The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase von ALTHAUS, I. W, GONZALES, A. J, DOWNEY, K. M, THOMAS, R. C, ARISTOFF, P. A, TARPLEY, W. G, REUSSER, F, CHOU, J. J, ROMERO, D. L, DEIBEL, M. R, KUO-CHEN CHOU, KEZDY, F. J, RESNICK, L, BUSSO, M. E, SO, A. G

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Kinetic studies of human immunodeficiency virus type 1 protease and its active-site hydrogen bond mutant A28S von Ido, E, Han, H P, Kezdy, F J, Tang, J

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Amphiphilic Secondary Structure: Design of Peptide Hormones von Kaiser, E. T., Kézdy, F. J.

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An activation-collision mechanism for cholesterol transfer between membranes von Steck, T L, Kezdy, F J, Lange, Y

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pH dependence of kinetic parameters of pepsin, rhizopuspepsin, and their active-site hydrogen bond mutants von LIN, YZ, FUSEK, M, LIN, XL, HARTSUCK, JA, KEZDY, FJ, TANG, J

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The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase von Althaus, Irene W., Chou, Kuo-Chen, Lemay, Richelle J., Franks, Kellie M., Deibel, Martin R., Kezdy, Ferenc J., Resnick, Lionel, Busso, Mariano E., So, Antero G., Downey, Kathleen M., Romero, Donna L., Thomas, Richard C., Aristoff, Paul A., Tarpley, W.Gary, Reusser, Fritz

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Kinetics of Processive Nucleic Acid Polymerases and Nucleases von Chou, K.C., Kezdy, F.J., Reusser, F.

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Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E von Althaus, I W, Chou, J J, Gonzales, A J, Deibel, M R, Chou, K C, Kezdy, F J, Romero, D L, Aristoff, P A, Tarpley, W G, Reusser, F

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Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E von Althaus, Irene W, Chou, James J, Gonzales, Andrea J, Deibel, Martin R, Chou, Kuo Chen, Kezdy, Ferenc J, Romero, Donna L, Palmer, John R, Thomas, Richard C

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[6] Chromogenic substrates and assay of phospholipases A2 von Cho, Wonhwa, Kézdy, Ferenc J.

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Transepithelial transport of aliphatic carboxylic acids studied in Madin Darby canine kidney (MDCK) cell monolayers von CHO, M. J, ADSON, A, KEZDY, F. J

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Dissociative inhibition of dimeric enzymes. Kinetic characterization of the inhibition of HIV-1 protease by its COOH-terminal tetrapeptide von Zhang, Z Y, Poorman, R A, Maggiora, L L, Heinrikson, R L, Kézdy, F J

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Molecular structure of deoxycytidyl-3'-methylphosphonate (Rp) 5'-deoxyguanidine, d[Cp(CH3)G]. A neutral dinucleotide with Watson-Crick base pairing and a right handed helical twist von HAN, F, WATT, W, DUCHAMP, D. J, CALLAHAN, L, KEZDY, F. J, AGARWAL, K

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Mode of interaction of phosphofructokinase with the erythrocyte membrane von Jenkins, J D, Kezdy, F J, Steck, T L

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Monolayers of long chain lecithins at the air/water interface and their hydrolysis by phospholipase A2 von YOKOYAMA, S, KEZDY, F. J

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A cumulative specificity model for proteases from human immunodeficiency virus types 1 and 2, inferred from statistical analysis of an extended substrate data base von POORMAN, R. A, TOMASSELLI, A. G, HEINRIKSON, R. L, KEZDY, F. J

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A synthetic amphiphilic .beta.-strand tridecapeptide: a model for apolipoprotein B von Osterman, David, Mora, Rene, Kezdy, F. J, Kaiser, E. T, Meredith, Stephen C

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Protein Nitration by Peroxynitrite: A Method for Monitoring Nitric Oxide Neurotoxicity von Althaus, J.S., Fici, G.J., Plaisted, S.M., Kezdy, F.J., Campbell, C.M., Hoogerheide, J.G., Von Voigtlander, P.F.

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Design, synthesis, and characterization of a cytotoxic peptide with melittin-like activity von DeGrado, William F, Kezdy, F. J, Kaiser, E. T

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The use of polymer-bound oximes for the synthesis of large peptides usable in segment condensation: synthesis of a 44 amino acid amphiphilic peptide model of apolipoprotein A-1 von Nakagawa, Satoe H, Lau, Herman S. H, Kezdy, F. J, Kaiser, E. T

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