The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61
about
The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repairRole of vascular endothelial growth factor in neuronal DNA damage and repair in rat brain following a transient cerebral ischemia.Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells.Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein.Cockayne syndrome group B cellular and biochemical functions.Molecular cloning and gene expression analysis of Ercc6l in Sika deer (Cervus nippon hortulorum).Early host cell reactivation of an oxidatively damaged adenovirus-encoded reporter gene requires the Cockayne syndrome proteins CSA and CSB.Persistent DNA damage inhibits S-phase and G2 progression, and results in apoptosisHuman Cockayne syndrome B protein reciprocally communicates with mitochondrial proteins and promotes transcriptional elongation.A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer.Nucleic acid binding activity of human Cockayne syndrome B protein and identification of Ca(2+) as a novel metal cofactorRNA polymerase between lesion bypass and DNA repair.Chromatin regulation of DNA damage repair and genome integrity in the central nervous system.Camptothecin (CPT) and its derivatives are known to target topoisomerase I (Top1) as their mechanism of action: did we miss something in CPT analogue molecular targets for treating human disease such as cancer?Genetic instability associated with loop or stem-loop structures within transcription units can be independent of nucleotide excision repair.ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelinationThe Cockayne syndrome protein B is involved in the repair of 5-AZA-2'-deoxycytidine-induced DNA lesions
P2860
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P2860
The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61
description
1996 nî lūn-bûn
@nan
1996 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@ast
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@en
The human CSB
@nl
type
label
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@ast
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@en
The human CSB
@nl
prefLabel
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@ast
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@en
The human CSB
@nl
P2093
P2860
P356
P1476
The human CSB (ERCC6) gene cor ...... ct in the CHO cell mutant UV61
@en
P2093
P2860
P304
P356
10.1093/NAR/24.17.3317
P407
P577
1996-09-01T00:00:00Z