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ALS mutant SOD1 interacts with G3BP1 and affects stress granule dynamics
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease. Mutations in Cu/Zn superoxide dismutase (SOD1) are responsible for approximately 20 % of the familial ALS cases. ALS-causing SOD1 mutants display a gain-of-toxicity phenotype, but the nature of this toxicity is still not fully...
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| Pubblicato in: | Acta Neuropathol |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer Berlin Heidelberg
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5023729/ https://ncbi.nlm.nih.gov/pubmed/27481264 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-016-1601-x |
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