Differential autophagy power in the spinal cord and muscle of transgenic ALS mice.

Amyotrophic lateral sclerosis (ALS) is a motoneuron disease characterized by misfolded proteins aggregation in affected motoneurons. In mutant SOD1 (mutSOD1) ALS models, aggregation correlates to impaired functions of proteasome and/or autophagy, both essential for the intracellular chaperone-mediat...

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Main Authors: Valeria eCrippa, Alessandra eBoncoraglio, Mariarita eGalbiati, Tanya eAggarwal, Paola eRusmini, Elisa eGiorgetti, Riccardo eCristofani, Serena eCarra, Maria ePennuto, Angelo ePoletti
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-11-01
Series:Frontiers in Cellular Neuroscience
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Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2013.00234/full

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