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Summary Anatomy Item Literature (6850) Expression Attributions Wiki
XB-ANAT-465

Papers associated with anatomical group (and gabarap)

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GABAA Receptor Subunit Composition Drives Its Sensitivity to the Insecticide Fipronil., Soualah Z., Front Neurosci. January 1, 2021; 15 768466.                


Novel Molecule Exhibiting Selective Affinity for GABAA Receptor Subtypes., Borghese CM., Sci Rep. July 24, 2017; 7 (1): 6230.        


GABAB receptor attenuation of GABAA currents in neurons of the mammalian central nervous system., Shen W., Physiol Rep. March 1, 2017; 5 (6):           


Zolpidem is a potent stoichiometry-selective modulator of α1β3 GABAA receptors: evidence of a novel benzodiazepine site in the α1-α1 interface., Che Has AT., Sci Rep. June 27, 2016; 6 28674.          


Direct evidence for GABAergic activity of Withania somnifera on mammalian ionotropic GABAA and GABAρ receptors., Candelario M., J Ethnopharmacol. August 2, 2015; 171 264-72.


A Multifaceted GABAA Receptor Modulator: Functional Properties and Mechanism of Action of the Sedative-Hypnotic and Recreational Drug Methaqualone (Quaalude)., Hammer H., Mol Pharmacol. August 1, 2015; 88 (2): 401-20.


Identification of amino acids involved in histamine potentiation of GABA A receptors., Thiel U., Front Pharmacol. May 26, 2015; 6 106.              


Pharmacological characterisation of murine α4β1δ GABAA receptors expressed in Xenopus oocytes., Villumsen IS., BMC Neurosci. March 5, 2015; 16 8.    


Benzodiazepine modulation of homomeric GABAAρ1 receptors: differential effects of diazepam and 4'-chlorodiazepam., Beltrán González AN., Eur J Pharmacol. November 15, 2014; 743 24-30.


A cycloartane glycoside derived from Actaea racemosa L. modulates GABAA receptors and induces pronounced sedation in mice., Strommer B., J Pharmacol Exp Ther. November 1, 2014; 351 (2): 234-42.


Unexpected Properties of δ-Containing GABAA Receptors in Response to Ligands Interacting with the α+ β- Site., Mirheydari P., Neurochem Res. June 1, 2014; 39 (6): 1057-1067.


GABA(A) receptor modulation by terpenoids from Sideritis extracts., Kessler A., Mol Nutr Food Res. April 1, 2014; 58 (4): 851-62.            


Generation of recombinant antibodies to rat GABAA receptor subunits by affinity selection on synthetic peptides., Koduvayur SP., PLoS One. February 19, 2014; 9 (2): e87964.          


Mutations at beta N265 in γ-aminobutyric acid type A receptors alter both binding affinity and efficacy of potent anesthetics., Stewart DS., PLoS One. January 1, 2014; 9 (10): e111470.              


Fractalkine/CX3CL1 modulates GABAA currents in human temporal lobe epilepsy., Roseti C., Epilepsia. October 1, 2013; 54 (10): 1834-44.


Do N-arachidonyl-glycine (NA-glycine) and 2-arachidonoyl glycerol (2-AG) share mode of action and the binding site on the β2 subunit of GABAA receptors?, Baur R., PeerJ. September 10, 2013; 1 e149.                  


New insights in endogenous modulation of ligand-gated ion channels: histamine is an inverse agonist at strychnine sensitive glycine receptors., Kletke O., Eur J Pharmacol. June 15, 2013; 710 (1-3): 59-66.


Benzodiazepine-induced spatial learning deficits in rats are regulated by the degree of modulation of α1 GABA(A) receptors., Joksimović S., Eur Neuropsychopharmacol. May 1, 2013; 23 (5): 390-9.


Potency of GABA at human recombinant GABA(A) receptors expressed in Xenopus oocytes: a mini review., Karim N., Amino Acids. April 1, 2013; 44 (4): 1139-49.


Partial agonism of taurine at gamma-containing native and recombinant GABAA receptors., Kletke O., PLoS One. January 1, 2013; 8 (4): e61733.            


A single amino acid determines the toxicity of Ginkgo biloba extracts., Thompson AJ., FASEB J. May 1, 2012; 26 (5): 1884-91.                    


The biochemical anatomy of cortical inhibitory synapses., Heller EA., PLoS One. January 1, 2012; 7 (6): e39572.            


Cloning and characterization of GABAA α subunits and GABAB subunits in Xenopus laevis during development., Kaeser GE., Dev Dyn. April 1, 2011; 240 (4): 862-73.                                          


Molecular characterization of agonists that bind to an insect GABA receptor., McGonigle I., Biochemistry. April 6, 2010; 49 (13): 2897-902.        


About a snail, a toad, and rodents: animal models for adaptation research., Roubos EW., Front Endocrinol (Lausanne). January 1, 2010; 1 4.      


Stoichiometry of a pore mutation that abolishes picrotoxin-mediated antagonism of the GABAA receptor., Sedelnikova A., J Physiol. December 1, 2006; 577 (Pt 2): 569-77.


A TM2 residue in the beta1 subunit determines spontaneous opening of homomeric and heteromeric gamma-aminobutyric acid-gated ion channels., Miko A., J Biol Chem. May 28, 2004; 279 (22): 22833-40.


Pharmacological properties of alpha 9 alpha 10 nicotinic acetylcholine receptors revealed by heterologous expression of subunit chimeras., Baker ER., Mol Pharmacol. February 1, 2004; 65 (2): 453-60.


Activation-dependent properties of pregnenolone sulfate inhibition of GABAA receptor-mediated current., Eisenman LN., J Physiol. August 1, 2003; 550 (Pt 3): 679-91.


Effects of gamma2S subunit incorporation on GABAA receptor macroscopic kinetics., Boileau AJ., Neuropharmacology. June 1, 2003; 44 (8): 1003-12.


Anesthetic properties of 4-iodopropofol: implications for mechanisms of anesthesia., Lingamaneni R., Anesthesiology. June 1, 2001; 94 (6): 1050-7.


Intravenous anesthetics differentially modulate ligand-gated ion channels., Flood P., Anesthesiology. May 1, 2000; 92 (5): 1418-25.


Response kinetics and pharmacological properties of heteromeric receptors formed by coassembly of GABA rho- and gamma 2-subunits., Qian H., Proc Biol Sci. December 7, 1999; 266 (1436): 2419-25.


Permeability and single channel conductance of human homomeric rho1 GABAC receptors., Wotring VE., J Physiol. December 1, 1999; 521 Pt 2 327-36.


A single amino acid confers barbiturate sensitivity upon the GABA rho 1 receptor., Belelli D., Br J Pharmacol. June 1, 1999; 127 (3): 601-4.


Sulfated and unsulfated steroids modulate gamma-aminobutyric acidA receptor function through distinct sites., Park-Chung M., Dev Biol. May 29, 1999; 830 (1): 72-87.


In vivo and in vitro toxicodynamic analyses of new quinolone-and nonsteroidal anti-inflammatory drug-induced effects on the central nervous system., Kita H., Antimicrob Agents Chemother. May 1, 1999; 43 (5): 1091-7.


Subunit dependent modulation of GABAA receptor function by neuroactive steroids., Maitra R., Dev Biol. February 20, 1999; 819 (1-2): 75-82.


Complementary regulation of anaesthetic activation of human (alpha6beta3gamma2L) and Drosophila (RDL) GABA receptors by a single amino acid residue., Pistis M., J Physiol. February 15, 1999; 515 ( Pt 1) 3-18.


A GABAA receptor alpha1 subunit tagged with green fluorescent protein requires a beta subunit for functional surface expression., Connor JX., J Biol Chem. October 30, 1998; 273 (44): 28906-11.


Functional characterization and visualization of a GABAA receptor-GFP chimera expressed in Xenopus oocytes., Bueno OF., Brain Res Mol Brain Res. August 31, 1998; 59 (2): 165-77.


GABAA-benzodiazepine receptors in the striatum are involved in the sedation produced by a moderate, but not an intoxicating ethanol dose in outbred Wistar rats., June HL., Dev Biol. May 25, 1998; 794 (1): 103-18.


Molecular composition of GABAC receptors., Enz R., Vision Res. May 1, 1998; 38 (10): 1431-41.


Differences in agonist/antagonist binding affinity and receptor transduction using recombinant human gamma-aminobutyric acid type A receptors., Ebert B., Mol Pharmacol. December 1, 1997; 52 (6): 1150-6.


The interaction of the general anesthetic etomidate with the gamma-aminobutyric acid type A receptor is influenced by a single amino acid., Belelli D., Proc Natl Acad Sci U S A. September 30, 1997; 94 (20): 11031-6.


Synaptic transmission in the pineal eye of young Xenopus laevis tadpoles: a role for NMDA and non-NMDA glutamate and non-glutaminergic receptors?, Jamieson D., J Comp Physiol A. August 1, 1997; 181 (2): 177-86.


Differential sensitivities of mammalian neuronal and muscle nicotinic acetylcholine receptors to general anesthetics., Violet JM., Anesthesiology. April 1, 1997; 86 (4): 866-74.


Alpha 4 beta 2 neuronal nicotinic acetylcholine receptors in the central nervous system are inhibited by isoflurane and propofol, but alpha 7-type nicotinic acetylcholine receptors are unaffected., Flood P., Anesthesiology. April 1, 1997; 86 (4): 859-65.


Actions of picrodendrin antagonists on dieldrin-sensitive and -resistant Drosophila GABA receptors., Hosie AM., Br J Pharmacol. December 1, 1996; 119 (8): 1569-76.


Design and in vitro pharmacology of a selective gamma-aminobutyric acidC receptor antagonist., Ragozzino D., Mol Pharmacol. October 1, 1996; 50 (4): 1024-30.

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