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Chemistry & Biology|February 1, 2011
Kinase inhibition that hinges on halogen bondsStephan K Grant, Elizabeth A LunneyMethods in Molecular Biology (Clifton, N.J.)|October 29, 2010
The design, annotation, and application of a kinase-targeted libraryHualin Xi, Elizabeth A LunneyExpert Opinion on Drug Discovery|March 20, 2013
Targeting the unactivated conformations of protein kinases for small molecule drug discoveryGordon R Alton, Elizabeth A LunneyJournal of Computer-Aided Molecular Design|December 31, 2013
Scaffold mining of kinase hinge binders in crystal structure databaseLi Xing, Brajesh Rai, Elizabeth A LunneyBMC Bioinformatics|November 27, 2008
Prediction of specificity-determining residues for small-molecule kinase inhibitorsDaniel R Caffrey, Elizabeth A Lunney, Deborah J MoshinskyBioorganic & Medicinal Chemistry|September 12, 2015
Kinase hinge binding scaffolds and their hydrogen bond patternsLi Xing, Jacquelyn Klug-Mcleod, Brajesh Rai, et al.BMC Bioinformatics|January 8, 2010
Statistical method on nonrandom clustering with application to somatic mutations in cancerJingjing Ye, Adam Pavlicek, Elizabeth A Lunney, et al.Journal of Biomolecular Screening|November 6, 2003
Development of novel assays for proteolytic enzymes using rhodamine-based fluorogenic substratesStephan K Grant, Joseph G Sklar, Richard T CummingsACS Chemical Biology|February 28, 2013
Substrate-specific conformational regulation of the receptor tyrosine kinase VEGFR2 catalytic domainJames Solowiej, Jeffrey H Chen, Helen Y Zou, et al.Protein Science : a Publication of the Protein Society|January 23, 2010
Drug binding and resistance mechanism of KIT tyrosine kinase revealed by hydrogen/deuterium exchange FTICR mass spectrometryHui-Min Zhang, Xiu Yu, Michael J Greig, et al.Pageof 3