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Distinct Roles for the XPB/p52 and XPD/p44 Subcomplexes of TFIIH in Damaged DNA Opening during Nucleotide Excision Repair

Molecular cell, 2007-04, Vol.26 (2), p.245-256

2007

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The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process

The EMBO journal, 2011-02, Vol.30 (3), p.468-479

2011

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XPG and XPF Endonucleases Trigger Chromatin Looping and DNA Demethylation for Accurate Expression of Activated Genes

Molecular cell, 2012-08, Vol.47 (4), p.622-632

2012

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Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome

Scientific reports, 2020-01, Vol.10 (1), p.1105-1105, Article 1105

2020

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Molecular insights into the recruitment of TFIIH to sites of DNA damage

The EMBO journal, 2009-10, Vol.28 (19), p.2971-2980

2009

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New functions of XPC in the protection of human skin cells from oxidative damage

The EMBO journal, 2006-09, Vol.25 (18), p.4305-4315

2006

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Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

The EMBO journal, 2006-05, Vol.25 (9), p.1915-1923

2006

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CSB protein is (a direct target of HIF-1 and) a critical mediator of the hypoxic response

The EMBO journal, 2008-10, Vol.27 (19), p.2545-2556

2008

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TFIIH Transcription Factor, a Target for the Rift Valley Hemorrhagic Fever Virus

Cell, 2004-02, Vol.116 (4), p.541-550

2004

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XPG Stabilizes TFIIH, Allowing Transactivation of Nuclear Receptors: Implications for Cockayne Syndrome in XP-G/CS Patients

Molecular cell, 2007-04, Vol.26 (2), p.231-243

2007

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The human DNA repair factor XPC-HR23B distinguishes stereoisomeric benzo[a]pyrenyl-DNA lesions

The EMBO journal, 2007-06, Vol.26 (12), p.2923-2932

2007

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Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH

Nature neuroscience, 2007-11, Vol.10 (11), p.1414-1422

2007

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A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A

Nature genetics, 2004-07, Vol.36 (7), p.714-719

2004

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Dysregulation of the Peroxisome Proliferator-Activated Receptor Target Genes by XPD Mutations

Molecular and Cellular Biology, 2005-07, Vol.25 (14), p.6065-6076

2005

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MED23 Mutation Links Intellectual Disability to Dysregulation of Immediate Early Gene Expression

Science (American Association for the Advancement of Science), 2011-08, Vol.333 (6046), p.1161-1163

2011

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DNA Repair and Transcriptional Deficiencies Caused by Mutations in the Drosophila p52 Subunit of TFIIH Generate Developmental Defects and Chromosome Fragility

Molecular and Cellular Biology, 2007-05, Vol.27 (10), p.3640-3650

2007

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TFIIH Enzymatic Activities in Transcription and Nucleotide Excision Repair

Methods in Enzymology, 2006, Vol.408, p.246-263

2006

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When transcription and repair meet: a complex system

Trends in genetics, 2006-08, Vol.22 (8), p.430-436

2006

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Sequential recruitment of the repair factors during NER: the role of XPG in initiating the resynthesis step

The EMBO journal, 2008-01, Vol.27 (1), p.155-167

2008

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A Ubiquitin-Binding Domain in Cockayne Syndrome B Required for Transcription-Coupled Nucleotide Excision Repair

Molecular cell, 2010-06, Vol.38 (5), p.637-648

2010

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Structural basis for group A trichothiodystrophy

Nature structural & molecular biology, 2008-09, Vol.15 (9), p.980-984

2008

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Phosphorylation of XPD drives its mitotic role independently of its DNA repair and transcription functions

Science advances, 2022-08, Vol.8 (33), p.eabp9457-eabp9457

2022

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p8/TTD-A as a Repair-Specific TFIIH Subunit

Molecular cell, 2006-01, Vol.21 (2), p.215-226

2006

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A Role for the TFIIH XPB DNA Helicase in Promoter Escape by RNA Polymerase II

The Journal of biological chemistry, 1999-08, Vol.274 (32), p.22127-22130

1999

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SUG1, a Putative Transcriptional Mediator and Subunit of the PA700 Proteasome Regulatory Complex, Is a DNA Helicase

The Journal of biological chemistry, 1997-03, Vol.272 (11), p.7122-7126

1997

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Distinct Roles for the XPB/p52 and XPD/p44 Subcomplexes of TFIIH in Damaged DNA Opening during Nucleotide Excision Repair

The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process

XPG and XPF Endonucleases Trigger Chromatin Looping and DNA Demethylation for Accurate Expression of Activated Genes

Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome

Molecular insights into the recruitment of TFIIH to sites of DNA damage

New functions of XPC in the protection of human skin cells from oxidative damage

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

CSB protein is (a direct target of HIF-1 and) a critical mediator of the hypoxic response

TFIIH Transcription Factor, a Target for the Rift Valley Hemorrhagic Fever Virus

XPG Stabilizes TFIIH, Allowing Transactivation of Nuclear Receptors: Implications for Cockayne Syndrome in XP-G/CS Patients

The human DNA repair factor XPC-HR23B distinguishes stereoisomeric benzo[a]pyrenyl-DNA lesions

Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH

A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A

Dysregulation of the Peroxisome Proliferator-Activated Receptor Target Genes by XPD Mutations

MED23 Mutation Links Intellectual Disability to Dysregulation of Immediate Early Gene Expression

DNA Repair and Transcriptional Deficiencies Caused by Mutations in the Drosophila p52 Subunit of TFIIH Generate Developmental Defects and Chromosome Fragility

TFIIH Enzymatic Activities in Transcription and Nucleotide Excision Repair

When transcription and repair meet: a complex system

Sequential recruitment of the repair factors during NER: the role of XPG in initiating the resynthesis step

A Ubiquitin-Binding Domain in Cockayne Syndrome B Required for Transcription-Coupled Nucleotide Excision Repair

Structural basis for group A trichothiodystrophy

Phosphorylation of XPD drives its mitotic role independently of its DNA repair and transcription functions

p8/TTD-A as a Repair-Specific TFIIH Subunit

A Role for the TFIIH XPB DNA Helicase in Promoter Escape by RNA Polymerase II

SUG1, a Putative Transcriptional Mediator and Subunit of the PA700 Proteasome Regulatory Complex, Is a DNA Helicase

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