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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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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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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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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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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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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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Effect of diet and vitamin C on DNA strand breakage in freshly-isolated human white blood cells

Mutation research, 1994-08, Vol.316 (2), p.91-102

1994

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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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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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The role of mammalian cell mutation assays in mutagenicity and carcinogenicity testing

Mutagenesis, 1988-11, Vol.3 (6), p.455-458

1988

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Human Disorders Showing Increased Sensitivity to the Induction of Genetic Damage

Annual review of genetics, 1978-01, Vol.12 (1), p.95-115

1978

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Human DNA repair defects

Journal of inherited metabolic disease, 1986-03, Vol.9 (S1), p.69-84

Arlett, C. F.

1986

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UV-C sensitivity of unstimulated and stimulated human lymphocytes from normal and xeroderma pigmentosum donors in the comet assay: A potential diagnostic technique

Mutation research, 1992-03, Vol.273 (2), p.137-144

1992

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Repair of cyclobutane pyrimidine dimers in unstimulated human mononuclear cells is deficient at very low fluences of ultraviolet B and is not enhanced by addition of deoxyribonucleosides

Mutagenesis, 1998-07, Vol.13 (4), p.353-356

1998

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Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophy

Mutation research, 1990-01, Vol.235 (1), p.33-40

1990

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Detection of somatic mutants in man: HPRT mutations in lymphocytes and hemoglobin mutations in erythrocytes

Mutation research, 1989-07, Vol.213 (1), p.73-82

1989

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Effect of deoxyribonucleosides on the hypersensitivity of human peripheral blood lymphocytes to UV-B and UV-C irradiation

Mutation research, 1994-07, Vol.315 (1), p.25-32

1994

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Inhibition of RNA and DNA synthesis in UV-irradiated normal human fibroblasts is correlated with pyrimidine (6-4) pyrimidone photoproduct formation

Mutation research, 1996-07, Vol.354 (1), p.87-94

1996

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A comparison of the agar cloning and microtitration techniques for assaying cell survival and mutation frequency in L5178Y mouse lymphoma cells

Mutation research, 1983-01, Vol.111 (3), p.371-386

1983

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The influence of the cytoplasm on mutation in Aspergillus nidulans

Mutation research, 1966-01, Vol.3 (5), p.410-419

Arlett, C F

1966

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The mutagenic potency of 1,8-dinitropyrene in cultured mouse lymphoma cells

Mutation research, 1982-03, Vol.93 (1), p.213-220

1982

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THE "MINUTE" CYTOPLASMIC VARIANT OF ASPERGILLUS NIDULANS

Heredity, 1964-02, Vol.19 (1), p.63-73

1964

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The fluctuation test as a more sensitive system for determining induced mutation in L5178Y mouse lymphoma cells

Mutation research, 1976-12, Vol.41 (2-3), p.377-386

1976

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The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation

Mutation research, 1975-12, Vol.33 (2-3), p.341-346

1975

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

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

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

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

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

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

Effect of diet and vitamin C on DNA strand breakage in freshly-isolated human white blood cells

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

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

The role of mammalian cell mutation assays in mutagenicity and carcinogenicity testing

Human Disorders Showing Increased Sensitivity to the Induction of Genetic Damage

Human DNA repair defects

UV-C sensitivity of unstimulated and stimulated human lymphocytes from normal and xeroderma pigmentosum donors in the comet assay: A potential diagnostic technique

Repair of cyclobutane pyrimidine dimers in unstimulated human mononuclear cells is deficient at very low fluences of ultraviolet B and is not enhanced by addition of deoxyribonucleosides

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophy

Detection of somatic mutants in man: HPRT mutations in lymphocytes and hemoglobin mutations in erythrocytes

Effect of deoxyribonucleosides on the hypersensitivity of human peripheral blood lymphocytes to UV-B and UV-C irradiation

Inhibition of RNA and DNA synthesis in UV-irradiated normal human fibroblasts is correlated with pyrimidine (6-4) pyrimidone photoproduct formation

A comparison of the agar cloning and microtitration techniques for assaying cell survival and mutation frequency in L5178Y mouse lymphoma cells

The influence of the cytoplasm on mutation in Aspergillus nidulans

The mutagenic potency of 1,8-dinitropyrene in cultured mouse lymphoma cells

THE "MINUTE" CYTOPLASMIC VARIANT OF ASPERGILLUS NIDULANS

The fluctuation test as a more sensitive system for determining induced mutation in L5178Y mouse lymphoma cells

The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation

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