Showing results (501-510 of 531) with videos related to
Sort By:
Pageof 54
American Journal of Medical Genetics. Part A|June 18, 2019
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathyLauren B Carter, Agatino Battaglia, Athena Cherry, et al.Bioorganic & Medicinal Chemistry Letters|April 1, 2008
2-Arylbenzoxazoles as novel cholesteryl ester transfer protein inhibitors: optimization via array synthesisLalgudi S Harikrishnan, Muthoni G Kamau, Timothy F Herpin, et al.Proceedings of the National Academy of Sciences of the United States of America|July 5, 2022
Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse modelAnna Axelsson Raja, Hiroko Wakimoto, Daniel M DeLaughter, et al.American Journal of Human Genetics|March 9, 2010
Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalitiesBlake C Ballif, Aaron Theisen, Jill A Rosenfeld, et al.Journal of Medicinal Chemistry|January 29, 2020
Identification of Reversible Small Molecule Inhibitors of Endothelial Lipase (EL) That Demonstrate HDL-C Increase In VivoGeorge Tora, Soong-Hoon Kim, Zulan Pi, et al.Med (New York, N.Y.)|November 14, 2023
The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human diseaseLeigh C Carmody, Michael A Gargano, Sabrina Toro, et al.Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
The Medical Action Ontology: A Tool for Annotating and Analyzing Treatments and Clinical Management of Human DiseaseLeigh C Carmody, Michael A Gargano, Sabrina Toro, et al.Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.Journal of Medicinal Chemistry|June 2, 2012
Diphenylpyridylethanamine (DPPE) derivatives as cholesteryl ester transfer protein (CETP) inhibitorsLalgudi S Harikrishnan, Heather J Finlay, Jennifer X Qiao, et al.Journal of Medical Genetics|March 7, 2009
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotypeT Kleefstra, W A van Zelst-Stams, W M Nillesen, et al.Pageof 54