Patient-derived olfactory mucosa for study of the non-neuronal contribution to amyotrophic lateral sclerosis pathology

Amyotrophic lateral sclerosis (ALS) is a degenerative motor neuron disease which currently has no cure. Research using rodent ALS models transgenic for mutant superoxide dismutase 1 (SOD1) has implicated that glial–neuronal interactions play a major role in the destruction of motor neurons, but the...

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Dettagli Bibliografici
Pubblicato in:J Cell Mol Med
Autori principali: García-Escudero, Vega, Rosales, María, Muñoz, José Luis, Scola, Esteban, Medina, Javier, Khalique, Hena, Garaulet, Guillermo, Rodriguez, Antonio, Lim, Filip
Natura: Artigo
Lingua:Inglês
Pubblicazione: BlackWell Publishing Ltd 2015
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4459844/
https://ncbi.nlm.nih.gov/pubmed/25807871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.12488
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