The predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complex (Q35563361)

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scientific article published on 11 August 2011

Language	Label	Description	Also known as
English	The predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complex	scientific article published on 11 August 2011

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

The predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complex (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

DNA mismatch repair

1 reference

based on heuristic

inferred from title

author name string

Jennifer L Cyr

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Graham D Brown

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Jennifer Stroop

3

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Christopher D Heinen

4

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

publication date

11 August 2011

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Molecular Carcinogenesis

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

51

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

647-658

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Evidence for an hMSH3 defect in familial hamartomatous polyps

1 reference

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MutLalpha and proliferating cell nuclear antigen share binding sites on MutSbeta

1 reference

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CUG start codon generates thioredoxin/glutathione reductase isoforms in mouse testes

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Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families

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Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

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Genetic Instability Caused by Loss of MutS Homologue 3 in Human Colorectal Cancer

1 reference

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12 July 2018

Hereditary cancer-associated missense mutations in hMSH6 uncouple ATP hydrolysis from DNA mismatch binding

1 reference

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Compound heterozygosity for two MSH2 mutations suggests mild consequences of the initiation codon variant c.1A>G of MSH2.

1 reference

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Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

1 reference

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Mechanisms and functions of DNA mismatch repair

1 reference

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Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes

1 reference

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Constitutive deficiency in DNA mismatch repair

1 reference

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Structure of the human MutSalpha DNA lesion recognition complex

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Saccharomyces cerevisiae MSH2-MSH3 and MSH2-MSH6 complexes display distinct requirements for DNA binding domain I in mismatch recognition

1 reference

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12 July 2018

The multifaceted mismatch-repair system

1 reference

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12 July 2018

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

1 reference

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12 July 2018

Dominant effects of an Msh6 missense mutation on DNA repair and cancer susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220760

12 July 2018

Differential specificities and simultaneous occupancy of human MutSalpha nucleotide binding sites

1 reference

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Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

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12 July 2018

An Msh2 point mutation uncouples DNA mismatch repair and apoptosis

1 reference

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12 July 2018

DNA repair and tumorigenesis: lessons from hereditary cancer syndromes

1 reference

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12 July 2018

Genetic instability in human mismatch repair deficient cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220760

12 July 2018

Complementation of an hMSH2 defect in human colorectal carcinoma cells by human chromosome 2 transfer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220760

12 July 2018

hMSH2-hMSH6 forms a hydrolysis-independent sliding clamp on mismatched DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220760

12 July 2018

DNA-dependent activation of the hMutSalpha ATPase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220760

12 July 2018

Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair

1 reference

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12 July 2018

Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer

1 reference

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Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls

1 reference

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The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch

1 reference

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Recognition of AUG and alternative initiator codons is augmented by G in position +4 but is not generally affected by the nucleotides in positions +5 and +6.

1 reference

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hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6

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Context effects and inefficient initiation at non-AUG codons in eucaryotic cell-free translation systems

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Lynch syndrome-associated mutations in MSH2 alter DNA repair and checkpoint response functions in vivo

1 reference

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HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions

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Preparation of heteroduplex enhanced green fluorescent protein plasmid for in vivo mismatch repair activity assay

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A precursor form of vascular endothelial growth factor arises by initiation from an upstream in-frame CUG codon

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Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer

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Dissociation of mismatch recognition and ATPase activity by hMSH2-hMSH3

1 reference

https://pubmed.ncbi.nlm.nih.gov/21837758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/MC.20838

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

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