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Vincent S Stoll

Showing results (11-20 of 40) with videos related to

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Communications Chemistry|October 29, 2023
Cryo-EM structure of human PAPP-A2 and mechanism of substrate recognitionJanani Sridar, Amirhossein Mafi, Russell A Judge, et al.
Nature Communications|June 9, 2021
Sugar phosphate activation of the stress sensor eIF2BQi Hao, Jin-Mi Heo, Boguslaw P Nocek, et al.
Blood|July 11, 2007
A potent erythropoietin-mimicking human antibody interacts through a novel binding siteZhihong Liu, Vincent S Stoll, Peter J Devries, et al.
Bioorganic & Medicinal Chemistry Letters|September 30, 2004
Synthesis and activity of 1-aryl-1'-imidazolyl methyl ethers as non-thiol farnesyltransferase inhibitorsQun Li, Gary T Wang, Tongmei Li, et al.
Bioorganic & Medicinal Chemistry|January 30, 2007
Design and synthesis of pyridine-pyrazolopyridine-based inhibitors of protein kinase B/AktGui-Dong Zhu, Jianchun Gong, Viraj B Gandhi, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strainsChen Zhao, Hing L Sham, Minghua Sun, et al.
Protein Science : a Publication of the Protein Society|December 3, 2005
Structure of MurF from Streptococcus pneumoniae co-crystallized with a small molecule inhibitor exhibits interdomain closureKenton L Longenecker, Geoffrey F Stamper, Philip J Hajduk, et al.
Journal of Medicinal Chemistry|October 22, 2009
Discovery of 3H-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as potent, highly selective, and orally bioavailable inhibitors of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM) kinasesZhi-Fu Tao, Lisa A Hasvold, Joel D Leverson, et al.
Chembiochem : a European Journal of Chemical Biology|January 10, 2018
Design of Aminobenzothiazole Inhibitors of Rho Kinases 1 and 2 by Using Protein Kinase A as a Structure SurrogateRussell A Judge, Anil Vasudevan, Victoria E Scott, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Hepatitis C NS5B polymerase inhibitors: functional equivalents for the benzothiadiazine moietyDouglas K Hutchinson, Charles A Flentge, Pamela L Donner, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Communications Chemistry|October 29, 2023
Cryo-EM structure of human PAPP-A2 and mechanism of substrate recognitionJanani Sridar, Amirhossein Mafi, Russell A Judge, et al.
Nature Communications|June 9, 2021
Sugar phosphate activation of the stress sensor eIF2BQi Hao, Jin-Mi Heo, Boguslaw P Nocek, et al.
Blood|July 11, 2007
A potent erythropoietin-mimicking human antibody interacts through a novel binding siteZhihong Liu, Vincent S Stoll, Peter J Devries, et al.
Bioorganic & Medicinal Chemistry Letters|September 30, 2004
Synthesis and activity of 1-aryl-1'-imidazolyl methyl ethers as non-thiol farnesyltransferase inhibitorsQun Li, Gary T Wang, Tongmei Li, et al.
Bioorganic & Medicinal Chemistry|January 30, 2007
Design and synthesis of pyridine-pyrazolopyridine-based inhibitors of protein kinase B/AktGui-Dong Zhu, Jianchun Gong, Viraj B Gandhi, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strainsChen Zhao, Hing L Sham, Minghua Sun, et al.
Protein Science : a Publication of the Protein Society|December 3, 2005
Structure of MurF from Streptococcus pneumoniae co-crystallized with a small molecule inhibitor exhibits interdomain closureKenton L Longenecker, Geoffrey F Stamper, Philip J Hajduk, et al.
Journal of Medicinal Chemistry|October 22, 2009
Discovery of 3H-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as potent, highly selective, and orally bioavailable inhibitors of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM) kinasesZhi-Fu Tao, Lisa A Hasvold, Joel D Leverson, et al.
Chembiochem : a European Journal of Chemical Biology|January 10, 2018
Design of Aminobenzothiazole Inhibitors of Rho Kinases 1 and 2 by Using Protein Kinase A as a Structure SurrogateRussell A Judge, Anil Vasudevan, Victoria E Scott, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Hepatitis C NS5B polymerase inhibitors: functional equivalents for the benzothiadiazine moietyDouglas K Hutchinson, Charles A Flentge, Pamela L Donner, et al.
Pageof 4