Dihydropyridine-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).
about
Calciseptine, a peptide isolated from black mamba venom, is a specific blocker of the L-type calcium channelNeuroleptics of the diphenylbutylpiperidine series are potent calcium channel inhibitorsCalcium currents, charge movement and dihydropyridine binding in fast- and slow-twitch muscles of rat and rabbitCalcium currents in embryonic and neonatal mammalian skeletal muscleDiversity and novel pharmacological properties of Ca2+ channels in Drosophila brain membranes.Ontogenesis and localization of Ca2+ channels in mammalian skeletal muscle in culture and role in excitation-contraction coupling.Dihydropyridine-sensitive skeletal muscle Ca channels in polarized planar bilayers. 1. Kinetics and voltage dependence of gating.Dihydropyridine-sensitive skeletal muscle Ca channels in polarized planar bilayers. 3. Effects of phosphorylation by protein kinase CMapacalcine protects mouse neurons against hypoxia by blocking cell calcium overload.Phosphorylation and dephosphorylation of dihydropyridine-sensitive voltage-dependent Ca2+ channel in skeletal muscle membranes by cAMP- and Ca2+-dependent processesInhibition of myocardial Ca2+ channels by three dihydropyridines with different structural features: potential-dependent blockade by Ro 18-3981.Single calcium channel behavior in native skeletal muscle.Effect of postnatal development on calcium currents and slow charge movement in mammalian skeletal muscleCytokinin stimulates dihydropyridine-sensitive calcium uptake in moss protoplasts.Molecular properties of structure and regulation of the calcium channel.Biochemistry, molecular pharmacology, and functional control of Ca2+ channels.Gating and permeation of different types of Ca channels.Evidence for an external location of the dihydropyridine agonist receptor site on smooth muscle and skeletal muscle calcium channels.A polypeptide toxin from the coral Goniopora. Purification and action on Ca2+ channels.Second messenger regulation of occlusion of the spinal neurocoel in the chick embryo.L-Type Ca2+ channels mediate the slow Ca2+-dependent afterhyperpolarization current in rat CA3 pyramidal cells in vitro.Endogenous DHP-sensitive Ca(2+) channels in Pleurodeles oocytes.Kinetics of inactivation and restoration from inactivation of the L-type calcium current in human myotubes.
P2860
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P2860
Dihydropyridine-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).
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@ast
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@en
type
label
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@ast
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@en
prefLabel
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@ast
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@en
P2093
P2860
P356
P1476
Dihydropyridine-sensitive Ca2+ ...... 4) and inhibitor (PN 200-110).
@en
P2093
P2860
P304
P356
10.1073/PNAS.83.5.1518
P407
P577
1986-03-01T00:00:00Z