Defective Oligodendroglial Lineage and Demyelination in Amyotrophic Lateral Sclerosis

Motor neurons and their axons reaching the skeletal muscle have long been considered as the best characterized targets of the degenerative process observed in amyotrophic lateral sclerosis (ALS). However, the involvement of glial cells was also more recently reported. Although oligodendrocytes have...

Descripción completa

Detalles Bibliográficos
Autores principales: Traiffort, Elisabeth, Morisset-Lopez, Séverine, Moussaed, Mireille, Zahaf, Amina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036314/
https://www.ncbi.nlm.nih.gov/pubmed/33810425
http://dx.doi.org/10.3390/ijms22073426

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036314/
https://www.ncbi.nlm.nih.gov/pubmed/33810425
http://dx.doi.org/10.3390/ijms22073426

Ejemplares similares