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Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome

Author

Isao Kuraoka

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

Date of publication: 2004-10-14

Language: ภาษาอังกฤษ

Main subject: Cockayne syndrome, UV-sensitive syndrome

Bibliographic databases:

Cites articles 26

Date

Title

Authors

1981-09-01

A new human photosensitive subject with a defect in the recovery of DNA synthesis after ultraviolet-light irradiation,A New Human Photosensitive Subject with a Defect in the Recovery of DNA Synthesis after Ultraviolet-light Irradiation
1982-04-01

Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum
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.
1992-04

Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21
1992-12-11

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

,
1992-01-01

Cockayne syndrome: review of 140 cases,Cockayne syndrome: Review of 140 cases
1993-11-01

Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome
1994-05-01

A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations
1995-06-01

UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I
1996-07-01

Xeroderma pigmentosum--Cockayne syndrome complex: a further case
1997-10-01

The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex
1997-07-01

Cockayne syndrome: defective repair of transcription?
1997-04-01

Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells
1997-06-01

Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24
1998-01

Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome
1999-06-01

The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta
1999-03-01

Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells
2000-04-01

Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome
2001-10-01

The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA
2002-12-01

Subpathways of nucleotide excision repair and their regulation
2002-10-01

CSB is a component of RNA pol I transcription

,
2002-06-01

Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases
2002-05-17

Premature aging in mice deficient in DNA repair and transcription
2002-08-01

Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers

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2002-06-11

The cockayne syndrome group B gene product is involved in cellular repair of 8-hydroxyadenine in DNA.
2003-01-01

Cell type-specific hypersensitivity to oxidative damage in CSB and XPA mice

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