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Disease Info Card
Mitochondrial Diseases
Information about Mitochondrial Diseases: 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 Mitochondrial Diseases
Most recent studies have shown that Mitochondrial Diseases shares some biological mechanisms with acidosis, acidosis-lactic, ataxia, atrophy, cardiomyopathies, chronic-progressive-external-ophthalmoplegia, diabetes-mellitus, encephalopathies, epilepsy, external-ophthalmoplegia, leigh-disease, melas-syndrome, mitochondrial-encephalomyopathies, mitochondrial-myopathies, myopathy, nervousness, neurodegenerative-disorders, ophthalmoplegia, parkinson-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mitochondrial Diseases, and have been seen in publications frequently: Aging, Autophagy, Cardiac Conduction, Cell Cycle, Cell Death, Dna Replication, Electron Transport, Electron Transport Chain, Fatty Acid Oxidation, Glycolysis, Localization, Mitochondrial Translation, Neuroprotection, Oxidative Phosphorylation, Pathogenesis, Programmed Cell Death, Secretion, Translation, Transport, Tricarboxylic Acid Cycle
Quite a number of genes have been found to play important roles in Mitochondrial Diseases, such as COX5A, COX8A, CPOX, CS, CSF2, CYCS, DGUOK, FXN, INS, LAMC2, NPTX2, OPA1, POLG, ROS1, SLC25A4, SOD1, TFAM, TYMP. 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.