miR-31 modulates dystrophin expression: new implications for Duchenne muscular dystrophy therapy

Duchenne muscular dystrophy (DMD)—which is caused by mutations in the dystrophin gene—is one of the most severe myopathies. Among therapeutic strategies, exon skipping allows the rescue of dystrophin synthesis through the production of a shorter but functional messenger RNA. Here, we report the iden...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Cacchiarelli, Davide, Incitti, Tania, Martone, Julie, Cesana, Marcella, Cazzella, Valentina, Santini, Tiziana, Sthandier, Olga, Bozzoni, Irene
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2011
Aiheet:
Scientific Reports
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3049433/
https://ncbi.nlm.nih.gov/pubmed/21212803
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/embor.2010.208
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