Modelling of promiscuous receptor–Gi/Gs-protein coupling and effector response
- 1 December 2001
- journal article
- review article
- Published by Elsevier in Trends in Pharmacological Sciences
- Vol. 22 (12) , 616-622
- https://doi.org/10.1016/s0165-6147(00)01864-2
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Role of G-protein availability in differential signaling by alpha 2-adrenoceptorsBiochemical Pharmacology, 2001
- Site‐Directed Mutations in the Third Intracellular Loop of the Serotonin 5‐HT1A Receptor Alter G Protein Coupling from Gi to Gs in a Ligand‐Dependent MannerJournal of Neurochemistry, 2000
- Molecular Basis of Receptor/G-Protein-Coupling SelectivityPharmacology & Therapeutics, 1998
- Selective inhibition of adenylyl cyclase by octopamine via a human cloned α2A‐adrenoceptorBritish Journal of Pharmacology, 1997
- The Second Intracellular Loop of the α2-Adrenergic Receptors Determines Subtype-specific Coupling to cAMP ProductionPublished by Elsevier ,1997
- Chimeric Mutagenesis of Putative G-protein Coupling Domains of the α2A-Adrenergic ReceptorPublished by Elsevier ,1996
- Inositol 1-,4-,5-trisphosphate-dependent Ca2+ signaling by the recombinant human PTH/PTHrP receptor stably expressed in a human kidney cell lineBone, 1996
- Diversity and Selectivity of Receptor-G Protein InteractionAnnual Review of Pharmacology and Toxicology, 1996
- The cloned human 5-HT1E receptor couples to inhibition and activation of adenylyl cyclase via two distinct pathways in transfected BS-C-1 cellsNeuropharmacology, 1994
- Coupling of human α2-adrenoceptor subtypes to regulation of cAMP production in transfected S115 cellsEuropean Journal of Pharmacology: Molecular Pharmacology, 1994