Heterogeneous ligand-mediated Ca++ responses at wt and mutant α2A-adrenoceptors suggest multiple ligand activation binding sites at the α2A-adrenoceptor
- 31 October 2000
- journal article
- Published by Elsevier in Neuropharmacology
- Vol. 39 (11) , 2101-2111
- https://doi.org/10.1016/s0028-3908(00)00040-x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Abnormal Regulation of the Sympathetic Nervous System in α2A-Adrenergic Receptor Knockout MiceMolecular Pharmacology, 1999
- Binding, gating, affinity and efficacy: The interpretation of structure‐activity relationships for agonists and of the effects of mutating receptorsBritish Journal of Pharmacology, 1998
- Ligand Efficacy and Potency at Recombinant α2 Adrenergic Receptors: Agonist-Mediated [35s]gtpγs BindingBiochemical Pharmacology, 1998
- Selective inhibition of adenylyl cyclase by octopamine via a human cloned α2A‐adrenoceptorBritish Journal of Pharmacology, 1997
- Adrenergic Receptors From Molecular Structure to in vivo functionTrends in Cardiovascular Medicine, 1997
- Central Hypotensive Effects of the α 2a -Adrenergic Receptor SubtypeScience, 1996
- Gα15 and Gα16 Couple a Wide Variety of Receptors to Phospholipase CPublished by Elsevier ,1995
- Regions of the alpha 1-adrenergic receptor involved in coupling to phosphatidylinositol hydrolysis and enhanced sensitivity of biological function.Proceedings of the National Academy of Sciences, 1990
- Receptors linked to inhibition of adenylate cyclase: additional signaling mechanismsThe FASEB Journal, 1988
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976