Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
about
Proton modulation of recombinant GABA(A) receptors: influence of GABA concentration and the beta subunit TM2-TM3 domainEnhanced macroscopic desensitization shapes the response of alpha4 subtype-containing GABAA receptors to synaptic and extrasynaptic GABAThe role of ovarian hormone-derived neurosteroids on the regulation of GABAA receptors in affective disordersA novel site on gamma 3 subunits important for assembly of GABA(A) receptorsAtomic force microscopy imaging demonstrates that P2X2 receptors are trimers but that P2X6 receptor subunits do not oligomerizeThe actions of ether, alcohol and alkane general anaesthetics on GABAA and glycine receptors and the effects of TM2 and TM3 mutationsGABA(A) receptor epsilon-subunit may confer benzodiazepine insensitivity to the caudal aspect of the nucleus tractus solitarii of the ratEvidence for the formation of functionally distinct alphabetagammaepsilon GABA(A) receptorsNeonatal development of the rat visual cortex: synaptic function of GABAA receptor alpha subunitsGABA receptor subunit distribution and FMRP-mGluR5 signaling abnormalities in the cerebellum of subjects with schizophrenia, mood disorders, and autism.Revealing Higher Order Protein Structure Using Mass Spectrometry.Adenosine-to-inosine RNA editing affects trafficking of the gamma-aminobutyric acid type A (GABA(A)) receptorStoichiometry of expressed alpha(4)beta(2)delta gamma-aminobutyric acid type A receptors depends on the ratio of subunit cDNA transfected.Atomic force microscopy reveals the stoichiometry and subunit arrangement of 5-HT3 receptors.Augmentation of Tonic GABA(A) Inhibition in Absence Epilepsy: Therapeutic Value of Inverse Agonists at Extrasynaptic GABA(A) ReceptorsPhosphorylation of GABAA receptors influences receptor trafficking and neurosteroid actions.Altering the relative abundance of GABA A receptor subunits changes GABA- and ethanol-responses in Xenopus oocytes.Gamma-aminobutyric acid increases the water accessibility of M3 membrane-spanning segment residues in gamma-aminobutyric acid type A receptorsZinc-mediated inhibition of GABA(A) receptors: discrete binding sites underlie subtype specificity.Positioning of the alpha-subunit isoforms confers a functional signature to gamma-aminobutyric acid type A receptors.Influence of GABA(A) receptor α subunit isoforms on the benzodiazepine binding siteAlcoholism: genes and mechanisms.Molecular analysis of the site for 2-arachidonylglycerol (2-AG) on the β₂ subunit of GABA(A) receptors.Tryptophan scanning mutagenesis in TM2 of the GABA(A) receptor alpha subunit: effects on channel gating and regulation by ethanol.Salicylidene salicylhydrazide, a selective inhibitor of beta 1-containing GABAA receptors.Implications for treatment: GABAA receptors in aging, Down syndrome and Alzheimer's disease.Different residues in the GABAA receptor benzodiazepine binding pocket mediate benzodiazepine efficacy and binding.Emerging themes in GABAergic synapse developmentThe GABAA receptor alpha+beta- interface: a novel target for subtype selective drugsThe dynamic modulation of GABA(A) receptor trafficking and its role in regulating the plasticity of inhibitory synapses.Neurosteroids and GABA-A Receptor Function.Identification of novel positive allosteric modulators and null modulators at the GABAA receptor α+β- interfaceNovel positive allosteric modulators of GABAA receptors with anesthetic activity.Zolpidem is a potent stoichiometry-selective modulator of α1β3 GABAA receptors: evidence of a novel benzodiazepine site in the α1-α1 interface.Neurochemical and physiological correlates of a critical period of respiratory development in the rat.Unexpected Properties of δ-Containing GABAA Receptors in Response to Ligands Interacting with the α+ β- Site.Low Expression in Xenopus Oocytes and Unusual Functional Properties of α1β2γ2 GABAA Receptors with Non-Conventional Subunit Arrangement.New insights into the molecular mechanisms of general anaesthetics.GABA(A) receptor and glycine receptor activation by paracrine/autocrine release of endogenous agonists: more than a simple communication pathway.A novel GABA(A) receptor pharmacology: drugs interacting with the α(+) β(-) interface.
P2860
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P2860
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@ast
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@en
type
label
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@ast
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@en
prefLabel
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@ast
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@en
P2093
P356
P1476
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer.
@en
P2093
Bonnert TP
McKernan RM
Whiting PJ
P304
10100-10104
P356
10.1074/JBC.274.15.10100
P407
P577
1999-04-01T00:00:00Z