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Bean,
Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state.
1984, Pubmed
Bean,
Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state.
1984,
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Berjukow,
Molecular mechanism of calcium channel block by isradipine. Role of a drug-induced inactivated channel conformation.
2000,
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Xenbase
Berjukow,
Endogenous calcium channels in human embryonic kidney (HEK293) cells.
1996,
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Berjukow,
Sequence differences between alpha1C and alpha1S Ca2+ channel subunits reveal structural determinants of a guarded and modulated benzothiazepine receptor.
1999,
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Brehm,
Calcium entry leads to inactivation of calcium channel in Paramecium.
1978,
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Catterall,
Molecular properties of a superfamily of plasma-membrane cation channels.
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Ertel,
Nomenclature of voltage-gated calcium channels.
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Frishman,
Use of calcium antagonists in patients with ischemic heart disease and systemic hypertension.
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Glossmann,
Assay for calcium channels.
1985,
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Grabner,
Transfer of 1,4-dihydropyridine sensitivity from L-type to class A (BI) calcium channels.
1996,
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Handrock,
Dihydropyridine enantiomers block recombinant L-type Ca2+ channels by two different mechanisms.
1999,
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Hering,
Molecular determinants of inactivation in voltage-gated Ca2+ channels.
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Hering,
Ca2+ channel block and inactivation: common molecular determinants.
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Ionic channels in excitable membranes. Current problems and biophysical approaches.
1978,
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Ito,
Transfer of the high affinity dihydropyridine sensitivity from L-type To non-L-type calcium channel.
1997,
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Lacinová,
Isradipine interacts with the open state of the L-type calcium channel at high concentrations.
1998,
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Lee,
Ca2+/calmodulin binds to and modulates P/Q-type calcium channels.
1999,
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Lund-Johansen,
Cardiac effects of isradipine in patients with hypertension.
1993,
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Mikami,
Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel.
1989,
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Peterson,
Molecular determinants of high affinity dihydropyridine binding in L-type calcium channels.
1996,
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Peterson,
Analysis of the dihydropyridine receptor site of L-type calcium channels by alanine-scanning mutagenesis.
1997,
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Sanguinetti,
Voltage-dependent block of calcium channel current in the calf cardiac Purkinje fiber by dihydropyridine calcium channel antagonists.
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Sinnegger,
Nine L-type amino acid residues confer full 1,4-dihydropyridine sensitivity to the neuronal calcium channel alpha1A subunit. Role of L-type Met1188.
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Striessnig,
Structural basis of drug binding to L Ca2+ channels.
1998,
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Tang,
Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action.
1993,
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Walker,
Subunit interaction sites in voltage-dependent Ca2+ channels: role in channel function.
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