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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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Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

Human molecular genetics, 2001-10, Vol.10 (22), p.2539-2547

2001

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Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy

American journal of human genetics, 1996-02, Vol.58 (2), p.263-270

1996

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Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells

Genes & development, 2001-01, Vol.15 (2), p.158-172

2001

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Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and cockayne syndrome

American journal of human genetics, 1995, Vol.56 (1), p.167-174

1995

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Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy

Nature genetics, 1994-06, Vol.7 (2), p.189-194

1994

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Molecular Analysis of Mutations in DNA Polymerase η in Xeroderma Pigmentosum-Variant Patients

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (2), p.815-820

2002

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Xeroderma Pigmentosum and Trichothiodystrophy are Associated with Different Mutations in the XPD (ERCC2) Repair/Transcription Gene

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (16), p.8658-8663

1997

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Localization of a DNA Repair Gene (XRCC5) Involved in Double-Strand-Break Rejoining to Human Chromosome 2

Proceedings of the National Academy of Sciences - PNAS, 1992-07, Vol.89 (14), p.6423-6427

1992

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Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels

Cancer research (Chicago, Ill.), 2000-04, Vol.60 (7), p.1974-1982

2000

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Mutations in the general transcription factor TFIIH result in β-thalassaemia in individuals with trichothiodystrophy

Human molecular genetics, 2001-11, Vol.10 (24), p.2797-2802

2001

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Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinical Severity

American journal of human genetics, 1998-10, Vol.63 (4), p.1036-1048

1998

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Cloning the RAD51 homologue of Schizosaccharomyces pombe

Nucleic acids research, 1993-09, Vol.21 (19), p.4586-4591

1993

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Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light

Cancer research (Chicago, Ill.), 1988-11, Vol.48 (21), p.6090-6096

1988

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Cells from an Immunodeficient Patient (46BR) with a Defect in DNA Ligation are Hypomutable but Hypersensitive to the Induction of Sister Chromatid Exchanges

Proceedings of the National Academy of Sciences - PNAS, 1985-04, Vol.82 (7), p.2044-2048

1985

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Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome

Cancer research (Chicago, Ill.), 1988-11, Vol.48 (22), p.6343-6347

1988

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Poly(ADP-ribosylation) reduces the steady-state level of breaks in DNA following treatment of human cells with alkylating agents

Carcinogenesis (New York), 1984-01, Vol.5 (1), p.117-119

1984

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Inhibition of DNA Replication by Ionizing Radiation is Mediated by a Trans-acting Factor

International journal of radiation biology, 1989, Vol.56 (2), p.125-130

1989

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DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells

Journal of investigative dermatology, 1996-10, Vol.107 (4), p.647-653

1996

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A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR)

Carcinogenesis (New York), 1983, Vol.4 (5), p.559-564

1983

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Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophy

Mutation research, 1990-01, Vol.235 (1), p.33-40

1990

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The ultraviolet sensitivity of Cockayne syndrome cells is not a consequence of reduced cellular NAD content

American journal of human genetics, 1984-03, Vol.36 (2), p.311-319

1984

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Cell killing and mutagenesis by 8-methoxypsoralen in mammalian (rodent) cells

Clinical and experimental dermatology, 1980-06, Vol.5 (2), p.147-158

1980

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An adaptive response to the cytotoxic effects of N-methyl- N-nitrosourea is apparently absent in normal human fibroblasts

Biochimie, 1982-08, Vol.64 (8), p.717-721

1982

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The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation

Mutation research, 1975-12, Vol.33 (2-3), p.341-346

1975

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Novel Human and Mouse Homologs of Saccharomyces cerevisiae DNA Polymerase η

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy

Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and cockayne syndrome

Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy

Molecular Analysis of Mutations in DNA Polymerase η in Xeroderma Pigmentosum-Variant Patients

Xeroderma Pigmentosum and Trichothiodystrophy are Associated with Different Mutations in the XPD (ERCC2) Repair/Transcription Gene

Localization of a DNA Repair Gene (XRCC5) Involved in Double-Strand-Break Rejoining to Human Chromosome 2

Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels

Mutations in the general transcription factor TFIIH result in β-thalassaemia in individuals with trichothiodystrophy

Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinical Severity

Cloning the RAD51 homologue of Schizosaccharomyces pombe

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light

Cells from an Immunodeficient Patient (46BR) with a Defect in DNA Ligation are Hypomutable but Hypersensitive to the Induction of Sister Chromatid Exchanges

Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome

Poly(ADP-ribosylation) reduces the steady-state level of breaks in DNA following treatment of human cells with alkylating agents

Inhibition of DNA Replication by Ionizing Radiation is Mediated by a Trans-acting Factor

DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells

A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR)

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophy

The ultraviolet sensitivity of Cockayne syndrome cells is not a consequence of reduced cellular NAD content

Cell killing and mutagenesis by 8-methoxypsoralen in mammalian (rodent) cells

An adaptive response to the cytotoxic effects of N-methyl- N-nitrosourea is apparently absent in normal human fibroblasts

The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation

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