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Atherosclerosis|December 7, 2010
Strong association of the APOA5-1131T>C gene variant and early-onset acute myocardial infarctionRaffaele De Caterina, Philippa J Talmud, Piera Angelica Merlini, et al.Plos One|August 11, 2012
Functional analysis of two PLA2G2A variants associated with secretory phospholipase A2-IIA levelsHolly J Exeter, Lasse Folkersen, Jutta Palmen, et al.Pediatrics|September 5, 2001
Age-related effects of genetic variation on lipid levels: The Columbia University BioMarkers StudyP J Talmud, L Berglund, E M Hawe, et al.European Heart Journal|March 30, 2011
Association of a sequence variant in DAB2IP with coronary heart diseaseSeamus C Harrison, Jackie A Cooper, Kawah Li, et al.Journal of Thrombosis and Haemostasis : JTH|August 26, 2010
Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK menG Ken-Dror, F Drenos, S E Humphries, et al.Pharmacogenetics|December 21, 2004
Response to micronized fenofibrate treatment is associated with the peroxisome-proliferator-activated receptors alpha G/C intron7 polymorphism in subjects with type 2 diabetesChristelle Foucher, Stephanie Rattier, David M Flavell, et al.Diabetologia|June 16, 2000
Variation in the PPARalpha gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjectsD M Flavell, I Pineda Torra, Y Jamshidi, et al.Biochimica Et Biophysica Acta|January 21, 2004
Association of apolipoprotein A5 variants with LDL particle size and triglyceride in Japanese AmericansMelissa A Austin, Philippa J Talmud, Federico M Farin, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2012
Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situA P Walker, R C Fowkes, F Saleh, et al.Kidney International|December 17, 2009
Circulating methylarginine levels and the decline in renal function in patients with chronic kidney disease are modulated by DDAH1 polymorphismsBen Caplin, Dorothea Nitsch, Herpreet Gill, et al.Pageof 23