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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Publicado no:Hum Mol Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4355022/
https://ncbi.nlm.nih.gov/pubmed/25468678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu605
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