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ALS-linked misfolded SOD1 species have divergent impacts on mitochondria
Approximately 20 % of familial Amyotrophic Lateral Sclerosis (ALS) is caused by mutations in superoxide dismutase (SOD1), which leads to misfolding of the SOD1 protein, resulting in a toxic gain of function. Several conformation-restricted antibodies have been generated that specifically recognize m...
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| Publicado no: | Acta Neuropathol Commun |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4847257/ https://ncbi.nlm.nih.gov/pubmed/27121871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-016-0313-8 |
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