c-Jun activation in Schwann cells protects against loss of sensory axons in inherited neuropathy

Charcot–Marie–Tooth disease type 1A is the most frequent inherited peripheral neuropathy. It is generally due to heterozygous inheritance of a partial chromosomal duplication resulting in over-expression of PMP22. A key feature of Charcot–Marie–Tooth disease type 1A is secondary death of axons. Prev...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Hantke, Janina, Carty, Lucy, Wagstaff, Laura J., Turmaine, Mark, Wilton, Daniel K., Quintes, Susanne, Koltzenburg, Martin, Baas, Frank, Mirsky, Rhona, Jessen, Kristján R.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2014
Matèries:
Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4208468/
https://ncbi.nlm.nih.gov/pubmed/25216747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awu257
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars