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The 0.8% ultraviolet B content of an ultraviolet A sunlamp induces 75% of cyclobutane pyrimidine dimers in human keratinocytes in vitro

British journal of dermatology (1951), 1999-06, Vol.140 (6), p.1023-1030

1999

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Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3

American journal of human genetics, 1994-02, Vol.54 (2), p.191-200

1994

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Defective repair of DNA double-strand breaks and chromosome damage in fibroblasts from a radiosensitive leukemia patient

Cancer research (Chicago, Ill.), 1995-03, Vol.55 (6), p.1232-1234

1995

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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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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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Hypersensitivity of human lymphocytes to UV-B and solar irradiation

Cancer research (Chicago, Ill.), 1993-02, Vol.53 (3), p.609-614

1993

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Extended-term cultures of human T-lymphocytes: a practical alternative to primary human lymphocytes for use in genotoxicity testing

Mutagenesis, 1995-05, Vol.10 (3), p.189-201

1995

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Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity

Human genetics, 1986-10, Vol.74 (2), p.107-112

1986

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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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An instance of clinical radiation morbidity and cellular radiosensitivity, not associated with ataxia-telangiectasia

British journal of radiology, 1990-08, Vol.63 (752), p.624-628

1990

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Induction of cyclobutane pyrimidine dimers, pyrimidine(6-4)pyrimidone photoproducts, and Dewar valence isomers by natural sunlight in normal human mononuclear cells

Cancer research (Chicago, Ill.), 1995-06, Vol.55 (11), p.2245-2248

1995

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Photocarcinogenesis and Inhibition of Intercellular Adhesion Molecule 1 Expression in Cells of DNA-Repair-Defective Individuals

Proceedings of the National Academy of Sciences - PNAS, 1997-06, Vol.94 (13), p.6837-6841

1997

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A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitivity in a patient with xeroderma pigmentosum

Journal of medical genetics, 2010-03, Vol.47 (3), p.176-181

2010

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Comments on the paper: the ATM gene and the radiobiology of ataxia-telangiectasia

International journal of radiation biology, 1997-04, Vol.71 (4), p.449-450

1997

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Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

Nature (London), 1975-12, Vol.258 (5534), p.427-429

1975

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Ultraviolet-B-Induced Apoptosis and Cytokine Release in Xeroderma Pigmentosum Keratinocytes

Journal of investigative dermatology, 2000-10, Vol.115 (4), p.687-693

2000

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Deficient recovery from potentially lethal damage in some gamma-irradiated human fibroblast cell strains

British journal of cancer. Supplement, 1984, Vol.6, p.227-232

1984

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The third UKEMS collaborative trial

Mutagenesis, 1990, Vol.5 (Supplement), p.3-4

1990

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Co-cultivation of CD4 + and CD8 + human T-cells leads to the appearance of CD4 cells expressing CD8 through de novo synthesis of the CD8 α-subunit

Human immunology, 1999-11, Vol.60 (11), p.1018-1027

1999

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Micronuclei: origins, applications and methodologies—a workshop sponsored by the Health and Safety Executive held in Manchester, May 23–25, 1988

Mutagenesis, 1989-11, Vol.4 (6), p.482-485

1989

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Repair of ultraviolet light damage in a variety of human fibroblast cell strains

Cancer research (Chicago, Ill.), 1977-03, Vol.37 (3), p.904-910

1977

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Variation in response to mutagens amongst normal and repair-defective human cells

Basic life sciences, 1983, Vol.23, p.249

1983

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An assessment of the radiosensitivity of ataxia-telangiectasia heterozygotes

Kroc Foundation series, 1985, Vol.19, p.101

1985

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Human genetic disorders with defects in the repair of deoxyribonucleic acid [proceedings]

Biochemical Society transactions, 1977, Vol.5 (4), p.1199-1203

1977

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Increased sensitivity to gamma irradiation of skin fibroblasts in Friedreich's ataxia

The Lancet (British edition), 1979-09, Vol.2 (8140), p.474

1979

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The 0.8% ultraviolet B content of an ultraviolet A sunlamp induces 75% of cyclobutane pyrimidine dimers in human keratinocytes in vitro

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3

Defective repair of DNA double-strand breaks and chromosome damage in fibroblasts from a radiosensitive leukemia patient

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

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

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

Extended-term cultures of human T-lymphocytes: a practical alternative to primary human lymphocytes for use in genotoxicity testing

Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity

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

An instance of clinical radiation morbidity and cellular radiosensitivity, not associated with ataxia-telangiectasia

Induction of cyclobutane pyrimidine dimers, pyrimidine(6-4)pyrimidone photoproducts, and Dewar valence isomers by natural sunlight in normal human mononuclear cells

Photocarcinogenesis and Inhibition of Intercellular Adhesion Molecule 1 Expression in Cells of DNA-Repair-Defective Individuals

A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitivity in a patient with xeroderma pigmentosum

Comments on the paper: the ATM gene and the radiobiology of ataxia-telangiectasia

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

Ultraviolet-B-Induced Apoptosis and Cytokine Release in Xeroderma Pigmentosum Keratinocytes

Deficient recovery from potentially lethal damage in some gamma-irradiated human fibroblast cell strains

The third UKEMS collaborative trial

Co-cultivation of CD4 + and CD8 + human T-cells leads to the appearance of CD4 cells expressing CD8 through de novo synthesis of the CD8 α-subunit

Micronuclei: origins, applications and methodologies—a workshop sponsored by the Health and Safety Executive held in Manchester, May 23–25, 1988

Repair of ultraviolet light damage in a variety of human fibroblast cell strains

Variation in response to mutagens amongst normal and repair-defective human cells

An assessment of the radiosensitivity of ataxia-telangiectasia heterozygotes

Human genetic disorders with defects in the repair of deoxyribonucleic acid [proceedings]

Increased sensitivity to gamma irradiation of skin fibroblasts in Friedreich's ataxia

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