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Clinical Chemistry and Laboratory Medicine|July 8, 2008
APOA5 Ala315>Val, identified in patients with severe hypertriglyceridemia, is a common mutation with no major effects on plasma lipid levelsJaroslav A Hubacek, Wu-Wei Wang, Zdena Skodová, et al.
Atherosclerosis|January 28, 2006
Lp-PLA2 activity and PLA2G7 A379V genotype in patients with diabetes mellitusP T E Wootton, J W Stephens, S J Hurel, et al.
Atherosclerosis|January 23, 2016
Post-GWAS methodologies for localisation of functional non-coding variants: ANGPTL3Federico Oldoni, Jutta Palmen, Claudia Giambartolomei, et al.
BMJ (Clinical Research Ed.)|January 16, 2010
Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort studyPhilippa J Talmud, Aroon D Hingorani, Jackie A Cooper, et al.
Social Psychiatry and Psychiatric Epidemiology|July 16, 2005
APOE polymorphism, socioeconomic status and cognitive function in mid-life--the Whitehall II longitudinal studyJ H Zhao, E J Brunner, M Kumari, et al.
The Journal of Biological Chemistry|January 15, 1990
Abetalipoproteinemia with an ApoB-100-lipoprotein(a) glycoprotein complex in plasma. Indication for an assembly defectH J Menzel, H Dieplinger, C Lackner, et al.
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