dc.creatorValenzuela, Vicente
dc.creatorNassif, Melissa
dc.creatorHetz Flores, Claudio
dc.date.accessioned2019-03-18T12:01:24Z
dc.date.available2019-03-18T12:01:24Z
dc.date.created2019-03-18T12:01:24Z
dc.date.issued2018
dc.identifierAutophagy, Volumen 14, Issue 4, 2018, Pages 733-737
dc.identifier15548635
dc.identifier15548627
dc.identifier10.1080/15548627.2018.1432327
dc.identifierhttps://repositorio.uchile.cl/handle/2250/167394
dc.description.abstract© 2018 Informa UK Limited, trading as Taylor & Francis Group. In recent years, the role of autophagy in the pathogenesis of most neurodegenerative diseases has transitioned into a limbo of protective or detrimental effects. Genetic evidence indicates that mutations in autophagy-regulatory genes can result in the occurrence of amyotrophic lateral sclerosis (ALS), suggesting a physiological role of the pathway to motoneuron function. However, experimental manipulation of autophagy in ALS models led to conflicting results depending on the intervention strategy and the disease model used. A recent work by the Maniatis group systematically explored the role of cell-specific autophagy in motoneurons at different disease stages, revealing surprising and unexpected findings. Autophagy activity at early stages may contribute to maintaining the structure and function of neuromuscular junctions, whereas at later steps of the disease it has a pathogenic activity possibly involving cell-nonautonomo
dc.languageen
dc.publisherTaylor and Francis Inc.
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceAutophagy
dc.subjectALS
dc.subjectamyotrophic lateral sclerosis
dc.subjectautophagy
dc.subjectcell-nonautonomous
dc.subjectmotoneuron
dc.subjectneuromuscular junction
dc.subjectSOD1
dc.titleUnraveling the role of motoneuron autophagy in ALS
dc.typeArtículo de revista


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