Cargando…
Contribution of RNA/DNA Binding Protein Dysfunction in Oligodendrocytes in the Pathogenesis of the Amyotrophic Lateral Sclerosis/Frontotemporal Lobar Degeneration Spectrum Diseases
Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are two incurable neurodegenerative disorders, often considered as the extreme manifestations of a disease spectrum, as they share similar pathomechanisms. In support of this, pathological aggregation of the RNA/DNA bin...
Autores principales: | Valori, Chiara F., Neumann, Manuela |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440855/ https://www.ncbi.nlm.nih.gov/pubmed/34539339 http://dx.doi.org/10.3389/fnins.2021.724891 |
Ejemplares similares
-
The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum
por: van Langenhove, Tim, et al.
Publicado: (2012) -
Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degenerations: Similarities in Genetic Background
por: Parobkova, Eva, et al.
Publicado: (2021) -
Retinal nerve fiber layer in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
por: Wong, Bryan M., et al.
Publicado: (2022) -
FUS Transgenic Rats Develop the Phenotypes of Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration
por: Huang, Cao, et al.
Publicado: (2011) -
Muscle sympathetic nerve activity in frontotemporal lobar degeneration is similar to amyotrophic lateral sclerosis
por: Shindo, Kazumasa, et al.
Publicado: (2015)