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BMC Molecular and Cell Biology|August 7, 2019
CD40/anti-CD40 antibody complexes which illustrate agonist and antagonist structural switchesMaria A Argiriadi, Lorenzo Benatuil, Ievgeniia Dubrovska, et al.Bioorganic & Medicinal Chemistry Letters|March 14, 2007
Lead optimization of methionine aminopeptidase-2 (MetAP2) inhibitors containing sulfonamides of 5,6-disubstituted anthranilic acidsGary T Wang, Robert A Mantei, Megumi Kawai, et al.Nature Communications|September 20, 2022
Structure of the PAPP-ABP5 complex reveals mechanism of substrate recognitionRussell A Judge, Janani Sridar, Kathryn Tunyasuvunakool, et al.ACS Medicinal Chemistry Letters|June 18, 2021
Structure-Based Design of A-1293102, a Potent and Selective BCL-XL InhibitorZhi-Fu Tao, Xilu Wang, Jun Chen, et al.Chembiochem : a European Journal of Chemical Biology|January 10, 2018
Design of Aminobenzothiazole Inhibitors of Rho Kinases 1 and 2 by Using Protein Kinase A as a Structure SurrogateRussell A Judge, Anil Vasudevan, Victoria E Scott, et al.Journal of Medicinal Chemistry|July 9, 2025
Discovery of Orally Efficacious Bridged Piperazines as smTNF ModulatorsZhiguo Bian, Robert G Schmidt, Noel S Wilson, et al.Scientific Reports|August 26, 2022
Identification and structure-based drug design of cell-active inhibitors of interleukin 17A at a novel C-terminal siteEric R Goedken, Maria A Argiriadi, Justin D Dietrich, et al.Chemical Biology & Drug Design|July 17, 2007
Discovery and design of novel HSP90 inhibitors using multiple fragment-based design strategiesJeffrey R Huth, Chang Park, Andrew M Petros, et al.Journal of Medicinal Chemistry|February 14, 2015
Structure-guided design of a series of MCL-1 inhibitors with high affinity and selectivityMilan Bruncko, Le Wang, George S Sheppard, et al.Molecular Cancer Therapeutics|March 20, 2024
Inhibition of MALT1 and BCL2 Induces Synergistic Antitumor Activity in Models of B-Cell LymphomaJoshua P Plotnik, Adam E Richardson, Haopeng Yang, et al.Pageof 4