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- Table of Contents
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Disease Info Card
Acidemia
Information about Acidemia: 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 Acidemia
Most recent studies have shown that Acidemia shares some biological mechanisms with acidosis, acidosis-lactic, anoxia, encephalopathies, fetal-diseases, hyperammonemia, hypercapnia, hypoglycemia, hypoxia, inborn-errors-of-metabolism, isovaleryl-coa-dehydrogenase-deficiency, ketosis, lactic-acidemia, malnutrition, mastitis-metritis-agalactia-syndrome, metabolic-acidosis, metabolic-diseases, methylmalonic-acidemia, propionic-acidemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acidemia, and have been seen in publications frequently: Brain Development, Coagulation, Diuresis, Electron Transport, Excretion, Fatty Acid Oxidation, Glomerular Filtration, Gluconeogenesis, Glycolysis, Inflammatory Response, Localization, Myelination, Oxidative Phosphorylation, Pathogenesis, Secretion, Translation, Transport, Urea Cycle, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Acidemia, such as AGA, AMY2A, AVP, BLOC1S6, C2, CYCS, ECHDC1, EPB42, ETFDH, G6PC, GCDH, GLS2, INS, IVD, MMD, PCCA, PCCB, PRH1. 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.