Spinocerebellar Ataxia Type 7: Disease Bioinformatics
Research of Spinocerebellar Ataxia Type 7 has been linked to Ataxia, Spinocerebellar, Ataxia, Neurodegenerative Disorders, Trinucleotide Repeat Expansion, Cerebellar Ataxia. The study of Spinocerebellar Ataxia Type 7 has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Spinocerebellar Ataxia Type 7 include Pathogenesis, Localization, Cell Death, Proteolysis, Histone Acetylation. These pathways complement our catalog of research reagents for the study of Spinocerebellar Ataxia Type 7 including antibodies and ELISA kits against CASPASE 7, CASPASE 3, CACNA1A, CASP3, CREBBP.
Top Research Reagents
We have 984 products for the study of Spinocerebellar Ataxia Type 7 that can be applied to Chromatin Immunoprecipitation, Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Spinocerebellar Ataxia Type 7 is also known as spinocerebellar ataxia type 7, olivopontocerebellar atrophy 3, opca with retinal degeneration, spinocerebellar ataxia 7, sca 7, sca7, opca with macular degeneration and external ophthalmoplegia, autosomal dominant cerebellar ataxia type 2, hereditary ataxia with retinal degeneration, spinocerebellar ataxia-7, ataxias, hereditary, adca type 2, opca3.