Identification of Diverse Microbial Metabolites as Potent Inhibitors of HIV-1 Tat Transactivation von Jayasuriya, Hiranthi, Zink, Deborah L., Polishook, Jon D., Bills, Gerald F., Dombrowski, Anne W., Genilloud, Olga, Pelaez, Fernando F., Herranz, Lucia, Quamina, Donette, Lingham, Russell B., Danzeizen, Renee, Graham, Pia L., Tomassini, Joanne E., Singh, Sheo B.

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Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure–activity relationships of 2-methoxystypandrone and its analogues von Singh, Sheo B, Graham, Pia L, Reamer, Robert A, Cordingley, Michael G

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Viral long terminal repeat substrate binding characteristics of the human immunodeficiency virus type 1 integrase von HAZUDA, D. J, WOLFE, A. L, HASTINGS, J. C, ROBBINS, H. L, GRAHAM, P. L, LAFEMINA, R. L, EMINI, E. A

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ChemInform Abstract: Discovery, Total Synthesis, HRV 3C-Protease Inhibitory Activity, and Structure-Activity Relationships of 2-Methoxystypandrone (VI) and Its Analogues von Singh, Sheo B., Graham, Pia L., Reamer, Robert A., Cordingley, Michael G.

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Sequence-Specific Interaction of Tat Protein and Tat Peptides with the Transactivation-Responsive Sequence Element of Human Immunodeficiency Virus Type 1 in vitro von Cordingley, Michael G., LaFemina, Robert L., Callahan, Pia L., Condra, Jon H., Sardana, Vinod V., Graham, Donald J., Nguyen, Tacy M., LeGrow, Kathleen, Gotlib, Leah, Schlabach, Abner J., Colonno, Richard J.

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