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R Hickey

Showing results (291-300 of 305) with videos related to

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Frontiers in Pharmacology|August 30, 2017
Reductive Metabolism Influences the Toxicity and Pharmacokinetics of the Hypoxia-Targeted Benzotriazine Di-Oxide Anticancer Agent SN30000 in MiceYongchuan Gu, Tony T-A Chang, Jingli Wang, et al.
Nature Aging|April 28, 2023
Dietary supplementation of clinically utilized PI3K p110α inhibitor extends the lifespan of male and female miceC P Hedges, B Shetty, S C Broome, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 9, 2014
G protein-coupled bile acid receptor 1 stimulation mediates arterial vasodilation through a K(Ca)1.1 (BK(Ca))-dependent mechanismRyan M Fryer, Khing Jow Ng, Suzanne G Nodop Mazurek, et al.
Plos One|June 27, 2014
A GPBAR1 (TGR5) small molecule agonist shows specific inhibitory effects on myeloid cell activation in vitro and reduces experimental autoimmune encephalitis (EAE) in vivoNuruddeen D Lewis, Lori A Patnaude, Josephine Pelletier, et al.
Molecular Pharmacology|April 14, 2019
Functional CRISPR and shRNA Screens Identify Involvement of Mitochondrial Electron Transport in the Activation of EvofosfamideFrancis W Hunter, Jules B L Devaux, Fanying Meng, et al.
Journal of Medicinal Chemistry|July 19, 2012
Identification of a potent sodium hydrogen exchanger isoform 1 (NHE1) inhibitor with a suitable profile for chronic dosing and demonstrated cardioprotective effects in a preclinical model of myocardial infarction in the ratJohn D Huber, Jörg Bentzien, Stephen J Boyer, et al.
The Journal of Thoracic and Cardiovascular Surgery|January 22, 1998
Perioperative effects of alpha-stat versus pH-stat strategies for deep hypothermic cardiopulmonary bypass in infantsA J du Plessis, R A Jonas, D Wypij, et al.
Journal of Medicinal Chemistry|May 29, 1999
Ligands for the tyrosine kinase p56lck SH2 domain: discovery of potent dipeptide derivatives with monocharged, nonhydrolyzable phosphate replacementsP L Beaulieu, D R Cameron, J M Ferland, et al.
Bioorganic & Medicinal Chemistry Letters|April 10, 2009
Discovery and characterization of the N-phenyl-N'-naphthylurea class of p38 kinase inhibitorsPier F Cirillo, Eugene R Hickey, Neil Moss, et al.
ACS Infectious Diseases|September 13, 2024
Identification of Chemical Scaffolds That Inhibit the <i>Mycobacterium tuberculosis</i> Respiratory Complex Succinate DehydrogenaseCara Adolph, Kiel Hards, Zoe C Williams, et al.
Pageof 31

Showing results (291-300 of 305) with videos related to

Sort By:
Pageof 31
Frontiers in Pharmacology|August 30, 2017
Reductive Metabolism Influences the Toxicity and Pharmacokinetics of the Hypoxia-Targeted Benzotriazine Di-Oxide Anticancer Agent SN30000 in MiceYongchuan Gu, Tony T-A Chang, Jingli Wang, et al.
Nature Aging|April 28, 2023
Dietary supplementation of clinically utilized PI3K p110α inhibitor extends the lifespan of male and female miceC P Hedges, B Shetty, S C Broome, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 9, 2014
G protein-coupled bile acid receptor 1 stimulation mediates arterial vasodilation through a K(Ca)1.1 (BK(Ca))-dependent mechanismRyan M Fryer, Khing Jow Ng, Suzanne G Nodop Mazurek, et al.
Plos One|June 27, 2014
A GPBAR1 (TGR5) small molecule agonist shows specific inhibitory effects on myeloid cell activation in vitro and reduces experimental autoimmune encephalitis (EAE) in vivoNuruddeen D Lewis, Lori A Patnaude, Josephine Pelletier, et al.
Molecular Pharmacology|April 14, 2019
Functional CRISPR and shRNA Screens Identify Involvement of Mitochondrial Electron Transport in the Activation of EvofosfamideFrancis W Hunter, Jules B L Devaux, Fanying Meng, et al.
Journal of Medicinal Chemistry|July 19, 2012
Identification of a potent sodium hydrogen exchanger isoform 1 (NHE1) inhibitor with a suitable profile for chronic dosing and demonstrated cardioprotective effects in a preclinical model of myocardial infarction in the ratJohn D Huber, Jörg Bentzien, Stephen J Boyer, et al.
The Journal of Thoracic and Cardiovascular Surgery|January 22, 1998
Perioperative effects of alpha-stat versus pH-stat strategies for deep hypothermic cardiopulmonary bypass in infantsA J du Plessis, R A Jonas, D Wypij, et al.
Journal of Medicinal Chemistry|May 29, 1999
Ligands for the tyrosine kinase p56lck SH2 domain: discovery of potent dipeptide derivatives with monocharged, nonhydrolyzable phosphate replacementsP L Beaulieu, D R Cameron, J M Ferland, et al.
Bioorganic & Medicinal Chemistry Letters|April 10, 2009
Discovery and characterization of the N-phenyl-N'-naphthylurea class of p38 kinase inhibitorsPier F Cirillo, Eugene R Hickey, Neil Moss, et al.
ACS Infectious Diseases|September 13, 2024
Identification of Chemical Scaffolds That Inhibit the <i>Mycobacterium tuberculosis</i> Respiratory Complex Succinate DehydrogenaseCara Adolph, Kiel Hards, Zoe C Williams, et al.
Pageof 31