Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study. - Wikidata - awgldk - TriplyDB

Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.

Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.

http://www.wikidata.org/entity/Q54445035

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MUTYH the base excision repair gene family member associated with colorectal cancer polyposis Systematic meta-analyses and field synopsis of genetic association studies in colorectal cancer Identifying alternative hyper-splicing signatures in MG-thymoma by exon arrays.Colorectal carcinomas in MUTYH-associated polyposis display histopathological similarities to microsatellite unstable carcinomas Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?Aberrant gene promoter methylation associated with sporadic multiple colorectal cancer Genetic testing for hereditary colorectal cancer.MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.A systems biology approach to the global analysis of transcription factors in colorectal cancer.A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.A high degree of LINE-1 hypomethylation is a unique feature of early-onset colorectal cancer.MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines.Familial colorectal cancer, beyond Lynch syndrome Colorectal carcinogenesis--update and perspectives.The genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Report from the OECI Oncology Days 2014 Multiple sporadic colorectal cancers display a unique methylation phenotype.Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.Serrated pathway colorectal cancer in the population: genetic consideration Molecular Features and Methylation Status in Early Onset (≤40 Years) Colorectal Cancer: A Population Based, Case-Control Study.A De Novo Germline APC Mutation (3927del5) in a Patient with Familial Adenomatous Polyposis: Case Report and Literature Review.Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients.Inheritance of Colorectal Cancer Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study.Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.MYH polyposis syndrome: clinical findings, genetics issues and management.A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.Hereditary and common familial colorectal cancer: evidence for colorectal screening.Familial colorectal cancer.Advances in Hereditary Colorectal and Pancreatic Cancers.High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis.Expression and clinical significance of the DNA repair enzyme MYH in esophageal squamous cell carcinoma.A perspective on bi-allelic MUTYH mutations in patients with hyperplastic polyposis syndrome.A bi-national perspective on the management of young patients with colorectal cancer.Hereditary Colorectal Tumors: A Literature Review on MUTYH-Associated Polyposis.Need to implement a coordinated and multidisciplinary care in the Spanish population at increased risk for colorectal cancer.

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P2860

Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.

http://www.wikidata.org/entity/Q54445035

description

2007 nî lūn-bûn

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Identification of MYH mutation ...... ntrol, population-based study.

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Identification of MYH mutation ...... ntrol, population-based study.

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Identification of MYH mutation ...... ntrol, population-based study.

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Identification of MYH mutation ...... ntrol, population-based study.

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J.CGH.2006.12.025

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Clinical Gastroenterology and Hepatology

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Identification of MYH mutation ...... ntrol, population-based study.

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Artemio Payá

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Cristina Alenda

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Elisenda Pons

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Francesc Balaguer

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Gastrointestinal Oncology Group of the Spanish Gastroenterological Association

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Jenifer Muñoz

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Josep M Piqué

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Montserrat Andreu

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Rodrigo Jover

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379-387

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10.1016/J.CGH.2006.12.025

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Javier P Gisbert

Antoni Castells

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2007-03-01T00:00:00Z

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17368238

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colorectal cancer