Papers associated with visual system (and grin2c)

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	Synthesis, binding affinity at glutamic acid receptors, neuroprotective effects, and molecular modeling investigation of novel dihydroisoxazole amino acids., Conti P., J Med Chem. October 6, 2005; 48 (20): 6315-25.
	Identification of subunit- and antagonist-specific amino acid residues in the N-Methyl-D-aspartate receptor glutamate-binding pocket., Kinarsky L., J Pharmacol Exp Ther. June 1, 2005; 313 (3): 1066-74.
	Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists., Morley RM., J Med Chem. April 7, 2005; 48 (7): 2627-37.
	The effect of competitive antagonist chain length on NMDA receptor subunit selectivity., Feng B., Neuropharmacology. March 1, 2005; 48 (3): 354-9.
	The micromolar zinc-binding domain on the NMDA receptor subunit NR2B., Rachline J., J Neurosci. January 12, 2005; 25 (2): 308-17.
	Characterization of two novel N-methyl-D-aspartate antagonists: EAA-090 (2-[8,9-dioxo-2,6-diazabicyclo [5.2.0]non-1(7)-en2-yl]ethylphosphonic acid) and EAB-318 (R-alpha-amino-5-chloro-1-(phosphonomethyl)-1H-benzimidazole-2-propanoic acid hydrochloride)., Sun L., J Pharmacol Exp Ther. August 1, 2004; 310 (2): 563-70.
	Structure-activity analysis of a novel NR2C/NR2D-preferring NMDA receptor antagonist: 1-(phenanthrene-2-carbonyl) piperazine-2,3-dicarboxylic acid., Feng B., Br J Pharmacol. February 1, 2004; 141 (3): 508-16.
	Clozapine inhibits isolated N-methyl-D-aspartate receptors expressed in xenopus oocytes in a subunit specific manner., Levine JB., Neurosci Lett. August 7, 2003; 346 (3): 125-8.

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