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Disease Info Card
Melas Syndrome
Information about Melas Syndrome: 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 Melas Syndrome
Most recent studies have shown that Melas Syndrome shares some biological mechanisms with acidosis, acidosis-lactic, cardiomyopathies, cerebrovascular-accident, cerebrovascular-disorders, chronic-progressive-external-ophthalmoplegia, complete-hearing-loss, diabetes-mellitus, encephalopathies, epilepsies-myoclonic, epilepsy, kearns-sayre-syndrome, merrf-syndrome, mitochondrial-diseases, mitochondrial-encephalomyopathies, mitochondrial-myopathies, myopathy, ophthalmoplegia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Melas Syndrome, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Death, Electron Transport, Electron Transport Chain, Excretion, Glycolysis, Insecticide Resistance, Insulin Secretion, Localization, Mating, Mitochondrial Translation, Muscle Atrophy, Oxidative Phosphorylation, Pathogenesis, Pigmentation, Secretion, Translation, Transport, Vasodilation
Quite a number of genes have been found to play important roles in Melas Syndrome, such as ACAT1, COX5A, COX8A, CPOX, CSF2, CYCS, INS, LAMC2, MRRF, NPTX2, POLG, RHO, RHOD, SLC25A5, 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.