbreviation]
Ophthalmologe
[Language]
ger
[Publication-type]
Comparative Study; English Abstract; Journal Article
[Publication-country]
Germany
[Chemical-registry-number]
0 / Cetrimonium Compounds; 0 / Contact Lens Solutions; 0 / Ophthalmic Solutions; 0 / Polymers; 0 / Polysaccharides; 0 / Preservatives, Pharmaceutical; 0 / hydroxypropyl guar; 3NXW29V3WO / Hypromellose Derivatives; 75345-27-6 / polyquaternium 1; 8L70Q75FXE / Adenosine Triphosphate; 9004-67-5 / Methylcellulose; EC 3.1.- / Esterases; Z7FF1XKL7A / cetrimonium
58.
Luo SJ, Johnson WE, David VA, Menotti-Raymond M, Stanyon R, Cai QX, Beck T, Yuhki N, Pecon-Slattery J, Smith JL, O'Brien SJ:
Development of Y chromosome intraspecific polymorphic markers in the Felidae.
J Hered
; 2007;98(5):400-13
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
We were able to identify new male-specific polymorphisms in the domestic cat Felis catus and 6 additional Felidae species with a combination of molecular genetic and cytogenetic approaches including 1) identifying domestic cat male-specific microsatellites from markers generated from a male cat microsatellite-enriched genomic library, a flow-sorted Y cosmid library, or a Y-specific cat bacteria artificial chromosome (
BAC
) clone, (2) constructing microsatellite-enriched libraries from flow-sorted Y chromosomes isolated directly from focal wildcat species, and (3) screening Y chromosome conserved anchored tagged sequences primers in Felidae species.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17646273.001).
[ISSN]
0022-1503
[Journal-full-title]
The Journal of heredity
[ISO-abbreviation]
J. Hered.
[Language]
eng
[Grant]
United States / NCI NIH HHS / CO / N01-CO-12400
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / DNA Primers
59.
Van Keuren ML, Gavrilina GB, Filipiak WE, Zeidler MG, Saunders TL:
Generating transgenic mice from bacterial artificial chromosomes: transgenesis efficiency, integration and expression outcomes.
Transgenic Res
; 2009 Oct;18(5):769-85
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Generating transgenic mice from
bacterial
artificial chromosomes: transgenesis efficiency, integration and expression outcomes.
Bacterial
artificial chromosome (
BAC
) transgenes direct gene expression at physiological levels with the same developmental timing and expression patterns as endogenous genes in transgenic animal models.
We generated 707 transgenic founders from 86
BAC
transgenes purified by three different methods.
Transgenesis efficiency was the same for all
BAC
DNA purification methods.
Polyamine microinjection buffer was essential for successful integration of intact
BAC
transgenes.
There was no correlation between
BAC
size and transgenic rate, birth rate, or transgenic efficiency.
Founders with complete
BAC
integrations were observed in all 47
BACs
for which multiple markers were tested.
Additional founders with
BAC
fragment integrations were observed for 65% of these
BACs
.
Expression data was available for 79
BAC
transgenes and expression was observed in transgenic founders from 63
BACs
(80%).
Consistent and reproducible success in
BAC
transgenesis required the combination of careful DNA purification, the use of polyamine buffer, and sensitive genotyping assays.
COS Scholar Universe.
author profiles
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Genome Res. 2000 Jan;10(1):116-28
[
10645956.001
]
[Cites]
Regul Pept. 2008 Nov 29;151(1-3):115-22
[
18456349.001
]
[Cites]
Dev Biol. 2001 May 1;233(1):214-24
[
11319870.001
]
[Cites]
Transgenic Res. 2001 Jun;10(3):211-21
[
11437278.001
]
[Cites]
Biotechnol Prog. 2002 Jan-Feb;18(1):82-7
[
11822904.001
]
[Cites]
Annu Rev Genet. 2002;36:361-88
[
12429697.001
]
[Cites]
Nat Biotechnol. 2003 Apr;21(4):443-7
[
12627172.001
]
[Cites]
Blood. 2003 Oct 15;102(8):2856-61
[
12855561.001
]
[Cites]
Nature. 2003 Oct 16;425(6959):721-7
[
14534547.001
]
[Cites]
Genes Dev. 2003 Nov 1;17(21):2664-74
[
14563677.001
]
[Cites]
Genesis. 2004 Jan;38(1):39-50
[
14755803.001
]
[Cites]
Development. 2004 Aug;131(16):3907-20
[
15289434.001
]
[Cites]
J Immunol. 2004 Nov 1;173(9):5531-9
[
15494502.001
]
[Cites]
J Mol Biol. 1975 Nov 5;98(3):503-17
[
1195397.001
]
[Cites]
Cell. 1983 Jul;33(3):705-16
[
6307525.001
]
[Cites]
Proc Natl Acad Sci U S A. 1985 Jul;82(13):4438-42
[
3892534.001
]
[Cites]
EMBO J. 1985 Jul;4(7):1715-23
[
2992937.001
]
[Cites]
J Cell Sci. 1986 Mar;81:143-62
[
3733894.001
]
[Cites]
Science. 1987 Jan 2;235(4784):53-8
[
2432657.001
]
[Cites]
Science. 1988 Jan 29;239(4839):487-91
[
2448875.001
]
[Cites]
Annu Rev Cell Biol. 1990;6:679-714
[
2275824.001
]
[Cites]
Proc Natl Acad Sci U S A. 1991 May 15;88(10):4123-7
[
2034658.001
]
[Cites]
Nature. 1993 Mar 18;362(6417):258-61
[
8459851.001
]
[Cites]
Transgenic Res. 1992 Jul;1(4):182-7
[
1301211.001
]
[Cites]
J Biol Chem. 1993 Nov 15;268(32):23747-50
[
8226902.001
]
[Cites]
Nucleic Acids Res. 1993 Oct 11;21(20):4783-7
[
8233827.001
]
[Cites]
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2130-4
[
8134359.001
]
[Cites]
J Mol Biol. 1995 Mar 3;246(4):486-92
[
7877169.001
]
[Cites]
Electrophoresis. 1995 Jan;16(1):1-7
[
7737080.001
]
[Cites]
Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):9067-72
[
8799155.001
]
[Cites]
Genomics. 1996 Aug 1;35(3):405-14
[
8812473.001
]
[Cites]
Reprod Nutr Dev. 1996;36(6):607-18
[
9021872.001
]
[Cites]
Cell. 1997 May 16;89(4):655-67
[
9160756.001
]
[Cites]
J Biol Chem. 1997 Nov 21;272(47):29752-8
[
9368045.001
]
[Cites]
Science. 1998 May 29;280(5368):1444-7
[
9603735.001
]
[Cites]
Lab Anim. 1998 Oct;32(4):407-13
[
9807753.001
]
[Cites]
J Exp Med. 2005 May 2;201(9):1459-66
[
15851486.001
]
[Cites]
Dev Dyn. 2006 May;235(5):1413-32
[
16586440.001
]
[Cites]
Nature. 2007 Jul 19;448(7151):313-7
[
17554338.001
]
[Cites]
Mamm Genome. 2007 Oct;18(10):693-708
[
17882484.001
]
[Cites]
Evol Dev. 2008 Jul-Aug;10(4):421-32
[
18638319.001
]
[Cites]
Genesis. 2008 Aug;46(8):390-5
[
18693271.001
]
[Cites]
Transgenic Res. 2001 Apr;10(2):83-103
[
11305364.001
]
(PMID = 19396621.001).
[ISSN]
1573-9368
[Journal-full-title]
Transgenic research
[ISO-abbreviation]
Transgenic Res.
[Language]
ENG
[Grant]
United States / NCI NIH HHS / CA / P30 CA046592; United States / NCI NIH HHS / CA / CA046592-14; United States / NIDDK NIH HHS / DK / DK034933; United States / NIDDK NIH HHS / DK / P30 DK034933; United States / NIAMS NIH HHS / AR / AR048310; United States / NCI NIH HHS / CA / P30 CA046592-14; United States / NIAMS NIH HHS / AR / P30 AR048310; United States / NIA NIH HHS / AG / P30 AG013283; United States / NCI NIH HHS / CA / CA046592; United States / NIA NIH HHS / AG / AG013283
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural
[Publication-country]
Netherlands
[Chemical-registry-number]
0 / DNA, Bacterial
[Other-IDs]
NLM/ NIHMS243268; NLM/ PMC3016422
60.
Dhingra A, Folta KM:
ASAP: amplification, sequencing & annotation of plastomes.
BMC Genomics
; 2005;6:176
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Traditionally, the first step in mining the valuable information within a chloroplast genome requires sequencing a chloroplast plasmid library or
BAC
clones.
These activities involve complicated preparatory procedures like chloroplast DNA isolation or identification of the appropriate
BAC
clones to be sequenced.
COS Scholar Universe.
author profiles
.
SILVA.
SILVA LSU Database
.
SILVA.
SILVA SSU Database
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Plant Cell. 2005 Mar;17(3):665-75
[
15705954.001
]
[Cites]
Methods Enzymol. 2005;395:348-84
[
15865976.001
]
[Cites]
Trends Biotechnol. 2005 May;23(5):238-45
[
15866001.001
]
[Cites]
Trends Plant Sci. 2005 May;10(5):203-9
[
15882651.001
]
[Cites]
Gene. 2005 May 9;350(2):117-28
[
15788152.001
]
[Cites]
BMC Plant Biol. 2005;5:12
[
15985176.001
]
[Cites]
Plant Mol Biol. 2005 Sep;59(2):309-22
[
16247559.001
]
[Cites]
Methods Mol Biol. 2006;323:245-62
[
16739583.001
]
[Cites]
DNA Res. 1999 Oct 29;6(5):283-90
[
10574454.001
]
[Cites]
DNA Res. 2000 Dec 31;7(6):323-30
[
11214967.001
]
[Cites]
Plant Mol Biol. 2001 Feb;45(3):307-15
[
11292076.001
]
[Cites]
Mol Genet Genomics. 2002 Jan;266(5):740-6
[
11810247.001
]
[Cites]
Mol Biol Evol. 2002 Sep;19(9):1602-12
[
12200487.001
]
[Cites]
DNA Res. 2003 Apr 30;10(2):59-65
[
12755170.001
]
[Cites]
Mol Biol Evol. 2003 Sep;20(9):1499-505
[
12832641.001
]
[Cites]
Mol Biol (Mosk). 2003 Sep-Oct;37(5):768-83
[
14593913.001
]
[Cites]
Plant Physiol. 2004 Sep;136(1):2843-54
[
15347789.001
]
[Cites]
Annu Rev Plant Biol. 2004;55:289-313
[
15377222.001
]
[Cites]
DNA Res. 2004 Apr 30;11(2):93-9
[
15449542.001
]
[Cites]
Trends Plant Sci. 2004 Oct;9(10):477-83
[
15465682.001
]
[Cites]
DNA Res. 2004 Aug 31;11(4):247-61
[
15500250.001
]
[Cites]
Annu Rev Genet. 1985;19:325-54
[
3936406.001
]
[Cites]
Mol Gen Genet. 1989 Jun;217(2-3):185-94
[
2770692.001
]
[Cites]
Nucleic Acids Res. 1991 Jul 25;19(14):4008
[
1861999.001
]
[Cites]
Biotechniques. 1992 Mar;12(3):332-4
[
1571138.001
]
[Cites]
J Mol Biol. 1995 Sep 1;251(5):614-28
[
7666415.001
]
[Cites]
Curr Genet. 1997 May;31(5):419-29
[
9162114.001
]
[Cites]
FEMS Microbiol Lett. 1999 May 15;174(2):247-50
[
10339815.001
]
[Cites]
Genome Res. 1999 Sep;9(9):868-77
[
10508846.001
]
[Cites]
Bioinformatics. 2004 Nov 22;20(17):3252-5
[
15180927.001
]
[Cites]
Plant Mol Biol. 2004 Sep;56(2):203-16
[
15604738.001
]
(PMID = 16336644.001).
[ISSN]
1471-2164
[Journal-full-title]
BMC genomics
[ISO-abbreviation]
BMC Genomics
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
England
[Chemical-registry-number]
0 / DNA Primers; 0 / DNA, Chloroplast; 0 / DNA, Plant
[Other-IDs]
NLM/ PMC1318494
61.
Tjia WM, Hu L, Zhang MY, Guan XY:
Characterization of rearrangements involving 4q, 13q and 16q in hepatocellular carcinoma cell lines using region-specific multiplex-FISH probes.
Cancer Lett
; 2007 May 18;250(1):92-9
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Characterization of rearrangements involving 4q, 13q and 16q in hepatocellular
carcinoma cell
lines using region-specific multiplex-FISH probes.
Deletions in 4q, 13q and 16q were frequently detected in hepatocellular
carcinoma
(HCC) by comparative genomic hybridization (CGH) studies.
Using CGH combined with multiplex-color FISH (M-FISH) with chromosome region-specific probes (CRPs), chromosome structural aberrations in 4q, 13q and 16q in six HCC
cell
lines were studied.
FISH with
BAC
probes was used to further characterize translocation breakpoints and deletions.
A breakpoint at 16q22 was localized at
a BAC
clone (RP11-341K23) and another breakpoint at 4q28 was localized within a 620 kb-region.
A minimal deleted region at 13q21 was found between
BAC
clones RP11-240M20 and RP11-435P18.
This study demonstrated that the combination of CGH, M-FISH and
BAC
-FISH is a very useful tool to detect and characterize translocation breakpoint.
[MeSH-major]
Carcinoma
, Hepatocellular / genetics. Chromosome Aberrations. Chromosomes, Human, Pair 13. Chromosomes, Human, Pair 16. Chromosomes, Human, Pair 4. In Situ Hybridization, Fluorescence / methods. Liver Neoplasms / genetics
[MeSH-minor]
Cell
Line, Tumor. Humans. Translocation, Genetic
MedlinePlus Health Information.
consumer health - Liver Cancer
.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17098359.001).
[ISSN]
0304-3835
[Journal-full-title]
Cancer letters
[ISO-abbreviation]
Cancer Lett.
[Language]
eng
[Publication-type]
Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Ireland
62.
Guo W, Cai C, Wang C, Zhao L, Wang L, Zhang T:
A preliminary analysis of genome structure and composition in Gossypium hirsutum.
BMC Genomics
; 2008;9:314
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Here, we employed GeneTrek and
BAC
tagging information approaches to predict the general composition and structure of the allotetraploid cotton genome.
RESULTS: 142
BAC
sequences from Gossypium hirsutum cv.
These
BAC
sequence analysis revealed that the tetraploid cotton genome contains over 70,000 candidate genes with duplicated gene copies in homoeologous A- and D-subgenome regions.
Twenty-one percent of the 142
BACs
lacked genes.
BAC
gene density ranged from 0 to 33.2 per 100 kb, whereas most gene islands contained only one gene with an average of 1.5 genes per island.
In addition, 166 polymorphic loci amplified with SSRs developed from 70
BAC
clones were tagged on our backbone genetic map.
Hai7124, and diploid G. herbaceum var. africanum and G. raimondii, 37
BACs
, 12 from
the A
- and 25 from the D-subgenome, were further anchored to their corresponding subgenome chromosomes.
After a large amount of genes sequence comparison from different subgenome
BACs
, the result showed that introns might have no contribution to different subgenome size in Gossypium.
[MeSH-major]
Chromosomes, Artificial,
Bacterial
. Genome, Plant. Gossypium / genetics. Polyploidy. Sequence Analysis, DNA
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Trends Genet. 2000 Sep;16(9):418-20
[
10973072.001
]
[Cites]
Plant Physiol. 2007 Dec;145(4):1303-10
[
18056866.001
]
[Cites]
Genome Res. 2001 Aug;11(8):1441-52
[
11483586.001
]
[Cites]
Plant Physiol. 2001 Dec;127(4):1361-6
[
11743074.001
]
[Cites]
Nat Genet. 2002 Feb;30(2):194-200
[
11799393.001
]
[Cites]
Mol Biol Evol. 2002 May;19(5):597-607
[
11961094.001
]
[Cites]
Genetics. 2002 Dec;162(4):1961-77
[
12524363.001
]
[Cites]
Theor Appl Genet. 2003 Feb;106(3):384-96
[
12589538.001
]
[Cites]
Mol Phylogenet Evol. 2003 Dec;29(3):380-95
[
14615181.001
]
[Cites]
Genome Res. 2004 Aug;14(8):1474-82
[
15256507.001
]
[Cites]
Curr Opin Plant Biol. 2004 Dec;7(6):732-6
[
15491923.001
]
[Cites]
Comput Chem. 1996 Mar;20(1):119-21
[
8867843.001
]
[Cites]
J Mol Biol. 1997 Apr 25;268(1):78-94
[
9149143.001
]
[Cites]
Nucleic Acids Res. 1998 Feb 15;26(4):1107-15
[
9461475.001
]
[Cites]
Genome Res. 1998 May;8(5):479-92
[
9582192.001
]
[Cites]
Mol Biol Evol. 1999 Apr;16(4):491-501
[
10331275.001
]
[Cites]
Nucleic Acids Res. 1999 Aug 1;27(15):3219-28
[
10454621.001
]
[Cites]
J Hered. 2005 Mar-Apr;96(2):132-44
[
15618303.001
]
[Cites]
Mol Genet Genomics. 2005 Nov;274(4):428-41
[
16187061.001
]
[Cites]
Plant Mol Biol. 2000 Jan;42(1):225-49
[
10688139.001
]
[Cites]
Plant Physiol. 2005 Dec;139(4):1612-24
[
16339807.001
]
[Cites]
Proc Natl Acad Sci U S A. 2005 Dec 27;102(52):19243-8
[
16357197.001
]
[Cites]
Genome Res. 2006 Mar;16(3):441-50
[
16478941.001
]
[Cites]
Plant J. 2006 Sep;47(5):761-75
[
16889650.001
]
[Cites]
Genome Res. 2006 Oct;16(10):1252-61
[
16954538.001
]
[Cites]
Genetics. 2007 May;176(1):527-41
[
17409069.001
]
[Cites]
Plant J. 2007 Jun;50(6):995-1006
[
17461788.001
]
[Cites]
Proc Natl Acad Sci U S A. 2007 Jul 10;104(28):11844-9
[
17615239.001
]
[Cites]
Evol Dev. 2001 Jan-Feb;3(1):3-17
[
11256432.001
]
(PMID = 18590573.001).
[ISSN]
1471-2164
[Journal-full-title]
BMC genomics
[ISO-abbreviation]
BMC Genomics
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / Genetic Markers; 0 / Retroelements
[Other-IDs]
NLM/ PMC2481271
63.
Vorstman JA, Jalali GR, Rappaport EF, Hacker AM, Scott C, Emanuel BS:
MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q.
Hum Mutat
; 2006 Aug;27(8):814-21
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
All samples in the training set have been previously characterized by fluorescence in situ hybridization (FISH) with cosmid or
BAC
clones and/or cytogenetic studies.
Given that MLPA is likely to be used as an initial screening method, a higher sensitivity, at the cost
of a
lower specificity, was deemed more appropriate.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Am J Hum Genet. 1999 Dec;65(6):1595-607
[
10577913.001
]
[Cites]
Genet Med. 2001 Jan-Feb;3(1):6-13
[
11339380.001
]
[Cites]
Clin Genet. 2005 Oct;68(4):373-8
[
16143025.001
]
[Cites]
Adv Pediatr. 2001;48:39-73
[
11480765.001
]
[Cites]
Nat Rev Genet. 2001 Oct;2(10):791-800
[
11584295.001
]
[Cites]
Curr Opin Pediatr. 2001 Dec;13(6):550-5
[
11753105.001
]
[Cites]
Nucleic Acids Res. 2002 Jun 15;30(12):e57
[
12060695.001
]
[Cites]
Am J Hum Genet. 2003 Mar;72(3):733-8
[
12557125.001
]
[Cites]
Pediatrics. 2003 Jul;112(1 Pt 1):101-7
[
12837874.001
]
[Cites]
Hum Mol Genet. 2003 Aug 1;12(15):1823-37
[
12874103.001
]
[Cites]
Hum Mol Genet. 2003 Nov 1;12(21):2817-25
[
12952865.001
]
[Cites]
Am J Hum Genet. 2003 Nov;73(5):1027-40
[
14526392.001
]
[Cites]
Hum Mutat. 2004 May;23(5):413-9
[
15108271.001
]
[Cites]
Science. 2004 Jul 23;305(5683):525-8
[
15273396.001
]
[Cites]
Br J Cancer. 2004 Sep 13;91(6):1155-9
[
15475941.001
]
[Cites]
Hum Genet. 1981;57(3):253-6
[
7250965.001
]
[Cites]
Science. 1986 May 2;232(4750):646-8
[
3961499.001
]
[Cites]
J Med Genet. 1996 Aug;33(8):719
[
8863171.001
]
[Cites]
J Med Genet. 1997 Oct;34(10):798-804
[
9350810.001
]
[Cites]
Cytogenet Cell Genet. 1997;78(3-4):247-52
[
9465898.001
]
[Cites]
Am J Med Genet. 1998 Apr 28;77(1):8-11
[
9557885.001
]
[Cites]
Arch Dis Child. 1998 Oct;79(4):348-51
[
9875047.001
]
[Cites]
J Pediatr. 1999 Feb;134(2):193-8
[
9931529.001
]
[Cites]
Genet Couns. 1999;10(1):11-24
[
10191425.001
]
[Cites]
Genet Couns. 1999;10(1):89-93
[
10191434.001
]
[Cites]
Hum Mol Genet. 1999 Jul;8(7):1157-67
[
10369860.001
]
[Cites]
Am J Med Genet. 1999 Jul 16;85(2):127-33
[
10406665.001
]
[Cites]
Am J Hum Genet. 2005 May;76(5):865-76
[
15800846.001
]
[Cites]
Am J Med Genet A. 2005 Aug 15;137(1):47-51
[
16007629.001
]
(PMID = 16791841.001).
[ISSN]
1098-1004
[Journal-full-title]
Human mutation
[ISO-abbreviation]
Hum. Mutat.
[Language]
ENG
[Grant]
United States / NCI NIH HHS / CA / CA 39926; United States / NICHD NIH HHS / HD / HD26979; United States / NICHD NIH HHS / HD / P30 HD026979; United States / NCI NIH HHS / CA / R01 CA039926-18; United States / NCI NIH HHS / CA / CA039926-18; United States / NIDCD NIH HHS / DC / DC02027; United States / NCI NIH HHS / CA / R01 CA039926; United States / NIDCD NIH HHS / DC / P01 DC002027
[Publication-type]
Evaluation Studies; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Other-IDs]
NLM/ NIHMS160121; NLM/ PMC2814414
64.
Park JH, Lee KS, Kim JH, Shim YM, Kim J, Choi YS, Yi CA:
Malignant pure pulmonary ground-glass opacity nodules: prognostic implications.
Korean J Radiol
; 2009 Jan-Feb;10(1):12-20
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Malignant
pure pulmonary ground-glass opacity nodules: prognostic implications.
OBJECTIVE: This study was designed to evaluate follow-up results in terms of patient prognosis for
malignant
pulmonary nodules depicted as pure ground-glass opacity (GGO) lesion observed at high-resolution CT (HRCT).
MATERIALS AND METHODS: Surgical removal for
malignant
GGO nodules was accomplished in 58 patients (26 men, 32 women; mean age, 57 years; age range, 29-78 years).
Differences in patient prognoses were compared for nodule number, size, surgical method, change in size before surgical removal, and histopathological
diagnosis
by use of Fisher's exact test and Pearson's chi-squared test.
RESULTS: Of the 58 patients, 40 patients (69%) were confirmed to have
a bronchioloalveolar carcinoma
(
BAC
) and 18 patients (31%) were confirmed to have an
adenocarcinoma
with a predominant
BAC
component.
Irrespective of nodule size, number, treatment method, change in size before surgical removal and histopathological
diagnosis
, neither local recurrence nor a metastasis occurred in any of these patients as determined at a follow-up period of 24 months (range; 12-65 months).
CONCLUSION: Prognoses in patients with pure GGO
malignant
pulmonary nodules are excellent, and not significantly different in terms of nodule number, size, surgical method, presence of size change before surgical removal and histopathological
diagnosis
.
[MeSH-major]
Lung
Neoplasms / radiography. Multiple Pulmonary Nodules / radiography. Solitary Pulmonary Nodule / radiography. Tomography, X-Ray Computed
[MeSH-minor]
Adenocarcinoma
/ pathology.
Adenocarcinoma
/ radiography.
Adenocarcinoma
/ surgery.
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ pathology.
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ radiography.
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ surgery. Adult. Female. Humans. Male. Middle Aged. Prognosis. Young Adult
MedlinePlus Health Information.
consumer health - CT Scans
.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Br J Radiol. 2000 Dec;73(876):1252-9
[
11205667.001
]
[Cites]
J Thorac Cardiovasc Surg. 2007 Oct;134(4):877-82
[
17903500.001
]
[Cites]
Ann Thorac Surg. 2002 Feb;73(2):386-92; discussion 392-3
[
11845847.001
]
[Cites]
AJR Am J Roentgenol. 2002 May;178(5):1053-7
[
11959700.001
]
[Cites]
Ann Thorac Surg. 2002 Apr;73(4):1071-5
[
11996243.001
]
[Cites]
Ann Thorac Surg. 2003 Oct;76(4):1016-22
[
14529977.001
]
[Cites]
J Comput Assist Tomogr. 2004 Jan-Feb;28(1):17-23
[
14716227.001
]
[Cites]
Clin Cancer Res. 2004 Jun 15;10(12 Pt 2):4205s-4209s
[
15217959.001
]
[Cites]
J Thorac Cardiovasc Surg. 2005 May;129(5):991-6
[
15867771.001
]
[Cites]
Semin Roentgenol. 2005 Apr;40(2):90-7
[
15898407.001
]
[Cites]
Ann Thorac Surg. 2006 Feb;81(2):413-9
[
16427823.001
]
[Cites]
J Clin Pathol. 2006 Jun;59(6):663-4
[
16731609.001
]
[Cites]
Eur J Cardiothorac Surg. 2006 Jul;30(1):160-3
[
16723239.001
]
[Cites]
Radiology. 2007 Feb;242(2):555-62
[
17255425.001
]
[Cites]
Korean J Radiol. 2007 Jan-Feb;8(1):22-31
[
17277560.001
]
[Cites]
Radiology. 2007 Oct;245(1):267-75
[
17885195.001
]
[Cites]
Cancer. 2001 Oct 25;93(5):330-6
[
11668468.001
]
(PMID = 19182498.001).
[ISSN]
1229-6929
[Journal-full-title]
Korean journal of radiology
[ISO-abbreviation]
Korean J Radiol
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Korea (South)
[Other-IDs]
NLM/ PMC2647178
65.
Kim YT, Kim TY, Lee DS, Park SJ, Park JY, Seo SJ, Choi HS, Kang HJ, Hahn S, Kang CH, Sung SW, Kim JH:
Molecular changes of epidermal growth factor receptor (EGFR) and KRAS and their impact on the clinical outcomes in surgically resected adenocarcinoma of the lung.
Lung Cancer
; 2008 Jan;59(1):111-8
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Molecular changes of epidermal growth factor receptor (EGFR) and KRAS and their impact on the clinical outcomes in surgically resected
adenocarcinoma of the lung
.
Recent studies have reported that clinical response to epidermal growth factor receptor (EGFR) inhibitors is associated with somatic changes of EGFR in the advanced stage
of lung cancer
.
However, there is no clear data demonstrating whether such molecular changes of EGFR per se can affect the clinical outcome of early stage
cancer
after surgical resection.
DNA mutations of EGFR and KRAS were investigated in 71
adenocarcinoma
patients who received surgical resection.
EGFR mutation was more frequently found in cases with
BAC
features (13/22 (59.1%):13/49 (26.5%); p=0.008) and in non-smokers (19/41 (46.3%):7/30 (23.3%); p=0.047).
KRAS mutations (p=0.000), male gender (p=0.001), absence
of BAC
feature (p=0.003), advanced stage (p=0.039), and smoking history (p=0.030) were poor prognostic factors for overall survival, whereas EGFR mutation (p=0.184) and amplification (p=0.756) were not.
The presence of EGFR mutation was not a prognostic factor of the clinical outcome of early
lung cancer
after surgical resection.
This result provides an important message for the protocol design of future trials of EGFR inhibitors in early
lung cancer
.
DNA mutations of EGFR and KRAS were investigated in 71
adenocarcinoma
patients who received surgical resection.
Whereas KRAS mutation was a poor prognostic factor, EGFR mutation was not, and its presence per se did not affect the clinical outcome of early
lung cancer
after surgical resection.
[MeSH-major]
Adenocarcinoma
/ genetics. Genes, ras.
Lung
Neoplasms / genetics. Mutation. Receptor, Epidermal Growth Factor / genetics
MedlinePlus Health Information.
consumer health - Lung Cancer
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17904685.001).
[ISSN]
0169-5002
[Journal-full-title]
Lung cancer (Amsterdam, Netherlands)
[ISO-abbreviation]
Lung Cancer
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Ireland
[Chemical-registry-number]
EC 2.7.10.1 / Receptor, Epidermal Growth Factor
66.
Domi A, Moss B:
Engineering of a vaccinia virus bacterial artificial chromosome in Escherichia coli by bacteriophage lambda-based recombination.
Nat Methods
; 2005 Feb;2(2):95-7
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Engineering
of a
vaccinia virus
bacterial
artificial chromosome in Escherichia coli by bacteriophage lambda-based recombination.
Here we describe how
a bacterial
artificial chromosome (
BAC
) containing the entire VAC genome can be engineered in Escherichia coli by homologous recombination using bacteriophage lambda-encoded enzymes.
[MeSH-major]
Bacteriophage lambda / genetics. Chromosomes, Artificial,
Bacterial
/ genetics. Escherichia coli / genetics. Escherichia coli / virology. Genetic Engineering / methods. Transfection / methods. Vaccinia / genetics
[MeSH-minor]
Cloning, Molecular / methods. Genome,
Bacterial
. Genome, Viral. Recombination, Genetic / genetics. Transformation,
Bacterial
/ genetics
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 15782205.001).
[ISSN]
1548-7091
[Journal-full-title]
Nature methods
[ISO-abbreviation]
Nat. Methods
[Language]
eng
[Publication-type]
Evaluation Studies; Journal Article
[Publication-country]
United States
67.
Serikawa T, Mashimo T, Takizawa A, Okajima R, Maedomari N, Kumafuji K, Tagami F, Neoda Y, Otsuki M, Nakanishi S, Yamasaki K, Voigt B, Kuramoto T:
National BioResource Project-Rat and related activities.
Exp Anim
; 2009 Jul;58(4):333-41
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
This review article introduces NBRP-Rat and highlights the phenome project, recombinant inbred strains,
BAC
clone libraries, and the ENU-mutant archive, named the Kyoto University Rat Mutant Archive (KURMA).
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19654430.001).
[ISSN]
1881-7122
[Journal-full-title]
Experimental animals
[ISO-abbreviation]
Exp. Anim.
[Language]
ENG
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Review
[Publication-country]
Japan
[Number-of-references]
29
68.
Pérez López ME, GarcÃa Mata J, GarcÃa Gómez J, Salgado Fernández M, FÃrvida Pérez JL:
[Prostate adenocarcinoma and synchcronous multiple myeloma: a case report].
Actas Urol Esp
; 2007 Feb;31(2):157-9
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
[Prostate
adenocarcinoma
and synchcronous multiple myeloma: a case report].
[Transliterated title]
Adenocarcinoma
prostático y mieloma múltiple sincrónicos: a propósito
de
un caso.
PURPOSE: To report a case of synchronous prostatic
cancer
with multiple myeloma as inusual neoplasm presentation.
To indicate the clinical data that they help to suspect the myeloma presence in the prostate bone metastatic
disease
.
CASE REPORT: Patient 63 years old diagnosed of prostatic
carcinoma
with bone metastasis and
BAC
good responsive, who have clinical deterioration, hypercalcemia and renal insufficiency.
[MeSH-major]
Adenocarcinoma
/
diagnosis
. Multiple Myeloma /
diagnosis
. Neoplasms, Multiple Primary /
diagnosis
. Prostatic Neoplasms /
diagnosis
Genetic Alliance.
consumer health - Multiple myeloma
.
MedlinePlus Health Information.
consumer health - Multiple Myeloma
.
MedlinePlus Health Information.
consumer health - Prostate Cancer
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17645096.001).
[ISSN]
0210-4806
[Journal-full-title]
Actas urologicas españolas
[ISO-abbreviation]
Actas Urol Esp
[Language]
spa
[Publication-type]
Case Reports; English Abstract; Journal Article
[Publication-country]
Spain
69.
Fan ZC, Bird RC:
Generation and characterization of an Npro-disrupted marker bovine viral diarrhea virus derived from a BAC cDNA.
J Virol Methods
; 2008 Aug;151(2):257-63
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Generation and characterization of an Npro-disrupted marker bovine viral diarrhea virus derived from
a BAC
cDNA.
In this study, an N(pro)-disrupted cDNA, pBSD1-N(pro)/eGFP2A, was constructed based on an infectious full-length
BAC
cDNA clone of NCP BVDV strain SD1, pBSD1.
In this clone, whole N(pro) gene except its first 57 nucleotides (nt) was in frame substituted with an eGFP2A sequence. eGFP2A was constructed by in frame fusing a foot-and-mouth
disease
virus 2A protease (FMDV 2A(pro)) to C-terminus of eGFP.
Intramolecular cleavage of FMDV 2A(pro) at its C-
terminal
glycine-proline dipeptide will release the viral nucleocapsid protein from the nascent viral polyprotein and the processed eGFP2A protein will then act as a marker protein.
The resulting
BAC
cDNA clone was propagated stably for at least 10 passages in E. coli strain XL1-blue as determined by sequencing the progeny plasmids.
[MeSH-minor]
Animals. Bovine Virus Diarrhea-Mucosal
Disease
/ epidemiology. Cattle.
Cell
Line. DNA Primers. DNA, Complementary. Genes, Reporter. Genetic Markers. Immunoblotting. Kidney. United States / epidemiology
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18555541.001).
[ISSN]
0166-0934
[Journal-full-title]
Journal of virological methods
[ISO-abbreviation]
J. Virol. Methods
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Netherlands
[Chemical-registry-number]
0 / DNA Primers; 0 / DNA, Complementary; 0 / DNA, Viral; 0 / Genetic Markers; 0 / Npro protein, bovine viral diarrhea virus; 0 / Viral Proteins
70.
Oldenburg RA, Kroeze-Jansema KH, Houwing-Duistermaat JJ, Bayley JP, Dambrot C, van Asperen CJ, van den Ouweland AM, Bakker B, van Beers EH, Nederlof PM, Vasen H, Hoogerbrugge N, Cornelisse CJ, Meijers-Heijboer H, Devilee P:
Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.
Genes Chromosomes Cancer
; 2008 Nov;47(11):947-56
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast
cancer
families identifies 9q21-22 as a putative breast
cancer
susceptibility locus.
Breast
cancer
accounts for over 20% of all female cancers.
A positive family history remains one of the most important risk factors for
the disease
, with first-degree relatives of patients having a twofold elevated risk.
Known breast
cancer
susceptibility genes such as BRCA1 and BRCA2 explain only 20-25% of this risk, suggesting the existence of other breast
cancer
susceptibility genes.
Here, we report the results
of a
genome-wide linkage scan in 55 high-risk Dutch breast
cancer
families with no mutations in BRCA1 and BRCA2.
Twenty-two of these families were also part
of a
previous linkage study by the Breast
Cancer
Linkage Consortium.
With CGH analyses we observed preferential copy number loss at
BAC
RP11-276H19, containing D9S167 in familial tumors as compared to sporadic tumors (P < 0.001).
[MeSH-major]
Breast Neoplasms / genetics. Chromosomes, Human, Pair 9 / genetics. Genetic Linkage. Genetic Predisposition to
Disease
. Genome, Human
Genetic Alliance.
consumer health - Hereditary Cancer
.
Genetic Alliance.
consumer health - Breast Cancer
.
MedlinePlus Health Information.
consumer health - Breast Cancer
.
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18663745.001).
[ISSN]
1098-2264
[Journal-full-title]
Genes, chromosomes & cancer
[ISO-abbreviation]
Genes Chromosomes Cancer
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / BRCA1 Protein; 0 / BRCA2 Protein
71.
Qiu SQ, Liu K, Jiang JX, Song X, Xu CG, Li XH, Zhang Q:
Delimitation of the rice wide compatibility gene S5 ( n ) to a 40-kb DNA fragment.
Theor Appl Genet
; 2005 Oct;111(6):1080-6
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
A physical map consisting of six overlapping
BAC
clones was formed, spanning a genomic region of 540-kb in length.
[MeSH-minor]
Aspartic Acid Endopeptidases / genetics. Chromosomes, Artificial,
Bacterial
. Crosses, Genetic. Fertility / genetics. Fucosyltransferases / genetics. Heat-Shock Proteins / genetics. Molecular Chaperones / genetics. Polymorphism, Restriction Fragment Length. Sequence Analysis, DNA
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Eur J Biochem. 1998 Jul 1;255(1):133-8
[
9692911.001
]
[Cites]
Nucleic Acids Res. 1980 Oct 10;8(19):4321-5
[
7433111.001
]
[Cites]
Genetics. 1994 Dec;138(4):1251-74
[
7896104.001
]
[Cites]
Nat Genet. 1994 Dec;8(4):365-72
[
7894488.001
]
[Cites]
Genomics. 1995 Feb 10;25(3):674-81
[
7759102.001
]
[Cites]
Theor Appl Genet. 1996 Apr;92(5):541-51
[
24166321.001
]
[Cites]
Planta. 1992 Feb;186(3):317-23
[
24186727.001
]
[Cites]
Curr Opin Cell Biol. 1995 Aug;7(4):523-9
[
7495572.001
]
[Cites]
Theor Appl Genet. 1996 Dec;93(8):1218-24
[
24162533.001
]
[Cites]
Mol Gen Genet. 1993 Oct;241(1-2):225-35
[
7901751.001
]
[Cites]
Theor Appl Genet. 2005 Jan;110(2):205-11
[
15672255.001
]
[Cites]
Theor Appl Genet. 1995 Feb;90(2):182-8
[
24173889.001
]
(PMID = 16177904.001).
[ISSN]
0040-5752
[Journal-full-title]
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik
[ISO-abbreviation]
Theor. Appl. Genet.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Germany
[Chemical-registry-number]
0 / Heat-Shock Proteins; 0 / Molecular Chaperones; 0 / molecular chaperone GRP78; EC 2.4.1.- / Fucosyltransferases; EC 2.4.1.- / xyloglucan 2-fucosyltransferase; EC 3.4.23.- / Aspartic Acid Endopeptidases
72.
Rajamohan F, Harris MS, Frisbie RK, Hoth LR, Geoghegan KF, Valentine JJ, Reyes AR, Landro JA, Qiu X, Kurumbail RG:
Escherichia coli expression, purification and characterization of functional full-length recombinant alpha2beta2gamma3 heterotrimeric complex of human AMP-activated protein kinase.
Protein Expr Purif
; 2010 Oct;73(2):189-97
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Escherichia coli expression, purification and characterization of functional full-length recombinant alpha2beta2gamma3 heterotrimeric
complex of
human AMP-activated protein kinase.
The muscle-specific AMPK heterotrimeric
complex
(alpha2beta2gamma3) is involved in glucose and fat metabolism in skeletal muscle and therefore has emerged as an attractive target for drug development for diabetes and metabolic syndrome.
Here we describe the expression, purification and biochemical characterization of functional full-length AMPK alpha2beta2gamma3 heterotrimeric
complex
using an Escherichia coli expression system.
All three subunits of AMPK alpha2beta2gamma3 were transcribed as a single tricistronic transcript driven by the T7 RNA polymerase promoter, allowing spontaneous formation of the heterotrimeric
complex
in
the bacterial
cytosol.
The self-assembled trimeric
complex
was purified from
the cell
lysate by nickel-ion chromatography using the hexahistidine tag fused exclusively at the N-terminus of the alpha 2 domain.
The final yield of the recombinant AMPK alpha2beta2gamma3
complex
was 1.1mg/L culture in shaker flasks.
The kinase activity of activated AMPK alpha2beta2gamma3
complex
was significantly enhanced by AMP (an allosteric activator) but not by thienopyridone A-769662, a known small molecule activator of AMPK.
Mass spectrometric characterization of recombinant AMPK alpha2beta2gamma3 showed significant heterogeneity before and after activation that could potentially hamper crystallographic studies of this
complex
.
Hazardous Substances Data Bank.
ADENOSINE 5'-PHOSPHATE
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
Copyright 2010 Elsevier Inc. All rights reserved.
(PMID = 20451617.001).
[ISSN]
1096-0279
[Journal-full-title]
Protein expression and purification
[ISO-abbreviation]
Protein Expr. Purif.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Chemical-registry-number]
0 / A 769662; 0 / Cyclic AMP-Dependent Protein Kinase RIIbeta Subunit; 0 / Protein Subunits; 0 / Pyrones; 0 / Recombinant Proteins; 0 / Thiophenes; 415SHH325A / Adenosine Monophosphate; EC 2.7.11.1 / AMP-Activated Protein Kinases; EC 2.7.11.1 / Protein-Serine-Threonine Kinases; EC 2.7.11.17 / Calcium-Calmodulin-Dependent Protein Kinase Kinase
73.
Khandani AH, Whitney KD, Keller SM, Isasi CR, Donald Blaufox M:
Sensitivity of FDG PET, GLUT1 expression and proliferative index in bronchioloalveolar lung cancer.
Nucl Med Commun
; 2007 Mar;28(3):173-7
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Sensitivity of FDG PET, GLUT1 expression and proliferative index in
bronchioloalveolar lung cancer
.
OBJECTIVE: To estimate the sensitivity of [F] fluorodeoxyglucose (FDG) positron emission tomography (PET) and to assess the expression of glucose transporter 1 (GLUT1) and proliferative index (PI) in
bronchioloalveolar lung cancer
(
BAC
).
METHODS: Twenty-four patients with resected
BAC
underwent preoperative PET between October 1996 and February 2003.
The surgical specimens were re-examined, and 18 patients who fulfilled the 1999 WHO definition for
BAC
were included in the study.
The pathology slides were stained with antibodies to GLUT1 and Proliferating
cell
nuclear
antigen
(PCNA) in order to determine GLUT1 expression and PI, respectively.
RESULTS: There were 13 cases of PET+
BAC
(sensitivity, 72%; confidence interval, 52-93%); seven of them were GLUT1+ cases and six were GLUT1-.
The stromal
cell
PI was significantly higher in GLUT1+
BAC
compared to GLUT-
BAC
(50.9+/-17.1 vs. 33.2+/-14.2, P=0.0286), and higher in PET+
BAC
compared to PET-
BAC
(45.5+/-15.3 vs. 29.6+/-19.6, P=0.0854).
CONCLUSION: After applying the 1999 WHO criteria, the sensitivity of PET for detecting
BAC
is still relatively low.
Other glucose transporters such as GLUT3 likely play a role in FDG uptake in
BAC
.
GLUT1+ or PET+
BAC
tumours have a higher stromal
cell
PI when compared to GLUT1-
BAC
or PET-
BAC
tumours, respectively.
[MeSH-major]
Bronchial Neoplasms /
diagnosis
. Glucose Transporter Type 1 / biosynthesis.
Lung
Neoplasms /
diagnosis
[MeSH-minor]
Cell
Proliferation. Cesium. Epithelial Cells / pathology. Fluorodeoxyglucose F18. Humans.
Lung
/ pathology. Positron-Emission Tomography. Proliferating
Cell
Nuclear
Antigen
/ biosynthesis. Proliferating
Cell
Nuclear
Antigen
/ genetics. Radiopharmaceuticals. Stromal Cells / pathology. Tomography, X-Ray Computed
Genetic Alliance.
consumer health - Lung Cancer
.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
CESIUM, ELEMENTAL
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17264775.001).
[ISSN]
0143-3636
[Journal-full-title]
Nuclear medicine communications
[ISO-abbreviation]
Nucl Med Commun
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
[Chemical-registry-number]
0 / Glucose Transporter Type 1; 0 / Proliferating Cell Nuclear Antigen; 0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18; 1KSV9V4Y4I / Cesium
74.
Yang Y, Gozen O, Vidensky S, Robinson MB, Rothstein JD:
Epigenetic regulation of neuron-dependent induction of astroglial synaptic protein GLT1.
Glia
; 2010 Feb;58(3):277-86
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
In this study, we established a procedure to selectively isolate a pure astrocyte population in vitro and in vivo from
BAC
GLT1 eGFP mice using an eGFP-based fluorescence-activated
cell
sorting approach.
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
GLUTAMIC ACID HYDROCHLORIDE
.
KOMP Repository.
gene/protein/disease-specific - KOMP Repository
(subscription/membership/fee required).
Mouse Genome Informatics (MGI).
Mouse Genome Informatics (MGI)
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
(c) 2009 Wiley-Liss, Inc.
[Cites]
Nat Neurosci. 2007 May;10(5):608-14
[
17435754.001
]
[Cites]
Nat Neurosci. 2007 May;10(5):615-22
[
17435755.001
]
[Cites]
J Neurosci. 2007 Jun 20;27(25):6607-19
[
17581948.001
]
[Cites]
J Neurosci. 2007 Nov 7;27(45):12255-66
[
17989291.001
]
[Cites]
Nat Neurosci. 2007 Nov;10(11):1355-60
[
17965655.001
]
[Cites]
Nat Neurosci. 2008 Mar;11(3):251-3
[
18246065.001
]
[Cites]
Nat Neurosci. 2009 Mar;12(3):311-7
[
19234456.001
]
[Cites]
Neuron. 2009 Mar 26;61(6):880-94
[
19323997.001
]
[Cites]
Prog Neurobiol. 2001 Sep;65(1):1-105
[
11369436.001
]
[Cites]
Neurobiol Dis. 2001 Oct;8(5):807-21
[
11592850.001
]
[Cites]
J Neurosci. 2002 Mar 15;22(6):2142-52
[
11896154.001
]
[Cites]
Bioinformatics. 2002 Nov;18(11):1427-31
[
12424112.001
]
[Cites]
J Neurosci. 2004 Feb 4;24(5):1136-48
[
14762132.001
]
[Cites]
Nat Neurosci. 2004 Mar;7(3):229-35
[
14770186.001
]
[Cites]
N Engl J Med. 1992 May 28;326(22):1464-8
[
1349424.001
]
[Cites]
Ann Neurol. 1996 May;39(5):676-9
[
8619555.001
]
[Cites]
Neuron. 1996 Mar;16(3):675-86
[
8785064.001
]
[Cites]
J Neurosci. 1997 Feb 1;17(3):932-40
[
8994048.001
]
[Cites]
Science. 1997 Jun 13;276(5319):1699-702
[
9180080.001
]
[Cites]
J Neurosci. 1997 Nov 1;17(21):8363-75
[
9334410.001
]
[Cites]
Nat Genet. 1999 Oct;23(2):185-8
[
10508514.001
]
[Cites]
EMBO J. 2005 Feb 9;24(3):510-20
[
15660126.001
]
[Cites]
Science. 2006 Jun 2;312(5778):1389-92
[
16741123.001
]
[Cites]
Glia. 2007 May;55(7):663-74
[
17311293.001
]
(PMID = 19672971.001).
[ISSN]
1098-1136
[Journal-full-title]
Glia
[ISO-abbreviation]
Glia
[Language]
ENG
[Grant]
United States / NINDS NIH HHS / NS / R01 NS036465; United States / NINDS NIH HHS / NS / R01 NS052179; United States / NINDS NIH HHS / NS / NS33958; United States / NINDS NIH HHS / NS / NS036465; United States / NINDS NIH HHS / NS / NS052179-05; United States / NINDS NIH HHS / NS / R01 NS033958-09; United States / NINDS NIH HHS / NS / R01 NS033958; United States / NINDS NIH HHS / NS / R01 NS052179-05; United States / NINDS NIH HHS / NS / NS033958-09
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / Excitatory Amino Acid Transporter 2; 0 / Neurotoxins; 0 / Repressor Proteins; 3KX376GY7L / Glutamic Acid
[Other-IDs]
NLM/ NIHMS136480; NLM/ PMC2794958
75.
Bonnet C, Grégoire MJ, Vibert M, Raffo E, Leheup B, Jonveaux P:
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.
J Hum Genet
; 2008;53(10):876-85
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced
de
novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.
Genetic investigations allowed the identification of an apparently balanced
de
novo reciprocal translocation, t(7;9)(q21;p23).
Breakpoint-region mapping using fluorescent in situ hybridization (FISH) analysis
of bacterial
artificial chromosome (
BAC
) clone probes identified microdeletions of 3.7 and 5.2 Mb within 7q21 and 9p23 breakpoint regions, respectively.
These results emphasize that the phenotypic abnormalities of apparently balanced
de
novo translocations can be due to cryptic deletions and that the precise mapping of these aneusomies may improve clinical management.
Genetic Alliance.
consumer health - Dystonia
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
Nature Publishing Group.
Nature Publishing Group
(subscription/membership/fee required).
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18651096.001).
[ISSN]
1434-5161
[Journal-full-title]
Journal of human genetics
[ISO-abbreviation]
J. Hum. Genet.
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Japan
[Chemical-registry-number]
0 / SGCE protein, human; 0 / Sarcoglycans
76.
Rossi MR, Laduca J, Cowell JK, Srivastava BI, Matsui S:
Genomic analysis of CD8+ NK/T cell line, 'SRIK-NKL', with array-based CGH (aCGH), SKY/FISH and molecular mapping.
Leuk Res
; 2008 Mar;32(3):455-63
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Genomic analysis of CD8+ NK/T
cell
line, 'SRIK-NKL', with array-based CGH (aCGH), SKY/FISH and molecular mapping.
We performed aCGH, SKY/FISH, molecular mapping and expression analyses on a permanent CD8+ NK/T
cell
line, 'SRIK-NKL' established from a lymphoma (ALL) patient, in attempt to define the fundamental genetic profile of its unique NK phenotypes. aCGH revealed hemizygous deletion of 6p containing genes responsible for hematopoietic functions.
The FISH analysis using
a BAC
which contains TRA@ and its flanking region further revealed a approximately 231kb deletion within 14q11 in the der(5) but not in the normal homologue of no. 14.
The RT
-PCR analysis detected mRNA for TRA@ transcripts which were extending across, but not including, the deleted region.
In addition to rcpt(5;14), aCGH identified novel copy number abnormalities suggesting that the unique phenotype of the SRIK-NKL
cell
line is not solely due to the TRA@ rearrangement.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Cold Spring Harb Symp Quant Biol. 1986;51 Pt 2:899-909
[
3495397.001
]
[Cites]
Blood. 1988 Nov;72(5):1560-6
[
3263151.001
]
[Cites]
Cell. 1991 Aug 23;66(4):649-61
[
1831692.001
]
[Cites]
Genes Chromosomes Cancer. 1991 Nov;3(6):461-7
[
1663780.001
]
[Cites]
Blood. 1991 Nov 15;78(10):2686-95
[
1824262.001
]
[Cites]
Genomics. 1993 Dec;18(3):486-95
[
8307557.001
]
[Cites]
Ann Hum Genet. 1995 Apr;59(Pt 2):233-41
[
7625768.001
]
[Cites]
Ann Hum Genet. 1996 May;60(Pt 3):213-20
[
8800437.001
]
[Cites]
Br J Haematol. 1997 Jun;97(3):621-5
[
9207410.001
]
[Cites]
Br J Haematol. 1997 Sep;98(4):922-6
[
9326190.001
]
[Cites]
Blood. 1997 Oct 15;90(8):3136-41
[
9376595.001
]
[Cites]
Cancer Genet Cytogenet. 1998 Aug;105(1):60-8
[
9689932.001
]
[Cites]
J Exp Med. 1998 Sep 7;188(5):953-60
[
9730896.001
]
[Cites]
J Exp Med. 1999 Mar 1;189(5):787-96
[
10049942.001
]
[Cites]
J Immunol. 1999 Jul 1;163(1):507-13
[
10384155.001
]
[Cites]
Leuk Lymphoma. 1999 Jul;34(3-4):241-50
[
10439361.001
]
[Cites]
Cancer Res. 2005 Feb 15;65(4):1570-6
[
15735047.001
]
[Cites]
Leuk Res. 2005 Jul;29(7):771-83
[
15927673.001
]
[Cites]
Leuk Res. 2005 Jul;29(7):813-20
[
15927677.001
]
[Cites]
Genes Chromosomes Cancer. 2006 Mar;45(3):290-303
[
16320246.001
]
[Cites]
J Exp Med. 1999 Nov 15;190(10):1505-16
[
10562324.001
]
[Cites]
Leukemia. 2000 May;14(5):777-82
[
10803505.001
]
[Cites]
Hum Pathol. 2000 Jun;31(6):771-4
[
10872675.001
]
[Cites]
Scand J Immunol. 2001 Feb;53(2):103-10
[
11169213.001
]
[Cites]
Oncogene. 2001 Aug 30;20(38):5378-92
[
11536051.001
]
[Cites]
Nat Genet. 2001 Nov;29(3):263-4
[
11687795.001
]
[Cites]
Hematology Am Soc Hematol Educ Program. 2001;:259-81
[
11722988.001
]
[Cites]
Leuk Res. 2002 Nov;26(11):977-8
[
12363463.001
]
[Cites]
Leuk Res. 2002 Nov;26(11):1027-33
[
12363472.001
]
[Cites]
Leuk Res. 2003 Oct;27(10):935-45
[
12860014.001
]
[Cites]
Gastroenterology. 2003 Aug;125(2):345-56
[
12891535.001
]
[Cites]
Nat Rev Cancer. 2003 Sep;3(9):666-75
[
12951585.001
]
[Cites]
J Exp Med. 2003 Oct 20;198(8):1201-12
[
14568979.001
]
[Cites]
Eur J Immunol. 2003 Dec;33(12):3439-47
[
14635054.001
]
[Cites]
J Immunol. 2004 Feb 1;172(3):1455-62
[
14734722.001
]
[Cites]
Cancer Genet Cytogenet. 2004 May;151(1):36-51
[
15120909.001
]
[Cites]
Cancer Res. 2004 Oct 1;64(19):6941-9
[
15466185.001
]
[Cites]
Somatic Cell Genet. 1975 Oct;1(4):397-400
[
1242069.001
]
[Cites]
Nature. 1983 Jan 27;301(5898):290-1
[
6823303.001
]
[Cites]
Cold Spring Harb Symp Quant Biol. 1986;51 Pt 2:891-8
[
3495396.001
]
(PMID = 17640729.001).
[ISSN]
0145-2126
[Journal-full-title]
Leukemia research
[ISO-abbreviation]
Leuk. Res.
[Language]
ENG
[Grant]
United States / NCI NIH HHS / CA / CA016056-31; United States / NCI NIH HHS / CA / P30 CA016056; United States / NCI NIH HHS / CA / CA 16056; United States / NCI NIH HHS / CA / P30 CA016056-31
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / Antigens, CD8
[Other-IDs]
NLM/ NIHMS42920; NLM/ PMC2855542
77.
Komura D, Shen F, Ishikawa S, Fitch KR, Chen W, Zhang J, Liu G, Ihara S, Nakamura H, Hurles ME, Lee C, Scherer SW, Jones KW, Shapero MH, Huang J, Aburatani H:
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Genome Res
; 2006 Dec;16(12):1575-84
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
In addition, the contribution of CNVs to human
disease
susceptibility may be greater than previously expected, although a complete understanding of the phenotypic consequences of CNVs is incomplete.
We have recently reported a comprehensive view of CNVs among 270 HapMap samples using high-density SNP genotyping arrays and
BAC
array CGH.
Independent testing
of a
subset of CNVs by quantitative PCR and mass spectrometry demonstrated a >90% verification rate.
COS Scholar Universe.
author profiles
.
Coriell Cell Repositories.
culture/stock collections - Coriell Cell Repositories
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Science. 2004 Jul 23;305(5683):525-8
[
15273396.001
]
[Cites]
Biotechniques. 2004 May;36(5):840-5
[
15152604.001
]
[Cites]
Nat Genet. 2004 Sep;36(9):949-51
[
15286789.001
]
[Cites]
Nature. 2004 Oct 21;431(7011):931-45
[
15496913.001
]
[Cites]
Science. 1991 Feb 15;251(4995):767-73
[
1990438.001
]
[Cites]
Nature. 1993 Aug 5;364(6437):555-6
[
7687751.001
]
[Cites]
Proc Natl Acad Sci U S A. 1994 May 24;91(11):5022-6
[
8197176.001
]
[Cites]
Hum Genomics. 2004 May;1(4):287-99
[
15588488.001
]
[Cites]
Science. 2005 Mar 4;307(5714):1434-40
[
15637236.001
]
[Cites]
Nat Methods. 2004 Nov;1(2):109-11
[
15782172.001
]
[Cites]
Bioinformatics. 2005 May 1;21(9):1958-63
[
15657097.001
]
[Cites]
Am J Hum Genet. 2005 Jul;77(1):78-88
[
15918152.001
]
[Cites]
Nucleic Acids Res. 2005;33(11):3455-64
[
15961730.001
]
[Cites]
Nat Genet. 2005 Jul;37(7):727-32
[
15895083.001
]
[Cites]
Biochem Biophys Res Commun. 2005 Aug 12;333(4):1309-14
[
15982637.001
]
[Cites]
Cancer Res. 2005 Jul 15;65(14):6071-9
[
16024607.001
]
[Cites]
Nat Rev Genet. 2005 Oct;6(10):782-92
[
16145555.001
]
[Cites]
Am J Hum Genet. 2005 Nov;77(5):709-26
[
16252233.001
]
[Cites]
Nature. 2005 Oct 27;437(7063):1299-320
[
16255080.001
]
[Cites]
Nucleic Acids Res. 2005;33(21):e183
[
16314297.001
]
[Cites]
PLoS Comput Biol. 2005 Nov;1(6):e65
[
16322765.001
]
[Cites]
Pharmacogenomics. 2006 Jan;7(1):25-9
[
16354122.001
]
[Cites]
Nat Genet. 2006 Jan;38(1):75-81
[
16327808.001
]
[Cites]
Nat Genet. 2006 Jan;38(1):82-5
[
16327809.001
]
[Cites]
Nat Rev Genet. 2006 Feb;7(2):85-97
[
16418744.001
]
[Cites]
Nat Genet. 2006 Jan;38(1):86-92
[
16468122.001
]
[Cites]
Nat Rev Genet. 2006 Mar;7(3):200-10
[
16485019.001
]
[Cites]
Hum Mol Genet. 2006 Apr 1;15(7):1159-67
[
16497726.001
]
[Cites]
BMC Bioinformatics. 2006;7:83
[
16504045.001
]
[Cites]
Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4534-9
[
16537408.001
]
[Cites]
Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R57-66
[
16651370.001
]
[Cites]
PLoS Comput Biol. 2006 May;2(5):e41
[
16699594.001
]
[Cites]
Am J Hum Genet. 2006 Aug;79(2):275-90
[
16826518.001
]
[Cites]
Genome Res. 2006 Aug;16(8):949-61
[
16809666.001
]
[Cites]
Oncogene. 2006 Sep 7;25(40):5581-90
[
16785998.001
]
[Cites]
In Silico Biol. 2006;6(1-2):79-92
[
16789916.001
]
[Cites]
Nature. 2006 Nov 23;444(7118):444-54
[
17122850.001
]
[Cites]
Annu Rev Genomics Hum Genet. 2002;3:199-242
[
12142364.001
]
[Cites]
Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16871-4
[
12475937.001
]
[Cites]
Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16928-33
[
12482934.001
]
[Cites]
Nat Biotechnol. 2003 Oct;21(10):1233-7
[
12960966.001
]
[Cites]
Genome Res. 2004 Feb;14(2):287-95
[
14762065.001
]
[Cites]
Genome Res. 2004 Mar;14(3):414-25
[
14993208.001
]
[Cites]
Cancer Res. 2004 May 1;64(9):3060-71
[
15126342.001
]
[Cites]
Nat Genet. 2004 Aug;36(8):861-6
[
15247918.001
]
(PMID = 17122084.001).
[ISSN]
1088-9051
[Journal-full-title]
Genome research
[ISO-abbreviation]
Genome Res.
[Language]
eng
[Databank-accession-numbers]
GEO/ GSE5013/ GSE5173
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
9007-49-2 / DNA
[Other-IDs]
NLM/ PMC1665641
78.
Szamalek JM, Goidts V, Chuzhanova N, Hameister H, Cooper DN, Kehrer-Sawatzki H:
Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosome.
Hum Genet
; 2005 Jul;117(2-3):168-76
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Breakpoint-spanning
BAC
clones were identified from both the human and chimpanzee genomes by fluorescence in situ hybridisation, and the precise locations of the breakpoints were determined by sequence comparisons.
[MeSH-minor]
Animals.
Cell
Line, Tumor. Humans. Karyotyping
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Genomics. 1998 Jun 15;50(3):368-72
[
9676431.001
]
[Cites]
Genome Res. 2003 Mar;13(3):341-6
[
12618364.001
]
[Cites]
Cytogenet Genome Res. 2005;108(1-3):161-74
[
15545726.001
]
[Cites]
Genome Res. 2001 Jul;11(7):1205-10
[
11435402.001
]
[Cites]
Genome Res. 2003 Mar;13(3):369-81
[
12618367.001
]
[Cites]
Genomics. 2004 Feb;83(2):193-202
[
14706448.001
]
[Cites]
Genome Res. 2005 Sep;15(9):1232-42
[
16140991.001
]
[Cites]
Genome Res. 1999 Dec;9(12):1184-8
[
10613840.001
]
[Cites]
Hum Genet. 2004 Jul;115(2):116-22
[
15133654.001
]
[Cites]
Science. 2002 Apr 12;296(5566):340-3
[
11951044.001
]
[Cites]
Hum Mutat. 2005 Jan;25(1):45-55
[
15580561.001
]
[Cites]
Genomics. 2005 May;85(5):542-50
[
15820305.001
]
[Cites]
Cytogenet Cell Genet. 1997;76(3-4):189-91
[
9186521.001
]
[Cites]
J Biol Chem. 2004 Nov 12;279(46):47411-4
[
15326170.001
]
[Cites]
Cytogenet Genome Res. 2005;108(1-3):91-7
[
15545720.001
]
[Cites]
Genome Biol. 2004;5(4):R23
[
15059256.001
]
[Cites]
Genomics. 2004 Mar;83(3):493-501
[
14962675.001
]
[Cites]
Nucleic Acids Res. 1990 Jan 11;18(1):1-11
[
2155393.001
]
[Cites]
Nature. 2004 Sep 16;431(7006):268-74
[
15372022.001
]
[Cites]
Int J Oncol. 2004 Jan;24(1):127-36
[
14654949.001
]
[Cites]
Genomics. 2004 Sep;84(3):458-67
[
15498453.001
]
[Cites]
Genome Biol. 2003;4(8):R50
[
12914658.001
]
[Cites]
Cytogenet Genome Res. 2005;108(1-3):217-22
[
15545733.001
]
[Cites]
Genomics. 2000 Feb 1;63(3):307-13
[
10704278.001
]
[Cites]
Mol Pathol. 2000 Aug;53(4):184-7
[
11040940.001
]
[Cites]
Hum Mutat. 2003 Sep;22(3):229-44
[
12938088.001
]
[Cites]
Genome Res. 2004 Nov;14(11):2209-20
[
15520286.001
]
[Cites]
Hum Genet. 2001 Jul;109(1):85-94
[
11479739.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Sep 28;101(39):14162-7
[
15377784.001
]
[Cites]
Cancer Genet Cytogenet. 2002 Jul 15;136(2):101-7
[
12237232.001
]
[Cites]
Am J Hum Genet. 2002 Jan;70(1):269-78
[
11731935.001
]
[Cites]
Am J Hum Genet. 2002 Aug;71(2):375-88
[
12094327.001
]
[Cites]
Mol Biol Evol. 2003 Sep;20(9):1506-12
[
12832646.001
]
[Cites]
Hum Genet. 1979 May 10;48(3):251-314
[
112030.001
]
[Cites]
Genome Res. 2004 Aug;14(8):1462-73
[
15289471.001
]
[Cites]
Cancer Res. 1996 Mar 15;56(6):1418-25
[
8640834.001
]
[Cites]
Proc Natl Acad Sci U S A. 2003 Oct 28;100(22):13030-5
[
14557539.001
]
[Cites]
Genomics. 1990 Oct;8(2):347-50
[
2249853.001
]
[Cites]
Genome Res. 2003 Jul;13(7):1619-30
[
12840040.001
]
[Cites]
Ann Genet. 1975 Sep;18(3):153-61
[
1080978.001
]
[Cites]
Science. 1982 Mar 19;215(4539):1525-30
[
7063861.001
]
[Cites]
J Med Genet. 2001 Mar;38(3):151-8
[
11238681.001
]
[Cites]
Cytogenet Genome Res. 2005;108(1-3):83-90
[
15545719.001
]
[Cites]
Bioinformatics. 1999 Dec;15(12):994-9
[
10745989.001
]
[Cites]
Genomics. 2002 Oct;80(4):395-401
[
12376093.001
]
[Cites]
Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):9051-5
[
1924367.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):2957-62
[
14976249.001
]
[Cites]
Cancer Genet Cytogenet. 2004 Aug;153(1):16-25
[
15325089.001
]
[Cites]
Genome Res. 2002 Nov;12(11):1651-62
[
12421751.001
]
(PMID = 15883840.001).
[ISSN]
0340-6717
[Journal-full-title]
Human genetics
[ISO-abbreviation]
Hum. Genet.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Germany
79.
Li L, Zhu W, Zhang P, Zhang Q, Zhang Z:
AC/O3-BAC processes for removing refractory and hazardous pollutants in raw water.
J Hazard Mater
; 2006 Jul 31;135(1-3):129-33
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
AC/O3-
BAC
processes for removing refractory and hazardous pollutants in raw water.
Granular activated carbon (AC)/O(3)-biological activated carbon (
BAC
) process was employed to treat raw water and compared to O(3)-
BAC
process in its optimum parameters (3 mg/L ozone dosage with 15 min oxidation time and 15 min empty bed contact time in
BAC
).
For dissolved organic carbon (DOC) removal, AC/O(3)-
BAC
was more efficient than O(3)-
BAC
and its synergetic effect could be noticed.
GC/MS analysis showed that AC/O(3)-
BAC
process was effective in removing phthalate esters (PAEs) and persistent organic pollutants (POPs).
MedlinePlus Health Information.
consumer health - Ozone
.
Hazardous Substances Data Bank.
OZONE
.
Hazardous Substances Data Bank.
CARBON
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 16386361.001).
[ISSN]
0304-3894
[Journal-full-title]
Journal of hazardous materials
[ISO-abbreviation]
J. Hazard. Mater.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Netherlands
[Chemical-registry-number]
0 / Water Pollutants, Chemical; 66H7ZZK23N / Ozone; 7440-44-0 / Carbon
80.
Chaves LD, Harry DE, Reed KM:
Genome-wide genetic diversity of 'Nici', the DNA source for the CHORI-260 turkey BAC library and candidate for whole genome sequencing.
Anim Genet
; 2009 Jun;40(3):348-52
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Genome-wide genetic diversity of 'Nici', the DNA source for the CHORI-260 turkey
BAC
library and candidate for whole genome sequencing.
Here we examined the source DNA [Nicholas inbred (Nici)] of the CHORI-260 turkey
bacterial
artificial chromosome (
BAC
) library through analysis of microsatellites and
BAC
sequences.
[MeSH-major]
Chromosomes, Artificial,
Bacterial
/ genetics. DNA / genetics. Turkeys / genetics
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19292710.001).
[ISSN]
1365-2052
[Journal-full-title]
Animal genetics
[ISO-abbreviation]
Anim. Genet.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
9007-49-2 / DNA
81.
Ng HY, Lee LY, Ong SL, Tao G, Viawanath B, Kekre K, Lay W, Seah H:
Treatment of RO brine-towards sustainable water reclamation practice.
Water Sci Technol
; 2008;58(4):931-6
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The proposed treatment consists of biological activated carbon (
BAC
) column followed by capacitive deionization (CDI) process for organic and inorganic removals, respectively.
Preliminary bench-scale study demonstrated about 20% TOC removal efficiency was achieved using
BAC
at 40 mins empty bed contact time (EBCT) while the CDI process was able to remove more than 90% conductivity reducing it from 2.19 mS/cm to only about 164 microS/cm.
More than 90% cations and anions in
the BAC
effluent were removed using CDI process.
COS Scholar Universe.
author profiles
.
Hazardous Substances Data Bank.
CARBON
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Copyright]
Copyright IWA Publishing 2008.
(PMID = 18776632.001).
[ISSN]
0273-1223
[Journal-full-title]
Water science and technology : a journal of the International Association on Water Pollution Research
[ISO-abbreviation]
Water Sci. Technol.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
England
[Chemical-registry-number]
0 / Inorganic Chemicals; 0 / Organic Chemicals; 0 / Water Pollutants, Chemical; 7440-44-0 / Carbon
82.
Lux R, Shi W:
A novel bacterial signalling system with a combination of a Ser/Thr kinase cascade and a His/Asp two-component system.
Mol Microbiol
; 2005 Oct;58(2):345-8
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
A novel
bacterial
signalling system with a combination
of a
Ser/Thr kinase cascade and a His/Asp two-component system.
Prokaryotes and eukaryotes have long been thought to use very different types of kinases (the His kinases of the '
bacterial
' two-component systems versus the 'eukaryotic' Ser/Thr/Tyr kinases) to carry out signal transduction.
Pioneering work on
bacterial
protein serine threonine kinases (PSTKs) has been performed in Myxococcus xanthus, a soil bacterium with
a complex
life cycle that possesses orthologues of signalling-related kinases 'typical' of both the prokaryotic and the eukaryotic kingdoms.
In the work reported in this volume of Molecular Microbiology, Nariya and Inouye describe a PSTK cascade that modulates the biochemical activity of MrpC, a CRP-like transcriptional regulator for essential developmental signalling pathways in M. xanthus whose transcription is under the control
of a
two-component system.
This is the first report of both a functional PSTK cascade in bacteria and the use of both PSTK and two-component systems to control a single
complex bacterial
signalling event.
[MeSH-minor]
Bacterial
Proteins / genetics.
Bacterial
Proteins / metabolism. Gene Expression Regulation,
Bacterial
. Transcription Factors / genetics. Transcription Factors / metabolism
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[CommentOn]
Mol Microbiol. 2005 Oct;58(2):367-79
[
16194226.001
]
(PMID = 16194223.001).
[ISSN]
0950-382X
[Journal-full-title]
Molecular microbiology
[ISO-abbreviation]
Mol. Microbiol.
[Language]
eng
[Grant]
United States / NIGMS NIH HHS / GM / GM54666
[Publication-type]
Comment; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
[Publication-country]
England
[Chemical-registry-number]
0 / Bacterial Proteins; 0 / MrpC protein, Myxococcus xanthus; 0 / Transcription Factors; EC 2.7.- / Protein Kinases; EC 2.7.11.1 / Protein-Serine-Threonine Kinases; EC 2.7.2.4 / Aspartate Kinase; EC 2.7.3.- / protein-histidine kinase
83.
Zhu ZY, Wang CM, Feng F, Yue GH:
Isolation and characterization of 51 microsatellites from BAC clones in Asian seabass, Lates calcarifer.
Anim Genet
; 2009 Feb;40(1):125-6
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Isolation and characterization of 51 microsatellites from
BAC
clones in Asian seabass, Lates calcarifer.
[MeSH-minor]
Animals. Chromosomes, Artificial,
Bacterial
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18945291.001).
[ISSN]
1365-2052
[Journal-full-title]
Animal genetics
[ISO-abbreviation]
Anim. Genet.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
84.
Mormino EC, Kluth JT, Madison CM, Rabinovici GD, Baker SL, Miller BL, Koeppe RA, Mathis CA, Weiner MW, Jagust WJ, Alzheimer's Disease Neuroimaging Initiative:
Episodic memory loss is related to hippocampal-mediated beta-amyloid deposition in elderly subjects.
Brain
; 2009 May;132(Pt 5):1310-23
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Although beta-amyloid (Abeta) plaques are a primary diagnostic criterion for Alzheimer's
disease
, this pathology is commonly observed in the brains of non-demented older individuals.
To explore the importance of this pathology in the absence of dementia, we compared levels of amyloid deposition (via 'Pittsburgh Compound-B' (PIB) positron emission tomography (PET) imaging) to hippocampus volume (HV) and episodic memory (EM) in three groups: (i) normal controls (NC) from the Berkeley Aging Cohort (
BAC
NC, n = 20);.
(ii) normal controls (NC) from the Alzheimer's
disease
neuroimaging initiative (ADNI NC, n = 17); and (iii) PIB+ mild cognitive impairment subjects from the ADNI (ADNI PIB+ MCI, n = 39).
In
BAC
NC, elevated PIB uptake was significantly associated with smaller aHV (P = 0.0016) and worse EM (P = 0.0086).
[MeSH-minor]
Age Factors. Aged. Aging / physiology. Alzheimer
Disease
/ diagnostic imaging. Alzheimer
Disease
/ pathology. Alzheimer
Disease
/ psychology. Aniline Compounds. Atrophy. Carbon Radioisotopes. Case-Control Studies. Educational Status. Female. Humans. Linear Models. Magnetic Resonance Imaging. Male. Middle Aged. Multivariate Analysis. Organ Size. Positron-Emission Tomography / methods. Psychiatric Status Rating Scales. Radiopharmaceuticals. Sex Factors. Thiazoles
MedlinePlus Health Information.
consumer health - Memory
.
COS Scholar Universe.
author profiles
.
Faculty of 1000.
commentaries/discussion - See the articles recommended by F1000Prime's Faculty of more than 8,000 leading experts in Biology and Medicine.
(subscription/membership/fee required).
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
J Cereb Blood Flow Metab. 1996 Sep;16(5):834-40
[
8784228.001
]
[Cites]
Nucl Med Biol. 1997 Jan;24(1):93-7
[
9080480.001
]
[Cites]
Neurobiol Aging. 1997 Jul-Aug;18(4):351-7
[
9330961.001
]
[Cites]
J Neuropathol Exp Neurol. 1998 Dec;57(12):1168-74
[
9862640.001
]
[Cites]
Neuroimage. 1999 Feb;9(2):179-94
[
9931268.001
]
[Cites]
Ann Neurol. 1999 Mar;45(3):358-68
[
10072051.001
]
[Cites]
J Neuropathol Exp Neurol. 1999 Apr;58(4):376-88
[
10218633.001
]
[Cites]
Neurology. 1999 Apr 22;52(7):1392-6
[
10227623.001
]
[Cites]
Neurology. 1999 Apr 22;52(7):1397-403
[
10227624.001
]
[Cites]
J Cereb Blood Flow Metab. 2005 Nov;25(11):1528-47
[
15944649.001
]
[Cites]
Hippocampus. 2005;15(8):997-1005
[
16281291.001
]
[Cites]
J Nucl Med. 1999 Dec;40(12):2053-65
[
10616886.001
]
[Cites]
Neuroimage. 2006 Jun;31(2):496-504
[
16473024.001
]
[Cites]
Neuroimage. 2006 Jul 1;31(3):968-80
[
16530430.001
]
[Cites]
Neurology. 2006 Jun 27;66(12):1837-44
[
16801647.001
]
[Cites]
Neurology. 2006 Aug 8;67(3):446-52
[
16894106.001
]
[Cites]
Alzheimer Dis Assoc Disord. 2006 Jul-Sep;20(3 Suppl 2):S69-74
[
16917199.001
]
[Cites]
Neurosci Biobehav Rev. 2006;30(6):730-48
[
16919333.001
]
[Cites]
Neuroimage. 2006 Oct 1;32(4):1591-607
[
16828315.001
]
[Cites]
Neurology. 2006 Nov 14;67(9):1575-80
[
16971697.001
]
[Cites]
Neurology. 2007 Apr 17;68(16):1268-73
[
17438217.001
]
[Cites]
Brain. 2007 Nov;130(Pt 11):2837-44
[
17928318.001
]
[Cites]
Arch Neurol. 2008 Jan;65(1):113-20
[
18195148.001
]
[Cites]
Ann Neurol. 2008 Jan;63(1):112-8
[
18023012.001
]
[Cites]
Nature. 2008 Feb 7;451(7179):720-4
[
18256671.001
]
[Cites]
J Int Neuropsychol Soc. 2008 Mar;14(2):266-78
[
18282324.001
]
[Cites]
Brain. 2008 Mar;131(Pt 3):665-80
[
18263627.001
]
[Cites]
J Magn Reson Imaging. 2008 Apr;27(4):685-91
[
18302232.001
]
[Cites]
Neuropsychologia. 2008;46(6):1688-97
[
18343463.001
]
[Cites]
Neurobiol Aging. 2008 Oct;29(10):1456-65
[
17499392.001
]
[Cites]
Arch Neurol. 2008 Nov;65(11):1509-17
[
19001171.001
]
[Cites]
Brain. 2007 Oct;130(Pt 10):2607-15
[
17698496.001
]
[Cites]
J Neurochem. 2007 Jun;101(5):1172-84
[
17286590.001
]
[Cites]
Arch Neurol. 2000 Jun;57(6):839-44
[
10867781.001
]
[Cites]
Neurology. 2000 Aug 8;55(3):370-6
[
10932270.001
]
[Cites]
Neurology. 2001 Feb 13;56(3):361-7
[
11171902.001
]
[Cites]
IEEE Trans Med Imaging. 2001 Jan;20(1):70-80
[
11293693.001
]
[Cites]
Neuron. 2002 Jan 31;33(3):341-55
[
11832223.001
]
[Cites]
Neurology. 2002 Mar 12;58(5):750-7
[
11889239.001
]
[Cites]
Ann Neurol. 2006 Mar;59(3):512-9
[
16372280.001
]
[Cites]
Arch Neurol. 2006 May;63(5):674-81
[
16682537.001
]
[Cites]
Arch Neurol. 2006 May;63(5):693-9
[
16682538.001
]
[Cites]
Neurology. 2007 May 15;68(20):1718-25
[
17502554.001
]
[Cites]
Science. 2002 Jul 19;297(5580):353-6
[
12130773.001
]
[Cites]
J Med Chem. 2003 Jun 19;46(13):2740-54
[
12801237.001
]
[Cites]
J Neuropathol Exp Neurol. 2003 Nov;62(11):1087-95
[
14656067.001
]
[Cites]
Cogn Behav Neurol. 2003 Dec;16(4):211-8
[
14665820.001
]
[Cites]
Ann Neurol. 2004 Mar;55(3):306-19
[
14991808.001
]
[Cites]
Arch Neurol. 2004 Mar;61(3):378-84
[
15023815.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Mar 30;101(13):4637-42
[
15070770.001
]
[Cites]
Neuroimage. 2004 Jul;22(3):1060-75
[
15219578.001
]
[Cites]
Neuroimage. 2004 Oct;23(2):724-38
[
15488422.001
]
[Cites]
J Neurol Sci. 1968 Sep-Oct;7(2):331-56
[
5707082.001
]
[Cites]
Neurology. 1984 Jul;34(7):939-44
[
6610841.001
]
[Cites]
J Pers Soc Psychol. 1986 Dec;51(6):1173-82
[
3806354.001
]
[Cites]
J Nucl Med. 1987 Jun;28(6):1037-40
[
3585494.001
]
[Cites]
Ann Neurol. 1988 Feb;23(2):138-44
[
2897823.001
]
[Cites]
Psychol Aging. 1991 Mar;6(1):118-27
[
2029360.001
]
[Cites]
Acta Neuropathol. 1991;82(4):239-59
[
1759558.001
]
[Cites]
Cereb Cortex. 1991 Jan-Feb;1(1):103-16
[
1822725.001
]
[Cites]
Psychiatry Res. 1993 Jun;50(2):121-39
[
8378488.001
]
[Cites]
Neurology. 1993 Nov;43(11):2412-4
[
8232972.001
]
[Cites]
Ann N Y Acad Sci. 1996 Jan 17;777:1-13
[
8624070.001
]
(PMID = 19042931.001).
[ISSN]
1460-2156
[Journal-full-title]
Brain : a journal of neurology
[ISO-abbreviation]
Brain
[Language]
eng
[Grant]
United States / NIA NIH HHS / AG / R01 AG034570; United States / NIA NIH HHS / AG / P50 AG023501; United States / NIA NIH HHS / AG / AG024904; United States / NIA NIH HHS / AG / R01 AG027342; United States / NIA NIH HHS / AG / U01 AG024904; United States / NIA NIH HHS / AG / U19 AG010483; United States / NIA NIH HHS / AG / R01 AG027859; United States / NIA NIH HHS / AG / K23 AG031861; United States / NIA NIH HHS / AG / AG027859; United Kingdom / Medical Research Council / / G0601846; United States / NIA NIH HHS / AG / P01 AG010491-14; United States / NIA NIH HHS / AG / P01 AG010491; United States / NIA NIH HHS / AG / P30 AG019610; United States / NIA NIH HHS / AG / R01 AG027859-02
[Publication-type]
Comparative Study; Journal Article; Research Support, N.I.H., Extramural
[Publication-country]
England
[Chemical-registry-number]
0 / 2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole; 0 / Amyloid beta-Peptides; 0 / Aniline Compounds; 0 / Carbon Radioisotopes; 0 / Radiopharmaceuticals; 0 / Thiazoles
[Other-IDs]
NLM/ PMC2677792
[Investigator]
Weiner M; Thal L; Weiner M; Thal L; Petersen R; Jack CR Jr; Jagust W; Trojanowki J; Toga AW; Beckett L; Green RC; Gamst A; Potter WZ; Green RC; Montine T; Petersen R; Thal L; Jack CR Jr; Anders D; Bernstein M; Felmlee J; Fox N; Thompson P; Schuff N; Alexander G; Jagust W; Bandy D; Koeppe RA; Foster N; Reiman EM; Chen K; Trojanowki J; Shaw L; Lee VM; Korecka M; Toga AW; Crawford K; Neu S; Beckett L; Harvey D; Gamst A; Kornak J; Kachaturian Z; Frank R; Snyder PJ; Molchan S; Kaye J; Vorobik R; Quinn J; Schneider L; Pawluczyk S; Spann B; Fleisher AS; Vanderswag H; Heidebrink JL; Lord JL; Petersen R; Johnson K; Doody RS; Villanueva-Meyer J; Chowdhury M; Stern Y; Honig LS; Bell KL; Morris JC; Mintun MA; Schneider S; Marson D; Griffith R; Badger B; Grossman H; Tang C; Stern J; deToledo-Morrell L; Shah RC; Bach J; Duara R; Isaacson R; Strauman S; Albert MS; Pedroso J; Toroney J; Rusinek H; de Leon MJ; De Santi SM; Doraiswamy PM; Petrella JR; Aiello M; Clark CM; Pham C; Nunez J; Smith CD; Given CA 2nd; Hardy P; DeKosky ST; Oakley M; Simpson DM; Ismail MS; Porsteinsson A; McCallum C; Cramer SC; Mulnard RA; McAdams-Ortiz C; Diaz-Arrastia R; Martin-Cook K; DeVous M; Levey AI; Lah JJ; Cellar JS; Burns JM; Anderson HS; Laubinger MM; Bartzokis G; Silverman DH; Lu PH; Fletcher R; Parfitt F; Johnson H; Farlow M; Herring S; Hake AM; van Dyck CH; MacAvoy MG; Bifano LA; Chertkow H; Bergman H; Hosein C; Black S; Graham S; Caldwell C; Feldman H; Assaly M; Hsiung GY; Kertesz A; Rogers J; Trost D; Bernick C; Gitelman D; Johnson N; Mesulam M; Sadowsky C; Villena T; Mesner S; Aisen PS; Johnson KB; Behan KE; Sperling RA; Rentz DM; Johnson KA; Rosen A; Tinklenberg J; Ashford W; Sabbagh M; Connor D; Obradov S; Green RC; Killiany R; Norbash A; Obisesan TO; Jayam-Trouth A; Wang P; Auchus AP; Huang J; Friedland RP; DeCarli C; Fletcher E; Carmichael O; Kittur S; Mirje S; Johnson SC; Borrie M; Lee TY; Asthana S; Carlsson CM; Potkin SG; Highum D; Preda A; Nguyen D; Tariot PN; Reiman EM; Hendin BA; Scharre DW; Kataki M; Beversdorf DQ; Zimmerman EA; Celmins D; Brown AD; Gandy S; Marenberg ME; Rovner BW; Pearlson G; Blank K; Anderson K; Saykin AJ; Santulli RB; Pare N; Williamson JD; Sink KM; Potter H; Raj BA; Giordano A; Ott BR; Wu CK; Cohen R; Wilks KL; Safirstein BE
85.
Kim HB, Ahn S, Jang HJ, Sim SB, Kim KW:
Evaluation of corrosion behaviors and surface profiles of platinum-coated electrodes by electrochemistry and complementary microscopy: biomedical implications for anticancer therapy.
Micron
; 2007;38(7):747-53
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
Furthermore, nude mice inoculated with
a bronchoalveolar cancer cell
line and exposed to direct electric field showed the deterioration of proliferated tumor cells, proving the efficacy of electrochemical treatment.
Hazardous Substances Data Bank.
PLATINUM
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17493825.001).
[ISSN]
0968-4328
[Journal-full-title]
Micron (Oxford, England : 1993)
[ISO-abbreviation]
Micron
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
[Chemical-registry-number]
49DFR088MY / Platinum
86.
Gandara DR, Aberle D, Lau D, Jett J, Akhurst T, Heelan R, Mulshine J, Berg C, Patz EF Jr:
Radiographic imaging of bronchioloalveolar carcinoma: screening, patterns of presentation and response assessment.
J Thorac Oncol
; 2006 Nov;1(9 Suppl):S20-6
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Radiographic imaging
of bronchioloalveolar carcinoma
: screening, patterns of presentation and response assessment.
Bronchioloalveolar carcinoma
(
BAC
) is a previously uncommon subset
of adenocarcinoma
with unique epidemiology, pathology, radiographic presentation, clinical features, and natural history compared with other non-small
cell lung cancer
(NSCLC) subtypes.
Classically,
BAC
demonstrates a relatively slow growth pattern and indolent clinical course.
However, in a subset of patients, rapid growth and death from bilateral diffuse consolidative
disease
occurs within months
of diagnosis
or recurrence.
Recent data suggest that the incidence
of BAC
is increasing, notably in younger nonsmoking women.
The initial radiographic presentation
of BAC
varies considerably, from single ground glass opacities (GGOs) or nodules of mixed ground glass and solid attenuation to diffuse consolidative or bilateral multinodular
disease
.
The rising incidence
of BAC
is also reflected in recent
lung cancer
screening studies employing helical computed tomography (CT), where the differential
diagnosis of
GGOs includes not only
BAC
and overt
adenocarcinoma
, but inflammatory
disease
, focal fibrosis, and atypical adenomatous hyperplasia.
Because advanced-stage
BAC
presents as measurable mass lesions in fewer than 50% of cases, determination of radiographic response to therapy by standard criteria is often difficult.
Here, we review current data regarding the radiographic imaging
of BAC
: its radiographic presentations in asymptomatic early-stage and in advanced-stage
disease
, the functional imaging characteristics
of BAC
, and challenges of response assessment, including evolving opportunities for computer-assisted image analysis.
[MeSH-major]
Adenocarcinoma
,
Bronchiolo
-
Alveolar
/ radiography.
Carcinoma
, Non-Small-
Cell Lung
/ radiography.
Lung
Neoplasms / radiography. Neoplasm Recurrence, Local / radiography. Tomography, Spiral Computed
[MeSH-minor]
Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Combined Modality Therapy.
Diagnosis
, Differential. Female. Follow-Up Studies. Humans. Male. Mass Screening / methods. Neoplasm Staging. Pneumonectomy / methods. Positron-Emission Tomography. Sensitivity and Specificity. Treatment Outcome
MedlinePlus Health Information.
consumer health - Lung Cancer
.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[ErratumIn]
J Thorac Oncol. 2007 Jan;2(1):11. Heelan, Robert [added]
(PMID = 17409997.001).
[ISSN]
1556-1380
[Journal-full-title]
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
[ISO-abbreviation]
J Thorac Oncol
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Review
[Publication-country]
United States
[Number-of-references]
65
87.
Inoue K, Wakakura M, Miyanaga Y, Tomita G:
[Microbial contamination of nipradiol with and without benzalkonium chloride].
Nippon Ganka Gakkai Zasshi
; 2010 Jul;114(7):604-11
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
PURPOSE: To compare microbial contamination of nipradiol both with and without benzalkonium chloride (
BAC
).
SUBJECTS AND METHODS: Twenty primary open angle glaucoma patients treated with nipradiol with
BAC
were studied.
The nipradiol with
BAC
was switched to nipradiol without
BAC
.
Four weeks after switching, the nipradiol without
BAC
was once again switched to nipradiol with
BAC
.
RESULTS: In nipradiol without
BAC
microorganisms were isolated from caps (30%), nozzles (50%), solutions (0%), and filters (15%), whereas in nipradiol with
BAC
they were isolated from caps (35%), nozzles (40%), and solutions (25%).
The microorganisms in the nipradiol without
BAC
were coagulase-negative Staphylococci (38.2%) and Propionibacterium acnes (29.4%), and in the nipradiol with
BAC
they were coagulase-negative Staphylococci (20.5%), Alcaligenes xylosoxidans (12.8%).
CONCLUSIONS: In nipradiol without
BAC
, the bacteria were detected outside the filters, but not in the solution.
The rate of microbial contamination of the nipradiol without
BAC
was similar to that of the nipradiol with
BAC
.
Both the bacteria detected from the nipradiol with and those detected in the solution without
BAC
consisted only
of bacterial
flora of the cul-
de
-sac and skin.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 20681256.001).
[ISSN]
0029-0203
[Journal-full-title]
Nippon Ganka Gakkai zasshi
[ISO-abbreviation]
Nippon Ganka Gakkai Zasshi
[Language]
jpn
[Publication-type]
English Abstract; Journal Article
[Publication-country]
Japan
[Chemical-registry-number]
0 / Anti-Infective Agents, Local; 0 / Benzalkonium Compounds; 0 / Ophthalmic Solutions; 0 / Propanolamines; FVM336I71Y / nipradilol
88.
McCartt AT, Hellinga LA, Wells JK:
Effects of a college community campaign on drinking and driving with a strong enforcement component.
Traffic Inj Prev
; 2009 Apr;10(2):141-7
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Effects
of a
college community campaign on drinking and driving with a strong enforcement component.
The effects on driving at various blood alcohol concentrations (
BACs
) were evaluated, particularly for drivers ages 16-24 targeted by the program.
METHODS: Objective measures of driver
BACs
were collected through nighttime roadside surveys before and during the program in the experimental college community and a comparison college community.
Logistic regression models estimated the program's effects on the likelihood of driving at various
BAC
thresholds in the program community, after accounting for
BAC
patterns in the comparison community.
RESULTS: Relative to the comparison community, consistent reductions in driving at various
BAC
levels (positive
BAC
and
BAC
at least 0.02, 0.05, or 0.08%) were achieved in the experimental community.
Reductions were greatest for 16- to 20-year-olds (from 66% for positive
BAC
to 94% for
BAC
> or = 0.05%), followed by 21- to 24-year-olds (from 32% for positive
BAC
to 71% for
BAC
> or = 0.08%) and drivers 25 and older (from 23% for positive
BAC
to 53% for
BAC
> or = 0.08%).
All reductions for 16- to 20-year-olds were significant (p < 0.05), and all except the reduction for
BAC
> or = 0.08 percent were significantly greater than the corresponding reductions for drivers 25 and older.
Reductions for 21- to 24-year-olds were significant for
BACs
at least 0.02, 0.05, and 0.08 percent, but they were not significantly greater than the corresponding reductions for drivers 25 and older.
MedlinePlus Health Information.
consumer health - Alcohol
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 19333826.001).
[ISSN]
1538-957X
[Journal-full-title]
Traffic injury prevention
[ISO-abbreviation]
Traffic Inj Prev
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
89.
Tao T, Su SK, Miao YG, Yue WF, Du HH, Chen SL, Liu F, Zhan Y:
Expression of apalbumin1 of Apis cerana cerana in the larvae of silkworm, Bombyx mori.
J Agric Food Chem
; 2008 Oct 22;56(20):9464-8
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
In this study, Bacmid- apalbumin1 was constructed for Apis cerana cerana using the newly established
Bac
-to-
Bac
/BmNPV baculovirus expression system (BES).
The r
Accapalbumin1 was then purified by Ni-NTA spin columns and subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting.
The peptide Ile-Phe was identified from trypsin production
of r
Accapalbumin1.
COS Scholar Universe.
author profiles
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 18800804.001).
[ISSN]
1520-5118
[Journal-full-title]
Journal of agricultural and food chemistry
[ISO-abbreviation]
J. Agric. Food Chem.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / Glycoproteins; 0 / Insect Proteins; 0 / apalbumin 1, honeybee
90.
Qin LT, Wang XJ, Hu S, Li ZZ, Chen WY, Ge JY, Liu SD, Bu ZG:
[Expression of porcine gamma-interferon in recombinant baculovirus and determination of its antiviral activity].
Sheng Wu Gong Cheng Xue Bao
; 2007 May;23(3):386-91
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The full-length porcine interferon gamma(PoIFN-gamma) cDNA, including the secretion signal peptide coding region was recloned into honor plasmid pFastBac 1
of Bac
-To-
Bac
Baculovirus Expression System.
[MeSH-minor]
Animals. Blotting, Western.
Cell
Line. Enzyme-Linked Immunosorbent Assay. Fluorescent Antibody Technique, Indirect. Gene Expression. Green Fluorescent Proteins / genetics. Green Fluorescent Proteins / metabolism. Immune Sera / immunology. Mice. Mice, Inbred BALB C. Microscopy, Fluorescence. Recombinant Proteins. Spodoptera. Swine. Vesiculovirus / genetics. Virus Replication / drug effects
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 17577980.001).
[ISSN]
1000-3061
[Journal-full-title]
Sheng wu gong cheng xue bao = Chinese journal of biotechnology
[ISO-abbreviation]
Sheng Wu Gong Cheng Xue Bao
[Language]
chi
[Publication-type]
English Abstract; Journal Article
[Publication-country]
China
[Chemical-registry-number]
0 / Antiviral Agents; 0 / Immune Sera; 0 / Recombinant Proteins; 147336-22-9 / Green Fluorescent Proteins; 82115-62-6 / Interferon-gamma
91.
Koina E, Graves JA:
Assignment of the glucose-6-phosphate dehydrogenase (G6PD) gene to tammar wallaby chromosome Xq by fluorescence in situ hybridization with a BAC clone.
Cytogenet Genome Res
; 2005;108(4):362
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Assignment of the glucose-6-phosphate dehydrogenase (G6PD) gene to tammar wallaby chromosome Xq by fluorescence in situ hybridization with
a BAC
clone.
[MeSH-major]
Chromosomes, Artificial,
Bacterial
/ genetics. Glucosephosphate Dehydrogenase / genetics. In Situ Hybridization, Fluorescence / methods. Macropodidae / genetics. X Chromosome / genetics
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
(PMID = 15628031.001).
[ISSN]
1424-859X
[Journal-full-title]
Cytogenetic and genome research
[ISO-abbreviation]
Cytogenet. Genome Res.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Switzerland
[Chemical-registry-number]
EC 1.1.1.49 / Glucosephosphate Dehydrogenase
92.
Gao M, Li G, McCombie WR, Quiros CF:
Comparative analysis of a transposon-rich Brassica oleracea BAC clone with its corresponding sequence in A. thaliana.
Theor Appl Genet
; 2005 Sep;111(5):949-55
[Fulltext service]
Get downloadable
fulltext PDFs
of
articles closely matching to this article
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Comparative analysis
of a
transposon-rich Brassica oleracea
BAC
clone with its corresponding sequence in A. thaliana.
We compared the sequence
of a
96.7 Kb-long
BAC
clone (B 19 N 3) from Brassica oleracea (broccoli) with its corresponding regions in Arabidopsis thaliana.
A contig for this region was constructed by primer walking and
BAC
-end-sequencing, revealing general gene colinearity between both species.
[MeSH-minor]
Base Sequence. Chromosome Mapping. Chromosomes, Artificial,
Bacterial
. Cloning, Molecular. Expressed Sequence Tags. Gene Library. Reproducibility of Results
COS Scholar Universe.
author profiles
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
The Arabidopsis Information Resource.
Linked Gene Data
(subscription/membership/fee required).
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
Plant Physiol. 2001 Nov;127(3):1077-88
[
11706188.001
]
[Cites]
Mol Gen Genet. 1999 Jul;261(6):883-91
[
10485278.001
]
[Cites]
Theor Appl Genet. 2003 Jun;107(1):168-80
[
12835942.001
]
[Cites]
Genetics. 1994 Oct;138(2):499-510
[
7828831.001
]
[Cites]
Genetics. 2001 Mar;157(3):1321-30
[
11238417.001
]
[Cites]
Genome. 2001 Oct;44(5):808-17
[
11681604.001
]
[Cites]
Genetics. 2002 Dec;162(4):1937-43
[
12524361.001
]
[Cites]
Genome Res. 2003 Jan;13(1):46-54
[
12529305.001
]
[Cites]
Mol Genet Genomics. 2003 Feb;268(5):656-65
[
12589440.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5589-94
[
15064405.001
]
[Cites]
Plant Mol Biol. 1996 Mar;30(6):1321-9
[
8704140.001
]
[Cites]
Genetics. 2003 May;164(1):359-72
[
12750346.001
]
[Cites]
J Mol Biol. 1997 Apr 25;268(1):78-94
[
9149143.001
]
[Cites]
Genome Res. 2000 Jun;10(6):776-88
[
10854410.001
]
[Cites]
Genomics. 1999 Jul 1;59(1):24-31
[
10395796.001
]
[Cites]
Plant J. 2000 Jul;23(2):233-43
[
10929117.001
]
[Cites]
Bioinformatics. 2000 Oct;16(10):944-5
[
11120685.001
]
[Cites]
Science. 1996 Nov 1;274(5288):765-8
[
8864112.001
]
[Cites]
Genome. 2004 Aug;47(4):666-79
[
15284871.001
]
[Cites]
Nature. 2000 Dec 14;408(6814):796-815
[
11130711.001
]
[Cites]
Trends Genet. 2001 Feb;17(2):89-93
[
11173118.001
]
[Cites]
J Mol Evol. 1999 May;48(5):597-604
[
10198125.001
]
[Cites]
Proc Natl Acad Sci U S A. 2003 Nov 25;100 Suppl 2:14587-92
[
14506289.001
]
[Cites]
Genetics. 1998 Nov;150(3):1217-28
[
9799273.001
]
[Cites]
Genetica. 1999;107(1-3):53-63
[
10952197.001
]
[Cites]
Genome. 1998 Feb;41(1):62-9
[
9549059.001
]
[Cites]
Nucleic Acids Res. 1997 Sep 1;25(17):3389-402
[
9254694.001
]
(PMID = 16044267.001).
[ISSN]
0040-5752
[Journal-full-title]
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik
[ISO-abbreviation]
Theor. Appl. Genet.
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Germany
[Chemical-registry-number]
0 / DNA Transposable Elements
93.
Huyghe A, Francois P, Charbonnier Y, Tangomo-Bento M, Bonetti EJ, Paster BJ, Bolivar I, Baratti-Mayer D, Pittet D, Schrenzel J, Geneva Study Group on Noma (GESNOMA):
Novel microarray design strategy to study complex bacterial communities.
Appl Environ Microbiol
; 2008 Mar;74(6):1876-85
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
[Title]
Novel microarray design strategy to study
complex bacterial
communities.
Assessing
bacterial
flora composition appears to be of increasing importance to fields as diverse as physiology, development, medicine, epidemiology, the environment, and the food industry.
We report here the development and validation of an original microarray strategy that allows analysis of the phylogenic composition
of complex bacterial
mixtures.
Probe design was performed by selecting oligonucleotide sequences specific to each node of the seven levels of the
bacterial
phylogenetic tree (domain, phylum, class, order, family, genus, and species).
This approach, based on sequence information, allows analysis of the
bacterial
contents
of complex bacterial
mixtures to detect both known and unknown microorganisms.
Initial proof-of-concept experiments were performed on oral
bacterial
communities.
COS Scholar Universe.
author profiles
.
The Lens.
Cited by Patents in
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
BMC Genomics. 2005;6:95
[
15963225.001
]
[Cites]
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D294-6
[
15608200.001
]
[Cites]
J Clin Microbiol. 2005 Nov;43(11):5721-32
[
16272510.001
]
[Cites]
Oral Microbiol Immunol. 2006 Feb;21(1):61-8
[
16390343.001
]
[Cites]
Nucleic Acids Res. 2006;34(1):e5
[
16407321.001
]
[Cites]
J Mol Diagn. 2005 Feb;7(1):105-10
[
15681481.001
]
[Cites]
Appl Environ Microbiol. 2005 Mar;71(3):1373-86
[
15746340.001
]
[Cites]
Environ Microbiol. 2006 Feb;8(2):289-307
[
16423016.001
]
[Cites]
Cell Microbiol. 2006 May;8(5):738-57
[
16611224.001
]
[Cites]
Science. 2006 Jun 2;312(5778):1355-9
[
16741115.001
]
[Cites]
Anal Chem. 2006 Jul 15;78(14):4794-802
[
16841897.001
]
[Cites]
Appl Environ Microbiol. 2006 Sep;72(9):6288-98
[
16957256.001
]
[Cites]
Environ Microbiol. 2006 Oct;8(10):1721-35
[
16958753.001
]
[Cites]
Microb Ecol. 2006 Aug;52(2):159-75
[
16897303.001
]
[Cites]
Nature. 2006 Dec 21;444(7122):1027-31
[
17183312.001
]
[Cites]
Proc Natl Acad Sci U S A. 2007 Jan 2;104(1):299-304
[
17182744.001
]
[Cites]
Environ Microbiol. 2007 Jan;9(1):81-92
[
17227414.001
]
[Cites]
FEMS Microbiol Ecol. 2007 Jan;59(1):81-94
[
17233746.001
]
[Cites]
Microb Ecol. 2007 Apr;53(3):371-83
[
17334858.001
]
[Cites]
J Clin Microbiol. 2007 Jun;45(6):1954-62
[
17409203.001
]
[Cites]
J Microbiol Methods. 2007 Jul;70(1):165-78
[
17543401.001
]
[Cites]
Appl Environ Microbiol. 2007 Aug;73(15):4707-16
[
17545322.001
]
[Cites]
Appl Environ Microbiol. 2007 Aug;73(16):5261-7
[
17586664.001
]
[Cites]
Proc Natl Acad Sci U S A. 2007 Aug 21;104(34):13780-5
[
17699621.001
]
[Cites]
ISME J. 2007 May;1(1):67-77
[
18043615.001
]
[Cites]
PLoS Biol. 2007 Jul;5(7):e177
[
17594176.001
]
[Cites]
Proc Natl Acad Sci U S A. 1999 Dec 7;96(25):14547-52
[
10588742.001
]
[Cites]
Am J Med Genet. 2000 Oct 9;96(5):604-15
[
11054767.001
]
[Cites]
J Bacteriol. 2001 Jun;183(12):3770-83
[
11371542.001
]
[Cites]
J Clin Microbiol. 2001 Oct;39(10):3578-82
[
11574575.001
]
[Cites]
Appl Environ Microbiol. 2001 Dec;67(12):5780-90
[
11722935.001
]
[Cites]
Genome Biol. 2002;3(2):REVIEWS0003
[
11864374.001
]
[Cites]
Appl Environ Microbiol. 2002 May;68(5):2535-41
[
11976131.001
]
[Cites]
Nucleic Acids Res. 2002 Jun 1;30(11):e51
[
12034852.001
]
[Cites]
J Clin Microbiol. 2002 Jun;40(6):2187-91
[
12037085.001
]
[Cites]
Toxicol Sci. 2002 Oct;69(2):383-90
[
12377987.001
]
[Cites]
Environ Microbiol. 2003 Jul;5(7):566-82
[
12823189.001
]
[Cites]
Infect Immun. 2004 Apr;72(4):2272-9
[
15039352.001
]
[Cites]
Science. 2004 Apr 2;304(5667):66-74
[
15001713.001
]
[Cites]
Biotechniques. 2004 Apr;36(4):664-70, 672, 674-5
[
15088384.001
]
[Cites]
Proc Natl Acad Sci U S A. 2004 Apr 20;101(16):6176-81
[
15067114.001
]
[Cites]
Appl Environ Microbiol. 2004 Jul;70(7):4303-17
[
15240314.001
]
[Cites]
Clin Microbiol Rev. 2004 Oct;17(4):840-62, table of contents
[
15489351.001
]
[Cites]
Proc Natl Acad Sci U S A. 1998 Feb 17;95(4):1460-5
[
9465037.001
]
[Cites]
J Bacteriol. 1998 Sep;180(18):4765-74
[
9733676.001
]
[Cites]
Nat Genet. 1999 Jan;21(1 Suppl):42-7
[
9915500.001
]
[Cites]
Am J Trop Med Hyg. 1999 Jan;60(1):150-6
[
9988340.001
]
[Cites]
Am J Trop Med Hyg. 1999 Feb;60(2):223-32
[
10072140.001
]
[Cites]
Appl Environ Microbiol. 2004 Dec;70(12):7161-72
[
15574913.001
]
[Cites]
Infect Immun. 2005 Sep;73(9):5367-78
[
16113252.001
]
(PMID = 18203854.001).
[ISSN]
1098-5336
[Journal-full-title]
Applied and environmental microbiology
[ISO-abbreviation]
Appl. Environ. Microbiol.
[Language]
ENG
[Grant]
United States / NIDCR NIH HHS / DE / R01 DE011443; United States / NIDCR NIH HHS / DE / DE-11443
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / RNA, Ribosomal, 16S
[Other-IDs]
NLM/ PMC2268287
94.
Taketa S, Matsuki K, Amano S, Saisho D, Himi E, Shitsukawa N, Yuo T, Noda K, Takeda K:
Duplicate polyphenol oxidase genes on barley chromosome 2H and their functional differentiation in the phenol reaction of spikes and grains.
J Exp Bot
; 2010 Sep;61(14):3983-93
[Fulltext service]
Download
fulltext PDF
of
this article and others
, as many as you want.
[Source]
The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
The full-lengths of the respective PPO genes were cloned using
a BAC
library, inverse-PCR, and 3'-RACE.
Subsequent
RT
-PCR experiments showed that PPO1 was expressed in hulls and awns, and that PPO2 was expressed in the caryopses.
In PPO1, amino acid substitutions of five types affecting functionally important motif(s) or C-
terminal
region(s) were identified in 40 of the 51 accessions tested.
An insertion
of a
hAT-family transposon in the promoter region of PPO2 may be responsible for different expression patterns of the duplicate PPO genes in barley.
National BioResource Project.
culture/stock collections - NBRP resources
.
[Email]
Email this result item
Email the results to the following email address:
[X] Close
[Cites]
J Agric Food Chem. 2006 Mar 22;54(6):2378-84
[
16536622.001
]
[Cites]
Funct Integr Genomics. 2005 Oct;5(4):185-200
[
15918034.001
]
[Cites]
J Agric Food Chem. 2006 Dec 27;54(26):9978-84
[
17177530.001
]
[Cites]
Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3289-94
[
17360640.001
]
[Cites]
Theor Appl Genet. 2007 May;114(7):1239-47
[
17468807.001
]
[Cites]
Theor Appl Genet. 2007 Jun;115(1):47-58
[
17426955.001
]
[Cites]
Mol Biol Evol. 2007 Aug;24(8):1596-9
[
17488738.001
]
[Cites]
Genetics. 2007 Nov;177(3):1765-76
[
17947416.001
]
[Cites]
Proc Natl Acad Sci U S A. 2008 Mar 11;105(10):4062-7
[
18316719.001
]
[Cites]
Plant Cell. 2008 Nov;20(11):2946-59
[
19033526.001
]
[Cites]
Plant J. 2009 Feb;57(3):413-25
[
18808453.001
]
[Cites]
BMC Plant Biol. 2009;9:94
[
19619287.001
]
[Cites]
Genetics. 2009 Dec;183(4):1315-25
[
19822730.001
]
[Cites]
Nucleic Acids Res. 2010 Jan;38(Database issue):D835-42
[
19854933.001
]
[Cites]
J Inorg Biochem. 2006 Jan;100(1):108-23
[
16332393.001
]
[Cites]
Plant Cell. 2000 May;12(5):637-46
[
10810140.001
]
[Cites]
Plant Physiol. 2000 Sep;124(1):285-95
[
10982443.001
]
[Cites]
Genetics. 2000 Dec;156(4):1997-2005
[
11102390.001
]
[Cites]
Planta. 2002 Jun;215(2):239-47
[
12029473.001
]
[Cites]
Cell Mol Biol Lett. 2002;7(2B):763-9
[
12378236.001