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Bioorganic & Medicinal Chemistry|July 23, 2018
Design and synthesis of novel anti-hyperalgesic agents based on 6-prenylnaringenin as the T-type calcium channel blockersHuy Du Nguyen, Takuya Okada, Shun Kitamura, et al.
European Journal of Pharmacology|September 19, 2020
Essential role of Cav3.2 T-type calcium channels in butyrate-induced colonic pain and nociceptor hypersensitivity in miceMaho Tsubota, Kazuki Matsui, Maki Nakano, et al.
European Journal of Pharmacology|April 24, 2025
HMGB1 derived from macrophages and enteric glial cells contributes to the butyrate-induced colonic hypersensitivity in miceMaho Tsubota, Kana Sasaki, Eunkyung Shin, et al.
Journal of Pharmacological Sciences|September 8, 2019
Genetic deletion of Cav3.2 T-type calcium channels abolishes H2S-dependent somatic and visceral pain signaling in C57BL/6 miceKazuki Matsui, Maho Tsubota, Saaya Fukushi, et al.
European Journal of Medicinal Chemistry|September 8, 2022
Discovery of pimozide derivatives as novel T-type calcium channel inhibitors with little binding affinity to dopamine D2 receptors for treatment of somatic and visceral painYoshihito Kasanami, Chihiro Ishikawa, Takahiro Kino, et al.
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