Synthesis of substituted 5[ H]phenanthridin-6-ones as potent poly(ADP-ribose)polymerase-1 (PARP1) inhibitors by Li, Jia-He, Serdyuk, Larisa, Ferraris, Dana V., Xiao, Ge, Tays, Kevin L., Kletzly, Paul W., Li, Weixing, Lautar, Susan, Zhang, Jie, Kalish, Vincent J.

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Design and Pharmacological Activity of Phosphinic Acid Based NAALADase Inhibitors by Jackson, Paul F, Tays, Kevin L, Maclin, Keith M, Ko, Yao-Sen, Li, Weixing, Vitharana, Dil, Tsukamoto, Takashi, Stoermer, Doris, Lu, Xi-Chun M, Wozniak, Krystyna, Slusher, Barbara S

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Identification of a Potent, Selective, and Orally Active Leukotriene A4 Hydrolase Inhibitor with Anti-Inflammatory Activity by Grice, Cheryl A, Tays, Kevin L, Savall, Brad M, Wei, Jianmei, Butler, Christopher R, Axe, Frank U, Bembenek, Scott D, Fourie, Anne M, Dunford, Paul J, Lundeen, Katherine, Coles, Fawn, Xue, Xiaohua, Riley, Jason P, Williams, Kacy N, Karlsson, Lars, Edwards, James P

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Identification of a Potent, Selective, and Orally Active Leukotriene A 4 Hydrolase Inhibitor with Anti-Inflammatory Activity by Grice, Cheryl A., Tays, Kevin L., Savall, Brad M., Wei, Jianmei, Butler, Christopher R., Axe, Frank U., Bembenek, Scott D., Fourie, Anne M., Dunford, Paul J., Lundeen, Katherine, Coles, Fawn, Xue, Xiaohua, Riley, Jason P., Williams, Kacy N., Karlsson, Lars, Edwards, James P.

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Discovery and SAR of 6-Alkyl-2,4-diaminopyrimidines as Histamine H 4 Receptor Antagonists by Savall, Brad M., Chavez, Frank, Tays, Kevin, Dunford, Paul J., Cowden, Jeffery M., Hack, Michael D., Wolin, Ronald L., Thurmond, Robin L., Edwards, James P.

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Two susceptibility loci identified for prostate cancer aggressiveness by Berndt, Sonja I., Wang, Zhaoming, Yeager, Meredith, Alavanja, Michael C., Albanes, Demetrius, Amundadottir, Laufey, Andriole, Gerald, Beane Freeman, Laura, Campa, Daniele, Cancel-Tassin, Geraldine, Canzian, Federico, Cornu, Jean-Nicolas, Cussenot, Olivier, Diver, W. Ryan, Gapstur, Susan M., Grönberg, Henrik, Haiman, Christopher A., Henderson, Brian, Hutchinson, Amy, Hunter, David J., Key, Timothy J., Kolb, Suzanne, Koutros, Stella, Kraft, Peter, Le Marchand, Loic, Lindström, Sara, Machiela, Mitchell J., Ostrander, Elaine A., Riboli, Elio, Schumacher, Fred, Siddiq, Afshan, Stanford, Janet L., Stevens, Victoria L., Travis, Ruth C., Tsilidis, Konstantinos K., Virtamo, Jarmo, Weinstein, Stephanie, Wilkund, Fredrik, Xu, Jianfeng, Lilly Zheng, S., Yu, Kai, Wheeler, William, Zhang, Han, Sampson, Joshua, Black, Amanda, Jacobs, Kevin, Hoover, Robert N., Tucker, Margaret, Chanock, Stephen J.

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Lower body mass index and age are predictive of improved pain and health utility scores following arthroscopic management of femoroacetabular impingement by Kay, Jeffrey, Simunovic, Nicole, Heels-Ansdell, Diane, Bhandari, Mohit, Ayeni, Olufemi R.

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Discovery and SAR of 6‑Alkyl-2,4-diaminopyrimidines as Histamine H4 Receptor Antagonists by Savall, Brad M, Chavez, Frank, Tays, Kevin, Dunford, Paul J, Cowden, Jeffery M, Hack, Michael D, Wolin, Ronald L, Thurmond, Robin L, Edwards, James P

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Diaminopyrimidines, diaminopyridines and diaminopyridazines as histamine H4 receptor modulators by Savall, Brad M., Meduna, Steven P., Tays, Kevin, Cai, Hui, Thurmond, Robin L., McGovern, Patricia, Gaul, Michael, Zhao, Bao-Ping, Edwards, James P.

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Diaminopyrimidines, diaminopyridines and diaminopyridazines as histamine H sub(4) receptor modulators by Savall, Brad M, Meduna, Steven P, Tays, Kevin, Cai, Hui, Thurmond, Robin L, McGovern, Patricia, Gaul, Michael, Zhao, Bao-Ping, Edwards, James P

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The SAR of 4-substituted (6,6-bicyclic) piperidine cathepsin S inhibitors by Grice, Cheryl A., Tays, Kevin, Khatuya, Haripada, Gustin, Darin J., Butler, Christopher R., Wei, Jianmei, Sehon, Clark A., Sun, Siquan, Gu, Yin, Jiang, Wen, Thurmond, Robin L., Karlsson, Lars, Edwards, James P.

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