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Updated: May 29, 2025

Dissection of the Transversus Abdominis Muscle for Whole-mount Neuromuscular Junction Analysis
Published on: January 11, 2014
Chaperone dysfunction in motor neuron disease: new insights from studies of the SMN complex
A Gregory Matera1,2,3
1Integrative Program for Biological and Genome Sciences, University of North Carolina School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 25799, USA.
Abstract:
Spinal muscular atrophy and amyotrophic lateral sclerosis are devastating neurodegenerative diseases characterized by motor neuron loss. Although these 2 disorders have distinct genetic origins, recent studies suggest that they share common etiological mechanisms rooted in proteostatic dysfunction. At the heart of this emerging understanding is the survival motor neuron (SMN) complex.
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