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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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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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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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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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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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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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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

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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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Four radiation hypersensitivity cases and their implications for clinical radiotherapy

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

2000

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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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Abnormal erythemal response and elevated T lymphocyte HRPT mutant frequency in Cockayne's syndrome

British journal of dermatology (1951), 1991-05, Vol.124 (5), p.453-460

1991

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Comparative Human Cellular Radiosensitivity: IV. The Increased Sensitivity of Human Neonatal Cord Blood Lymphocytes to γ-irradiation Compared with Lymphocytes from Children and Adults

International journal of radiation biology, 1991, Vol.59 (3), p.767-776

1991

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Defective Recovery from Potentially Lethal Damage in Some Human Fibroblast Cell Strains

International journal of radiation biology, 1983-01, Vol.43 (2), p.157-167

1983

Volltextzugriff (PDF)

Possible Effects of Sunlight on Human Lymphocytes

Journal of Epidemiology, 1999, Vol.9(6sup), pp.48-57

1999

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Transplacental effects of chemical mutagens detected by the micronucleus test

Nature (London), 1979-01, Vol.277 (5694), p.317-318

1979

Volltextzugriff (PDF)

Immune Function, Mutant Frequency, and Cancer Risk in the DNA Repair Defective Genodermatoses Xeroderma Pigmentosum, Cockayne's Syndrome, and Trichothiodystrophy

Journal of investigative dermatology, 1990-01, Vol.94 (1), p.94-100

1990

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Survey of radiosensitivity in a variety of human cell strains

Cancer research (Chicago, Ill.), 1980-03, Vol.40 (3), p.926

1980

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Lack of discernible effect of diagnostic ultrasound on the chromosomes of cord blood lymphocytes exposed in utero

British journal of radiology, 1986-05, Vol.59 (701), p.499-503

1986

Volltextzugriff (PDF)

Risk of Breast Cancer in Ataxia–Telangiectasia

The New England journal of medicine, 1992-05, Vol.326 (20), p.1357-1361

1992

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Cloning efficiency and spontaneous mutant frequency in circulating T-lymphocytes in ataxia-telangiectasia patients

International journal of radiation biology, 1994-12, Vol.66 (6 Suppl), p.S123

1994

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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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Observations on the growth in vitro of myeloid progenitor cells and fibroblasts from hemizygotes and heterozygotes for “complete” and “partial” hypoxanthine-guanine phosphoribosyltransferase (HGPRT) deficiency, and their relevance to the pathogenesis of brain damage in the Lesch-Nyhan syndrome

Journal of the neurological sciences, 1974-06, Vol.22 (2), p.183-195

1974

Volltextzugriff (PDF)

Prolonged expression of the γ‐H2AX DNA repair biomarker correlates with excess acute and chronic toxicity from radiotherapy treatment

International journal of cancer, 2011-12, Vol.129 (12), p.2928-2934

2011

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

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

Neurological symptoms and natural course of xeroderma pigmentosum

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

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

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

Photosensitivity associated with the Smith-Lemli-Opitz syndrome

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

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

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

Abnormal erythemal response and elevated T lymphocyte HRPT mutant frequency in Cockayne's syndrome

Comparative Human Cellular Radiosensitivity: IV. The Increased Sensitivity of Human Neonatal Cord Blood Lymphocytes to γ-irradiation Compared with Lymphocytes from Children and Adults

Defective Recovery from Potentially Lethal Damage in Some Human Fibroblast Cell Strains

Possible Effects of Sunlight on Human Lymphocytes

Transplacental effects of chemical mutagens detected by the micronucleus test

Immune Function, Mutant Frequency, and Cancer Risk in the DNA Repair Defective Genodermatoses Xeroderma Pigmentosum, Cockayne's Syndrome, and Trichothiodystrophy

Survey of radiosensitivity in a variety of human cell strains

Lack of discernible effect of diagnostic ultrasound on the chromosomes of cord blood lymphocytes exposed in utero

Risk of Breast Cancer in Ataxia–Telangiectasia

Cloning efficiency and spontaneous mutant frequency in circulating T-lymphocytes in ataxia-telangiectasia patients

An assessment of the radiosensitivity of ataxia-telangiectasia heterozygotes

Prolonged expression of the γ‐H2AX DNA repair biomarker correlates with excess acute and chronic toxicity from radiotherapy treatment

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