Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Fumihiro Nakamori"'
Autor:
Hiroyuki Usuda, Fumihiro Nakamori, Takayuki Inoue, Hiroaki Tominaga, Yutaka Nakajima, Masamichi Inami, Ayako Moritomo, Misato Ito, Jun Maeda, Takeshi Hondo, Yasuyuki Higashi, Hiroki Morio, Koji Nakamura, Shohei Shirakami, Hiroaki Yamagishi
Publikováno v:
Bioorganic & Medicinal Chemistry. 25:5311-5326
Janus kinases (JAKs) play a crucial role in cytokine mediated signal transduction. JAK inhibitors have emerged as effective immunomodulative agents for the prevention of transplant rejection. We previously reported that the tricyclic imidazo-pyrrolop
Autor:
Yuji Ohishi, Ken-ichi Fukumoto, Fumihiro Nakamori, Shinsuke Yamanaka, Hiroaki Muta, Ken Kurosaki
Publikováno v:
Journal of Nuclear Science and Technology. 54:1267-1273
In order to conduct defueling operations for the decommissioning of the reactor at the Fukushima Daiichi nuclear power plant, an understanding of the physical properties of ZrSiO4 is of extreme imp...
Publikováno v:
Journal of Nuclear Materials. 487:121-127
During a molten core–concrete interaction, molten oxides consisting of molten core materials (UO2 and ZrO2) and concrete (Al2O3, SiO2, CaO) are formed. Reliable data on the physical properties of the molten oxides will allow us to accurately predic
Autor:
Shinsuke Yamanaka, Fumihiro Nakamori, Ken-ichi Fukumoto, Yuji Ohishi, Masaya Kumagai, Ken Kurosaki, Hiroaki Muta
Publikováno v:
Transactions of the Atomic Energy Society of Japan. 15:223-228
Autor:
Hiroaki Muta, Yuji Ohishi, Ken-ichi Fukumoto, Ken Kurosaki, Shinsuke Yamanaka, Fumihiro Nakamori
Publikováno v:
Journal of Nuclear Materials. 467:612-617
ZrB 2 appears to have formed in the fuel debris at the Fukushima Daiichi nuclear disaster site, through the reaction between Zircaloy cladding materials and the control rod material B 4 C. Since ZrB 2 has a high melting point of 3518 K, the ceramic h
Autor:
Katsuhiro Yamano, Fumihiro Nakamori, Takako Furukawa, Kazuhiro Tetsuka, Yoichi Naritomi, Kenji Tabata, Shigeyuki Terashita, Hiroyuki Moriguchi, Toshio Teramura
Publikováno v:
Xenobiotica. 44:205-216
1. Glucuronidation via UDP-glucuronosyltransferase (UGT) in the intestine has been reported to influence the pharmacokinetics (PK) of drugs; however, information concerning the differences in activity between species is limited. Here, we investigated
Autor:
Takayuki Inoue, Hiroshi Sasaki, Fumie Takahashi, Fumihiro Nakamori, Masamichi Inami, Yutaka Nakajima, Misato Ito, Koji Nakamura, Naohiro Aoyama, Keiko Hatanaka, Shohei Shirakami, Ayako Moritomo
Publikováno v:
Bioorganicmedicinal chemistry. 24(19)
In organ transplantation, T cell-mediated immune responses play a key role in the rejection of allografts. Janus kinase 3 (JAK3) is specifically expressed in hematopoietic cells and associated with regulation of T cell development via interleukin-2 s
Autor:
Katsuhiro Yamano, Keitaro Kadono, Hiroyuki Moriguchi, Fumihiro Nakamori, Shigeyuki Terashita, Yoichi Naritomi, Toshio Teramura, Kazuhiro Tetsuka, Ken Ichi Hosoya, Takako Furukawa
Publikováno v:
Drug Metabolism and Disposition. 40:1771-1777
We investigated whether the effects of intestinal glucuronidation on the first-pass effect can be predicted from in vitro data for UDP-glucuronosyltransferase (UGT) substrates. Human in vitro intrinsic glucuronidation clearance (CL(int, UGT)) for 11
Autor:
Katsuhiro Yamano, Toshio Teramura, Kazuhiro Tetsuka, Fumihiro Nakamori, Shigeyuki Terashita, Takako Furukawa, Yoichi Naritomi, Hiroyuki Moriguchi
Publikováno v:
Drug Metabolism and Pharmacokinetics. 27:171-180
UDP-glucuronosyltransferase (UGT) is highly expressed in the small intestine and catalyzes the glucuronidation of small molecules, which may affect the oral bioavailability of drugs. However, no method of predicting the in vivo observed fraction of a
Autor:
Shigeyuki Terashita, Fumihiro Nakamori, Fujiko Takamura, Hiroya Miura, Hidetsugu Murai, Toshio Teramura, Yoichi Naritomi, Masako Furutani
Publikováno v:
Drug Metabolism and Pharmacokinetics. 26:465-473
A method for quantitatively predicting the hepatic clearance of drugs by UDP-glucuronosyltransferases (UGTs) from in vitro data has not yet been established. We examined the relationship between in vitro and in vivo intrinsic clearance by rat hepatic