Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
about
Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindredsEarly-onset colorectal cancer: a separate subset of colorectal cancerOptimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes.Distinct clinical features associated with microsatellite instability in colorectal cancers of young patients.Approach to early-onset colorectal cancer: clinicopathological, familial, molecular and immunohistochemical characteristics.Haploinsufficiency of Flap endonuclease (Fen1) leads to rapid tumor progressionGermline MLH1 and MSH2 mutational spectrum including frequent large genomic aberrations in Hungarian hereditary non-polyposis colorectal cancer families: implications for genetic testingPathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.Early-onset colorectal cancer: a sporadic or inherited disease?Improving the ascertainment of families at high risk of colorectal cancer: a prospective GP register studyCompound heterozygosity for two MSH2 mutations suggests mild consequences of the initiation codon variant c.1A>G of MSH2.Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome.MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancerPrevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer.Novel DNA variants and mutation frequencies of hMLH1 and hMSH2 genes in colorectal cancer in the Northeast China populationReview article: genetic testing and counselling for hereditary colorectal cancer.The predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complexFrequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patientsPathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing.The germline MLH1 K618A variant and susceptibility to Lynch syndrome-associated tumorsGuidance on large bowel surveillance for people with two first degree relatives with colorectal cancer or one first degree relative diagnosed with colorectal cancer under 45 years.Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach.Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposisEarly-onset colorectal cancer patients without family history are "at very low risk" for lynch syndrome.Evidence for an age-related influence of microsatellite instability on colorectal cancer survival.Colorectal cancer in the very young: a comparative study of tumor markers, pathology and survival in early onset and adult onset patients.Cancer at ages 15-29 years: the contrasting incidence in India and England.Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genes.Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report.A bi-national perspective on the management of young patients with colorectal cancer.The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer.Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.Managing young colorectal cancer: a UK and Irish perspective.Early-onset colorectal cancer is an easy and effective tool to identify retrospectively Lynch syndrome.Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes.AfterhMSH2 andhMLH1?what next? Analysis of three-generational, population-based, early-onset colorectal cancer familiesScreening of patients at high risk of colorectal cancerEarly-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomesClinical Definition of Hereditary Non-polyposis Colorectal Cancer: A Search for the Impossible?
P2860
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P2860
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
description
1998 nî lūn-bûn
@nan
1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@ast
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@en
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@nl
type
label
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@ast
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@en
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@nl
prefLabel
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@ast
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@en
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@nl
P2093
P356
P1476
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
@en
P2093
D J Robbins
J D Burczak
J Lin-Goerke
S M Farrington
P304
P356
10.1086/301996
P407
P577
1998-09-01T00:00:00Z