Cargando…
Brain inflammation is accompanied by peripheral inflammation in Cstb(−/−) mice, a model for progressive myoclonus epilepsy
Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is an autosomal recessively inherited childhood-onset neurodegenerative disorder, characterized by myoclonus, seizures, and ataxia. Mutations in the cystatin B gene (CSTB) underlie EPM1. The CSTB-deficient (Cstb (−/−)) mouse model rec...
Autores principales: | Okuneva, Olesya, Li, Zhilin, Körber, Inken, Tegelberg, Saara, Joensuu, Tarja, Tian, Li, Lehesjoki, Anna-Elina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127053/ https://www.ncbi.nlm.nih.gov/pubmed/27894304 http://dx.doi.org/10.1186/s12974-016-0764-7 |
Ejemplares similares
-
Gene Expression Alterations in the Cerebellum and Granule Neurons of Cstb(−/−) Mouse Are Associated with Early Synaptic Changes and Inflammation
por: Joensuu, Tarja, et al.
Publicado: (2014) -
Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb(-/-) Microglia
por: Körber, Inken, et al.
Publicado: (2016) -
Progressive Volume Loss and White Matter Degeneration in Cstb-Deficient Mice: A Diffusion Tensor and Longitudinal Volumetry MRI Study
por: Manninen, Otto, et al.
Publicado: (2014) -
Cystatin B deficiency results in sustained histone H3 tail cleavage in postnatal mouse brain mediated by increased chromatin-associated cathepsin L activity
por: Daura, Eduard, et al.
Publicado: (2022) -
Progressive myoclonus epilepsy associated with SACS gene mutations
por: Nascimento, Fábio A., et al.
Publicado: (2016)