Familial endometrial cancer in female carriers of MSH6 germline mutations - Wikidata - awgldk - TriplyDB

Familial endometrial cancer in female carriers of MSH6 germline mutations

Familial endometrial cancer in female carriers of MSH6 germline mutations

http://www.wikidata.org/entity/Q28145436

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Current hypotheses on how microsatellite instability leads to enhanced survival of Lynch Syndrome patients MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas HNPCC: six new pathogenic mutations Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesis Hereditary Syndromes Manifesting as Endometrial Carcinoma: How Can Pathological Features Aid Risk Assessment?Carcinogenesis and microsatellite instability: the interrelationship between genetics and epigenetics A review of the clinical relevance of mismatch-repair deficiency in ovarian cancer DNA replication fidelity and cancer Coevolution between simple sequence repeats (SSRs) and virus genome size The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.Multilineage progression of genetically unstable tumor subclones in cutaneous T-cell lymphoma.Mouse models of colorectal cancer.Comparison of lifestyle, hormonal and medical factors in women with sporadic and Lynch syndrome-associated endometrial cancer: A retrospective case-case study.Current and emerging trends in Lynch syndrome identification in women with endometrial cancer.Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions.Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity Genomic and epigenetic instability in colorectal cancer pathogenesis.Cooperative nuclear localization sequences lend a novel role to the N-terminal region of MSH6.Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term.The PWWP domain: a potential protein-protein interaction domain in nuclear proteins influencing differentiation?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 gene.The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype.Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.Microsatellite instability and mutational analysis of transforming growth factor beta receptor type II gene (TGFBR2) in sporadic ovarian cancer.Haploinsufficiency of Flap endonuclease (Fen1) leads to rapid tumor progression Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.Induction of HSF1 expression is associated with sporadic colorectal cancer.Mouse models of inherited cancer syndromes New facial papules in a 66-year-old woman with bladder cancer Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.Cancer genetics: risks and mechanisms of cancer in women with inherited susceptibility to epithelial ovarian cancer Pathogenesis and clinical management of hereditary non-polyposis colorectal cancer.Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management.Functional analysis in mouse embryonic stem cells reveals wild-type activity for three MSH6 variants found in suspected Lynch syndrome patients.Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers.Molecular pathogenesis and prognostic factors in endometrial carcinoma.Detection of germline mutations of hMLH1 and hMSH2 based on cDNA sequencing in China Aberrant crypt foci as microscopic precursors of colorectal cancer.Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability

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P2860

Familial endometrial cancer in female carriers of MSH6 germline mutations

http://www.wikidata.org/entity/Q28145436

description

1999 nî lūn-bûn

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1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի հոտեմբերին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

Familial endometrial cancer in female carriers of MSH6 germline mutations

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Familial endometrial cancer in female carriers of MSH6 germline mutations

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Familial endometrial cancer in female carriers of MSH6 germline mutations

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type

label

Familial endometrial cancer in female carriers of MSH6 germline mutations

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Familial endometrial cancer in female carriers of MSH6 germline mutations

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Familial endometrial cancer in female carriers of MSH6 germline mutations

@nl

prefLabel

Familial endometrial cancer in female carriers of MSH6 germline mutations

@ast

Familial endometrial cancer in female carriers of MSH6 germline mutations

@en

Familial endometrial cancer in female carriers of MSH6 germline mutations

@nl

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Familial endometrial cancer in female carriers of MSH6 germline mutations

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Bröcker-Vriends A

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Cornelisse C

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Menko F

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Morreau H

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Möslein G

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Vossen S

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Wu Y

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142-144

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scholarly article

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10.1038/13773

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2

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23

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Hanne Meijers-Heijboer

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1999-10-01T00:00:00Z

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12790980

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10508506

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