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A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity
Transgenic mouse models expressing mutant superoxide dismutase 1 (SOD1) have been critical in furthering our understanding of amyotrophic lateral sclerosis (ALS). However, such models generally overexpress the mutant protein, which may give rise to phenotypes not directly relevant to the disorder. H...
Autores principales: | Joyce, Peter I., Mcgoldrick, Philip, Saccon, Rachele A., Weber, William, Fratta, Pietro, West, Steven J., Zhu, Ning, Carter, Sarah, Phatak, Vinaya, Stewart, Michelle, Simon, Michelle, Kumar, Saumya, Heise, Ines, Bros-Facer, Virginie, Dick, James, Corrochano, Silvia, Stanford, Macdonnell J., Luong, Tu Vinh, Nolan, Patrick M., Meyer, Timothy, Brandner, Sebastian, Bennett, David L.H., Ozdinler, P. Hande, Greensmith, Linda, Fisher, Elizabeth M.C., Acevedo-Arozena, Abraham |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355022/ https://www.ncbi.nlm.nih.gov/pubmed/25468678 http://dx.doi.org/10.1093/hmg/ddu605 |
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