Cargando…
C9ORF72-related cellular pathology in skeletal myocytes derived from ALS-patient induced pluripotent stem cells
Amyotrophic lateral sclerosis (ALS) is a late-onset neuromuscular disease with no cure and limited treatment options. Patients experience a gradual paralysis leading to death from respiratory complications on average only 2-5 years after diagnosis. There is increasing evidence that skeletal muscle i...
Autores principales: | Lynch, Eileen, Semrad, Theran, Belsito, Vincent S., FitzGibbons, Claire, Reilly, Megan, Hayakawa, Koji, Suzuki, Masatoshi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737948/ https://www.ncbi.nlm.nih.gov/pubmed/31439573 http://dx.doi.org/10.1242/dmm.039552 |
Ejemplares similares
-
A Novel Protocol for Directed Differentiation of C9orf72-Associated Human Induced Pluripotent Stem Cells Into Contractile Skeletal Myotubes
por: Swartz, Elliot W., et al.
Publicado: (2016) -
C9ORF72 expression and cellular localization over mouse development
por: Atkinson, Rachel A K, et al.
Publicado: (2015) -
Commentary: The C9orf72 Repeat Expansion Disrupts Nucleocytoplasmic Transport
por: Munteanu, Tudor, et al.
Publicado: (2016) -
Erratum: C9ORF72 expression and cellular localization over mouse development
por: Atkinson, Rachel A. K., et al.
Publicado: (2016) -
Modeling the C9ORF72 repeat expansion mutation using human induced pluripotent stem cells
por: Selvaraj, Bhuvaneish T., et al.
Publicado: (2017)