Potentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms.
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Phospholemman modulates the gating of cardiac L-type calcium channels.The cardiac alpha(1C) subunit can support excitation-triggered Ca2+ entry in dysgenic and dyspedic myotubesFPL 64176 modification of Ca(V)1.2 L-type calcium channels: dissociation of effects on ionic current and gating current.Properties of Na+ currents conducted by a skeletal muscle L-type Ca2+ channel pore mutant (SkEIIIK).Potentiated L-type Ca2+ channels rectifyDistinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1.The skeletal L-type Ca(2+) current is a major contributor to excitation-coupled Ca(2+) entry.The alpha(1S) III-IV loop influences 1,4-dihydropyridine receptor gating but is not directly involved in excitation-contraction coupling interactions with the type 1 ryanodine receptor.Modulation of single channels underlying hippocampal L-type current enhancement by agonists depends on the permeant ion.High-voltage-activated calcium channels in Muller cells acutely isolated from tiger salamander retina.
P2860
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P2860
Potentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms.
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Potentiation of the cardiac L- ...... occur via distinct mechanisms.
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Potentiation of the cardiac L- ...... occur via distinct mechanisms.
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type
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Potentiation of the cardiac L- ...... occur via distinct mechanisms.
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Potentiation of the cardiac L- ...... occur via distinct mechanisms.
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prefLabel
Potentiation of the cardiac L- ...... occur via distinct mechanisms.
@ast
Potentiation of the cardiac L- ...... occur via distinct mechanisms.
@en
P2093
P2860
P356
P1476
Potentiation of the cardiac L- ...... occur via distinct mechanisms.
@en
P2093
P2860
P304
P356
10.1085/JGP.118.5.495
P577
2001-11-01T00:00:00Z