about
Molecular organization and dynamics of the melatonin MT₁ receptor/RGS20/G(i) protein complex reveal asymmetry of receptor dimers for RGS and G(i) couplingInhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetineThe selective antagonist EPPTB reveals TAAR1-mediated regulatory mechanisms in dopaminergic neurons of the mesolimbic systemSlow modal gating of single G protein-activated K+ channels expressed in Xenopus oocytesEthanol action on dopaminergic neurons in the ventral tegmental area: interaction with intrinsic ion channels and neurotransmitter inputs.Functional and biochemical evidence for G-protein-gated inwardly rectifying K+ (GIRK) channels composed of GIRK2 and GIRK3Mapping the Gbetagamma-binding sites in GIRK1 and GIRK2 subunits of the G protein-activated K+ channelIdentification of native atrial G-protein-regulated inwardly rectifying K+ (GIRK4) channel homomultimersIncreased inwardly rectifying potassium currents in HEK-293 cells expressing murine transient receptor potential 4Eicosanoids inhibit the G-protein-gated inwardly rectifying potassium channel (Kir3) at the Na+/PIP2 gating site.Kir3.1/3.2 encodes an I(KACh)-like current in gastrointestinal myocytesG-protein-coupled inwardly rectifying potassium channels are targets of alcohol actionIdentification of the structural determinant responsible for the phosphorylation of G-protein activated potassium channel 1 by cAMP-dependent protein kinaseActivation and inhibition of G protein-coupled inwardly rectifying potassium (Kir3) channels by G protein beta gamma subunits.Receptor-mediated inhibition of G protein-coupled inwardly rectifying potassium channels involves G(alpha)q family subunits, phospholipase C, and a readily diffusible messenger.Receptor-independent activation of atrial muscarinic potassium channels in the absence of nucleotides.Mapping a barbiturate withdrawal locus to a 0.44 Mb interval and analysis of a novel null mutant identify a role for Kcnj9 (GIRK3) in withdrawal from pentobarbital, zolpidem, and ethanol.Functional characterization of bursicon receptor and genome-wide analysis for identification of genes affected by bursicon receptor RNAiMouse bestrophin-2 is a bona fide Cl(-) channel: identification of a residue important in anion binding and conduction.Voltage affects the dissociation rate constant of the m2 muscarinic receptor.Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.The GIRK1 brain variant GIRK1d and its functional impact on heteromultimeric GIRK channels.A real-time screening assay for GIRK1/4 channel blockers.Ethanol actions on multiple ion channels: which are important?Fast inactivation of a brain K+ channel composed of Kv1.1 and Kvbeta1.1 subunits modulated by G protein beta gamma subunits.G-protein mediated gating of inward-rectifier K+ channels.Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil.Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants.TrkB activation by brain-derived neurotrophic factor inhibits the G protein-gated inward rectifier Kir3 by tyrosine phosphorylation of the channel.Single channel analysis of the regulation of GIRK1/GIRK4 channels by protein phosphorylation.SDF and GABA interact to regulate axophilic migration of GnRH neurons.Contribution of GIRK2-mediated postsynaptic signaling to opiate and alpha 2-adrenergic analgesia and analgesic sex differences.Hydrogen-bonding dynamics between adjacent blades in G-protein beta-subunit regulates GIRK channel activationN-terminal tyrosine residues within the potassium channel Kir3 modulate GTPase activity of Galphai.A novel fast mechanism for GPCR-mediated signal transduction--control of neurotransmitter release.The polarization of the G-protein activated potassium channel GIRK5 to the vegetal pole of Xenopus laevis oocytes is driven by a di-leucine motifAltered heart rate control in transgenic mice carrying the KCNJ6 gene of the human chromosome 21.Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac).Muscarinic regulation of cardiac ion channels.Naringin directly activates inwardly rectifying potassium channels at an overlapping binding site to tertiapin-Q.
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Signalling via the G protein-activated K+ channels
@ast
Signalling via the G protein-activated K+ channels
@en
Signalling via the G protein-activated K+ channels
@nl
type
label
Signalling via the G protein-activated K+ channels
@ast
Signalling via the G protein-activated K+ channels
@en
Signalling via the G protein-activated K+ channels
@nl
prefLabel
Signalling via the G protein-activated K+ channels
@ast
Signalling via the G protein-activated K+ channels
@en
Signalling via the G protein-activated K+ channels
@nl
P921
P1433
P1476
Signalling via the G protein-activated K+ channels
@en
P2093
P304
P356
10.1016/S0898-6568(97)00095-8
P407
P577
1997-12-01T00:00:00Z