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Altered mRNA Splicing in SMN-Depleted Motor Neuron-Like Cells

Spinal muscular atrophy (SMA) is an intractable neurodegenerative disease afflicting 1 in 6–10,000 live births. One of the key functions of the SMN protein is regulation of spliceosome assembly. Reduced levels of the SMN protein that are observed in SMA have been shown to result in aberrant mRNA spl...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Custer, Sara K., Gilson, Timra D., Li, Hongxia, Todd, A. Gary, Astroski, Jacob W., Lin, Hai, Liu, Yunlong, Androphy, Elliot J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2016
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5063418/
https://ncbi.nlm.nih.gov/pubmed/27736905
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0163954
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