about
Base-excision repair of oxidative DNA damageA novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype.Colorectal cancer: molecular features and clinical opportunitiesLower gastrointestinal tract cancer predisposition syndromesColorectal Cancer Incidence Rates in the Louisiana Acadian Parishes Demonstrated to be Among the Highest in the United States.MUTYH Associated Polyposis (MAP).Identification of patients at risk for hereditary colorectal cancerThe genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Cross-species comparison of human and mouse intestinal polyps reveals conserved mechanisms in adenomatous polyposis coli (APC)-driven tumorigenesis.miR-211 suppresses epithelial ovarian cancer proliferation and cell-cycle progression by targeting Cyclin D1 and CDK6.The signatures of autozygosity among patients with colorectal cancer.Aberrations Involving Chromosome 1 as a Possible Predictor of Odds Ratio for Colon Cancer--Results from the Krakow Case-Control Study.The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia.The genetic basis of colonic adenomatous polyposis syndromesColorectal cancer risks in relatives of young-onset cases: is risk the same across all first-degree relatives?The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.Multiple primary cancers as a guide to heritability.AXIN1 and AXIN2 variants in gastrointestinal cancers.Familial colorectal cancer.Identification of an APC Variant in a Patient with Clinical Attenuated Familial Adenomatous Polyposis.Colonic polyposis in a 15 year-old boy: Challenges and lessons from a rural resource-poor area.Tumor suppressor genes in familial adenomatous polyposisClinical Characteristics of Multiple Colorectal Adenoma Patients Without Germline APC or MYH Mutations.Allele-specific expression of APC in adenomatous polyposis families.Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.Barrett's esophagus in the patients with familial adenomatous polyposis.A survey of APC mutations in Quebec.[Colorectal polyposis syndrome: a guide to diagnosis].Oncogenic KRAS is not necessary for Wnt signalling activation in APC-associated FAP adenomas
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
The genetics of FAP and FAP-like syndromes.
@ast
The genetics of FAP and FAP-like syndromes.
@en
type
label
The genetics of FAP and FAP-like syndromes.
@ast
The genetics of FAP and FAP-like syndromes.
@en
prefLabel
The genetics of FAP and FAP-like syndromes.
@ast
The genetics of FAP and FAP-like syndromes.
@en
P1433
P1476
The genetics of FAP and FAP-like syndromes.
@en
P2093
Lara Lipton
P2860
P2888
P304
P356
10.1007/S10689-005-5673-3
P577
2006-01-01T00:00:00Z