Foundational Grounding and Creaturely Freedom von Pearce, Kenneth L

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A novel small molecule screening assay using normal human chondrocytes toward osteoarthritis drug discovery von Coryell, Philip R, Hardy, Paul B, Chubinskaya, Susan, Pearce, Kenneth H, Loeser, Richard F

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Anthony Collins’s Non-Vindication of the Divine Attributes von Pearce, Kenneth L

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KRAS Suppression-Induced Degradation of MYC Is Antagonized by a MEK5-ERK5 Compensatory Mechanism von Vaseva, Angelina V., Blake, Devon R., Gilbert, Thomas S.K., Ng, Serina, Hostetter, Galen, Azam, Salma H., Ozkan-Dagliyan, Irem, Gautam, Prson, Bryant, Kirsten L., Pearce, Kenneth H., Herring, Laura E., Han, Haiyong, Graves, Lee M., Witkiewicz, Agnieszka K., Knudsen, Erik S., Pecot, Chad V., Rashid, Naim, Houghton, Peter J., Wennerberg, Krister, Cox, Adrienne D., Der, Channing J.

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Degradation of Polycomb Repressive Complex 2 with an EED-Targeted Bivalent Chemical Degrader von Potjewyd, Frances, Turner, Anne-Marie W., Beri, Joshua, Rectenwald, Justin M., Norris-Drouin, Jacqueline L., Cholensky, Stephanie H., Margolis, David M., Pearce, Kenneth H., Herring, Laura E., James, Lindsey I.

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PCNA-binding activity separates RNF168 functions in DNA replication and DNA double-stranded break signaling von Yang, Yang, Jayaprakash, Deepika, Jhujh, Satpal S, Reynolds, John J, Chen, Steve, Gao, Yanzhe, Anand, Jay Ramanlal, Mutter-Rottmayer, Elizabeth, Ariel, Pablo, An, Jing, Cheng, Xing, Pearce, Kenneth H, Blanchet, Sophie-Anne, Nandakumar, Nandana, Zhou, Pei, Fradet-Turcotte, Amélie, Stewart, Grant S, Vaziri, Cyrus

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Crystal structure of MAGEA4 MHD-RAD18 R6BD reveals a flipped binding mode compared to AlphaFold2 prediction von Forker, Karly, Fleming, Matthew C, Pearce, Kenneth H, Vaziri, Cyrus, Bowers, Albert A, Zhou, Pei

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In silico fragment-based discovery of CIB1-directed anti-tumor agents by FRASE-bot von An, Yi, Lim, Jiwoong, Glavatskikh, Marta, Wang, Xiaowen, Norris-Drouin, Jacqueline, Hardy, P. Brian, Leisner, Tina M., Pearce, Kenneth H., Kireev, Dmitri

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Author Correction: A neomorphic cancer cell-specific role of MAGE-A4 in trans-lesion synthesis von Gao, Yanzhe, Mutter-Rottmayer, Elizabeth, Greenwalt, Alicia M., Goldfarb, Dennis, Yan, Feng, Yang, Yang, Martinez-Chacin, Raquel C., Pearce, Kenneth H., Tateishi, Satoshi, Major, Michael B., Vaziri, Cyrus

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Intentionality, belief, and the logical problem of evil von PEARCE, KENNETH L.

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Development of Novel IP6K Inhibitors for the Treatment of Obesity and Obesity-Induced Metabolic Dysfunctions von Zhou, Yubai, Mukherjee, Sandip, Huang, Daowei, Chakraborty, Molee, Gu, Chunfang, Zong, Guangning, Stashko, Michael A., Pearce, Kenneth H., Shears, Stephen B., Chakraborty, Anutosh, Wang, Huanchen, Wang, Xiaodong

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A neomorphic cancer cell-specific role of MAGE-A4 in trans-lesion synthesis von Gao, Yanzhe, Mutter-Rottmayer, Elizabeth, Greenwalt, Alicia M., Goldfarb, Dennis, Yan, Feng, Yang, Yang, Martinez-Chacin, Raquel C., Pearce, Kenneth H., Tateishi, Satoshi, Major, Michael B., Vaziri, Cyrus

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Discovery and Characterization of a Cellular Potent Positive Allosteric Modulator of the Polycomb Repressive Complex 1 Chromodomain, CBX7 von Lamb, Kelsey N., Bsteh, Daniel, Dishman, Sarah N., Moussa, Hagar F., Fan, Huitao, Stuckey, Jacob I., Norris, Jacqueline L., Cholensky, Stephanie H., Li, Dongxu, Wang, Jingkui, Sagum, Cari, Stanton, Benjamin Z., Bedford, Mark T., Pearce, Kenneth H., Kenakin, Terry P., Kireev, Dmitri B., Wang, Gang Greg, James, Lindsey I., Bell, Oliver, Frye, Stephen V.

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Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM von Bashore, Frances M, Katis, Vittorio L, Du, Yuhong, Sikdar, Arunima, Wang, Dongxue, Bradshaw, William J, Rygiel, Karolina A, Leisner, Tina M, Chalk, Rod, Mishra, Swati, Williams, C Andrew, Gileadi, Opher, Brennan, Paul E, Wiley, Jesse C, Gockley, Jake, Cary, Gregory A, Carter, Gregory W, Young, Jessica E, Pearce, Kenneth H, Fu, Haian, Axtman, Alison D

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Rev-erbα, a Heme Sensor That Coordinates Metabolic and Circadian Pathways von Yin, Lei, Wu, Nan, Curtin, Joshua C, Qatanani, Mohammed, Szwergold, Nava R, Reid, Robert A, Waitt, Gregory M, Parks, Derek J, Pearce, Kenneth H, Wisely, G. Bruce, Lazar, Mitchell A

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Identification of Covalent Cyclic Peptide Inhibitors in mRNA Display von Iskandar, Sabrina E., Chiou, Lilly F., Leisner, Tina M., Shell, Devan J., Norris-Drouin, Jacqueline L., Vaziri, Cyrus, Pearce, Kenneth H., Bowers, Albert A.

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William King on Free Will von Pearce, Kenneth L

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Discovery and Structural Basis of the Selectivity of Potent Cyclic Peptide Inhibitors of MAGE-A4 von Fleming, Matthew C., Chiou, Lilly F., Tumbale, Percy P., Droby, Gaith N., Lim, Jiwoong, Norris-Drouin, Jacqueline L., Williams, Jason G., Pearce, Kenneth H., Williams, R. Scott, Vaziri, Cyrus, Bowers, Albert A.

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Peter Browne on the Metaphysics of Knowledge von Pearce, Kenneth L.

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Targeting Regorafenib-Induced Toxicity through Inhibition of Gut Microbial β‑Glucuronidases von Ervin, Samantha M, Hanley, Ronan P, Lim, Lauren, Walton, William G, Pearce, Kenneth H, Bhatt, Aadra P, James, Lindsey I, Redinbo, Matthew R

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