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Article

A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis

1 Jul 1995

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7797014
DOI: 10.1016/0016-5085(95)90280-5

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Related research

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A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitisPMID 7797014Read ↗

Novel germline and somatic mutations of the MSH2 gene in hereditary non-polyposis colorectal cancer.Semantic proximity Read ↗

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Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an American Founder Genomic Deletion of the MSH2 GeneSemantic proximity Read ↗

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Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeSemantic proximity Read ↗

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillanceSemantic proximity Read ↗

Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition.Semantic proximity Read ↗

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Analysis of the Expression and Prognostic Value of MSH2 in Pan-Cancer Based on Bioinformatics.Semantic proximity Read ↗

Thirty-nine-year-old with familial colon cancer, and variant of undetermined significance in MSH6.Semantic proximity Read ↗

Splice site mutations in mismatch repair genes and risk of cancer in the general population.Semantic proximity Read ↗

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