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α-COP binding to the survival motor neuron protein SMN is required for neuronal process outgrowth

Spinal muscular atrophy (SMA), a heritable neurodegenerative disease, results from insufficient levels of the survival motor neuron (SMN) protein. α-COP binds to SMN, linking the COPI vesicular transport pathway to SMA. Reduced levels of α-COP restricted development of neuronal processes in NSC-34 c...

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Publicado en:Hum Mol Genet
Autores principales: Li, Hongxia, Custer, Sara K., Gilson, Timra, Hao, Le Thi, Beattie, Christine E., Androphy, Elliot J.
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2015
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4664168/
https://ncbi.nlm.nih.gov/pubmed/26464491
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv428
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