Cargando…
Non-coding RNA in C9orf72-related amyotrophic lateral sclerosis and frontotemporal dementia: A perfect storm of dysfunction
A hexanucleotide repeat expansion in the first intron/promoter region of C9orf72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Both sense and antisense transcripts exist at the C9orf72 locus but the function of the antisense lncRNA is unkn...
Autor principal: | Douglas, Andrew G.L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260478/ https://www.ncbi.nlm.nih.gov/pubmed/30533567 http://dx.doi.org/10.1016/j.ncrna.2018.09.001 |
Ejemplares similares
-
Glial Cell Dysfunction in C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
por: Ghasemi, Mehdi, et al.
Publicado: (2021) -
C9orf72 amyotrophic lateral sclerosis and frontotemporal dementia: gain or loss of function?
por: Mizielinska, Sarah, et al.
Publicado: (2014) -
The Development of C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Disorders
por: Yang, Qijie, et al.
Publicado: (2020) -
Modeling C9orf72-Related Frontotemporal Dementia and Amyotrophic Lateral Sclerosis in Drosophila
por: Sharpe, Joanne L., et al.
Publicado: (2021) -
Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit
por: Sattler, Rita, et al.
Publicado: (2023)