Cargando…
Impaired Nucleoporins Are Present in Sporadic Amyotrophic Lateral Sclerosis Motor Neurons that Exhibit Mislocalization of the 43-kDa TAR DNA-Binding Protein
BACKGROUND AND PURPOSE: Disruption of nucleoporins has been reported in the motor neurons of patients with sporadic amyotrophic lateral sclerosis (sALS). However, the precise changes in the morphology of nucleoporins associated with the pathology of the 43-kDa TAR DNA-binding protein (TDP-43) in the...
Autores principales: | Aizawa, Hitoshi, Yamashita, Takenari, Kato, Haruhisa, Kimura, Takashi, Kwak, Shin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325357/ https://www.ncbi.nlm.nih.gov/pubmed/30618218 http://dx.doi.org/10.3988/jcn.2019.15.1.62 |
Ejemplares similares
-
Co-Occurrence of TDP-43 Mislocalization with Reduced Activity of an RNA Editing Enzyme, ADAR2, in Aged Mouse Motor Neurons
por: Hideyama, Takuto, et al.
Publicado: (2012) -
Extracellular RNAs as Biomarkers of Sporadic Amyotrophic Lateral Sclerosis and Other Neurodegenerative Diseases
por: Hosaka, Takashi, et al.
Publicado: (2019) -
The role of TDP-43 mislocalization in amyotrophic lateral sclerosis
por: Suk, Terry R., et al.
Publicado: (2020) -
Neurotoxic 43-kDa TAR DNA-binding Protein (TDP-43) Triggers Mitochondrion-dependent Programmed Cell Death in Yeast
por: Braun, Ralf J., et al.
Publicado: (2011) -
Effect of Serum Perampanel Concentration on Sporadic Amyotrophic Lateral Sclerosis Progression
por: Kato, Haruhisa, et al.
Publicado: (2023)