Tsutsumi R - Search Results

1

Functional characterization of YM928, a novel moncompetitive alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist.

Ohno K, Tsutsumi R, Matsumoto N, Yamashita H, Amada Y, Shishikura J, Yatsugi HI, Okada M, Sakamoto S, Yamaguchi T. Ohno K, et al. Among authors: tsutsumi r. J Pharmacol Exp Ther. 2003 Jul;306(1):66-72. doi: 10.1124/jpet.103.049973. Epub 2003 Mar 26. J Pharmacol Exp Ther. 2003. PMID: 12660313

2

The AMPA-receptor antagonist YM90K reduces AMPA receptor-mediated excitotoxicity in rat hippocampal cultures.

Ohno K, Okada M, Tsutsumi R, Sakamoto S, Yamaguchi T. Ohno K, et al. Among authors: tsutsumi r. Jpn J Pharmacol. 1998 Jan;76(1):105-8. doi: 10.1254/jjp.76.105. Jpn J Pharmacol. 1998. PMID: 9517411 Free article.

3

Characterization of cyclothiazide-enhanced kainate excitotoxicity in rat hippocampal cultures.

Ohno K, Okada M, Tsutsumi R, Matsumoto N, Yamaguchi T. Ohno K, et al. Among authors: tsutsumi r. Neurochem Int. 1998 Mar;32(3):265-71. doi: 10.1016/s0197-0186(97)00098-3. Neurochem Int. 1998. PMID: 9587920

4

In-vitro characterization of YM872, a selective, potent and highly water-soluble alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate receptor antagonist.

Kohara A, Okada M, Tsutsumi R, Ohno K, Takahashi M, Shimizu-Sasamata M, Shishikura J, Inami H, Sakamoto S, Yamaguchi T. Kohara A, et al. Among authors: tsutsumi r. J Pharm Pharmacol. 1998 Jul;50(7):795-801. doi: 10.1111/j.2042-7158.1998.tb07142.x. J Pharm Pharmacol. 1998. PMID: 9720630

5

Kainate excitotoxicity is mediated by AMPA- but not kainate-preferring receptors in embryonic rat hippocampal cultures.

Ohno K, Okada M, Tsutsumi R, Kohara A, Yamaguchi T. Ohno K, et al. Among authors: tsutsumi r. Neurochem Int. 1997 Nov;31(5):715-22. doi: 10.1016/s0197-0186(97)00011-9. Neurochem Int. 1997. PMID: 9364457

6

Control of calcium oscillations by phosphorylation of metabotropic glutamate receptors.

Kawabata S, Tsutsumi R, Kohara A, Yamaguchi T, Nakanishi S, Okada M. Kawabata S, et al. Among authors: tsutsumi r. Nature. 1996 Sep 5;383(6595):89-92. doi: 10.1038/383089a0. Nature. 1996. PMID: 8779726

7

Diversity of calcium signaling by metabotropic glutamate receptors.

Kawabata S, Kohara A, Tsutsumi R, Itahana H, Hayashibe S, Yamaguchi T, Okada M. Kawabata S, et al. Among authors: tsutsumi r. J Biol Chem. 1998 Jul 10;273(28):17381-5. doi: 10.1074/jbc.273.28.17381. J Biol Chem. 1998. PMID: 9651322 Free article.

8

Pharmacological profile of (R)-1-[2,3-dihydro-1-(2'-methylphenacyl)-2-oxo- 5-phenyl-1H-1,4-benzodiazepin-3-yl]-3-(3-methylphenyl)urea (YM022), a new potent and selective gastrin/cholecystokinin-B receptor antagonist, in vitro and in vivo.

Nishida A, Miyata K, Tsutsumi R, Yuki H, Akuzawa S, Kobayashi A, Kamato T, Ito H, Yamano M, Katuyama Y, et al. Nishida A, et al. Among authors: tsutsumi r. J Pharmacol Exp Ther. 1994 May;269(2):725-31. J Pharmacol Exp Ther. 1994. PMID: 7910212

9

Pharmacologic profile of (R)-5-[(1-methyl-3-indolyl)carbonyl]-4,5,6,7-tetrahydro-1H- benzimidazole hydrochloride (YM060), a potent and selective 5-hydroxytryptamine3 receptor antagonist, and its enantiomer in the isolated tissue.

Miyata K, Kamato T, Nishida A, Ito H, Katsuyama Y, Iwai A, Yuki H, Yamano M, Tsutsumi R, Ohta M, et al. Miyata K, et al. Among authors: tsutsumi r. J Pharmacol Exp Ther. 1991 Oct;259(1):15-21. J Pharmacol Exp Ther. 1991. PMID: 1656016

10

Serotonin (5-HT)3 receptor blocking activities of YM060, a novel 4,5,6,7-tetrahydrobenzimidazole derivative, and its enantiomer in anesthetized rats.

Miyata K, Kamato T, Yamano M, Nishida A, Ito H, Katsuyama Y, Yuki H, Tsutsumi R, Ohta M, Takeda M, et al. Miyata K, et al. Among authors: tsutsumi r. J Pharmacol Exp Ther. 1991 Nov;259(2):815-9. J Pharmacol Exp Ther. 1991. PMID: 1941629

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