The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease
about
Germline INDELs and CNVs in a cohort of colorectal cancer patients: their characteristics, associations with relapse-free survival time, and potential time-varying effects on the risk of relapseGene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X.Familial colon cancer syndromes: an update of a rapidly evolving fieldColorectal Cancer Incidence Rates in the Louisiana Acadian Parishes Demonstrated to be Among the Highest in the United States.Examining the polymorphisms in the hypoxia pathway genes in relation to outcome in colorectal cancer.MTHFR Glu429Ala and ERCC5 His46His polymorphisms are associated with prognosis in colorectal cancer patients: analysis of two independent cohorts from Newfoundland.Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms.A genome wide association study on Newfoundland colorectal cancer patients' survival outcomesA Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal CancerMitochondrial DNA polymorphisms, its copy number change and outcome in colorectal cancer.Next-generation sequencing for genetic testing of familial colorectal cancer syndromes.Determining the frequency of de novo germline mutations in DNA mismatch repair genes.Clinico-pathologic Parameters for Prediction of Microsatellite Instability in Colorectal Cancer.Dietary patterns and colorectal cancer recurrence and survival: a cohort study.Hereditary colorectal cancer registries in Canada: report from the Colorectal Cancer Association of Canada consensus meeting; Montreal, Quebec; October 28, 2011No associations of a set of SNPs in the Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloproteinase (MMP) genes with survival of colorectal cancer patientsEndobiogeny: a global approach to systems biology (part 1 of 2).Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).Influence of pre-diagnostic cigarette smoking on colorectal cancer survival: overall and by tumour molecular phenotype.Familial colorectal cancer type X: genetic profiles and phenotypic features.Vitamin D receptor and calcium-sensing receptor polymorphisms and colorectal cancer survival in the Newfoundland population.Identification of a novel deletion mutant strain in Saccharomyces cerevisiae that results in a microsatellite instability phenotype.Familial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description.Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: a Norwegian population-based study.Community Practice Implementation of a Self-administered Version of PREMM1,2,6 to Assess Risk for Lynch Syndrome.Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.XRCC3 Thr241Met and TYMS variable number tandem repeat polymorphisms are associated with time-to-metastasis in colorectal cancer.Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort.Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.Association of rs2282679 A>C polymorphism in vitamin D binding protein gene with colorectal cancer risk and survival: effect modification by dietary vitamin D intake.A population-based study of hereditary non-polyposis colorectal cancer: evidence of pathologic and genetic heterogeneity.Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers.Two functional indel polymorphisms in the promoter region of the Brahma gene (BRM) and disease risk and progression-free survival in colorectal cancer.
P2860
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P2860
The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
The genetic basis of colorecta ...... high rate of familial disease
@ast
The genetic basis of colorecta ...... high rate of familial disease
@en
The genetic basis of colorecta ...... high rate of familial disease
@nl
type
label
The genetic basis of colorecta ...... high rate of familial disease
@ast
The genetic basis of colorecta ...... high rate of familial disease
@en
The genetic basis of colorecta ...... high rate of familial disease
@nl
prefLabel
The genetic basis of colorecta ...... high rate of familial disease
@ast
The genetic basis of colorecta ...... high rate of familial disease
@en
The genetic basis of colorecta ...... high rate of familial disease
@nl
P2093
P2860
P356
P1433
P1476
The genetic basis of colorecta ...... high rate of familial disease
@en
P2093
A de la Chapelle
H B Younghusband
J McLaughlin
M Clendenning
P2860
P304
P356
10.1136/GUT.2010.208462
P407
P577
2010-08-03T00:00:00Z