Search Results - Nomura, Tamako

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  1. 1
    Inactivation of a Novel Neuropeptide Y/Peptide YY Receptor Gene in Primate Species

    Inactivation of a Novel Neuropeptide Y/Peptide YY Receptor Gene in Primate Species by Matsumoto, Mitsuyuki, Nomura, Tamako, Momose, Kazuhiro, Ikeda, Yasushi, Kondou, Yutaka, Akiho, Hiraku, Togami, Junji, Kimura, Yasuharu, Okada, Masamichi, Yamaguchi, Tokio

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  2. 2
    Synthesis and Pharmacological Characterization of Novel 6-Fluorochroman Derivatives as Potential 5-HT1A Receptor Antagonists

    Synthesis and Pharmacological Characterization of Novel 6-Fluorochroman Derivatives as Potential 5-HT1A Receptor Antagonists by Yasunaga, Tomoyuki, Kimura, Takenori, Naito, Ryo, Kontani, Toru, Wanibuchi, Fumikazu, Yamashita, Hiroshi, Nomura, Tamako, Tsukamoto, Shin-ichi, Yamaguchi, Tokio, Mase, Toshiyasu

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  3. 3
    In vitro pharmacological profile of YM‐43611, a novel D2‐like receptor antagonist with high affinity and selectivity for dopamine D3 and D4 receptors

    In vitro pharmacological profile of YM‐43611, a novel D2‐like receptor antagonist with high affinity and selectivity for dopamine D3 and D4 receptors by Hidaka, Kazuyuki, Tada, Shoko, Matsumoto, Mitsuyuki, Ohmori, Junya, Tasaki, Yoshikazu, Nomura, Tamako, Usuda, Shinji, Yamaguchi, Tokio

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  4. 4
    In vitro pharmacological profile of YM‐43611, a novel D 2 ‐like receptor antagonist with high affinity and selectivity for dopamine D 3 and D 4 receptors

    In vitro pharmacological profile of YM‐43611, a novel D 2 ‐like receptor antagonist with high affinity and selectivity for dopamine D 3 and D 4 receptors by Hidaka, Kazuyuki, Tada, Shoko, Matsumoto, Mitsuyuki, Ohmori, Junya, Tasaki, Yoshikazu, Nomura, Tamako, Usuda, Shinji, Yamaguchi, Tokio

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  5. 5
    N -[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines:  Synthesis and Wide Range of Antagonism at the Human 5-HT 1A Receptor

    N -[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines:  Synthesis and Wide Range of Antagonism at the Human 5-HT 1A Receptor by Yasunaga, Tomoyuki, Naito, Ryo, Kontani, Toru, Tsukamoto, Shin-ichi, Nomura, Tamako, Yamaguchi, Tokio, Mase, Toshiyasu

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  6. 6
    Synthesis and Pharmacological Characterization of Novel 6-Fluorochroman Derivatives as Potential 5-HT 1A Receptor Antagonists

    Synthesis and Pharmacological Characterization of Novel 6-Fluorochroman Derivatives as Potential 5-HT 1A Receptor Antagonists by Yasunaga, Tomoyuki, Kimura, Takenori, Naito, Ryo, Kontani, Toru, Wanibuchi, Fumikazu, Yamashita, Hiroshi, Nomura, Tamako, Tsukamoto, Shin-ichi, Yamaguchi, Tokio, Mase, Toshiyasu

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  7. 7
    N-[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines:  Synthesis and Wide Range of Antagonism at the Human 5-HT1A Receptor

    N-[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines:  Synthesis and Wide Range of Antagonism at the Human 5-HT1A Receptor by Yasunaga, Tomoyuki, Naito, Ryo, Kontani, Toru, Tsukamoto, Shin-ichi, Nomura, Tamako, Yamaguchi, Tokio, Mase, Toshiyasu

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