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Elevated expression of artemis in human fibroblast cells is associated with cellular radiosensitivity and increased apoptosis

British journal of cancer, 2012-10, Vol.107 (9), p.1506-1513

2012

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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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Hypersensitivity of ataxia telangiectasia fibroblasts to ionizing radiation is associated with a repair deficiency of DNA double-strand breaks

International journal of radiation biology, 1997-09, Vol.72 (3), p.271-283

FORAY, A. PRIESTLEY, G. ALSBEIH, C. BADIE, E. P. CAPULAS, C. F. ARLETT and E. P. MALAISE, N.

1997

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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, 2008-01, 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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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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Underestimation of the small residual damage when measuring DNA double-strand breaks (DSB): is the repair of radiation-induced DSB complete?

International journal of radiation biology, 1999, Vol.75 (12), p.1589-1595

Foray, C. F. Arlett, E. P. Malaise, N.

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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Radiation-induced DNA double-strand breaks and the radiosensitivity of human cells: A closer look

Biochimie, 1997-10, Vol.79 (9), p.567-575

1997

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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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The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect

Cancer research (Chicago, Ill.), 2000-01, Vol.60 (2), p.431-438

2000

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A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype

Cancer research (Chicago, Ill.), 1997-10, Vol.57 (20), p.4600-4607

1997

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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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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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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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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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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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Elevated expression of artemis in human fibroblast cells is associated with cellular radiosensitivity and increased apoptosis

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

Hypersensitivity of ataxia telangiectasia fibroblasts to ionizing radiation is associated with a repair deficiency of DNA double-strand breaks

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

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

Underestimation of the small residual damage when measuring DNA double-strand breaks (DSB): is the repair of radiation-induced DSB complete?

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

Radiation-induced DNA double-strand breaks and the radiosensitivity of human cells: A closer look

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

The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect

A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype

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

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

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

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

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

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