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Molecular Pharmacology|March 18, 2005
Identification and pharmacological characterization of prokineticin 2 beta as a selective ligand for prokineticin receptor 1Jingcai Chen, Chester Kuei, Steven Sutton, et al.
European Journal of Pharmacology|June 28, 2008
Identification of the domains in RXFP4 (GPCR142) responsible for the high affinity binding and agonistic activity of INSL5 at RXFP4 compared to RXFP3 (GPCR135)Jessica Zhu, Chester Kuei, Steven Sutton, et al.
European Journal of Pharmacology|May 3, 2005
Molecular and pharmacological characterization of serotonin 5-HT2A and 5-HT2B receptor subtypes in dogPascal Bonaventure, Diane Nepomuceno, Kirsten Miller, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 16, 2004
Pharmacological characterization of relaxin-3/INSL7 receptors GPCR135 and GPCR142 from different mammalian speciesJingcai Chen, Chester Kuei, Steven W Sutton, et al.
The Journal of Biological Chemistry|October 3, 2003
Identification of relaxin-3/INSL7 as an endogenous ligand for the orphan G-protein-coupled receptor GPCR135Changlu Liu, Elo Eriste, Steven Sutton, et al.
Plos One|February 21, 2020
The PAR2 signal peptide prevents premature receptor cleavage and activationBelinda Liu, Grace Lee, Jiejun Wu, et al.
Annals of the New York Academy of Sciences|May 7, 2009
Metabolic and neuroendocrine responses to RXFP3 modulation in the central nervous systemSteven W Sutton, Jonathan Shelton, Craig Smith, et al.
Pharmacology Research & Perspectives|February 19, 2019
Mutagenesis of GPR139 reveals ways to create gain or loss of function receptorsLien Wang, Grace Lee, Amy Shih, et al.
The Journal of Biological Chemistry|August 10, 2005
A novel form of neurotensin post-translationally modified by arginylationElo Eriste, Ake Norberg, Diane Nepomuceno, et al.
ACS Medicinal Chemistry Letters|September 24, 2015
Identification and SAR of Glycine Benzamides as Potent Agonists for the GPR139 ReceptorCurt A Dvorak, Heather Coate, Diane Nepomuceno, et al.
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