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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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A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

Science (American Association for the Advancement of Science), 1995-06, Vol.268 (5218), p.1749-1753

1995

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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.510-517

2006

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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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Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia

British journal of cancer, 1999-03, Vol.79 (7-8), p.1304-1307

1999

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

British journal of radiology, 2008, Vol.81 (961), p.51-58

2008

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Short Tandem Repeat Profiling Provides an International Reference Standard for Human Cell Lines

Proceedings of the National Academy of Sciences - PNAS, 2001-07, Vol.98 (14), p.8012-8017

2001

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Induction of Interleukin-6 Production by Ultraviolet Radiation in Normal Human Epidermal Keratinocytes and in a Human Keratinocyte Cell Line is Mediated by DNA Damage

Journal of investigative dermatology, 1998-09, Vol.111 (3), p.354-359

1998

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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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Characterization of photosensitivity in the Smith-Lemli-Opitz syndrome: a new congenital photosensitivity syndrome

British journal of dermatology (1951), 1999-09, Vol.141 (3), p.406-414

1999

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A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy

American journal of human genetics, 1993-10, Vol.53 (4), p.817-821

1993

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V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder

The Journal of biological chemistry, 1993-09, Vol.268 (27), p.20105-20109

1993

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Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I gene

The Lancet (British edition), 1992-06, Vol.339 (8808), p.1508-1509

1992

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Photosensitivity associated with the Smith-Lemli-Opitz syndrome

British journal of dermatology (1951), 1998-05, Vol.138 (5), p.885-888

1998

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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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Frequencies of hprt– mutations and bcl-2 translocations in circulating human lymphocytes are correlated with United Kingdom sunlight records

Mutagenesis, 1999-11, Vol.14 (6), p.527-532

1999

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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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Repair of radiation-induced DNA double-strand breaks in human fibroblasts is consistent with a continuous spectrum of repair probability

International journal of radiation biology, 1998, Vol.74 (5), p.551-560

FORAY, N.

1998

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Possible association between mutant frequency in peripheral lymphocytes and domestic radon concentrations

The Lancet (British edition), 1991-05, Vol.337 (8751), p.1187-1189

1991

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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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Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line

Journal of molecular biology, 1991-01, Vol.217 (2), p.217-222

1991

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Apoptosis and cytokine release induced by ionizing or ultraviolet B radiation in primary and immortalized human keratinocytes

Carcinogenesis (New York), 2000-06, Vol.21 (6), p.1087-1095

2000

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The use of dubious cell lines in research: is trust enough?

The lancet oncology, 2001-08, Vol.2 (8), p.467-467

Arlett, Colin F

2001

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

A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

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

Neurological symptoms and natural course of xeroderma pigmentosum

Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia

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

Short Tandem Repeat Profiling Provides an International Reference Standard for Human Cell Lines

Induction of Interleukin-6 Production by Ultraviolet Radiation in Normal Human Epidermal Keratinocytes and in a Human Keratinocyte Cell Line is Mediated by DNA Damage

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

Characterization of photosensitivity in the Smith-Lemli-Opitz syndrome: a new congenital photosensitivity syndrome

A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy

V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder

Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I gene

Photosensitivity associated with the Smith-Lemli-Opitz syndrome

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

Frequencies of hprt– mutations and bcl-2 translocations in circulating human lymphocytes are correlated with United Kingdom sunlight records

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

Repair of radiation-induced DNA double-strand breaks in human fibroblasts is consistent with a continuous spectrum of repair probability

Possible association between mutant frequency in peripheral lymphocytes and domestic radon concentrations

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line

Apoptosis and cytokine release induced by ionizing or ultraviolet B radiation in primary and immortalized human keratinocytes

The use of dubious cell lines in research: is trust enough?

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

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