Total Synthesis of (−)-7-Epicylindrospermopsin, a Toxic Metabolite of the Freshwater Cyanobacterium Aphanizomenon ovalisporum, and Assignment of Its Absolute Configuration von WHITE, James D., HANSEN, Joshua D.

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Discovery of CRBN E3 Ligase Modulator CC-92480 for the Treatment of Relapsed and Refractory Multiple Myeloma von Hansen, Joshua D, Correa, Matthew, Nagy, Mark A, Alexander, Matt, Plantevin, Veronique, Grant, Virginia, Whitefield, Brandon, Huang, Dehua, Kercher, Timothy, Harris, Roy, Narla, Rama Krishna, Leisten, Jim, Tang, Yang, Moghaddam, Mehran, Ebinger, Katalin, Piccotti, Joseph, Havens, Courtney G, Cathers, Brian, Carmichael, James, Daniel, Thomas, Vessey, Rupert, Hamann, Lawrence G, Leftheris, Katerina, Mendy, Derek, Baculi, Frans, LeBrun, Laurie A, Khambatta, Gody, Lopez-Girona, Antonia

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Evolution of Cereblon-Mediated Protein Degradation as a Therapeutic Modality von Chamberlain, Philip P, D’Agostino, Laura A, Ellis, J. Michael, Hansen, Joshua D, Matyskiela, Mary E, McDonald, Joseph J, Riggs, Jennifer R, Hamann, Lawrence G

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Asymmetric Synthesis of Epicylindrospermopsin via Intramolecular Nitrone Cycloaddition. Assignment of Absolute Configuration von White, James D, Hansen, Joshua D

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Pyrazolopyridine inhibitors of B-RafV600E. Part 2: Structure–activity relationships von Wenglowsky, Steve, Ahrendt, Kateri A., Buckmelter, Alex J., Feng, Bainian, Gloor, Susan L., Gradl, Stefan, Grina, Jonas, Hansen, Joshua D., Laird, Ellen R., Lunghofer, Paul, Mathieu, Simon, Moreno, David, Newhouse, Brad, Ren, Li, Risom, Tyler, Rudolph, Joachim, Seo, Jeongbeob, Sturgis, Hillary L., Voegtli, Walter C., Wen, Zhaoyang

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Proximity-dependent proteomics of the Chlamydia trachomatis inclusion membrane reveals functional interactions with endoplasmic reticulum exit sites von Dickinson, Mary S, Anderson, Lindsey N, Webb-Robertson, Bobbie-Jo M, Hansen, Joshua R, Smith, Richard D, Wright, Aaron T, Hybiske, Kevin

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CC-90009: A Cereblon E3 Ligase Modulating Drug That Promotes Selective Degradation of GSPT1 for the Treatment of Acute Myeloid Leukemia von Hansen, Joshua D, Correa, Matthew, Alexander, Matt, Nagy, Mark, Huang, Dehua, Sapienza, John, Lu, Gang, LeBrun, Laurie A, Cathers, Brian E, Zhang, Weihong, Tang, Yang, Ammirante, Massimo, Narla, Rama K, Piccotti, Joseph R, Pourdehnad, Michael, Lopez-Girona, Antonia

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Design and Synthesis of Novel Cereblon Binders for Use in Targeted Protein Degradation von Norris, Stephen, Ba, Xiaochu, Rhodes, Jayce, Huang, Dehua, Khambatta, Gody, Buenviaje, Jennifer, Nayak, Surendra, Meiring, Joseph, Reiss, Samantha, Xu, Shuichan, Shi, Lihong, Whitefield, Brandon, Alexander, Matt, Horn, Evan J., Correa, Matthew, Tehrani, Lida, Hansen, Joshua D., Papa, Patrick, Mortensen, Deborah S.

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Correction to “Design and Synthesis of Novel Cereblon Binders for Use in Targeted Protein Degradation” von Norris, Stephen, Ba, Xiaochu, Rhodes, Jayce, Huang, Dehua, Khambatta, Gody, Buenviaje, Jennifer, Nayak, Surendra, Meiring, Joseph, Reiss, Samantha, Xu, Shuichan, Shi, Lihong, Whitefield, Brandon, Alexander, Matt, Horn, Evan J., Correa, Matthew, Tehrani, Lida, Hansen, Joshua D., Papa, Patrick, Mortensen, Deborah S., Brazeau, Jean-François

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Protein Degradation via CRL4 CRBN Ubiquitin Ligase: Discovery and Structure-Activity Relationships of Novel Glutarimide Analogs That Promote Degradation of Aiolos and/or GSPT1 von Hansen, Joshua D, Condroski, Kevin, Correa, Matthew, Muller, George, Man, Hon-Wah, Ruchelman, Alexander, Zhang, Weihong, Vocanson, Fan, Crea, Tim, Liu, Wei, Lu, Gang, Baculi, Frans, LeBrun, Laurie, Mahmoudi, Afshin, Carmel, Gilles, Hickman, Matt, Lu, Chin-Chun

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Racemic and chiral lactams as potent, selective and functionally active CCR4 antagonists von Newhouse, Bradley, Allen, Shelley, Fauber, Benjamin, Anderson, Aaron S., Eary, C. Todd, Hansen, Joshua D., Schiro, Justin, Gaudino, John J., Laird, Ellen, Chantry, David, Eberhardt, Christine, Burgess, Laurence E.

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Walleye growth declines following zebra mussel and Bythotrephes invasion von Hansen, Gretchen J. A., Ahrenstorff, Tyler D., Bethke, Bethany J., Dumke, Joshua D., Hirsch, Jodie, Kovalenko, Katya E., LeDuc, Jaime F., Maki, Ryan P., Rantala, Heidi M., Wagner, Tyler

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Potent and Selective Aminopyrimidine-Based B-Raf Inhibitors with Favorable Physicochemical and Pharmacokinetic Properties von Mathieu, Simon, Gradl, Stefan N, Ren, Li, Wen, Zhaoyang, Aliagas, Ignacio, Gunzner-Toste, Janet, Lee, Wendy, Pulk, Rebecca, Zhao, Guiling, Alicke, Bruno, Boggs, Jason W, Buckmelter, Alex J, Choo, Edna F, Dinkel, Victoria, Gloor, Susan L, Gould, Stephen E, Hansen, Joshua D, Hastings, Gregg, Hatzivassiliou, Georgia, Laird, Ellen R, Moreno, David, Ran, Yingqing, Voegtli, Walter C, Wenglowsky, Steve, Grina, Jonas, Rudolph, Joachim

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Highly potent and selective 3-N-methylquinazoline-4(3H)-one based inhibitors of B-Raf(V600E) kinase von Wenglowsky, Steve, Ren, Li, Grina, Jonas, Hansen, Joshua D, Laird, Ellen R, Moreno, David, Dinkel, Victoria, Gloor, Susan L, Hastings, Gregg, Rana, Sumeet, Rasor, Kevin, Sturgis, Hillary L, Voegtli, Walter C, Vigers, Guy, Willis, Brandon, Mathieu, Simon, Rudolph, Joachim

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Trophic complexity of small fish in nearshore food webs von Wellard Kelly, Holly A., Kovalenko, Katya E., Ahrenstorff, Tyler D., Bethke, Bethany J., Brady, Valerie J., Dumke, Joshua D., Hansen, Gretchen J. A., Rantala, Heidi M.

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Non-oxime pyrazole based inhibitors of B-Raf kinase von Newhouse, Bradley J., Hansen, Joshua D., Grina, Jonas, Welch, Mike, Topalov, George, Littman, Nicole, Callejo, Michele, Martinson, Matthew, Galbraith, Sarah, Laird, Ellen R., Brandhuber, Barbara J., Vigers, Guy, Morales, Tony, Woessner, Rich, Randolph, Nikole, Lyssikatos, Joseph, Olivero, Alan

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Potent and selective pyrazole-based inhibitors of B-Raf kinase von Hansen, Joshua D., Grina, Jonas, Newhouse, Brad, Welch, Mike, Topalov, George, Littman, Nicole, Callejo, Michele, Gloor, Susan, Martinson, Matthew, Laird, Ellen, Brandhuber, Barbara J., Vigers, Guy, Morales, Tony, Woessner, Rich, Randolph, Nikole, Lyssikatos, Joseph, Olivero, Alan

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Walleye and yellow perch resource use in large lakes invaded by spiny water fleas and zebra mussels von Bethke, Bethany J., Rantala, Heidi M., Ahrenstorff, Tyler D., Kelly, Holly A. Wellard, Kovalenko, Katya E., Maki, Ryan P., Hirsch, Jodene K., Dumke, Joshua D., Brady, Valerie J., LeDuc, Jaime F., Hansen, Gretchen J. A.

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Pyrazolopyridine Inhibitors of B-RafV600E. Part 1: The Development of Selective, Orally Bioavailable, and Efficacious Inhibitors von Wenglowsky, Steve, Ren, Li, Ahrendt, Kateri A, Laird, Ellen R, Aliagas, Ignacio, Alicke, Bruno, Buckmelter, Alex J, Choo, Edna F, Dinkel, Victoria, Feng, Bainian, Gloor, Susan L, Gould, Stephen E, Gross, Stefan, Gunzner-Toste, Janet, Hansen, Joshua D, Hatzivassiliou, Georgia, Liu, Bonnie, Malesky, Kim, Mathieu, Simon, Newhouse, Brad, Raddatz, Nicholas J, Ran, Yingqing, Rana, Sumeet, Randolph, Nikole, Risom, Tyler, Rudolph, Joachim, Savage, Scott, Selby, LeAnn T, Shrag, Michael, Song, Kyung, Sturgis, Hillary L, Voegtli, Walter C, Wen, Zhaoyang, Willis, Brandon S, Woessner, Richard D, Wu, Wen-I, Young, Wendy B, Grina, Jonas

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Pyrazolopyridine Inhibitors of B-Raf(V600E). Part 1: The Development of Selective, Orally Bioavailable, and Efficacious Inhibitors von Wenglowsky, Steve, Ren, Li, Ahrendt, Kateri A, Laird, Ellen R, Aliagas, Ignacio, Alicke, Bruno, Buckmelter, Alex J, Choo, Edna F, Dinkel, Victoria, Feng, Bainian, Gloor, Susan L, Gould, Stephen E, Gross, Stefan, Gunzner-Toste, Janet, Hansen, Joshua D, Hatzivassiliou, Georgia, Liu, Bonnie, Malesky, Kim, Mathieu, Simon, Newhouse, Brad, Raddatz, Nicholas J, Ran, Yingqing, Rana, Sumeet, Randolph, Nikole, Risom, Tyler, Rudolph, Joachim, Savage, Scott, Selby, LeAnn T, Shrag, Michael, Song, Kyung, Sturgis, Hillary L, Voegtli, Walter C, Wen, Zhaoyang, Willis, Brandon S, Woessner, Richard D, Wu, Wen-I, Young, Wendy B, Grina, Jonas

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