Sphingomyelin Deacylase, the Enzyme Involved in the Pathogenesis of Atopic Dermatitis, Is Identical to the beta-Subunit of Acid Ceramidase von Teranishi, Yasuhiro, Kuwahara, Hiroshi, Ueda, Masaru, Takemura, Tadashi, Kusumoto, Masanori, Nakamura, Keiji, Sakai, Jun, Kimura, Toru, Furutani, Yasuji, Kawashima, Makoto, Imokawa, Genji, Nogami-Itoh, Mari

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Discovery of a Novel and Potent Human and Rat β3-Adrenergic Receptor Agonist, [3-[(2R)-[[(2R)-(3-Chlorophenyl)-2-hydroxyethyl]amino]propyl]-1H-indol-7-yloxy]acetic Acid von Harada, Hiroshi, Hirokawa, Yoshimi, Suzuki, Kenji, Hiyama, Yoichi, Oue, Mayumi, Kawashima, Hitoshi, Kato, Hiroshi, Yoshida, Naoyuki, Furutani, Yasuji, Kato, Shiro

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Voreloxin, formerly SNS-595, has potent activity against a broad panel of cancer cell lines and in vivo tumor models von Hoch, Ute, Lynch, Jennifer, Sato, Yuji, Kashimoto, Shigeki, Kajikawa, Fumie, Furutani, Yasuji, Silverman, Jeffrey A

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Tryptamine-based human β3-adrenergic receptor agonists. Part 2: SAR of the methylene derivatives von SAWA, Masaaki, TATEISHI, Hirotaka, MIZUNO, Kazuhiro, HARADA, Hiroshi, OUE, Mayumi, TSUJIUCHI, Hiroshi, FURUTANI, Yasuji, KATO, Shiro

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Cloning and sequencing of the cDNA for human monocyte chemotactic and activating factor (MCAF) von Furutani, Yasuji, Nomura, Hideki, Notake, Mitsue, Oyamada, Yoshihiro, Fukui, Toshikazu, Yamada, Masaaki, Larsen, Christian G., Oppenheim, Joost J., Matsushima, Kouji

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Discovery of a novel and potent human and rat beta3-adrenergic receptor agonist, [3-[(2R)-[[(2R)-(3-chlorophenyl)-2-hydroxyethyl]amino]propyl]-1H-indol-7-yloxy]acetic acid von Harada, Hiroshi, Hirokawa, Yoshimi, Suzuki, Kenji, Hiyama, Yoichi, Oue, Mayumi, Kawashima, Hitoshi, Kato, Hiroshi, Yoshida, Naoyuki, Furutani, Yasuji, Kato, Shiro

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Structural homology of Torpedo californica acetylcholine receptor subunits von Noda, Masaharu, Takahashi, Hideo, Tanabe, Tsutomu, Toyosato, Mitsuyoshi, Kikyotani, Sho, Furutani, Yasuji, Hirose, Tadaaki, Takashima, Hideaki, Inayama, Seiichi, Miyata, Takashi, Numa, Shosaku

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Cloning and sequence analysis of cDNA for bovine adrenal preproenkephalin von Noda, Masaharu, Furutani, Yasuji, Takahashi, Hideo, Toyosato, Mitsuyoshi, Hirose, Tadaaki, Inayama, Seiichi, Nakanishi, Shigetada, Numa, Shosaku

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Mechanism of Amelioration of Insulin Resistance by β3-Adrenoceptor Agonist AJ-9677 in the KK-Ay/Ta Diabetic Obese Mouse Model von KATO, Hiroshi, OHUE, Mayumi, KATO, Kaori, NOMURA, Akinori, TOYOSAWA, Kaoru, FURUTANI, Yasuji, KIMURA, Satoshi, KADOWAKI, Takashi

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Cloning and characterization of the cDNAs for human and rabbit interleukin-1 precursor von Furutani, Yasuji, Notake, Mitsue, Yamayoshi, Michiko, Yamagishi, Jun-ichi, Nomura, Hideki, Ohue, Mayumi, Furuta, Ryuji, Fukui, Toshikazu, Yamada, Masaaki, Nakamura, Shinichi

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Cloning and sequence analysis of cDNA for rat corticotropin-releasing factor precursor von Jingami, Hisato, Mizuno, Noboru, Takahashi, Hideo, Shibahara, Shigeki, Furutani, Yasuji, Imura, Hiroo, Numa, Shosaku

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Novel benzodiazepine receptor ligand AC-4402 is an inverse agonist for GABAAR with pro-cognitive effect in vivo von Hatayama, Yuki, Kiyoshi, Tomoko, Kohayakawa, Hitoshi, Ochi, Yoshiaki, Hashimoto, Takashi, Yoshida, Naoyuki, Furutani, Yasuji

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P3‐435: Novel benzodiazepine receptor ligand AC‐4402 is an inverse agonist for GABAAR with pro‐cognitive effect in vivo von Hatayama, Yuki, Kiyoshi, Tomoko, Kohayakawa, Hitoshi, Ochi, Yoshiaki, Hashimoto, Takashi, Yoshida, Naoyuki, Furutani, Yasuji

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Novel and potent human and rat β3-Adrenergic receptor agonists containing substituted 3-indolylalkylamines von HARADA, Hiroshi, HIROKAWA, Yoshimi, SUZUKI, Kenji, HIYAMA, Yoichi, OUE, Mayumi, KAWASHIMA, Hitoshi, YOSHIDA, Naoyuki, FURUTANI, Yasuji, KATO, Shiro

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Ranirestat (AS-3201), A Potent Aldose Reductase Inhibitor, Normalizes Nerve Sorbitol Levels and Ameliorates Nerve Dysfunction in Diabetic Rats and Patients with Diabetic Sensorimot... von Matsumoto, Takafumi, Ono, Yoshiyuki, Hirose, Toshiyuki, Furutani, Yasuji, Bril, Vera

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Discovery of 1,7-cyclized indoles as a new class of potent and highly selective human β 3-adrenergic receptor agonists with high cell permeability von Mizuno, Kazuhiro, Sawa, Masaaki, Harada, Hiroshi, Taoka, Ikuko, Yamashita, Haruhisa, Oue, Mayumi, Tsujiuchi, Hiroshi, Arai, Yukiyo, Suzuki, Shinya, Furutani, Yasuji, Kato, Shiro

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Tryptamine-based human β 3-adrenergic receptor agonists. Part 1: SAR studies of the 7-position of the indole ring von Mizuno, Kazuhiro, Sawa, Masaaki, Harada, Hiroshi, Tateishi, Hirotaka, Oue, Mayumi, Tsujiuchi, Hiroshi, Furutani, Yasuji, Kato, Shiro

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Tryptamine-based human β 3-adrenergic receptor agonists. Part 2: SAR of the methylene derivatives von Sawa, Masaaki, Tateishi, Hirotaka, Mizuno, Kazuhiro, Harada, Hiroshi, Oue, Mayumi, Tsujiuchi, Hiroshi, Furutani, Yasuji, Kato, Shiro

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Tryptamine-based human β3-adrenergic receptor agonists. Part 3: Improved oral bioavailability via modification of the sulfonamide moiety von SAWA, Masaaki, MIZUNO, Kazuhiro, HARADA, Hiroshi, TATEISHI, Hirotaka, ARAI, Yukiyo, SUZUKI, Shinya, OUE, Mayumi, TSUJIUCHI, Hiroshi, FURUTANI, Yasuji, KATO, Shiro

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Tryptamine-based human β 3-adrenergic receptor agonists. Part 3: Improved oral bioavailability via modification of the sulfonamide moiety von Sawa, Masaaki, Mizuno, Kazuhiro, Harada, Hiroshi, Tateishi, Hirotaka, Arai, Yukiyo, Suzuki, Shinya, Oue, Mayumi, Tsujiuchi, Hiroshi, Furutani, Yasuji, Kato, Shiro

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