This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Abetalipoproteinemia
Information about Abetalipoproteinemia: 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 Abetalipoproteinemia
Most recent studies have shown that Abetalipoproteinemia shares some biological mechanisms with acanthocytosis, anemia, ataxia, celiac-disease, familial-hypobetalipoproteinemia, hereditary-diseases, hypercholesterolemia, hypercholesterolemia-familial, hyperlipidemia, hypobetalipoproteinemias, hypolipoproteinemias, liver-diseases, malabsorption-syndrome, nervous-system-disorder, refsum-disease, retinitis-pigmentosa, tangier-disease, vitamin-e-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Abetalipoproteinemia, and have been seen in publications frequently: Cholesterol Esterification, Chylomicron Assembly, Coagulation, Dna Repair, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Glycosylation, Intestinal Absorption, Lipid Binding, Lipid Storage, Lipid Transport, Localization, Pathogenesis, Platelet Aggregation, Reflex, Regeneration, Secretion, Secretory Pathway, Transport
Quite a number of genes have been found to play important roles in Abetalipoproteinemia, such as ABL1, APOA1, APOA2, APOB, APOE, CETP, HADHA, LCAT, LDLR, LPA, LPL, MT1B, MTTP, POMC, SEPSECS, TTPA, TXNDC15. 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.