RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns

Spinal Muscular Atrophy (SMA) is a neuromuscular disorder caused by insufficient levels of the Survival of Motor Neuron (SMN) protein. SMN is expressed ubiquitously and functions in RNA processing pathways that include trafficking of mRNA and assembly of snRNP complexes. Importantly, SMA severity is...

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Detalles Bibliográficos
Autores principales: Doktor, Thomas Koed, Hua, Yimin, Andersen, Henriette Skovgaard, Brøner, Sabrina, Liu, Ying Hsiu, Wieckowska, Anna, Dembic, Maja, Bruun, Gitte Hoffmann, Krainer, Adrian R., Andresen, Brage Storstein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224493/
https://www.ncbi.nlm.nih.gov/pubmed/27557711
http://dx.doi.org/10.1093/nar/gkw731

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224493/
https://www.ncbi.nlm.nih.gov/pubmed/27557711
http://dx.doi.org/10.1093/nar/gkw731

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