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

Bertrand Dirié

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
ACS Chemical Biology|August 14, 2010
Exploring drug target flexibility using in situ click chemistry: application to a mycobacterial transcriptional regulatorNicolas Willand, Matthieu Desroses, Patrick Toto, et al.
Bioorganic & Medicinal Chemistry|September 10, 2014
From human immunodeficiency virus non-nucleoside reverse transcriptase inhibitors to potent and selective antitrypanosomal compoundsMuthusamy Venkatraj, Kevin K Ariën, Jan Heeres, et al.
Bioorganic & Medicinal Chemistry|September 21, 2011
Novel diarylpyridinones, diarylpyridazinones and diarylphthalazinones as potential HIV-1 nonnucleoside reverse transcriptase inhibitors (NNRTIs)Muthusamy Venkatraj, Kevin K Ariën, Jan Heeres, et al.
Nature Medicine|May 5, 2009
Synthetic EthR inhibitors boost antituberculous activity of ethionamideNicolas Willand, Bertrand Dirié, Xavier Carette, et al.
Nucleic Acids Research|December 14, 2011
Structural activation of the transcriptional repressor EthR from Mycobacterium tuberculosis by single amino acid change mimicking natural and synthetic ligandsXavier Carette, Nicolas Blondiaux, Eve Willery, et al.
Journal of Medicinal Chemistry|March 23, 2011
Ethionamide boosters: synthesis, biological activity, and structure-activity relationships of a series of 1,2,4-oxadiazole EthR inhibitorsMarion Flipo, Matthieu Desroses, Nathalie Lecat-Guillet, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
ACS Chemical Biology|August 14, 2010
Exploring drug target flexibility using in situ click chemistry: application to a mycobacterial transcriptional regulatorNicolas Willand, Matthieu Desroses, Patrick Toto, et al.
Bioorganic & Medicinal Chemistry|September 10, 2014
From human immunodeficiency virus non-nucleoside reverse transcriptase inhibitors to potent and selective antitrypanosomal compoundsMuthusamy Venkatraj, Kevin K Ariën, Jan Heeres, et al.
Bioorganic & Medicinal Chemistry|September 21, 2011
Novel diarylpyridinones, diarylpyridazinones and diarylphthalazinones as potential HIV-1 nonnucleoside reverse transcriptase inhibitors (NNRTIs)Muthusamy Venkatraj, Kevin K Ariën, Jan Heeres, et al.
Nature Medicine|May 5, 2009
Synthetic EthR inhibitors boost antituberculous activity of ethionamideNicolas Willand, Bertrand Dirié, Xavier Carette, et al.
Nucleic Acids Research|December 14, 2011
Structural activation of the transcriptional repressor EthR from Mycobacterium tuberculosis by single amino acid change mimicking natural and synthetic ligandsXavier Carette, Nicolas Blondiaux, Eve Willery, et al.
Journal of Medicinal Chemistry|March 23, 2011
Ethionamide boosters: synthesis, biological activity, and structure-activity relationships of a series of 1,2,4-oxadiazole EthR inhibitorsMarion Flipo, Matthieu Desroses, Nathalie Lecat-Guillet, et al.
Pageof 1