Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.
暂无分享,去创建一个
H. Steingrimsdottir | A. Natarajan | A. Lehmann | C. Arlett | M. Stefanini | B. Broughton | S. A. Harcourt | S. Green | R. Taylor | A. Malcolm
[1] M. Stefanini,et al. The Association of Xeroderma Pigmentosum with Trichothiodystrophy: A Clue to a Better Understanding of XP-D? , 1989 .
[2] M. Stefanini,et al. Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity. , 1987, Mutation research.
[3] P. Hanawalt,et al. Preferential DNA repair of an active gene in human cells. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[4] C. Haipek,et al. (6-4)Photoproducts are removed from the DNA of UV-irradiated mammalian cells more efficiently than cyclobutane pyrimidine dimers. , 1985, Mutation research.
[5] A. Lehmann,et al. PRENATAL DIAGNOSIS OF COCKAYNE'S SYNDROME , 1985, The Lancet.
[6] M. King,et al. Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases. , 1984, Journal of medical genetics.
[7] D. Mitchell,et al. The use of an immunological probe to measure the kinetics of DNA repair in normal and UV-sensitive mammalian cell lines. , 1983, Mutation research.
[8] C. Arlett,et al. Variation in response to mutagens amongst normal and repair-defective human cells. , 1983, Basic life sciences.
[9] T. Beals,et al. Neurotrichosis: Hair‐shaft Abnormalities associated with Neurological Diseases , 1982, Developmental medicine and child neurology.
[10] A. Lehmann,et al. Three complementation groups in Cockayne syndrome. , 1982, Mutation research.
[11] A. Lehmann,et al. Excision repair in Cockayne syndrome. , 1982, Mutation research.
[12] S. Squires,et al. Initial rates of DNA incision in UV-irradiated human cells: differences between normal, xeroderma pigmentosum and tumour cells. , 1982, Mutation research.
[13] R. G. Crounse,et al. Ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature (IBIDS syndrome) , 1982, The British journal of dermatology.
[14] A. Lehmann,et al. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum. , 1982, Cancer research.
[15] A. Natarajan,et al. Chromosomal damage induced by furocoumarins and UVA in hamster and human cells including cells from patients with ataxia telangiectasia and xeroderma pigmentosum. , 1981, Mutation research.
[16] P. Hanawalt,et al. Sensitive determination of pyrimidine dimers in DNA of UV-irradiated mammalian cells. Introduction of T4 endonuclease V into frozen and thawed cells. , 1981, Mutation research.
[17] B. Bridges. How important are somatic mutations and immune control in skin cancer? Reflections on xeroderma pigmentosum. , 1981, Carcinogenesis.
[18] V. Price,et al. Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex. , 1980, Archives of dermatology.
[19] A. Lehmann,et al. A rapid procedure for measurement of DNA repair in human fibroblasts and for complementation analysis of xeroderma pigmentosum cells. , 1980, Mutation research.
[20] P. J. Abrahams,et al. A seventh complementation group in excision-deficient xeroderma pigmentosum. , 1979, Mutation research.
[21] F. Giannelli,et al. Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum. , 1979, The Quarterly journal of medicine.
[22] J. Robbins,et al. Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation. , 1978, Proceedings of the National Academy of Sciences of the United States of America.
[23] D. Bootsma,et al. Induction of sister chromatid exchanges in xeroderma pigmentosum cells after exposure to ultraviolet light. , 1977, Mutation research.
[24] D. Hull,et al. THE EFFECT OF ULTRAVIOLET LIGHT ON ARRESTED HUMAN DIPLOID CELL POPULATIONS , 1977, Photochemistry and photobiology.
[25] A. Lehmann,et al. Repair of ultraviolet light damage in a variety of human fibroblast cell strains. , 1977, Cancer research.
[26] P. Hanawalt,et al. Repair replication in cultured normal and transformed human fibroblasts. , 1976, Biochimica et biophysica acta.
[27] L. Weiss,et al. The physicochemical properties of hair in the BIDS syndrome. , 1976, American journal of human genetics.
[28] K. Kraemer,et al. Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[29] L. Weiss,et al. "Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred. , 1974, Pediatrics.
[30] R. Pollitt,et al. Sibs with mental and physical retardation and trichorrhexis nodosa with abnormal amino acid composition of the hair. , 1968, Archives of disease in childhood.