A novel series of potent and selective small molecule inhibitors of the complement component C1s von Subasinghe, Nalin L., Ali, Farah, Illig, Carl R., Jonathan Rudolph, M., Klein, Scott, Khalil, Ehab, Soll, Richard M., Bone, Roger F., Spurlino, John C., DesJarlais, Renee L., Crysler, Carl S., Cummings, Maxwell D., Morris, Philip E., Kilpatrick, John M., Sudhakara Babu, Y.

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Discovery of novel FMS kinase inhibitors as anti-inflammatory agents von Illig, Carl R., Chen, Jinsheng, Wall, Mark J., Wilson, Kenneth J., Ballentine, Shelley K., Rudolph, M. Jonathan, DesJarlais, Renee L., Chen, Yanmin, Schubert, Carsten, Petrounia, Ioanna, Crysler, Carl S., Molloy, Christopher J., Chaikin, Margery A., Manthey, Carl L., Player, Mark R., Tomczuk, Bruce E., Meegalla, Sanath K.

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Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors von WILSON, Kenneth J, ILLIG, Carl R, ZHANG, Marie, LEWANDOWSKI, Frank A, ZHAO ZHOU, SHARP, Celia, MAGUIRE, Diane, GRASBERGER, Bruce, DESJARLAIS, Renee L, SPURLINO, John, SUBASINGHE, Nalin, HOFFMAN, James B, RUDOLPH, M. Jonathan, SOLL, Richard, MOLLOY, Christopher J, BONE, Roger, GREEN, David, RANDALL, Troy

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Design and Synthesis of 4,5-Disubstituted-thiophene-2-amidines as Potent Urokinase Inhibitors von Rudolph, M.Jonathan, Illig, Carl R., Subasinghe, Nalin L., Wilson, Kenneth J., Hoffman, James B., Randle, Troy, Green, David, Molloy, Chris J., Soll, Richard M., Lewandowski, Frank, Zhang, Marie, Bone, Roger, Spurlino, John C., Deckman, Ingrid C., Manthey, Carl, Sharp, Celia, Maguire, Diane, Grasberger, Bruce L., DesJarlais, Renée L., Zhou, Zhao

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Synthesis of thiophene-2-carboxamidines containing 2-amino-thiazoles and their biological evaluation as urokinase inhibitors von Wilson, Kenneth J., Illig, Carl R., Subasinghe, Nalin, Hoffman, James B., Jonathan Rudolph, M., Soll, Richard, Molloy, Christopher J., Bone, Roger, Green, David, Randall, Troy, Zhang, Marie, Lewandowski, Frank A., Zhou, Zhao, Sharp, Celia, Maguire, Diane, Grasberger, Bruce, DesJarlais, Renee L., Spurlino, John

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Structure-Based design, synthesis and sAR of a novel series of thiopheneamidine urokinase plasminogen activator inhibitors von Subasinghe, Nalin L., Illig, Carl, Hoffman, James, Rudolph, M.Jonathan, Wilson, Kenneth J., Soll, Richard, Randle, Troy, Green, David, Lewandowski, Frank, Zhang, Marie, Bone, Roger, Spurlino, John, DesJarlais, Renee, Deckman, Ingrid, Molloy, Christopher J., Manthey, Carl, Zhou, Zhau, Sharp, Celia, Maguire, Diane, Crysler, Carl, Grasberger, Bruce

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Preparation of oligonucleotide-peptide conjugates von Tung, Ching Hsuan, Rudolph, M. Jonathan, Stein, Stanley

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PHOSPHONOACETATE DERIVATIVES OF OLIGODEOXYRIBONUCLEOTIDES von Jonathan Rudolph, M, Reitman, Michael S., MacMillan, Eric W, Cook, Alan F.

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Synthesis and Properties of Combinatorial Libraries of Phosphoramidates von Fathi, Reza, Rudolph, M. Jonathan, Gentles, Robert G, Patel, Rina, MacMillan, Eric W, Reitman, Michael S, Pelham, David, Cook, Alan F

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Photochemistry of stilbenes. 8. Eliminative photocyclization of o-methoxystilbenes von Mallory, Frank B, Rudolph, M. Jonathan, Oh, Soon M

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INHIBITORS OF C-FMS KINASE von MOLLOY, Christopher, ILLIG, Carl R, MEEGALLA, Sanath, CHEN, Jinsheng, WALL, Mark J, MANTHEY, Carl, FLORES, Christopher, RUDOLPH, M. Jonathan, WILSON, Ken, BALLENTINE, Shelley K, DESJARLAIS, Renee

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INHIBITORS OF C-FMS KINASE von CHEN JINSHENG, ILLIG CARL R, WILSON KEN, DESJARLAIS RENEE, BALLENTINE SHELLEY K, MANTHEY CARL, FLORES CHRISTOPHER, MEEGALLA SANATH, WALL MARK J, RUDOLPH M. JONATHAN, MOLLOY CHRISTOPHER

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INHIBITORER AF C-FMS KINASE von MOLLOY, Christopher, ILLIG, Carl R, MEEGALLA, Sanath, CHEN, Jinsheng, MANTHEY, Carl, WALL, Mark J, FLORES, Christopher, WILSON, Ken, RUDOLPH, M. Jonathan, DESJARLAIS, Renee, BALLENTINE, Shelley K

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INHIBITORS OF C-FMS KINASE von M. JONATHAN RUDOLPH, SANATH MEEGALLA, MARK J. WALL, CARL MANTHEY, CARL R. ILLIG, KEN WILSON, JINSHENG CHEN, CHRISTOPHER MOLLOY, CHRISTOPHER FLORES, RENEE DESJARLAIS, SHELLEY K. BALLENTINE

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Inhibitorer av c-fms kinase von Chen, Jinsheng, Meegalla, Sanath, Molloy, Christopher, Ballentine, Shelley, Wilson, Ken, Illig, Carl R, Rudolph, Jonathan M, Manthey, Carl, Wall, Mark, Desjarlais, Renee, Flores, Christopher

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INHIBITORS OF C-FMS KINASE von BALLENTINE, SHELLEY K, WALL, MARK J, MOLLOY, CHRISTOPHER, CHEN, JINSHENG, FLORES, CHRISTOPHER, ILLIG, CARL R, RUDOLPH, M. JONATHAN, DESJARLAIS, RENEE, MEEGALLA, SANATH, WILSON, KEN, MANTHEY, CARL

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METHOD OF INHIBITING FLT3 KINASE von BALLENTINE, SHELLEY K, WILSON, KENNETH, WALL, MARK J, BAUMANN, CHRISTIAN ANDREW, ILLIG, CARL R, RUDOLPH, M. JONATHAN, TUMAN, ROBERT W, CHEN, JINGSHENG, MEEGALLA, SANETH, JOHNSON, DANA L

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Method of inhibiting C-KIT kinase von Molloy Christopher J, Manthey Carl M, Chen Jinsheng, Ballentine Shelley K, Meegalla Sanath K, Illig Carl R, Wall Mark J, Wilson Kenneth J, Rudolph M. Jonathan, Desjarlais Renee Louise

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métodos para reduzir e inibir atividade cinase de c-kit em uma célula von M. JONATHAN RUDOLPH, CARL L. MANTHEY, RENEE L. DESJARLAIS, MARK J. WALL, CARL R. ILLIG, KENNETH WILSON, JINGSHENG CHEN, CHRISTOPHER FLORES, Sanath K. Meegalla, CHRISTOPHER J. MOLLOY, SHELLEY K. BALLENTINE

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métodos para reduzir e inibir atividade cinase de ckit em uma célula von Christopher J. Molloy, M. JONATHAN RUDOLPH, CARL L. MANTHEY, Shelley K. Ballentine, Renee L. Desjarlais, Carl R. Illig, CHRISTOPHER FLORES, Mark J. Wall, Sanath K. Meegalla, Kenneth Wilson, Jingsheng Chen

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