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Elizabeth A Lunney

Showing results (1-10 of 13) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|October 29, 2010
The design, annotation, and application of a kinase-targeted libraryHualin Xi, Elizabeth A Lunney
Expert Opinion on Drug Discovery|March 20, 2013
Targeting the unactivated conformations of protein kinases for small molecule drug discoveryGordon R Alton, Elizabeth A Lunney
Chemistry & Biology|February 1, 2011
Kinase inhibition that hinges on halogen bondsStephan K Grant, Elizabeth A Lunney
Journal of Computer-Aided Molecular Design|December 31, 2013
Scaffold mining of kinase hinge binders in crystal structure databaseLi Xing, Brajesh Rai, Elizabeth A Lunney
BMC Bioinformatics|November 27, 2008
Prediction of specificity-determining residues for small-molecule kinase inhibitorsDaniel R Caffrey, Elizabeth A Lunney, Deborah J Moshinsky
Bioorganic & 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.
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.
Bioorganic & Medicinal Chemistry Letters|March 31, 2009
Synthesis and SAR of 4-substituted-2-aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitorsPaul S Humphries, Jennifer A Lafontaine, Charles S Agree, et al.
Journal of Medicinal Chemistry|August 4, 2006
4-Phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione inhibitors of the checkpoint kinase Wee1. Structure-activity relationships for chromophore modification and phenyl ring substitutionBrian D Palmer, Andrew M Thompson, R John Booth, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|October 29, 2010
The design, annotation, and application of a kinase-targeted libraryHualin Xi, Elizabeth A Lunney
Expert Opinion on Drug Discovery|March 20, 2013
Targeting the unactivated conformations of protein kinases for small molecule drug discoveryGordon R Alton, Elizabeth A Lunney
Chemistry & Biology|February 1, 2011
Kinase inhibition that hinges on halogen bondsStephan K Grant, Elizabeth A Lunney
Journal of Computer-Aided Molecular Design|December 31, 2013
Scaffold mining of kinase hinge binders in crystal structure databaseLi Xing, Brajesh Rai, Elizabeth A Lunney
BMC Bioinformatics|November 27, 2008
Prediction of specificity-determining residues for small-molecule kinase inhibitorsDaniel R Caffrey, Elizabeth A Lunney, Deborah J Moshinsky
Bioorganic & 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.
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.
Bioorganic & Medicinal Chemistry Letters|March 31, 2009
Synthesis and SAR of 4-substituted-2-aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitorsPaul S Humphries, Jennifer A Lafontaine, Charles S Agree, et al.
Journal of Medicinal Chemistry|August 4, 2006
4-Phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione inhibitors of the checkpoint kinase Wee1. Structure-activity relationships for chromophore modification and phenyl ring substitutionBrian D Palmer, Andrew M Thompson, R John Booth, et al.
Pageof 2