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Profilin 1 mutants form aggregates that induce accumulation of prion-like TDP-43

Mutations in the profilin 1 (PFN1) gene have been identified as a cause of familial amyotrophic lateral sclerosis (ALS), and neuropathological studies indicate that TDP-43 is accumulated in brains of patients with PFN1 mutation. Here, we investigated the role of PFN1 mutations in the formation of pr...

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Библиографические подробности
Опубликовано в: :Prion
Главные авторы: Tanaka, Yoshinori, Hasegawa, Masato
Формат: Artigo
Язык:Inglês
Опубликовано: Taylor & Francis 2016
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5082967/
https://ncbi.nlm.nih.gov/pubmed/27432186
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2016.1207033
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