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Methods in Molecular Biology (Clifton, N.J.)|October 1, 2011
Kinase inhibitor profiling using chemoproteomicsMarkus Schirle, Eugene C Petrella, Scott M Brittain, et al.Proteome Science|July 21, 2017
Examining the influence of specificity ligands and ATP-competitive ligands on the overall effectiveness of bivalent kinase inhibitorsMargaret L Wong, Jason Murphy, Edmund Harrington, et al.ACS Chemical Biology|March 20, 2023
Targeted Protein Degradation through E2 RecruitmentNafsika Forte, Dustin Dovala, Matthew J Hesse, et al.BMC Biochemistry|January 26, 2008
Blocking binding of Bacillus thuringiensis Cry1Aa to Bombyx mori cadherin receptor results in only a minor reduction of toxicityTaek H You, Mi K Lee, Jeremy L Jenkins, et al.Nature|July 22, 2014
Structure of the DDB1-CRBN E3 ubiquitin ligase in complex with thalidomideEric S Fischer, Kerstin Böhm, John R Lydeard, et al.Journal of Medicinal Chemistry|December 13, 2006
Bridging chemical and biological space: "target fishing" using 2D and 3D molecular descriptorsJames H Nettles, Jeremy L Jenkins, Andreas Bender, et al.ACS Omega|September 18, 2018
Indolyl-Pyridinyl-Propenone-Induced Methuosis through the Inhibition of PIKFYVEHyelim Cho, Erin Geno, Maude Patoor, et al.Journal of Chemical Information and Modeling|November 28, 2006
"Bayes affinity fingerprints" improve retrieval rates in virtual screening and define orthogonal bioactivity space: when are multitarget drugs a feasible concept?Andreas Bender, Jeremy L Jenkins, Meir Glick, et al.Biorxiv : the Preprint Server for Biology|July 17, 2026
Stereoselective Covalent Targeting of BTK(C481S) and Kinases with β-Lactone ElectrophilesCeline D Wang, Polina E Barzova, Julian Robles, et al.Cell Chemical Biology|March 10, 2023
Chemoproteomics-enabled discovery of a covalent molecular glue degrader targeting NF-κBElizabeth A King, Yoojin Cho, Nathan S Hsu, et al.Pageof 14