Papers associated with kidney (and gabarap)

Limit to papers also referencing gene:
Show all kidney papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	Dissecting the Molecular Determinants of GABAA Receptors Current Rundown, a Hallmark of Refractory Human Epilepsy., Cifelli P., Brain Sci. March 30, 2021; 11 (4):
	A Benzodiazepine Ligand with Improved GABAA Receptor α5-Subunit Selectivity Driven by Interactions with Loop C., Simeone X., Mol Pharmacol. January 1, 2021; 99 (1): 39-48.
	Diversity of Nicotinic Acetylcholine Receptor Positive Allosteric Modulators Revealed by Mutagenesis and a Revised Structural Model., Newcombe J., Mol Pharmacol. February 1, 2018; 93 (2): 128-140.
	Signal Transduction at the Domain Interface of Prokaryotic Pentameric Ligand-Gated Ion Channels., Bertozzi C., PLoS Biol. March 4, 2016; 14 (3): e1002393.
	11-trifluoromethyl-phenyldiazirinyl neurosteroid analogues: potent general anesthetics and photolabeling reagents for GABAA receptors., Chen ZW., Psychopharmacology (Berl). September 1, 2014; 231 (17): 3479-91.
	GABA(A) receptor modulation by terpenoids from Sideritis extracts., Kessler A., Mol Nutr Food Res. April 1, 2014; 58 (4): 851-62.
	Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans., Bianchi MT., J Neurosci. July 1, 2002; 22 (13): 5321-7.
	Intravenous anesthetics differentially modulate ligand-gated ion channels., Flood P., Anesthesiology. May 1, 2000; 92 (5): 1418-25.
	The actions of ether, alcohol and alkane general anaesthetics on GABAA and glycine receptors and the effects of TM2 and TM3 mutations., Krasowski MD., Br J Pharmacol. February 1, 2000; 129 (4): 731-43.
	Permeability and single channel conductance of human homomeric rho1 GABAC receptors., Wotring VE., J Physiol. December 1, 1999; 521 Pt 2 327-36.
	Subunit-selective modulation of GABAA receptors by the non-steroidal anti-inflammatory agent, mefenamic acid., Halliwell RF., Eur J Neurosci. August 1, 1999; 11 (8): 2897-905.
	Residues at positions 206 and 209 of the alpha1 subunit of gamma-aminobutyric AcidA receptors influence affinities for benzodiazepine binding site ligands., Buhr A., Mol Pharmacol. October 1, 1997; 52 (4): 676-82.
	A point mutation in the gamma2 subunit of gamma-aminobutyric acid type A receptors results in altered benzodiazepine binding site specificity., Buhr A., Proc Natl Acad Sci U S A. August 5, 1997; 94 (16): 8824-9.
	Subtle changes in residue 77 of the gamma subunit of alpha1beta2gamma2 GABAA receptors drastically alter the affinity for ligands of the benzodiazepine binding site., Buhr A., J Biol Chem. May 2, 1997; 272 (18): 11799-804.
	3 alpha-Hydroxy-3 beta-trifluoromethyl-5 alpha-pregnan-20-one (Co 2-1970): a partial agonist at the neuroactive steroid site of the gamma-aminobutyric acidA receptor., Hawkinson JE., Mol Pharmacol. May 1, 1996; 49 (5): 897-906.
	Site-directed mutagenesis of N-linked glycosylation sites on the gamma-aminobutyric acid type A receptor alpha 1 subunit., Buller AL., Mol Pharmacol. November 1, 1994; 46 (5): 858-65.
	Small N-terminal deletion by splicing in cerebellar alpha 6 subunit abolishes GABAA receptor function., Korpi ER., J Neurochem. September 1, 1994; 63 (3): 1167-70.
	Regulation of GABAA receptor function by protein kinase C phosphorylation., Krishek BJ., Neuron. May 1, 1994; 12 (5): 1081-95.
	Pharmacological and Electrophysiological Properties of Recombinant GABAA Receptors Comprising the alpha3, beta1 and gamma2 Subunits., Knoflach F., Eur J Neurosci. October 1, 1992; 4 (1): 1-9.

???pagination.result.page??? 1