鳥取大学における染色体医工学研究の歩み

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59-63, 19902. Ishizaki K., Oshimura M., Sasaki M.S., Nakamura Y., Ikenaga M.: Human chromosome 9 can complement UV-sensitivity of xeroderma pigmentosum group A cells. Mutation Res., 235: 209-215, 19903. Ejima Y., Oshimura M., Sasaki, M.S.: Establishment of a novel immortalized cell line from ataxia telangiectasia fi broblasts and its use for the chromosomal assignment of radiosensitivity gene. Int. J. Rad. Biol., 58: 989-997, 1990 4. Ejima Y., Oshimura M., Sasaki M.S.: Determination of the chromosomal site for the human radiosensitive ataxia telangiectasia gene by chromosome transfer. Mutation Res., 250: 337-343, 1991 5. Parshad R., Price F.M., Oshimura M., Barrett J.C., Satoh H., Weissman B.E., Stanbridge E.J., Sanford, K.K.: Complementation of a DNA repair defi ciency in six human tumor cell lines by chromosome 11. Hum. Genet., 88: 524-528, 19926. Kodama S., Komatsu K., Okumura Y., Oshimura M.: Suppression of X-ray-induced chromosome aberrations in ataxia telangiectasia cells by introduction of a normal human chromosome 11. Mutation Res., 293: 31-37, 19927. Chen D.J., Park M.S., Campbell E., Oshimura M., Liu P., Zhao Y., White B.F., Siciliano M.J.: Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2. Genomics 13:1088-1094, 19928. Kurimasa A., Ohno K., Oshimura M.: Restoration of the cholesterol metabolism in 3T3 cell lines derived from the sphingomyelinosis mouse (spm/spm) by transfer of a human chromosome 18. Hum. Genet., 92: 157-162, 19939. Ejima Y., Oshimura M., Sasaki M. S.: Use of microcell hybrids for analysis of the 11q23 region and improved localization of the A-T Group A/C genes. Ataxia-Telangiectasia. Cell Biology, 77: 75-85, 199310. Zdzienicka M.Z., Verhaegh G.W.C.T., Jongmans W., Jaspers N.G.J., Oshimura M., James M.R., Lohman, P.H.M.: At-like radiosensitive rodent cell mutants: An alternative approach to the isolation of the AT gene(s). Ataxia-Telangiectasia. Cell Biology, 77: 87-97, 199311. Jongmans W., Wigant J., Oshimura M., James M.R., Lohman P.H.M., Zdzienicka M.Z.: Human chromosome 11 does not complement the defect in AT-like Chinese hamster V79 cell mutants. Human Genet., 92: 259-264, 199312. Kurimasa A., Nagata Y., Shimizu M., Emi M., Nakamura Y., Oshimura M.: A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1→q11.1. Hum. Genet., 93: 21-26, 199413. 押村光雄:染色体移入による細胞老化遺伝子のマッピング 細胞工学 12:180-184, 199314. Kurimasa A., Ohno K., Oshimura M.: Restoration of the cholesterol metabolism in 3T3 cell lines derived from the sphingomyelinosis mouse (spm/spm) by transfer of a human chromosome 18. Hum. Genet., 92: 157-162, 199315. 押村光雄:染色体導入による不死化細胞の老化誘導 組織培養 19: 450-454, 199316. Ejima Y., Oshimura M., Sasaki M. S.: Use of microcell hybrids for analysis of the 11q23 region and improved localization of the A-T Group A/C genes. Ataxia-Telangiectasia. Cell Biology, 77: 75-85, 199317. Zdzienicka M.Z., Verhaegh G.W.C.T., Jongmans W., Morolli B., Jaspers N.G.J., Oshimura M.: Functional complementation studies with X-ray-sensitive mutants of Chinese hamster cells closely resembling ataxia-telangiectasia cells. Int. J. Radiat. Biol., 66: S189-S195, 199418. Peterson S.R., Kurimasa A., Oshimura M., Dynan W.S., Bradbury E.M., Chen, D.J.: Loss of the catalytic subunit of the DNA-dependent protein kinase in DNA double-strand-break-repair mutant mammalian cells. Proc. Natl. Acad. Sci. USA, 92: 3171-3174, 199519. Zenklusen J.C., Oshimura M., Barrett J.C., Conti C.J.: Human chromosome 11 inhibits tumorigenicity of a murine squamous cell carcinoma cell line. Genes, Chromosomes and Cancer, 13: 47-53, 199520. Zdzienicka M.Z., Jongmans W., Oshimura M., Priestley A. Whitemore G.F., Jeggo P.A.: 156

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