Stokke, M <br/><br/>
Stable guanosine 5'-triphosphate-analogues inhibit specific (+)-[3H]isradipine binding in rat hearts by a Ca(2+)-lowering, G protein-independent mechanism.  [electronic resource] 

 -  Pharmacology & toxicology  Jan 1996 
 - 28-36 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0901-9928 
<br/><br/><label>Standard No.: </label>10.1111/j.1600-0773.1996.tb00176.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Calcium--metabolism<br/>Calcium Channels--drug effects<br/>Cyclic AMP-Dependent Protein Kinases--metabolism<br/>GTP-Binding Proteins--metabolism<br/>Guanosine 5'-O-(3-Thiotriphosphate)--pharmacology<br/>Guanylyl Imidodiphosphate--pharmacology<br/>Heart--drug effects<br/>In Vitro Techniques<br/>Isradipine--pharmacokinetics<br/>Magnesium--pharmacology<br/>Male<br/>Membranes--drug effects<br/>Myocardium--cytology<br/>Radioligand Assay<br/>Rats<br/>Rats, Wistar<br/>Temperature<br/>Vasodilator Agents--pharmacokinetics