(+)- and (-)-cis-2-Aminomethylcyclopropanecarboxylic Acids Show Opposite Pharmacology at Recombinant ρ1 and ρ2 GABAC Receptors
- 29 July 2008
- journal article
- research article
- Published by Wiley in Journal of Neurochemistry
- Vol. 75 (6) , 2602-2610
- https://doi.org/10.1046/j.1471-4159.2000.0752602.x
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Ligand Recognition Sites on P2XReceptors Studied by Quantitative Autoradiography of [3H]α,β-Methylene-ATP Binding in Rat BrainBiochemical and Biophysical Research Communications, 1998
- Sequences in the Amino Termini of GABA ρ and GABAA Subunits Specify Their Selective Interaction In VitroJournal of Neurochemistry, 1998
- Insensitivity to anaesthetic agents conferred by a class of GABAA receptor subunitNature, 1997
- The first selective antagonist for a GABAC receptorBioorganic & Medicinal Chemistry Letters, 1996
- GABAc receptorsTrends in Neurosciences, 1995
- Tiagabine, SK&F 89976-A, CI-966, and NNC-711 are selective for the cloned GABA transporter GAT-1European Journal of Pharmacology: Molecular Pharmacology, 1994
- GABA ρ2 receptor pharmacological profile: GABA recognition site similarities to ρ1European Journal of Pharmacology: Molecular Pharmacology, 1993
- Synthesis of Analogues of GABA. XIII. An Alternative Route to (Z)-4-Aminocrotonic AcidAustralian Journal of Chemistry, 1985
- Liberation of amino acids during the preparation of brain slicesBrain Research, 1975
- HIGH AFFINITY UPTAKE OF TRANSMITTERS: STUDIES ON THE UPTAKE OF l‐ASPARTATE, GABA, l‐GLUTAMATE AND GLYCINE IN CAT SPINAL CORDJournal of Neurochemistry, 1973