鳥取大学における染色体医工学研究の歩み

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M., McAuley E.Z., Caff rey T.M., Timmusk T., Pruunsild P., Koppel I., Lind P.A., Matsumoto-Itaba N., Nicod J., Xiong L., Joober R., Enard W., Krinsky B., Nanba E., Richardson A.J., Riley B.P., Martin N.G., Strittmatter S.M., Moller H.J., Rujescu D., St. Clair D., Muglia P., Roos J.L., Fisher S.E., Wade-Martins R., Rouleau G.A., Stein J.F., Karayiorgou M., Geschwind D.H., Ragoussis J., Kendler K.S., Airaksinen M.S., Oshimura M., Delisi L.E., Monaco A.P.: LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry, 12:1129-39, 200758. Nguyen P., Cui H., Bisht KS., Sun L., Patel K., Lee RS., Kugoh H., Oshimura M., Feinberg AP., Gius D.CTCFL/BORIS is a methylation-independent DNA-binding protein that preferentially binds to the paternal H19 diff erentially methylated region. Cancer Res., 68:5546-51, 200859. Yotova IY, Vlatkovic IM, Pauler FM, Warczok KE, Ambros PF, Oshimura M, Theussl HC, Gessler M, Wagner EF, Barlow DP.: Identifi cation of the human homolog of the imprinted mouse Air non-coding RNA. Genomics, 92:464-73. 2008 60. Meguro-Horike M, Yasui DH, Powell W, Schroeder DI, Oshimura M, Lasalle JM, Horike S.: Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome. Hum Mol Genet. 20:3798-3810, 201161. Itoh M., Tahimic C.G., Ide S., Otsuki A., Sasaoka T., Noguchi S., Oshimura M., Goto Y., Kurimasa A.: J Biol Chem. 287:13859-13867, 2012 I: DNA marker and mapping(DNAマーカーとマッピング)1. Yamakawa K., Takahashi E., Saito H., Sato T., Oshimura M., Hori, T. and Nakamura, Y.: Isolation and mapping of 75 new DNA markers on human chromosome 3. Genomics, 9: 536-543, 19912. Seya T., Okada M., Hara T., Matsumoto M., Miyagawa S., Oshimura M.: Human complement regulatory proteins expressed on mouse A9 cells containing a human chromosome 1. Immunology, 74: 719-724, 1991 3. Hosoya M., Kimura C., Ogi K., Ohkubo S., Miyamoto Y., Kugoh H., Shimizu M., Onda H., Oshimura M., Arimura A., Fujino M.: Structure of the human pituitary adenylate cyclase activating polypeptide (PACAP) gene. Biochem. Biophys. Acta., 1129: 199-206, 19924. Sugino H., Oshimura M., Matsubara K.: Banding profiles of LTR of human endogenous retrovirus HERV-A in 24 chromosomes in somatic cell hybrids. Genomics, 13: 461-464, 19925. Iizuka M., Mashiyama S., Oshimura M., Sekiya T., Hayashi, K.: Cloning and polymerase chain reaction-single-strand conformation polymorphism analysis of anonymous alu repeats on chromosome 11. Genomics, 12: 139-146, 19926. Saito S., Okui K., Tokino T., Oshimura M., Nakamura Y.: Isolation and mapping of 68 RFLP markers on human chromosome 6. Am. J. Hum. Genet., 50: 65-70, 19927. Tamari M., Hamaguchi M., Shimizu M., Oshimura M., Takayama H., Kohno T., Yamaguchi N., Sugimura T., Terada M., Yokota J.: Ordering of human chromosome 3p markers by radiation hybrid mapping. Genomics, 13: 705-712, 19928. Jinno Y., Harada N., Yoshiura K., Ohta T., Tohma T., Hirota T. Tsukamoto K., Deng H., Oshimura M., Niikawa N.: A simple and efficient amplification method of DNA with unknown sequences and its application to microdissection/ microcloning. J. Biochem., 112: 75-80, 19929. Emi M., Takahashi E., Koyama K., Okui K., Oshimura M., Nakamura Y.: Isolation and mapping of 88 new RFLP markers on human chromosome 8. Genomics, 13: 1261-1266, 199210. Yamakawa K., Takahashi E., Saito H., Sato T., Oshimura M., Hori T., Nakamura Y.: Isolation and mapping of 75 new DNA markers on human chromosome 3. Genomics, 9: 536-543, 199111. 押村光雄,栗政明弘,清水素行:微小核融合細胞のゲノム解析への利用 蛋白質 核酸 酵素 38: 563-572, 199312. Yamamoto K., Seto M., Akao Y., Iida S., Nakazawa S., Oshimura M., Takahashi M., Takahashi T., Ueda R.: 166

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