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Disease Info Card
Fraxa Syndrome
Information about Fraxa 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 Fraxa Syndrome
Most recent studies have shown that Fraxa Syndrome shares some biological mechanisms with ataxia, ataxia-spinocerebellar, atrophy, autistic-disorder, chromosome-fragility, dystrophy, fragile-x-syndrome, fraxe-syndrome, hereditary-diseases, huntington-disease, myotonic-dystrophy, neurodegenerative-disorders, ovarian-failure-premature, premature-menopause, sex-chromosome-aberrations, trinucleotide-repeat-expansion, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Fraxa Syndrome, and have been seen in publications frequently: Aging, Brain Development, Cell Cycle, Demethylation, Dna Deamination, Dna Demethylation, Dna Hypermethylation, Dna Methylation, Dna Repair, Dna Replication, Fertilization, Interphase, Localization, Menopause, Metaphase, Methylation, Pathogenesis, S Phase, Translation, Transport
Quite a number of genes have been found to play important roles in Fraxa Syndrome, such as AFF2, AR, ATN1, ATXN1, ATXN3, CBL, DIAPH2, DLG3, DMPK, F8, F9, FMR1, FOSL1, HTT, IDS, MECP2, RABEP2. 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.