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

David C Tully

Showing results (1-10 of 24) with videos related to

Pageof 3
Sort By:
Chemistry & Biology|October 19, 2004
PNA-encoded protease substrate microarraysNicolas Winssinger, Robert Damoiseaux, David C Tully, et al.
Biochemical and Biophysical Research Communications|October 12, 2004
Biochemical characterization of prostasin, a channel activating proteaseAaron Shipway, Henry Danahay, Jennifer A Williams, et al.
Protein Science : a Publication of the Protein Society|April 24, 2009
Active site conformational changes of prostasin provide a new mechanism of protease regulation by divalent cationsGlen Spraggon, Michael Hornsby, Aaron Shipway, et al.
The Journal of Biological Chemistry|June 4, 2005
Functional profiling of recombinant NS3 proteases from all four serotypes of dengue virus using tetrapeptide and octapeptide substrate librariesJun Li, Siew Pheng Lim, David Beer, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2006
Arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 2: Optimization of P1 and N-arylPhillip B Alper, Hong Liu, Arnab K Chatterjee, et al.
Bioorganic & Medicinal Chemistry Letters|September 27, 2005
Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1Hong Liu, David C Tully, Robert Epple, et al.
Bioorganic & Medicinal Chemistry Letters|March 27, 2007
Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin SArnab K Chatterjee, Hong Liu, David C Tully, et al.
Bioorganic & Medicinal Chemistry Letters|August 30, 2008
Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based designDavid C Tully, Agnès Vidal, Arnab K Chatterjee, et al.
Elife|May 23, 2015
Chemical activation of the mechanotransduction channel Piezo1Ruhma Syeda, Jie Xu, Adrienne E Dubin, et al.
Journal of Medicinal Chemistry|July 23, 2025
Discovery and Optimization of a Novel Series of Influenza A Virus Replication Inhibitors Targeting the Nucleoprotein Protein-Protein InteractionBenjamin R Taft, Matthew J Hesse, Mulugeta Mamo, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Chemistry & Biology|October 19, 2004
PNA-encoded protease substrate microarraysNicolas Winssinger, Robert Damoiseaux, David C Tully, et al.
Biochemical and Biophysical Research Communications|October 12, 2004
Biochemical characterization of prostasin, a channel activating proteaseAaron Shipway, Henry Danahay, Jennifer A Williams, et al.
Protein Science : a Publication of the Protein Society|April 24, 2009
Active site conformational changes of prostasin provide a new mechanism of protease regulation by divalent cationsGlen Spraggon, Michael Hornsby, Aaron Shipway, et al.
The Journal of Biological Chemistry|June 4, 2005
Functional profiling of recombinant NS3 proteases from all four serotypes of dengue virus using tetrapeptide and octapeptide substrate librariesJun Li, Siew Pheng Lim, David Beer, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2006
Arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 2: Optimization of P1 and N-arylPhillip B Alper, Hong Liu, Arnab K Chatterjee, et al.
Bioorganic & Medicinal Chemistry Letters|September 27, 2005
Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1Hong Liu, David C Tully, Robert Epple, et al.
Bioorganic & Medicinal Chemistry Letters|March 27, 2007
Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin SArnab K Chatterjee, Hong Liu, David C Tully, et al.
Bioorganic & Medicinal Chemistry Letters|August 30, 2008
Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based designDavid C Tully, Agnès Vidal, Arnab K Chatterjee, et al.
Elife|May 23, 2015
Chemical activation of the mechanotransduction channel Piezo1Ruhma Syeda, Jie Xu, Adrienne E Dubin, et al.
Journal of Medicinal Chemistry|July 23, 2025
Discovery and Optimization of a Novel Series of Influenza A Virus Replication Inhibitors Targeting the Nucleoprotein Protein-Protein InteractionBenjamin R Taft, Matthew J Hesse, Mulugeta Mamo, et al.
Pageof 3