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Showing results (321-330 of 383) with videos related to

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Bioorganic & Medicinal Chemistry Letters|March 29, 2011
Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymeraseRobert G Gentles, Steven Sheriff, Brett R Beno, et al.
Bioorganic & Medicinal Chemistry Letters|October 27, 2016
Discovery of fluorobenzimidazole HCV NS5A inhibitorsJohn T Randolph, Charles A Flentge, Pamela Donner, et al.
JAMA Network Open|September 18, 2023
Pediatric vs Adult or Mixed Trauma Centers in Children Admitted to Hospitals Following Trauma: A Systematic Review and Meta-AnalysisLynne Moore, Gabrielle Freire, Alexis F Turgeon, et al.
Plos One|August 11, 2012
High-throughput screening and rapid inhibitor triage using an infectious chimeric Hepatitis C virusMichael J Wichroski, Jie Fang, Betsy J Eggers, et al.
Journal of Medicinal Chemistry|August 5, 2024
Atropisomerism Observed in Galactose-Based Monosaccharide Inhibitors of Galectin-3 Comprising 2-Methyl-4-phenyl-2,4-dihydro-3<i>H</i>-1,2,4-triazole-3-thioneDavid S Yoon, Chunjian Liu, Prasada Rao Jalagam, 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.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffoldDominique Potin, Michele Launay, Eric Nicolai, et al.
Journal of Medicinal Chemistry|September 3, 2011
Small molecule receptor protein tyrosine phosphatase γ (RPTPγ) ligands that inhibit phosphatase activity via perturbation of the tryptophan-proline-aspartate (WPD) loopSteven Sheriff, Brett R Beno, Weixu Zhai, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2012
Synthesis and SAR studies of novel heteroaryl fused tetracyclic indole-diamide compounds: potent allosteric inhibitors of the hepatitis C virus NS5B polymeraseMin Ding, Feng He, Thomas W Hudyma, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|December 15, 2025
Access to pediatric trauma centres in Canada: a population-based retrospective cohort studyAlexandra Lapierre, Carmel Awlise, Gabrielle Freire, et al.
Pageof 39

Showing results (321-330 of 383) with videos related to

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Pageof 39
Bioorganic & Medicinal Chemistry Letters|March 29, 2011
Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymeraseRobert G Gentles, Steven Sheriff, Brett R Beno, et al.
Bioorganic & Medicinal Chemistry Letters|October 27, 2016
Discovery of fluorobenzimidazole HCV NS5A inhibitorsJohn T Randolph, Charles A Flentge, Pamela Donner, et al.
JAMA Network Open|September 18, 2023
Pediatric vs Adult or Mixed Trauma Centers in Children Admitted to Hospitals Following Trauma: A Systematic Review and Meta-AnalysisLynne Moore, Gabrielle Freire, Alexis F Turgeon, et al.
Plos One|August 11, 2012
High-throughput screening and rapid inhibitor triage using an infectious chimeric Hepatitis C virusMichael J Wichroski, Jie Fang, Betsy J Eggers, et al.
Journal of Medicinal Chemistry|August 5, 2024
Atropisomerism Observed in Galactose-Based Monosaccharide Inhibitors of Galectin-3 Comprising 2-Methyl-4-phenyl-2,4-dihydro-3<i>H</i>-1,2,4-triazole-3-thioneDavid S Yoon, Chunjian Liu, Prasada Rao Jalagam, 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.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffoldDominique Potin, Michele Launay, Eric Nicolai, et al.
Journal of Medicinal Chemistry|September 3, 2011
Small molecule receptor protein tyrosine phosphatase γ (RPTPγ) ligands that inhibit phosphatase activity via perturbation of the tryptophan-proline-aspartate (WPD) loopSteven Sheriff, Brett R Beno, Weixu Zhai, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2012
Synthesis and SAR studies of novel heteroaryl fused tetracyclic indole-diamide compounds: potent allosteric inhibitors of the hepatitis C virus NS5B polymeraseMin Ding, Feng He, Thomas W Hudyma, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|December 15, 2025
Access to pediatric trauma centres in Canada: a population-based retrospective cohort studyAlexandra Lapierre, Carmel Awlise, Gabrielle Freire, et al.
Pageof 39