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Disease Info Card
Opca, Menzel Type
Information about Opca, Menzel Type: 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 Opca, Menzel Type
Most recent studies have shown that Opca, Menzel Type shares some biological mechanisms with ataxia, ataxia-spinocerebellar, atrophy, cerebellar-ataxia, dentatorubral-pallidoluysian-atrophy, dystrophy, friedreich-ataxia, hereditary-ataxia-unspecified, huntington-disease, machado-joseph-disease, muscular-atrophy, myotonic-dystrophy, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders, olivopontocerebellar-atrophies, spinal-and-bulbar-muscular-atrophy-x-linked-1, spinocerebellar-degeneration, trinucleotide-repeat-expansion.
Among the many pathways, these few ones have gauged particular interests from scientists studying Opca, Menzel Type, and have been seen in publications frequently: Aging, Cell Death, Dna Repair, Glucose Homeostasis, Localization, Methylation, Nuclear Export, Pathogenesis, Pigmentation, Protein Folding, Protein Phosphorylation, Proteolysis, Reflex, Rna Interference, Rna Processing, Segmentation, Spermatogenesis, Synaptic Transmission, Transport, Virulence
Quite a number of genes have been found to play important roles in Opca, Menzel Type, such as ANP32A, AR, ATN1, ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, CALB1, CASP3, CAT, CRAT, DMPK, FANCA, FXN, GLYAT, HTT, LY6E, YWHAQ. 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.