Cargando…
Inhibition of colony-stimulating factor 1 receptor early in disease ameliorates motor deficits in SCA1 mice
BACKGROUND: Polyglutamine (polyQ) expansion in the protein Ataxin-1 (ATXN1) causes spinocerebellar ataxia type 1 (SCA1), a fatal dominantly inherited neurodegenerative disease characterized by motor deficits, cerebellar neurodegeneration, and gliosis. Currently, there are no treatments available to...
Autores principales: | Qu, Wenhui, Johnson, Andrea, Kim, Joo Hyun, Lukowicz, Abigail, Svedberg, Daniel, Cvetanovic, Marija |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445366/ https://www.ncbi.nlm.nih.gov/pubmed/28545543 http://dx.doi.org/10.1186/s12974-017-0880-z |
Ejemplares similares
-
Inhibition of NF-κB signaling in IKKβ(F/F);LysM Cre mice causes motor deficits but does not alter pathogenesis of Spinocerebellar ataxia type 1
por: Ferro, Austin, et al.
Publicado: (2018) -
VEGF ameliorates the ataxic phenotype in spinocerebellar ataxia type 1 (SCA1) mice
por: Cvetanovic, Marija, et al.
Publicado: (2011) -
Brain Derived Neurotrophic Factor (BDNF) Delays Onset of Pathogenesis in Transgenic Mouse Model of Spinocerebellar Ataxia Type 1 (SCA1)
por: Mellesmoen, Aaron, et al.
Publicado: (2019) -
Altered calcium signaling in Bergmann glia contributes to spinocerebellar ataxia type-1 in a mouse model of SCA1
por: Nanclares, Carmen, et al.
Publicado: (2023) -
Motor neuron degeneration correlates with respiratory dysfunction in SCA1
por: Orengo, James P., et al.
Publicado: (2018)