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Disease Info Card
Hyperlipidemia, Familial Combined
Information about Hyperlipidemia, Familial Combined: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Hyperlipidemia, Familial Combined
Most recent studies have shown that Hyperlipidemia, Familial Combined shares some biological mechanisms with arteriosclerosis, atherosclerosis, cardiovascular-diseases, combined-hyperlipidaemia, coronary-artery-disease, coronary-heart-disease, diabetes-mellitus, diabetes-mellitus-non-insulin-dependent, dyslipidemias, heart-diseases, hypercholesterolemia, hypercholesterolemia-familial, hyperlipidemia, hyperlipoproteinemia-type-iib, hyperlipoproteinemia-type-iv, hyperlipoproteinemias, hypertensive-disease, insulin-resistance, lipid-metabolism-disorders, obesity.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hyperlipidemia, Familial Combined, and have been seen in publications frequently: Aging, Cell Adhesion, Cholesterol Esterification, Cholesterol Transport, Coagulation, Excretion, Fatty Acid Oxidation, Fibrinolysis, Gallstone Formation, Glucose Homeostasis, Insulin Secretion, Lipid Homeostasis, Lipid Storage, Localization, Pathogenesis, Platelet Activation, Reverse Cholesterol Transport, Secretion, Transport, Vasodilation
Quite a number of genes have been found to play important roles in Hyperlipidemia, Familial Combined, such as APOA1, APOA2, APOB, APOC3, APOE, C3, CD55, CETP, CFH, INS, LCP1, LDLR, LIPC, LPA, LPL, TCN2, TG, USF1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.