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ACS Medicinal Chemistry Letters|June 6, 2014
Synthesis and Agonistic Activity at the GPR35 of 5,6-Dihydroxyindole-2-carboxylic Acid AnaloguesHuayun Deng, Ye FangPharmacology|April 11, 2012
Anti-inflammatory gallic Acid and wedelolactone are G protein-coupled receptor-35 agonistsHuayun Deng, Ye FangNaunyn-Schmiedeberg'S Archives of Pharmacology|April 25, 2012
Aspirin metabolites are GPR35 agonistsHuayun Deng, Ye FangPharmaceuticals (Basel, Switzerland)|November 27, 2013
The Three Catecholics Benserazide, Catechol and Pyrogallol are GPR35 AgonistsHuayun Deng, Ye FangJournal of Pharmacological and Toxicological Methods|August 13, 2013
Label-free cell phenotypic assessment of the biased agonism and efficacy of agonists at the endogenous muscarinic M3 receptorsHuayun Deng, Haiyan Sun, Ye FangMethods in Molecular Biology (Clifton, N.J.)|July 19, 2016
Label-Free Cell Phenotypic Identification of D-Luciferin as an Agonist for GPR35Heidi Hu, Huayun Deng, Ye FangScientific Reports|April 24, 2012
Multiple tyrosine metabolites are GPR35 agonistsHuayun Deng, Haibei Hu, Ye FangPlos One|April 19, 2012
Label-free phenotypic profiling identified D-luciferin as a GPR35 agonistHaibei Hu, Huayun Deng, Ye FangAnalytical Chemistry|September 8, 2012
Probing biochemical mechanisms of action of muscarinic M3 receptor antagonists with label-free whole cell assaysHuayun Deng, Chaoming Wang, Ming Su, et al.Pageof 4