Matrix metalloproteinase–activated doxorubicin prodrugs inhibit HT1080 xenograft growth better than doxorubicin with less toxicity by Albright, Charles F, Graciani, Nilsa, Han, Wei, Yue, Eddy, Stein, Ross, Lai, Zhihong, Diamond, Melody, Dowling, Randine, Grimminger, Lisa, Zhang, Shu-Yun, Behrens, Davette, Musselman, Amy, Bruckner, Robert, Zhang, Mingzhu, Jiang, Xiang, Hu, Daniel, Higley, Anne, Dimeo, Susan, Rafalski, Maria, Mandlekar, Sandya, Car, Bruce, Yeleswaram, Swamy, Stern, Andrew, Copeland, Robert A, Combs, Andrew, Seitz, Steve P, Trainor, George L, Taub, Rebecca, Huang, Pearl, Oliff, Allen

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Synthesis and Evaluation of Indenopyrazoles as Cyclin-Dependent Kinase Inhibitors. 3. Structure Activity Relationships at C3 by Yue, Eddy W, Higley, C. Anne, DiMeo, Susan V, Carini, David J, Nugiel, David A, Benware, Carrie, Benfield, Pamela A, Burton, Catherine R, Cox, Sarah, Grafstrom, Robert H, Sharp, Diane M, Sisk, Lisa M, Boylan, John F, Muckelbauer, Jodi K, Smallwood, Angela M, Chen, Haiying, Chang, Chong-Hwan, Seitz, Steven P, Trainor, George L

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Development of a Scalable Synthesis toward a KRAS G12C Inhibitor Building Block Bearing an All-Carbon Quaternary Stereocenter, Part 2: Asymmetric Synthesis via Shi Epoxidation by Tan, Zhulin, Ju, Xuan, Wu, Hao, Dong, Weitong, Leung, Joyce C., Hou, Xiaowen, Lee, Heewon, Granger, Alice, Paolillo, Joshua M., DiMeo, Susan V., Chen, Chengsheng, Wu, Linglin, Lorenz, Jon C., Sarvestani, Max, Buono, Frederic, Frutos, Rogelio, Tampone, Thomas G., Huang, Xiaojun, Zhang, Gulin, Wang, Yuwen, Spinelli, Earl, Lei, Zhen, Song, Jinhua J.

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Development of a Scalable Synthesis toward a KRAS G12C Inhibitor Building Block Bearing an All-Carbon Quaternary Stereocenter, Part 1: From Discovery Route to Kilogram-Scale Produc... by Leung, Joyce C., Xu, Yibo, Radomkit, Suttipol, Lee, Jaehee, Kim, Wan Shin, Reeves, Jonathan T., Dong, Weitong, Jang, Hwanjong, Hou, Xiaowen, Lorenz, Jon C., Shao, Xiaole, Byrne, Denis, Johnson, Joe, Brundage, Anthony, Valentin, Clement, Beyer, Phouvieng, DiMeo, Susan V., Qu, Bo, Li, Ruoshi, Sarvestani, Max, Song, Jinhua J.

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Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3 by Yue, Eddy W., DiMeo, Susan V., Higley, C.Anne, Markwalder, Jay A., Burton, Catherine R., Benfield, Pamela A., Grafstrom, Robert H., Cox, Sarah, Muckelbauer, Jodi K., Smallwood, Angela M., Chen, Haiying, Chang, Chong-Hwan, Trainor, George L., Seitz, Steven P.

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National outbreak of Acanthamoeba keratitis associated with use of a contact lens solution, United States by VERANI, J.R, LORICK, S.A, YODER, J.S, BEACH, M.J, BRADEN, C.R, ROBERTS, J.M, CONOVER, C.S, CHEN, S, MCCONNELL, K.A, CHANG, D.C

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Micromachined chemical sensor with dual-transduction mechanisms by Chen, Ing-Shin, Stawasz, Michele, DiMascio, Susan K., Welch, James J., Neuner, Jeffrey W., Chen, Philip S. H., DiMeo, Frank

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(Imidazolylphenyl)pyrrol-2-one inhibitors of cardiac cAMP phosphodiesterase by Lampe, John W, Chou, Yuo Ling, Hanna, Reda G, Di Meo, Susan V, Erhardt, Paul W, Hagedorn, Alfred A, Ingebretsen, William R, Cantor, Elinor

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Heteroaryl-Fused 2-Phenylisothiazolone Inhibitors of Cartilage Breakdown by Wright, Stephen W, Petraitis, Joseph J, Abelman, Matthew M, Batt, Douglas G, Bostrom, Lori L, Corbett, Ronald L, Decicco, Carl P, Di Meo, Susan V, Freimark, Bruce

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Metabolism resistant isothiazolone inhibitors of cartilage breakdown by Wright, Stephen W., Petraitis, Joseph J., Batt, Douglas G., Corbett, Ronald L., Di Meo, Susan V., Freimark, Bruce, Giannaras, John V., Orwat, Michael J., Pinto, Donald J., Pratta, Michael A., Sherk, Susan R., Stampfli, Herman F., Williams, Jean M., Magolda, Ronald L., Arner, Elizabeth C.

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Synthesis and cardiac electrophysiological activity of N-substituted-4-(1H-imidazol-1-yl)benzamides - new selective class III agents by Morgan, Thomas K, Lis, Randall, Lumma, William C, Nickisch, Klaus, Wohl, Ronald A, Phillips, Gary B, Gomez, Robert P, Lampe, John W, Di Meo, Susan V

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Synthesis and pharmacological studies of N-[4-[2-hydroxy-3-[[2-[4-(1H-imidazol-1-yl)phenoxy]ethyl]amino]propoxy]phenyl]methanesulfonamide, a novel antiarrhythmic agent with class I... by Morgan, Thomas K, Lis, Randall, Lumma, William C, Wohl, Ronald A, Nickisch, Klaus, Phillips, Gary B, Lind, Joan M, Lampe, John W, Di Meo, Susan V

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