(Q28505404)

24 January 2017

title

Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice (English)

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24 January 2017

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GOA release 2020-03-11

K. Manley

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24 January 2017

T. L. Shirley

series ordinal

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24 January 2017

L. Flaherty

series ordinal

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24 January 2017

A. Messer

series ordinal

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24 January 2017

language of work or name

English

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publication date

1 December 1999

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24 January 2017

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24 January 2017

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24 January 2017

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24 January 2017

page(s)

471–473

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

24 January 2017

cites work

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7 January 2021

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

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7 January 2021

Rethinking genotype and phenotype correlations in polyglutamine expansion disorders

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7 January 2021

Inactivation of the mouse Huntington's disease gene homolog Hdh

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7 January 2021

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

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7 January 2021

Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset

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7 January 2021

Somatic expansion of the (CAG)n repeat in Huntington disease brains

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7 January 2021

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

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7 January 2021

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

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7 January 2021

Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse

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7 January 2021

Glutamine repeats and neurodegenerative diseases: molecular aspects

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7 January 2021

Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agent.

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7 January 2021

Tumors of DNA mismatch repair-deficient hosts exhibit dramatic increases in genomic instability

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7 January 2021

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

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7 January 2021

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

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7 January 2021

Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum

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7 January 2021

Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene

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7 January 2021

Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriers

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7 January 2021

Instability of the CAG repeat in immortalized fibroblast cell cultures from Huntington's disease transgenic mice

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7 January 2021

hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6

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7 January 2021

Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases

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7 January 2021

Role of Saccharomyces cerevisiae Msh2 and Msh3 repair proteins in double-strand break-induced recombination

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7 January 2021

A polymorphic trinucleotide repeat sequence mapping to distal mouse chromosome 4

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7 January 2021

Cloning of novel trinucleotide-repeat (CAG) containing genes in mouse brain

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7 January 2021

Identifiers

DOI

10.1038/70598

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Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1028338403

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Fatcat ID

release_x3bjrcalevfnzfs3uogui4lrcy

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Fatcat

https://api.fatcat.wiki/v0/release/x3bjrcalevfnzfs3uogui4lrcy

24 November 2022

mapped directly with Wikidata item

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017