Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history. - Wikidata - awgldk - TriplyDB

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

http://www.wikidata.org/entity/Q33910331

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Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome Risks of Lynch syndrome cancers for MSH6 mutation carriers.Current and emerging trends in Lynch syndrome identification in women with endometrial cancer.Loss of the mismatch repair protein MSH6 in human glioblastomas is associated with tumor progression during temozolomide treatment.Evaluation of clinical criteria for the identification of Lynch syndrome among unselected patients with endometrial cancer.Low prevalence of germline hMSH6 mutations in colorectal cancer families from Spain Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.Hereditary non-polyposis colon cancer Recently identified colon cancer predispositions: MYH and MSH6 mutations.Immunohistochemistry and microsatellite instability analysis in molecular subtyping of colorectal carcinoma based on mismatch repair competency.Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part II. The utility of microsatellite instability testing Prediction of germline mutations and cancer risk in the Lynch syndrome Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers.Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.A two-antibody mismatch repair protein immunohistochemistry screening approach for colorectal carcinomas, skin sebaceous tumors, and gynecologic tract carcinomas.Lynch syndrome diagnostics: decision-making process for germ-line testing.Association between MSH6 G39E polymorphism and cancer susceptibility: a meta-analysis of 7,046 cases and 34,554 controls.Is prostate cancer a Lynch syndrome cancer?

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P2860

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

http://www.wikidata.org/entity/Q33910331

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2004 nî lūn-bûn

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2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2004 թվականի ապրիլին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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Alison J Whelan

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Barbara M Buttin

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David G Mutch

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Janet S Rader

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Matthew A Powell

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Thomas J Herzog

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P2860

hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

Familial endometrial cancer in female carriers of MSH6 germline mutations

Germ-line msh6 mutations in colorectal cancer families

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

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

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

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10.1086/421332

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