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Showing results (41-50 of 51) with videos related to

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Nature Chemical Biology|August 24, 2023
Structural snapshots along K48-linked ubiquitin chain formation by the HECT E3 UBR5Laura A Hehl, Daniel Horn-Ghetko, J Rajan Prabu, et al.
BMC Public Health|August 27, 2005
Patterns of HIV prevalence among injecting drug users in the cross-border area of Lang Son Province, Vietnam, and Ning Ming County, Guangxi Province, ChinaDon C Des Jarlais, Patrick Johnston, Patricia Friedmann, et al.
Bioorganic & Medicinal Chemistry Letters|February 6, 1999
Design and synthesis of novel conformationally restricted HIV protease inhibitorsF G Salituro, C T Baker, J J Court, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|February 25, 2015
Effects of rare-earth size on the electronic structure of La1−xLuxVO3B Chen, J Laverock, D Newby, et al.
Nature Structural & Molecular Biology|April 11, 2024
Noncanonical assembly, neddylation and chimeric cullin-RING/RBR ubiquitylation by the 1.8 MDa CUL9 E3 ligase complexDaniel Horn-Ghetko, Linus V M Hopf, Ishita Tripathi-Giesgen, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506D M Armistead, M C Badia, D D Deininger, et al.
Molecular Cell|December 19, 2023
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assembliesJakub Chrustowicz, Dawafuti Sherpa, Jerry Li, et al.
Bioorganic & Medicinal Chemistry Letters|March 10, 2004
Inhibitors of hepatitis C virus NS3.4A protease 2. Warhead SAR and optimizationRobert B Perni, Janos Pitlik, Shawn D Britt, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
Inhibitors of hepatitis C virus NS3.4A protease 1. Non-charged tetrapeptide variantsRobert B Perni, Shawn D Britt, John C Court, et al.
Antimicrobial Agents and Chemotherapy|February 24, 2006
Preclinical profile of VX-950, a potent, selective, and orally bioavailable inhibitor of hepatitis C virus NS3-4A serine proteaseRobert B Perni, Susan J Almquist, Randal A Byrn, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Nature Chemical Biology|August 24, 2023
Structural snapshots along K48-linked ubiquitin chain formation by the HECT E3 UBR5Laura A Hehl, Daniel Horn-Ghetko, J Rajan Prabu, et al.
BMC Public Health|August 27, 2005
Patterns of HIV prevalence among injecting drug users in the cross-border area of Lang Son Province, Vietnam, and Ning Ming County, Guangxi Province, ChinaDon C Des Jarlais, Patrick Johnston, Patricia Friedmann, et al.
Bioorganic & Medicinal Chemistry Letters|February 6, 1999
Design and synthesis of novel conformationally restricted HIV protease inhibitorsF G Salituro, C T Baker, J J Court, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|February 25, 2015
Effects of rare-earth size on the electronic structure of La1−xLuxVO3B Chen, J Laverock, D Newby, et al.
Nature Structural & Molecular Biology|April 11, 2024
Noncanonical assembly, neddylation and chimeric cullin-RING/RBR ubiquitylation by the 1.8 MDa CUL9 E3 ligase complexDaniel Horn-Ghetko, Linus V M Hopf, Ishita Tripathi-Giesgen, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506D M Armistead, M C Badia, D D Deininger, et al.
Molecular Cell|December 19, 2023
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assembliesJakub Chrustowicz, Dawafuti Sherpa, Jerry Li, et al.
Bioorganic & Medicinal Chemistry Letters|March 10, 2004
Inhibitors of hepatitis C virus NS3.4A protease 2. Warhead SAR and optimizationRobert B Perni, Janos Pitlik, Shawn D Britt, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
Inhibitors of hepatitis C virus NS3.4A protease 1. Non-charged tetrapeptide variantsRobert B Perni, Shawn D Britt, John C Court, et al.
Antimicrobial Agents and Chemotherapy|February 24, 2006
Preclinical profile of VX-950, a potent, selective, and orally bioavailable inhibitor of hepatitis C virus NS3-4A serine proteaseRobert B Perni, Susan J Almquist, Randal A Byrn, et al.
Pageof 6