Molecular Mechanism of Calcium Channel Block by Isradipine
Open Access
- 1 July 2000
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 275 (29), 22114-22120
- https://doi.org/10.1074/jbc.m908836199
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Sequence Differences between α1C and α1S Ca2+ Channel Subunits Reveal Structural Determinants of a Guarded and Modulated Benzothiazepine ReceptorPublished by Elsevier ,1999
- Ca2+ channel sensitivity towards the blocker isradipine is affected by alternative splicing of the human α1C subunit geneFEBS Letters, 1998
- Nine L-type Amino Acid Residues Confer Full 1,4-Dihydropyridine Sensitivity to the Neuronal Calcium Channel α1ASubunitPublished by Elsevier ,1997
- Molecular Studies on the Voltage Dependence of Dihydropyridine Action on L-type Ca2+ ChannelsJournal of Biological Chemistry, 1997
- Analysis of the Dihydropyridine Receptor Site ofl-type Calcium Channels by Alanine-scanning MutagenesisPublished by Elsevier ,1997
- β Subunit Heterogeneity in Neuronal L-type Ca2+ChannelsPublished by Elsevier ,1997
- Transfer of 1,4-Dihydropyridine Sensitivity from L-Type to Class A (BI) Calcium ChannelsNeuron, 1996
- Molecular properties of a superfamily of plasma-membrane cation channelsCurrent Opinion in Cell Biology, 1994
- Molecular localization of regions in the L-type calcium channel critical for dihydropyridine actionNeuron, 1993
- Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channelNature, 1989