Research ArticleNEUROPHARMACOLOGY
Novel Structure Having Antagonist Actions at Both the Glycine Site of the N-Methyl-d-Aspartate Receptor and Neuronal Voltage-Sensitive Sodium Channels: Biochemical, Electrophysiological, and Behavioral Characterization
Lawrence D. Snell, David J. Claffey, James A. Ruth, C. Fernando Valenzuela, Rita Cardoso, Zejun Wang, Simon R. Levinson, William A. Sather, Anna V. Williamson, Nan C. Ingersoll, Larissa Ovchinnikova, Sanjiv V. Bhave, Paula L. Hoffman and Boris Tabakoff
Journal of Pharmacology and Experimental Therapeutics January 2000, 292 (1) 215-227;
Lawrence D. Snell
David J. Claffey
James A. Ruth
C. Fernando Valenzuela
Rita Cardoso
Zejun Wang
Simon R. Levinson
William A. Sather
Anna V. Williamson
Nan C. Ingersoll
Larissa Ovchinnikova
Sanjiv V. Bhave
Paula L. Hoffman
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In this issue
Journal of Pharmacology and Experimental Therapeutics
Vol. 292, Issue 1
1 Jan 2000
Research ArticleNEUROPHARMACOLOGY
Novel Structure Having Antagonist Actions at Both the Glycine Site of the N-Methyl-d-Aspartate Receptor and Neuronal Voltage-Sensitive Sodium Channels: Biochemical, Electrophysiological, and Behavioral Characterization
Lawrence D. Snell, David J. Claffey, James A. Ruth, C. Fernando Valenzuela, Rita Cardoso, Zejun Wang, Simon R. Levinson, William A. Sather, Anna V. Williamson, Nan C. Ingersoll, Larissa Ovchinnikova, Sanjiv V. Bhave, Paula L. Hoffman and Boris Tabakoff
Journal of Pharmacology and Experimental Therapeutics January 1, 2000, 292 (1) 215-227;
Research ArticleNEUROPHARMACOLOGY
Novel Structure Having Antagonist Actions at Both the Glycine Site of the N-Methyl-d-Aspartate Receptor and Neuronal Voltage-Sensitive Sodium Channels: Biochemical, Electrophysiological, and Behavioral Characterization
Lawrence D. Snell, David J. Claffey, James A. Ruth, C. Fernando Valenzuela, Rita Cardoso, Zejun Wang, Simon R. Levinson, William A. Sather, Anna V. Williamson, Nan C. Ingersoll, Larissa Ovchinnikova, Sanjiv V. Bhave, Paula L. Hoffman and Boris Tabakoff
Journal of Pharmacology and Experimental Therapeutics January 1, 2000, 292 (1) 215-227;
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