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Bioorganic & Medicinal Chemistry Letters|July 13, 2010
Enhanced selectivity profile of pyrazole-urea based DFG-out p38alpha inhibitorsHu Liu, Cyrille Kuhn, Frederic Feru, et al.
ACS Medicinal Chemistry Letters|June 24, 2015
Aryl Pyrazoles as Potent Inhibitors of Arginine Methyltransferases: Identification of the First PRMT6 Tool CompoundLorna H Mitchell, Allison E Drew, Scott A Ribich, et al.
ACS Medicinal Chemistry Letters|March 18, 2016
Novel Oxindole Sulfonamides and Sulfamides: EPZ031686, the First Orally Bioavailable Small Molecule SMYD3 InhibitorLorna H Mitchell, P Ann Boriack-Sjodin, Sherri Smith, et al.
Cell Reports|January 17, 2019
Modeling Tumor Phenotypes In Vitro with Three-Dimensional BioprintingEllen M Langer, Brittany L Allen-Petersen, Shelby M King, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2009
KIT kinase mutants show unique mechanisms of drug resistance to imatinib and sunitinib in gastrointestinal stromal tumor patientsKetan S Gajiwala, Joe C Wu, James Christensen, et al.
Scientific Reports|December 23, 2017
Identification of a CARM1 Inhibitor with Potent In Vitro and In Vivo Activity in Preclinical Models of Multiple MyelomaAllison E Drew, Oscar Moradei, Suzanne L Jacques, et al.
Plos One|June 2, 2018
Small molecule inhibitors and CRISPR/Cas9 mutagenesis demonstrate that SMYD2 and SMYD3 activity are dispensable for autonomous cancer cell proliferationMichael J Thomenius, Jennifer Totman, Darren Harvey, et al.
Nature Chemical Biology|April 28, 2015
A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL modelsElayne Chan-Penebre, Kristy G Kuplast, Christina R Majer, et al.
Biodiversity Data Journal|July 14, 2025
Vascular plants of Reserva Biológica do Tinguá, Rio de Janeiro, Brazil: leveraging herbarium databases to address knowledge gaps in the Atlantic ForestThuane Bochorny, Alexandre Quinet, Ana Carolina D Castello, et al.
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