Sistare, F D <br/><br/>
P2 purinergic receptors potentiate parathyroid hormone receptor-mediated increases in intracellular calcium and inositol trisphosphate in UMR-106 rat osteoblasts.  [electronic resource] 

 -  Endocrinology  Oct 1995 
 - 4489-97 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0013-7227 
<br/><br/><label>Standard No.: </label>10.1210/endo.136.10.7664669  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Diphosphate--pharmacology<br/>Alkaloids--pharmacology<br/>Animals<br/>Calcium--metabolism<br/>Inositol 1,4,5-Trisphosphate--metabolism<br/>Ionomycin--pharmacology<br/>Osteoblasts--metabolism<br/>Parathyroid Hormone--pharmacology<br/>Peptide Fragments--pharmacology<br/>Rats<br/>Receptors, Parathyroid Hormone--physiology<br/>Receptors, Purinergic P2--physiology<br/>Staurosporine<br/>Teriparatide<br/>Tumor Cells, Cultured<br/>Uridine Triphosphate--pharmacology