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Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy
LMNA mutations in patients are responsible for a dilated cardiomyopathy. Molecular mechanisms underlying the origin and development of the pathology are unknown. Herein, using mouse pluripotent embryonic stem cells (ESCs) and a mouse model both harboring the p.H222P Lmna mutation, we found early def...
Guardat en:
| Publicat a: | J Clin Invest |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7773358/ https://ncbi.nlm.nih.gov/pubmed/33393499 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI136488 |
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