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Publications by W. T. Birdsong
Buprenorphine Is a Weak Partial Agonist That Inhibits Opioid Receptor Desensitization
Journal of Neuroscience
Neuroscience
Related publications
6′-Guanidinonaltrindole (6′-Gnti) Is a G Protein-Biased Κ-Opioid Receptor Agonist That Inhibits Arrestin Recruitment
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
An Opioid Agonist That Does Not Induce -Opioid Receptor--Arrestin Interactions or Receptor Internalization
Molecular Pharmacology
Molecular Medicine
Pharmacology
Μ Opioid Receptor Phosphorylation, Desensitization, and Ligand Efficacy
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
The Mu Opioid Receptor Is Involved in Buprenorphine-Induced Locomotor Stimulation and Conditioned Place Preference
Neuropharmacology
Molecular Neuroscience
Cellular
Pharmacology
Opioid Kappa Receptor Selective Agonist TRK-820 (Nalfurafine Hydrochloride)
Growth in Buprenorphine Waivers for Physicians Increased Potential Access to Opioid Agonist Treatment, 2002-11
Health Affairs
Medicine
Health Policy
Optimal Agonist/Antagonist Combinations Maintain Receptor Response by Preventing Rapid SS1-Adrenergic Receptor Desensitization
International Journal of Pharmacology
Pharmacology
Opioid Peptidomimetics: Leads for the Design of Bioavailable Mixed Efficacy Μ Opioid Receptor (MOR) Agonist/Δ Opioid Receptor (DOR) Antagonist Ligands
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Characterization of Methadone as a Β-Arrestin-Biased Μ-Opioid Receptor Agonist
Molecular Pain
Molecular Medicine
Anesthesiology
Pain Medicine
Cellular
Molecular Neuroscience
