Molecular mechanism of pharmacological activation of BK channels.
about
BK channels: multiple sensors, one activation gateResin-acid derivatives as potent electrostatic openers of voltage-gated K channels and suppressors of neuronal excitabilityBK channel activators and their therapeutic perspectivesCalcium- and voltage-gated potassium (BK) channel activators in the 5β-cholanic acid-3α-ol analogue series with modifications in the lateral chainBK channels reveal novel phosphate sensitivity in SNr neurons.Molecular mechanisms underlying the effect of the novel BK channel opener GoSlo: involvement of the S4/S5 linker and the S6 segment.Two distinct effects of PIP2 underlie auxiliary subunit-dependent modulation of Slo1 BK channels.Effects of the novel BK (KCa 1.1) channel opener GoSlo-SR-5-130 are dependent on the presence of BKβ subunits.Single Channel Recordings Reveal Differential β2 Subunit Modulations Between Mammalian and Drosophila BKCa(β2) Channels.Genetic activation of BK currents in vivo generates bidirectional effects on neuronal excitability.Spontaneous and evoked contractions are regulated by PKC-mediated signaling in detrusor smooth muscle: involvement of BK channels.Single-channel biophysical and pharmacological characterizations of native human large-conductance calcium-activated potassium channels in freshly isolated detrusor smooth muscle cells.DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunit.Modulation of BK Channel Function by Auxiliary Beta and Gamma Subunits.Regulation of BK channels by auxiliary γ subunits.2014 Conway review lecture, Royal Academy of Medicine in Ireland: “S6, drugs and RCK and Bowl”.Molecular Determinants of BK Channel Functional Diversity and Functioning.The smooth muscle-type β1 subunit potentiates activation by DiBAC4(3) in recombinant BK channels.The Slo(w) path to identifying the mitochondrial channels responsible for ischemic protection.Differential efficacy of GoSlo-SR compounds on BKα and BKαγ1-4 channels.Big conductance calcium-activated potassium channel openers control spasticity without sedation.BK channel agonist represents a potential therapeutic approach for lysosomal storage diseases.Multilevel regulation: Controlling BK channels in central clock neurons.CO-independent modification of K+ channels by tricarbonyldichlororuthenium(II) dimer (CORM-2).
P2860
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P2860
Molecular mechanism of pharmacological activation of BK channels.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
@zh-cn
name
Molecular mechanism of pharmacological activation of BK channels.
@ast
Molecular mechanism of pharmacological activation of BK channels.
@en
type
label
Molecular mechanism of pharmacological activation of BK channels.
@ast
Molecular mechanism of pharmacological activation of BK channels.
@en
prefLabel
Molecular mechanism of pharmacological activation of BK channels.
@ast
Molecular mechanism of pharmacological activation of BK channels.
@en
P2093
P2860
P356
P1476
Molecular mechanism of pharmacological activation of BK channels
@en
P2093
Guido Gessner
Malle Soom
Tomohiko Ohwada
Toshinori Hoshi
Yong-Mei Cui
Yuko Otani
P2860
P304
P356
10.1073/PNAS.1114321109
P407
P577
2012-02-13T00:00:00Z