Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis. - Wikidata - wikimedia - TriplyDB

Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.

Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.

http://www.wikidata.org/entity/Q37400731

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Lessons from Lynch syndrome: a tumor biology-based approach to familial colorectal cancer.Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study.Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry.A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry.Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).

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Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.

http://www.wikidata.org/entity/Q37400731

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 25 February 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Analysis of families with Lync ...... review and pedigree analysis.

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Analysis of families with Lync ...... review and pedigree analysis.

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type

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Analysis of families with Lync ...... review and pedigree analysis.

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Analysis of families with Lync ...... review and pedigree analysis.

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Analysis of families with Lync ...... review and pedigree analysis.

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Analysis of families with Lync ...... review and pedigree analysis.

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S10689-009-9238-8

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Familial Cancer

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Analysis of families with Lync ...... y review and pedigree analysis

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Andrew R Ruszkiewicz

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Diane McKeone

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Finlay Macrae

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Graeme K Suthers

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Graeme P Young

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Jack Goldblatt

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Jeremy R Jass

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Jillian George

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Joanne P Young

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John L Hopper

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P2860

BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal 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

Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines

Comparison of microsatellite instability, CpG island methylation phenotype, BRAF and KRAS status in serrated polyps and traditional adenomas indicates separate pathways to distinct colorectal carcinoma end points.

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.

DNA microsatellite instability and mismatch repair protein loss in adenomas presenting in hereditary non-polyposis colorectal cancer.

Methylation patterns define two types of hyperplastic polyp associated with colorectal cancer

BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum

Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis

Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancers

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s10689-009-9238-8

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