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Molecular Pharmacology Fast Forward. Published on April 22, 2014 as doi:10.1124/mol.113.090563
MOL #90563
Discovery and characterization of a G protein-biased agonist that inhibits
β-arrestin recruitment to the D2 dopamine receptor
R. Benjamin Free, Lani S. Chun, Amy E. Moritz, Brittney Miller, Trevor B. Doyle, Jennie L. Conroy, Adrian
Padron, Julie A. Meade, Jingbo Xiao, Xin Hu, Andrés E. Dulcey, Yang Han, Lihua Duan, Steve Titus, Melanie
Bryant-Genevier, Elena Barnaeva, Marc Ferrer, Jonathan A. Javitch, Thijs Beuming, Lei Shi, Noel Southall,
Juan J. Marugan, and David R. Sibley
Molecular Neuropharmacology Section, National Institute of Neurological Disorders and Stroke, National
Institutes of Health, Bethesda, MD (RBF, LSC, AEM, BM, TDB, JLC, AP, JAM, DRS)
National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD (JX, XH,
AED, ST, MBG, EB, MF, NS, JJM)
Center for Molecular Recognition and Departments of Psychiatry and Pharmacology, Columbia University
College of Physicians and Surgeons, New York, NY. Division of Molecular Therapeutics, New York State
Psychiatric Institute, New York, NY (YH, LD, JAJ)
Schrödinger Inc., New York, NY (TB)
Department of Physiology and Biophysics and Institute for Computational Biomedicine, Weill Medical College
of Cornell University, New York, NY (LS)
1
Copyright 2014 by the American Society for Pharmacology and Experimental Therapeutics.
MOL #90563
Running Title: G Protein-Biased D Receptor Agonist
2
Corresponding Author:
R. Benjamin Free, Ph.D.
Molecular Neuropharmacology Section
National Institute of Neurological Disorders and Stroke,
National Institutes of Health
5625 Fishers Lane, Room 4S-04
Bethesda, MD 20892-940
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