miR-146a deficiency does not aggravate muscular dystrophy in mdx mice

Duchenne muscular dystrophy (DMD) is a genetic disease evoked by a mutation in the dystrophin gene. It is associated with progressive muscle degeneration and increased inflammation. Up to this date, mainly anti-inflammatory treatment is available for patients suffering from DMD. miR-146a is known to...

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Detalles Bibliográficos
Autores principales: Bronisz-Budzyńska, Iwona, Chwalenia, Katarzyna, Mucha, Olga, Podkalicka, Paulina, Karolina-Bukowska-Strakova, Józkowicz, Alicja, Łoboda, Agnieszka, Kozakowska, Magdalena, Dulak, Józef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693262/
https://www.ncbi.nlm.nih.gov/pubmed/31412923
http://dx.doi.org/10.1186/s13395-019-0207-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693262/
https://www.ncbi.nlm.nih.gov/pubmed/31412923
http://dx.doi.org/10.1186/s13395-019-0207-0

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