Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Shunsuke Nakazawa"'
Autor:
Yuka Kimura, Shunsuke Nakazawa, Kantaro Nishigori, Yuki Mori, Junji Ichihara, Yoshichika Yoshioka
Publikováno v:
Pharmacology Research & Perspectives, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract The dopamine D1 receptor (D1R) is associated with schizophrenia, Parkinson's disease, and attention deficit hyperactivity disorder. Although the receptor is considered a therapeutic target for these diseases, its neurophysiological function
Externí odkaz:
https://doaj.org/article/1218c93d99e040d4b942b565981e822b
Autor:
Shunsuke Nakazawa, Akira Haramiishi, Kohei Fukuda, Yukie Kanayama, Toshinori Watanabe, Masahiro Yuki, Moriya Ohkuma, Kazuhiro Takeda, Kazuhide Kimbara, Masaki Shintani
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0191393 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0186248.].
Externí odkaz:
https://doaj.org/article/6bbb54772d3b4f1cad3a5c28ef441ae3
Autor:
Shunsuke Nakazawa, Akira Haramiishi, Kohei Fukuda, Yukie Kanayama, Toshinori Watanabe, Masahiro Yuki, Moriya Ohkuma, Kazuhiro Takeda, Kazuhide Kimbara, Masaki Shintani
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186248 (2017)
Self-transmissible plasmids are classified into two types based on their sex pili: short and rigid pili, and long and flexible pili. The transferability of two plasmids with different types of sex pili, pBP136 and pCAR1, was compared in stirring liqu
Externí odkaz:
https://doaj.org/article/4fb85f5b8a2a4a6d888e68ef46553e19
Autor:
Shunsuke NAKAZAWA, Yuki SAKAI
Publikováno v:
Journal of Structural and Construction Engineering (Transactions of AIJ). 87:680-689
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1528350d408b11c8d58eceb9dfc6d453
https://doi.org/10.3130/aijs.87.680
https://doi.org/10.3130/aijs.87.680
Autor:
Yuka Kimura, Shunsuke Nakazawa, Kantaro Nishigori, Yuki Mori, Junji Ichihara, Yoshichika Yoshioka
Publikováno v:
Pharmacology Research & Perspectives. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc9a56ace9c3a57a4359e2791ffe83a7
https://doi.org/10.1002/prp2.1055
https://doi.org/10.1002/prp2.1055
Autor:
Shunsuke Nakazawa
Publikováno v:
Social Science Japan Journal. 19:244-247
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::511aebcfac14dcf2866f9445ccb6d63f
https://doi.org/10.1093/ssjj/jyw031
https://doi.org/10.1093/ssjj/jyw031
Publikováno v:
Journal of Japan Association for Earthquake Engineering. 20:6_65-6_84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8083028c6913b2f76828fac79cc550d
https://doi.org/10.5610/jaee.20.6_65
https://doi.org/10.5610/jaee.20.6_65
Publikováno v:
Journal of Japan Association for Earthquake Engineering. 19:7_67-7_104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1301e6b2867b5f640b5833014aebbc09
https://doi.org/10.5610/jaee.19.7_67
https://doi.org/10.5610/jaee.19.7_67
Autor:
Satoshi Tanaka, Noriyasu Hirasawa, Kazuyuki Furuta, Yasushi Okuno, Mayuko Natsuhara, Kazuhisa Nakayama, Soken Tsuchiya, Hirotsugu Takano, Mariko Sakanaka, Yukihiko Sugimoto, Hiroshi Ohtsu, Shunsuke Nakazawa, Masahiro Nishibori, Robin L. Thurmond, Atsushi Ichikawa
Publikováno v:
European Journal of Immunology. 44:204-214
Mast cells are the major sources of histamine, which is released in response to immunological stimulations. The synthesis of histamine is catalyzed by histidine decarboxylase (HDC). Previous studies have shown that Hdc(-/-) mast cells exhibit aberran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76f82dbf2793ece97f5546163148859f
https://doi.org/10.1002/eji.201343838
https://doi.org/10.1002/eji.201343838
Autor:
Hiroshi Mizuma, Hirotaka Onoe, Tomoko Horisawa, Shunsuke Nakazawa, Akihiro Kawasaki, Naohiro Nishimura, Hisashi Doi, Chihiro Yokoyama
Publikováno v:
Psychopharmacology. 225:329-339
Lurasidone is a novel antipsychotic drug with potent binding affinity for dopamine D2 and serotonin (5-hydroxytryptamine, 5-HT)2A, 5-HT7, and 5-HT1A receptors. Previous pharmacological studies have revealed that lurasidone exhibits a preferable profi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a16512c8981a7c65ca63955cd30fafec
https://doi.org/10.1007/s00213-012-2815-9
https://doi.org/10.1007/s00213-012-2815-9