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W Friesen

Showing results (31-40 of 52) with videos related to

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Bioorganic & Medicinal Chemistry Letters|October 7, 2008
Optimization and structure-activity relationship of a series of 1-phenyl-1,8-naphthyridin-4-one-3-carboxamides: identification of MK-0873, a potent and effective PDE4 inhibitorDaniel Guay, Louise Boulet, Richard W Friesen, et al.
FEMS Microbiology Ecology|July 24, 2012
The mercury resistance (mer) operon in a marine gliding flavobacterium, Tenacibaculum discolor 9A5Rachel C Allen, Yen-Kuei Tu, Michael J Nevarez, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2005
Inhibitors of the inducible microsomal prostaglandin E2 synthase (mPGES-1) derived from MK-886Denis Riendeau, Renee Aspiotis, Diane Ethier, et al.
Biochemistry|July 18, 2002
The structure of PTP-1B in complex with a peptide inhibitor reveals an alternative binding mode for bisphosphonatesErnest Asante-Appiah, Sangita Patel, Claude Dufresne, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 6, 2008
MF63 [2-(6-chloro-1H-phenanthro[9,10-d]imidazol-2-yl)-isophthalonitrile], a selective microsomal prostaglandin E synthase-1 inhibitor, relieves pyresis and pain in preclinical models of inflammationDaigen Xu, Steven E Rowland, Patsy Clark, et al.
Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Substituted 4-(2,2-diphenylethyl)pyridine-N-oxides as phosphodiesterase-4 inhibitors: SAR study directed toward the improvement of pharmacokinetic parametersRichard Frenette, Marc Blouin, Christine Brideau, et al.
Bioorganic & Medicinal Chemistry Letters|May 17, 2003
Substituted 2-pyridinemethanol derivatives as potent and selective phosphodiesterase-4 inhibitorsYves Ducharme, Richard W Friesen, Marc Blouin, et al.
Immunology Letters|September 13, 2005
The C3a receptor antagonist SB 290157 has agonist activityMarie-Claude Mathieu, Nicole Sawyer, Gillian M Greig, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
The discovery of setileuton, a potent and selective 5-lipoxygenase inhibitorYves Ducharme, Marc Blouin, Christine Brideau, et al.
Biochemical Society Transactions|February 15, 2001
Utility of the Arabidopsis FAE1 and yeast SLC1-1 genes for improvements in erucic acid and oil content in rapeseedV Katavic, W Friesen, D L Barton, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

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Pageof 6
Bioorganic & Medicinal Chemistry Letters|October 7, 2008
Optimization and structure-activity relationship of a series of 1-phenyl-1,8-naphthyridin-4-one-3-carboxamides: identification of MK-0873, a potent and effective PDE4 inhibitorDaniel Guay, Louise Boulet, Richard W Friesen, et al.
FEMS Microbiology Ecology|July 24, 2012
The mercury resistance (mer) operon in a marine gliding flavobacterium, Tenacibaculum discolor 9A5Rachel C Allen, Yen-Kuei Tu, Michael J Nevarez, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2005
Inhibitors of the inducible microsomal prostaglandin E2 synthase (mPGES-1) derived from MK-886Denis Riendeau, Renee Aspiotis, Diane Ethier, et al.
Biochemistry|July 18, 2002
The structure of PTP-1B in complex with a peptide inhibitor reveals an alternative binding mode for bisphosphonatesErnest Asante-Appiah, Sangita Patel, Claude Dufresne, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 6, 2008
MF63 [2-(6-chloro-1H-phenanthro[9,10-d]imidazol-2-yl)-isophthalonitrile], a selective microsomal prostaglandin E synthase-1 inhibitor, relieves pyresis and pain in preclinical models of inflammationDaigen Xu, Steven E Rowland, Patsy Clark, et al.
Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Substituted 4-(2,2-diphenylethyl)pyridine-N-oxides as phosphodiesterase-4 inhibitors: SAR study directed toward the improvement of pharmacokinetic parametersRichard Frenette, Marc Blouin, Christine Brideau, et al.
Bioorganic & Medicinal Chemistry Letters|May 17, 2003
Substituted 2-pyridinemethanol derivatives as potent and selective phosphodiesterase-4 inhibitorsYves Ducharme, Richard W Friesen, Marc Blouin, et al.
Immunology Letters|September 13, 2005
The C3a receptor antagonist SB 290157 has agonist activityMarie-Claude Mathieu, Nicole Sawyer, Gillian M Greig, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
The discovery of setileuton, a potent and selective 5-lipoxygenase inhibitorYves Ducharme, Marc Blouin, Christine Brideau, et al.
Biochemical Society Transactions|February 15, 2001
Utility of the Arabidopsis FAE1 and yeast SLC1-1 genes for improvements in erucic acid and oil content in rapeseedV Katavic, W Friesen, D L Barton, et al.
Pageof 6