Sargeant, P <br/><br/>
Calcium influx evoked by Ca2+ store depletion in human platelets is more susceptible to cytochrome P-450 inhibitors than receptor-mediated calcium entry.  [electronic resource] 

 -  Cell calcium  Oct 1992 
 - 553-64 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0143-4160 
<br/><br/><label>Standard No.: </label>10.1016/0143-4160(92)90035-q  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Diphosphate--pharmacology<br/>Blood Platelets--drug effects<br/>Calcium--metabolism<br/>Calcium Channels--drug effects<br/>Calcium-Transporting ATPases--antagonists & inhibitors<br/>Cell Compartmentation<br/>Cytochrome P-450 Enzyme Inhibitors<br/>Cytochrome P-450 Enzyme System--physiology<br/>Econazole--pharmacology<br/>Humans<br/>Hydroquinones--pharmacology<br/>Inositol 1,4,5-Trisphosphate--physiology<br/>Intracellular Fluid--metabolism<br/>Ion Channel Gating--drug effects<br/>Manganese--metabolism<br/>Miconazole--pharmacology<br/>Osmolar Concentration<br/>Platelet Activating Factor--pharmacology<br/>Platelet Activation--drug effects<br/>Receptors, Cholinergic--physiology<br/>Ryanodine Receptor Calcium Release Channel<br/>Signal Transduction<br/>Terpenes--pharmacology<br/>Thapsigargin<br/>Thrombin--pharmacology<br/>Vasopressins--pharmacology