Strategic Design of Catalytic Lysine‐Targeting Reversible Covalent BCR‐ABL Inhibitors von Quach, David, Tang, Guanghui, Anantharajan, Jothi, Baburajendran, Nithya, Poulsen, Anders, Wee, John L. K., Retna, Priya, Li, Rong, Liu, Boping, Tee, Doris H. Y., Kwek, Perlyn Z., Joy, Joma K., Yang, Wan‐Qi, Zhang, Chong‐Jing, Foo, Klement, Keller, Thomas H., Yao, Shao Q.

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The crystal structure of the non-liganded 14-3-3σ protein： insights into determinants of isoform specific ligand binding and dimerization von BENZINGER, Anne, POPOWICZ, Grzegorz M, JOY, Joma K, MAJUMDAR, Sudipta, HOLAK, Tad A, HERMEKING, Heiko

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Strategic Design of Catalytic Lysine‐Targeting Reversible Covalent BCR‐ABL Inhibitors von Quach, David, Tang, Guanghui, Anantharajan, Jothi, Baburajendran, Nithya, Poulsen, Anders, Wee, John L. K., Retna, Priya, Li, Rong, Liu, Boping, Tee, Doris H. Y., Kwek, Perlyn Z., Joy, Joma K., Yang, Wan‐Qi, Zhang, Chong‐Jing, Foo, Klement, Keller, Thomas H., Yao, Shao Q.

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Solid-phase synthesis and screening of a library of C-terminal arginine peptide aldehydes against Murray Valley encephalitis virus protease von Ede, Nicholas J., Hill, Jeffrey, Joy, Joma K., Ede, Anne-Marie, Koppens, Merran L.

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NMR and mass spectrometry studies of putative interactions of cell cycle proteins pRb and CDK6 with cell differentiation proteins MyoD and ID-2 von Smialowski, Pawel, Singh, Mahavir, Mikolajka, Aleksandra, Majumdar, Sudipta, Joy, Joma K., Nalabothula, Narasimharao, Krajewski, Marcin, Degenkolbe, Roland, Bernard, Hans-Ulrich, Holak, Tad A.

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The crystal structure of the non-liganded 14-3-3sigma protein: insights into determinants of isoform specific ligand binding and dimerization von Benzinger, Anne, Popowicz, Grzegorz M, Joy, Joma K, Majumdar, Sudipta, Holak, Tad A, Hermeking, Heiko

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The crystal structure of the non-liganded 14-3-3[sigma] protein: insights into determinants of isoform specific ligand binding and dimerization von Benzinger, Anne, Popowicz, Grzegorz M, Joy, Joma K, Majumdar, Sudipta, Holak, Tad A, Hermeking, Heiko

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Discovery of Irreversible Inhibitors Targeting Histone Methyltransferase, SMYD3 von Huang, Chuhui, Liew, Si Si, Lin, Grace R, Poulsen, Anders, Ang, Melgious J. Y, Chia, Brian C. S, Chew, Sin Yin, Kwek, Zekui P, Wee, John L. K, Ong, Esther H, Retna, Priya, Baburajendran, Nithya, Li, Rong, Yu, Weixuan, Koh-Stenta, Xiaoying, Ngo, Anna, Manesh, Sravanthy, Fulwood, Justina, Ke, Zhiyuan, Chung, Hwa Hwa, Sepramaniam, Sugunavathi, Chew, Xin Hui, Dinie, Nurul, Lee, May Ann, Chew, Yun Shan, Low, Choon Bing, Pendharkar, Vishal, Manoharan, Vithya, Vuddagiri, Susmitha, Sangthongpitag, Kanda, Joy, Joma, Matter, Alex, Hill, Jeffrey, Keller, Thomas H, Foo, Klement

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Identification of covalent active site inhibitors of dengue virus protease von Koh-Stenta, Xiaoying, Joy, Joma, Wang, Si Fang, Kwek, Perlyn Zekui, Wee, John Liang Kuan, Wan, Kah Fei, Gayen, Shovanlal, Chen, Angela Shuyi, Kang, CongBao, Lee, May Ann, Poulsen, Anders, Vasudevan, Subhash G, Hill, Jeffrey, Nacro, Kassoum

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Correction to “Discovery of Irreversible Inhibitors Targeting Histone Methyltransferase, SMYD3” von Huang, Chuhui, Liew, Si Si, Lin, Grace R, Poulsen, Anders, Ang, Melgious J. Y, Chia, Brian C. S, Chew, Sin Yin, Kwek, Zekui P, Wee, John L. K, Ong, Esther H, Retna, Priya, Baburajendran, Nithya, Li, Rong, Yu, Weixuan, Koh-Stenta, Xiaoying, Ngo, Anna, Manesh, Sravanthy, Fulwood, Justina, Ke, Zhiyuan, Chung, Hwa Hwa, Sepramaniam, Sugunavathi, Chew, Xin Hui, Dinie, Nurul, Lee, May Ann, Chew, Yun Shan, Low, Choon Bing, Pendharkar, Vishal, Manoharan, Vithya, Vuddagiri, Susmitha, Sangthongpitag, Kanda, Joy, Joma, Matter, Alex, Hill, Jeffrey, Keller, Thomas H, Foo, Klement

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