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Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodeling

Published in: Proceedings of the National Academy of Sciences of the United States of America

Date of publication: 2006-06-20

Language: ਅੰਗਰੇਜ਼ੀ

Main subject: Cockayne syndrome

Bibliographic databases:

Cites articles 60

Date

Title

Authors

1990-06-01

The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.
1992-12-11

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

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1992-01-01

Cockayne syndrome: review of 140 cases,Cockayne syndrome: Review of 140 cases
1995-06

p53 modulation of TFIIH-associated nucleotide excision repair activity,p53 modulation of TFIIH–associated nucleotide excision repair activity

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1996-10-15

UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells
1997-12

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes
1997-10-14

Cockayne syndrome group B protein enhances elongation by RNA polymerase II
1997-01-17

Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II
1998-05-01

Biochemical and biological characterization of wild-type and ATPase-deficient Cockayne syndrome B repair protein

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1998-11-01

Both Rb/p16INK4a inactivation and telomerase activity are required to immortalize human epithelial cells

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1999

A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy
1999

A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy
2000-05

Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes
2000-05-01

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium

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2000-11-01

Cockayne syndrome and xeroderma pigmentosum
2000-11-01

Activation of the p21WAF1/CIP1 promoter independent of p53 by the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) through the Sp1 sites
2000-10-01

ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor

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2000-06-01

Interference of transcriptional activation by the antineoplastic drug ecteinascidin-743

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2000-03-01

Whole-genome expression analysis of snf/swi mutants of Saccharomyces cerevisiae
2001-05

The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux
2001-04

Enhanceosomes
2001-12-01

Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II
2001-08-01

Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair
2001-05-01

A weak signal for strong responses: interferon-alpha/beta revisited
2001-02-01

Role of T antigen interactions with p53 in tumorigenesis
2002-06-28

Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. implications for Cockayne syndrome
2002-05-03

TFIIH plays an essential role in RNA polymerase I transcription

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2002-01-01

Translocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repair
2002-10-01

CSB is a component of RNA pol I transcription

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2002-06-01

Ecteinascidin-743 inhibits activated but not constitutive transcription
2002-03-04

Transcriptional regulation of cyclooxygenase-1 by histone deacetylase inhibitors in normal human astrocyte cells
2002-02-01

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

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