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Molecular Pharmacology|December 1, 1993
Role of the beta subunit in determining the pharmacology of human gamma-aminobutyric acid type A receptorsK L Hadingham, P B Wingrove, K A Wafford, et al.Proceedings of the National Academy of Sciences of the United States of America|July 15, 1992
Stable expression of mammalian type A gamma-aminobutyric acid receptors in mouse cells: demonstration of functional assembly of benzodiazepine-responsive sitesK L Hadingham, P C Harkness, R M McKernan, et al.Journal of Medicinal Chemistry|July 18, 1997
4-Heterocyclylpiperidines as selective high-affinity ligands at the human dopamine D4 receptorM Rowley, I Collins, H B Broughton, et al.The Journal of Pharmacology and Experimental Therapeutics|February 12, 1998
L-745,870, a subtype selective dopamine D4 receptor antagonist, does not exhibit a neuroleptic-like profile in rodent behavioral testsL J Bristow, N Collinson, G P Cook, et al.Journal of Neurochemistry|June 1, 1996
Generation and characterisation of stable cell lines expressing recombinant human N-methyl-D-aspartate receptor subtypesS Grimwood, B Le Bourdellès, J R Atack, et al.The Journal of Pharmacology and Experimental Therapeutics|November 14, 1997
Biological profile of L-745,870, a selective antagonist with high affinity for the dopamine D4 receptorS Patel, S Freedman, K L Chapman, et al.Nature Neuroscience|May 18, 2000
Sedative but not anxiolytic properties of benzodiazepines are mediated by the GABA(A) receptor alpha1 subtypeR M McKernan, T W Rosahl, D S Reynolds, et al.Pageof 10