Mechanisms of Neuroprotection by Protein Disulphide Isomerase in Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterised by the progressive loss of motor neurons, leading to paralysis and death within several years of onset. Although protein misfolding is a key feature of ALS, the upstream triggers of disease remain elusive. R...

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Detalles Bibliográficos
Autores principales: Walker, Adam K., Atkin, Julie D.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096316/
https://www.ncbi.nlm.nih.gov/pubmed/21603027
http://dx.doi.org/10.1155/2011/317340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096316/
https://www.ncbi.nlm.nih.gov/pubmed/21603027
http://dx.doi.org/10.1155/2011/317340

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