Substituted Diphenyl Ethers as a Novel Chemotherapeutic Platform against Burkholderia pseudomallei von CUMMINGS, Jason E, BEAUPRE, Adam J, SCHWEIZER, Herbert P, TONGE, Peter J, SLAYDEN, Richard A, KNUDSON, Susan E, LIU, Nina, WEIXUAN YU, NECKLES, Carla, HUI WANG, KHANNA, Avinash, BOMMINENI, Gopal R, TRUNCK, Lily A

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Fusion transcripts: Unexploited vulnerabilities in cancer? von Neckles, Carla, Sundara Rajan, Soumya, Caplen, Natasha J.

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HNRNPH1-dependent splicing of a fusion oncogene reveals a targetable RNA G-quadruplex interaction von Neckles, Carla, Boer, Robert E, Aboreden, Nicholas, Cross, Allison M, Walker, Robert L, Kim, Bong-Hyun, Kim, Suntae, Schneekloth, Jr, John S, Caplen, Natasha J

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Abstract 4494: HNRNPH1-dependent splicing of a fusion oncogene reveals a targetable RNA G-quadruplex interaction von Neckles, Carla, Boer, Robert, Aboreden, Nicholas, Walker, Robert L., Kim, Bong-Hyun, Kim, Suntae, Schneekloth, John S., Caplen, Natasha J.

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Abstract B25: HNRNPH1-dependent splicing of the fusion oncogene EWS-FLI1 reveals a targetable RNA G-quadruplex interaction von Neckles, Carla, Boer, Robert E., Aboreden, Nicholas, Cross, Allison M., Walker, Robert L., Kim, Bong-Hyun, Kim, Suntae, Schneekloth, John S., Caplen, Natasha J.

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A [32P]NAD+-based method to identify and quantitate long residence time enoyl-acyl carrier protein reductase inhibitors von Yu, Weixuan, Neckles, Carla, Chang, Andrew, Bommineni, Gopal Reddy, Spagnuolo, Lauren, Zhang, Zhuo, Liu, Nina, Lai, Christina, Truglio, James, Tonge, Peter J.

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Rational Optimization of Diphenyl Ether Binding Kinetics to the Enoyl-ACP Reductase FabI1 from Burkholderia pseudomallei von Neckles, Carla, Eltschkner, Sandra, Cummings, Jason E., Hirschbeck, Maria, Daryaee, Fereidoon, Bommineni, Gopal R., Zhang, Zhuo, Spagnuolo, Lauren, Yu, Weixuan, Davoodi, Shabnam, Slayden, Richard A., Kisker, Caroline, Tonge, Peter J.

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Rationalizing the Binding Kinetics for the Inhibition of the Burkholderia pseudomallei FabI1 Enoyl-ACP Reductase von Neckles, Carla, Eltschkner, Sandra, Cummings, Jason E, Hirschbeck, Maria, Daryaee, Fereidoon, Bommineni, Gopal R, Zhang, Zhuo, Spagnuolo, Lauren, Yu, Weixuan, Davoodi, Shabnam, Slayden, Richard A, Kisker, Caroline, Tonge, Peter J

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Selectivity of Pyridone- and Diphenyl Ether-Based Inhibitors for the Yersinia pestis FabV Enoyl-ACP Reductase von Neckles, Carla, Pschibul, Annica, Lai, Cheng-Tsung, Hirschbeck, Maria, Kuper, Jochen, Davoodi, Shabnam, Zou, Junjie, Liu, Nina, Pan, Pan, Shah, Sonam, Daryaee, Fereidoon, Bommineni, Gopal R, Lai, Cristina, Simmerling, Carlos, Kisker, Caroline, Tonge, Peter J

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A [32P]-NAD+-based method to identify and quantitate long residence time enoyl-ACP reductase inhibitors von Yu, Weixuan, Neckles, Carla, Chang, Andrew, Bommineni, Gopal Reddy, Spagnuolo, Lauren, Zhang, Zhuo, Liu, Nina, Lai, Christina, Truglio, James, Tonge, Peter J.

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Structure of the Yersinia pestis FabV Enoyl-ACP Reductase and Its Interaction with Two 2-Pyridone Inhibitors von Hirschbeck, Maria W., Kuper, Jochen, Lu, Hao, Liu, Nina, Neckles, Carla, Shah, Sonam, Wagner, Steffen, Sotriffer, Christoph A., Tonge, Peter J., Kisker, Caroline

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Structure of the Yersinia pestis FabV enoyl-ACP reductase and its interaction with two novel 2-pyridone inhibitors von Hirschbeck, Maria W., Kuper, Jochen, Lu, Hao, Liu, Nina, Neckles, Carla, Shah, Sonam, Wagner, Steffen, Sotriffer, Christoph A., Tonge, Peter J., Kisker, Caroline

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