Differential gene expression of S100 protein family in leukocytes from patients with Kawasaki disease von EBIHARA, Takashi, ENDO, Rika, KIKUTA, Hideaki, ISHIGURO, Nobuhisa, XIAOMING MA, SHIMAZU, Mitsunobu, OTOGURO, Takao, KOBAYASHI, Kunihiko

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Lowe syndrome in a 20-year-old male: the clinical course and genetic analysis in OCRL1 von Tsuji, Yuichirou, Murata, Takahiro, Watanabe, Hiroshi, Shinbo, Toshikazu, Ishiguro, Sei, Shimazu, Mitsunobu

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Flow Cytometric Characteristics of CD34+ Cells in Refractory Anemia: Their Diagnostic Value von Ogata, Kiyoyuki, Kishikawa, Yoshifumi, Shimazaki, Tomoko, Satoh, Chikako, Tamura, Hideto, Otsuka, Yoshihiko, Dan, Kazuo, Hayashi, Akio, Shimazu, Mitsunobu

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Decision Support for Internet Users von Fujimoto, Kazunori, Shimazu, Mitsunobu

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Decision Support for Internet Users: 個人ページの利用価値とプロトタイプの構築を中心に von Fujimoto, Kazunori, Shimazu, Mitsunobu

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SAMPLE SLIDE FOR GENETIC TEST von WAKAMATSU HIROTAKE, SHIMAZU MITSUNOBU

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Decision Support for Internet Users: On Research Progress and Challenge Toward Building Mathematical Models von Fujimoto, Kazunori, Shimazu, Mitsunobu, Yamamoto, Yutaka

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Decision Support for Internet Users von Fujimoto, Kazunori, Shimazu, Mitsunobu, Yamamoto, Yutaka

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Prenatal diagnosis of ornithine transcarbamylase deficiency by using a single nucleated erythrocyte from maternal blood von WATANABE, A, SEKIZAWA, A, TAGUCHI, A, SAITO, H, YANAIHARA, T, SHIMAZU, M, MATSUDA, I

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Identification of two novel mutations in the OCRL1 gene in Japanese families with Lowe syndrome von KUBOTA, T, SAKURAI, A, ARAKAWA, K, SHIMAZU, M, WAKUI, K, FURIHATA, K, FUKUSHIMA, Y

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METHOD FOR DETECTING GENE MUTATION WITH HIGH ACCURACY von WAKAMATSU HIROTAKE, HOSOKAWA YUKI, SHIMAZU MITSUNOBU, NOGAMI YOHEI, TERASAKI KOJI

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Decision Support for Internet Users: On Availability of Personal WebPages and A Prototype Development von Fujimoto, Kazunori, Shimazu, Mitsunobu

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DETECTION METHOD OF TISSUE INJURY OR CELL PROLIFERATIVE DISEASE von SHIMAZU MITSUNOBU, MATSUDA KOICHIRO, FUJIOKA YUICHIRO

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Decision Support for Internet Users: On Research Progress and Challenge Toward Building Mathematical Models von Fujimoto, Kazunori, Shimazu, Mitsunobu, Yamamoto, Yutaka

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Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent’sJapan disease von Igarashi, Takashi, Günther, Willy, Sekine, Takashi, Inatomi, Jun, Shiraga, Hiroshi, Takahashi, Shouri, Suzuki, Junzou, Tsuru, Noboru, Yanagihara, Toshio, Shimazu, Mitsunobu, Jentsch, Thomas J., Thakker, Rajesh V.

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Lowe症候群の1例: OCRL-1遺伝子解析と20年の臨床経過 von 辻, 祐一郎, 村田, 敬寛, 渡辺, 博, 新保, 敏和, 石黒, 精, 島津, 光伸

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METHOD FOR DETECTING TISSUE INJURY OR CELL PROLIFERATIVE DISORDER OF PANCREAS von SHIMAZU MITSUNOBU, MATSUDA KOICHIRO, FUJIOKA YUICHIRO

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Stabilization by the mini-F fragment of a pBR322 derivative bearing the tryptophan operon in Escherichia coli von YUKAWA, Hideaki, KURUSU, Yasurou, SHIMAZU, Mitsunobu, TERASAWA, Masato, OHTA, Akinori, SHIBUYA, Isao

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METHOD, DEVICE AND PROGRAM FOR ACQUIRING KNOWLEDGE AND RECORDING MEDIUM RECORDING THE PROGRAM von SHIMAZU MITSUNOBU, FUJIMOTO KAZUNORI

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DETECTION METHOD FOR TISSUE DAMAGE OR CELL PROLIFERATIVE DISORDER von SHIMAZU MITSUNOBU, MATSUDA KOICHIRO, FUJIOKA YUICHIRO

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