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ACS Chemical Biology|August 30, 2012
Irreversible inhibitors of c-Src kinase that target a nonconserved cysteineFrank E Kwarcinski, Christel C Fox, Michael E Steffey, et al.
ACS Medicinal Chemistry Letters|August 20, 2015
Discovery of Bivalent Kinase Inhibitors via Enzyme-Templated Fragment ElaborationFrank E Kwarcinski, Michael E Steffey, Christel C Fox, et al.
The Journal of Biological Chemistry|February 21, 2003
Cell surface expression of the melanocortin-4 receptor is dependent on a C-terminal di-isoleucine sequence at codons 316/317Donald VanLeeuwen, Michael E Steffey, Christopher Donahue, et al.
ACS Chemical Biology|May 19, 2012
Development of a highly selective c-Src kinase inhibitorKristoffer R Brandvold, Michael E Steffey, Christel C Fox, et al.
ACS Medicinal Chemistry Letters|September 10, 2013
Development of a chimeric c-Src kinase and HDAC inhibitorKristin S Ko, Michael E Steffey, Kristoffer R Brandvold, et al.
Angewandte Chemie (International Ed. in English)|May 7, 2014
Substrate activity screening with kinases: discovery of small-molecule substrate-competitive c-Src inhibitorsMeghan E Breen, Michael E Steffey, Eric J Lachacz, et al.
ACS Chemical Biology|March 21, 2015
Exquisitely specific bisubstrate inhibitors of c-Src kinaseKristoffer R Brandvold, Shana M Santos, Meghan E Breen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 8, 2016
UM-164: A Potent c-Src/p38 Kinase Inhibitor with In Vivo Activity against Triple-Negative Breast CancerRabia A Gilani, Sameer Phadke, Li Wei Bao, et al.
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