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The role of Cockayne syndrome group A (CSA) protein in transcription-coupled nucleotide excision repair

Mechanisms of ageing and development, 2013-05, Vol.134 (5-6), p.196-201

Saijo, Masafumi

2013

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The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair

The Journal of biological chemistry, 2016-01, Vol.291 (3), p.1387-1397

2016

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Inhibition of UVSSA ubiquitination suppresses transcription‐coupled nucleotide excision repair deficiency caused by dissociation from USP7

The FEBS journal, 2018-03, Vol.285 (5), p.965-976

2018

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Structural basis of ubiquitin recognition by the winged-helix domain of Cockayne syndrome group B protein

Nucleic acids research, 2019-04, Vol.47 (7), p.3784

2019

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Xeroderma pigmentosum A homolog from Hydra partially complements DNA repair defect in human XPA-deficient cells

Journal of biosciences, 2021-06, Vol.46 (2), Article 48

2021

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UV-Induced Ubiquitylation of XPC Protein Mediated by UV-DDB-Ubiquitin Ligase Complex

Cell, 2005-05, Vol.121 (3), p.387-400

2005

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DDB2 Complex-Mediated Ubiquitylation around DNA Damage Is Oppositely Regulated by XPC and Ku and Contributes to the Recruitment of XPA

Molecular and Cellular Biology, 2010-06, Vol.30 (11), p.2708-2723

2010

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Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome

Molecular and cellular biology, 2015-09, Vol.35 (18), p.3178-3188

2015

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Camptothecin compromises transcription recovery and cell survival against cisplatin and ultraviolet irradiation regardless of transcription-coupled nucleotide excision repair

DNA repair, 2022-05, Vol.113, p.103318-103318, Article 103318

2022

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The Ubiquitin Ligase Activity in the DDB2 and CSA Complexes Is Differentially Regulated by the COP9 Signalosome in Response to DNA Damage

Cell, 2003-05, Vol.113 (3), p.357-367

2003

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BRCA1 contributes to transcription‐coupled repair of DNA damage through polyubiquitination and degradation of Cockayne syndrome B protein

Cancer science, 2011-10, Vol.102 (10), p.1840-1847

2011

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DGCR8 Mediates Repair of UV-Induced DNA Damage Independently of RNA Processing

Cell reports (Cambridge), 2017-04, Vol.19 (1), p.162-174

2017

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Isolation of XAB2 Complex Involved in Pre-mRNA Splicing, Transcription, and Transcription-coupled Repair

The Journal of biological chemistry, 2008-01, Vol.283 (2), p.940-950

2008

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Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS

Journal of human genetics, 2015-05, Vol.60 (5), p.259-265

2015

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Xeroderma pigmentosum group F protein binds to Eg5 and is required for proper mitosis: implications for XP‐F and XFE

Genes to cells : devoted to molecular & cellular mechanisms, 2012-03, Vol.17 (3), p.173-185

2012

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Functional TFIIH Is Required for UV-Induced Translocation of CSA to the Nuclear Matrix

Molecular and Cellular Biology, 2007-04, Vol.27 (7), p.2538-2547

2007

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Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I‐DNA covalent complex

Genes to cells : devoted to molecular & cellular mechanisms, 2011-01, Vol.16 (1), p.101-114

2011

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Translocation of Cockayne Syndrome Group A Protein to the Nuclear Matrix: Possible Relevance to Transcription-Coupled DNA Repair

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (1), p.201-206

2002

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A Japanese trichothiodystrophy patient with XPD mutations

Journal of human genetics, 2011-01, Vol.56 (1), p.77-79

2011

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Stabilization of Ultraviolet (UV)-stimulated Scaffold Protein A by Interaction with Ubiquitin-specific Peptidase 7 Is Essential for Transcription-coupled Nucleotide Excision Repair

The Journal of biological chemistry, 2016-06, Vol.291 (26), p.13771-13779

2016

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Inhibition of UVSSA ubiquitination suppresses transcription‐coupled nucleotide excision repair deficiency caused by dissociation from USP 7

The FEBS journal, 2018-03, Vol.285 (5), p.965-976

2018

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XAB2, a Novel Tetratricopeptide Repeat Protein Involved in Transcription-coupled DNA Repair and Transcription

The Journal of biological chemistry, 2000-11, Vol.275 (45), p.34931-34937

2000

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Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA

Nature structural & molecular biology, 1998-08, Vol.5 (8), p.701-706

1998

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Three novel mutations responsible for Cockayne syndrome group A

Genes & Genetic Systems, 2003, Vol.78(1), pp.93-102

2003

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Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair

Nature genetics, 2012-05, Vol.44 (5), p.593-597

2012

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The role of Cockayne syndrome group A (CSA) protein in transcription-coupled nucleotide excision repair

The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair

Inhibition of UVSSA ubiquitination suppresses transcription‐coupled nucleotide excision repair deficiency caused by dissociation from USP7

Structural basis of ubiquitin recognition by the winged-helix domain of Cockayne syndrome group B protein

Xeroderma pigmentosum A homolog from Hydra partially complements DNA repair defect in human XPA-deficient cells

UV-Induced Ubiquitylation of XPC Protein Mediated by UV-DDB-Ubiquitin Ligase Complex

DDB2 Complex-Mediated Ubiquitylation around DNA Damage Is Oppositely Regulated by XPC and Ku and Contributes to the Recruitment of XPA

Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome

Camptothecin compromises transcription recovery and cell survival against cisplatin and ultraviolet irradiation regardless of transcription-coupled nucleotide excision repair

The Ubiquitin Ligase Activity in the DDB2 and CSA Complexes Is Differentially Regulated by the COP9 Signalosome in Response to DNA Damage

BRCA1 contributes to transcription‐coupled repair of DNA damage through polyubiquitination and degradation of Cockayne syndrome B protein

DGCR8 Mediates Repair of UV-Induced DNA Damage Independently of RNA Processing

Isolation of XAB2 Complex Involved in Pre-mRNA Splicing, Transcription, and Transcription-coupled Repair

Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS

Xeroderma pigmentosum group F protein binds to Eg5 and is required for proper mitosis: implications for XP‐F and XFE

Functional TFIIH Is Required for UV-Induced Translocation of CSA to the Nuclear Matrix

Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I‐DNA covalent complex

Translocation of Cockayne Syndrome Group A Protein to the Nuclear Matrix: Possible Relevance to Transcription-Coupled DNA Repair

A Japanese trichothiodystrophy patient with XPD mutations

Stabilization of Ultraviolet (UV)-stimulated Scaffold Protein A by Interaction with Ubiquitin-specific Peptidase 7 Is Essential for Transcription-coupled Nucleotide Excision Repair

Inhibition of UVSSA ubiquitination suppresses transcription‐coupled nucleotide excision repair deficiency caused by dissociation from USP 7

XAB2, a Novel Tetratricopeptide Repeat Protein Involved in Transcription-coupled DNA Repair and Transcription

Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA

Three novel mutations responsible for Cockayne syndrome group A

Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair

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