Zobrazeno 1 - 10
of 501
pro vyhledávání: '"F, Kanai"'
Autor:
F Kanai
Publikováno v:
Hepatology. 23:1359-1368
Autor:
M. Todaka, Narito Morii, Takanobu Imanaka, S. Kamohara, Shuh Narumiya, Kazuhiro Kishi, Motoaki Shichiri, Yasumasa Mitani, Yousuke Ebina, F Kanai, Hideki Hayashi, Keisuke Tamaoka
Publikováno v:
Scopus-Elsevier
Insulin, guanosine 5´-[γ-thio]triphospate (GTP[S]) and phorbol 12-myristate 13-acetate (PMA) trigger the translocation of GLUT4 (type 4 glucose transporter; insulin-sensitive glucose transporter) from an intracellular pool to the cell surface. We h
Autor:
M. Kan, F. Kanai, M. Iida, H. Jinnouchi, M. Todaka, T. Imanaka, K. Ito, Y. Nishioka, T. Ohnishi, S. Kamohara, al. et
Publikováno v:
Diabetes. 44:1081-1086
Autor:
Yousuke Ebina, Naotake Hashimoto, Takashi Murakami, Hiroyuki Sano, F Kanai, Masaharu Kan, M. Todaka, Mitsuru Iida, Hideaki Jinnouchi, S. Kamohara, Takanobu Imanaka, Hideichi Makino, Sho Yoshida, Tetsuo Ohnishi, Kimio Ito, Yasuhiko Nishioka, Susumu Kagawa, Hideki Hayashi
Publikováno v:
Diabetes. 44:1081-1086
To examine the prevalence of abnormalities in the insulin receptor structure gene in Japanese Patients with non-insulin-dependent diabetes mellitus (NIDDM), a population of 51 patients with NIDDM was screened for mutations in this gene. Patient genom
Autor:
F Kanai, M. Todaka, Satomi Saito, Hideki Hayashi, Takashi Murakami, M Shichiri, K. Ito, Kazuo Ishii, T Nishiyama, Masaharu Kan
Publikováno v:
Journal of Biological Chemistry. 269:29265-29270
We identified two enhancer elements of the mouse GLUT1 gene responsive to serum, growth factor, and oncogenes; the first enhancer element (enhancer-1) is located 2.7 kilobases upstream of the cap site of the gene, and the second one (enhancer-2) is l
Publikováno v:
Methods in molecular medicine. 45
Selective gene therapy represents a potent approach in cancer treatment that utilizes a cell's own nontoxic suicide genes. Currently, the suicide genes under investigation mediate sensitivity by encoding viral or bacterial enzymes that convert inacti
Publikováno v:
Scopus-Elsevier
Stimulation of glucose transport is the main physiological effect of insulin in target tissues. This effect is linked to translocation of the GLUT4 glucose transporter from an intracellular pool to the cell surface. To elucidate the molecular mechani
Autor:
N Miyake, F Shibasaki, S. Kamohara, T Takenawa, Hideki Hayashi, Yousuke Ebina, Yasuhiko Nishioka, Yoshihiro Fukui, F Kanai
Publikováno v:
Journal of Biological Chemistry. 267:22575-22580
After adding insulin to cells overexpressing the insulin receptor, the activity of phosphatidylinositol (PI) 3-kinase in the anti-phosphotyrosine immunoprecipitates was rapidly and greatly increased. This enzyme may therefore be a substrate for the i
Publikováno v:
Biochemical Journal. 280:769-775
Insulin causes a dramatic and rapid increase in phosphatidylinositol 3-kinase activity in the anti-phosphotyrosine immunoprecipitates of cells overexpressing the human insulin receptor. This enzyme may therefore be a mediator of insulin signal transd
Autor:
F Kanai, Yasuo Shinohara, Masataka Mori, Eiichi Araki, Fumio Shimada, Yousuke Ebina, Tetsuya Shirotani, Motoaki Shichiri, Takashi Murakami
Publikováno v:
Journal of Biological Chemistry. 266:3944-3948
Fragments of 5'-flanking sequences of the human insulin receptor gene were analyzed in transient expression assays after transfection of cell lines with expression assays after transfection of cell lines with an improved low background chloramphenico