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Disease Info Card
High Density Lipoprotein Deficiency
Information about High Density Lipoprotein Deficiency: 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 High Density Lipoprotein Deficiency
Most recent studies have shown that High Density Lipoprotein Deficiency shares some biological mechanisms with arteriosclerosis, atherosclerosis, cardiovascular-diseases, coronary-artery-disease, coronary-heart-disease, cystic-fibrosis, fish-eye-disease, heart-diseases, hereditary-diseases, hypercatabolism, hypoalphalipoproteinemia-familial, hypolipoproteinemias, infarction, lecithin-acyltransferase-deficiency, liver-diseases, myocardial-infarction, tangier-disease, xanthoma, xanthomatosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying High Density Lipoprotein Deficiency, and have been seen in publications frequently: Aging, Cell Adhesion, Cholesterol Efflux, Cholesterol Esterification, Cholesterol Homeostasis, Cholesterol Transport, Drug Resistance, Insulin Secretion, Intracellular Cholesterol Transport, Ion Homeostasis, Keratinization, Lipid Binding, Lipid Homeostasis, Localization, Phospholipid Efflux, Platelet Activation, Reverse Cholesterol Transport, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in High Density Lipoprotein Deficiency, such as ABCA1, ABCA4, ABCC8, APOA1, APOA2, APOC3, ATP6V0A1, CDC42, CLU, LCAT, LPA, LPL, RFC1, RFC2, RFC4, WASL. 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.