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Journal of Medicinal Chemistry|June 24, 2015
Optimization of a Series of Triazole Containing Mammalian Target of Rapamycin (mTOR) Kinase Inhibitors and the Discovery of CC-115Deborah S Mortensen, Sophie M Perrin-Ninkovic, Graziella Shevlin, et al.
Journal of Medicinal Chemistry|June 18, 2015
Discovery of mammalian target of rapamycin (mTOR) kinase inhibitor CC-223Deborah S Mortensen, Sophie M Perrin-Ninkovic, Graziella Shevlin, et al.
Journal of Medicinal Chemistry|August 6, 2021
Discovery of the Selective Protein Kinase C-θ Kinase Inhibitor, CC-90005Patrick Papa, Brandon Whitefield, Deborah S Mortensen, et al.
Nature Genetics|March 11, 2008
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndromeCarmen C Leitch, Norann A Zaghloul, Erica E Davis, et al.
American Journal of Human Genetics|August 4, 2016
Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl SyndromeAnna Lindstrand, Stephan Frangakis, Claudia M B Carvalho, et al.
Human Genetics|June 24, 2006
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivityErica R Eichers, Muhammad M Abd-El-Barr, Richard Paylor, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2012
Discovery of CC-930, an orally active anti-fibrotic JNK inhibitorVéronique Plantevin Krenitsky, Lisa Nadolny, Mercedes Delgado, et al.
American Journal of Human Genetics|March 10, 2009
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosaHui Wang, Anneke I den Hollander, Yalda Moayedi, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 15, 2011
Reporting adverse events in a surgical trial for complex congenital heart disease: the Pediatric Heart Network experienceLisa Virzi, Victoria Pemberton, Richard G Ohye, et al.
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