Mutational analysis of molecular requirements for the actions of general anaesthetics at the gamma-aminobutyric acidA receptor subtype, alpha1beta2gamma2
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Mutations at beta N265 in γ-aminobutyric acid type A receptors alter both binding affinity and efficacy of potent anestheticsIs the Brain a Quantum Computer?Mapping the contribution of beta3-containing GABAA receptors to volatile and intravenous general anesthetic actionsGamma-amino butyric acid type A receptor mutations at beta2N265 alter etomidate efficacy while preserving basal and agonist-dependent activitySpecificity of intersubunit general anesthetic-binding sites in the transmembrane domain of the human α1β3γ2 γ-aminobutyric acid type A (GABAA) receptor.A propofol binding site on mammalian GABAA receptors identified by photolabelingMultiple Non-Equivalent Interfaces Mediate Direct Activation of GABAA Receptors by Propofol.Comparative pharmacology of flatworm and roundworm glutamate-gated chloride channels: Implications for potential anthelmintics.Clinical and molecular pharmacology of etomidate.An allosteric coagonist model for propofol effects on α1β2γ2L γ-aminobutyric acid type A receptors.Flavan-3-ol esters: new agents for exploring modulatory sites on GABA(A) receptors.Molecular and neuronal substrates for general anaesthetics.Novel positive allosteric modulators of GABAA receptors with anesthetic activity.Cysteine substitutions define etomidate binding and gating linkages in the α-M1 domain of γ-aminobutyric acid type A (GABAA) receptorsDistinct structural changes in the GABAA receptor elicited by pentobarbital and GABA.Propofol modulation of α1 glycine receptors does not require a structural transition at adjacent subunits that is crucial to agonist-induced activationGABAA-R α4 subunits are required for the low dose locomotor stimulatory effect of alphaxalone, but not for several other behavioral responses to alphaxalone, etomidate or propofolGamma-aminobutyric acid (GABA) and pentobarbital induce different conformational rearrangements in the GABA A receptor alpha1 and beta2 pre-M1 regions.Major role for tonic GABAA conductances in anesthetic suppression of intrinsic neuronal excitability.Alphaxalone Binds in Inner Transmembrane β+-α- Interfaces of α1β3γ2 γ-Aminobutyric Acid Type A Receptors.Potentiating effect of glabridin from Glycyrrhiza glabra on GABAA receptors.Structural basis of neurosteroid anesthetic action on GABA receptors
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P2860
Mutational analysis of molecular requirements for the actions of general anaesthetics at the gamma-aminobutyric acidA receptor subtype, alpha1beta2gamma2
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2003 nî lūn-bûn
@nan
2003 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
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2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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label
Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
@ast
Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
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P2093
P2860
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Mutational analysis of molecul ...... tor subtype, alpha1beta2gamma2
@en
P2093
Karin Krähenbühl
Roberta Siegwart
Sachar Lambert
Uwe Rudolph
P2860
P2888
P3181
P356
10.1186/1471-2210-3-13
P407
P577
2003-11-12T00:00:00Z
P5875
P6179
1047036801