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收藏分享 收藏 Suppression of a pituitary-ovarian axis by chronic oral administration of a novel nonpeptide gonadotropin-releasing hormone antagonist, TAK-013, in cynomolgus monkeys
Hara, T; Araki, H; Kusaka, M; Harada, M; Cho, N; Suzuki, N; Furuya, S; Fujino, M 分享 收藏 A G protein-coupled receptor responsive to bile acids一种对胆汁酸有反应的g蛋白偶联受体Kawamata, Y; Fujii, R; Hosoya, M; Harada, M; Yoshida, H; Miwa, M; Fukusumi, S; Habata, Y; Itoh, T; Shintani, Y; Hinuma, S; Fujisawa, Y; Fujino, M 分享 收藏 分享 收藏 Identification of a neuropeptide modified with bromine as an endogenous ligand for GPR7Fujii, R; Yoshida, H; Fukusumi, S; Habata, Y; Hosoya, M; Kawamata, Y; Yano, T; Hinuma, S; Kitada, C; Asami, T; Mori, M; Fujisawa, Y; Fujino, M 分享 收藏 Identification of neuropeptide W as the endogenous ligand for orphan G-protein-coupled receptors GPR7 and GPR8Shimomura, Y; Harada, M; Goto, M; Sugo, T; Matsumoto, Y; Abe, M; Watanabe, T; Asami, T; Kitada, C; Mori, M; Onda, H; Fujino, M 分享 收藏 Increased expression of the human Ca2+-activated Cl- channel 1 (CaCC1) gene in the asthmatic airwayHoshino, M; Morita, S; Iwashita, H; Sagiya, Y; Nagi, T; Nakanishi, A; Ashida, Y; Nishimura, O; Fujisawa, Y; Fujino, M 分享 收藏 T-226296: a novel, orally active and selective melanin-concentrating hormone receptor antagonistTakekawa, S; Asami, A; Ishihara, Y; Terauchi, J; Kato, K; Shimomura, Y; Mori, M; Murakoshi, H; Kato, K; Suzuki, N; Nishimura, O; Fujino, M 分享 收藏 Novel betacellulin derivatives - Separation of the differentiation activity from the mitogenic activityItoh, T; Kondo, M; Tanaka, Y; Kobayashi, M; Sasada, R; Igarashi, K; Suenaga, M; Koyama, N; Nishimura, O; Fujino, M 分享 收藏 分享 收藏 Apelin, the natural ligand of the orphan seven-transmembrane receptor APJ, inhibits human immunodeficiency virus type 1 entryCayabyab, M; Hinuma, S; Farzan, M; Choe, H; Fukusumi, S; Kitada, C; Nishizawa, N; Hosoya, M; Nishimura, O; Messele, T; Pollakis, G; Goudsmit, J; Fujino, M; Sodroski, J 分享 收藏 New neuropeptides containing carboxy-terminal RFamide and their receptor in mammalsHinuma, S; Shintani, Y; Fukusumi, S; Iijima, N; Matsumoto, Y; Hosoya, M; Fujii, R; Watanabe, T; Kikuchi, K; Terao, Y; Yano, T; Yamamoto, T; Kawamata, Y; Habata, Y; Asada, M; Kitada, C; Kurokawa, T; Onda, H; Nishimura, O; Tanaka, M; Ibata, Y; Fujino, M 分享 收藏 Identification and functional characterization of a novel subtype of neuromedin U receptorHosoya, M; Moriya, T; Kawamata, Y; Ohkubo, S; Fujii, R; Matsui, H; Shintani, Y; Fukusumi, S; Habata, Y; Hinuma, S; Onda, H; Nishimura, O; Fujino, M 分享 收藏 分享 收藏 Molecular and functional characteristics of APJ - Tissue distribution of mRNA and interaction with the endogenous ligand apelinHosoya, M; Kawamata, Y; Fukusumi, S; Fujii, R; Habata, Y; Hinuma, S; Kitada, C; Honda, S; Kurokawa, T; Onda, H; Nishimura, O; Fujino, M 分享 收藏 Discovery of novel, potent, and selective small-molecule CCR5 antagonists as anti-HIV-1 agents: Synthesis and biological evaluation of anilide derivatives with a quaternary ammonium moietyShiraishi, M; Aramaki, Y; Seto, M; Imoto, H; Nishikawa, Y; Kanzaki, N; Okamoto, M; Sawada, H; Nishimura, O; Baba, M; Fujino, M 分享 收藏 Isolation and cDNA cloning of a novel galanin-like peptide (GALP) from porcine hypothalamusOhtaki, T; Kumano, S; Ishibashi, Y; Ogi, K; Matsui, H; Harada, M; Kitada, C; Kurokawa, T; Onda, H; Fujino, M 分享 收藏 A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activityBaba, M; Nishimura, O; Kanzaki, N; Okamoto, M; Sawada, H; Iizawa, Y; Shiraishi, M; Aramaki, Y; Okonogi, K; Ogawa, Y; Meguro, K; Fujino, M 分享 收藏 Discovery of a novel, potent, and orally active nonpeptide antagonist of the human luteinizing hormone-releasing hormone (LHRH) receptorCho, NB; Harada, M; Imaeda, T; Imada, T; Matsumoto, H; Hayase, Y; Sasaki, S; Furuya, S; Suzuki, N; Okubo, S; Ogi, K; Endo, S; Onda, H; Fujino, M 分享 收藏 
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