Remodeling of astrocyte secretome in amyotrophic lateral sclerosis: uncovering novel targets to combat astrocyte-mediated toxicity

Amyotrophic lateral sclerosis (ALS) is an adult-onset paralytic disease characterized by progressive degeneration of upper and lower motor neurons in the motor cortex, brainstem and spinal cord. Motor neuron degeneration is typically caused by a combination of intrinsic neuronal (cell autonomous) de...

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Detalles Bibliográficos
Autores principales: Ng, Winanto, Ng, Shi-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791755/
https://www.ncbi.nlm.nih.gov/pubmed/36567359
http://dx.doi.org/10.1186/s40035-022-00332-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791755/
https://www.ncbi.nlm.nih.gov/pubmed/36567359
http://dx.doi.org/10.1186/s40035-022-00332-y

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