Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients. - Wikidata - wikimedia - TriplyDB

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients.

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients.

http://www.wikidata.org/entity/Q35791897

about

MUTYH DNA glycosylase: the rationale for removing undamaged bases from the DNA Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer Role of inherited defects of MYH in the development of sporadic colorectal cancer Germline susceptibility to colorectal cancer due to base-excision repair gene defects.Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk Gastrointestinal tract cancers: Genetics, heritability and germ line mutations Genetic testing for hereditary colorectal cancer.The Swedish family-cancer database: update, application to colorectal cancer and clinical relevance.MUTYH Mutations Do Not Cause HNPCC or Late Onset Familial Colorectal Cancer MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.MUTYH Associated Polyposis (MAP).The genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.Simple and complex genetics of colorectal cancer susceptibility.Molecular basis and diagnostics of hereditary colorectal cancers.Serrated pathway colorectal cancer in the population: genetic consideration ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes Recently identified colon cancer predispositions: MYH and MSH6 mutations.The genetics of FAP and FAP-like syndromes.The role of MYH and microsatellite instability in the development of sporadic colorectal cancer.Genetic alterations in sporadic and hereditary colorectal cancer: implementations for screening and follow-up.Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study.Pathological features of colorectal carcinomas in MYH-associated polyposis.Prevalence of MYH-associated polyposis related to three recurrent mutations in Morocco.Frequent mutation in North African patients with MUTYH-associated polyposis.Association of MUTYH and colorectal cancer.Colorectal cancer risk in monoallelic carriers of MYH variants.ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.Oxidative DNA damage and DNA repair enzyme expression are inversely related in murine models of fatty liver disease.Association between genetic polymorphisms of the base excision repair gene MUTYH and increased colorectal cancer risk in a Japanese population.Germline MYH mutations in a clinic-based series of Canadian multiple colorectal adenoma patients.Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer.MYH mutations are rare in prostate cancer.Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer.MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations.Implication of MYH in colorectal polyposis.

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Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients.

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The American Journal of Pathology

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Anu Suomalainen

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Auli Karhu

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Heikki J Järvinen

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Lara Lipton

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Matti Eskelinen

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Susa Enholm

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Tuija Hienonen

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P2860

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

Cloning and expression of cDNA for a human enzyme that hydrolyzes 8-oxo-dGTP, a mutagenic substrate for DNA synthesis

Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage

Mutation of a mutL homolog in hereditary colon cancer

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH

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

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10599254

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colorectal cancer

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1868242

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