Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Minoru, Seto"'
Autor:
Asako Hitomi, Steven K. Feske, Koh Kawasaki, Yasuo Sasaki, Galen V. Henderson, Farzaneh A. Sorond, James K. Liao, Toshio Asano, Minoru Seto
Publikováno v:
Brain Research. 1257:89-93
Background Rho-kinase (ROCK) is a downstream effector of Rho GTPase that is known to regulate various pathological processes important to the development of ischemic stroke, such as thrombus formation, inflammation, and vasospasm. Inhibition of ROCK
Autor:
Kazuo Yano, Koh Kawasaki, Yuji Ohtsuka, Shunsuke Tawara, Hiroshi Kuriyama, Yuki Yoshino, Toshio Asano, Kunie Sasaki, Minoru Seto, Shin'ichi Satoh, Ichiro Ikegaki
Publikováno v:
Journal of Molecular Neuroscience. 39:59-68
Whether Rho-kinase activity is really associated with the pathogenesis of cerebral infarction remains unclear. To consider this question, we investigated correspondences between severity of neurological deficit, infarct size, amount of various marker
Autor:
Mamunur Rashid, Minoru Seto, Hiroaki Shimokawa, Kazuo Yano, Yoshihiro Fukumoto, Shunsuke Tawara
Publikováno v:
Circulation Journal. 73:361-370
Background The pleiotropic effects of HMG-CoA reductase inhibitors (statins) are thought to be mediated through inhibition of small GTP-binding proteins; however, it remains to be examined whether clinical concentrations/doses of statins actually exe
Autor:
Yoshio Suzuki, Minoru Seto, Shin'ichi Satoh, Hirotoshi Sugiyama, Kintomo Takakura, Masato Shibuya
Publikováno v:
Neurologia medico-chirurgica. 48:241-248
Sub-analysis of the fasudil post-marketing surveillance study compared the safety and efficacy of fasudil plus ozagrel to fasudil only. A total of 3690 patients received fasudil and 1138 received fasudil plus ozagrel between 1995 and 2000. The occurr
Publikováno v:
Journal of Cardiovascular Pharmacology. 50:17-24
The Rho kinase (ROCK) isoforms, ROCK1 and ROCK2, were initially discovered as downstream targets of the small GTP-binding protein Rho. Because ROCKs mediate various important cellular functions such as cell shape, motility, secretion, proliferation,
Autor:
Yasuo Mori, Yuji Kiuchi, Shunichi Shimizu, Minoru Wakamori, Masakazu Ishii, Katsuhiko Sakurada, Takaharu Okada, Masami Takahashi, Takashi Yoshida, Minoru Seto
Publikováno v:
The Journal of Physiology. 570:219-235
Mammalian homologues of Drosophila transient receptor potential (TRP) proteins are responsible for receptor-activated Ca2+ influx in vertebrate cells. We previously reported the involvement of intracellular Ca2+ in the receptor-mediated activation of
Publikováno v:
Journal of the Neurological Sciences. 238:31-39
Background: A multicenter, double-blind, placebo-controlled study was conducted to assess the efficacy and safety of fasudil, a Rhokinase inhibitor (RKI), in the treatment of acute ischemic stroke. Methods: A total of 160 patients, who were able to r
Autor:
Hideaki Karaki, Masatoshi Hori, Yoon-Sun Kim, Hiroshi Ozaki, Makoto Egawa, Minoru Seto, Hideharu Kanzaki, Hiroshi Nakazawa, Katsuhiko Yasuda
Publikováno v:
British Journal of Pharmacology. 140:1303-1312
Activation of protein kinase C (PKC) by phorbol 12,13-dibutylate (PDBu, 1 μM) induced sustained contractions with no increase in [Ca2+]i in nonpregnant and pregnant human myometria. The contractile effects of PDBu in pregnant myometrium were much gr
Autor:
Quang-Dé Nguyen, Sandrine Faivre, Christian Gespach, Takeshi Endo, Christine Rivat, Erik Bruyneel, Shahin Emami, Minoru Seto, Marc Mareel
Publikováno v:
The FASEB Journal. 16:565-576
Thrombin and proteinase-activated receptors (PAR) specifically regulate several functions that markedly enhance the transformation phenotype such as inflammation, cell proliferation, tumor growth, and metastasis. We recently reported that thrombin in
Autor:
Ling Pan, Minoru Seto, Hiroshi Watanabe, Quang-Kim Tran, Kazuhiko Takeuchi, Kyoichi Ohashi, Hong-Yen Le
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 21:509-515
Abstract —Monocytes/macrophages are present in all stages of atherosclerosis. Although many of their activities depend to various extents on changes in intracellular Ca 2+ concentration ([Ca 2+ ] i ), mechanisms regulating [Ca 2+ ] i in these cells