Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
about
The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repairXAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcriptionA novel cytoplasmic GTPase XAB1 interacts with DNA repair protein XPATranslocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repairCockayne syndrome protein B interacts with and is phosphorylated by c-Abl tyrosine kinaseCockayne syndrome: defective repair of transcription?Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndromeRecruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexesDifferential role of basal keratinocytes in UV-induced immunosuppression and skin cancerA common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG functionFunctional TFIIH is required for UV-induced translocation of CSA to the nuclear matrixRequirement of ELC1 for RNA polymerase II polyubiquitylation and degradation in response to DNA damage in Saccharomyces cerevisiaeEvidence that the transcription elongation function of Rpb9 is involved in transcription-coupled DNA repair in Saccharomyces cerevisiae.The C-terminal repeat domain of Spt5 plays an important role in suppression of Rad26-independent transcription coupled repair.Rad26p regulates the occupancy of histone H2A-H2B dimer at the active genes in vivoTranscription factor TFIIH and DNA endonuclease Rad2 constitute yeast nucleotide excision repair factor 3: implications for nucleotide excision repair and Cockayne syndrome.RAD26, the yeast homolog of human Cockayne's syndrome group B gene, encodes a DNA-dependent ATPase.RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.Modulation of Rad26- and Rpb9-mediated DNA repair by different promoter elements.RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62The defect in transcription-coupled repair displayed by a Saccharomyces cerevisiae rad26 mutant is dependent on carbon source and is not associated with a lack of transcriptionDifferent effects of CSA and CSB deficiency on sensitivity to oxidative DNA damageRetinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndromeDifferential role of transcription-coupled repair in UVB-induced G2 arrest and apoptosis in mouse epidermisPersistently stalled replication forks inhibit nucleotide excision repair in trans by sequestering Replication protein A.DNA damage stabilizes interaction of CSB with the transcription elongation machinery.Recruitment of DNA damage checkpoint proteins to damage in transcribed and nontranscribed sequences.Initiation of DNA repair mediated by a stalled RNA polymerase IIO.Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase IIDifferential 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.Decreased transcription-coupled nucleotide excision repair capacity is associated with increased p53- and MLH1-independent apoptosis in response to cisplatin.Transcription-coupled DNA repair in yeast transcription factor IIE (TFIIE) mutants.Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein.The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complexDeletion of the CSB homolog, RAD26, yields Spt(-) strains with proficient transcription-coupled repair.Terminally differentiated human neurons repair transcribed genes but display attenuated global DNA repair and modulation of repair gene expression.Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage.Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.USF-1 is critical for maintaining genome integrity in response to UV-induced DNA photolesions.On the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutations
P2860
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P2860
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
description
1993 nî lūn-bûn
@nan
1993 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@ast
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@en
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@nl
type
label
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@ast
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@en
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@nl
prefLabel
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@ast
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@en
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@nl
P2093
P2860
P356
P1476
Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
@en
P2093
A A van Zeeland
A T Natarajan
A van Hoffen
L H Mullenders
P2860
P304
P356
10.1093/NAR/21.25.5890
P407
P577
1993-12-01T00:00:00Z