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The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy

Spinal muscular atrophy (SMA) is a common autosomal recessive neurodegenerative disorder in humans. Amongst the earliest signs of neurodegeneration are severe and progressive defects of the neuromuscular synapse. These defects, characterized by poor terminal arborization and immature motor endplates...

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Библиографические подробности
Главные авторы: Kariya, Shingo, Mauricio, Rina, Dai, Ya, Monani, Umrao R.
Формат: Artigo
Язык:Inglês
Опубликовано: 2008
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2671206/
https://ncbi.nlm.nih.gov/pubmed/19010394
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2008.10.107
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