Structure, function and regulation of CSB: a multi-talented gymnast
about
Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiencyTranscriptional and Posttranslational Regulation of Nucleotide Excision Repair: The Guardian of the Genome against Ultraviolet RadiationA novel ERCC6 splicing variant associated with a mild Cockayne syndrome phenotypeNAP1L1 accelerates activation and decreases pausing to enhance nucleosome remodeling by CSBCSB interacts with SNM1A and promotes DNA interstrand crosslink processingElements That Regulate the DNA Damage Response of Proteins Defective in Cockayne SyndromeRegulation of the Rhp26ERCC6/CSB chromatin remodeler by a novel conserved leucine latch motifThe sequence-specific transcription factor c-Jun targets Cockayne syndrome protein B to regulate transcription and chromatin structure.Body mass index is associated with gene methylation in estrogen receptor-positive breast tumors.The transcription-coupled repair protein ERCC6/CSB also protects against repeat expansion in a mouse model of the fragile X premutation.The Repeat Expansion Diseases: The dark side of DNA repair.The Cellular Response to Oxidatively Induced DNA Damage and Polymorphism of Some DNA Repair Genes Associated with Clinicopathological Features of Bladder Cancer.The CSB chromatin remodeler and CTCF architectural protein cooperate in response to oxidative stress.DNA excision repair at telomeres.The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair.Mfd as a central partner of transcription coupled repair.The role of Cockayne Syndrome Protein B in transcription regulationOverexpression of parkin rescues the defective mitochondrial phenotype and the increased apoptosis of Cockayne Syndrome A cells.Chromatin Architectural Changes during Cellular Senescence and Aging.ROS-induced R loops trigger a transcription-coupled but BRCA1/2-independent homologous recombination pathway through CSBNovel frame shift mutation in ERCC6 leads to a severe form of Cockayne syndrome with postnatal growth failure and early death: A case report and brief literature reviewPolymorphism of DNA repair genes OGG1, XRCC1, XPD and ERCC6 in bladder cancer in BelarusFirst molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene
P2860
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P2860
Structure, function and regulation of CSB: a multi-talented gymnast
description
2013 nî lūn-bûn
@nan
2013 թուականին հրատարակուած գիտական յօդուած
@hyw
2013 թվականին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Structure, function and regulation of CSB: a multi-talented gymnast
@ast
Structure, function and regulation of CSB: a multi-talented gymnast
@en
Structure, function and regulation of CSB: a multi-talented gymnast
@nl
type
label
Structure, function and regulation of CSB: a multi-talented gymnast
@ast
Structure, function and regulation of CSB: a multi-talented gymnast
@en
Structure, function and regulation of CSB: a multi-talented gymnast
@nl
prefLabel
Structure, function and regulation of CSB: a multi-talented gymnast
@ast
Structure, function and regulation of CSB: a multi-talented gymnast
@en
Structure, function and regulation of CSB: a multi-talented gymnast
@nl
P2860
P1476
Structure, function and regulation of CSB: a multi-talented gymnast
@en
P2093
Hua-Ying Fan
Robert J. Lake
P2860
P304
P356
10.1016/J.MAD.2013.02.004
P407
P577
2013-01-01T00:00:00Z