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Aggregated SOD1 causes selective death of cultured human motor neurons
Most human neurodegenerative diseases share a phenotype of neuronal protein aggregation. In Amyotrophic Lateral Sclerosis (ALS), the abundant protein superoxide dismutase (SOD1) or the TAR-DNA binding protein TDP-43 can aggregate in motor neurons. Recently, numerous studies have highlighted the abil...
Autores principales: | Benkler, Chen, O’Neil, Alison L., Slepian, Susannah, Qian, Fang, Weinreb, Paul H., Rubin, Lee L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219543/ https://www.ncbi.nlm.nih.gov/pubmed/30401824 http://dx.doi.org/10.1038/s41598-018-34759-z |
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