Cargando…
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
Spinocerebellar Ataxia type 1 (SCA1) is a fatal neurodegenerative genetic disease that is characterized by pronounced neuronal loss and gliosis in the cerebellum. We have previously demonstrated microglial activation, measured as an increase in microglial density in cerebellar cortex and an increase...
Autores principales: | Ferro, Austin, Qu, Wenhui, Lukowicz, Abigail, Svedberg, Daniel, Johnson, Andrea, Cvetanovic, Marija |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033432/ https://www.ncbi.nlm.nih.gov/pubmed/29975753 http://dx.doi.org/10.1371/journal.pone.0200013 |
Ejemplares similares
-
Is LysM-Cre a good candidate Cre for knocking out Atg5 gene in mice?
por: Wen, Jun-Hao, et al.
Publicado: (2022) -
Inhibition of colony-stimulating factor 1 receptor early in disease ameliorates motor deficits in SCA1 mice
por: Qu, Wenhui, et al.
Publicado: (2017) -
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) -
Mood alterations in mouse models of Spinocerebellar Ataxia type 1
por: Asher, Melissa, et al.
Publicado: (2021) -
LysM Receptor-Like Kinase and LysM Receptor-Like Protein Families: An Update on Phylogeny and Functional Characterization
por: Buendia, Luis, et al.
Publicado: (2018)