Lataa...
Megf10 deficiency impairs skeletal muscle stem cell migration and muscle regeneration
Biallelic loss‐of‐function MEGF10 mutations lead to MEGF10 myopathy, also known as early onset myopathy with areflexia, respiratory distress, and dysphagia (EMARDD). MEGF10 is expressed in muscle satellite cells, but the contribution of satellite cell dysfunction to MEGF10 myopathy is unclear. Myofi...
Tallennettuna:
| Julkaisussa: | FEBS Open Bio |
|---|---|
| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2020
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7780119/ https://ncbi.nlm.nih.gov/pubmed/33159715 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/2211-5463.13031 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|