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Human Flap Endonuclease Structures, DNA Double-Base Flipping, and a Unified Understanding of the FEN1 Superfamily

Cell, 2011-04, Vol.145 (2), p.198-211

2011

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A versatile viral system for expression and depletion of proteins in mammalian cells

PloS one, 2009-08, Vol.4 (8), p.e6529-e6529

2009

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Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency

PLoS genetics, 2014-10, Vol.10 (10), p.e1004686-e1004686

2014

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Non-catalytic Roles for XPG with BRCA1 and BRCA2 in Homologous Recombination and Genome Stability

Molecular cell, 2016-02, Vol.61 (4), p.535-546

2016

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Repair complexes of FEN1 endonuclease, DNA, and Rad9-Hus1-Rad1 are distinguished from their PCNA counterparts by functionally important stability

Proceedings of the National Academy of Sciences - PNAS, 2012-05, Vol.109 (22), p.8528-8533

2012

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Recognition of RNA Polymerase II and Transcription Bubbles by XPG, CSB, and TFIIH: Insights for Transcription-Coupled Repair and Cockayne Syndrome

Molecular cell, 2005-10, Vol.20 (2), p.187-198

2005

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Conserved XPB Core Structure and Motifs for DNA Unwinding: Implications for Pathway Selection of Transcription or Excision Repair

Molecular cell, 2006-04, Vol.22 (1), p.27-37

2006

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DNA repair: dynamic defenders against cancer and aging

PLoS biology, 2006-06, Vol.4 (6), p.e203-e203

2006

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DNA glycosylase NEIL2 functions in multiple cellular processes

Progress in biophysics and molecular biology, 2021-09, Vol.164, p.72-80

2021

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The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome

Cell cycle (Georgetown, Tex.), 2011-06, Vol.10 (12), p.1998-2007

2011

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Human XPG nuclease structure, assembly, and activities with insights for neurodegeneration and cancer from pathogenic mutations

Proceedings of the National Academy of Sciences - PNAS, 2020-06, Vol.117 (25), p.14127-14138

2020

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XPD Helicase Structures and Activities: Insights into the Cancer and Aging Phenotypes from XPD Mutations

Cell, 2008-05, Vol.133 (5), p.789-800

2008

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The Single-Strand DNA Binding Activity of Human PC4 Prevents Mutagenesis and Killing by Oxidative DNA Damage

Molecular and Cellular Biology, 2004-07, Vol.24 (13), p.6084-6093

2004

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Dose-Dependent Misrejoining of Radiation-Induced DNA Double-Strand Breaks in Human Fibroblasts: Experimental and Theoretical Study for High- and Low-LET Radiation

Radiation research, 2005-05, Vol.163 (5), p.526-534

2005

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Thirdhand smoke exposure causes replication stress and impaired transcription in human lung cells

Environmental and molecular mutagenesis, 2020-07, Vol.61 (6), p.635-646

2020

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Repair of X-Ray-Induced DNA Double-Strand Breaks in Specific Not I Restriction Fragments in Human Fibroblasts: Joining of Correct and Incorrect Ends

Proceedings of the National Academy of Sciences - PNAS, 1995-12, Vol.92 (26), p.12050-12054

1995

Volltextzugriff (PDF)

A Common Mutational Pattern in Cockayne Syndrome Patients from Xeroderma Pigmentosum Group G: Implications for a Second XPG Function

Proceedings of the National Academy of Sciences - PNAS, 1997-04, Vol.94 (7), p.3116-3121

1997

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WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing

Nature structural & molecular biology, 2006-05, Vol.13 (5), p.414-422

2006

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Structural analysis of flexible proteins in solution by small angle X-ray scattering combined with crystallography

Journal of structural biology, 2007-05, Vol.158 (2), p.214-223

2007

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Defective Transcription-Coupled Repair of Oxidative Base Damage in Cockayne Syndrome Patients from XP Group G

Science (American Association for the Advancement of Science), 1997-02, Vol.275 (5302), p.990-993

1997

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Artemis deficiency confers a DNA double-strand break repair defect and Artemis phosphorylation status is altered by DNA damage and cell cycle progression

DNA repair, 2005-05, Vol.4 (5), p.556-570

2005

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DNA double-strand break and chromosomal rejoining defects with misrejoining in Nijmegen breakage syndrome cells

DNA repair, 2008, Vol.7 (1), p.108-118

2008

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Transcription-Coupled Repair of 8-oxoguanine: Requirement for XPG, TFIIH, and CSB and Implications for Cockayne Syndrome

Cell, 2005-11, Vol.123 (4), p.711-711

2005

Volltextzugriff (PDF)

Comparative TFIIS-mediated transcript cleavage by mammalian RNA polymerase II arrested at a lesion in different transcription systems

DNA repair, 2005-09, Vol.4 (10), p.1075-1087

2005

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Spatial Distribution and Yield of DNA Double-Strand Breaks Induced by 3–7 MeV Helium Ions in Human Fibroblasts

Radiation research, 2002-07, Vol.158 (1), p.32-42

2002

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Human Flap Endonuclease Structures, DNA Double-Base Flipping, and a Unified Understanding of the FEN1 Superfamily

A versatile viral system for expression and depletion of proteins in mammalian cells

Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency

Non-catalytic Roles for XPG with BRCA1 and BRCA2 in Homologous Recombination and Genome Stability

Repair complexes of FEN1 endonuclease, DNA, and Rad9-Hus1-Rad1 are distinguished from their PCNA counterparts by functionally important stability

Recognition of RNA Polymerase II and Transcription Bubbles by XPG, CSB, and TFIIH: Insights for Transcription-Coupled Repair and Cockayne Syndrome

Conserved XPB Core Structure and Motifs for DNA Unwinding: Implications for Pathway Selection of Transcription or Excision Repair

DNA repair: dynamic defenders against cancer and aging

DNA glycosylase NEIL2 functions in multiple cellular processes

The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome

Human XPG nuclease structure, assembly, and activities with insights for neurodegeneration and cancer from pathogenic mutations

XPD Helicase Structures and Activities: Insights into the Cancer and Aging Phenotypes from XPD Mutations

The Single-Strand DNA Binding Activity of Human PC4 Prevents Mutagenesis and Killing by Oxidative DNA Damage

Dose-Dependent Misrejoining of Radiation-Induced DNA Double-Strand Breaks in Human Fibroblasts: Experimental and Theoretical Study for High- and Low-LET Radiation

Thirdhand smoke exposure causes replication stress and impaired transcription in human lung cells

Repair of X-Ray-Induced DNA Double-Strand Breaks in Specific Not I Restriction Fragments in Human Fibroblasts: Joining of Correct and Incorrect Ends

A Common Mutational Pattern in Cockayne Syndrome Patients from Xeroderma Pigmentosum Group G: Implications for a Second XPG Function

WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing

Structural analysis of flexible proteins in solution by small angle X-ray scattering combined with crystallography

Defective Transcription-Coupled Repair of Oxidative Base Damage in Cockayne Syndrome Patients from XP Group G

Artemis deficiency confers a DNA double-strand break repair defect and Artemis phosphorylation status is altered by DNA damage and cell cycle progression

DNA double-strand break and chromosomal rejoining defects with misrejoining in Nijmegen breakage syndrome cells

Transcription-Coupled Repair of 8-oxoguanine: Requirement for XPG, TFIIH, and CSB and Implications for Cockayne Syndrome

Comparative TFIIS-mediated transcript cleavage by mammalian RNA polymerase II arrested at a lesion in different transcription systems

Spatial Distribution and Yield of DNA Double-Strand Breaks Induced by 3–7 MeV Helium Ions in Human Fibroblasts

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