Empty mesoporous silica particles significantly delay disease progression and extend survival in a mouse model of ALS

Amyotrophic lateral sclerosis (ALS) is a devastating incurable neurological disorder characterized by motor neuron (MN) death and muscle dysfunction leading to mean survival time after diagnosis of only 2–5 years. A potential ALS treatment is to delay the loss of MNs and disease progression by the d...

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Detalles Bibliográficos
Autores principales: Leyton-Jaimes, Marcel F., Ivert, Patrik, Hoeber, Jan, Han, Yilin, Feiler, Adam, Zhou, Chunfang, Pankratova, Stanislava, Shoshan-Barmatz, Varda, Israelson, Adrian, Kozlova, Elena N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691331/
https://www.ncbi.nlm.nih.gov/pubmed/33244084
http://dx.doi.org/10.1038/s41598-020-77578-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691331/
https://www.ncbi.nlm.nih.gov/pubmed/33244084
http://dx.doi.org/10.1038/s41598-020-77578-x

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