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RAN Translation Regulated by Muscleblind Proteins in Myotonic Dystrophy Type 2

Several microsatellite-expansion diseases are characterized by the accumulation of RNA foci and RAN proteins raising the possibility of a mechanistic connection. We explored this question using myotonic dystrophy type 2, a multisystemic disease thought to be primarily caused by RNA gain-of-function...

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Bibliografski detalji
Izdano u:Neuron
Glavni autori: Zu, Tao, Cleary, John D., Liu, Yuanjing, Bañez-Coronel, Monica, Bubenik, Jodi L., Ayhan, Fatma, Ashizawa, Tetsuo, Xia, Guangbin, Clark, H. Brent, Yachnis, Anthony T., Swanson, Maurice S., Ranum, Laura P.W.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5951173/
https://ncbi.nlm.nih.gov/pubmed/28910618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2017.08.039
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