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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Articles
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

Internet

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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