Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Yumiko Sakakibara"'
Autor:
Junko, FUKADA, Yuki, KUMAZAWA, Yayoi, KAMAKURA, Maya, NUNOTANI, Yumiko, SAKAKIBARA, Junichi, TURUTA, Kayoko, YAMADA, Chigusa, HYOUDO
Publikováno v:
愛知県立大学看護学部紀要 = Bulletin of Aichi Prefectural University School of Nursing & Health. 17:25-32
Publikováno v:
Journal of Bronchology. 11:37-39
Publikováno v:
Chemical and Pharmaceutical Bulletin. 40:588-592
Indenestrol A (IA) is a metabolite of diethylstilbestrol (DES), and indenestrol B (IB) is an analog of IA. IA was simply obtained from E,E-dienestrol in the presence of dilute sulfuric acid, and a mixture of IA and IB was formed by thermal cyclizatio
Autor:
Kiyoshi Hasegawa, Aiko Hirata, Taiko Oda, Yoshihiro Sato, Michio Matsuhashi, Yumiko Sakakibara, Hazime Saitô, Masahiko Kodama
Publikováno v:
Biochemical Pharmacology. 39:167-172
We previously reported on the inhibition of microtubule polymerization and the formation of ribbon structures by synthetic estrogens [Sato et al., J Biochem101: 1247–1252, 1987]. The present investigation aimed to analyse these effects in vitro on
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:3419-3422
We have reported that meso-hexestrol, a synthetic estrogen, inhibits microtubule assembly and induces microtubule proteins into twisted ribbon structures. On the other hand, Serrano et al. proved that S-tubulin, which lacks the C-terminal moiety of t
Publikováno v:
Biologicalpharmaceutical bulletin. 18(10)
We have previously reported the inhibitory effects of diethylstilbestrol (1) and optically active indenestrol derivatives on microtubule polymerization in vitro and their disruptive effect on cytoplasmic microtubules and cytotoxicity in cultured Chin
Publikováno v:
Mutation research. 289(2)
We have reported that (+)-, (−)- and (±)-indenestrols A and B (IA and IB respectively) inhibit the polymerization of microtubule proteins isolated from porcine brain in vitro. In this study, the effects of (+)-, (−)- and (±)-IA and IB on the re
Publikováno v:
Chemicalpharmaceutical bulletin. 40(10)
The effects of 32-oxygenated lanosterol derivatives on 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase activity and cholesterol biosynthesis from [24,25-3H]24,25-dihydrolanosterol were studied. Among the derivatives, 3 beta-hydroxylanost-7-
Autor:
Hiroshi Tsujibo, Yoshihiro Sato, Izumi Saito, Yoshihiko Inamori, Taiko Oda, Yumiko Sakakibara
Publikováno v:
Chemicalpharmaceutical bulletin. 40(8)
We examined the inhibitory activities of 3,3'-dihydroxy-alpha,beta-diethylstilbene (DDS) and 3,3',4,5'-tetrahydroxystilbene (THS) on microtubule assembly in vitro and their effects on chromosome number and cellular microtubule networks in Chinese ham