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Adenomatous polyposis coli (APC) is required for normal development of skin and thymusInherited colorectal cancer syndromesDECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesGenetic risks and familial associations of small bowel carcinomaClinical Genetic Testing in GastroenterologyGastric cancer: descriptive epidemiology, risk factors, screening, and preventionStem cell dynamics and pretumor progression in the intestinal tractEpigenetic regulation of the intestinal epitheliumSurgical resection for non-familial adenomatous polyposis-related intra-abdominal fibromatosisColorectal cancer and genetic alterations in the Wnt pathwayThe Rising Incidence of Younger Patients With Colorectal Cancer: Questions About Screening, Biology, and Treatment.The UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variations.Identification of 5 novel germline APC mutations and characterization of clinical phenotypes in Japanese patients with classical and attenuated familial adenomatous polyposis.Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseqClinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.Application of a spontaneously closed protective stoma in an ileal pouch-anal anastomosis: a preliminary study.A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.Gastrointestinal tract cancers: Genetics, heritability and germ line mutationsThe differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.Inducible loss of one Apc allele in Lrig1-expressing progenitor cells results in multiple distal colonic tumors with features of familial adenomatous polyposis.Lower gastrointestinal tract cancer predisposition syndromesOral manifestations of hereditary nonpolyposis colorectal cancer syndrome: a family case series.Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling.Pancreatic ductal adenocarcinoma: risk factors, screening, and early detection.Familial adenomatous polyposis: ileo-anal pouch versus ileo-rectal anastomosis.Extra-intestinal manifestations of familial adenomatous polyposisMUTYH Associated Polyposis (MAP).Colorectal carcinoma: Pathologic aspectsIdentification of patients at risk for hereditary colorectal cancerThe genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Colorectal Cancer Incidence Among Young Adults in CaliforniaIsolation and characterization of the TIGA genes, whose transcripts are induced by growth arrestClinics in diagnostic imaging. 159. Jejunal intussusception due to Peutz-Jeghers syndromeThe prognosis of clinical course and the analysis of the frequency of the inflammation and dysplasia in the intestinal J-pouch at the patients after restorative proctocolectomy due to FAP.Large intron 14 rearrangement in APC results in splice defect and attenuated FAP.Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?Oral manifestations in patients with familial adenomatous polyposis: A systematic review and meta-analysis.Two Metachronous Neoplasms in the Radiotherapy Fields of a Young Man With Familial Adenomatous PolyposisAspirin for the prevention of colorectal cancerDevelopment of a Novel Scoring System for Predicting the Risk of Colorectal Neoplasia: A Retrospective Study
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P2860
description
article
@en
im Februar 2006 veröffentlichter wissenschaftlicher Artikel
@de
наукова стаття, опублікована в лютому 2006
@uk
ലേഖനം
@ml
name
Familial Adenomatous Polyposis
@en
type
label
Familial Adenomatous Polyposis
@en
prefLabel
Familial Adenomatous Polyposis
@en
P2860
P1476
Familial adenomatous polyposis
@en
P2093
Polymnia Galiatsatos
P2860
P304
P356
10.1111/J.1572-0241.2006.00375.X
P407
P577
2006-02-01T00:00:00Z