Anxiogenic properties of an inverse agonist selective forα3 subunit-containing GABAAreceptors

Author:

Atack John R,Hutson Peter H,Collinson Neil,Marshall George,Bentley Graham,Moyes Christopher,Cook Susan M,Collins Ian,Wafford Keith,McKernan Ruth M,Dawson Gerard R

Publisher

Wiley

Subject

Pharmacology

Reference54 articles.

1. Regional differences in the inhibition of mouse in vivo[3H]Ro 15-1788 binding reflect selectivity for α1 versus α2 and α3 subunit-containing GABAA receptors;ATACK;Neuropharmacology,1999

2. Comparison of benzodiazepine (BZ) receptor agonists in two rodent activity tests;BAYLEY;J. Psychopharmacol.,1996

3. Pharmacological characterization of a novel cell line expressing human α4β3δ GABAA receptors;BROWN;Br. J. Pharmacol.,2002

4. Identification of amino acid residues responsible for the α5 subunit binding selectivity of L-655,708, a benzodiazepine binding site ligand at the GABAA receptor;CASULA;J. Neurochem.,2001

5. 6,7-Dihydro-2-benzothiophen-4(5H)-ones: a novel class of GABA-A α5 receptor inverse agonists;CHAMBERS;J. Med. Chem.,2002

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