In vivo somatic mutations in humans: measurement and analysis.
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R. Albertini | J. Nicklas | J. O’Neill | S. Robison | J. O'neill | R J Albertini | J P O'Neill | S H Robison | R. J. Albertini
[1] L. B. Russell,et al. Radiation-Induced Presumed Somatic Mutations in the House Mouse. , 1957, Genetics.
[2] G. Stamatoyannopoulos,et al. F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F. , 1975, Blood.
[3] G. Stamatoyannopoulos,et al. A new form of hereditary persistence of fetal hemoglobin in blacks and its association with sickle cell trait. , 1975, Blood.
[4] J. Lawrence,et al. Localization of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay , 1977, Cell.
[5] R. Albertini,et al. T-cell cloning to detect the mutant 6-thioguanine-resistant lymphocytes present in human peripheral blood. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[6] R. Albertini,et al. 15 – 6-THIOGUANINE-RESISTANT LYMPHOCYTES IN HUMAN BLOOD , 1984 .
[7] D. Ledbetter,et al. Organization of the HPRT gene and related sequences in the human genome , 1984, Somatic cell and molecular genetics.
[8] Kevin J. Trainor,et al. Mutation frequency in human lymphocytes increases with age , 1984, Mechanisms of Ageing and Development.
[9] K. Messing,et al. In vivo mutant frequency rises among breast cancer patients after exposure to high doses of gamma-radiation. , 1985, Mutation research.
[10] P. Nowell,et al. Location of gene for beta subunit of human T-cell receptor at band 7q35, a region prone to rearrangements in T cells. , 1985, Science.
[11] T. Waldmann,et al. Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7 , 1985, Nature.
[12] R. Albertini. Somatic gene mutations in vivo as indicated by the 6-thioguanine-resistant T-lymphocytes in human blood. , 1985, Mutation research.
[13] A. Morley,et al. Methods for study of mutations and mutagenesis in human lymphocytes. , 1985, Mutation research.
[14] B. Davidson,et al. A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in man. , 1986, The Journal of clinical investigation.
[15] K. Messing,et al. In vivo mutant frequency of technicians professionally exposed to ionizing radiation. , 1986, Progress in clinical and biological research.
[16] K. Messing,et al. Molecular characterization of 15 rearrangements among 90 human in vivo somatic mutants shows that deletions predominate , 1987, Molecular and cellular biology.
[17] R. Albertini,et al. Molecular analyses of in vivo hprt mutations in human T-lymphocytes. I. Studies of low frequency 'spontaneous' mutants by Southern blots. , 1987, Mutagenesis.
[18] R. Tice,et al. The use of bromodeoxyuridine labeling in the human lymphocyte HGPRT somatic mutation assay. , 1987, Mutation research.
[19] R. Albertini,et al. Refinement of a T-lymphocyte cloning assay to quantify the in vivo thioguanine-resistant mutant frequency in humans. , 1987, Mutagenesis.
[20] M. Green,et al. A further assessment of factors influencing measurements of thioguanine-resistant mutant frequency in circulating T-lymphocytes. , 1988, Mutation research.
[21] A. Morley,et al. Karyotypic abnormality of the X chromosome is rare in mutant HPRT-lymphocyte clones. , 1988, Mutation research.
[22] A. Morley,et al. Mutations in human lymphocytes commonly involve gene duplication and resemble those seen in cancer cels. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[23] R. Albertini,et al. Mutagenicity monitoring in humans by autoradiographic assay for mutant T lymphocytes. , 1988, Mutation research.
[24] A. Morley,et al. Mutations in human lymphocytes studied by an HLA selection system. , 1988, Mutation research.
[25] B. Davidson,et al. Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome. , 1989, The Journal of clinical investigation.
[26] S. Kudo,et al. Structural organization of glycophorin A and B genes: glycophorin B gene evolved by homologous recombination at Alu repeat sequences. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[27] B. Lambert,et al. Hprt mutations and karyotype abnormalities in T-cell clones from healthy subjects and melphalan-treated ovarian carcinoma patients. , 1989, Mutation research.
[28] W. Bigbee,et al. Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia. , 1989, American journal of human genetics.
[29] A. Morley,et al. The HLA-A mutation assay: improved technique and normal results. , 1989, Mutation research.
[30] W. Bigbee,et al. Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[31] R. Albertini,et al. Longitudinal study of the in vivo hprt mutant frequency in human T‐lymphocytes as determined by a cell cloning assay , 1989, Environmental and molecular mutagenesis.
[32] M. Akiyama,et al. Detection of somatic mutations at the glycophorin A locus in erythrocytes of atomic bomb survivors using a single beam flow sorter. , 1989, Cancer research.
[33] M. Akiyama,et al. Molecular analyses of in vivo hprt mutant T cells from atomic bomb survivors , 1989, Environmental and molecular mutagenesis.
[34] A. Tates,et al. Detection of somatic mutants in man: HPRT mutations in lymphocytes and hemoglobin mutations in erythrocytes. , 1989, Mutation research.
[35] 6-Thioguanine resistant T-lymphocyte determination as a possible indicator of human ionizing radiation exposure. , 1989, Boletin de estudios medicos y biologicos.
[36] B. Davidson,et al. Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in ten subjects determined by direct sequencing of amplified transcripts. , 1989, The Journal of clinical investigation.
[37] W. Bigbee,et al. Flow cytometric analysis of erythrocyte populations in Tn syndrome blood using monoclonal antibodies to glycophorin A and the Tn antigen. , 1990, Cytometry.
[38] A. Tates,et al. Mutations affecting RNA splicing in man are detected more frequently in somatic than in germ cells. , 1990, Mutation research.
[39] R. Albertini,et al. Molecular analysis of in vivo hprt mutations in human T lymphocytes. V. Effects of total body irradiation secondary to radioimmunoglobulin therapy (RIT) , 1990, Mutagenesis.
[40] T. Skopek,et al. DNA sequence analysis of in vivo hprt mutation in human T lymphocytes. , 1990, Mutagenesis.
[41] J. Schöneich,et al. Increased frequency of 6-thioguanine-resistant lymphocytes in peripheral blood of workers employed in cyclophosphamide production. , 1990, Mutation research.
[42] A. Wyrobek,et al. The effect of chemotherapy on the in vivo frequency of glycophorin A 'null' variant erythrocytes. , 1990, Mutation research.