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- Table of Contents
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Disease Info Card
Acidosis, Lactic
Information about Acidosis, Lactic: 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 Acidosis, Lactic
Most recent studies have shown that Acidosis, Lactic shares some biological mechanisms with acidosis, cerebrovascular-accident, diabetes-mellitus, diabetes-mellitus-non-insulin-dependent, encephalopathies, epilepsy, hiv-infections, hyperglycemia, hypoglycemia, hypoxia, ischemia, kidney-failure, melas-syndrome, metabolic-acidosis, mitochondrial-diseases, mitochondrial-encephalomyopathies, mitochondrial-myopathies, myopathy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acidosis, Lactic, and have been seen in publications frequently: Cell Death, Coagulation, Electron Transport, Electron Transport Chain, Excretion, Fermentation, Gluconeogenesis, Glycolysis, Hypersensitivity, Inflammatory Response, Insulin Secretion, Mitochondrial Translation, Oxidative Phosphorylation, Oxygen Transport, Pathogenesis, Pyruvate Oxidation, Secretion, Translation, Transport, Tricarboxylic Acid Cycle
Quite a number of genes have been found to play important roles in Acidosis, Lactic, such as ALB, BCHE, C2, CD4, COX5A, COX8A, CPOX, CSF2, CYCS, DLD, F2, G6PC, GCG, INS, LAMC2, PC, PDP1, 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.