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Information about Medium-chain Acyl-coenzyme A Dehydrogenase 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.
Most recent studies have shown that Medium-chain Acyl-coenzyme A Dehydrogenase Deficiency shares some biological mechanisms with acidemia, comatose, deficiency-of-butyryl-coa-dehydrogenase, encephalopathies, fatty-liver, heart-failure, hypertrophy, hypoglycemia, inborn-errors-of-metabolism, lethargy, long-chain-acyl-coa-dehydrogenase-deficiency, metabolic-diseases, multiple-acyl-coenzyme-a-dehydrogenase-deficiency, phenylketonurias, reye-syndrome, sudden-death, sudden-infant-death-syndrome, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Medium-chain Acyl-coenzyme A Dehydrogenase Deficiency, and have been seen in publications frequently: Aging, Cell Activation, Electron Transport, Electron Transport Chain, Energy Homeostasis, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Fatty Acid Transport, Glucose Homeostasis, Glucose Transport, Glycolysis, Lipid Oxidation, Lipid Storage, Localization, Mast Cell Activation, Oxidative Phosphorylation, Pathogenesis, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Medium-chain Acyl-coenzyme A Dehydrogenase Deficiency, such as ACADL, ACADM, ACADS, ACADVL, BRCA2, CALD1, CDH15, CPT2, ESRRA, FANCD2, IVD, NBN, NME1, PPARA, PPARG, PSEN1, SLC2A4, TEAD2. 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.