MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions. (Q54419188)

29 May 2018

title

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

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29 May 2018

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8

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Jean-François Fléjou

6

object named as

Jean-Francois Flejou

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29 May 2018

Carolina Bonilla

4

object named as

Carolina Bonilla

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29 May 2018

author name string

Jérémie H Lefevre

1

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29 May 2018

Chrystelle Colas

2

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29 May 2018

Florence Coulet

3

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29 May 2018

Najat Mourra

5

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29 May 2018

Emmanuel Tiret

7

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29 May 2018

Florent Soubrier

9

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29 May 2018

Yann Parc

10

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29 May 2018

publication date

1 December 2010

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29 May 2018

published in

Familial Cancer

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volume

9

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29 May 2018

page(s)

589-594

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issue

4

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https://scigraph.springernature.com/pub.10.1007/s10689-010-9367-0

exact match

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cites work

The interacting pathways for prevention and repair of oxidative DNA damage

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Crossref

https://api.crossref.org/works/10.1007%2FS10689-010-9367-0

A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma

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1 reference

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Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway

1 reference

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Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors

1 reference

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Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

1 reference

12 December 2020

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

1 reference

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Efficiency of the revised Bethesda guidelines (2003) for the detection of mutations in mismatch repair genes in Austrian HNPCC patients

1 reference

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Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families

1 reference

12 December 2020

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

1 reference

12 December 2020

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.

1 reference

12 December 2020

Implication of MYH in colorectal polyposis.

1 reference

12 December 2020

The mammalian mismatch repair pathway removes DNA 8-oxodGMP incorporated from the oxidized dNTP pool

1 reference

12 December 2020

Immunohistochemistry for MSH2 and MHL1: a method for identifying mismatch repair deficient colorectal cancer

1 reference

12 December 2020

Prognostic significance of microsatellite instability determined by immunohistochemical staining of MSH2 and MLH1 in sporadic T3N0M0 colon cancer

1 reference

12 December 2020

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

1 reference

12 December 2020

No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer

1 reference

12 December 2020

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

1 reference

12 December 2020

Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6

1 reference

12 December 2020

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing

1 reference

12 December 2020

The role of MYH and microsatellite instability in the development of sporadic colorectal cancer

1 reference

12 December 2020

10.1007/S10689-010-9367-0

Identifiers

DOI

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29 May 2018

PubMed ID

20640893

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29 May 2018