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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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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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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.3784-3794

2019

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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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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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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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Nucleotide Excision Repair by Mutant Xeroderma Pigmentosum Group A (XPA) Proteins with Deficiency in Interaction with RPA

The Journal of biological chemistry, 2011-02, Vol.286 (7), p.5476-5483

2011

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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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Three novel mutations responsible for Cockayne syndrome group A

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

2003

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DNA Damage Recognition by XPA Protein Promotes Efficient Recruitment of Transcription Factor II H

The Journal of biological chemistry, 1997-09, Vol.272 (37), p.22991-22994

1997

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Analysis of the conserved NER helicases (XPB and XPD) and UV-induced DNA damage in Hydra

Biochimica et biophysica acta. General subjects, 2018-09, Vol.1862 (9), p.2031-2042

2018

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DNA Repair Protein XPA Binds Replication Protein A (RPA)

The Journal of biological chemistry, 1995-02, Vol.270 (8), p.4152-4157

1995

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Generation of splice switching oligonucleotides targeting the Cockayne syndrome group B gene product in order to change the diseased cell state

Biochemical and biophysical research communications, 2018-06, Vol.500 (2), p.163-169

2018

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Resonance Assignments, Solution Structure, and Backbone Dynamics of the DNA- and RPA-Binding Domain of Human Repair Factor XPA

Journal of biochemistry (Tokyo), 1999-03, Vol.125 (3), p.495-506

1999

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DDB2, the xeroderma pigmentosum group E gene product, is directly ubiquitylated by Cullin 4A-based ubiquitin ligase complex

DNA repair, 2005-05, Vol.4 (5), p.537-545

2005

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Inhibition of nucleotide excision repair by anti-XPA monoclonal antibodies which interfere with binding to RPA, ERCC1, and TFIIH

Biochemical and biophysical research communications, 2004-09, Vol.321 (4), p.815-822

2004

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Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex: Mutant CSB inhibits repair of Top1-cc

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

2011

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High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene

Nature (London), 1995-09, Vol.377 (6545), p.165-168

1995

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Mutations in theXPD gene leading to xeroderma pigmentosum symptoms

Human mutation, 1997, Vol.9 (4), p.322-331

1997

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Sequential binding of DNA repair proteins RPA and ERCC1 to XPA in vitro

Nucleic acids research, 1996-12, Vol.24 (23), p.4719-4724

1996

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

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

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

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

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

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

Nucleotide Excision Repair by Mutant Xeroderma Pigmentosum Group A (XPA) Proteins with Deficiency in Interaction with RPA

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

Three novel mutations responsible for Cockayne syndrome group A

DNA Damage Recognition by XPA Protein Promotes Efficient Recruitment of Transcription Factor II H

Analysis of the conserved NER helicases (XPB and XPD) and UV-induced DNA damage in Hydra

DNA Repair Protein XPA Binds Replication Protein A (RPA)

Generation of splice switching oligonucleotides targeting the Cockayne syndrome group B gene product in order to change the diseased cell state

Resonance Assignments, Solution Structure, and Backbone Dynamics of the DNA- and RPA-Binding Domain of Human Repair Factor XPA

DDB2, the xeroderma pigmentosum group E gene product, is directly ubiquitylated by Cullin 4A-based ubiquitin ligase complex

Inhibition of nucleotide excision repair by anti-XPA monoclonal antibodies which interfere with binding to RPA, ERCC1, and TFIIH

Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex: Mutant CSB inhibits repair of Top1-cc

High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene

Mutations in theXPD gene leading to xeroderma pigmentosum symptoms

Sequential binding of DNA repair proteins RPA and ERCC1 to XPA in vitro

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