Synthesis of novel IP agonists via N-aminoethyl cyclic amines prepared by decarboxylative ring-opening reactions von Morita, Yasuhiro, Ishigaki, Takeshi, Kawamura, Kuniaki, Hayashi, Ryoji, Isogaya, Masafumi, Kitsukawa, Mika, Miyamoto, Mitsuko, Uchida, Masashi, Iseki, Katsuhiko

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Design and synthesis of selective α1B adrenoceptor antagonists von HAYASHI, Ryoji, OHMORI, Eiji, ISOGAYA, Masafumi, MORIWAKI, Mitsuhiro, KUMAGAI, Hiroki

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Indolylpiperidine derivatives as potent and selective α1B adrenoceptor antagonists von Hayashi, Ryoji, Ohmori, Eiji, Moriwaki, Mitsuhiro, Kumagai, Hiroki, Isogaya, Masafumi

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Piperidine derivatives as nonprostanoid IP receptor agonists von Hayashi, Ryoji, Sakagami, Hideki, Koiwa, Masakazu, Ito, Hiroaki, Miyamoto, Mitsuko, Isogaya, Masafumi

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Piperidine derivatives as nonprostanoid IP receptor agonists 2 von Hayashi, Ryoji, Ito, Hiroaki, Ishigaki, Takeshi, Morita, Yasuhiro, Miyamoto, Mitsuko, Isogaya, Masafumi

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Differential contribution of two serine residues of wild type and constitutively active β 2 ‐adrenoceptors to the interaction with β 2 ‐selective agonists von Kikkawa, Hideo, Kurose, Hitoshi, Isogaya, Masafumi, Sato, Yoji, Nagao, Taku

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Efficient synthesis of a novel m-phenylene derivative as a selective EP₄ agonist inducing follicular growth and maturation in the ovary von Hayashi, Ryoji, Hosono, Yutaka, Nakatsuji, Koji, Tanaka, Yoichiro, Mori, Takeshi, Kanno, Takami, Makita, Kei, Moriwaki, Mitsuhiro, Ohyama, Tomofumi, Ochi, Yasuo, Inada, Chifumi, Isogaya, Masafumi

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Efficient synthesis of a novel m-phenylene derivative as a selective EP 4 agonist inducing follicular growth and maturation in the ovary von Hayashi, Ryoji, Hosono, Yutaka, Nakatsuji, Koji, Tanaka, Yoichiro, Mori, Takeshi, Kanno, Takami, Makita, Kei, Moriwaki, Mitsuhiro, Ohyama, Tomofumi, Ochi, Yasuo, Inada, Chifumi, Isogaya, Masafumi

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Design and synthesis of selective alpha1B adrenoceptor antagonists von Hayashi, Ryoji, Ohmori, Eiji, Isogaya, Masafumi, Moriwaki, Mitsuhiro, Kumagai, Hiroki

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Inhibition of Restenosis by Beraprost Sodium (a Prostaglandin I2 Analogue) in the Atherosclerotic Rabbit Artery After Angioplasty von Isogaya, Masafumi, Yamada, Naohiro, Koike, Hiroshi, Ueno, Yuji, Kumagai, Hiroki, Ochi, Yasuo, Okazaki, Seiji, Nishio, Shintaro

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Design and synthesis of selective α 1B adrenoceptor antagonists von Hayashi, Ryoji, Ohmori, Eiji, Isogaya, Masafumi, Moriwaki, Mitsuhiro, Kumagai, Hiroki

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Design and synthesis of selective alpha sub(1B) adrenoceptor antagonists von Hayashi, Ryoji, Ohmori, Eiji, Isogaya, Masafumi, Moriwaki, Mitsuhiro, Kumagai, Hiroki

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Enhanced cAMP Response of Naturally Occurring Mutant of Human β3-Adrenergic Receptor von Isogaya, Masafumi, Nagao, Taku, Kurose, Hitoshi

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Enhanced cAMP Response of Naturally Occurring Mutant of Human β-Adrenergic Receptor von Isogaya, Masafumi, Nagao, Taku, Kurose, Hitoshi

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Differential contribution of two serine residues of wild type and constitutively active β2‐adrenoceptors to the interaction with β2‐selective agonists von Kikkawa, Hideo, Kurose, Hitoshi, Isogaya, Masafumi, Sato, Yoji, Nagao, Taku

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Molecular characterization of pharmacological properties of T-0509 for β-adrenoceptors von Sato, Yoji, Kurose, Hitoshi, Isogaya, Masafumi, Nagao, Taku

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Enhanced cAMP response of naturally occurring mutant of human beta3-adrenergic receptor von Isogaya, Masafumi, Nagao, Taku, Kurose, Hitoshi

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Domains of β1 and β2 adrenergic receptors to bind subtype selective agonists von Kurose, Hitoshi, Isogaya, Masafumi, Kikkawa, Hideo, Nagao, Taku

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The Role of the Seventh Transmembrane Region in High Affinity Binding of a β2-Selective Agonist TA-2005 von Hideo Kikkawa, Masafumi Isogaya, Taku Nagao, Hitoshi Kurose

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Binding Pockets of the β 1 - and β 2 -Adrenergic Receptors for Subtype-Selective Agonists von Isogaya, Masafumi, Sugimoto, Yoshiyuki, Tanimura, Ryuji, Tanaka, Rie, Kikkawa, Hideo, Nagao, Taku, Kurose, Hitoshi

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