The COPI vesicle complex binds and moves with survival motor neuron within axons

Spinal muscular atrophy (SMA), an inherited disease of motor neuron dysfunction, results from insufficient levels of the survival motor neuron (SMN) protein. Movement of the SMN protein as granules within cultured axons suggests that the pathogenesis of SMA may involve defects in neuronal transport,...

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Detalhes bibliográficos
Main Authors: Peter, Cyril Jayakumar, Evans, Matthew, Thayanithy, Venugopal, Taniguchi-Ishigaki, Naoko, Bach, Ingolf, Kolpak, Adrianne, Bassell, Gary J., Rossoll, Wilfried, Lorson, Christian L., Bao, Zheng-Zheng, Androphy, Elliot J.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3071668/
https://ncbi.nlm.nih.gov/pubmed/21300694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr046
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