Dihydropyridine derivatives prolong the open state of Ca channels in cultured cardiac cells.
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Structural Basis for Pharmacology of Voltage-Gated Sodium and Calcium ChannelsPurified skeletal muscle 1,4-dihydropyridine receptor forms phosphorylation-dependent oligomeric calcium channels in planar bilayers.(R)-roscovitine prolongs the mean open time of unitary N-type calcium channel currents.Physiologic gating properties of unitary cardiac L-type Ca2+ channels.Ca channel kinetics during the spontaneous heart beat in embryonic chick ventricle cells.Dihydropyridine-sensitive skeletal muscle Ca channels in polarized planar bilayers. 1. Kinetics and voltage dependence of gating.Molecular basis for the inhibition of 1,4-dihydropyridine calcium channel drugs binding to their receptors by a nonspecific site interaction mechanism.Dihydropyridine-sensitive skeletal muscle Ca channels in polarized planar bilayers. 3. Effects of phosphorylation by protein kinase CFast activation of cardiac Ca++ channel gating charge by the dihydropyridine agonist, BAY K 8644.Ion concentration-dependence of rat cardiac unitary L-type calcium channel conductance.Modulation of the conductance of unitary cardiac L-type Ca(2+) channels by conditioning voltage and divalent ions.Agonists Bay-K8644 and CGP-28392 open calcium channels reconstituted from skeletal muscle transverse tubulesEffects of the calcium channel agonist, BAY K 8644, on electrical activity in mouse pancreatic B-cellsStructural analysis of drug molecules in biological membranesCalcium channels of amphibian stomach and mammalian aorta smooth muscle cellsPartitioning and location of Bay K 8644, 1,4-dihydropyridine calcium channel agonist, in model and biological membranesAmino acid substitutions in the pore of the Ca(V)1.2 calcium channel reduce barium currents without affecting calcium currentsCyclosporin and Timothy syndrome increase mode 2 gating of CaV1.2 calcium channels through aberrant phosphorylation of S6 helicesQuercetin as a novel activator of L-type Ca(2+) channels in rat tail artery smooth muscle cellsMefenamic acid as a novel activator of L-type voltage-dependent Ca2+ channels in smooth muscle cells from pig proximal urethraIncorporation of calcium channels from cardiac sarcolemmal membrane vesicles into planar lipid bilayersDihydropyridine-sensitive Ca2+ channels in mammalian skeletal muscle cells in culture: electrophysiological properties and interactions with Ca2+ channel activator (Bay K8644) and inhibitor (PN 200-110).Release from the cone ribbon synapse under bright light conditions can be controlled by the opening of only a few Ca(2+) channelsThe Ca2+ -antagonist and binding properties of the phenylalkylamine, anipamil.Blockade of the inotropic effect of Bay K 8644 by cytochalasin-B and phloretinPharmacological analysis of the effects of Bay K 8644 and organic calcium antagonists on the mouse isolated distal colon.Mechanical and electrophysiological effects of 8-oxoberberine (JKL1073A) on atrial tissueStimulation rate modulates effects of the dihydropyridine CGP 28 392 on cardiac calcium-dependent action potentialsRS 30026: a potent and effective calcium channel agonist.Cellular mechanisms of early afterdepolarizations.Nonmodal gating of cardiac calcium channels as revealed by dihydropyridinesVoltage-dependent modulation of Ca channel current in heart cells by Bay K8644.Cardiac calcium channels in planar lipid bilayers. L-type channels and calcium-permeable channels open at negative membrane potentials.Nonlinear charge movement in mammalian cardiac ventricular cells. Components from Na and Ca channel gatingPotentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms.Construction of a high-affinity receptor site for dihydropyridine agonists and antagonists by single amino acid substitutions in a non-L-type Ca2+ channelSERCA2 activity is involved in the CNP-mediated functional responses in failing rat myocardium.Mevinolin, an inhibitor of cholesterol biosynthesis, drastically depresses Ca2+ channel activity and uncouples excitation from contraction in cardiac cells in cultureBeta-adrenergic stimulation of calcium channels occurs by potentiation of high-activity gating modesLong-opening mode of gating of neuronal calcium channels and its promotion by the dihydropyridine calcium agonist Bay K 8644.
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Dihydropyridine derivatives prolong the open state of Ca channels in cultured cardiac cells.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 1984
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@en
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@nl
type
label
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@en
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@nl
prefLabel
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@en
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@nl
P2860
P356
P1476
Dihydropyridine derivatives pr ...... els in cultured cardiac cells.
@en
P2093
P2860
P304
P356
10.1073/PNAS.81.15.4824
P407
P577
1984-08-01T00:00:00Z