A. Kohara

发表

Control of calcium oscillations by phosphorylation of metabotropic glutamate receptors

Shigetada Nakanishi, S. Nakanishi, Tokio Yamaguchi, 1996, Nature.

Radioligand Binding Properties and Pharmacological Characterization of 6-Amino-N-cyclohexyl-N,3-dimethylthiazolo[3,2-a]benzimidazole-2-carboxamide (YM-298198), a High-Affinity, Selective, and Noncompetitive Antagonist of Metabotropic Glutamate Receptor Type 1

Seiji Tamura, Y. Shitaka, S. Kawabata, 2005, Journal of Pharmacology and Experimental Therapeutics.

Neuroprotective effects of the selective type 1 metabotropic glutamate receptor antagonist YM-202074 in rat stroke models

Seiji Tamura, Shigeki Kawabata, Shigeki Kawabata, 2008, Brain Research.

The unique feature of dog liver cytosolic glutathione S-transferases. An isozyme not retained on the affinity column has the highest activity toward 1,2-dichloro-4-nitrobenzene.

T. Igarashi, T. Satoh, A. Kohara, 1991, The Journal of biological chemistry.

YM872: a selective, potent and highly water-soluble alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor antagonist.

A. Kohara, Tokio Yamaguchi, M. Okada, 2006, CNS drug reviews.

Synthesis and biological evaluation of 3-biphenyl-4-yl-4-phenyl-4H-1,2,4-triazoles as novel glycine transporter 1 inhibitors.

A. Kohara, S. Tsukamoto, S. Sakamoto, 2011, Journal of medicinal chemistry.

Substituent effect of a fluorine atom on the mutagenicity of nitroquinolines.

A. Kohara, A. Hakura, K. Saeki, 1999, Mutation research.

Allodynia and Hyperalgesia in Adjuvant-Induced Arthritic Rats: Time Course of Progression and Efficacy of Analgesics

A. Kohara, Tokio Yamaguchi, M. Okada, 2003, Journal of Pharmacology and Experimental Therapeutics.

Antinociceptive profile of a selective metabotropic glutamate receptor 1 antagonist YM-230888 in chronic pain rodent models.

H. Itahana, Y. Shitaka, A. Kohara, 2007, European journal of pharmacology.

Amelioration of Neuropathic Pain by Novel Transient Receptor Potential Vanilloid 1 Antagonist AS1928370 in Rats without Hyperthermic Effect

T. Aoki, N. Matsuoka, A. Kohara, 2011, Journal of Pharmacology and Experimental Therapeutics.

In‐vitro Characterization of YM872, a Selective, Potent and Highly Water‐soluble α‐Amino‐3‐hydroxy‐5‐methylisoxazole‐4‐propionate Receptor Antagonist

R. Tsutsumi, A. Kohara, Tokio Yamaguchi, 1998, The Journal of pharmacy and pharmacology.

Diversity of Calcium Signaling by Metabotropic Glutamate Receptors*

H. Itahana, S. Kawabata, R. Tsutsumi, 1998, The Journal of Biological Chemistry.

Characterization of YM90K, a selective and potent antagonist of AMPA receptors, in rat cortical mRNA-injected Xenopus oocytes.

A. Kohara, M. Okada, T. Yamaguchi, 1996, European journal of pharmacology.

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

R. Tsutsumi, A. Kohara, Tokio Yamaguchi, 1997, Neurochemistry International.

JPET #050781 1 Title page Title: Allodynia and Hyperalgesia in Adjuvant-Induced Arthritic Rats: Time-Course of Their Progression and Efficacy of Analgesics for Them

A. Kohara, A. Iwai, T. Toya, 2003 .

Amelioration of Neuropathic Pain by Novel Transient Receptor Potential Vanilloid 1 Antagonist AS1928370 in Rats without Hyperthermic Effect

T. Aoki, N. Matsuoka, A. Kohara, 2011, Journal of Pharmacology and Experimental Therapeutics.

CNS Drug Reviews

G. Perrault, H. Schoemaker, G. Griebel, 2000 .