APC gene: database of germline and somatic mutations in human tumors and cell lines
about
EB3, a novel member of the EB1 family preferentially expressed in the central nervous system, binds to a CNS-specific APC homologueGermline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomasColorectal cancer and genetic alterations in the Wnt pathwaySingle nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in TaiwanSerum Levels of Glycoproteins are Elevated in Patients with Ovarian CancerLimited importance of the dominant-negative effect of TP53 missense mutationsVariable expressivity and mutation databases: The androgen receptor gene mutations database.Readthrough of premature termination codons in the adenomatous polyposis coli gene restores its biological activity in human cancer cellsCadherin and catenin alterations in human cancer.Frequent alteration of the tumor suppressor gene APC in sporadic canine colorectal tumors.Review article: genetic testing and counselling for hereditary colorectal cancer.Current and evolving strategies for colorectal cancer screening.Pathological features and genetic alterations in colorectal carcinomas with characteristics of nonpolypoid growthAnalysis of masked mutations in familial adenomatous polyposisThe C-terminus of Apc does not influence intestinal adenoma development or progression.The nucleoside analog clitocine is a potent and efficacious readthrough agent.Extracellular inhibitors can attenuate tumorigenic Wnt pathway activity in adenomatous polyposis coli mutants: Predictions of a validated mathematical modelDetecting colorectal cancer in stool with the use of multiple genetic targets.Adenomatous polyposis coli is down-regulated by the ubiquitin-proteasome pathway in a process facilitated by Axin.UMD (Universal mutation database): a generic software to build and analyze locus-specific databases.Investigation of pathogenic mechanisms in multiple colorectal adenoma patients without germline APC or MYH/MUTYH mutations.Nasopharyngeal angiofibroma: a manifestation of familial adenomatous polyposis.The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations.Dental anomalies in pediatric patients with familial adenomatous polyposis.A survey of APC mutations in Quebec.APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations.
P2860
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P2860
APC gene: database of germline and somatic mutations in human tumors and cell lines
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh-hant
name
APC gene: database of germline and somatic mutations in human tumors and cell lines
@en
APC gene: database of germline and somatic mutations in human tumors and cell lines
@nl
type
label
APC gene: database of germline and somatic mutations in human tumors and cell lines
@en
APC gene: database of germline and somatic mutations in human tumors and cell lines
@nl
prefLabel
APC gene: database of germline and somatic mutations in human tumors and cell lines
@en
APC gene: database of germline and somatic mutations in human tumors and cell lines
@nl
P50
P356
P1476
APC gene: database of germline and somatic mutations in human tumors and cell lines
@en
P304
P356
10.1093/NAR/26.1.269
P407
P577
1998-01-01T00:00:00Z