Cargando…
Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease
AIMS: Cerebellar ataxia is common in patients with mitochondrial disease, and despite previous neuropathological investigations demonstrating vulnerability of the olivocerebellar pathway in patients with mitochondrial disease, the exact neurodegenerative mechanisms are still not clear. We use quanti...
Autores principales: | Chrysostomou, Alexia, Grady, John P., Laude, Alex, Taylor, Robert W., Turnbull, Doug M., Lax, Nichola Z. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973693/ https://www.ncbi.nlm.nih.gov/pubmed/26337858 http://dx.doi.org/10.1111/nan.12282 |
Ejemplares similares
-
Development of passive CLARITY and immunofluorescent labelling of multiple proteins in human cerebellum: understanding mechanisms of neurodegeneration in mitochondrial disease
por: Phillips, Jonathan, et al.
Publicado: (2016) -
Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease
por: Lax, Nichola Z., et al.
Publicado: (2015) -
The mitochondrial brain: From mitochondrial genome to neurodegeneration
por: Turnbull, Helen E., et al.
Publicado: (2010) -
Mitochondrial Mutations: Newly Discovered Players in Neuronal Degeneration
por: Lax, Nichola Z., et al.
Publicado: (2011) -
The genetics and pathology of mitochondrial disease
por: Alston, Charlotte L, et al.
Publicado: (2016)