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Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a fatal disease characterized by complex neuronal and glial phenotypes. Recently, RNA-based mechanisms have been linked to ALS via RNA-binding proteins such as TDP-43, which has been studied in vivo using models ranging from yeast to rodents. We have developed...
Autores principales: | Estes, Patricia S., Daniel, Scott G., Mccallum, Abigail P., Boehringer, Ashley V., Sukhina, Alona S., Zwick, Rebecca A., Zarnescu, Daniela C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Limited
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634655/ https://www.ncbi.nlm.nih.gov/pubmed/23471911 http://dx.doi.org/10.1242/dmm.010710 |
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