Cargando…
RNP2 of RNA Recognition Motif 1 Plays a Central Role in the Aberrant Modification of TDP-43
Phosphorylated and truncated TAR DNA-binding protein-43 (TDP-43) is a major component of ubiquitinated cytoplasmic inclusions in neuronal and glial cells of two TDP-43 proteinopathies, amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Modifications of TDP-43 are thus considered to...
Autores principales: | Takagi, Shinnosuke, Iguchi, Yohei, Katsuno, Masahisa, Ishigaki, Shinsuke, Ikenaka, Kensuke, Fujioka, Yusuke, Honda, Daiyu, Niwa, Jun-ichi, Tanaka, Fumiaki, Watanabe, Hirohisa, Adachi, Hiroaki, Sobue, Gen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695991/ https://www.ncbi.nlm.nih.gov/pubmed/23840565 http://dx.doi.org/10.1371/journal.pone.0066966 |
Ejemplares similares
-
The ALS/FTLD-related RNA-binding proteins TDP-43 and FUS have common downstream RNA targets in cortical neurons()
por: Honda, Daiyu, et al.
Publicado: (2013) -
Corrigendum to “The ALS/FTLD-related RNA-binding proteins TDP-43 and FUS have common downstream RNA targets in cortical neurons” [FEBS Open Bio 4 (2014) 1–10]
por: Honda, Daiyu, et al.
Publicado: (2014) -
TDP-43 Proteinopathy and Tauopathy: Do They Have Pathomechanistic Links?
por: Riku, Yuichi, et al.
Publicado: (2022) -
Disruption of Axonal Transport in Motor Neuron Diseases
por: Ikenaka, Kensuke, et al.
Publicado: (2012) -
Pathway from TDP-43-Related Pathology to Neuronal Dysfunction in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration
por: Riku, Yuichi, et al.
Publicado: (2021)