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Journal of the American Chemical Society|October 26, 2017
Cell-Surface Receptor-Ligand Interaction Analysis with Homogeneous Time-Resolved FRET and Metabolic Glycan Engineering: Application to Transmembrane and GPI-Anchored ReceptorsHenning Stockmann, Viktor Todorovic, Paul L Richardson, et al.Analytical Biochemistry|August 11, 2004
Fluorescence assay of SIRT protein deacetylases using an acetylated peptide substrate and a secondary trypsin reactionPatrick A Marcotte, Paul L Richardson, Paul R Richardson, et al.Biochemistry|November 23, 2006
Interactions of two monoclonal antibodies with BNP: high resolution epitope mapping using fluorescence correlation spectroscopySergey Y Tetin, Qiaoqiao Ruan, Sylvia C Saldana, et al.Biochemistry|July 23, 2003
Investigating the origin of the slow-binding inhibition of HCV NS3 serine protease by a novel substrate based inhibitorYaya Liu, Ayda Saldivar, Joshua Bess, et al.The Journal of Biological Chemistry|November 29, 2017
Quantitative ligand and receptor binding studies reveal the mechanism of interleukin-36 (IL-36) pathway activationLi Zhou, Viktor Todorovic, Steve Kakavas, et al.Npj Imaging|July 2, 2025
Increased imaging ligand hydrophilicity and improved pharmacokinetic properties provides enhanced in vivo targeting of fibroblast activation proteinRadhika Narain, Ian Nessler, Paul L Richardson, et al.SLAS Discovery : Advancing Life Sciences R & D|August 16, 2024
Development of a sensitive high-throughput enzymatic assay capable of measuring sub-nanomolar inhibitors of SARS-CoV2 MproPeter Kovar, Paul L Richardson, Alla Korepanova, et al.Analytical Biochemistry|July 24, 2007
Longer wavelength fluorescence resonance energy transfer depsipeptide substrates for hepatitis C virus NS3 proteaseAlex K Konstantinidis, Paul L Richardson, Kevin A Kurtz, et al.Journal of Biomolecular Screening|March 10, 2004
Microarrayed compound screening (microARCS) to identify activators and inhibitors of AMP-activated protein kinaseSteven N Anderson, Barbara L Cool, Lemma Kifle, et al.Bioorganic & Medicinal Chemistry Letters|May 17, 2003
Indole amide hydroxamic acids as potent inhibitors of histone deacetylasesYujia Dai, Yan Guo, Jun Guo, et al.Pageof 4