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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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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

2006

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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

2008

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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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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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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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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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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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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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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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Induction of mutagenic DNA damage in human fibroblasts after exposure to artificial tanning lamps

British journal of dermatology (1951), 1997-11, Vol.137 (5), p.687-692

1997

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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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Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

Cancer research (Chicago, Ill.), 2000-09, Vol.60 (17), p.4881-4888

2000

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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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Mutant frequencies in workers at the Sellafield installation

Health physics (1958), 1995-03, Vol.68 (3), p.388

1995

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Long-term survival and preservation of natural killer cell activity in a xeroderma pigmentosum patient with spontaneous regression and multiple deposits of malignant melanoma

British journal of dermatology (1951), 1991-09, Vol.125 (3), p.272-278

1991

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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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Biomonitoring of possible human exposure to environmental genotoxic chemicals: Lessons from a study following the wreck of the oil tanker Braer

Environmental and molecular mutagenesis, 1997, Vol.30 (2), p.97-111

1997

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

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

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

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

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

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

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

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

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

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

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

Induction of mutagenic DNA damage in human fibroblasts after exposure to artificial tanning lamps

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

Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

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

Mutant frequencies in workers at the Sellafield installation

Long-term survival and preservation of natural killer cell activity in a xeroderma pigmentosum patient with spontaneous regression and multiple deposits of malignant melanoma

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

Biomonitoring of possible human exposure to environmental genotoxic chemicals: Lessons from a study following the wreck of the oil tanker Braer

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