Kamohara S - Search Results

1

Insulin treatment stimulates the tyrosine phosphorylation of the alpha-type 85-kDa subunit of phosphatidylinositol 3-kinase in vivo.

Hayashi H, Kamohara S, Nishioka Y, Kanai F, Miyake N, Fukui Y, Shibasaki F, Takenawa T, Ebina Y. Hayashi H, et al. Among authors: kamohara s. J Biol Chem. 1992 Nov 5;267(31):22575-80. J Biol Chem. 1992. PMID: 1385401 Free article.

2

Direct demonstration of insulin-induced GLUT4 translocation to the surface of intact cells by insertion of a c-myc epitope into an exofacial GLUT4 domain.

Kanai F, Nishioka Y, Hayashi H, Kamohara S, Todaka M, Ebina Y. Kanai F, et al. Among authors: kamohara s. J Biol Chem. 1993 Jul 5;268(19):14523-6. J Biol Chem. 1993. PMID: 7686158 Free article.

3

Platelet-derived growth factor triggers translocation of the insulin-regulatable glucose transporter (type 4) predominantly through phosphatidylinositol 3-kinase binding sites on the receptor.

Kamohara S, Hayashi H, Todaka M, Kanai F, Ishii K, Imanaka T, Escobedo JA, Williams LT, Ebina Y. Kamohara S, et al. Proc Natl Acad Sci U S A. 1995 Feb 14;92(4):1077-81. doi: 10.1073/pnas.92.4.1077. Proc Natl Acad Sci U S A. 1995. PMID: 7862637 Free PMC article.

4

Epidermal growth factor triggers the translocation of insulin-responsive glucose transporter (GLUT4).

Ishii K, Kamohara S, Hayashi H, Todaka M, Kanai F, Imanaka T, Ebina Y. Ishii K, et al. Among authors: kamohara s. Biochem Biophys Res Commun. 1994 Nov 30;205(1):857-63. doi: 10.1006/bbrc.1994.2743. Biochem Biophys Res Commun. 1994. PMID: 7999123

5

The alpha-type 85-kDa subunit of phosphatidylinositol 3-kinase is phosphorylated at tyrosines 368, 580, and 607 by the insulin receptor.

Hayashi H, Nishioka Y, Kamohara S, Kanai F, Ishii K, Fukui Y, Shibasaki F, Takenawa T, Kido H, Katsunuma N, et al. Hayashi H, et al. Among authors: kamohara s. J Biol Chem. 1993 Apr 5;268(10):7107-17. J Biol Chem. 1993. PMID: 8385099 Free article.

6

Insulin-stimulated GLUT4 translocation is relevant to the phosphorylation of IRS-1 and the activity of PI3-kinase.

Kanai F, Ito K, Todaka M, Hayashi H, Kamohara S, Ishii K, Okada T, Hazeki O, Ui M, Ebina Y. Kanai F, et al. Among authors: kamohara s. Biochem Biophys Res Commun. 1993 Sep 15;195(2):762-8. doi: 10.1006/bbrc.1993.2111. Biochem Biophys Res Commun. 1993. PMID: 8396927

We had already developed a novel cell line to detect GLUT4 on the cell surface, directly and sensitively (Kanai, F., Nishioka, Y., Hayashi, H., Kamohara, S., Todaka, M., and Ebina, Y. (1993) J. Biol. Chem. 268, 14523-14526). We stably expressed a mutant insulin rece …

We had already developed a novel cell line to detect GLUT4 on the cell surface, directly and sensitively (Kanai, F., Nishioka, Y., Hayashi, …

7

Gq-coupled receptors transmit the signal for GLUT4 translocation via an insulin-independent pathway.

Kishi K, Hayashi H, Wang L, Kamohara S, Tamaoka K, Shimizu T, Ushikubi F, Narumiya S, Ebina Y. Kishi K, et al. Among authors: kamohara s. J Biol Chem. 1996 Oct 25;271(43):26561-8. doi: 10.1074/jbc.271.43.26561. J Biol Chem. 1996. PMID: 8900127 Free article.

8

Possible domains responsible for intracellular targeting and insulin-dependent translocation of glucose transporter type 4.

Ishii K, Hayashi H, Todaka M, Kamohara S, Kanai F, Jinnouchi H, Wang L, Ebina Y. Ishii K, et al. Among authors: kamohara s. Biochem J. 1995 Aug 1;309 ( Pt 3)(Pt 3):813-23. doi: 10.1042/bj3090813. Biochem J. 1995. PMID: 7543750 Free PMC article.

9

Frequency of mutations of insulin receptor gene in Japanese patients with NIDDM.

Kan M, Kanai F, Iida M, Jinnouchi H, Todaka M, Imanaka T, Ito K, Nishioka Y, Ohnishi T, Kamohara S, et al. Kan M, et al. Among authors: kamohara s. Diabetes. 1995 Sep;44(9):1081-6. doi: 10.2337/diab.44.9.1081. Diabetes. 1995. PMID: 7657032

10

[Molecular mechanisms of insulin-stimulated glucose uptake and PI3-kinase].

Hayashi H, Kamohara S, Ishii K, Todaka M, Kanai F, Ebina Y. Hayashi H, et al. Among authors: kamohara s. Nihon Rinsho. 1994 Oct;52(10):2665-72. Nihon Rinsho. 1994. PMID: 7983796 Review. Japanese. No abstract available.

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