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Disease Info Card
Trinucleotide Repeat Expansion
Information about Trinucleotide Repeat Expansion: 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 Trinucleotide Repeat Expansion
Most recent studies have shown that Trinucleotide Repeat Expansion shares some biological mechanisms with ataxia, ataxia-spinocerebellar, atrophy, cerebellar-ataxia, dystrophy, fragile-x-syndrome, friedreich-ataxia, hereditary-diseases, huntington-disease, machado-joseph-disease, malignant-neoplasms, muscular-atrophy, myotonic-dystrophy, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders, spinal-and-bulbar-muscular-atrophy-x-linked-1, spinocerebellar-degeneration.
Among the many pathways, these few ones have gauged particular interests from scientists studying Trinucleotide Repeat Expansion, and have been seen in publications frequently: Aging, Autophagy, Cell Death, Cognition, Dna Methylation, Dna Repair, Dna Replication, Gene Silencing, Localization, Meiosis, Methylation, Mismatch Repair, Muscle Atrophy, Nuclear Export, Pathogenesis, Proteolysis, Rna Interference, Rna Processing, Translation, Transport
Quite a number of genes have been found to play important roles in Trinucleotide Repeat Expansion, such as AKR1B1, AR, AREG, ATN1, ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, DMPK, FDXR, FMR1, FXN, GAA, HTT, LY6E, SLC6A4, TBP. 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.