(Q83394008)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21309037%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Characterization of MSH2 variants by endogenous gene modification in mouse embryonic stem cells (English)

1 reference

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22 January 2020

author name string

Eva A L Wielders

1

1 reference

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22 January 2020

Rob J Dekker

2

1 reference

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22 January 2020

Ian Holt

3

1 reference

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22 January 2020

Glenn E Morris

4

1 reference

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22 January 2020

Hein te Riele

5

1 reference

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22 January 2020

publication date

8 March 2011

1 reference

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22 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21309037%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

volume

32

1 reference

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22 January 2020

issue

4

1 reference

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22 January 2020

page(s)

389-396

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21309037%20AND%20SRC:MED&resulttype=core&format=json

Generation of a mouse mutant by oligonucleotide-mediated gene modification in ES cells.

22 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Identification of germline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Met688Ile and Leu390Phe of the MSH2 gene are not functional mutations, but polymorphisms in Japanese individuals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Microsatellite instability analysis in hereditary non-polyposis colon cancer using the Bethesda consensus panel of microsatellite markers in the absence of proband normal tissue

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Methylation tolerance in mismatch repair proficient cells with low MSH2 protein level

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

MSH2 missense mutations alter cisplatin cytotoxicity and promote cisplatin-induced genome instability

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Mutator phenotypes of common polymorphisms and missense mutations in MSH2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

MSH2 sequence variations and inherited colorectal cancer susceptibility

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Functional characterization of pathogenic human MSH2 missense mutations in Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

AfterhMSH2 andhMLH1?what next? Analysis of three-generational, population-based, early-onset colorectal cancer families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

The multifaceted mismatch-repair system

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

In silico and in vivo splicing analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

The use of microsatellite instability, immunohistochemistry and other variables in determining the clinical significance of MLH1 and MSH2 unclassified variants in Lynch syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Functional analysis of HNPCC-related missense mutations in MSH2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Evidence for sequential action of two ATPase active sites in yeast Msh2-Msh6.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Production of homozygous mutant ES cells with a single targeting construct

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Enhanced detection of deleterious and other germline mutations of hMSH2 and hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Functional genetic tests of DNA mismatch repair protein activity in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Highly efficient gene targeting in embryonic stem cells through homologous recombination with isogenic DNA constructs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Consecutive inactivation of both alleles of the pim-1 proto-oncogene by homologous recombination in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21448

7 January 2021

Identifiers

DOI

10.1002/HUMU.21448

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21309037%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference