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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,
Pubmed Berjukow,
Molecular mechanism of calcium channel block by isradipine. Role of a drug-induced inactivated channel conformation.
2000,
Pubmed
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Xenbase Berjukow,
Sequence differences between alpha1C and alpha1S Ca2+ channel subunits reveal structural determinants of a guarded and modulated benzothiazepine receptor.
1999,
Pubmed Berjukow,
Endogenous calcium channels in human embryonic kidney (HEK293) cells.
1996,
Pubmed Brehm,
Calcium entry leads to inactivation of calcium channel in Paramecium.
1978,
Pubmed Catterall,
Molecular properties of a superfamily of plasma-membrane cation channels.
1994,
Pubmed Ertel,
Nomenclature of voltage-gated calcium channels.
2000,
Pubmed Frishman,
Use of calcium antagonists in patients with ischemic heart disease and systemic hypertension.
1997,
Pubmed Glossmann,
Assay for calcium channels.
1985,
Pubmed Grabner,
Transfer of 1,4-dihydropyridine sensitivity from L-type to class A (BI) calcium channels.
1996,
Pubmed Handrock,
Dihydropyridine enantiomers block recombinant L-type Ca2+ channels by two different mechanisms.
1999,
Pubmed Hering,
Ca2+ channel block and inactivation: common molecular determinants.
1998,
Pubmed Hering,
Molecular determinants of inactivation in voltage-gated Ca2+ channels.
2000,
Pubmed Hille,
Ionic channels in excitable membranes. Current problems and biophysical approaches.
1978,
Pubmed Ito,
Transfer of the high affinity dihydropyridine sensitivity from L-type To non-L-type calcium channel.
1997,
Pubmed Lacinová,
Isradipine interacts with the open state of the L-type calcium channel at high concentrations.
1998,
Pubmed Lee,
Ca2+/calmodulin binds to and modulates P/Q-type calcium channels.
1999,
Pubmed Lund-Johansen,
Cardiac effects of isradipine in patients with hypertension.
1993,
Pubmed Mikami,
Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel.
1989,
Pubmed
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Xenbase Peterson,
Analysis of the dihydropyridine receptor site of L-type calcium channels by alanine-scanning mutagenesis.
1997,
Pubmed Peterson,
Molecular determinants of high affinity dihydropyridine binding in L-type calcium channels.
1996,
Pubmed Sanguinetti,
Voltage-dependent block of calcium channel current in the calf cardiac Purkinje fiber by dihydropyridine calcium channel antagonists.
1984,
Pubmed 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.
1997,
Pubmed
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Xenbase Striessnig,
Structural basis of drug binding to L Ca2+ channels.
1998,
Pubmed Tang,
Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action.
1993,
Pubmed
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Xenbase Walker,
Subunit interaction sites in voltage-dependent Ca2+ channels: role in channel function.
1998,
Pubmed
