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Disease Info Card
Brain Diseases, Metabolic, Inborn
Information about Brain Diseases, Metabolic, Inborn: 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 Brain Diseases, Metabolic, Inborn
Most recent studies have shown that Brain Diseases, Metabolic, Inborn shares some biological mechanisms with ataxia, atrophy, brain-injuries, combined-d-2--and-l-2-hydroxyglutaric-aciduria, developmental-delay-(disorder), developmental-disabilities, encephalopathies, epilepsy, glutaric-aciduria-type-1, inborn-errors-of-metabolism, metabolic-diseases, movement-disorders, muscle-hypotonia, nerve-degeneration, nervous-system-disorder, nervousness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Brain Diseases, Metabolic, Inborn, and have been seen in publications frequently: Brain Development, Cell Death, Cell Proliferation, Creatine Transport, Energy Homeostasis, Excretion, Fatty Acid Oxidation, Glucose Transport, Glycosylation, Hyperphosphorylation, Lipid Storage, Localization, Myelination, Oxidative Phosphorylation, Pathogenesis, Pyruvate Oxidation, Translation, Transport, Tricarboxylic Acid Cycle, Urea Cycle
Quite a number of genes have been found to play important roles in Brain Diseases, Metabolic, Inborn, such as ADSL, AGA, ALDH5A1, CAT, COX5A, COX8A, CPOX, CSF2, ETHE1, GAMT, GCDH, GLS2, GLUL, L2HGDH, LAMC2, PHGDH, SLC2A1, SLC6A8, SUOX. 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.