Article
A mitochondrial tipping point couples early hyperexcitability to late-stage failure in patient-derived ALS motor neurons
2026-03-23
Abstract excerpt
<h4>SUMMARY</h4> Amyotrophic lateral sclerosis (ALS) is a motor neuron (MN) disease characterized by profound alterations in energy metabolism and progressive degeneration of MNs. Evidence from patients and model systems point to MN hyperexcitability as an early hallmark of ALS. How altered electrical activity intersects with energy metabolism, however, remains largely unexplored. To directly examine this relatio...
Topics
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- Amyotrophic Lateral Sclerosis Research
- ATP Synthase and ATPases Research
- Autophagy in Disease and Therapy
- Cholinesterase and Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Mitochondrial Function and Pathology
- Neurogenetic and Muscular Disorders Research
- Parkinson's Disease Mechanisms and Treatments
Identifiers and source
- Literature Corpus work
- 9b423154-b378-52d7-b696-86f5b59954b6
- DOI
- 10.64898/2026.03.20.713134
