Suchergebnisse - Sunghyun Kang

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  1. 1
    Identification of a sequence within U5 required for human immunodeficiency virus type 1 to stably maintain a primer binding site complementary to tRNA(Met)

    Identification of a sequence within U5 required for human immunodeficiency virus type 1 to stably maintain a primer binding site complementary to tRNA(Met) von Sunghyun Kang, Zhixin Zhang, Casey D. Morrow

    Veröffentlicht 1997
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  2. 2
    Selective inhibition of calcineurin-NFAT signaling by blocking protein–protein interaction with small organic molecules

    Selective inhibition of calcineurin-NFAT signaling by blocking protein–protein interaction with small organic molecules von Michael H. A. Roehrl, Sunghyun Kang, J. A. Aramburu, Gerhard Wagner, Anjana Rao, Patrick G. Hogan

    Veröffentlicht 2004
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  3. 3
    Potent and Orally Active Small-Molecule Inhibitors of the MDM2−p53 Interaction

    Potent and Orally Active Small-Molecule Inhibitors of the MDM2−p53 Interaction von Shanghai Yu, Dongguang Qin, Sanjeev Shangary, Jianyong Chen, Guoping Wang, Ke Ding, Donna McEachern, Su Qiu, Zaneta Nikolovska‐Coleska, Rebecca S. Miller, Sunghyun Kang, Dajun Yang, Shaomeng Wang

    Veröffentlicht 2009
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  4. 4
    Inhibition of urease-mediated ammonia production by 2-octynohydroxamic acid in hepatic encephalopathy

    Inhibition of urease-mediated ammonia production by 2-octynohydroxamic acid in hepatic encephalopathy von Diana Evstafeva, Filip Ilievski, Yinyin Bao, Zhi Luo, Boris Abramovic, Sunghyun Kang, Christian Steuer, Elita Montanari, Tommaso Casalini, Dunja Simičić, Dario Sessa, Stefanita-Octavian Mitrea, Katarzyna Pierzchała, Cristina Cudalbu, Chelsie E. Armbruster, Jean‐Christophe Leroux

    Veröffentlicht 2024
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  5. 5
    A Potent and Orally Active Antagonist (SM-406/AT-406) of Multiple Inhibitor of Apoptosis Proteins (IAPs) in Clinical Development for Cancer Treatment

    A Potent and Orally Active Antagonist (SM-406/AT-406) of Multiple Inhibitor of Apoptosis Proteins (IAPs) in Clinical Development for Cancer Treatment von Qian Cai, Haiying Sun, Yuefeng Peng, Jianfeng Lü, Zaneta Nikolovska‐Coleska, Donna McEachern, Liu Liu, Su Qiu, Chao‐Yie Yang, Rebecca S. Miller, Yi Han, Tao Zhang, Duxin Sun, Sunghyun Kang, Ming Guo, Lance Leopold, Dajun Yang, Shaomeng Wang

    Veröffentlicht 2011
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  6. 6
    Temporal activation of p53 by a specific MDM2 inhibitor is selectively toxic to tumors and leads to complete tumor growth inhibition

    Temporal activation of p53 by a specific MDM2 inhibitor is selectively toxic to tumors and leads to complete tumor growth inhibition von Sanjeev Shangary, Dongguang Qin, Donna McEachern, Meilan Liu, Rebecca S. Miller, Su Qiu, Zaneta Nikolovska‐Coleska, Ke Ding, Guoping Wang, Jianyong Chen, Denzil Bernard, Jian Zhang, Yipin Lu, Qingyang Gu, Rajal B. Shah, Kenneth J. Pienta, Xiaolan Ling, Sunghyun Kang, Ming Guo, Yi Sun, Dajun Yang, Shaomeng Wang

    Veröffentlicht 2008
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