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Dysregulated mitochondrial Ca(2+) and ROS signaling in skeletal muscle of ALS mouse model

Amyotrophic lateral sclerosis (ALS) is a devastating neuromuscular disease characterized by motor neuron loss and prominent skeletal muscle wasting. Despite more than one hundred years of research efforts, the pathogenic mechanisms underlying neuromuscular degeneration in ALS remain elusive. While t...

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Detaylı Bibliyografya
Yayımlandı:Arch Biochem Biophys
Asıl Yazarlar: Zhou, Jingsong, Li, Ang, Li, Xuejun, Yi, Jianxun
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2019
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6506190/
https://ncbi.nlm.nih.gov/pubmed/30682329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.abb.2019.01.024
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