Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation. (Q51772302)

12 April 2018

title

Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation. (English)

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12 April 2018

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3

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author name string

Hanifa Bouzourene

1

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12 April 2018

Pierre Hutter

2

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12 April 2018

Patricia Martin

4

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12 April 2018

Jean Benhattar

5

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12 April 2018

publication date

1 June 2010

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12 April 2018

published in

Familial Cancer

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volume

9

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issue

2

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page(s)

167-172

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https://scigraph.springernature.com/pub.10.1007/s10689-009-9302-4

exact match

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cites work

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

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Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term

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

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Methylation-sensitive single-strand conformation analysis: a rapid method to screen for and analyze DNA methylation

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Genetic predisposition to colorectal cancer

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Methylation of hMLH1 promoter correlates with the gene silencing with a region-specific manner in colorectal cancer

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12 December 2020

Testing for defective DNA mismatch repair in colorectal carcinoma: a practical guide

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Activated BRAF targets proximal colon tumors with mismatch repair deficiency and MLH1 inactivation

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Mutations of the BRAF gene in human cancer

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Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability

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Morphology of sporadic colorectal cancer with DNA replication errors

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12 December 2020

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

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12 December 2020

Differential involvement of the hypermethylator phenotype in hereditary and sporadic colorectal cancers with high-frequency microsatellite instability.

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12 December 2020

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

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New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

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Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome

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Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes.

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

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12 December 2020

Mutations of BRAF are associated with extensive hMLH1 promoter methylation in sporadic colorectal carcinomas.

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12 December 2020

The role of hypermethylation of the hMLH1 promoter region in HNPCC versus MSI+ sporadic colorectal cancers

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Population-based molecular detection of hereditary nonpolyposis colorectal cancer

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12 December 2020

Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer

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Microsatellite instability in cancer of the proximal colon

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12 December 2020

HNPCC and sporadic MSI-H colorectal cancer: a review of the morphological similarities and differences

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Promoter hypermethylation frequency and BRAF mutations distinguish hereditary non-polyposis colon cancer from sporadic MSI-H colon cancer.

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12 December 2020

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

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12 December 2020

Hereditary colorectal cancer

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12 December 2020

RAF/RAS oncogenes and mismatch-repair status

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Tumor microsatellite instability and clinical outcome in young patients with colorectal cancer

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Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives.

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A cost-effective algorithm for hereditary nonpolyposis colorectal cancer detection.

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Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

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Decrease in mortality in Lynch syndrome families because of surveillance.

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Microsatellite instability phenotype of tumors: genotyping or immunohistochemistry? The jury is still out

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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

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Causes of microsatellite instability in colorectal tumors

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Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications

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Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

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BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair

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12 December 2020

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

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12 December 2020

Methylation pattern of different regions of theMLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer

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12 December 2020

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

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Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.

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Distinction between familial and sporadic forms of colorectal cancer showing DNA microsatellite instability

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12 December 2020

Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.

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12 December 2020

Distinction of hereditary nonpolyposis colorectal cancer and sporadic microsatellite-unstable colorectal cancer through quantification of MLH1 methylation by real-time PCR

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12 December 2020

10.1007/S10689-009-9302-4

Identifiers

DOI

1 reference

12 April 2018

release_bb2mkw44dzdsjdz3u67adhr3uq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/bb2mkw44dzdsjdz3u67adhr3uq

24 November 2022

mapped directly with Wikidata item

PubMed ID

19949877

1 reference

12 April 2018