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Disease Info Card
Mitochondrial Dna Depletion
Information about Mitochondrial Dna Depletion: 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 Dna Depletion
Most recent studies have shown that Mitochondrial Dna Depletion shares some biological mechanisms with acidosis, acidosis-lactic, alpers-syndrome-(disorder), chronic-progressive-external-ophthalmoplegia, dysmyelopoietic-syndromes, external-ophthalmoplegia, hiv-infections, liver-diseases, liver-failure, malignant-neoplasms, mitochondrial-damage, mitochondrial-diseases, mitochondrial-encephalomyopathies, mitochondrial-myopathies, muscle-hypotonia, myopathy, neoplasms, ophthalmoplegia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mitochondrial Dna Depletion, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Growth, Cell Migration, Cell Proliferation, Dna Repair, Dna Replication, Drug Resistance, Electron Transport, Electron Transport Chain, Glycolysis, Localization, Mitochondrial Dna Replication, Mitochondrial Translation, Oxidative Phosphorylation, Pathogenesis, Regeneration, Translation, Transport
Quite a number of genes have been found to play important roles in Mitochondrial Dna Depletion, such as ASXL1, CS, CYCS, DGKB, DGKE, DGUOK, MPV17, PAFAH1B1, POLG, RHO, RRM2B, SF3B1, SUCLA2, SUCLG1, TFAM, TK1, TK2, TYMP, YWHAE. 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.