Contributions of the non-alpha subunit residues (loop D) to agonist binding and channel gating in the muscle nicotinic acetylcholine receptor.
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5-HT3 receptorsCrystal Structures of a Cysteine-modified Mutant in Loop D of Acetylcholine-binding ProteinAllosteric activation mechanism of the cys-loop receptorsHighly fatal fast-channel syndrome caused by AChR ε subunit mutation at the agonist binding siteEnergetics of gating at the apo-acetylcholine receptor transmitter binding site.Maximum likelihood estimation of ion channel kinetics from macroscopic currentsγ-aminobutyric acid type A α4, β2, and δ subunits assemble to produce more than one functionally distinct receptor type.Design and control of acetylcholine receptor conformational changeEnergetic contributions to channel gating of residues in the muscle nicotinic receptor β1 subunit.Functional characterization of the α5(Asn398) variant associated with risk for nicotine dependence in the α3β4α5 nicotinic receptor.Synaptic-type α1β2γ2L GABAA receptors produce large persistent currents in the presence of ambient GABA and anesthetic drugs.Mechanisms of potentiation of the mammalian GABAA receptor by the marine cembranoid eupalmerin acetateLong-range coupling in an allosteric receptor revealed by mutant cycle analysisThe benzodiazepine diazepam potentiates responses of α1β2γ2L γ-aminobutyric acid type A receptors activated by either γ-aminobutyric acid or allosteric agonists.Hydrogen bonding between the 17beta-substituent of a neurosteroid and the GABA(A) receptor is not obligatory for channel potentiation.Differential Contribution of Subunit Interfaces to α9α10 Nicotinic Acetylcholine Receptor Function.Aromatic Residues {epsilon}Trp-55 and {delta}Trp-57 and the Activation of Acetylcholine Receptor Channels.Activation and block of the adult muscle-type nicotinic receptor by physostigmine: single-channel studies.A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties.Activation of heteroliganded mouse muscle nicotinic receptors.Neuroactive steroids have multiple actions to potentiate GABAA receptors.Activation of GABA(A) receptors containing the alpha4 subunit by GABA and pentobarbital.Activation and block of mouse muscle-type nicotinic receptors by tetraethylammonium.Neurosteroid migration to intracellular compartments reduces steroid concentration in the membrane and diminishes GABA-A receptor potentiation.
P2860
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P2860
Contributions of the non-alpha subunit residues (loop D) to agonist binding and channel gating in the muscle nicotinic acetylcholine receptor.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Contributions of the non-alpha ...... otinic acetylcholine receptor.
@en
type
label
Contributions of the non-alpha ...... otinic acetylcholine receptor.
@en
prefLabel
Contributions of the non-alpha ...... otinic acetylcholine receptor.
@en
P2860
P1476
Contributions of the non-alpha ...... otinic acetylcholine receptor.
@en
P2093
Gustav Akk
P2860
P304
P356
10.1113/JPHYSIOL.2002.029413
P407
P577
2002-11-01T00:00:00Z