Altered Immunomodulatory Responses in the CX3CL1/CX3CR1 Axis Mediated by hMSCs in an Early In Vitro SOD1(G93A) Model of ALS

Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron (MN) disease characterized by progressive MN loss and muscular atrophy resulting in rapidly progressive paralysis and respiratory failure. Human mesenchymal stem/stromal cell (hMSC)-based therapy has been suggested to prolong MN survival vi...

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Detalles Bibliográficos
Autores principales: Sarikidi, Anastasia, Kefalakes, Ekaterini, Falk, Christine S., Esser, Ruth, Ganser, Arnold, Thau-Habermann, Nadine, Petri, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688016/
https://www.ncbi.nlm.nih.gov/pubmed/36428484
http://dx.doi.org/10.3390/biomedicines10112916

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688016/
https://www.ncbi.nlm.nih.gov/pubmed/36428484
http://dx.doi.org/10.3390/biomedicines10112916

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