miR-708-5p and miR-34c-5p are involved in nNOS regulation in dystrophic context

BACKGROUND: Duchenne (DMD) and Becker (BMD) muscular dystrophies are caused by mutations in the DMD gene coding for dystrophin, a protein being part of a large sarcolemmal protein scaffold that includes the neuronal nitric oxide synthase (nNOS). The nNOS was shown to play critical roles in a variety...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Skelet Muscle
Päätekijät: Guilbaud, Marine, Gentil, Christel, Peccate, Cécile, Gargaun, Elena, Holtzmann, Isabelle, Gruszczynski, Carole, Falcone, Sestina, Mamchaoui, Kamel, Ben Yaou, Rabah, Leturcq, France, Jeanson-Leh, Laurence, Piétri-Rouxel, France
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2018
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5924477/
https://ncbi.nlm.nih.gov/pubmed/29703249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13395-018-0161-2
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