鳥取大学における染色体医工学研究の歩み

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Gene rearrangement and truncated mRNA in cell with 11q23 translocation. Oncogene, 8: 479-485, 199313. Kohno T., Takayama H., Hamaguchi M., Takano H., Yamaguchi N., Tsuda H., Hirohashi S., Vissing H., Shimizu M., Oshimura M., Yokota J.: Deletion mapping of chromosome 3p in human uterine cervical cancer. Oncogene, 8: 1825-1832, 199314. Ohe N., Yamasaki Y., Sogawa K., Inazawa J., Ariyama T., Oshimura M., Fujii -K.Y.: Chromosomal localization and cDNA sequence of human BTEB, a GC box binding protein. Somatic cell and Mol. Genet., 19: 499-503, 199315. Fujiwara Y., Ohata H., Emi M., Okui K., Koyama K., Tsuchiya E., Nakajima T., Moden M., Mori T., Kurimasa A., Oshimura M., Nakamura Y.: A3-Mb physical map of the chromosome region 8p21.3-p22, including a 600-kb region commonly deleted in Human Hepatocellular Carcinoma, colorectal cancer, and Non-small Cell Lung Cancer. Genes, Chromosomes and Cancer, 10: 7-14, 199416. Ema M., Matsushita N., Sogawa K., Ariyama T., Inazawa J., Nemoto T., Ota M., Oshimura M., Fujii-Kuriyama Y.: Human arylhydrocarbon receptor: functional expression and chromosomal assignment to 7p21. J. Biochem., 116: 845-851, 199417. Horikawa I., Tanaka H., Yuasa Y., Suzuki M., Oshimura M.: Molecular cloning of a novel human cDNA on chromosome 1q21 and its mouse homolog encoding a nuclear protein with DNA-binding ability. Biochem. Biophys. Res. Commun., 208: 999-1007, 199518. Kugoh H., Nakagawa Y., Mitsuya K., Mita T., Suzuki M., Suzuki N., Uejima H., Yuasa Y. Oshimura M.: Isolation and mapping of 186 new DNA markers on human chromosome 1. Genomics, 27: 207-210, 199519. Urimasa A., Suzuki N., Kumano S., Li H., Wells D., Wagner M. J., Chen F., Chen D. J., Oshimura M.: Construction of 110 cosmid markers and a 4.5 Mb YAC contig on human chromosome 8p12-q11. Genomics, 28: 147-153, 199520. Katoh M., Nakagawa Y., Yawata T., Kumano S., Kobayashi E., Kurimasa A., Kugoh H., Oshimura M.: Cosmids and transcribed sequences from chromosome 11q23. Jpn. J. Hum. Genet., 40: 307-317, 199521. Kitagawa K., Hatada I., Wang X., Yamaoka T., Nojima H., Inazawa J., Abe T., Mitsuya K., Oshimura M., Murata A., Monden M., Mukai T.: Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1. Genomics, 30: 257-263, 199522. Kobayashi D., Ieiri I., Hirota T., Takane H., Maegawa S., Kigawa J., Suzuki H., Nanba E., Oshimura M., Terakawa N., Otsubo K., Mine K., Sugiyama Y.: Functional assessment of abcg2 (bcrp) gene polymorphisms to proteinExpressi onin human placenta. Drug Metabolisum and Disposition, 33:94-101, 200423. Nguyen G., Bukanov N., Oshimura M., Smith CL.: Cloneless genomic DNA analysis: an effi cient and simple methods for de novo genomic sequencing projects and gap fi lling. Biomol Eng., 21:135-44.200524. Spence J.M., Fournier R.E., Oshimura M., Regnier V., Farr C.J.: Topoisomerase II cleavage activity within the human D11Z1 and DXZ1 alpha-satellite arrays. Chromosome Res., 13:637-48, 2005J: Others(その他)1. 長田愉以子,押村光雄:遺伝性癌と非遺伝性癌の相違 臨床科学 28: 1311-1315, 19922. Kohno T., Sekine T., Tobisu K., Oshimura M., Yokota J.: Chromosome 3p deletion in a cell carcinoma cell line established from a patient with von Hippel-Lindau desease Jpn. J. Clin. Oncol., 23: 226-231, 19933. Suzuki N., Sugawara M., Sugimoto M., Oshimura M., Furuichi Y.: Gene expression of transferred human chromosome 8 in mouse cell lines. Biochem. Biophys. Res. Commun., 230: 315-319, 19974. Mukaida N., Kodama S., Suzuki K., Oshimura M., Watanabe M.: Transmission of genomic instability from a single irradiated human chromosome to the progeny of unirradiated cells, Radiat Res., 167:675-81, 20075. Kai Y., Wang CC., Kishigami S., Kazuki Y., Abe S., Takiguchi M., Shirayoshi Y., Inoue T., Ito H., 167

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