(Q51528432)

6 April 2018

title

Influence of eight unclassified missense variants of the MLH1 gene on Lynch syndrome susceptibility. (English)

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6 April 2018

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Yimei Fan

1

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6 April 2018

Jinyun Chen

2

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6 April 2018

Wei Wang

3

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6 April 2018

Puyuan Wu

4

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6 April 2018

Wenxian Zhi

5

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6 April 2018

Binshuang Xue

6

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6 April 2018

Wanfen Zhang

7

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6 April 2018

Yaping Wang

8

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6 April 2018

publication date

28 September 2011

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6 April 2018

published in

Biochemical Genetics

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6 April 2018

volume

50

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6 April 2018

page(s)

84-93

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6 April 2018

issue

1-2

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6 April 2018

https://scigraph.springernature.com/pub.10.1007/s10528-011-9467-z

exact match

0 references

cites work

Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional features.

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

SIFT: Predicting amino acid changes that affect protein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Germline mutations and polymorphic variants in MMR, E-cadherin and MYH genes associated with familial gastric cancer in Jiangsu of China.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

Interpretation of Genetic Test Results for Hereditary Nonpolyposis Colorectal Cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10528-011-9467-Z

10.1007/S10528-011-9467-Z

21 January 2018

Identifiers

DOI

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6 April 2018

PubMed ID

21952876

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6 April 2018