Hyperexcitability in synaptic and firing activities of spinal motoneurons in an adult mouse model of amyotrophic lateral sclerosis

Hyperexcitability is hypothesized to contribute to the degeneration of spinal motoneurons (MNs) in amyotrophic lateral sclerosis (ALS). Studies, thus far, have not linked hyperexcitability to the intrinsic properties of MNs in the adult ALS mouse model with the G93A-mutated SOD1 protein (mSOD1(G93A)...

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Detaylı Bibliyografya
Yayımlandı:Neuroscience
Asıl Yazarlar: Jiang, Mingchen C., Adimula, Adesoji, Birch, Derin, Heckman, Charles J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2017
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5614896/
https://ncbi.nlm.nih.gov/pubmed/28844763
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2017.08.041
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