The Buprenorphine Analogue BU10119 Attenuates Drug-Primed and Stress-Induced Cocaine Reinstatement in Mice
Todd M. Hillhouse(University of Wisconsin–Green Bay), John R. Traynor(University of Michigan), Emily M. Jutkiewicz(University of Wisconsin–Green Bay), Mehrnoosh Ostovar(University of Bath), James E. Hallahan(University of Wisconsin–Green Bay), Keith M. Olson(University of Michigan), Joshua L. West(University of Wisconsin–Green Bay), Bryan Sears(University of Wisconsin–Green Bay), Claire Meurice(University of Wisconsin–Green Bay), Stephen M. Husbands(University of Bath), Peyton O. Koppenhaver(University of Wisconsin–Green Bay), Lauren Rysztak(University of Wisconsin–Green Bay)
Cited by 10
Related Papers
The novel μ‐opioid receptor agonist PZM21 depresses respiration and induces tolerance to antinociception
|British Journal of Pharmacology|2018|174
Endogenous RGS Protein Action Modulates μ-Opioid Signaling through Gαo
|Journal of Biological Chemistry|2003|107
Role of G Protein–Coupled Receptor Kinases 2 and 3 in μ-Opioid Receptor Desensitization and Internalization
|Molecular Pharmacology|2015|93
Discovery, Synthesis, and Molecular Pharmacology of Selective Positive Allosteric Modulators of the δ-Opioid Receptor
|Journal of Medicinal Chemistry|2015|75
Activities of mixed NOP and μ‐opioid receptor ligands
|British Journal of Pharmacology|2007|62