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Thomas Machleidt

Showing results (31-40 of 53) with videos related to

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ACS Chemical Biology|May 27, 2015
NanoBRET--A Novel BRET Platform for the Analysis of Protein-Protein InteractionsThomas Machleidt, Carolyn C Woodroofe, Marie K Schwinn, et al.
ACS Chemical Biology|September 12, 2017
CRISPR-Mediated Tagging of Endogenous Proteins with a Luminescent PeptideMarie K Schwinn, Thomas Machleidt, Kris Zimmerman, et al.
Nature Methods|June 2, 2015
Application of BRET to monitor ligand binding to GPCRsLeigh A Stoddart, Elizabeth K M Johnstone, Amanda J Wheal, et al.
Bioorganic & Medicinal Chemistry|March 14, 2009
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitorsSurya K De, Li-Hsing Chen, John L Stebbins, et al.
Journal of Biomolecular Screening|October 13, 2009
Generation of site-specific retargeting platform cell lines for drug discovery using phiC31 and R4 integrasesPauline T Lieu, Thomas Machleidt, Bhaskar Thyagarajan, et al.
Journal of Medicinal Chemistry|March 11, 2009
Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinaseSurya K De, John L Stebbins, Li-Hsing Chen, et al.
Analytical Biochemistry|August 18, 2015
A luminescent assay for real-time measurements of receptor endocytosis in living cellsMatthew B Robers, Brock F Binkowski, Mei Cong, et al.
ACS Chemical Biology|March 20, 2026
A Modular Platform for Quantitative Two-Color Bioluminescence Combining NanoLuc and Red-Shifted NanoPrism LuciferasesKarilyn Porter, Mike Killoran, Robin Hurst, et al.
Bioorganic & Medicinal Chemistry|January 5, 2010
Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitorsSurya K De, Vida Chen, John L Stebbins, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 17, 2008
Identification of a new JNK inhibitor targeting the JNK-JIP interaction siteJohn L Stebbins, Surya K De, Thomas Machleidt, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
ACS Chemical Biology|May 27, 2015
NanoBRET--A Novel BRET Platform for the Analysis of Protein-Protein InteractionsThomas Machleidt, Carolyn C Woodroofe, Marie K Schwinn, et al.
ACS Chemical Biology|September 12, 2017
CRISPR-Mediated Tagging of Endogenous Proteins with a Luminescent PeptideMarie K Schwinn, Thomas Machleidt, Kris Zimmerman, et al.
Nature Methods|June 2, 2015
Application of BRET to monitor ligand binding to GPCRsLeigh A Stoddart, Elizabeth K M Johnstone, Amanda J Wheal, et al.
Bioorganic & Medicinal Chemistry|March 14, 2009
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitorsSurya K De, Li-Hsing Chen, John L Stebbins, et al.
Journal of Biomolecular Screening|October 13, 2009
Generation of site-specific retargeting platform cell lines for drug discovery using phiC31 and R4 integrasesPauline T Lieu, Thomas Machleidt, Bhaskar Thyagarajan, et al.
Journal of Medicinal Chemistry|March 11, 2009
Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinaseSurya K De, John L Stebbins, Li-Hsing Chen, et al.
Analytical Biochemistry|August 18, 2015
A luminescent assay for real-time measurements of receptor endocytosis in living cellsMatthew B Robers, Brock F Binkowski, Mei Cong, et al.
ACS Chemical Biology|March 20, 2026
A Modular Platform for Quantitative Two-Color Bioluminescence Combining NanoLuc and Red-Shifted NanoPrism LuciferasesKarilyn Porter, Mike Killoran, Robin Hurst, et al.
Bioorganic & Medicinal Chemistry|January 5, 2010
Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitorsSurya K De, Vida Chen, John L Stebbins, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 17, 2008
Identification of a new JNK inhibitor targeting the JNK-JIP interaction siteJohn L Stebbins, Surya K De, Thomas Machleidt, et al.
Pageof 6