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Xenobiotica; the Fate of Foreign Compounds in Biological Systems|June 12, 2012
Acute arsenic toxicity alters cytochrome P450 and soluble epoxide hydrolase and their associated arachidonic acid metabolism in C57Bl/6 mouse heartAnwar Anwar-Mohamed, Ahmed A El-Sherbeni, Seok H Kim, et al.
Biological Trace Element Research|May 17, 2024
Alteration of Hepatic Cytochrome P450 Expression and Arachidonic Acid Metabolism by Arsenic Trioxide (ATO) in C57BL/6 MiceMahmoud A El-Ghiaty, Mohammed A Alqahtani, Sara R El-Mahrouk, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|February 2, 2011
The effect of Nrf2 knockout on the constitutive expression of drug metabolizing enzymes and transporters in C57Bl/6 mice liversAnwar Anwar-Mohamed, Owen S Degenhardt, Mohamed A M El Gendy, et al.
Drug Development Research|July 12, 2024
Identification of aryl hydrocarbon receptor allosteric antagonists from clinically approved drugsFarag E S Mosa, Mohammed A Alqahtani, Mahmoud A El-Ghiaty, et al.
Archives of Biochemistry and Biophysics|July 11, 2024
Modulation of aryl hydrocarbon receptor activity by tyrosine kinase inhibitors (ponatinib and tofacitinib)Farag E S Mosa, Mohammed A Alqahtani, Mahmoud A El-Ghiaty, et al.
Journal of Cardiovascular Pharmacology|April 25, 2017
Inhibition of Mid-chain HETEs Protects Against Angiotensin II-induced Cardiac HypertrophySamya Elkhatali, Zaid H Maayah, Ahmed A El-Sherbeni, et al.
Prostaglandins & Other Lipid Mediators|August 28, 2012
Differential effects of soluble epoxide hydrolase inhibition and CYP2J2 overexpression on postischemic cardiac function in aged miceKetul R Chaudhary, Beshay N M Zordoky, Matthew L Edin, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|February 16, 2013
Acute arsenic treatment alters cytochrome P450 expression and arachidonic acid metabolism in lung, liver and kidney of C57Bl/6 miceAnwar Anwar-Mohamed, Ahmed El-Sherbeni, Seok Hee Kim, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|November 20, 2014
Design and synthesis of resveratrol-salicylate hybrid derivatives as CYP1A1 inhibitorsFahad S Aldawsari, Osama H Elshenawy, Mohamed A M El Gendy, et al.
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