Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Eric F Johnson

Showing results (51-60 of 122) with videos related to

Pageof 13
Sort By:
The Journal of Biological Chemistry|June 15, 2016
20-Hydroxyeicosatetraenoic Acid (HETE)-dependent Hypertension in Human Cytochrome P450 (CYP) 4A11 Transgenic Mice: NORMALIZATION OF BLOOD PRESSURE BY SODIUM RESTRICTION, HYDROCHLOROTHIAZIDE, OR BLOCKADE OF THE TYPE 1 ANGIOTENSIN II RECEPTORÜzen Savas, Shouzou Wei, Mei-Hui Hsu, et al.
The Journal of Biological Chemistry|July 19, 2002
The CYP4A isoforms hydroxylate epoxyeicosatrienoic acids to form high affinity peroxisome proliferator-activated receptor ligandsL Ashley Cowart, Shouzuo Wei, Mei-Hui Hsu, et al.
The Journal of Biological Chemistry|June 8, 2004
The structure of human cytochrome P450 2C9 complexed with flurbiprofen at 2.0-A resolutionMichael R Wester, Jason K Yano, Guillaume A Schoch, et al.
The Journal of Biological Chemistry|February 22, 2007
Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2Stefaan Sansen, Jason K Yano, Rosamund L Reynald, et al.
The Journal of Biological Chemistry|April 16, 2009
Opposing roles of peroxisome proliferator-activated receptor alpha and growth hormone in the regulation of CYP4A11 expression in a transgenic mouse modelÜzen Savas, Daniel E W Machemer, Mei-Hui Hsu, et al.
The Journal of Biological Chemistry|May 24, 2017
Heme-thiolate sulfenylation of human cytochrome P450 4A11 functions as a redox switch for catalytic inhibitionMatthew E Albertolle, Donghak Kim, Leslie D Nagy, et al.
The Journal of Biological Chemistry|October 25, 2011
1-Benzyl-3-cetyl-2-methylimidazolium iodide (NH125) induces phosphorylation of eukaryotic elongation factor-2 (eEF2): a cautionary note on the anticancer mechanism of an eEF2 kinase inhibitorZehan Chen, Sujatha M Gopalakrishnan, Mai-Ha Bui, et al.
Biochemistry|August 23, 2008
Single mutations change CYP2F3 from a dehydrogenase of 3-methylindole to an oxygenaseJaya S Kartha, Konstantine W Skordos, Hao Sun, et al.
Bioorganic & Medicinal Chemistry Letters|October 12, 2005
Scaffold oriented synthesis. Part 1: Design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitorsIrini Akritopoulou-Zanze, Daria Darczak, Kathy Sarris, et al.
The Journal of Biological Chemistry|September 6, 2011
Ubiquitin-specific cysteine protease 2a (USP2a) regulates the stability of Aurora-AYan Shi, Larry R Solomon, Ana Pereda-Lopez, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
The Journal of Biological Chemistry|June 15, 2016
20-Hydroxyeicosatetraenoic Acid (HETE)-dependent Hypertension in Human Cytochrome P450 (CYP) 4A11 Transgenic Mice: NORMALIZATION OF BLOOD PRESSURE BY SODIUM RESTRICTION, HYDROCHLOROTHIAZIDE, OR BLOCKADE OF THE TYPE 1 ANGIOTENSIN II RECEPTORÜzen Savas, Shouzou Wei, Mei-Hui Hsu, et al.
The Journal of Biological Chemistry|July 19, 2002
The CYP4A isoforms hydroxylate epoxyeicosatrienoic acids to form high affinity peroxisome proliferator-activated receptor ligandsL Ashley Cowart, Shouzuo Wei, Mei-Hui Hsu, et al.
The Journal of Biological Chemistry|June 8, 2004
The structure of human cytochrome P450 2C9 complexed with flurbiprofen at 2.0-A resolutionMichael R Wester, Jason K Yano, Guillaume A Schoch, et al.
The Journal of Biological Chemistry|February 22, 2007
Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2Stefaan Sansen, Jason K Yano, Rosamund L Reynald, et al.
The Journal of Biological Chemistry|April 16, 2009
Opposing roles of peroxisome proliferator-activated receptor alpha and growth hormone in the regulation of CYP4A11 expression in a transgenic mouse modelÜzen Savas, Daniel E W Machemer, Mei-Hui Hsu, et al.
The Journal of Biological Chemistry|May 24, 2017
Heme-thiolate sulfenylation of human cytochrome P450 4A11 functions as a redox switch for catalytic inhibitionMatthew E Albertolle, Donghak Kim, Leslie D Nagy, et al.
The Journal of Biological Chemistry|October 25, 2011
1-Benzyl-3-cetyl-2-methylimidazolium iodide (NH125) induces phosphorylation of eukaryotic elongation factor-2 (eEF2): a cautionary note on the anticancer mechanism of an eEF2 kinase inhibitorZehan Chen, Sujatha M Gopalakrishnan, Mai-Ha Bui, et al.
Biochemistry|August 23, 2008
Single mutations change CYP2F3 from a dehydrogenase of 3-methylindole to an oxygenaseJaya S Kartha, Konstantine W Skordos, Hao Sun, et al.
Bioorganic & Medicinal Chemistry Letters|October 12, 2005
Scaffold oriented synthesis. Part 1: Design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitorsIrini Akritopoulou-Zanze, Daria Darczak, Kathy Sarris, et al.
The Journal of Biological Chemistry|September 6, 2011
Ubiquitin-specific cysteine protease 2a (USP2a) regulates the stability of Aurora-AYan Shi, Larry R Solomon, Ana Pereda-Lopez, et al.
Pageof 13