Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors (Q44884428)

7 December 2017

Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors (English)

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Armelle Bardier-Dupas

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object named as

Armelle Bardier-Dupas

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Magali Svrcek

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Isabelle Sourrouille

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Florence Coulet

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Chrystelle Colas

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Mélanie Eyries

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Yann Parc

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Florent Soubrier

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1 March 2013

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https://scigraph.springernature.com/pub.10.1007/s10689-012-9568-9

7 December 2017

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Microsatellite instability in colorectal cancer

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Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

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Intestinal inflammation and cancer

21 January 2018

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A meta-analysis of the prevalence of somatic mutations in the hMLH1 and hMSH2 genes in colorectal cancer

21 January 2018

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Determining the frequency of de novo germline mutations in DNA mismatch repair genes

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MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions.

21 January 2018

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Immunohistochemical staining for mismatch repair proteins, and its relevance in the diagnosis of hereditary non-polyposis colorectal cancer

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

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Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based ApproachVersusMolecular Screening

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Exome sequencing: expanding the genetic testing toolbox

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12 December 2020

Somatic mosaicism in a patient with Lynch syndrome

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12 December 2020

Toward a consensus in molecular diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome)

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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

Screening for Lynch syndrome in colorectal cancer: are we doing enough?

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12 December 2020

Microsatellite instability and hMLH1/hMSH2 expression in young endometrial carcinoma patients: associations with family history and histopathology

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12 December 2020

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes

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12 December 2020

10.1007/S10689-012-9568-9

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DOI

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7 December 2017

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