Cargando…
Current Advances and Limitations in Modeling ALS/FTD in a Dish Using Induced Pluripotent Stem Cells
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two age-dependent multifactorial neurodegenerative disorders, which are typically characterized by the selective death of motor neurons and cerebral cortex neurons, respectively. These two diseases share many clinical, genetic...
Autores principales: | Guo, Wenting, Fumagalli, Laura, Prior, Robert, Van Den Bosch, Ludo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733489/ https://www.ncbi.nlm.nih.gov/pubmed/29326542 http://dx.doi.org/10.3389/fnins.2017.00671 |
Ejemplares similares
-
Editorial: Current Concept and Translational Study in ALS–FTD Spectrum: From Genetics, Neuroinflammation to Neurodegeneration
por: Guo, Wenting, et al.
Publicado: (2022) -
Motor Neuron Susceptibility in ALS/FTD
por: Ragagnin, Audrey M. G., et al.
Publicado: (2019) -
C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD?
por: Braems, Elke, et al.
Publicado: (2020) -
Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent ISR in C9ORF72 FTD/ALS
por: Parameswaran, Janani, et al.
Publicado: (2023) -
Linking hnRNP Function to ALS and FTD Pathology
por: Purice, Maria D., et al.
Publicado: (2018)