Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Kyle V Butler

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Current Pharmaceutical Design|March 14, 2008
Chemical origins of isoform selectivity in histone deacetylase inhibitorsKyle V Butler, Alan P Kozikowski
Medchemcomm|August 23, 2016
Non-Substrate Based, Small Molecule Inhibitors of the Human Isoprenylcysteine Carboxyl MethyltransferaseKyle V Butler, Kelsey Bohn, Christine A Hrycyna, et al.
Journal of Chemical Information and Modeling|October 17, 2017
Report and Application of a Tool Compound Data SetKyle V Butler, Ian A MacDonald, Nathaniel A Hathaway, et al.
ACS Synthetic Biology|October 28, 2017
Targeted Gene Repression Using Novel Bifunctional Molecules to Harness Endogenous Histone Deacetylation ActivityKyle V Butler, Anna M Chiarella, Jian Jin, et al.
Scientific Reports|May 11, 2017
Development of a S-adenosylmethionine analog that intrudes the RNA-cap binding site of Zika methyltransferaseRinku Jain, Kyle V Butler, Javier Coloma, et al.
Journal of Medicinal Chemistry|December 15, 2011
Second-generation histone deacetylase 6 inhibitors enhance the immunosuppressive effects of Foxp3+ T-regulatory cellsJay H Kalin, Kyle V Butler, Tatiana Akimova, et al.
Medchemcomm|January 3, 2015
Structure-activity relationship studies of SETD8 inhibitorsAnqi Ma, Wenyu Yu, Yan Xiong, et al.
Journal of Visualized Experiments : Jove|October 9, 2018
Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic ModifiersAnna M Chiarella, Tiffany A Wang, Kyle V Butler, et al.
Chemmedchem|June 25, 2009
Stereoselective HDAC inhibition from cysteine-derived zinc-binding groupsKyle V Butler, Rong He, Kathryn McLaughlin, et al.
Journal of the American Chemical Society|July 10, 2010
Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin AKyle V Butler, Jay Kalin, Camille Brochier, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Current Pharmaceutical Design|March 14, 2008
Chemical origins of isoform selectivity in histone deacetylase inhibitorsKyle V Butler, Alan P Kozikowski
Medchemcomm|August 23, 2016
Non-Substrate Based, Small Molecule Inhibitors of the Human Isoprenylcysteine Carboxyl MethyltransferaseKyle V Butler, Kelsey Bohn, Christine A Hrycyna, et al.
Journal of Chemical Information and Modeling|October 17, 2017
Report and Application of a Tool Compound Data SetKyle V Butler, Ian A MacDonald, Nathaniel A Hathaway, et al.
ACS Synthetic Biology|October 28, 2017
Targeted Gene Repression Using Novel Bifunctional Molecules to Harness Endogenous Histone Deacetylation ActivityKyle V Butler, Anna M Chiarella, Jian Jin, et al.
Scientific Reports|May 11, 2017
Development of a S-adenosylmethionine analog that intrudes the RNA-cap binding site of Zika methyltransferaseRinku Jain, Kyle V Butler, Javier Coloma, et al.
Journal of Medicinal Chemistry|December 15, 2011
Second-generation histone deacetylase 6 inhibitors enhance the immunosuppressive effects of Foxp3+ T-regulatory cellsJay H Kalin, Kyle V Butler, Tatiana Akimova, et al.
Medchemcomm|January 3, 2015
Structure-activity relationship studies of SETD8 inhibitorsAnqi Ma, Wenyu Yu, Yan Xiong, et al.
Journal of Visualized Experiments : Jove|October 9, 2018
Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic ModifiersAnna M Chiarella, Tiffany A Wang, Kyle V Butler, et al.
Chemmedchem|June 25, 2009
Stereoselective HDAC inhibition from cysteine-derived zinc-binding groupsKyle V Butler, Rong He, Kathryn McLaughlin, et al.
Journal of the American Chemical Society|July 10, 2010
Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin AKyle V Butler, Jay Kalin, Camille Brochier, et al.
Pageof 2