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Histone acetyltransferase inhibition rescues differentiation of emerin-deficient myogenic progenitors
INTRODUCTION: Emery-Dreifuss muscular dystrophy (EDMD) is a disease characterized by skeletal muscle wasting, major tendon contractures, and cardiac conduction defects. Mutations in the gene encoding emerin cause EDMD1. Our previous studies suggested that emerin activation of histone deacetylase 3 (...
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| Gepubliceerd in: | Muscle Nerve |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7382944/ https://ncbi.nlm.nih.gov/pubmed/32304242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mus.26892 |
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