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An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity
Mutations in TARDBP, encoding TAR DNA-binding protein-43 (TDP-43), are associated with TDP-43 proteinopathies, including amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). We compared wild-type TDP-43 and an ALS-associated mutant TDP-43 in vitro and in vivo. The A315T...
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3357956/ https://ncbi.nlm.nih.gov/pubmed/21666678 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nsmb.2053 |
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