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Increased steady state levels of CUGBP1 in Myotonic Dystrophy 1 are due to PKC-mediated hyper-phosphorylation

The genetic basis of myotonic dystrophy type 1 (DM1) is a CTG expansion in the 3' untranslated region (UTR) of DMPK. The pathogenic mechanism involves an RNA gain of function in which the repeat containing transcripts accumulate in nuclei and alter the functions of RNA binding proteins such as...

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Détails bibliographiques
Auteurs principaux: Kuyumcu-Martinez, N. Muge, Wang, Guey-Shin, Cooper, Thomas A.
Format: Artigo
Langue:Inglês
Publié: 2007
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2083558/
https://ncbi.nlm.nih.gov/pubmed/17936705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molcel.2007.07.027
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