C. Tsai

发表

CGS 8216: receptor binding characteristics of a potent benzodiazepine antagonist.

R. A. Lovell, A. Czernik, W. D. Cash, 1982, Life sciences.

CPP, a selective N-methyl-D-aspartate (NMDA)-type receptor antagonist: characterization in vitro and in vivo.

J. Lehmann, D. A. Bennett, D. Murphy, 1987, The Journal of pharmacology and experimental therapeutics.

Trans-2-carboxy-3-pyrrolidineacetic acid (CPAA), a novel agonist at NMDA-type receptors

J. Lehmann, C. Tsai, J. Schneider, 1988, Neuroscience Letters.

Enhancement of the antiviral and interferon-inducing activities of poly r(A-U) by carminic acid.

S. Kitareewan, K. Rosenthal, C. Tsai, 1988, Life sciences.

Enhancement of the antiviral activity of poly r(A-U) by ametantrone and mitoxantrone.

C. Tsai, J. Jamison, K. Krabill, 1990, Life Science.

CGS 19755, a selective and competitive N-methyl-D-aspartate-type excitatory amino acid receptor antagonist.

C. Sinton, M. Williams, J. Lehmann, 1988, The Journal of pharmacology and experimental therapeutics.

Glycine-evoked release of [3H]acetylcholine from rat striatal slices is independent of the NMDA receptor

J. Lehmann, C. Tsai, Cynthia A. Taylor, 1988, Naunyn-Schmiedeberg's Archives of Pharmacology.

Homocysteic Acid as a Putative Excitatory Amino Acid Neurotransmitter: I. Postsynaptic Characteristics at N‐Methyl‐D‐Aspartate‐Type Receptors on Striatal Cholinergic Interneurons

P. Wood, J. Lehmann, C. Tsai, 1988, Journal of neurochemistry.

ALX 5407: a potent, selective inhibitor of the hGlyT1 glycine transporter.

V. Ognyanov, S. Lechner, M. De Vivo, 2001, Molecular pharmacology.

CGS 19755 is a potent and competitive antagonist at NMDA-type receptors.

P. Wood, B. Meldrum, J. Lehmann, 1988, European journal of pharmacology.

Serotonin 5-HT1A receptors mediate inhibition of tyrosine hydroxylation in rat striatum.

A. Azzaro, C. Tsai, E. A. Johnson, 1993, The Journal of pharmacology and experimental therapeutics.