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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Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2011
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On-line přístup: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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