DNA repair: Pathways and defects
暂无分享,去创建一个
[1] C. Bartram,et al. Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts. , 1980, American journal of human genetics.
[2] R. N. Schimke. Elemente der klinischen genetik , 1980 .
[3] P. Smith,et al. Enhanced radiosensitivity of cultured fibroblasts from ataxia telangiectasia heterozygotes manifested by defective colony-forming ability and reduced DNA repair replication after hypoxic gamma-irradiation. , 1979, Cancer research.
[4] D. Bootsma,et al. Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair , 1979, Clinical genetics.
[5] J. Cleaver,et al. Postreplication repair: questions of its definition and possible alteration in xeroderma pigmentosum cell strains. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[6] P. J. Abrahams,et al. A seventh complementation group in excision-deficient xeroderma pigmentosum. , 1979, Mutation research.
[7] A. Moshell,et al. DNA repair processes protect human beings from premature solar skin damage: evidence from studies on xeroderma pigmentosum. , 1979, The Journal of investigative dermatology.
[8] S. Goldstein. Studies on age-related diseases in cultured skin fibroblasts. , 1979, The Journal of investigative dermatology.
[9] H. Hoehn,et al. Normalisation of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridisation , 1979, Nature.
[10] M. Swift,et al. Cancer in families with xeroderma pigmentosum. , 1979, Journal of the National Cancer Institute.
[11] C. Bartram,et al. Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cells , 1979, Human Genetics.
[12] J. Cleaver. DNA repair and its coupling to DNA replication in eukaryotic cells. , 1978, Biochimica et biophysica acta.
[13] M. Ichihashi,et al. Werner's syndrome: in vivo and in vitro characteristics as a model of aging. , 1978, The American journal of medicine.
[14] D. Hoar,et al. DNA repair in Cockayne syndrome. , 1978, American journal of human genetics.
[15] M. Lavin,et al. Identification of ataxia telangiectasia heterozygotes, a cancer prone population , 1978, Nature.
[16] C. Bartram,et al. Chromosomenanomalien bei malignen Tumoren , 1978, Klinische Wochenschrift.
[17] A. Taylor. Unrepaired DNA strand breaks in irradiated ataxia telangiectasia lymphocytes suggested from cytogenetic observations. , 1978, Mutation research.
[18] J. Marx. DNA repair: new clues to carcinogenesis. , 1978, Science.
[19] 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.
[20] R. Setlow,et al. Defective and enhanced postreplication repair in classical and variant xeroderma pigmentosum cells treated with N-acetoxy-2-acetylaminofluorene. , 1978, Cancer research.
[21] S. Linn,et al. Xeroderma pigmentosum fibroblasts of the D group lack an apurinic DNA endonuclease species with a low apparent Km. , 1978, Nucleic acids research.
[22] R. Setlow. Repair deficient human disorders and cancer , 1978, Nature.
[23] R. Weichselbaum,et al. Deficient recovery from potentially lethal radiation damage in ataxia telangiectasia and xeroderma pigmentosum , 1978, Nature.
[24] Rüdiger Hw. Genetically determined risk factors for malignant tumors in man , 1978 .
[25] A. Auerbach,et al. Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells , 1978, Nature.
[26] T. Inoue,et al. DNA repair enzymes in ataxia telangiectasia and Bloom's syndrome fibroblasts. , 1977, Biochimica et biophysica acta.
[27] M. Sasaki. Sister chromatid exchange and chromatid interchange as possible manifestation of different DNA repair processes , 1977, Nature.
[28] E. Passarge,et al. Bloom's syndrome. V. Surveillance for cancer in affected families , 1977, Clinical genetics.
[29] Y. Fujiwara,et al. A retarded rate of DNA replication and normal level of DNA repair in Werner's syndrome fibroblasts in culture , 1977, Journal of cellular physiology.
[30] J. Trosko,et al. Cockayne syndrome: a cellular sensitivity to ultraviolet light. , 1977, Pediatrics.
[31] Y. Fujiwara,et al. Cross-link repair in human cells and its possible defect in Fanconi's anemia cells. , 1977 .
[32] K. Tanaka,et al. Specific action of T4 endonuclease V on damaged DNA in xeroderma pigmentosum cells in vivo. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[33] H. Ochs,et al. Autoimmunity in the relatives of patients with immunodeficiency diseases. , 1977, Clinical and experimental immunology.
[34] R. Goth-Goldstein. Repair of DNA damaged by alkylating carcinogens is defective in xeroderma pigmentosum-derived fibroblasts , 1977, Nature.
[35] J. German,et al. Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes. , 1977, American journal of human genetics.
[36] A. Schönwald,et al. UV-light induced sister chromatid exchanges in xeroderma pigmentosum lymphocytes , 1977, Human Genetics.
[37] J. Mccormick,et al. Caffeine enhancement of the cytotoxic and mutagenic effect of ultraviolet irradiation in a xeroderma pigmentosum variant strain of human cells. , 1976, Biochemical and biophysical research communications.
[38] C. Bartram,et al. Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderrna pigmentosum , 1976, Annals of human genetics.
[39] J. Robbins,et al. RELATION OF D.N.A. REPAIR PROCESSES TO PATHOLOGICAL AGEING OF THE NERVOUS SYSTEM IN XERODERMA PIGMENTOSUM , 1976, The Lancet.
[40] A. Auerbach,et al. Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens , 1976, Nature.
[41] D. Hoar,et al. Chemical mutagen hypersensitivity in ataxia telangiectasia , 1976, Nature.
[42] E. Hook,et al. Sister chromatid exchanges in ataxia telangiectasia. , 1976, Mutation research.
[43] S. Linn,et al. An altered apurinic DNA endonuclease activity in group A and group D xeroderma pigmentosum fibroblasts. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[44] M. Paterson,et al. Defective excision repair of γ-ray-damaged DNA in human (ataxia telangiectasia) fibroblasts , 1976, Nature.
[45] K. Sperling,et al. Cytogenetic investigations in a new case of Bloom's syndrome , 1976, Human Genetics.
[46] J. Mccormick,et al. Synergistic effect of caffeine on the cytotoxicity of ultraviolet irradiation and of hydrocarbon epoxides in strains of Xeroderma pigmentosum , 1975, Nature.
[47] A. Taylor,et al. Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity , 1975, Nature.
[48] S. Latt,et al. Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[49] W. Schmid,et al. The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts , 1975, Humangenetik.
[50] F. Hecht,et al. Somatic rearrangement of chromosome 14 in human lymphocytes. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[51] E. Friedberg,et al. Human diseases with genetically altered DNA repair processes. , 1975, Genetics.
[52] A. Cameron,et al. Radiosensitivity in ataxia-telangiectasia. , 1975, The British journal of radiology.
[53] J. German,et al. Bloom's syndrome and Fanconi's anemia: Demonstration of two distinctive patterns of chromosome disruption and rearrangement , 1974, Humangenetik.
[54] J. German,et al. A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. , 1974, Proceedings of the National Academy of Sciences of the United States of America.
[55] F. Giannelli,et al. Prenatal diagnosis of xeroderma pigmentosum. Report of the first successful case. , 1974, Lancet.
[56] B. Sutherland. Photoreactivating enzyme from human leukocytes , 1974, Nature.
[57] K. Kraemer,et al. Xeroderma Pigmentosum: An Inherited Disease with Sun Sensitivity, Multiple Cutaneous Neoplasms, and Abnormal DNA Repair , 1974 .
[58] S. Latt. Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[59] M. Sasaki. DNA repair capacity and susceptibility to chromosome breakage in xeroderma pigmentosum cells. , 1973, Mutation research.
[60] F. Hecht,et al. Ataxia-telangiectasia--clonal growth of translocation lymphocytes. , 1973, The New England journal of medicine.
[61] M. Sasaki,et al. A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents. , 1973, Cancer research.
[62] J. Little,et al. Deficient DNA repair in human progeroid cells. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[63] A. Lehmann. Postreplication repair of DNA in ultraviolet-irradiated mammalian cells. , 1972, Journal of molecular biology.
[64] M. Swift. Fanconi's Anaemia in the Genetics of Neoplasia , 1971, Nature.
[65] R. Setlow,et al. Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. , 1969, Proceedings of the National Academy of Sciences of the United States of America.
[66] J. L. Morgan,et al. Radiation reaction in ataxia telangiectasia. , 1968, American journal of diseases of children.
[67] J. Cleaver. Defective Repair Replication of DNA in Xeroderma Pigmentosum , 1968, Nature.
[68] S. Gotoff,et al. Ataxia Telangiectasia: Neoplasia, Untoward Response to X -Irradiation, and Tuberous Sclerosis , 1967 .
[69] J. Cook,et al. Photoreactivating-enzyme activity in metazoa. , 1967, Proceedings of the National Academy of Sciences of the United States of America.
[70] M. Shearn,et al. Immunoglobulin deficiency in Bloom's syndrome. , 1967, American journal of diseases of children.
[71] C. Epstein,et al. A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process , 1966 .
[72] W. Reed,et al. CONGENITAL LIPODYSTROPHIC DIABETES WITH ACANTHOSIS NIGRICANS: THE SEIP-LAWRENCE SYNDROME. , 1965, Archives of dermatology.
[73] W. Reed,et al. XERODERMA PIGMENTOSUM WITH NEUROLOGICAL COMPLICATIONS: THE DE SANCTIS-CACCHIONE SYNDROME. , 1965 .
[74] P. Hanawalt,et al. EVIDENCE FOR REPAIR-REPLICATION OF ULTRAVIOLET DAMAGED DNA IN BACTERIA. , 1964, Journal of molecular biology.
[75] K. Fitch,et al. Cockayne's syndrome. An heredo-familial disorder of growth and development. , 1960, Pediatrics.
[76] E. Boder,et al. Ataxia-telangiectasia; a familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection. , 1958, Pediatrics.
[77] E. Cockayne. Dwarfism with retinal atrophy and deafness , 1936, Archives of disease in childhood.
[78] R. Wegner,et al. Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemia , 2004, Humangenetik.
[79] G. Thomas,et al. Clinical characteristics, DNA repair, and complementation groups in xeroderma pigmentosum patients from Egypt. , 1980, Cancer research.
[80] C. Arlett,et al. Increased sensitivity of cell strains from Cockayne's syndrome to sister-chromatid-exchange induction and cell killing by UV light. , 1980, Mutation research.
[81] S. Arase,et al. A sixth complementation group in xeroderma pigmentosum. , 1979, Mutation research.
[82] R. Chaganti,et al. Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods. , 1979, American journal of human genetics.
[83] A. Lehmann,et al. Human disorders showing increased sensitivity to the induction of genetic damage. , 1978, Annual review of genetics.
[84] M. Daly,et al. Epidemiological factors related to the malignant neoplasms in ataxia-telangiectasia families. , 1978, Journal of chronic diseases.
[85] M. Paterson,et al. Ataxia Telangiectasia: An Inherited Human Disease Involving Radiosensitivity, Malignancy and Defective DNA Repair , 1977 .
[86] A. Sandberg,et al. Increased sister chromatid exchange in bone marrow and blood cells from Bloom's syndrome. , 1976, Cytogenetics and cell genetics.
[87] C. Bartram,et al. Somatic recombination as possible prelude to malignant transformation. , 1976, Birth defects original article series.
[88] M. Swift,et al. Malignant neoplasms in the families of patients with ataxia-telangiectasia. , 1976, Cancer research.
[89] M. Swift. Malignant disease in heterozygous carriers. , 1976, Birth defects original article series.
[90] 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.
[91] H. Evans,et al. Sister chromatid exchange in human chromosomes from normal individuals and patients with ataxia telangiectasia. , 1975, Cytogenetics and cell genetics.
[92] B. Sutherland,et al. Xeroderma pigmentosum cells contain low levels of photoreactivating enzyme. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[93] D. Bootsma,et al. Xeroderma pigmentosum: biochemical and genetic characteristics. , 1975, Annual review of genetics.
[94] M. Paterson,et al. Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[95] J. Cleaver. Repair Processes for Photochemical Damage in Mammalian Cells , 1974 .
[96] J. German. Genes which increase chromosomal instability in somatic cells and predispose to cancer. , 1972, Progress in medical genetics.
[97] J. Lawton,et al. Flames augmented by Inductive Coupling of Electrical Energy , 1971, Nature.
[98] E. Witkin. Ultraviolet-induced mutation and DNA repair. , 1969, Annual review of microbiology.