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Biorxiv : the Preprint Server for Biology|September 16, 2024
Next generation APOBEC3 inhibitors: Optimally designed for potency and nuclease stabilityAdam K Hedger, Wazo Myint, Jeong Min Lee, et al.European Journal of Medicinal Chemistry|December 25, 2025
Fluorinated HIV-1 protease inhibitors containing chiral hydroxyethylbenzene and indanol as P2' ligands with potent activity against drug-resistant variantsJagroop Kaur, Ean Spielvogel, Desaboini Nageswara Rao, et al.The Journal of Biological Chemistry|January 30, 2026
Engineered IgA-Fc fusion protein with bioactive nanobody neutralizes SARS-CoV-2 variants with mucosal delivery potentialRachel M Golonka, Lauren E Intravaia, Ala M Shaqra, et al.ACS Infectious Diseases|June 30, 2023
Systematic Analyses of the Resistance Potential of Drugs Targeting SARS-CoV-2 Main ProteaseJulia M Flynn, Qiu Yu J Huang, Sarah N Zvornicanin, et al.Mabs|September 26, 2024
FcRn-enhancing mutations lead to increased and prolonged levels of the HIV CCR5-blocking monoclonal antibody leronlimab in the fetuses and newborns of pregnant rhesus macaquesJoanna Zikos, Gabriela M Webb, Helen L Wu, et al.Nature Communications|June 21, 2022
Defining the substrate envelope of SARS-CoV-2 main protease to predict and avoid drug resistanceAla M Shaqra, Sarah N Zvornicanin, Qiu Yu J Huang, et al.Biorxiv : the Preprint Server for Biology|August 6, 2025
Cooperativity and Communication between the Active Sites of the Dimeric SARS-CoV-2 Main ProteaseSarah N Zvornicanin, Ala M Shaqra, Julia Flynn, et al.Science Advances|January 16, 2026
Cooperativity and communication between the active sites of the dimeric SARS-CoV-2 main proteaseSarah N Zvornicanin, Ala M Shaqra, Julia Flynn, et al.Science (New York, N.Y.)|November 9, 2023
Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitorsMelissa L Boby, Daren Fearon, Matteo Ferla, et al.Pageof 2