Aminopyridine-Based c-Jun N-Terminal Kinase Inhibitors with Cellular Activity and Minimal Cross-Kinase Activity von Szczepankiewicz, Bruce G, Kosogof, Christi, Nelson, Lissa T. J, Liu, Gang, Liu, Bo, Zhao, Hongyu, Serby, Michael D, Xin, Zhili, Liu, Mei, Gum, Rebecca J, Haasch, Deanna L, Wang, Sanyi, Clampit, Jill E, Johnson, Eric F, Lubben, Thomas H, Stashko, Michael A, Olejniczak, Edward T, Sun, Chaohong, Dorwin, Sarah A, Haskins, Kristi, Abad-Zapatero, Cele, Fry, Elizabeth H, Hutchins, Charles W, Sham, Hing L, Rondinone, Cristina M, Trevillyan, James M

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Toxicological Evaluation of Thiol-Reactive Compounds Identified Using a La Assay To Detect Reactive Molecules by Nuclear Magnetic Resonance von Huth, Jeffrey R, Song, Danying, Mendoza, Renaldo R, Black-Schaefer, Candice L, Mack, Jamey C, Dorwin, Sarah A, Ladror, Uri S, Severin, Jean M, Walter, Karl A, Bartley, Diane M, Hajduk, Philip J

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Discovery and Design of Novel HSP90 Inhibitors Using Multiple Fragment-based Design Strategies von Huth, Jeffrey R., Park, Chang, Petros, Andrew M., Kunzer, Aaron R., Wendt, Michael D., Wang, Xilu, Lynch, Christopher L., Mack, Jamey C., Swift, Kerry M., Judge, Russell A., Chen, Jun, Richardson, Paul L., Jin, Sha, Tahir, Stephen K., Matayoshi, Edward D., Dorwin, Sarah A., Ladror, Uri S., Severin, Jean M., Walter, Karl A., Bartley, Diane M., Fesik, Stephen W., Elmore, Steven W., Hajduk, Philip J.

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From Bacterial Genomes to Novel Antibacterial Agents: Discovery, Characterization, and Antibacterial Activity of Compounds that Bind to HI0065 (YjeE) from Haemophilus influenzae von Lerner, Claude G., Hajduk, Philip J., Wagner, Rolf, Wagenaar, Frank L., Woodall, Charlotte, Gu, Yu‐Gui, Searle, Xenia B., Florjancic, Alan S., Zhang, Tianyuan, Clark, Richard F., Cooper, Curt S., Mack, Jamey C., Yu, Liping, Cai, Mengli, Betz, Steven F., Chovan, Linda E., McCall, J. Owen, Black‐Schaefer, Candace L., Kakavas, Stephan J., Schurdak, Mark E., Comess, Kenneth M., Walter, Karl A., Edalji, Rohinton, Dorwin, Sarah A., Smith, Richard A., Hebert, Eric J., Harlan, John E., Metzger, Randy E., Merta, Philip J., Baranowski, John L., Coen, Michael L., Thornewell, Susan J., Shivakumar, Annapur G., Saiki, Anne Y., Soni, Niru, Bui, Mai, Balli, Darlene J., Sanders, William J., Nilius, Angela M., Holzman, Thomas F., Fesik, Stephen W., Beutel, Bruce A.

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Preparation of synthetic polypeptide domains of carcinoembryonic antigen and their use in epitope mapping von HASS, G. M, BOLLING, T. J, KINDERS, R. J, HENSLEE, J. G, MANDECKI, W, DORWIN, S. A, SHIVELY, J. E

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ASELACINS, NOVEL COMPOUNDS THAT INHIBIT BINDING OF ENDOTHELIN TO ITS RECEPTOR: II. ISOLATION AND ELUCIDATION OF STRUCTURES von HOCHLOWSKI, JILL E., HILL, PRESTON, WHITTERN, DAVID N., SCHERR, MICHAEL H., RASMUSSEN, RONALD R., DORWIN, SARAH A., MCALPINE, JAMES B.

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Cloning and Expression of the Adenosine Kinase Gene from Rat and Human Tissues von McNally, Teresa, Helfrich, Rosalind J., Cowart, Marlon, Dorwin, Sarah A., Meuth, Joseph L., Idler, Kenneth B., Klute, Kimberly A., Simmer, Robert L., Kowaluk, Elizabeth A., Halbert, Donald N.

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The matrix metalloproteinase pump-1 catalyzes formation of low molecular weight (pro)urokinase in cultures of normal human kidney cells von MARCOTTE, P. A, KOZAN, I. M, DORWIN, S. A, RYAN, J. M

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Domain structure analysis of elongation factor‐3 from saccharomyces cerevisiae by limited proteolysis and differential scanning calorimetry von Ladror, Uri S., Egan, David A., Snyder, Seth W., Capobianco, John O., Goldman, Robert C., Dorwin, Sarah A., Johnson, Robert W., Edalji, Rohinton, Sarthy, Aparna V., Mcgonigal, Tom, Walter, Karl A., Holzman, Thomas F.

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Discovery of a potent and selective Bcl-2 inhibitor using SAR by NMR von Petros, Andrew M., Huth, Jeffrey R., Oost, Thorsten, Park, Cheol-Min, Ding, Hong, Wang, Xilu, Zhang, Haichao, Nimmer, Paul, Mendoza, Renaldo, Sun, Chaohong, Mack, Jamey, Walter, Karl, Dorwin, Sarah, Gramling, Emily, Ladror, Uri, Rosenberg, Saul H., Elmore, Steven W., Fesik, Stephen W., Hajduk, Philip J.

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Species Specificity of Amidine-Based Urokinase Inhibitors von Klinghofer, Vered, Stewart, Kent, McGonigal, Tom, Smith, Richard, Sarthy, Aparna, Nienaber, Vicki, Butler, Chris, Dorwin, Sarah, Richardson, Paul, Weitzberg, Moshe, Wendt, Mike, Rockway, Todd, Zhao, Xumiao, Hulkower, Keren I, Giranda, Vincent L

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Protein fragmentation via liquid chromatography–quadrupole time-of-flight mass spectrometry: The use of limited sequence information in structural characterization von Johnson, Robert W., Ahmed, Tanveer F., Miesbauer, Laura J., Edalji, Rohinton, Smith, Richard, Harlan, John, Dorwin, Sarah, Walter, Karl, Holzman, Tom

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