MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice
about
EMAST is a Form of Microsatellite Instability That is Initiated by Inflammation and Modulates Colorectal Cancer ProgressionRepeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disordersA MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?Ups and Downs: Mechanisms of Repeat Instability in the Fragile X-Related DisordersModulation of trinucleotide repeat instability by DNA polymerase β polymorphic variant R137Q.Gender and cell-type-specific effects of the transcription-coupled repair protein, ERCC6/CSB, on repeat expansion in a mouse model of the fragile X-related disordersA selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington's disease miceRNA-protein interactions in unstable microsatellite diseases.Natural genetic variation determines susceptibility to aggregation or toxicity in a C. elegans model for polyglutamine disease.Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approachesModifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes.Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.Parental age effects, but no evidence for an intrauterine effect in the transmission of myotonic dystrophy type 1.Repeat instability during DNA repair: Insights from model systemsMSH3 Promotes Dynamic Behavior of Trinucleotide Repeat Tracts In Vivo.The Repeat Expansion Diseases: The dark side of DNA repair.DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesCrosstalk between MSH2-MSH3 and polβ promotes trinucleotide repeat expansion during base excision repair.Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort studyThe mismatch repair protein MSH2 is rate limiting for repeat expansion in a fragile X premutation mouse model.Close encounters: Moving along bumps, breaks, and bubbles on expanded trinucleotide tracts.MutSβ abundance and Msh3 ATP hydrolysis activity are important drivers of CTG•CAG repeat expansions.LncRNA lnc-RI regulates homologous recombination repair of DNA double-strand breaks by stabilizing RAD51 mRNA as a competitive endogenous RNA.Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders.Genetic instability associated with loop or stem-loop structures within transcription units can be independent of nucleotide excision repair.Huntington diseaseRegulatory mechanisms of incomplete huntingtin mRNA splicing
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P2860
MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice
description
2013 nî lūn-bûn
@nan
2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年学术文章
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2013年学术文章
@zh-cn
2013年学术文章
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2013年学术文章
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2013年学术文章
@zh-sg
2013年學術文章
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name
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@ast
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@en
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@nl
type
label
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@ast
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@en
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@nl
prefLabel
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@ast
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@en
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@nl
P2093
P2860
P1433
P1476
MSH3 polymorphisms and protein ...... y in Huntington's disease mice
@en
P2093
Anne Messer
Christopher E Pearson
Greg W Clark
Jodie P Simard
Kevin Manley
Meera Swami
Meghan M Slean
Peggy F Shelbourne
Stéphanie Tomé
P2860
P304
P356
10.1371/JOURNAL.PGEN.1003280
P577
2013-02-28T00:00:00Z