Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Kiyoko Bando"'
Autor:
Yukari Fujiwara, Dong-sik Ham, Byung Hyune Choi, Yat P. Tsui, James Ooi, Yoshie Tsurumaki, Tomohiro Yoneda, Feng-Cheng Chou, Pawan Gupta, Yongjun Liu, Takeshi Watanabe, Joo Y. Lee, Yuu Moriya, Yoshiteru Kamiyama, Chih-Yuan Ho, Kou Omura, Ling-Mei Wang, Kiyoko Bando, Guangyang Liu, Yohan Bae, Masayuki Kanki, Hiroshi Karasawa
Publikováno v:
Cytotherapy. 23:874-885
Background aims Cell-based regenerative medicine is an innovative field that can potentially alter the overall survival and quality of life of patients with devastating diseases. Several cell therapy products (CTPs) have been approved within the last
Autor:
Tomohiro Yoneda, Toshimitsu Tanaka, Kiyoko Bando, Byung Hyune Choi, Ryan Chang, Yukari Fujiwara, Pawan Kumar Gupta, Dong-sik Ham, Hiroshi Karasawa, Shinobu Kuwae, Shing-mou Lee, Yuu Moriya, Koji Takakura, Yoshie Tsurumaki, Takeshi Watanabe, Keiji Yoshimura, Masayuki Nomura
Publikováno v:
Cytotherapy. 24(9)
The 4th Asia Partnership Conference of Regenerative Medicine (APACRM) was held online on April 15, 2021, to promote regulatory harmonization of regenerative medicine products throughout Asia. Recognizing domestic regulatory guidelines within each cou
Autor:
Akihiko Kiyoshi, Isao Shimizu, Yasunori Katsura, Tadashi Tsubouchi, Kiyoko Bando, Seiko Oku, Shinji Tsujimoto, Toru Yamada, Kazuhiro Chihara, Yukiko Mine, Takeshi Kunimatsu
Publikováno v:
European Journal of Pharmacology. 826:96-105
The pharmacological activity of DSP-6952, a novel compound was investigated, compared to that of clinically efficacious gastrointestinal (GI) prokinetic 5-hydroxytryptamine 4 (5-HT 4 ) receptor agonists. DSP-6952 had a strong affinity of K i = 51.9 n
Autor:
Eiichiro Ogimura, Tetsuya Nakagawa, Mayuko Tokizono, Kousei Ito, Shuichi Sekine, Kiyoko Bando
Publikováno v:
Journal of Pharmaceutical Sciences. 106:2509-2514
We previously reported a cell-based toxicity assay using sandwich-cultured hepatocytes in combination with a titrated amount of human bile acid (BA) species. In this assay, test compound-induced inhibition of BA efflux from sandwich-cultured hepatocy
Autor:
Toru Yamada, Izumi Matsumoto, Mami Kouchi, Yuta Fujii, Tomoaki Tochitani, Izuru Miyawaki, Akihito Yamashita, Kiyoko Bando
Publikováno v:
Toxicologic Pathology. 45:756-763
The aim of this study was to evaluate the usefulness of simultaneous measurement of plasma steroids, including precursors, for the evaluation of drug effects on adrenal steroidogenesis in vivo. Plasma concentrations of corticosterone and its precurso
Publikováno v:
Toxicological Sciences. 158:347-355
Troglitazone and pioglitazone were developed as thiazolidinedione-type antidiabetes drugs, but only troglitazone was withdrawn from the markets due to severe liver injury. As both troglitazone and its sulfate metabolite are strong inhibitors of the b
Publikováno v:
The Journal of Toxicological Sciences. 42:519-527
Monitoring dramatic changes in intracellular calcium ion levels during cardiac contraction and relaxation, known as calcium transient, in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) would be an attractive strategy for asses
Publikováno v:
The AAPS Journal. 21
Accurate prediction of human pharmacokinetics for drugs remains challenging, especially for non-cytochrome P450 (P450) substrates. Hepatocytes might be suitable for predicting hepatic intrinsic clearance (CLint) of new chemical entities, because they
Publikováno v:
Biopharmaceuticsdrug disposition. 40(5-6)
The metabolism and pharmacokinetics of DSP-0565 [2-(2'-fluoro[1,1'-biphenyl]-2-yl)acetamide], an antiepileptic drug candidate, was investigated in rats, dogs, and humans. In human hepatocytes, [14 C]DSP-0565 was primarily metabolized via amide bond h
Autor:
Tadashi, Tsubouchi, Takeshi, Kunimatsu, Shinji, Tsujimoto, Akihiko, Kiyoshi, Yasunori, Katsura, Seiko, Oku, Kazuhiro, Chihara, Yukiko, Mine, Toru, Yamada, Isao, Shimizu, Kiyoko, Bando
Publikováno v:
European journal of pharmacology. 826
The pharmacological activity of DSP-6952, a novel compound was investigated, compared to that of clinically efficacious gastrointestinal (GI) prokinetic 5-hydroxytryptamine