ANIMAL CELL;
ARTICLE;
CHLORIDE CURRENT;
CONTROLLED STUDY;
DRUG EFFECT;
DRUG EFFICACY;
DRUG POTENCY;
DRUG SPECIFICITY;
DRUG STRUCTURE;
FEMALE;
MICROELECTRODE;
MODULATION;
MOUSE;
NONHUMAN;
OOCYTE;
PERFUSION;
PRIORITY JOURNAL;
PROTEIN EXPRESSION;
VOLTAGE CLAMP;
XENOPUS LAEVIS;
ANIMAL;
CHEMISTRY;
International Union of Pharmacology. XV. Subtypes of gamma-aminobutyric acidA receptors: Classification on the basis of subunit structure and receptor function
Barnard EA, Skolnick P, Olsen RW, Mohler H, Sieghart W, Biggio G, Braestrup C, Bateson AN, and Langer SZ (1998) International Union of Pharmacology. XV. Subtypes of gamma-aminobutyric acidA receptors: classification on the basis of subunit structure and receptor function. Pharmacol Rev 50:291-313.
GABAA receptor subtypes differentiated by their gamma-subunit variants: Prevalence, pharmacology and subunit architecture
Benke D, Honer M, Michel C, and Mohler H (1996) GABAA receptor subtypes differentiated by their gamma-subunit variants: prevalence, pharmacology and subunit architecture. Neuropharmacology 35:1413-1423.
Structural determinants of fast desensitization and desensitization- deactivation coupling in GABAa receptors
Bianchi MT, Haas KF, and Macdonald RL (2001) Structural determinants of fast desensitization and desensitization-deactivation coupling in GABAa receptors. J Neurosci 21:1127-1136.
Effects of gamma2S subunit incorporation on GABAA receptor macroscopic kinetics
Boileau AJ, Li T, Benkwitz C, Czajkowski C, and Pearce RA (2003) Effects of gamma2S subunit incorporation on GABAA receptor macroscopic kinetics. Neuropharmacology 44:1003-1012.
Subtle changes in residue 77 of the γ subunit of α1β2γ2 GABAA receptors drastically alter the affinity for ligands of the benzodiazepine binding site
Buhr A, Baur R, and Sigel E (1997) Subtle changes in residue 77 of the γ subunit of α1β2γ2 GABAA receptors drastically alter the affinity for ligands of the benzodiazepine binding site. J Biol Chem 272:11799-11804.
Transfer of 1,4-dihydropyridine sensitivity from L-type to class A (BI) calcium channels
Grabner M, Wang Z, Hering S, Striessnig J, and Glossmann H (1996) Transfer of 1,4-dihydropyridine sensitivity from L-type to class A (BI) calcium channels. Neuron 16:207-218.
The diversity of GABAA receptors. Pharmacological and electrophysiological properties of GABAA channel subtypes
Hevers W and Luddens H (1998) The diversity of GABAA receptors. Pharmacological and electrophysiological properties of GABAA channel subtypes. Mol Neurobiol 18:35-86.
Patch clamp measurements on Xenopus laevis oocytes: Currents through endogenous channels and implanted acetylcholine receptor and sodium channels
Methfessel C, Witzemann V, Takahashi T, Mishina M, Numa S, and Sakmann B (1986) Patch clamp measurements on Xenopus laevis oocytes: currents through endogenous channels and implanted acetylcholine receptor and sodium channels. Pflueg Arch Eur J Physiol 407:577-588.
Functional comparison of the role of subunits in recombinant human γ-aminobutyric acidA/benzodiazepine receptors
Wafford KA, Bain CJ, Whiting PJ, and Kemp JA (1993) Functional comparison of the role of subunits in recombinant human γ-aminobutyric acidA/benzodiazepine receptors. Mol Pharmacol 44:437-442.
Benzodiazepines act on GABAA receptors via two distinct and separable mechanisms
Walters RJ, Hadley SH, Morris KD, and Amin J (2000) Benzodiazepines act on GABAA receptors via two distinct and separable mechanisms. Nat Neurosci 3:1274-1281.
Mechanism of alpha-subunit selectivity of benzodiazepine pharmacology at gamma-aminobutyric acid type A receptors
Wingrove PB, Safo P, Wheat L, Thompson SA, Wafford KA, and Whiting PJ (2002) Mechanism of alpha-subunit selectivity of benzodiazepine pharmacology at gamma-aminobutyric acid type A receptors. Eur J Pharmacol 437:31-39.