MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
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MUTYH the base excision repair gene family member associated with colorectal cancer polyposisNOMO-1 gene is deleted in early-onset colorectal cancer.Early-onset colorectal cancer: a sporadic or inherited disease?Biallelic MUTYH mutations can mimic Lynch syndromeA high degree of LINE-1 hypomethylation is a unique feature of early-onset colorectal cancer.Functional analysis in mouse embryonic stem cells reveals wild-type activity for three MSH6 variants found in suspected Lynch syndrome patients.Multiple sporadic colorectal cancers display a unique methylation phenotype.Colorectal cancers with microsatellite instability display unique miRNA profiles.Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family RegistryMolecular Features and Methylation Status in Early Onset (≤40 Years) Colorectal Cancer: A Population Based, Case-Control Study.Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancerEarly-onset colorectal cancer patients without family history are "at very low risk" for lynch syndrome.Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review.Colorectal cancer in young adults.Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.Recent discoveries in the molecular genetics of Lynch syndrome.Clinicopathological characteristics of colorectal cancer presenting under the age of 50.ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).Germline Genetic Features of Young Individuals with Colorectal Cancer.Colorectal cancer in patients under the age of 40 years: experience from a tertiary care centre in the Czech Republic.Prevalence and clinicopathologic/molecular characteristics of mismatch repair-deficient colorectal cancer in the under-50-year-old Japanese population.Deficient mismatch repair and RAS mutation in colorectal carcinoma patients: a retrospective study in Eastern China.
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P2860
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին 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
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@ast
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@en
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@nl
type
label
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@ast
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@en
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@nl
prefLabel
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@ast
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@en
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@nl
P2093
P2860
P1476
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
@en
P2093
Anna Petit
Antoni Castells
C Richard Boland
Francesc Balaguer
Jenifer Muñoz
José María Enríquez-Navascués
Leticia Moreira
Luis Bujanda
María Dolores Giráldez
P2860
P304
P356
10.1158/1078-0432.CCR-10-1491
P407
P577
2010-10-05T00:00:00Z