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Disease Info Card
Neuroaxonal Dystrophies
Information about Neuroaxonal Dystrophies: 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 Neuroaxonal Dystrophies
Most recent studies have shown that Neuroaxonal Dystrophies shares some biological mechanisms with abnormal-degeneration, ataxia, atrophy, brain-diseases, cns-disorder, dementia, demyelinating-diseases, diabetes-mellitus, diabetes-mellitus-experimental, diabetic-neuropathies, dystrophy, gliosis, hallervorden-spatz-syndrome, infantile-neuroaxonal-dystrophy, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neuroaxonal Dystrophies, and have been seen in publications frequently: Aging, Brain Development, Cell Activation, Cell Death, Conjugation, Excretion, Glycolysis, Innervation, Localization, Myelination, Pathogenesis, Pigmentation, Proteolysis, Reflex, Regeneration, Reverse Transcription, Senescence, Superoxide Anion Generation, Synapse Maturation, Transport
Quite a number of genes have been found to play important roles in Neuroaxonal Dystrophies, such as APP, IGF1, INS, NAGA, NPY, NTF3, PANK2, PLA2G1B, PLA2G6, PLB1, PRNP, SAMD4A, SNCA, SNRPG, SORD, UCHL1, YWHAZ. 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.