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USP7 is essential for maintaining Rad18 stability and DNA damage tolerance

Oncogene, 2016-02, Vol.35 (8), p.965-976

2016

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Patients with xeroderma pigmentosum complementation groups C, E and V do not have abnormal sunburn reactions

British journal of dermatology (1951), 2013-12, Vol.169 (6), p.1279-1287

2013

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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases

Genes & development, 2001-01, Vol.15 (1), p.15-23

Lehmann, A R

2001

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Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

Human mutation, 2010-02, Vol.31 (2), p.113-126

2010

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Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice

Current biology, 2000-04, Vol.10 (8), p.479-482

2000

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Decreased colorectal atypia among a cohort of gout patients

Scandinavian journal of rheumatology, 2018-01, Vol.47 (1), p.81-82

2018

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DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

Biochimie, 2003-11, Vol.85 (11), p.1101-1111

Lehmann, Alan R.

2003

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Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

Current biology, 1999-07, Vol.9 (13), p.699,S1-702,S2

1999

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The rad18 gene of Schizosaccharomyces pombe defines a new subgroup of the SMC superfamily involved in DNA repair

Molecular and Cellular Biology, 1995-12, Vol.15 (12), p.7067-7080

1995

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Molecular and biochemical characterization of xrs mutants defective in Ku80

Molecular and Cellular Biology, 1997-03, Vol.17 (3), p.1264-1273

1997

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Interaction of Human DNA Polymerase η with Monoubiquitinated PCNA: A Possible Mechanism for the Polymerase Switch in Response to DNA Damage

Molecular cell, 2004-05, Vol.14 (4), p.491-500

2004

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A novel mutation in the XPA gene associated with unusually mild clinical features in a patient who developed a spindle cell melanoma

British journal of dermatology (1951), 2006-07, Vol.155 (1), p.81-88

2006

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Identification and characterization of new elements involved in checkpoint and feedback controls in fission yeast

Molecular biology of the cell, 1994-02, Vol.5 (2), p.147-160

1994

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Ku80: Product of the XRCC5 Gene and Its Role in DNA Repair and V(D)J Recombination

Science (American Association for the Advancement of Science), 1994-09, Vol.265 (5177), p.1442-1445

1994

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Splitting the ATM: distinct repair and checkpoint defects in ataxia–telangiectasia

Trends in genetics, 1998-08, Vol.14 (8), p.312-316

1998

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Identification of a Nonsense Mutation in the Carboxyl-Terminal Region of DNA-Dependent Protein Kinase Catalytic Subunit in the scid Mouse

Proceedings of the National Academy of Sciences - PNAS, 1996-09, Vol.93 (19), p.10285-10290

1996

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Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum

British journal of radiology, 2006-06, Vol.79 (942), p.510

2006

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Novel Human and Mouse Homologs of Saccharomyces cerevisiae DNA Polymerase η

Genomics (San Diego, Calif.), 1999-08, Vol.60 (1), p.20-30

1999

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Neurological symptoms and natural course of xeroderma pigmentosum

Brain (London, England : 1878), 2008-08, Vol.131 (8), p.1979-1989

2008

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Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts

British journal of radiology, 2008-01, Vol.81 (961), p.51

2008

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Characterization of the alternative excision repair pathway of UV-damaged DNA in Schizosaccharomyces pombe

Nucleic acids research, 1997-04, Vol.25 (8), p.1553

1997

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Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome

American journal of human genetics, 1998-01, Vol.62 (1), p.77-85

1998

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Structural and functional conservation of the human homolog of the Schizosaccharomyces pombe rad2 gene, which is required for chromosome segregation and recovery from DNA damage

Molecular and Cellular Biology, 1994-07, Vol.14 (7), p.4878-4888

1994

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Alterations in the CSB Gene in Three Italian Patients with the Severe Form of Cockayne Syndrome (CS) But Without Clinical Photosensitivity

Human molecular genetics, 1999-05, Vol.8 (5), p.935-941

1999

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Identical mutations in the CSB gene associated with either cockayne syndrome or the DeSanctis-Cacchione variant of xeroderma pigmentosum

Human molecular genetics, 2000-05, Vol.9 (8), p.1171-1175

2000

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USP7 is essential for maintaining Rad18 stability and DNA damage tolerance

Patients with xeroderma pigmentosum complementation groups C, E and V do not have abnormal sunburn reactions

The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases

Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice

Decreased colorectal atypia among a cohort of gout patients

DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

The rad18 gene of Schizosaccharomyces pombe defines a new subgroup of the SMC superfamily involved in DNA repair

Molecular and biochemical characterization of xrs mutants defective in Ku80

Interaction of Human DNA Polymerase η with Monoubiquitinated PCNA: A Possible Mechanism for the Polymerase Switch in Response to DNA Damage

A novel mutation in the XPA gene associated with unusually mild clinical features in a patient who developed a spindle cell melanoma

Identification and characterization of new elements involved in checkpoint and feedback controls in fission yeast

Ku80: Product of the XRCC5 Gene and Its Role in DNA Repair and V(D)J Recombination

Splitting the ATM: distinct repair and checkpoint defects in ataxia–telangiectasia

Identification of a Nonsense Mutation in the Carboxyl-Terminal Region of DNA-Dependent Protein Kinase Catalytic Subunit in the scid Mouse

Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum

Novel Human and Mouse Homologs of Saccharomyces cerevisiae DNA Polymerase η

Neurological symptoms and natural course of xeroderma pigmentosum

Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts

Characterization of the alternative excision repair pathway of UV-damaged DNA in Schizosaccharomyces pombe

Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome

Structural and functional conservation of the human homolog of the Schizosaccharomyces pombe rad2 gene, which is required for chromosome segregation and recovery from DNA damage

Alterations in the CSB Gene in Three Italian Patients with the Severe Form of Cockayne Syndrome (CS) But Without Clinical Photosensitivity

Identical mutations in the CSB gene associated with either cockayne syndrome or the DeSanctis-Cacchione variant of xeroderma pigmentosum

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