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Disease Info Card
Canavan Disease
Information about Canavan Disease: 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 Canavan Disease
Most recent studies have shown that Canavan Disease shares some biological mechanisms with adrenoleukodystrophy, alexander-disease, brain-diseases, brain-diseases-metabolic, cns-disorder, demyelinating-diseases, demyelination, diffuse-cerebral-sclerosis-of-schilder, edema, inborn-errors-of-metabolism, leukodystrophy, leukoencephalopathies, macrocephaly, muscle-hypotonia, nerve-degeneration, nervousness, neurodegenerative-disorders, spongy-degeneration.
Among the many pathways, these few ones have gauged particular interests from scientists studying Canavan Disease, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Cycle, Cell Death, Cell Motility, Developmental Process, Excretion, Immune Response, Inflammatory Response, Localization, Malate-aspartate Shuttle, Muscle Atrophy, Muscle Contraction, Myelination, Oxidative Phosphorylation, Pathogenesis, Protein Oxidation, Transport, Tricarboxylic Acid Cycle, Tropism
Quite a number of genes have been found to play important roles in Canavan Disease, such as ABCD1, ASPA, BRCA1, CALB2, CAT, CD55, CDKN1A, CR2, CSF2, DHRS4, ITGA2B, LAMC2, MBP, MLC1, MYL4, PLP1, QPCT, TDGF1, TNIP1. 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.