Binding Site Elucidation of Hydantoin-Based Antagonists of LFA-1 Using Multidisciplinary Technologies:  Evidence for the Allosteric Inhibition of a Protein−Protein Interaction von Last-Barney, Kathleen, Davidson, Walter, Cardozo, Mario, Frye, Leah L, Grygon, Christine A, Hopkins, Jerry L, Jeanfavre, Deborah D, Pav, Susan, Qian, Chungeng, Stevenson, James M, Tong, Liang, Zindell, Renee, Kelly, Terence A

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A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket von Tong, Liang, Pav, Susan, White, Della M., Rogers, Sheri, Crane, Kathy M., Cywin, Charles L., Brown, Maryanne L., Pargellis, Christopher A.

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Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site von Pargellis, Christopher, Tong, Liang, Churchill, Laurie, Cirillo, Pier F., Gilmore, Thomas, Graham, Anne G., Grob, Peter M., Hickey, Eugene R., Moss, Neil, Pav, Susan, Regan, John

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Vitamin D 25OH deficiency in COVID-19 patients admitted to a tertiary referral hospital von Cereda, Emanuele, Bogliolo, Laura, Klersy, Catherine, Lobascio, Federica, Masi, Sara, Crotti, Silvia, De Stefano, Ludovico, Bruno, Raffaele, Corsico, Angelo Guido, Di Sabatino, Antonio, Perlini, Stefano, Montecucco, Carlomaurizio, Caccialanza, Riccardo, Belliato, Mirko, Ludovisi, Serena, Mariani, Francesca, Ferrari, Alessandra, Musella, Valeria, Muggia, Chiara, Croce, Gabriele, Barteselli, Chiara, Mambella, Jacopo, Di Terlizzi, Francesco

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Pyrazole Urea-Based Inhibitors of p38 MAP Kinase:  From Lead Compound to Clinical Candidate von Regan, John, Breitfelder, Steffen, Cirillo, Pier, Gilmore, Thomas, Graham, Anne G, Hickey, Eugene, Klaus, Bernhard, Madwed, Jeffrey, Moriak, Monica, Moss, Neil, Pargellis, Chris, Pav, Sue, Proto, Alfred, Swinamer, Alan, Tong, Liang, Torcellini, Carol

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Crystal Structure of Human Immunodeficiency Virus (HIV) Type 2 Protease in Complex with a Reduced Amide Inhibitor and Comparison with HIV-1 Protease Structures von Tong, Liang, Pav, Susan, Pargellis, Christopher, Do, Florence, Lamarre, Daniel, Anderson, Paul C.

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Potent HIV Protease Inhibitors Containing a Novel (Hydroxyethyl)amide Isostere von Beaulieu, Pierre L, Wernic, Dominik, Abraham, Anderson, Paul C, Bogri, Tibor, Bousquet, Yves, Croteau, Gilbert, Guse, Ingrid, Lamarre, Daniel, Liard, Francine, Paris, William, Thibeault, Diane, Pav, Susan, Tong, Liang

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Crystallization and preliminary crystallographic analysis of recombinant human p38 MAP kinase von Pav, S., White, D.M., Rogers, S., Crane, K.M., Cywin, C.L., Hopkins, J., Brown, M.L., Pargellis, C.A., Tong, L., Davidson, W.

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Frailty and anticoagulants in older subjects with atrial fibrillation: the EUROSAF study von Pilotto, Alberto, Veronese, Nicola, Polidori, Maria Cristina, Strandberg, Timo, Topinkova, Eva, Cruz-Jentoft, Alfonso J, Custodero, Carlo, Barbagallo, Mario, Maggi, Stefania

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Design and Synthesis of Dipeptide Nitriles as Reversible and Potent Cathepsin S Inhibitors von Ward, Yancey D, Thomson, David S, Frye, Leah L, Cywin, Charles L, Morwick, Tina, Emmanuel, Michel J, Zindell, Renée, McNeil, Daniel, Bekkali, Younes, Hrapchak, Matt, DeTuri, Molly, Crane, Kathy, White, Della, Pav, Susan, Wang, Yong, Hao, Ming-Hong, Grygon, Christine A, Labadia, Mark E, Freeman, Dorothy M, Davidson, Walter, Hopkins, Jerry L, Brown, Maryanne L, Spero, Denice M

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DB2 PureXML Cookbook: Master the Power of the IBM Hybrid Data Server von Nicola, Matthias, Kumar-Chatterjee, Pav

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Administração de nitroglicerina no tratamento convencional refratário do edema pulmonar cardiogênico em cão von Velasquez, Omar Gutierrez, Gimenes, André Martins

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Optimization of 2-Phenylaminoimidazo[4,5-h]isoquinolin-9-ones:  Orally Active Inhibitors of lck Kinase von Goldberg, Daniel R, Butz, Tanja, Cardozo, Mario G, Eckner, Robert J, Hammach, Abdelhakim, Huang, Jessica, Jakes, Scott, Kapadia, Suresh, Kashem, Mohammed, Lukas, Susan, Morwick, Tina M, Panzenbeck, Maret, Patel, Usha, Pav, Susan, Peet, Gregory W, Peterson, Jeffrey D, Prokopowicz, Anthony S, Snow, Roger J, Sellati, Rosemarie, Takahashi, Hidenori, Tan, Jonathan, Tschantz, Matt A, Wang, Xiao-Jun, Wang, Yong, Wolak, John, Xiong, Pla, Moss, Neil

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Preliminary Crystallographic Studies of Human Mitochondrial NAD(P)+-Dependent Malic Enzyme von Bhargava, Girija, Mui, Suet, Pav, Susan, Wu, Hao, Loeber, Gerhard, Tong, Liang

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2‘,6‘-Dimethylphenoxyacetyl:  A New Achiral High Affinity P 3 -P 2 Ligand for Peptidomimetic-Based HIV Protease Inhibitors von Beaulieu, Pierre L., Anderson, Paul C., Cameron, Dale R., Croteau, Gilbert, Gorys, Vida, Grand-Maître, Chantal, Lamarre, Daniel, Liard, Francine, Paris, William, Plamondon, Louis, Soucy, François, Thibeault, Diane, Wernic, Dominik, Yoakim, Christiane, Pav, Susan, Tong, Liang

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2‘,6‘-Dimethylphenoxyacetyl:  A New Achiral High Affinity P3-P2 Ligand for Peptidomimetic-Based HIV Protease Inhibitors von Beaulieu, Pierre L, Anderson, Paul C, Cameron, Dale R, Croteau, Gilbert, Gorys, Vida, Grand-Maître, Chantal, Lamarre, Daniel, Liard, Francine, Paris, William, Plamondon, Louis, Soucy, François, Thibeault, Diane, Wernic, Dominik, Yoakim, Christiane, Pav, Susan, Tong, Liang

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Crystal structures of HIV-2 protease in complex with inhibitors containing the hydroxyethylamine dipeptide isostere von Tong, Liang, Pav, Susan, Mui, Suet, Lamarre, Daniel, Yoakim, Christiane, Beaulieu, Pierre, Anderson, Paul C

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Design and Synthesis of Dipeptide Nitriles as Reversible and Potent Cathepsin S Inhibitors von Ward, Yancey D, Thomson, David S, Frye, Leah L, Cywin, Charles L, Morwick, Tina, Emmanuel, Michel J, Zindell, Renée, McNeil, Daniel, Bekkali, Younes, Girardot, Marc, Hrapchak, Matt, DeTuri, Molly, Crane, Kathy, White, Della, Pav, Susan, Wang, Yong, Hao, Ming-Hong, Grygon, Christine A, Labadia, Mark E, Freeman, Dorothy M, Davidson, Walter, Hopkins, Jerry L, Brown, Maryanne L, Spero, Denice M

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High Resolution Crystal Structures of Recombinant Human Renin in Complex with Polyhydroxymonoamide Inhibitors von Tong, Liang, Pav, Susan, Lamarre, Daniel, Pilote, Louise, LaPlante, Steven, Anderson, Paul C., Jung, Grace

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