In vitro and in vivo activities of SCH 42427, the active enantiomer of the antifungal agent SCH 39304 by LOEBENBERG, D, CACCIAPUOTI, A, PARMEGIANI, R, MOSS, E. L, MENZEL, F. JR, ANTONACCI, B, NORRIS, C, YAROSH-TOMAINE, T, HARE, R. S, MILLER, G. H

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Posaconazole Is a Potent Inhibitor of Sterol 14α-Demethylation in Yeasts and Molds by Munayyer, Hanan K, Mann, Paul A, Chau, Andrew S, Yarosh-Tomaine, Taisa, Greene, Jonathan R, Hare, Roberta S, Heimark, Larry, Palermo, Robert E, Loebenberg, David, McNicholas, Paul M

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Comparison of SCH 39304, fluconazole, and ketoconazole for treatment of systemic infections in mice by Cacciapuoti, A, Loebenberg, D, Parmegiani, R, Antonacci, B, Norris, C, Moss, Jr, E L, Menzel, Jr, F, Yarosh-Tomaine, T, Hare, R S, Miller, G H

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Crystal Structure of the Catalytic Domain of Human ADAM33 by Orth, Peter, Reichert, Paul, Wang, Wenyan, Prosise, Winifred W., Yarosh-Tomaine, Taisa, Hammond, Gerald, Ingram, Richard N., Xiao, Li, Mirza, Urooj A., Zou, Jun, Strickland, Corey, Taremi, S.Shane, Le, Hung V., Madison, Vincent

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In vitro and in vivo activities of SCH 56592 (Posaconazole), a new triazole antifungal agent, against Aspergillus and Candida by CACCIAPUOTI, A, LOEBENBERG, D, ARNOLD, B, ANTONACCI, B, PARMEGIANI, R, YAROSH-TOMAINE, T, MILLER, G. H, HARE, R. S, CORCORAN, E, MENZEL, F. JR, MOSS, E. L, NORRIS, C, MICHALSKI, M, RAYNOR, K, HALPERN, J, MENDRICK, C

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Comparative in vitro and in vivo evaluation of N-D-ornithyl amphotericin B methyl ester, amphotericin B methyl ester, and amphotericin B by PARMEGIANI, R. M, LOEBENBERG, D, ANTONACCI, B, YAROSH-TOMAINE, T, SCUPP, R, WRIGHT, J. J, CHIU, P. J. S, MILLER, G. H

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Mechanism of azole antifungal activity as determined by liquid chromatographic/mass spectrometric monitoring of ergosterol biosynthesis by Heimark, Larry, Shipkova, Petia, Greene, Jonathan, Munayyer, Hanan, Yarosh-Tomaine, Taisa, DiDomenico, Beth, Hare, Roberta, Pramanik, Birendra N.

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Protease domain of human ADAM33 produced by Drosophila S2 cells by Prosise, Winifred W., Yarosh-Tomaine, Taisa, Lozewski, Zia, Ingram, Richard N., Zou, Jun, Liu, Jian-Jun, Zhu, Feng, Taremi, S. Shane, Le, Hung V., Wang, Wenyan

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Relationship among physicochemical properties, skin permeability, and topical activity of the racemic compound and pure enantiomers of a new antifungal by WEARLEY, L, ANTONACCI, B, SEQUEIRA, J, YAROSH-TOMAINE, T, CACCIAPUOTI, A, ASSENZA, S, CHAUDRY, I, ECKHART, C, LEVINE, N, LOEBENBERG, D, NORRIS, C, PARMEGIANI, R

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Comparison of SCH 39304, fluconazole, and ketaconazole for treatment of systemic infectious in mice by CACCIAPUOTI, A.°, LOEBENBERG, D, PARMEGIANI, R, ANTONACCI, B, NORRIS, C, MOSS, E. L, MENZEL, F. JR, YAROSH-TOMAINE, T, HARE, R. S, MILLER, G. H

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Discovery of the HCV NS3/4A Protease Inhibitor (1R,5S)-N-[3-Amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]-3- [2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl... by Prongay, Andrew J, Guo, Zhuyan, Yao, Nanhua, Pichardo, John, Fischmann, Thierry, Strickland, Corey, Myers, Joseph, Weber, Patricia C, Beyer, Brian M, Ingram, Richard, Hong, Zhi, Prosise, Winifred W, Ramanathan, Lata, Taremi, S. Shane, Yarosh-Tomaine, Taisa, Zhang, Rumin, Senior, Mary, Yang, Rong-Sheng, Malcolm, Bruce, Arasappan, Ashok, Bennett, Frank, Bogen, Stephane L, Chen, Kevin, Jao, Edwin, Liu, Yi-Tsung, Lovey, Raymond G, Saksena, Anil K, Venkatraman, Srikanth, Girijavallabhan, Viyyoor, Njoroge, F. George, Madison, Vincent

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Key steps in the structure-based optimization of the hepatitis C virus NS3/4A protease inhibitor SCH503034 by Madison, Vincent, Prongay, Andrew J., Guo, Zhuyan, Yao, Nanhua, Pichardo, John, Fischmann, Thierry, Strickland, Corey, Myers Jr, Joseph, Weber, Patricia C., Beyer, Brian M., Ingram, Richard, Hong, Zhi, Prosise, Winifred W., Ramanathan, Lata, Taremi, S. Shane, Yarosh-Tomaine, Taisa, Zhang, Rumin, Senior, Mary, Yang, Rong-Sheng, Malcolm, Bruce, Arasappan, Ashok, Bennett, Frank, Bogen, Stephane L., Chen, Kevin, Jao, Edwin, Liu, Yi-Tsung, Lovey, Raymond G., Saksena, Anil K., Venkatraman, Srikanth, Girijavallabhan, Viyyoor, Njoroge, F. George

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In Vitro and In Vivo Activities of SCH 56592 (Posaconazole), a New Triazole Antifungal Agent, againstAspergillus and Candida by Cacciapuoti, Anthony, Loebenberg, David, Corcoran, Erik, Menzel, Fred, Moss, Eugene L, Norris, Christine, Michalski, Monika, Raynor, Kimberly, Halpern, Judith, Mendrick, Cara, Arnold, Brian, Antonacci, Barry, Parmegiani, Raulo, Yarosh-Tomaine, Taisa, Miller, George H, Hare, Roberta S

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Posaconazole is a potent inhibitor of sterol 14alpha-demethylation in yeasts and molds by Munayyer, Hanan K, Mann, Paul A, Chau, Andrew S, Yarosh-Tomaine, Taisa, Greene, Jonathan R, Hare, Roberta S, Heimark, Larry, Palermo, Robert E, Loebenberg, David, McNicholas, Paul M

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