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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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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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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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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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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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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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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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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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

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

1993

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Use of Fluorescence in Situ Hybridization to Determine the Relationship between Chromosome Aberrations and Cell Survival in Eight Human Fibroblast Strains

International journal of radiation biology, 1995, Vol.68 (2), p.185-196

1995

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Four radiation hypersensitivity cases and their implications for clinical radiotherapy

Radiotherapy and oncology, 2000-11, Vol.57 (2), p.143-154

2000

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Dose-rate effect on induction and repair rate of radiation-induced DNA double-strand breaks in a normal and an ataxia telangiectasia human fibroblast cell line

Biochimie, 1995, Vol.77 (11), p.900-905

1995

Volltextzugriff (PDF)

Cloning Efficiency and Spontaneous Mutant Frequency in Circulating T-lymphocytes in Ataxia-telangiectasia Patients

International journal of radiation biology, 1994, Vol.66 (6), p.S123-S131

1994

Volltextzugriff (PDF)

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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

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

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

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

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

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

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

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

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

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

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

Use of Fluorescence in Situ Hybridization to Determine the Relationship between Chromosome Aberrations and Cell Survival in Eight Human Fibroblast Strains

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

Four radiation hypersensitivity cases and their implications for clinical radiotherapy

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

Dose-rate effect on induction and repair rate of radiation-induced DNA double-strand breaks in a normal and an ataxia telangiectasia human fibroblast cell line

Cloning Efficiency and Spontaneous Mutant Frequency in Circulating T-lymphocytes in Ataxia-telangiectasia Patients

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