Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Hirokazu Ishikawa"'
Autor:
Kazuhiko Namekata, Naoki Tsuji, Xiaoli Guo, Euido Nishijima, Sari Honda, Yuta Kitamura, Atsushi Yamasaki, Masamichi Kishida, Jun Takeyama, Hirokazu Ishikawa, Youichi Shinozaki, Atsuko Kimura, Chikako Harada, Takayuki Harada
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-8 (2023)
Abstract Dedicator of cytokinesis 3 (DOCK3) is an atypical member of the guanine nucleotide exchange factors (GEFs) and plays important roles in neurite outgrowth. DOCK3 forms a complex with Engulfment and cell motility protein 1 (Elmo1) and effectiv
Externí odkaz:
https://doaj.org/article/2c0459c1ded845d2905aa9f9482ad0c3
Autor:
Kumiko Koyama, Hirokazu Ishikawa, Manabu Abe, Yoshinobu Shiose, Suguru Ueno, Yang Qiu, Kenji Nakamaru, Masato Murakami
Publikováno v:
PLoS ONE, Vol 17, Iss 5 (2022)
ErbB3 (HER3), a member of the HER family, is overexpressed in various cancers and plays an important role in cell proliferation and survival. Certain HER3 mutations have also been identified as oncogenic drivers, making them potential therapeutic tar
Externí odkaz:
https://doaj.org/article/c5db8888d872468a953ab15144af6a21
Publikováno v:
Nihon Toseki Igakkai Zasshi. 54:303-307
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports
Scientific Reports
Fumarate hydratase (FH) is an enzyme in the tricarboxylic acid (TCA) cycle, biallelic loss-of-function mutations of which are associated with hereditary leiomyomatosis and renal cell cancer. However, how FH defect modulates intracellular metabolic fl
Autor:
Yoshinobu Shiose, Suguru Ueno, Manabu Abe, Kenji Nakamaru, Hirokazu Ishikawa, Kumiko Koyama, Masato Murakami
Publikováno v:
Cancer Research. 80:5201-5201
Background: U3-1402, a novel HER3-targeting antibody-drug conjugate (ADC) composed of a fully human anti-HER3 antibody (patritumab), tetrapeptide-based linker, and topoisomerase I inhibitor payload, is currently being studied in clinical trials for p
Autor:
Kiyoshi Arai, Yuka Morikawa, Tsuyoshi Homma, Naoko Ubukata, Toshio Sada, Hiyoyuki Tsuruoka, Hirokazu Ishikawa, Makoto Mizuno, Aoki Kazumasa
Publikováno v:
European Journal of Pharmacology. 761:226-234
The present study was designed to characterize the pharmacological profile of CS-3150, a novel non-steroidal mineralocorticoid receptor antagonist. In the radioligand-binding assay, CS-3150 inhibited (3)H-aldosterone binding to mineralocorticoid rece
Publikováno v:
Biological and Pharmaceutical Bulletin. 27:288-294
RS-7897 is a novel antianginal nitrate containing an L-2-oxothiazolidine-4-carboxylic acid (OTCA) and unlike other organic nitrates does not induce nitrate tolerance. OTCA is known to be converted to L-cysteine (L-Cys) by rat 5-oxo-prolinase (5-OPase
Publikováno v:
British Journal of Pharmacology. 139:1085-1094
We studied the effect of a new angiotensin II type 1 (AT1) receptor antagonist, olmesartan medoxomil (olmesartan), on the fibrogenic responses in rat hepatic stellate cells (HSCs) and liver fibrogenesis. Olmesartan (1 mg kg−1 per day) was orally ad
Publikováno v:
PROCEEDINGS OF CIVIL ENGINEERING IN THE OCEAN. 19:457-462
Publikováno v:
PROCEEDINGS OF CIVIL ENGINEERING IN THE OCEAN. 19:451-456