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Molecular chaperone Hsp110 rescues a vesicle transport defect produced by an ALS-associated mutant SOD1 protein in squid axoplasm

Mutant human Cu/Zn superoxide dismutase 1 (SOD1) is associated with motor neuron toxicity and death in an inherited form of amyotrophic lateral sclerosis (ALS; Lou Gehrig disease). One aspect of toxicity in motor neurons involves diminished fast axonal transport, observed both in transgenic mice and...

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Detalhes bibliográficos
Main Authors: Song, Yuyu, Nagy, Maria, Ni, Weiming, Tyagi, Navneet K., Fenton, Wayne A., López-Giráldez, Francesc, Overton, John D., Horwich, Arthur L., Brady, Scott T.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3619309/
https://ncbi.nlm.nih.gov/pubmed/23509252
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1303279110
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