Llwytho...

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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Hantke, Janina, Carty, Lucy, Wagstaff, Laura J., Turmaine, Mark, Wilton, Daniel K., Quintes, Susanne, Koltzenburg, Martin, Baas, Frank, Mirsky, Rhona, Jessen, Kristján R.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2014
Pynciau:
Mynediad Ar-lein: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
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