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

Minghan Wang

Showing results (71-80 of 79) with videos related to

Pageof 8
Sort By:
You have reached the last page of results.This site can display upto 79 results.
The Journal of Biological Chemistry|August 28, 2002
Protein kinase A site-specific phosphorylation regulates ATP-binding cassette A1 (ABCA1)-mediated phospholipid effluxRaymond H See, Rosalinda A Caday-Malcolm, Roshni R Singaraja, et al.
Journal of Medicinal Chemistry|April 19, 2008
2-amino-1,3-thiazol-4(5H)-ones as potent and selective 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: enzyme-ligand co-crystal structure and demonstration of pharmacodynamic effects in C57Bl/6 miceLars Johansson, Christopher Fotsch, Michael D Bartberger, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2013
Metabolism-guided discovery of a potent and orally bioavailable urea-based calcimimetic for the treatment of secondary hyperparathyroidismPaul M Wehn, Paul E Harrington, Timothy J Carlson, et al.
Bioorganic & Medicinal Chemistry Letters|October 9, 2007
The discovery of 2-anilinothiazolones as 11beta-HSD1 inhibitorsChester Yuan, David J St Jean, Qingyian Liu, et al.
Science Translational Medicine|December 1, 2012
Treating diabetes and obesity with an FGF21-mimetic antibody activating the βKlotho/FGFR1c receptor complexIan N Foltz, Sylvia Hu, Chadwick King, et al.
Journal of Medicinal Chemistry|December 5, 2008
Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic modelChristopher Fotsch, Michael D Bartberger, Eric A Bercot, et al.
Journal of Medicinal Chemistry|May 15, 2010
Discovery of a potent, orally active 11beta-hydroxysteroid dehydrogenase type 1 inhibitor for clinical study: identification of (S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (AMG 221)Murielle M Véniant, Clarence Hale, Randall W Hungate, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2010
The discovery of an orally efficacious positive allosteric modulator of the calcium sensing receptor containing a dibenzylamine corePaul E Harrington, David J St Jean, Jeffrey Clarine, et al.
Nature|November 15, 2013
Antidiabetic effects of glucokinase regulatory protein small-molecule disruptorsDavid J Lloyd, David J St Jean, Robert J M Kurzeja, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
The Journal of Biological Chemistry|August 28, 2002
Protein kinase A site-specific phosphorylation regulates ATP-binding cassette A1 (ABCA1)-mediated phospholipid effluxRaymond H See, Rosalinda A Caday-Malcolm, Roshni R Singaraja, et al.
Journal of Medicinal Chemistry|April 19, 2008
2-amino-1,3-thiazol-4(5H)-ones as potent and selective 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: enzyme-ligand co-crystal structure and demonstration of pharmacodynamic effects in C57Bl/6 miceLars Johansson, Christopher Fotsch, Michael D Bartberger, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2013
Metabolism-guided discovery of a potent and orally bioavailable urea-based calcimimetic for the treatment of secondary hyperparathyroidismPaul M Wehn, Paul E Harrington, Timothy J Carlson, et al.
Bioorganic & Medicinal Chemistry Letters|October 9, 2007
The discovery of 2-anilinothiazolones as 11beta-HSD1 inhibitorsChester Yuan, David J St Jean, Qingyian Liu, et al.
Science Translational Medicine|December 1, 2012
Treating diabetes and obesity with an FGF21-mimetic antibody activating the βKlotho/FGFR1c receptor complexIan N Foltz, Sylvia Hu, Chadwick King, et al.
Journal of Medicinal Chemistry|December 5, 2008
Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic modelChristopher Fotsch, Michael D Bartberger, Eric A Bercot, et al.
Journal of Medicinal Chemistry|May 15, 2010
Discovery of a potent, orally active 11beta-hydroxysteroid dehydrogenase type 1 inhibitor for clinical study: identification of (S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (AMG 221)Murielle M Véniant, Clarence Hale, Randall W Hungate, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2010
The discovery of an orally efficacious positive allosteric modulator of the calcium sensing receptor containing a dibenzylamine corePaul E Harrington, David J St Jean, Jeffrey Clarine, et al.
Nature|November 15, 2013
Antidiabetic effects of glucokinase regulatory protein small-molecule disruptorsDavid J Lloyd, David J St Jean, Robert J M Kurzeja, et al.
Pageof 8