Pages that link to "Q73325079"

The following pages link to Lipoprotein lipase gene variants and risk of coronary disease: a quantitative analysis of population-based studies (Q73325079):

Displaying 25 items.

• A novel endothelial-derived lipase that modulates HDL metabolism (Q22009153) (← links)
• Genetic determinants of plasma triglycerides: impact of rare and common mutations (Q28609419) (← links)
• Genes influencing HDL metabolism: new perspectives and implications for atherosclerosis prevention (Q33877037) (← links)
• Common mutations of the lipoprotein lipase gene and their clinical significance (Q34107183) (← links)
• High-density lipoprotein metabolism: molecular targets for new therapies for atherosclerosis (Q34107511) (← links)
• Triglyceride-rich lipoproteins and high-density lipoprotein cholesterol in patients at high risk of cardiovascular disease: evidence and guidance for management (Q34181381) (← links)
• Molecular genetics and gene expression in atherosclerosis. (Q34386072) (← links)
• Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency (Q34388982) (← links)
• Lipases and HDL metabolism (Q34594298) (← links)
• Regulation of reverse cholesterol transport and clinical implications (Q35212558) (← links)
• Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci (Q37567281) (← links)
• Common variants in the genes of triglyceride and HDL-C metabolism lack association with coronary artery disease in the Pakistani subjects (Q37615850) (← links)
• Enhancing reverse cholesterol transport/raising HDL cholesterol: new options for prevention and treatment of cardiovascular disease (Q42339302) (← links)
• The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease (Q43782371) (← links)
• Relative contribution of low-density lipoprotein receptor and lipoprotein lipase gene mutations to angiographically assessed coronary artery disease among French Canadians. (Q47671233) (← links)
• Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women. (Q51558850) (← links)
• Evidence of a major locus for lipoprotein lipase (LPL) activity in addition to a pleiotropic locus for both LPL and fasting insulin: results from the HERITAGE Family Study. (Q51562313) (← links)
• Substitution of asparagine for aspartic acid at residue 9 (D9N) of lipoprotein lipase markedly augments risk of ischaemic heart disease in male smokers. (Q53838842) (← links)
• Genetic Aspects of Obesity. (Q54963578) (← links)
• Human lipoprotein lipase HindIII polymorphism in young patients with myocardial infarction. (Q64999111) (← links)
• Effect of obesity on HDL and LDL particle sizes in carriers of the null P207L or defective D9N mutation in the lipoprotein lipase gene: the Québec LipD Study (Q73293556) (← links)
• Lack of Association of Lipoprotein Lipase Gene Polymorphisms With Coronary Artery Disease in the Saudi Arab Population (Q73303502) (← links)
• Association of pre-eclampsia with common coding sequence variations in the lipoprotein lipase gene (Q73356668) (← links)
• A Common Truncated Variant of Lipoprotein Lipase in the Japanese Population Is Characterized by Pattern B Phenotype (Q79212069) (← links)
• . Association of HindIII and PvuII genetic polymorphisms of lipoprotein lipase with lipid metabolism and macrovascular events in type 2 diabetic patients (Q79787012) (← links)