Heterodimerization of ORL1 and Opioid Receptors and Its Consequences for N-type Calcium Channel Regulation
Open Access
- 1 January 2010
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 285 (2) , 1032-1040
- https://doi.org/10.1074/jbc.m109.040634
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Two Distinct Mechanisms Mediate Acute μ-Opioid Receptor Desensitization in Native NeuronsJournal of Neuroscience, 2009
- Constitutive Dimerization of the G-Protein Coupled Receptor, Neurotensin Receptor 1, Reconstituted into Phospholipid BilayersBiophysical Journal, 2009
- The Third Intracellular Loop Stabilizes the Inactive State of the Neuropeptide Y1 ReceptorJournal of Biological Chemistry, 2008
- β-Adrenergic Receptor Activation Induces Internalization of Cardiac Cav1.2 Channel Complexes through a β-Arrestin 1-mediated PathwayJournal of Biological Chemistry, 2008
- How and why do GPCRs dimerize?Trends in Pharmacological Sciences, 2008
- ORL1 receptor–mediated internalization of N-type calcium channelsNature Neuroscience, 2005
- ORL1, a novel member of the opioid receptor familyPublished by Wiley ,2001
- Molecular cloning and tissue distribution of a putative member of the rat opioid receptor gene family that is not a μ, δ or κ opioid receptor typePublished by Wiley ,2001
- Opioid receptor-like (ORL1) receptor distribution in the rat central nervous system: Comparison of ORL1 receptor mRNA expression with125I-[14Tyr]-orphanin FQ bindingJournal of Comparative Neurology, 1999
- Localization of orphanin FQ (nociceptin) peptide and messenger RNA in the central nervous system of the ratJournal of Comparative Neurology, 1999