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1. Varela M, Spencer TE, Palmarini M, Arnaud F: Friendly viruses: the special relationship between endogenous retroviruses and their host. Ann N Y Acad Sci; 2009 Oct;1178:157-72
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  • [Title] Friendly viruses: the special relationship between endogenous retroviruses and their host.
  • Endogenous retroviruses (ERVs) are present in the genome of all vertebrates and have coevolved with their hosts for millions of years.
  • Some ERVs play a critical role in placental development, contribute to genome plasticity, and protect the host against infection of related pathogenic and exogenous retroviruses, thus some ERVs have been positively selected and maintained in the host genome.
  • The sheep genome contains 27 endogenous retroviruses (enJSRVs) related to the pathogenic Jaagsiekte sheep retrovirus (JSRV), the causative agent of a transmissible lung cancer in sheep. enJSRVs are able to protect their host against JSRV infection by blocking different steps of the viral replication cycle.
  • In addition, enJSRVs are absolutely required for sheep placental development.
  • Thus, enJSRVs-JSRV provides a unique and interesting model to study the symbiotic relationship and interplay between host ERVs and evolution.
  • This review will provide some examples of the biological functions of ERvs. In particular, the role of ERVs in reproductive biology and in protecting the host against pathogenic retrovirus infections will be emphasized using enJSRVs/JSRV and the sheep as a model.

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  • (PMID = 19845636.001).
  • [ISSN] 1749-6632
  • [Journal-full-title] Annals of the New York Academy of Sciences
  • [ISO-abbreviation] Ann. N. Y. Acad. Sci.
  • [Language] ENG
  • [Grant] United States / NICHD NIH HHS / HD / R01 HD052745; United States / NICHD NIH HHS / HD / HD052745; United Kingdom / Wellcome Trust / /
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS634039; NLM/ PMC4199234
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2. Ruys AT, Alderlieste YA, Gouma DJ, Dekker E, Mathus-Vliegen EM: Jejunal cancer in patients with familial adenomatous polyposis. Clin Gastroenterol Hepatol; 2010 Aug;8(8):731-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Jejunal cancer in patients with familial adenomatous polyposis.
  • BACKGROUND & AIMS: Familial adenomatous polyposis (FAP) is an inherited disease affecting approximately 1:10,000 newborns, characterized by the formation of numerous adenomas in the digestive tract.
  • RESULTS: Three patients with FAP aged 71, 57, and 59 years developed advanced duodenal adenomatosis and a jejunal carcinoma, which was associated with poor prognosis in 2 patients.
  • [MeSH-major] Adenocarcinoma / diagnosis. Adenoma / diagnosis. Adenomatous Polyposis Coli / complications. Jejunal Neoplasms / diagnosis


3. Cajaiba MM, Sarita-Reyes C, Zambrano E, Reyes-Múgica M: Mesenchymal hamartoma of the liver associated with features of Beckwith-Wiedemann syndrome and high serum alpha-fetoprotein levels. Pediatr Dev Pathol; 2007 May-Jun;10(3):233-8
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  • In addition, we analyze the unusual pancreatic lesion (focal endocrine adenomatosis) leading to severe hyperinsulinemic hypoglycemia in a patient with possible BWS.

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  • [CommentIn] Pediatr Dev Pathol. 2008 Jul-Aug;11(4):264-5 [17990933.001]
  • (PMID = 17535089.001).
  • [ISSN] 1093-5266
  • [Journal-full-title] Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
  • [ISO-abbreviation] Pediatr. Dev. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / alpha-Fetoproteins
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4. Hardy OT, Hernandez-Pampaloni M, Saffer JR, Suchi M, Ruchelli E, Zhuang H, Ganguly A, Freifelder R, Adzick NS, Alavi A, Stanley CA: Diagnosis and localization of focal congenital hyperinsulinism by 18F-fluorodopa PET scan. J Pediatr; 2007 Feb;150(2):140-5
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  • Pathology results confirmed that all 11 had focal adenomatosis, and the locations of these lesions matched the areas of increased [18F]-DOPA uptake on the PET scans in all of the cases.

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  • [CommentIn] J Pediatr. 2007 Feb;150(2):122-4 [17236885.001]
  • (PMID = 17236890.001).
  • [ISSN] 1097-6833
  • [Journal-full-title] The Journal of pediatrics
  • [ISO-abbreviation] J. Pediatr.
  • [Language] eng
  • [Grant] United States / NCRR NIH HHS / RR / M01-RR-00240; United States / NIDDK NIH HHS / DK / R01-DK-56268; United States / NIDDK NIH HHS / DK / T32-DK63688
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
  • [Chemical-registry-number] 2C598205QX / fluorodopa F 18; 63-84-3 / Dihydroxyphenylalanine
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5. Kwon JE, Park YN: [Hepatic adenomatosis in glycogen storage disease]. Korean J Hepatol; 2008 Mar;14(1):108-12
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  • [Title] [Hepatic adenomatosis in glycogen storage disease].

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  • (PMID = 18367864.001).
  • [ISSN] 1738-222X
  • [Journal-full-title] The Korean journal of hepatology
  • [ISO-abbreviation] Korean J Hepatol
  • [Language] kor
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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6. Berkhout M, Roelofs HM, te Morsche RH, Dekker E, van Krieken JH, Nagengast FM, Peters WH: Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis. Br J Surg; 2008 Apr;95(4):499-505
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis.
  • BACKGROUND: Patients with familial adenomatous polyposis (FAP) are at high risk of developing duodenal adenomas and carcinomas.
  • Besides germline mutations in the adenomatous polyposis coli (APC) gene, additional factors may influence the age of onset and number of duodenal adenomas.
  • The polymorphisms investigated had no predictive value for the severity of duodenal adenomatosis in patients with FAP.
  • CONCLUSION: Although the variant genotypes of UGT1A3 were less common in patients with FAP than in those without, this did not modulate the severity of duodenal adenomatosis.
  • [MeSH-major] Adenomatous Polyposis Coli / enzymology. Duodenal Neoplasms / enzymology. Genes, APC. Glucuronosyltransferase / genetics. Glutathione Transferase / genetics. Polymorphism, Genetic / genetics


7. Henopp T, Anlauf M, Schmitt A, Schlenger R, Zalatnai A, Couvelard A, Ruszniewski P, Schaps KP, Jonkers YM, Speel EJ, Pellegata NS, Heitz PU, Komminoth P, Perren A, Klöppel G: Glucagon cell adenomatosis: a newly recognized disease of the endocrine pancreas. J Clin Endocrinol Metab; 2009 Jan;94(1):213-7
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  • [Title] Glucagon cell adenomatosis: a newly recognized disease of the endocrine pancreas.
  • BACKGROUND: Glucagon-producing tumors are either solitary neoplasms of the pancreas, occasionally associated with a glucagonoma syndrome, or multiple neoplasms associated with multiple endocrine neoplasia type 1 (MEN1).
  • METHODS: Pancreatic tissue from four patients showing multiple neuroendocrine microadenomas and in two cases also macrotumors were screened for hormones using immunohistochemical and morphometric methods.
  • CONCLUSIONS: The findings are sufficiently distinctive to suggest a new neoplastic disease of the endocrine pancreas that we recommend calling glucagon cell adenomatosis.

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  • (PMID = 18957496.001).
  • [ISSN] 0021-972X
  • [Journal-full-title] The Journal of clinical endocrinology and metabolism
  • [ISO-abbreviation] J. Clin. Endocrinol. Metab.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / MEN1 protein, human; 0 / Proto-Oncogene Proteins; 147604-94-2 / Cyclin-Dependent Kinase Inhibitor p27; 9007-92-5 / Glucagon; EC 6.3.2.19 / VHL protein, human; EC 6.3.2.19 / Von Hippel-Lindau Tumor Suppressor Protein
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8. Herrejón A, Cervera A, Maciá M, Ferrer R, Blanquer R: [Bronchioloalveolar adenoma associated with bronchiolitis obliterans and leishmaniasis with lung involvement in acquired immunodeficiency syndrome]. Arch Bronconeumol; 2005 Apr;41(4):233-5
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  • In addition, the transbronchial biopsy findings were consistent with a diagnosis of bronchioloalveolar adenoma with radiographic evidence of multiple nodules.
  • [MeSH-major] Acquired Immunodeficiency Syndrome / complications. Adenomatosis, Pulmonary / diagnosis. Bronchiolitis Obliterans / diagnosis. Leishmaniasis / diagnosis. Lung Diseases, Parasitic / diagnosis


9. Kim JC, Cho YK, Roh SA, Yu CS, Gong G, Jang SJ, Kim SY, Kim YS: Individual tumorigenesis pathways of sporadic colorectal adenocarcinomas are associated with the biological behavior of tumors. Cancer Sci; 2008 Jul;99(7):1348-54
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  • Individual steps in the tumorigenesis pathway, that is, adenomatosis polyposis coli (APC), Wnt-activated, base excision repair mutations, mismatch repair defects, RAF-mediated, transforming growth factor (TGF)-beta-suppressed, bone morphogenic protein (BMP)-suppressed, and p53 alterations, were examined in terms of genetic and epigenetic changes, as well as protein expression.

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  • [ErratumIn] Cancer Sci. 2008 Jul;99(7):1499
  • (PMID = 18422752.001).
  • [ISSN] 1349-7006
  • [Journal-full-title] Cancer science
  • [ISO-abbreviation] Cancer Sci.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] EC 2.7.11.1 / raf Kinases
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10. Komaba H, Takeda Y, Shin J, Tanaka R, Kakuta T, Tominaga Y, Fukagawa M: Reversed whole PTH/intact PTH ratio as an indicator of marked parathyroid enlargement: five case studies and a literature review. NDT Plus; 2008 Aug;1(Suppl 3):iii54-iii58
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  • In the case of a single enlarged gland, the pathological pattern and heterogeneous expression of parathyroid adenomatosis 1/cyclin D1 suggested it to be a single nodule of uraemic hyperparathyroidism rather than sporadic primary adenoma.

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  • (PMID = 25983975.001).
  • [ISSN] 1753-0784
  • [Journal-full-title] NDT plus
  • [ISO-abbreviation] NDT Plus
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC4421125
  • [Keywords] NOTNLM ; N-PTH / intact PTH / secondary hyperparathyroidism / single nodule / whole PTH
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11. Di Sandro S, Slim AO, Lauterio A, Giacomoni A, Mangoni I, Aseni P, Pirotta V, Aldumour A, Mihaylov P, De Carlis L: Liver adenomatosis: a rare indication for living donor liver transplantation. Transplant Proc; 2009 May;41(4):1375-7
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  • [Title] Liver adenomatosis: a rare indication for living donor liver transplantation.
  • Liver adenomatosis (LA) is a rare benign disease of the liver with unclear pathogenesis, which is characterized by multiple hepatic adenomas.
  • A 48-year-old woman developed multiple liver adenomas.
  • Thirty-four months later, she developed recurrence of multiple hepatic adenomas and 2 nodules were highly suspect for hepatocellular carcinoma.


12. de Ferro SM, Suspiro A, Fidalgo P, Lage P, Rodrigues P, Fragoso S, Vitoriano I, Baltazar C, Albuquerque C, Bettencourt A, Leitão CN: Aggressive phenotype of MYH-associated polyposis with jejunal cancer and intra-abdominal desmoid tumor: report of a case. Dis Colon Rectum; 2009 Apr;52(4):742-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Aggressive phenotype of MYH-associated polyposis with jejunal cancer and intra-abdominal desmoid tumor: report of a case.
  • MYH-associated polyposis is an inherited autosomal recessive disease, linked to biallelic germline MYH mutations, which predisposes to the development of multiple colorectal adenomas and cancer.
  • We report the case of a young male patient with an aggressive MYH-associated polyposis phenotype.
  • He presented at aged 30 years with more than 100 colonic polyps and 4 colonic adenocarcinomas.
  • At aged 35 years, Spigelman Stage IV duodenal adenomatosis was detected.
  • Based on this report, we believe that screening of the entire small bowel should be recommended in MYH-associated polyposis patients, especially in those with duodenal adenomas.
  • Similar to patients with familial adenomatous polyposis, desmoid tumors also may be part of the clinical spectrum of MYH-associated polyposis and may prove to be a significant clinical problem in patients submitted to prophylactic colectomy.
  • [MeSH-major] Adenomatous Polyposis Coli / genetics. Colorectal Neoplasms / genetics. Fibromatosis, Aggressive / genetics. Jejunal Neoplasms / genetics. Neoplasms, Multiple Primary / genetics. Peritoneal Neoplasms / genetics


13. Kaufmann C, Brechbühl M, Oevermann A, Müller S, Zimmer K, Schönmann M, Leroux C, Weibel D, Bertoni G: [Enzootic nasal adenocarcinoma in a dairy sheep flock]. Schweiz Arch Tierheilkd; 2008 Jun;150(6):297-302
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  • The significance of the disease in Switzerland is discussed, also in the context of lung adenomatosis.
  • [MeSH-major] Adenocarcinoma / veterinary. Jaagsiekte sheep retrovirus / isolation & purification. Nose Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / diagnosis. Sheep Diseases / diagnosis

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  • (PMID = 18605021.001).
  • [ISSN] 0036-7281
  • [Journal-full-title] Schweizer Archiv für Tierheilkunde
  • [ISO-abbreviation] Schweiz. Arch. Tierheilkd.
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Switzerland
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14. Oyama T, Yamada Y, Hata K, Tomita H, Hirata A, Sheng H, Hara A, Aoki H, Kunisada T, Yamashita S, Mori H: Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Carcinogenesis; 2008 Mar;29(3):666-72
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  • Apc(Min/+) mouse, a mouse model for human familial adenomatosis polyposis, contains a truncating mutation in the Apc gene and spontaneously develops intestinal tumors.

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  • (PMID = 18204079.001).
  • [ISSN] 1460-2180
  • [Journal-full-title] Carcinogenesis
  • [ISO-abbreviation] Carcinogenesis
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Dkk1 protein, mouse; 0 / Intercellular Signaling Peptides and Proteins; 0 / T Cell Transcription Factor 1; 0 / Wnt Proteins; 0 / beta Catenin
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15. Haase M, Willenberg HS: Adrenal cortical tumors and multiple endocrine neoplasia-related syndromes. Minerva Endocrinol; 2009 Jun;34(2):123-35
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  • [Title] Adrenal cortical tumors and multiple endocrine neoplasia-related syndromes.
  • These syndromes and diseases include the Carney complex, the McCune-Albright syndrome, multiple endocrine neoplasia type 1, familial adenomatosis coli, congenital adrenal hyperplasia, familial forms of primary aldosteronism, the Beckwith-Wiedemann syndrome, and the Li-Fraumeni syndrome.
  • [MeSH-major] Adrenal Cortex Neoplasms / genetics. Multiple Endocrine Neoplasia / genetics. Mutation
  • [MeSH-minor] Adenomatous Polyposis Coli / genetics. Adrenal Hyperplasia, Congenital / genetics. Beckwith-Wiedemann Syndrome / genetics. Fibrous Dysplasia, Polyostotic / genetics. Heart Neoplasms / genetics. Humans. Hyperaldosteronism / genetics. Li-Fraumeni Syndrome / genetics. Multiple Endocrine Neoplasia Type 1 / genetics. Myxoma / genetics. Pigmentation Disorders / genetics

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  • (PMID = 19471237.001).
  • [ISSN] 0391-1977
  • [Journal-full-title] Minerva endocrinologica
  • [ISO-abbreviation] Minerva Endocrinol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] Italy
  • [Number-of-references] 100
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16. Marín Hernández C, Robles Campos R, López Conesa A, Parrilla P: [Multiple liver adenomatosis treated with surgical resection and radiofrequency]. Cir Esp; 2010 Nov;88(5):337-8
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  • [Title] [Multiple liver adenomatosis treated with surgical resection and radiofrequency].
  • [Transliterated title] Adenomatosis hepática múltiple tratada con resección quirúrgica y radiofrecuencia.

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  • (PMID = 20206344.001).
  • [ISSN] 1578-147X
  • [Journal-full-title] Cirugía española
  • [ISO-abbreviation] Cir Esp
  • [Language] spa
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Spain
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17. Tei R, Morimoto T, Miyamoto K, Aketa S, Shimokawara T, Shin Y, Hironaka Y: Intradural extramedullary ganglioneuroma associated with multiple hamartoma syndrome. Neurol Med Chir (Tokyo); 2007 Nov;47(11):513-5
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  • [Title] Intradural extramedullary ganglioneuroma associated with multiple hamartoma syndrome.
  • A 51-year-old woman presented with a rare completely intradural and extramedullary spinal ganglioneuroma associated with multiple hamartoma syndrome and manifesting as complaints of neck pain and dizziness persisting for 8 months.
  • She also suffered from multiple facial trichilemmomas, thyroid goiter, multiple polyposis of the gastrointestinal tract, and pulmonary hamartoma indicating multiple hamartoma syndrome.
  • [MeSH-major] Ganglioneuroma / pathology. Hamartoma Syndrome, Multiple / pathology. Spinal Cord Neoplasms / pathology

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  • (PMID = 18037807.001).
  • [ISSN] 0470-8105
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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18. Beaton MD, Taylor B, Driman D, Ainsworth P, Adams PC: Colonic interposition in a woman with attenuated familial adenomatosis polyposis: does the location of the colon affect polyp formation? Can J Gastroenterol; 2008 Jul;22(7):634-6
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  • [Title] Colonic interposition in a woman with attenuated familial adenomatosis polyposis: does the location of the colon affect polyp formation?
  • Attenuated familial adenomatous polyposis (AFAP) is a rare but well-established cause of colorectal carcinoma and multiple polyps.
  • While she had developed adenomatous polyps in her native cecum, there was no evidence of polyps or cancer in the segment of large intestine interposed between her upper esophagus and stomach.
  • [MeSH-major] Adenomatous Polyposis Coli / pathology. Colonic Polyps / pathology

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  • [Cites] Gut. 1999 Dec;45(6):829-33 [10562580.001]
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  • (PMID = 18629394.001).
  • [ISSN] 0835-7900
  • [Journal-full-title] Canadian journal of gastroenterology = Journal canadien de gastroenterologie
  • [ISO-abbreviation] Can. J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Canada
  • [Other-IDs] NLM/ PMC2661270
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19. Idogawa M, Yamada T, Honda K, Sato S, Imai K, Hirohashi S: Poly(ADP-ribose) polymerase-1 is a component of the oncogenic T-cell factor-4/beta-catenin complex. Gastroenterology; 2005 Jun;128(7):1919-36
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  • PARP-1 was overexpressed in the intestinal adenomas of patients with familial adenomatous polyposis and multiple intestinal polyposis mice.

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  • (PMID = 15940627.001).
  • [ISSN] 0016-5085
  • [Journal-full-title] Gastroenterology
  • [ISO-abbreviation] Gastroenterology
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CTNNB1 protein, human; 0 / Cytoskeletal Proteins; 0 / DNA-Binding Proteins; 0 / TCF Transcription Factors; 0 / TCF7L2 protein, human; 0 / Tcf7l2 protein, mouse; 0 / Trans-Activators; 0 / Transcription Factor 7-Like 2 Protein; 0 / Transcription Factors; 0 / beta Catenin; EC 2.4.2.30 / PARP1 protein, human; EC 2.4.2.30 / Poly(ADP-ribose) Polymerases
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20. Zlobec I, Terracciano L, Jass JR, Lugli A: Value of staining intensity in the interpretation of immunohistochemistry for tumor markers in colorectal cancer. Virchows Arch; 2007 Oct;451(4):763-9
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  • A tissue microarray of 1,197 colorectal cancers was immunostained for p53, Her2/neu, epidermal growth factor receptor (EGFR), adenomatosis polyposis coli (APC), and beta-catenin.
  • [MeSH-minor] Adenomatous Polyposis Coli Protein / metabolism. Humans. Multivariate Analysis. Neoplasm Staging. Receptor, Epidermal Growth Factor / metabolism. Receptor, ErbB-2 / metabolism. Tumor Suppressor Protein p53 / metabolism. beta Catenin / metabolism


21. Siderits R, Hanna I, Baig Z, Godyn JJ: Sporadic ganglioneuromatosis of esophagogastric junction in a patient with gastro-esophageal reflux disorder and intestinal metaplasia. World J Gastroenterol; 2006 Dec 28;12(48):7874-7
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  • Biopsies showed prominent intestinal metaplasia of Barrett's type without dysplasia, chronic inflammation and multiple aggregates of large cells within the mucosal lamina propria, some with spindle shaped nuclei.
  • No genetic syndromes were identified in the patient including familial adenomatous polyposis and multiple endocrine neoplasia type IIb (MEN IIb).

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  • (PMID = 17203537.001).
  • [ISSN] 1007-9327
  • [Journal-full-title] World journal of gastroenterology
  • [ISO-abbreviation] World J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC4087559
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22. Sun S, Schiller JH, Gazdar AF: Lung cancer in never smokers--a different disease. Nat Rev Cancer; 2007 Oct;7(10):778-90
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  • [MeSH-minor] Adenocarcinoma / epidemiology. Adenocarcinoma / genetics. Adenocarcinoma / pathology. Animals. Carcinoma, Small Cell / epidemiology. Carcinoma, Small Cell / genetics. Carcinoma, Small Cell / pathology. Carcinoma, Squamous Cell / epidemiology. Carcinoma, Squamous Cell / genetics. Carcinoma, Squamous Cell / pathology. Causality. Comorbidity. Cooking. Environmental Exposure / statistics & numerical data. Estrogens / metabolism. Female. Genetic Predisposition to Disease / epidemiology. Global Health. Humans. Incidence. Male. Mutation. Papillomavirus Infections / epidemiology. Polycyclic Hydrocarbons, Aromatic. Pulmonary Adenomatosis, Ovine / epidemiology. Radon. Risk Factors. Sex Distribution. Sheep. Smoking / epidemiology. Smoking / pathology. Tobacco Smoke Pollution / statistics & numerical data

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  • (PMID = 17882278.001).
  • [ISSN] 1474-1768
  • [Journal-full-title] Nature reviews. Cancer
  • [ISO-abbreviation] Nat. Rev. Cancer
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / P50 CA070907
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Estrogens; 0 / Polycyclic Hydrocarbons, Aromatic; 0 / Tobacco Smoke Pollution; Q74S4N8N1G / Radon
  • [Number-of-references] 163
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23. Müller MW, Dahmen R, Köninger J, Michalski CW, Hinz U, Hartel M, Kadmon M, Kleeff J, Büchler MW, Friess H: Is there an advantage in performing a pancreas-preserving total duodenectomy in duodenal adenomatosis? Am J Surg; 2008 Jun;195(6):741-8
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  • [Title] Is there an advantage in performing a pancreas-preserving total duodenectomy in duodenal adenomatosis?
  • BACKGROUND: Duodenal adenomatosis is a premalignant condition often not treatable by local resection or endoscopy.
  • Since the introduction of pancreas-preserving total duodenectomy (PPTD), the question has arisen whether a pp-Whipple resection is still needed to treat duodenal adenomatosis.
  • PATIENTS AND METHODS: In a 5-year period 23 PPTDs were performed for duodenal adenomatosis.
  • CONCLUSIONS: PPTD is a safe surgical procedure for duodenal adenomatosis that avoids pancreatic head resection, provides high quality of life, and shows advantages over the pp-Whipple procedure.


24. Svrcek M, Jeannot E, Arrivé L, Poupon R, Fromont G, Fléjou JF, Zucman-Rossi J, Bouchard P, Wendum D: Regressive liver adenomatosis following androgenic progestin therapy withdrawal: a case report with a 10-year follow-up and a molecular analysis. Eur J Endocrinol; 2007 Jun;156(6):617-21
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  • [Title] Regressive liver adenomatosis following androgenic progestin therapy withdrawal: a case report with a 10-year follow-up and a molecular analysis.
  • On the contrary, their contribution to liver adenomatosis (LA) development is still a debatable issue.

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  • (PMID = 17535860.001).
  • [ISSN] 0804-4643
  • [Journal-full-title] European journal of endocrinology
  • [ISO-abbreviation] Eur. J. Endocrinol.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Contraceptives, Oral, Synthetic; 0 / Hepatocyte Nuclear Factor 1-alpha; 0 / Receptors, Androgen; 0 / Receptors, Estrogen; 0 / Receptors, Progesterone; N2Z8ALG4U5 / Lynestrenol
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25. Griffiths DJ, Martineau HM, Cousens C: Pathology and pathogenesis of ovine pulmonary adenocarcinoma. J Comp Pathol; 2010 May;142(4):260-83
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  • [MeSH-major] Adenocarcinoma / virology. Jaagsiekte sheep retrovirus / physiology. Pulmonary Adenomatosis, Ovine. Sheep Diseases / virology

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  • [Copyright] Copyright 2010 Elsevier Ltd. All rights reserved.
  • (PMID = 20163805.001).
  • [ISSN] 1532-3129
  • [Journal-full-title] Journal of comparative pathology
  • [ISO-abbreviation] J. Comp. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Number-of-references] 171
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26. Hudachek SF, Kraft SL, Thamm DH, Bielefeldt-Ohmann H, DeMartini JC, Miller AD, Dernell WS: Lung tumor development and spontaneous regression in lambs coinfected with Jaagsiekte sheep retrovirus and ovine lentivirus. Vet Pathol; 2010 Jan;47(1):148-62
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Jaagsiekte sheep retrovirus. Lentivirus Infections / veterinary. Lentiviruses, Ovine-Caprine. Lung Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / pathology. Sheep Diseases / virology

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  • (PMID = 20080496.001).
  • [ISSN] 1544-2217
  • [Journal-full-title] Veterinary pathology
  • [ISO-abbreviation] Vet. Pathol.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA 59116
  • [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, Viral
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27. McGee-Estrada K, Palmarini M, Hallwirth C, Fan H: A Moloney murine leukemia virus driven by the Jaagsiekte sheep retrovirus enhancers shows enhanced specificity for infectivity in lung epithelial cells. Virus Genes; 2005 Dec;31(3):257-63
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  • [MeSH-minor] Animals. Cell Line. Enhancer Elements, Genetic. Epithelial Cells / virology. Genes, Viral. Mice. Plasmids / genetics. Pulmonary Adenomatosis, Ovine / etiology. Pulmonary Adenomatosis, Ovine / virology. Sheep. Terminal Repeat Sequences. Transfection. Virulence / genetics

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  • (PMID = 16175331.001).
  • [ISSN] 0920-8569
  • [Journal-full-title] Virus genes
  • [ISO-abbreviation] Virus Genes
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA85264; United States / NCI NIH HHS / CA / T32 CA09054
  • [Publication-type] 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
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28. Giovanoli O, Heim M, Terracciano L, Bongartz G, Ledermann HP: MRI of hepatic adenomatosis: initial observations with gadoxetic acid contrast agent in three patients. AJR Am J Roentgenol; 2008 May;190(5):W290-3
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  • [Title] MRI of hepatic adenomatosis: initial observations with gadoxetic acid contrast agent in three patients.
  • OBJECTIVE: The purpose of our study was to describe the MR signal characteristics of histologically proven liver adenomatosis in three patients using gadoxetic acid, a newly developed liver-specific MR contrast agent.

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  • (PMID = 18430814.001).
  • [ISSN] 1546-3141
  • [Journal-full-title] AJR. American journal of roentgenology
  • [ISO-abbreviation] AJR Am J Roentgenol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media; 0 / gadolinium ethoxybenzyl DTPA; K2I13DR72L / Gadolinium DTPA
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29. Vivarelli M, Lauro A, Cucchetti A, D'Errico A, Pironi L, Pinna AD: Effect of total enterectomy, pancreatectomy, and portal vein ligation on liver function and histology: a case report. Transplant Proc; 2007 Jan-Feb;39(1):300-2
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  • Herein a 32-year-old woman with familial adenomatous polyposis and multiple desmoid tumors involving the mesentery and the retroperitoneum underwent total enterectomy and pancreatectomy followed by en bloc transplantation of the stomach, small bowel, and pancreas.

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  • (PMID = 17275528.001).
  • [ISSN] 0041-1345
  • [Journal-full-title] Transplantation proceedings
  • [ISO-abbreviation] Transplant. Proc.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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30. Kok NF, Terkivatan T, Ijzermans JN: Regarding 'Liver cell adenoma and liver cell adenomatosis' by Ludger Barthelmes and Iain S. Tait. HPB (Oxford); 2006;8(1):71-2
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  • [Title] Regarding 'Liver cell adenoma and liver cell adenomatosis' by Ludger Barthelmes and Iain S. Tait.

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  • [Cites] Am J Surg Pathol. 2005 Dec;29(12):1600-8 [16327432.001]
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  • (PMID = 18333245.001).
  • [ISSN] 1365-182X
  • [Journal-full-title] HPB : the official journal of the International Hepato Pancreato Biliary Association
  • [ISO-abbreviation] HPB (Oxford)
  • [Language] eng
  • [Publication-type] Comment; Letter
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2131360
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31. Karoui M, Tresallet C, Brouquet A, Radvanyi H, Penna C: [Colorectal carcinogenesis. 1. Hereditary predisposition and colorectal cancer]. J Chir (Paris); 2007 Jan-Feb;144(1):13-8
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  • The two best defined forms of inherited CRC-familial multiple polyposis (FMP) and Hereditary Non-Polyposis Colon Cancer (HNPCC) account respectively for<1% and 2-3% of CRC.
  • [MeSH-minor] Adenomatous Polyposis Coli / genetics. Colorectal Neoplasms, Hereditary Nonpolyposis / genetics. Environment. Genes, Tumor Suppressor. Humans. Mutation / genetics. Penetrance. Peutz-Jeghers Syndrome / genetics


32. Summers C, Norval M, De Las Heras M, Gonzalez L, Sharp JM, Woods GM: An influx of macrophages is the predominant local immune response in ovine pulmonary adenocarcinoma. Vet Immunol Immunopathol; 2005 Jul 15;106(3-4):285-94
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  • [MeSH-major] Macrophages / immunology. Pulmonary Adenomatosis, Ovine / immunology

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  • (PMID = 15878202.001).
  • [ISSN] 0165-2427
  • [Journal-full-title] Veterinary immunology and immunopathology
  • [ISO-abbreviation] Vet. Immunol. Immunopathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Antigens, CD14; 0 / Histocompatibility Antigens Class II; 82115-62-6 / Interferon-gamma
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33. Dakessian RM, Inoshima Y, Fan H: Tumors in mice transgenic for the envelope protein of Jaagsiekte sheep retrovirus. Virus Genes; 2007 Aug;35(1):73-80
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  • [MeSH-major] Adenocarcinoma / genetics. Genes, env. Jaagsiekte sheep retrovirus / genetics. Lung Neoplasms / genetics. Pulmonary Adenomatosis, Ovine / genetics

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  • (PMID = 17043760.001).
  • [ISSN] 0920-8569
  • [Journal-full-title] Virus genes
  • [ISO-abbreviation] Virus Genes
  • [Language] eng
  • [Grant] United States / PHS HHS / / 82564; United States / NCI NIH HHS / CA / CA94188
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
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34. Leroux C, Girard N, Cottin V, Greenland T, Mornex JF, Archer F: Jaagsiekte Sheep Retrovirus (JSRV): from virus to lung cancer in sheep. Vet Res; 2007 Mar-Apr;38(2):211-28
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  • [MeSH-major] Jaagsiekte sheep retrovirus / physiology. Lung Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / virology. Sheep / virology

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  • (PMID = 17257570.001).
  • [ISSN] 0928-4249
  • [Journal-full-title] Veterinary research
  • [ISO-abbreviation] Vet. Res.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 93
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35. Dekker E, Boparai KS, Poley JW, Mathus-Vliegen EM, Offerhaus GJ, Kuipers EJ, Fockens P, Dees J: High resolution endoscopy and the additional value of chromoendoscopy in the evaluation of duodenal adenomatosis in patients with familial adenomatous polyposis. Endoscopy; 2009 Aug;41(8):666-9
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  • [Title] High resolution endoscopy and the additional value of chromoendoscopy in the evaluation of duodenal adenomatosis in patients with familial adenomatous polyposis.
  • BACKGROUND AND STUDY AIM: Duodenal polyposis occurs in approximately 90 % of patients with familial adenomatous polyposis (FAP) and 5 % - 10 % develop duodenal cancer.
  • Novel imaging techniques may improve evaluation of duodenal polyposis using the Spigelman classification.
  • We aimed to analyze the value of high resolution endoscopy (HRE) and the additional value of chromoendoscopy in the evaluation of duodenal polyposis in FAP.
  • After number and size of adenomas had been scored, indigo carmine 0.5 % was sprayed onto the mucosa, polyps were scored again and biopsies taken from the larger lesions.
  • Therefore, a combination of forward-viewing HRE and chromoendoscopy with side-viewing endoscopy for the periampullary region seems useful for surveillance of duodenal adenomatosis in FAP.
  • [MeSH-major] Adenoma / diagnosis. Adenomatous Polyposis Coli / complications. Duodenal Neoplasms / diagnosis. Duodenoscopy / methods


36. Buttrick GJ, Beaumont LM, Leitch J, Yau C, Hughes JR, Wakefield JG: Akt regulates centrosome migration and spindle orientation in the early Drosophila melanogaster embryo. J Cell Biol; 2008 Feb 11;180(3):537-48
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  • We show that Akt is enriched at the embryonic cortex and is required for phosphorylation of the glycogen synthase kinase-3beta homologue Zeste-white 3 kinase (Zw3) and for the cortical localizations of the adenomatosis polyposis coli (APC)-related protein APC2/E-APC and the MT + Tip protein EB1.

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  • (PMID = 18268102.001).
  • [ISSN] 1540-8140
  • [Journal-full-title] The Journal of cell biology
  • [ISO-abbreviation] J. Cell Biol.
  • [Language] eng
  • [Grant] United Kingdom / Biotechnology and Biological Sciences Research Council / / BBS/B/08019
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / APC2 protein, Drosophila; 0 / Armadillo Domain Proteins; 0 / Drosophila Proteins; 0 / Transcription Factors; 0 / Tumor Suppressor Proteins; 0 / armadillo protein, Drosophila; EC 2.7.11.1 / Proto-Oncogene Proteins c-akt; EC 2.7.11.1 / shaggy protein, Drosophila; EC 2.7.11.26 / Glycogen Synthase Kinase 3
  • [Other-IDs] NLM/ PMC2234228
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37. Kalimutho M, Blanco Gdel V, Gravina P, Cretella M, Mannucci L, Mannisi E, Formosa A, Pallone F, Federici G, Bernardini S: Quantitative denaturing high performance liquid chromatography (Q-dHPLC) detection of APC long DNA in faeces from patients with colorectal cancer. Clin Chem Lab Med; 2010 Sep;48(9):1303-11
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  • Adenomatosis polyposis coli (APC)-Long-DNA and its mutations were analysed using dHPLC and the Sanger sequencing method.

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  • (PMID = 20504269.001).
  • [ISSN] 1437-4331
  • [Journal-full-title] Clinical chemistry and laboratory medicine
  • [ISO-abbreviation] Clin. Chem. Lab. Med.
  • [Language] ENG
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Actins; 9007-49-2 / DNA
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38. Kámory E, Olasz J, Csuka O: Somatic APC inactivation mechanisms in sporadic colorectal cancer cases in Hungary. Pathol Oncol Res; 2008 Mar;14(1):51-6
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  • The role of germline inactivation of the adenomatosis polyposis coli (APC) gene in hereditary colorectal cancer is well known, being the most important cause of familial adenomatosus polyposis (FAP) syndrome.

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  • (PMID = 18369740.001).
  • [ISSN] 1219-4956
  • [Journal-full-title] Pathology oncology research : POR
  • [ISO-abbreviation] Pathol. Oncol. Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
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39. Upadhyay G, Goessling W, North TE, Xavier R, Zon LI, Yajnik V: Molecular association between beta-catenin degradation complex and Rac guanine exchange factor DOCK4 is essential for Wnt/beta-catenin signaling. Oncogene; 2008 Oct 2;27(44):5845-55
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  • Biochemical studies demonstrate that DOCK4 interacts with the beta-catenin degradation complex, consisting of the proteins adenomatosis polyposis coli, Axin and glycogen synthase kinase 3beta (GSK3beta).


40. Morandi L, Asioli S, Cavazza A, Pession A, Damiani S: Genetic relationship among atypical adenomatous hyperplasia, bronchioloalveolar carcinoma and adenocarcinoma of the lung. Lung Cancer; 2007 Apr;56(1):35-42
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  • [Title] Genetic relationship among atypical adenomatous hyperplasia, bronchioloalveolar carcinoma and adenocarcinoma of the lung.
  • Atypical adenomatous hyperplasia (AAH) has been recently defined by WHO as a small lesion, not exceeding 5mm in major axis, composed of slightly enlarged alveolar septa lined by pneumocytes with plump, atypical nuclei.
  • In particular, it is not clear whether multiple foci of AAH and of adenocarcinoma in the same patients are clonally related to each other or represent independent neoplastic foci.
  • [MeSH-major] Adenocarcinoma / genetics. Adenocarcinoma, Bronchiolo-Alveolar / genetics. Adenomatosis, Pulmonary / genetics. Lung Neoplasms / genetics. Precancerous Conditions / genetics

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  • (PMID = 17241687.001).
  • [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 / DNA, Mitochondrial
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41. Fearnhead NS, Winney B, Bodmer WF: Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model. Cell Cycle; 2005 Apr;4(4):521-5
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  • Recent evidence suggests that a quarter of patients with multiple adenomatous polyps are due to rare but functionally important variants in just five genes.
  • [MeSH-minor] Adenomatous Polyps / pathology. Base Pair Mismatch. DNA Repair. Disease Susceptibility. Genetic Variation. Humans. Intestinal Polyps. Multifactorial Inheritance. Risk. Wnt Proteins / metabolism

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  • (PMID = 15753653.001).
  • [ISSN] 1551-4005
  • [Journal-full-title] Cell cycle (Georgetown, Tex.)
  • [ISO-abbreviation] Cell Cycle
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Wnt Proteins
  • [Number-of-references] 62
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42. Cousens C, Graham M, Sales J, Dagleish MP: Evaluation of the efficacy of clinical diagnosis of ovine pulmonary adenocarcinoma. Vet Rec; 2008 Jan 19;162(3):88-90
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  • [MeSH-major] Jaagsiekte sheep retrovirus / isolation & purification. Lung / pathology. Pulmonary Adenomatosis, Ovine / diagnosis

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  • (PMID = 18204033.001).
  • [ISSN] 0042-4900
  • [Journal-full-title] The Veterinary record
  • [ISO-abbreviation] Vet. Rec.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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43. Grazioli L, Morana G, Kirchin MA, Schneider G: Accurate differentiation of focal nodular hyperplasia from hepatic adenoma at gadobenate dimeglumine-enhanced MR imaging: prospective study. Radiology; 2005 Jul;236(1):166-77
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  • PURPOSE: To prospectively determine the accuracy of differentiating benign focal nodular hyperplasia (FNH) from hepatic adenoma (HA) and liver adenomatosis (LA) by using gadobenate dimeglumine-enhanced magnetic resonance (MR) imaging.

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  • [Copyright] Copyright RSNA, 2005
  • (PMID = 15955857.001).
  • [ISSN] 0033-8419
  • [Journal-full-title] Radiology
  • [ISO-abbreviation] Radiology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media; 0 / Organometallic Compounds; 15G12L5X8K / gadobenic acid; 6HG8UB2MUY / Meglumine
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44. Voigt K, Krämer U, Brügmann M, Dewar P, Sharp JM, Ganter M: Eradication of ovine pulmonary adenocarcinoma by motherless rearing of lambs. Vet Rec; 2007 Jul 28;161(4):129-32
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  • [MeSH-major] Animal Husbandry / methods. Jaagsiekte sheep retrovirus / isolation & purification. Pulmonary Adenomatosis, Ovine / prevention & control

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  • (PMID = 17660466.001).
  • [ISSN] 0042-4900
  • [Journal-full-title] The Veterinary record
  • [ISO-abbreviation] Vet. Rec.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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45. Langers AM, De Vos tot Nederveen Cappel WH, Veenendaal RA, Bonsing BA, Hardwick JC, Vasen HF: Double balloon endoscopy for detection of small-bowel adenomas in familial adenomatous polyposis after pancreaticoduodenectomy according to Whipple. Endoscopy; 2008 Sep;40(9):773-4
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  • [Title] Double balloon endoscopy for detection of small-bowel adenomas in familial adenomatous polyposis after pancreaticoduodenectomy according to Whipple.
  • Patients with familial adenomatous polyposis (FAP) have a 5%-10% lifetime risk of developing duodenal cancer.
  • In severe duodenal polyposis, pancreaticoduodenectomy according to Whipple has been considered the only way to cure duodenal polyposis.
  • However, polyps recur even after surgery.
  • We describe a patient with severe adenomatosis of the small bowel in the afferent loop of a Roux-en-Y anastomosis after a Whipple procedure, detected by double balloon endoscopy (DBE).
  • [MeSH-major] Adenoma / diagnosis. Adenoma / surgery. Adenomatous Polyposis Coli / complications. Duodenal Neoplasms / diagnosis. Duodenal Neoplasms / surgery. Endoscopy / methods
  • [MeSH-minor] Anastomosis, Roux-en-Y. Catheterization. Cholangiopancreatography, Endoscopic Retrograde. Duodenal Diseases / surgery. Duodenoscopy. Humans. Intestinal Polyps / surgery. Male. Middle Aged. Pancreaticoduodenectomy. Polyps / surgery. Recurrence


46. Plevová P, Drobcinská L, Stekrová J, Silhánová E: [Single nucleotide c.645+32c&gt;T substitution in the APC gene is a non-pathogenic polymorphism appearing in about 16% of the Czech population]. Cas Lek Cesk; 2008;147(5):266-8
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  • BACKGROUND: Familial adenomatous polyposis is an autosomal dominant disease characterised by predisposition to colon polyposis and colorectal cancer and caused by germline mutations in the APC gene.
  • The aim of the study was to establish the frequency of c.645+32C>T substitution in intron 5 of the APC gene in patients with multiple colon polyposis and in the general population and to determine if this substitution is a nonpathogenic polymorphism or a pathogenic mutation associated with multiple polyposis coli.
  • METHODS AND RESULTS: The frequency of c.645+32C>T substitution in the APC gene was established in 170 patients with the clinical phenotype of familial adenomatous polyposis or its attenuated form using denaturating gradient gel electrophoresis and direct sequencing.
  • The c.645+32C>T substitution was detected in 27 of 170 patients with multiple colon polyposis (i.e. 15.9%).
  • The difference between patients with polyposis and the control group was not statistically significant (p = 0.979; chí-square test).
  • [MeSH-major] Adenomatous Polyposis Coli / genetics. Genes, APC. Polymorphism, Single Nucleotide

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  • (PMID = 18630182.001).
  • [ISSN] 0008-7335
  • [Journal-full-title] Casopís lékar̆ů c̆eských
  • [ISO-abbreviation] Cas. Lek. Cesk.
  • [Language] cze
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Czech Republic
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47. Berger BM, Schroy PC 3rd, Rosenberg JL, Lai-Goldman M, Eisenberg M, Brown T, Rochelle RB, Billings PR: Colorectal cancer screening using stool DNA analysis in clinical practice: early clinical experience with respect to patient acceptance and colonoscopic follow-up of abnormal tests. Clin Colorectal Cancer; 2006 Jan;5(5):338-43
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  • An abnormal stool DNA test correlated with a colonoscopically demonstrable abnormality in 49% of cases (34 of 69).
  • Abnormal findings, including CRC in 3 patients (4%; 1 with Dukes A and 2 with Dukes B disease), single or multiple adenomatous polyps in 23 patients (33%), hyperplastic polyps in 3 patients (4%), and colitis in 5 patients (7%).
  • CONCLUSION: Stool DNA testing provides an acceptable noninvasive alternative for CRC screening that can identify early-stage CRCs and adenomatous polyps in routine clinical practice.


48. Bambha K, Nagorney D, Sanderson S, Gores GJ: Hepatic adenomatosis in a young woman with glucose intolerance. Nat Clin Pract Gastroenterol Hepatol; 2006 Sep;3(9):526-31; quiz (following 531)
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  • [Title] Hepatic adenomatosis in a young woman with glucose intolerance.
  • DIAGNOSIS: Hepatic adenomatosis.

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  • (PMID = 16951669.001).
  • [ISSN] 1743-4378
  • [Journal-full-title] Nature clinical practice. Gastroenterology & hepatology
  • [ISO-abbreviation] Nat Clin Pract Gastroenterol Hepatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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49. Amemori H, Hyakutake M, Maeda Y, Tomita Y, Mitsumizo S, Oishi H, Koizumi S, Nakashima M, Araki K: Survival case of Vibrio vulnificus infection with multiple endocrine neoplasia type I. Fukuoka Igaku Zasshi; 2007 Sep;98(9):346-52
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  • [Title] Survival case of Vibrio vulnificus infection with multiple endocrine neoplasia type I.
  • A 35-year-old female with malabsorption syndrome who underwent a pancreatoduodenectomy for multiple endocrine adenomatosis 13 years prior was admitted to our hospital with diarrhea, general fatigue, high fever, and eruption in the lower legs.
  • [MeSH-major] Immunocompromised Host. Multiple Endocrine Neoplasia Type 1 / complications. Vibrio Infections / etiology. Vibrio Infections / therapy. Vibrio vulnificus

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  • (PMID = 17974078.001).
  • [ISSN] 0016-254X
  • [Journal-full-title] Fukuoka igaku zasshi = Hukuoka acta medica
  • [ISO-abbreviation] Fukuoka Igaku Zasshi
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Anti-Bacterial Agents; 0 / Catecholamines; 9M416Z9QNR / Ceftazidime; FYY3R43WGO / Minocycline; IY9XDZ35W2 / Glucose
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50. Kazanjian A, Noah T, Brown D, Burkart J, Shroyer NF: Atonal homolog 1 is required for growth and differentiation effects of notch/gamma-secretase inhibitors on normal and cancerous intestinal epithelial cells. Gastroenterology; 2010 Sep;139(3):918-28, 928.e1-6
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  • METHODS: We studied mice with intestine-specific disruption of Atoh1 (Atoh1(Deltaintestine)), the adenomatosis polyposis coli (APC)(min) mutation, both mutations (Atoh1(Deltaintestine); APC(min)), or littermate controls; mice were given GSI or vehicle.

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  • [Copyright] Copyright © 2010 AGA Institute. Published by Elsevier Inc. All rights reserved.
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  • (PMID = 20621629.001).
  • [ISSN] 1528-0012
  • [Journal-full-title] Gastroenterology
  • [ISO-abbreviation] Gastroenterology
  • [Language] eng
  • [Grant] United States / NIDDK NIH HHS / DK / K01 DK071686; United States / NIDDK NIH HHS / DK / K01 DK071686; United States / NIDDK NIH HHS / DK / P30 DK078392; United States / NCI NIH HHS / CA / R01 CA142826; United States / NCI NIH HHS / CA / R01 CA142826; United States / NCI NIH HHS / CA / R01 CA142826-01; United States / NIDDK NIH HHS / DK / R03 DK084167; United States / NIDDK NIH HHS / DK / R03 DK084167-01; United States / NIDDK NIH HHS / DK / T35 DK060444
  • [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 / ATOH1 protein, human; 0 / Antineoplastic Agents; 0 / Atoh1 protein, mouse; 0 / Basic Helix-Loop-Helix Transcription Factors; 0 / RNA, Messenger; 0 / Receptors, Notch; EC 3.4.- / Amyloid Precursor Protein Secretases
  • [Other-IDs] NLM/ NIHMS215773; NLM/ PMC3197859
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51. Cadigan KM, Liu YI: Wnt signaling: complexity at the surface. J Cell Sci; 2006 Feb 1;119(Pt 3):395-402
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  • Activation of Fz-LRP promotes the stability and nuclear localization of beta-catenin by compromising the ability of a multiprotein complex containing axin, adenomatosis polyposis coli (APC) and glycogen synthase kinase 3 (GSK3) to target it for degradation and block its nuclear import.
  • The Fz-LRP receptor complex probably accomplishes this by generating multiple signals in the cytoplasm.

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  • (PMID = 16443747.001).
  • [ISSN] 0021-9533
  • [Journal-full-title] Journal of cell science
  • [ISO-abbreviation] J. Cell. Sci.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA95869; United States / NIGMS NIH HHS / GM / R01 GM59846
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Low Density Lipoprotein Receptor-Related Protein-1; 0 / Multiprotein Complexes; 0 / Receptors, Neurotransmitter; 0 / Wnt Proteins
  • [Number-of-references] 131
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52. Gradowski JF, Mantha GS, Hunt JL, Dacic S: Molecular alterations in atypical adenomatous hyperplasia occurring in benign and cancer-bearing lungs. Diagn Mol Pathol; 2007 Jun;16(2):87-90
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  • [Title] Molecular alterations in atypical adenomatous hyperplasia occurring in benign and cancer-bearing lungs.
  • Atypical adenomatous hyperplasia (AAH) is considered to be a precursor lesion of the lung adenocarcinoma.
  • [MeSH-major] Adenocarcinoma / genetics. Adenomatosis, Pulmonary / genetics. Loss of Heterozygosity. Lung / pathology. Lung Neoplasms / genetics. Precancerous Conditions / genetics

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  • (PMID = 17525677.001).
  • [ISSN] 1052-9551
  • [Journal-full-title] Diagnostic molecular pathology : the American journal of surgical pathology, part B
  • [ISO-abbreviation] Diagn. Mol. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA, Neoplasm; 0 / Genetic Markers
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53. Bioulac-Sage P, Laumonier H, Laurent C, Zucman-Rossi J, Balabaud C: Hepatocellular adenoma: what is new in 2008. Hepatol Int; 2008 Sep;2(3):316-21
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  • Adenomatosis is frequently detected in this context.

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  • (PMID = 19669260.001).
  • [ISSN] 1936-0533
  • [Journal-full-title] Hepatology international
  • [ISO-abbreviation] Hepatol Int
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2716879
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54. Bliznashki I, Minev M, Mikhova A, Velev M: [A rare case of Gardner's syndrome complicated with rectal carcinoma]. Khirurgiia (Sofiia); 2007;(3):60-3
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  • Gardner's syndrome is a rare variant of the Familial Adenomatous Polyposis (FAP) in which affected individuals develop thousands of polyps within the gastrointestinal tract, with a 100 % risk of eventual malignant change.
  • Gardner's syndrome is an autosomal dominant disease, caused by mutations in APC ( adenomatous polyposis coli ) gene, which is located in chromosomal locus 5q21- q22.
  • They have investigated a family of 51 members with polyposis, some of them with multiple epidermoid cysts, fibromas and jaw osteomas.
  • He had multiple adenomatous polyposis of colon, rectal cancer, osteomas of skull bones, subcutaneous fibromas and lipomas.
  • We discovered also by ultrasound examination a polyp of gall bladder.
  • His father has had also multiple polyposis with malignancy and metastatic lesions and he has died at age of 49 years.
  • [MeSH-minor] Adenomatous Polyposis Coli / diagnosis. Adenomatous Polyposis Coli / genetics. Adenomatous Polyposis Coli / surgery. Adult. Cholecystectomy. Epidermal Cyst / diagnosis. Epidermal Cyst / genetics. Epidermal Cyst / surgery. Humans. Male. Osteoma / diagnosis. Osteoma / genetics. Osteoma / surgery. Proctocolectomy, Restorative

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  • (PMID = 18437113.001).
  • [ISSN] 0450-2167
  • [Journal-full-title] Khirurgii︠a︡
  • [ISO-abbreviation] Khirurgiia (Sofiia)
  • [Language] bul
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Bulgaria
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55. Lepistö A, Kiviluoto T, Halttunen J, Järvinen HJ: Surveillance and treatment of duodenal adenomatosis in familial adenomatous polyposis. Endoscopy; 2009 Jun;41(6):504-9
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  • [Title] Surveillance and treatment of duodenal adenomatosis in familial adenomatous polyposis.
  • BACKGROUND AND STUDY AIMS: Patients with familial adenomatous polyposis (FAP) are at increased risk for duodenal cancer whereas colorectal cancer is largely prevented by prophylactic colectomy.
  • We analyzed the results of endoscopic surveillance and different treatment modalities of duodenal adenomatosis in patients with FAP.
  • The cumulative incidences of duodenal adenomatosis and severe dysplasia and cancer were calculated using Kaplan-Meier analysis.
  • RESULTS: By the age of 60 years, the cumulative incidence was 80% for any adenomatosis and 23% for severe dysplasia or cancer.
  • CONCLUSIONS: The high incidence of severe dysplasia and cancer in duodenal polyps suggests that endoscopic surveillance is essential.
  • High-risk patients with Spigelman IV adenomatosis or adenomas with persisting severe dysplasia should undergo surgery with pylorus-preserving pancreaticoduodenectomy before invasive cancer develops.
  • [MeSH-major] Adenomatous Polyposis Coli / complications. Duodenal Neoplasms / diagnosis. Duodenal Neoplasms / epidemiology. Intestinal Polyps / complications


56. Scurry J, van der Putte SC, Pyman J, Chetty N, Szabo R: Mammary-like gland adenoma of the vulva: review of 46 cases. Pathology; 2009;41(4):372-8
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  • Unusual architectural patterns resembled breast lesions such as erosive adenomatosis, sclerosing adenosis and ductal adenoma.
  • The ductal cell and a site compatible with and/or the presence of adjacent normal MLG are the most characteristic features.
  • Unusual vulvar tumours, which have been previously reported as erosive adenomatosis, sclerosing adenosis, papillary adenofibroma, syringocystadenoma papilliferans, etc., are variants of MLG adenomas.

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  • (PMID = 19404851.001).
  • [ISSN] 1465-3931
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 46
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57. Ku BS, Kwon OE, Kim DC, Song KH, Lee CW, Kim KH: A case of erosive adenomatosis of nipple treated with total excision using purse-string suture. Dermatol Surg; 2006 Aug;32(8):1093-6
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  • [Title] A case of erosive adenomatosis of nipple treated with total excision using purse-string suture.

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  • [CommentIn] Dermatol Surg. 2007 Aug;33(8):1001 [17661951.001]
  • (PMID = 16918575.001).
  • [ISSN] 1076-0512
  • [Journal-full-title] Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
  • [ISO-abbreviation] Dermatol Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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58. Rosoff PM, Larrier N, Rice HE: Intra-abdominal desmoid tumor after successful treatment for Hodgkin disease. Pediatr Blood Cancer; 2005 Oct 15;45(5):728-31
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  • The tumor did not occur at either a surgical site or within a radiation field.
  • She did not carry a mutation for familial adenomatosis polypoli.

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  • (PMID = 16035093.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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59. Madani M, Madani F: Gardner's syndrome presenting with dental complaints. Arch Iran Med; 2007 Oct;10(4):535-9
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  • There are three distinctive features associated with this syndrome: familial intestinal polyposis or adenomatosis, surface tumors of hard tissues particularly osteoma in the skull, maxillae, and mandible, and finally surface tumors of the soft tissue.
  • The intestinal polyps have a 100% risk of undergoing malignant transformation if not treated.
  • In this article an 18-year-old male patient with previously undiagnosed Gardner's syndrome who presented for removal of multiple impacted and unerupted teeth is reported to illustrate the importance of early detection and proper referral.

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  • (PMID = 17903064.001).
  • [ISSN] 1029-2977
  • [Journal-full-title] Archives of Iranian medicine
  • [ISO-abbreviation] Arch Iran Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Iran
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60. Hsiao HP, Kirschner LS, Bourdeau I, Keil MF, Boikos SA, Verma S, Robinson-White AJ, Nesterova M, Lacroix A, Stratakis CA: Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors. J Clin Endocrinol Metab; 2009 Aug;94(8):2930-7
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  • For three patients with AIMAH, there was family history of CS; germline mutations were identified in three other patients in the genes for menin (one), fumarate hydratase (one), and adenomatosis polyposis coli (APC) (one); a PDE11A gene variant was found in another.

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  • (PMID = 19509103.001).
  • [ISSN] 1945-7197
  • [Journal-full-title] The Journal of clinical endocrinology and metabolism
  • [ISO-abbreviation] J. Clin. Endocrinol. Metab.
  • [Language] ENG
  • [Grant] United States / NICHD NIH HHS / HD / Z01 HD000642; United States / NICHD NIH HHS / HD / Z01-HD-000642-04
  • [Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Glucocorticoids; 7S5I7G3JQL / Dexamethasone; 9002-60-2 / Adrenocorticotropic Hormone; 9015-71-8 / Corticotropin-Releasing Hormone; EC 3.6.1.- / GNAS protein, human; EC 3.6.5.1 / GTP-Binding Protein alpha Subunits, Gs
  • [Other-IDs] NLM/ PMC2730864
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61. Brunt EM, Wolverson MK, Di Bisceglie AM: Benign hepatocellular tumors (adenomatosis) in nonalcoholic steatohepatitis: a case report. Semin Liver Dis; 2005;25(2):230-6
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  • [Title] Benign hepatocellular tumors (adenomatosis) in nonalcoholic steatohepatitis: a case report.

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  • (PMID = 15918151.001).
  • [ISSN] 0272-8087
  • [Journal-full-title] Seminars in liver disease
  • [ISO-abbreviation] Semin. Liver Dis.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD34
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62. Kogan EA, Tyong FV, Demura SA: [The mechanism of lung tissue remodeling in the progression of idiopathic pulmonary fibrosis]. Arkh Patol; 2010 Jul-Aug;72(4):30-6
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  • Thus, lung tissue remodeling in the progression of IPF from the early to late stage of the disease comprises interrelated processes that are largely localized in the BATZ, such as immune inflammation with pathological reparation, neoangiogenesis, apoptosis, and proliferation of epitheliocytes and myofibroblasts, which lead to the development of interstitial fibrosis and adenomatosis of the lung.


63. Lewin M, Handra-Luca A, Arrivé L, Wendum D, Paradis V, Bridel E, Fléjou JF, Belghiti J, Tubiana JM, Vilgrain V: Liver adenomatosis: classification of MR imaging features and comparison with pathologic findings. Radiology; 2006 Nov;241(2):433-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Liver adenomatosis: classification of MR imaging features and comparison with pathologic findings.
  • PURPOSE: To retrospectively compare the clinical manifestation and magnetic resonance (MR) imaging features of liver adenomatosis with pathologic findings.
  • Twenty patients were classified on the basis of pathologic findings into three groups: those with a steatotic, those with a peliotic, and those with a mixed (steatotic and peliotic) form of liver adenomatosis.
  • CONCLUSION: There are three patterns of MR imaging features of liver adenomatosis that are associated with three pathologic forms (steatotic, peliotic, and mixed).

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  • (PMID = 16966481.001).
  • [ISSN] 0033-8419
  • [Journal-full-title] Radiology
  • [ISO-abbreviation] Radiology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media; 0 / Organometallic Compounds; 0 / gadoterate meglumine; 6HG8UB2MUY / Meglumine
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64. Caporale M, Centorame P, Giovannini A, Sacchini F, Di Ventura M, De las Heras M, Palmarini M: Infection of lung epithelial cells and induction of pulmonary adenocarcinoma is not the most common outcome of naturally occurring JSRV infection during the commercial lifespan of sheep. Virology; 2005 Jul 20;338(1):144-53
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Adenocarcinoma / veterinary. Jaagsiekte sheep retrovirus / pathogenicity. Lung Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / etiology. Sheep Diseases / etiology

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  • (PMID = 15950254.001).
  • [ISSN] 0042-6822
  • [Journal-full-title] Virology
  • [ISO-abbreviation] Virology
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA95706-01
  • [Publication-type] 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] 0 / DNA, Viral
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65. Parés D, García-Ruiz A, Biondo S, Blanco I, Llort G, Arriol E, de Oca J, del Río C, Osorio A, Navarro M, Martí-Ragué J, Jaurrieta E: [Current status of follow-up of the upper digestive tract in familial adenomatous polyposis]. Gastroenterol Hepatol; 2006 Jan;29(1):15-20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Current status of follow-up of the upper digestive tract in familial adenomatous polyposis].
  • [Transliterated title] Estado actual del seguimiento del área gastroduodenal en la poliposis adenomatosa familiar.
  • Familiar adenomatous polyposis (FAP) is a hereditary disease characterized by the development of multiple adenomatous polyps in the gastrointestinal tract and colorectal cancer in practically all patients who do not receive appropriate treatment.
  • Because of the possibility of malignant transformation of these polyps, adequate monitoring is required, even though the optimal follow-up schedule has not yet been defined.
  • Subsequently, a follow-up schedule should be designed, according to the number and histological characteristics of the polyps observed.
  • [MeSH-major] Adenocarcinoma / etiology. Adenomatous Polyposis Coli / complications. Stomach Neoplasms / etiology


66. Belingheri M, Ghio L, Sala A, Menni F, Trespidi L, Ferraresso M, Berardinelli L, Rossi G, Edefonti A, Parini R: Combined liver-kidney transplantation in glycogen storage disease Ia: a case beyond the guidelines. Liver Transpl; 2007 May;13(5):762-4
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  • Liver transplantation is the only radical treatment, for which the main indications are hepatic adenomatosis, hepatocellular carcinoma, or severe hepatic dysfunction.


67. van Esch AA, Drenth JP, te Morsche RH, Jansen JB, Nagengast FM: Recurrent idiopathic pancreatitis in familial adenomatous polyposis: report of a case-series and review of the literature. Fam Cancer; 2007;6(3):275-80
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  • [Title] Recurrent idiopathic pancreatitis in familial adenomatous polyposis: report of a case-series and review of the literature.
  • Familial adenomatous polyposis (FAP) is characterized by the development of multiple adenomatous polyps predominantly in the colon but also in the duodenum.
  • [MeSH-major] Adenomatous Polyposis Coli / complications. Duodenal Neoplasms / complications. Pancreatitis, Chronic / complications. Polyps / complications


68. Hardy OT, Hernandez-Pampaloni M, Saffer JR, Scheuermann JS, Ernst LM, Freifelder R, Zhuang H, MacMullen C, Becker S, Adzick NS, Divgi C, Alavi A, Stanley CA: Accuracy of [18F]fluorodopa positron emission tomography for diagnosing and localizing focal congenital hyperinsulinism. J Clin Endocrinol Metab; 2007 Dec;92(12):4706-11
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  • OBJECTIVES: Focal lesions in infants with congenital hyperinsulinism (HI) represent areas of adenomatosis that express a paternally derived ATP-sensitive potassium channel mutation due to embryonic loss of heterozygosity for the maternal 11p region.
  • The positive predictive value of [18F]DOPA in diagnosing focal adenomatosis was 100%, and the negative predictive value was 81%.
  • These results suggest that [18F]DOPA PET imaging provides a useful guide to surgical resection of focal adenomatosis and should be considered as a guide to surgery in all infants with congenital HI who have medically uncontrollable disease.
  • [MeSH-minor] Biopsy. Humans. Image Interpretation, Computer-Assisted. Infant. Infant, Newborn. Islets of Langerhans / pathology. Kidney / pathology. Multiple Endocrine Neoplasia / pathology. Multiple Endocrine Neoplasia / radionuclide imaging. Pancreatectomy. Pancreatic Neoplasms / pathology. Pancreatic Neoplasms / radionuclide imaging. Positron-Emission Tomography. Sample Size

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  • (PMID = 17895314.001).
  • [ISSN] 0021-972X
  • [Journal-full-title] The Journal of clinical endocrinology and metabolism
  • [ISO-abbreviation] J. Clin. Endocrinol. Metab.
  • [Language] eng
  • [Grant] United States / NCRR NIH HHS / RR / M01-RR-00240; United States / NIDDK NIH HHS / DK / R01-DK-56268; United States / NIDDK NIH HHS / DK / T32-DK63688
  • [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; 2C598205QX / fluorodopa F 18; 63-84-3 / Dihydroxyphenylalanine
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69. Chan OT, Haghighi P: Hamartomatous polyps of the colon: ganglioneuromatous, stromal, and lipomatous. Arch Pathol Lab Med; 2006 Oct;130(10):1561-6
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  • [Title] Hamartomatous polyps of the colon: ganglioneuromatous, stromal, and lipomatous.
  • Intestinal ganglioneuromas comprise benign, hamartomatous polyps characterized by an overgrowth of nerve ganglion cells, nerve fibers, and supporting cells in the gastrointestinal tract.
  • This polyposis has been divided into 3 subgroups, each with a different degree of ganglioneuroma formation: polypoid ganglioneuroma, ganglioneuromatous polyposis, and diffuse ganglioneuromatosis.
  • The ganglioneuromatous polyposis subgroup is not known to coexist with systemic disorders that often have an associated intestinal polyposis, such as multiple endocrine neoplasia type IIb, neurofibromatosis type I, and Cowden syndrome.
  • We report a case of ganglioneuromatous polyposis plus cutaneous lipomatosis in a 41-year-old man with no established systemic disease.
  • This case report and brief review of the literature provide an overview of intestinal ganglioneuromatosis in relation to the hereditary polyposis syndromes and describe the individual ganglioneuromatosis subgroups.
  • [MeSH-major] Colonic Neoplasms / pathology. Ganglioneuroma / pathology. Hamartoma / pathology. Intestinal Polyposis / pathology. Lipomatosis / complications. Skin Neoplasms / complications. Stromal Cells / pathology

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  • (PMID = 17090203.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 47
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70. Peters WH, te Morsche RH, Roelofs HM, Mathus-Vliegen EM, Berkhout M, Nagengast FM: COX-2 polymorphisms in patients with familial adenomatous polyposis. Oncol Res; 2009;17(8):347-51
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  • [Title] COX-2 polymorphisms in patients with familial adenomatous polyposis.
  • We investigated whether functional genetic polymorphisms in COX-2 may have a risk-modifying effect on duodenal adenomatosis in patients with familial adenomatous polyposis (FAP).
  • The COX-2 genotypes showed no association with the severity of duodenal adenomatosis.
  • [MeSH-major] Adenomatous Polyposis Coli / enzymology. Adenomatous Polyposis Coli / genetics. Cyclooxygenase 2 / genetics. Genetic Predisposition to Disease. Polymorphism, Single Nucleotide

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  • (PMID = 19544971.001).
  • [ISSN] 0965-0407
  • [Journal-full-title] Oncology research
  • [ISO-abbreviation] Oncol. Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] EC 1.14.99.1 / Cyclooxygenase 2
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71. Brambilla E, Lantuejoul S: Telomerase activation in adenocarcinoma-bronchioloalveolar carcinoma. Eur Respir J; 2006 Jun;27(6):1079-81
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Adenocarcinoma / genetics. Adenocarcinoma, Bronchiolo-Alveolar / genetics. Disease Models, Animal. Jaagsiekte sheep retrovirus / genetics. Lung Neoplasms / genetics. Pulmonary Adenomatosis, Ovine / genetics. Telomerase / genetics

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  • [CommentOn] Eur Respir J. 2006 Jun;27(6):1175-82 [16455826.001]
  • (PMID = 16772385.001).
  • [ISSN] 0903-1936
  • [Journal-full-title] The European respiratory journal
  • [ISO-abbreviation] Eur. Respir. J.
  • [Language] eng
  • [Publication-type] Comment; Editorial
  • [Publication-country] Denmark
  • [Chemical-registry-number] EC 2.7.7.49 / Telomerase
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72. Zhang W, Chuang YJ, Jin T, Swanson R, Xiong Y, Leung L, Olson ST: Antiangiogenic antithrombin induces global changes in the gene expression profile of endothelial cells. Cancer Res; 2006 May 15;66(10):5047-55
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  • In contrast, most up-regulated genes (e.g., caspase-3, p21, tissue inhibitor of metalloproteinases 1, 2, and 3, and adenomatosis polyposis coli) are known for their antiangiogenic functions which include the promotion of cell apoptosis and cell cycle arrest and the inhibition of tumor growth and metastasis.

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  • (PMID = 16707426.001).
  • [ISSN] 0008-5472
  • [Journal-full-title] Cancer research
  • [ISO-abbreviation] Cancer Res.
  • [Language] eng
  • [Grant] United States / NHLBI NIH HHS / HL / HL-39888
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Angiogenesis Inhibitors; 0 / Antithrombins; 103107-01-3 / Fibroblast Growth Factor 2
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73. Greaves WO, Bhattacharya B: Hepatic adenomatosis. Arch Pathol Lab Med; 2008 Dec;132(12):1951-5
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  • [Title] Hepatic adenomatosis.
  • Hepatic adenomatosis was first described in 1985 by Flejou et al as multiple adenomas, arbitrarily more than 10, in an otherwise normal liver parenchyma.

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  • (PMID = 19061298.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Hepatocyte Nuclear Factor 1-alpha
  • [Number-of-references] 30
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74. Bober A: Passing it on: should health care professionals be permitted to disclose patients' genetic information to their reproductive partners? J Law Med; 2006 Nov;14(2):262-81
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  • The issue is addressed with reference to four genetic disorders (Huntington Disease, Familial Adenomatous Polyposis, Multiple Endocrine Neoplasia Type 2A and Cystic Fibrosis) which illustrate differences in inheritance traits and availability of effective treatments.
  • [MeSH-minor] Adenomatous Polyposis Coli / genetics. Australia. Cystic Fibrosis / genetics. Humans. Huntington Disease / genetics. Multiple Endocrine Neoplasia Type 2a / genetics

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  • (PMID = 17153530.001).
  • [ISSN] 1320-159X
  • [Journal-full-title] Journal of law and medicine
  • [ISO-abbreviation] J Law Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Australia
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75. Ivanov SV, Zhabin SN, Gorbacheva OS, Barsukov VS, Denisova EIu: [Multifactor analysis of nodular goiter by the method of artificial neural network]. Klin Med (Mosk); 2008;86(4):49-50
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  • Study of 297 patients with preparative methods of nontoxic nodular goiter and cytological diagnose "adenomatosis" with the use of artificial neural network (ANN) were analyzed.
  • Painless elastic nodules with sonographically iso- o hyperechogenic structure, with clear outline and cytologically determined adenomatosis in combination with colloid can be interpreted as benign lesion of thyroid gland.

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  • (PMID = 18494287.001).
  • [ISSN] 0023-2149
  • [Journal-full-title] Klinicheskaia meditsina
  • [ISO-abbreviation] Klin Med (Mosk)
  • [Language] rus
  • [Publication-type] Comparative Study; English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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76. Chen R, Axell L, Klein C: Attenuated familial adenomatosis polyposis. J Clin Oncol; 2007 Feb 20;25(6):724-5
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  • [Title] Attenuated familial adenomatosis polyposis.
  • [MeSH-major] Adenomatous Polyposis Coli / diagnosis. Adenomatous Polyposis Coli / genetics. Genes, APC. Genetic Predisposition to Disease

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  • (PMID = 17308276.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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77. Shimomura Y, Agalliu D, Vonica A, Luria V, Wajid M, Baumer A, Belli S, Petukhova L, Schinzel A, Brivanlou AH, Barres BA, Christiano AM: APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex. Nature; 2010 Apr 15;464(7291):1043-7
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  • Using genetic linkage analysis, we mapped a new locus for the disease to chromosome 18p11.22, and identified a mutation (Leu9Arg) in the adenomatosis polyposis down-regulated 1 (APCDD1) gene in three families.


78. Kim YT, Park JY, Jeon YK, Park SJ, Song JY, Kang CH, Sung SW, Kim JH: Aberrant promoter CpG island hypermethylation of the adenomatosis polyposis coli gene can serve as a good prognostic factor by affecting lymph node metastasis in squamous cell carcinoma of the esophagus. Dis Esophagus; 2009;22(2):143-50
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  • [Title] Aberrant promoter CpG island hypermethylation of the adenomatosis polyposis coli gene can serve as a good prognostic factor by affecting lymph node metastasis in squamous cell carcinoma of the esophagus.
  • CpG island hypermethylations were observed in 10% for p16, 34% for RARbetaP2, 46% for adenomatosis polyposis coli (APC), 14% for RASSF1A, 84% for FHIT, and 8% for hMLH1.

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  • (PMID = 18847451.001).
  • [ISSN] 1442-2050
  • [Journal-full-title] Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus
  • [ISO-abbreviation] Dis. Esophagus
  • [Language] ENG
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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79. Miller MJ, Reuter BK, Wallace JL, Sharkey KA: A unique therapeutic approach to emesis and itch with a proanthocyanidin-rich genonutrient. J Transl Med; 2008;6:3
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  • In the ApcMinmouse model of precancerous adenomatosis polyposis, mice received Zangrado (100 mug/ml in drinking water) from the age of 6 - 16 weeks for effects on polyp number.

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  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
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  • (PMID = 18205911.001).
  • [ISSN] 1479-5876
  • [Journal-full-title] Journal of translational medicine
  • [ISO-abbreviation] J Transl Med
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / AM 251; 0 / Antiemetics; 0 / Antipruritics; 0 / Morphine Derivatives; 0 / Piperidines; 0 / Plant Extracts; 0 / Proanthocyanidins; 0 / Pyrazoles; 0 / Receptor, Cannabinoid, CB1; 18206-61-6 / proanthocyanidin; 20290-10-2 / morphine-6-glucuronide
  • [Other-IDs] NLM/ PMC2254379
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80. Kim H, Kim HJ, Chi SG, Lee SK, Joo GR, Dong SH, Kim BH, Chang YW, Lee JI, Chang R: Absence of MutY homologue mutation in patients with multiple sporadic adenomatous polyps in Korea. World J Gastroenterol; 2006 Feb 14;12(6):951-5
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  • [Title] Absence of MutY homologue mutation in patients with multiple sporadic adenomatous polyps in Korea.
  • AIM: Recently, germ-line mutation in the base excision repair gene MYH has been identified to cause a novel autosomal recessive form of familial adenomatous polyposis (FAP).
  • In this study, we screened 30 patients with multiple adenomatous polyps for MYH mutations to assess its prevalence and ethnic specificity in Korea.
  • METHODS: Thirty patients (21 men and 9 women; mean age 62.3 years) with multiple adenomatous polyps were examined for MYH mutations.
  • CONCLUSION: Mutation in MYH may be rarely involved in the pathogenesis of multiple sporadic colorectal adenomas in Korean population, although a large-scale analysis will be required to clarify the presence of specific MYH variants in a subset of patients and their role in the predisposition of multiple colorectal adenomas in Korean population.
  • [MeSH-major] Adenomatous Polyposis Coli / genetics. DNA Glycosylases / genetics. Mutation

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  • (PMID = 16521226.001).
  • [ISSN] 1007-9327
  • [Journal-full-title] World journal of gastroenterology
  • [ISO-abbreviation] World J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / DNA Primers; EC 3.2.2.- / DNA Glycosylases; EC 3.2.2.- / mutY adenine glycosylase
  • [Other-IDs] NLM/ PMC4066163
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81. Kadzhaia NR, Virsaladze DK, Tkeshelashvili BD, Dzhavashvili LV, Dzhugeli MK: [Endocrine-metabolic peculiarities in women of reproductive age with hyperplastic processes of cervix and mammary glands]. Georgian Med News; 2006 May;(134):60-3
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  • 72 patients with hyperplastic processes in endomyometrium, uterine cervix (hyperplasia, polyposis, myoma) and mammary glands (fibroadenomatosis, adenomatosis) were selected in main group.


82. Esteban JM, Gutiérrez del Olmo A, Baki W, Fernández S, Soria MT, Díaz Mediavilla J, Ramírez Armengol JA: Colonic mucosa-associated lymphoid tissue lymphoma presenting as multiple polyposis. Gastrointest Endosc; 2005 Jun;61(7):928-30
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  • [Title] Colonic mucosa-associated lymphoid tissue lymphoma presenting as multiple polyposis.
  • [MeSH-major] Colonic Neoplasms / pathology. Colonic Polyps / pathology. Intestinal Polyposis / pathology. Lymphoma, B-Cell, Marginal Zone / pathology

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  • (PMID = 15933708.001).
  • [ISSN] 0016-5107
  • [Journal-full-title] Gastrointestinal endoscopy
  • [ISO-abbreviation] Gastrointest. Endosc.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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83. Grazioli L, Bondioni MP, Faccioli N, Gambarini S, Tinti R, Schneider G, Kirchin M: Solid focal liver lesions: dynamic and late enhancement patterns with the dual phase contrast agent gadobenate dimeglumine. J Gastrointest Cancer; 2010 Dec;41(4):221-32
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  • IMAGING FINDINGS: Unenhanced T2- and T1-weighted, dynamic T1-weighted (arterial, portal-venous, and equilibrium) and late phase (1-3 h) Gd-BOPTA-enhanced MR imaging of different focal liver lesions (nodular regenerative hyperplasia, hepatic adenoma, liver adenomatosis, hepatocellular carcinoma, peripheral cholangiocarcinoma, hypervascular metastases, and hypovascular metastases) are shown.

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  • (PMID = 20405242.001).
  • [ISSN] 1941-6636
  • [Journal-full-title] Journal of gastrointestinal cancer
  • [ISO-abbreviation] J Gastrointest Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media; 0 / Organometallic Compounds; 15G12L5X8K / gadobenic acid; 6HG8UB2MUY / Meglumine
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84. Arnaud F, Varela M, Spencer TE, Palmarini M: Coevolution of endogenous betaretroviruses of sheep and their host. Cell Mol Life Sci; 2008 Nov;65(21):3422-32
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  • [Title] Coevolution of endogenous betaretroviruses of sheep and their host.
  • Sheep betaretroviruses offer a unique model system to study the complex interaction between retroviruses and their host.
  • Jaagsiekte sheep retrovirus (JSRV) is a pathogenic exogenous retrovirus and the causative agent of ovine pulmonary adenocarcinoma.
  • The sheep genome contains at least 27 copies of endogenous retroviruses (enJSRVs) highly related to JSRV. enJSRVs have played several roles in the evolution of the domestic sheep as they are able to block the JSRV replication cycle and play a critical role in sheep conceptus development and placental morphogenesis.
  • Available data strongly suggest that some dominant negative enJSRV proviruses (i.e. able to block JSRV replication) have been positively selected during evolution.
  • Interestingly, viruses escaping the transdominant enJSRV loci have recently emerged (less than 200 years ago).
  • Thus, endogenization of these retroviruses may still be occurring today.
  • Therefore, sheep provide an exciting and unique system to study retrovirus-host coevolution. (Part of a multi-author review).

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  • (PMID = 18818869.001).
  • [ISSN] 1420-9071
  • [Journal-full-title] Cellular and molecular life sciences : CMLS
  • [ISO-abbreviation] Cell. Mol. Life Sci.
  • [Language] ENG
  • [Grant] United States / NICHD NIH HHS / HD / R01 HD052745; United States / NICHD NIH HHS / HD / HD052745
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Retroviridae Proteins, Oncogenic
  • [Number-of-references] 73
  • [Other-IDs] NLM/ NIHMS634040; NLM/ PMC4207369
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85. Nakanishi K, Matsuo H, Kanai Y, Endou H, Hiroi S, Tominaga S, Mukai M, Ikeda E, Ozeki Y, Aida S, Kawai T: LAT1 expression in normal lung and in atypical adenomatous hyperplasia and adenocarcinoma of the lung. Virchows Arch; 2006 Feb;448(2):142-50
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  • [Title] LAT1 expression in normal lung and in atypical adenomatous hyperplasia and adenocarcinoma of the lung.
  • No previous study has investigated neutral large amino acid transporter type 1 (LAT1) in normal lung cells, or in atypical adenomatous hyperplasia(s) (AAH) and nonmucinous bronchioloalveolar carcinoma(s) (NMBAC) of the lung.
  • [MeSH-major] Adenocarcinoma, Bronchiolo-Alveolar / pathology. Adenomatosis, Pulmonary / pathology. Large Neutral Amino Acid-Transporter 1 / genetics. Lung / metabolism. Lung Neoplasms / pathology

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  • (PMID = 16175382.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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86. Wellen JR, Anderson CD, Doyle M, Shenoy S, Nadler M, Turmelle Y, Shepherd R, Chapman WC, Lowell JA: The role of liver transplantation for hepatic adenomatosis in the pediatric population: case report and review of the literature. Pediatr Transplant; 2010 May;14(3):E16-9
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  • [Title] The role of liver transplantation for hepatic adenomatosis in the pediatric population: case report and review of the literature.
  • These tumors are often solitary but can also be multiple in which case this is referred to as hepatic adenomatosis (HA).


87. Sa Cunha A, Blanc JF, Lazaro E, Mellottee L, Le Bail B, Zucman-Rossi J, Balabaud C, Bioulac-Sage P: Inflammatory syndrome with liver adenomatosis: the beneficial effects of surgical management. Gut; 2007 Feb;56(2):307-9
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  • [Title] Inflammatory syndrome with liver adenomatosis: the beneficial effects of surgical management.

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88. Ek ET, Ek EW, Moulton CA, Mackay S: Incidental discovery of massive hepatic adenomatosis. ANZ J Surg; 2005 Jan-Feb;75(1-2):90-1
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  • [Title] Incidental discovery of massive hepatic adenomatosis.

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  • (PMID = 15740530.001).
  • [ISSN] 1445-1433
  • [Journal-full-title] ANZ journal of surgery
  • [ISO-abbreviation] ANZ J Surg
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Australia
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89. Flemming P, Lehmann U, Steinemann D, Kreipe H, Wilkens L: [Hepatocellular adenoma. Malignancy potential and differentiation from hepatocellular carcinoma]. Pathologe; 2006 Jul;27(4):238-43
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  • A limitation of particular HCA in genetic and metabolic diseases, children, adult males, adenomatosis, and HCA-like tumors with known risk factors of HCC would seem pragmatically meaningful.

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  • (PMID = 16736176.001).
  • [ISSN] 0172-8113
  • [Journal-full-title] Der Pathologe
  • [ISO-abbreviation] Pathologe
  • [Language] ger
  • [Publication-type] Comparative Study; English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 39
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90. Okegawa T, Nutahara K, Higashihara E: Association of circulating tumor cells with tumor-related methylated DNA in patients with hormone-refractory prostate cancer. Int J Urol; 2010 May;17(5):466-75
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  • Hypermethylation at adenomatosis polyposis coli, glutathione-S-transferase-pi, prostaglandin-endoperoxide synthase 2, multidrug resistance 1 and Ras association domain family 1 isoform A was analyzed using a sensitive SYBR green methylation-specific polymerase chain reaction.
  • [MeSH-minor] Adenomatous Polyposis Coli Protein / genetics. Aged. Aged, 80 and over. Antineoplastic Agents, Hormonal / therapeutic use. Biopsy. Cell Count. CpG Islands / physiology. Drug Resistance, Neoplasm. Glutathione S-Transferase pi / genetics. Humans. Kaplan-Meier Estimate. Male. Middle Aged. P-Glycoprotein / genetics. Prognosis. Proportional Hazards Models. Prostaglandin-Endoperoxide Synthases / genetics. Reverse Transcriptase Polymerase Chain Reaction. Tumor Suppressor Proteins / genetics

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  • (PMID = 20337729.001).
  • [ISSN] 1442-2042
  • [Journal-full-title] International journal of urology : official journal of the Japanese Urological Association
  • [ISO-abbreviation] Int. J. Urol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Adenomatous Polyposis Coli Protein; 0 / Antineoplastic Agents, Hormonal; 0 / Biomarkers, Tumor; 0 / DNA, Neoplasm; 0 / P-Glycoprotein; 0 / RASSF1 protein, human; 0 / Tumor Suppressor Proteins; EC 1.14.99.1 / Prostaglandin-Endoperoxide Synthases; EC 2.5.1.18 / Glutathione S-Transferase pi
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91. Chimenos-Küstner E, Pascual M, Blanco I, Finestres F: Hereditary familial polyposis and Gardner's syndrome: contribution of the odonto-stomatology examination in its diagnosis and a case description. Med Oral Patol Oral Cir Bucal; 2005 Nov-Dec;10(5):402-9
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  • [Title] Hereditary familial polyposis and Gardner's syndrome: contribution of the odonto-stomatology examination in its diagnosis and a case description.
  • Familial Adenomatous Polyposis (FAP) and its phenotype variant, Gardner's syndrome, constitute a rare autosomal dominant inherited disorder.
  • They are characterised by the development, generally during the second and third decades of life, of multiple adenomatous polyps in the colon and rectum.
  • These polyps have a high risk of subsequently becoming malignant, which normally occurs in the third and fourth decades of life.
  • As well as colorectal polyps, these individuals can present with extra-colonic symptoms, among which are particularly: gastro-duodenal polyps, dermoid and epidermoid cysts, desmoid tumours, congenital hypertrophy of the retinal pigment epithelium, disorders of the maxillary and skeletal bones and dental anomalies.
  • [MeSH-major] Adenomatous Polyposis Coli / diagnosis. Jaw Neoplasms / etiology. Osteoma / etiology
  • [MeSH-minor] Adenomatous Polyposis Coli Protein / genetics. Adult. Cementoma / diagnosis. Cementoma / etiology. Codon, Nonsense. Diagnosis, Differential. Early Diagnosis. Epidermal Cyst / diagnosis. Epidermal Cyst / etiology. Female. Fibroma / diagnosis. Fibroma / etiology. Gardner Syndrome / complications. Gardner Syndrome / diagnosis. Gardner Syndrome / genetics. Genes, APC. Humans. Hypertrophy. Pedigree. Pigment Epithelium of Eye / abnormalities. Prognosis

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  • (PMID = 16264375.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng; spa
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Spain
  • [Chemical-registry-number] 0 / Adenomatous Polyposis Coli Protein; 0 / Codon, Nonsense
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92. Durno CA, Holter S, Sherman PM, Gallinger S: The gastrointestinal phenotype of germline biallelic mismatch repair gene mutations. Am J Gastroenterol; 2010 Nov;105(11):2449-56
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  • More than one-third of patients had multiple colorectal adenomas (>10 polyps).
  • This distinct phenotype includes multiple adenomatous polyps and CAL skin lesions.

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  • (PMID = 20531397.001).
  • [ISSN] 1572-0241
  • [Journal-full-title] The American journal of gastroenterology
  • [ISO-abbreviation] Am. J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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93. Kobayashi S, Sakaguchi H, Takatsuka M, Suekane T, Iwai S, Morikawa H, Enomoto M, Tamori A, Kawada N: Two cases of hepatocellular adenomatosis treated with transcatheter arterial embolization. Hepatol Int; 2009 Jun;3(2):416-20
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  • [Title] Two cases of hepatocellular adenomatosis treated with transcatheter arterial embolization.
  • Surgical resection is considered to be the best choice of treatment, when adenomas are increasing in size, while resection is difficult to perform when multiple adenomas develop throughout the liver.
  • Here, we report two cases of multiple hepatocellular adenomatosis.
  • These cases suggest that TAE is an effective treatment of hepatocellular adenomatosis.

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  • (PMID = 19669369.001).
  • [ISSN] 1936-0533
  • [Journal-full-title] Hepatology international
  • [ISO-abbreviation] Hepatol Int
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2716763
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94. Radford IR, Lobachevsky PN: Clustered DNA lesion sites as a source of mutations during human colorectal tumourigenesis. Mutat Res; 2008 Nov 10;646(1-2):60-8
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  • We used statistical analyses to search for sets of dinucleotide sequences (designated target sequences) that are present at and in close proximity to mutation sites in four genes associated with human colorectal tumourigenesis (adenomatosis polyposis coli (APC), v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS), phosphoinositide-3-kinase, catalytic, alpha polypeptide (PIK3CA), and tumour protein p53 (TP53)).
  • Our results strongly suggest a statistical association between the presence of multiple, clustered target sequences and mutational events.

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  • (PMID = 18824008.001).
  • [ISSN] 0027-5107
  • [Journal-full-title] Mutation research
  • [ISO-abbreviation] Mutat. Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Tumor Suppressor Protein p53; 9007-49-2 / DNA; EC 2.7.1.- / Phosphatidylinositol 3-Kinases; EC 2.7.1.137 / PIK3CA protein, human
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95. Veteläinen R, Erdogan D, de Graaf W, ten Kate F, Jansen PL, Gouma DJ, van Gulik TM: Liver adenomatosis: re-evaluation of aetiology and management. Liver Int; 2008 Apr;28(4):499-508
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  • [Title] Liver adenomatosis: re-evaluation of aetiology and management.
  • BACKGROUND: Liver adenomatosis (LA) is a rare benign parenchymal liver disease with unknown aetiology.
  • CONCLUSION: Liver adenomatosis is a progressive, benign parenchymal disease mainly occurring in females.

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  • [CommentIn] Liver Int. 2009 Jan;29(1):142 [18828785.001]
  • (PMID = 18339077.001).
  • [ISSN] 1478-3231
  • [Journal-full-title] Liver international : official journal of the International Association for the Study of the Liver
  • [ISO-abbreviation] Liver Int.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 57
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96. Barreda Costa C, Vila Gutierrez S, Salazar Cabrera F, Barriga Calle E, Velarde Criado H, Barriga Briceño J: [Advanced adenoma in 3700 colonoscopies]. Rev Gastroenterol Peru; 2010 Apr-Jun;30(2):113-20
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  • OBJECTIVES: To determine the prevalence of colon polyps, distribution in the colon, as well as their histological characteristics, with special mention on advanced adenomas, in an adult population at an endoscopy center in Lima.
  • Each polyp was studied separately and its histological findings recorded.
  • RESULTS: 3,701 colonoscopies were done in 3,690 patients; 1,492 (40,4%) had polyps and were included in the study.
  • 997 (27%) had adenomatous polyps and 495 (13.4%) non adenomatous polyps.
  • Adenomatous polyps were found throughout the colon, with a predominance of hyperplasic polyps in the rectum.
  • 78% of the adenomatous polyps and 84% of the advanced adenomas were found in patients older than 50 years old.
  • In this group of patients, significant risk factors were: prior history of adenomas or colorectal cancer (46/203 vs. 63/495; p<0.01), and multiple adenomatous polyps found during colonoscopy (67/203 vs. 121/794; p<0.01).
  • CONCLUSIONS: Adenomatous polyps were the most frequently found polyps in our study; approximately 20% were advanced lesions, especially in patients older than 50 years old.
  • [MeSH-major] Adenocarcinoma / epidemiology. Adenoma / epidemiology. Colonic Neoplasms / epidemiology. Colonic Polyps / epidemiology. Colonoscopy / statistics & numerical data. Rectal Neoplasms / epidemiology
  • [MeSH-minor] Adenomatous Polyps / diagnosis. Adenomatous Polyps / epidemiology. Adenomatous Polyps / pathology. Adult. Age Factors. Aged. Aged, 80 and over. Early Diagnosis. Humans. Hyperplasia. Middle Aged. Motivation. Neoplasms, Multiple Primary / diagnosis. Neoplasms, Multiple Primary / epidemiology. Neoplasms, Multiple Primary / pathology. Organ Specificity. Peru / epidemiology. Prospective Studies. Young Adult

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  • (PMID = 20644602.001).
  • [ISSN] 1609-722X
  • [Journal-full-title] Revista de gastroenterología del Perú : órgano oficial de la Sociedad de Gastroenterología del Perú
  • [ISO-abbreviation] Rev Gastroenterol Peru
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Peru
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97. Widimský J Jr, Zelinka T, Petrák O, Strauch B, Safarík L, Kasalický M, Vranková A, Holaj R: [Diagnostic and therapeutic procedures in pheochromocytoma: current trends]. Vnitr Lek; 2007 Apr;53(4):428-33
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  • 5 gene mutations have so far been identified that may be responsible for the familial form of pheochromacytoma: mutation of the von Hippel-Lindau (VHL) gene, leading to the onset of VHL syndrome, mutation of the RET-proto-oncogene in multiple endocrine adenomatosis type 2, mutation of the type 1 gene for neurofibromatosis, which is associated with von Recklinghausen's disease and finally mutation of the genes encoding the B and D subunits of succinated hydrogenase (SDHB, SDHD), which are associated with familial paragangliomas and pheochromacytoma.
  • The diagnosis of extraadrenal or multiple forms can use not only CT/MR but also imaging using the radiopharmaceutical 123I-Metaiodobenzylguanidine (MIBG) or 18F-fluorodopamine PET (only available in the USA).
  • [MeSH-minor] Humans. Hypertension / etiology. Multiple Endocrine Neoplasia Type 2a / diagnosis. Neurofibromatosis 1 / diagnosis. Paraganglioma / diagnosis. von Hippel-Lindau Disease / diagnosis. von Hippel-Lindau Disease / etiology

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  • (PMID = 17578179.001).
  • [ISSN] 0042-773X
  • [Journal-full-title] Vnitr̆ní lékar̆ství
  • [ISO-abbreviation] Vnitr Lek
  • [Language] cze
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Czech Republic
  • [Number-of-references] 25
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98. Entz-Werlé N, Choquet P, Neuville A, Kuchler-Bopp S, Clauss F, Danse JM, Simo-Noumbissie P, Guérin E, Gaub MP, Freund JN, Boehm N, Constantinesco A, Lutz P, Guenot D, Perrin-Schmitt F: Targeted apc;twist double-mutant mice: a new model of spontaneous osteosarcoma that mimics the human disease. Transl Oncol; 2010;3(6):344-53
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  • TWIST and adenomatosis polyposis coli (APC) are critical signaling factors in normal bone development.

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  • (PMID = 21151473.001).
  • [ISSN] 1936-5233
  • [Journal-full-title] Translational oncology
  • [ISO-abbreviation] Transl Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3000459
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99. Kang MS, Lu H, Yasui T, Sharpe A, Warren H, Cahir-McFarland E, Bronson R, Hung SC, Kieff E: Epstein-Barr virus nuclear antigen 1 does not induce lymphoma in transgenic FVB mice. Proc Natl Acad Sci U S A; 2005 Jan 18;102(3):820-5
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  • [Title] Epstein-Barr virus nuclear antigen 1 does not induce lymphoma in transgenic FVB mice.
  • The lymphoma-inducing potential of Ig heavy-chain enhancer- and promoter-regulated Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA1) was evaluated in three transgenic FVB mouse lineages.
  • EBNA1 was expressed at a higher level in transgenic B220(+) splenocytes than in EBV-infected lymphoblastoid cell lines.
  • EBNA1 was also expressed in B220(-) transgenic splenocytes and thymocytes.
  • Before killing and assessments at 18-26 months, EBNA1-transgenic mice did not differ from control mice in mortality.
  • At 18-26 months EBNA1-transgenic mice did not differ from littermate control in ultimate body weight, in spleen size or weight, in lymph node, kidney, liver, or spleen histology, in splenocyte fractions positive for cluster of differentiation (CD)3epsilon, CD4, CD8, CD62L, B220, CD5, IgM, IgD, MHC class II, CD11b, or CD25, or in serum IgM, IgG, or total Ig levels.
  • Lymphomas were not found in spleens or other organs of 18- to 26-month-old EBNA1-transgenic (n=86) or control (n=45) FVB mice.
  • EBNA1-transgenic lineages had a higher pulmonary adenoma prevalence than did littermate controls (39% versus 7%).
  • However, the adenoma prevalence was not higher in EBNA1-transgenic mice than has been described for FVB mice, and EBNA1 was not expressed in normal pulmonary epithelia or adenomas.

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  • (PMID = 15640350.001).
  • [ISSN] 0027-8424
  • [Journal-full-title] Proceedings of the National Academy of Sciences of the United States of America
  • [ISO-abbreviation] Proc. Natl. Acad. Sci. U.S.A.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / R01 CA047006; United States / NCI NIH HHS / CA / R35 CA047006; United States / NCI NIH HHS / CA / CA47006
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / EBV-encoded nuclear antigen 1; 0 / Epstein-Barr Virus Nuclear Antigens; EC 3.1.3.48 / Antigens, CD45
  • [Other-IDs] NLM/ PMC545574
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100. Lejeune S, Guillemot F, Triboulet JP, Cattan S, Mouton C, PAFNORD Group, Porchet N, Manouvrier S, Buisine MP: Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis. Hum Mutat; 2006 Oct;27(10):1064
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  • [Title] Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
  • Familial adenomatous polyposis has been linked to germline mutations in the APC tumor suppressor gene.
  • However, a number of patients with familial adenomatous polyposis (with either classical or attenuated phenotype) have no APC mutation.
  • Moreover, biallelic mutations in the base excision repair gene MUTYH have been associated with polyposis and early-onset colorectal cancer.
  • AXIN2 and MUTYH genes were screened for germline mutations by PCR and direct sequencing in 39 unrelated patients with multiple adenomas or colorectal cancer without evidence of APC mutation nor mismatch repair defect.
  • Two novel AXIN2 variants were detected in one patient with multiple adenomas, but no clearly pathogenic mutation.
  • Biallelic MUTYH mutations were only found in patients with multiple adenomatous polyposis (7 out of 22 (32%)).
  • Moreover, one patient with biallelic MUTYH mutations presented with multiple adenomas and severe tooth agenesis.
  • Therefore, germline mutations are rare in AXIN2 but frequent in MUTYH in patients with multiple adenomas.
  • [MeSH-major] Adenomatous Polyposis Coli / genetics. Cytoskeletal Proteins / genetics. DNA Glycosylases / genetics. Mutation / genetics

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  • (PMID = 16941501.001).
  • [ISSN] 1098-1004
  • [Journal-full-title] Human mutation
  • [ISO-abbreviation] Hum. Mutat.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / AXIN2 protein, human; 0 / Axin Protein; 0 / Cytoskeletal Proteins; EC 3.2.2.- / DNA Glycosylases; EC 3.2.2.- / mutY adenine glycosylase
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