The autoimmune MRL/lpr mouse strain, a model for systemic lupus erythematosus, exhibited an unusual plasma lipoprotein profile, suggesting a possible interaction of autoimmune disease and lipoprotein metabolism. In an effort to examine the genetic basis of such interactions, and to study their relationship to atherogenesis, we performed a quantitative trait locus analysis using a total of 272 (MRL/lprxBALB/cJ) second generation (F2) intercross mice. These mice were examined for levels of total plasma cholesterol, HDL cholesterol, VLDL and LDL cholesterol, unesterified cholesterol, autoantibodies, and aortic fatty streak lesions. Using a genome scan approach, we identified 4 quantitative trait loci controlling plasma lipoprotein levels on ch...
To identify genes controlling plasma HDL and triglyceride levels, quantitative trait locus (QTL) ana...
Susceptibility to atherosclerosis is determined by both environmental and genetic factors. Its genet...
HDL levels identified in mice by controlling for Apoa2 allelic effects: confirmation of a chromosome...
To investigate the quantitative trait loci (QTL) regulating plasma cholesterol, the female progeny o...
To identify genetic determinants of lipoprotein levels, we are performing quantitative trait locus (...
To investigate genetic contributions to individual variations of lipoprotein cholesterol concentrati...
A higher incidence of coronary artery disease is associated with a lower level of HDL-cholesterol. W...
Common forms of atherosclerosis involve multiple genetic and environmental factors. While human geno...
To determine the genetic contribution to variation among lipoprotein cholesterol levels, we performe...
To identify additional loci that influence lipoprotein cholesterol levels, we performed quantitative...
To identify additional loci that influence lipoprotein cholesterol levels, we performed quantitative...
AbstractTo identify quantitative trait loci (QTLs) responsible for regulating plasma lipid concentra...
The plasma lipid concentrations and obesity of C57BL/6J (B6) and 129S1/SvImJ (129) inbred mouse stra...
Susceptibility to atherosclerosis is determined by both environmental and genetic factors. Its genet...
OBJECTIVE: Summarizing the many discovered mouse and human quantitative trait loci (QTL) for high de...
To identify genes controlling plasma HDL and triglyceride levels, quantitative trait locus (QTL) ana...
Susceptibility to atherosclerosis is determined by both environmental and genetic factors. Its genet...
HDL levels identified in mice by controlling for Apoa2 allelic effects: confirmation of a chromosome...
To investigate the quantitative trait loci (QTL) regulating plasma cholesterol, the female progeny o...
To identify genetic determinants of lipoprotein levels, we are performing quantitative trait locus (...
To investigate genetic contributions to individual variations of lipoprotein cholesterol concentrati...
A higher incidence of coronary artery disease is associated with a lower level of HDL-cholesterol. W...
Common forms of atherosclerosis involve multiple genetic and environmental factors. While human geno...
To determine the genetic contribution to variation among lipoprotein cholesterol levels, we performe...
To identify additional loci that influence lipoprotein cholesterol levels, we performed quantitative...
To identify additional loci that influence lipoprotein cholesterol levels, we performed quantitative...
AbstractTo identify quantitative trait loci (QTLs) responsible for regulating plasma lipid concentra...
The plasma lipid concentrations and obesity of C57BL/6J (B6) and 129S1/SvImJ (129) inbred mouse stra...
Susceptibility to atherosclerosis is determined by both environmental and genetic factors. Its genet...
OBJECTIVE: Summarizing the many discovered mouse and human quantitative trait loci (QTL) for high de...
To identify genes controlling plasma HDL and triglyceride levels, quantitative trait locus (QTL) ana...
Susceptibility to atherosclerosis is determined by both environmental and genetic factors. Its genet...
HDL levels identified in mice by controlling for Apoa2 allelic effects: confirmation of a chromosome...