Pharmacological and functional properties of voltagemi independent Ca2+ channels
- 1 April 1996
- journal article
- review article
- Published by Elsevier in Cell Calcium
- Vol. 19 (4) , 269-279
- https://doi.org/10.1016/s0143-4160(96)90068-8
Abstract
No abstract availableKeywords
This publication has 128 references indexed in Scilit:
- LU52396, an inhibitor of the store-dependent (capacitative) Ca2+ influxEuropean Journal of Pharmacology: Molecular Pharmacology, 1995
- Nitric oxide modulates agonist-evoked Ca2+ release and influx responses in PC12-64 cellsEuropean Journal of Pharmacology: Molecular Pharmacology, 1995
- Modulation of cytosolic Ca2+ concentration by thapsigargin and cyclopiazonic acid in human aortic endothelial cellsEuropean Journal of Pharmacology: Molecular Pharmacology, 1995
- Tetrandrine: A new ligand to block voltage-dependent Ca2+ and Ca2+-activated K+ channelsLife Sciences, 1994
- TRH-evoked entry of extracellular calcium in GH4C1 cells: Possible importance of arachidonic acid metabolitesMolecular and Cellular Endocrinology, 1994
- Depletion of InsP3 stores activates a Ca2+ and K+ current by means of a phosphatase and a diffusible messengerNature, 1993
- Inhibition of human brain tumor cell growth by a receptor-operated Ca2+ channel blockerCancer Letters, 1993
- Calcium influx evoked by Ca2+ store depletion in human platelets is more susceptible to cytochrome P-450 inhibitors than receptor-mediated calcium entryCell Calcium, 1992
- Intracellular Ca2+ release by flufenamic acid and other blockers of the non‐selective cation channelFEBS Letters, 1992
- Multiple actions of SC 38249: the blocker of both voltage-operated and second messenger-operated Ca2+ channels also inhibits Ca2+ extrusionEuropean Journal of Pharmacology: Molecular Pharmacology, 1990