Detection of hMSH2 and hMLH1 mutations in Chinese hereditary non-polyposis colorectal cancer kindreds. - Wikidata - wikimedia - TriplyDB

Detection of hMSH2 and hMLH1 mutations in Chinese hereditary non-polyposis colorectal cancer kindreds.

Detection of hMSH2 and hMLH1 mutations in Chinese hereditary non-polyposis colorectal cancer kindreds.

http://www.wikidata.org/entity/Q37174196

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Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer.Advances in the study of Lynch syndrome in China Missense mutations of MLH1 and MSH2 genes detected in patients with gastrointestinal cancer are associated with exonic splicing enhancers and silencers.

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Detection of hMSH2 and hMLH1 mutations in Chinese hereditary non-polyposis colorectal cancer kindreds.

http://www.wikidata.org/entity/Q37174196

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

@en

Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

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type

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Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

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Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

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Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

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Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

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World Journal of Gastroenterology

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Detection of hMSH2 and hMLH1 m ...... is colorectal cancer kindreds.

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Chang-Hua Zhang

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Chuang-Qi Chen

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Dong-Jie Yang

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Fang-Jin Wang

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Shi-Rong Cai

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Wen-Hua Zhan

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Wu Song

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Xi-Yu Yuan

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Yu-Long He

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P2860

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.

Founding mutations and Alu-mediated recombination in hereditary colon cancer.

Cancer risk in mutation carriers of DNA-mismatch-repair genes.

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review.

Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1.

Cancer risk in mismatch repair gene mutation carriers.

Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors.

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298-302

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scholarly article

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10.3748/WJG.14.298

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2008-01-01T00:00:00Z

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18186571

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colorectal cancer

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2675130

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