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JHEP Reports : Innovation in Hepatology|December 11, 2023
A missense variant in human perilipin 2 (PLIN2 Ser251Pro) reduces hepatic steatosis in miceEleonora Scorletti, Yedidya Saiman, Sookyoung Jeon, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 18, 2010
Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcificationHaiqing Shen, Lawrence F Bielak, Jane F Ferguson, et al.
The Journal of Clinical Investigation|July 2, 2010
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 functionSebastian Zeissig, Stephanie K Dougan, Duarte C Barral, et al.
Journal of the American College of Cardiology|June 6, 2020
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery DiseaseKrishna G Aragam, Amanda Dobbyn, Renae Judy, et al.
Journal of the American College of Cardiology|April 8, 2017
ANGPTL3 Deficiency and Protection Against Coronary Artery DiseaseNathan O Stitziel, Amit V Khera, Xiao Wang, et al.
Plos One|May 26, 2012
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe projectKiran Musunuru, Simon P R Romaine, Guillaume Lettre, et al.
Nature Genetics|January 9, 2007
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionAgnar Helgason, Snaebjörn Pálsson, Gudmar Thorleifsson, et al.
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