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Craig M Crews

Showing results (81-90 of 155) with videos related to

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Journal of the American Chemical Society|November 17, 2018
Addressing Kinase-Independent Functions of Fak via PROTAC-Mediated DegradationPhilipp M Cromm, Kusal T G Samarasinghe, John Hines, et al.
Organic Letters|July 10, 2007
Synthesis of the C3-C18 fragment of amphidinolides G and HAndreas F Petri, John S Schneekloth, Amit K Mandal, et al.
ACS Central Science|September 3, 2020
Targeted Degradation of Oncogenic KRAS<sup>G12C</sup> by VHL-Recruiting PROTACsMichael J Bond, Ling Chu, Dhanusha A Nalawansha, et al.
Molecular Biology of the Cell|June 6, 2019
Protein folding state-dependent sorting at the Golgi apparatusDoris Hellerschmied, Yevgeniy V Serebrenik, Lin Shao, et al.
Bioorganic & Medicinal Chemistry Letters|December 28, 2019
Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic propertiesSaul Jaime-Figueroa, Alexandru D Buhimschi, Momar Toure, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 24, 2010
Reversal of TNP-470-induced endothelial cell growth arrest by guanine and guanine nucleosidesJohn Hines, Rong Ju, Ginger E Dutschman, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2002
Inhibitors of NF-kappaB signaling: design and synthesis of a biotinylated isopanepoxydone affinity reagentJ Brad Shotwell, Brian Koh, Hui Won Choi, et al.
Journal of the American Chemical Society|August 12, 2009
Total synthesis and structure-activity investigation of the marine natural product neopeltolideDaniel W Custar, Thomas P Zabawa, John Hines, et al.
Molecular Biosystems|August 2, 2006
Myriaporone 3/4 structure--activity relationship studies define a pharmacophore targeting eukaryotic protein synthesisJohn Hines, Myriam Roy, Hua Cheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 2010
Activation of the planar cell polarity formin DAAM1 leads to inhibition of endothelial cell proliferation, migration, and angiogenesisRong Ju, Pasquale Cirone, Shengda Lin, et al.
Pageof 16

Showing results (81-90 of 155) with videos related to

Sort By:
Pageof 16
Journal of the American Chemical Society|November 17, 2018
Addressing Kinase-Independent Functions of Fak via PROTAC-Mediated DegradationPhilipp M Cromm, Kusal T G Samarasinghe, John Hines, et al.
Organic Letters|July 10, 2007
Synthesis of the C3-C18 fragment of amphidinolides G and HAndreas F Petri, John S Schneekloth, Amit K Mandal, et al.
ACS Central Science|September 3, 2020
Targeted Degradation of Oncogenic KRAS<sup>G12C</sup> by VHL-Recruiting PROTACsMichael J Bond, Ling Chu, Dhanusha A Nalawansha, et al.
Molecular Biology of the Cell|June 6, 2019
Protein folding state-dependent sorting at the Golgi apparatusDoris Hellerschmied, Yevgeniy V Serebrenik, Lin Shao, et al.
Bioorganic & Medicinal Chemistry Letters|December 28, 2019
Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic propertiesSaul Jaime-Figueroa, Alexandru D Buhimschi, Momar Toure, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 24, 2010
Reversal of TNP-470-induced endothelial cell growth arrest by guanine and guanine nucleosidesJohn Hines, Rong Ju, Ginger E Dutschman, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2002
Inhibitors of NF-kappaB signaling: design and synthesis of a biotinylated isopanepoxydone affinity reagentJ Brad Shotwell, Brian Koh, Hui Won Choi, et al.
Journal of the American Chemical Society|August 12, 2009
Total synthesis and structure-activity investigation of the marine natural product neopeltolideDaniel W Custar, Thomas P Zabawa, John Hines, et al.
Molecular Biosystems|August 2, 2006
Myriaporone 3/4 structure--activity relationship studies define a pharmacophore targeting eukaryotic protein synthesisJohn Hines, Myriam Roy, Hua Cheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 2010
Activation of the planar cell polarity formin DAAM1 leads to inhibition of endothelial cell proliferation, migration, and angiogenesisRong Ju, Pasquale Cirone, Shengda Lin, et al.
Pageof 16