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Disease Info Card
Lactic Acidemia
Information about Lactic 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 Lactic Acidemia
Most recent studies have shown that Lactic Acidemia shares some biological mechanisms with acidemia, acidosis, acidosis-lactic, atrophy, encephalopathies, glycogen-storage-disease, glycogen-storage-disease-type-i, hepatomegaly, hypoglycemia, inborn-errors-of-metabolism, leigh-disease, metabolic-acidosis, metabolic-diseases, mitochondrial-diseases, mitochondrial-myopathies, muscle-hypotonia, myopathy, pyruvate-dehydrogenase-complex-deficiency-disease, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Lactic Acidemia, and have been seen in publications frequently: Brain Development, Coagulation, Developmental Process, Electron Transport, Electron Transport Chain, Excretion, Fatty Acid Oxidation, Gluconeogenesis, Glucose Homeostasis, Glycolysis, Inflammatory Response, Localization, Muscle Atrophy, Oxidative Phosphorylation, Pathogenesis, Pyruvate Oxidation, Response To Hypoxia, Transport, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Lactic Acidemia, such as ALDH9A1, BCHE, CELA3B, CSF2, CYCS, DBT, DLD, ENOPH1, G6PC, GCG, INS, LAMC2, LILRA3, PC, PDP1, POLG, TNF. 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.