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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...
Shranjeno v:
| izdano v: | Arch Biochem Biophys |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2019
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| Teme: | |
| Online dostop: | 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 |
| Oznake: |
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