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YAP plays a crucial role in the development of cardiomyopathy in lysosomal storage diseases
Lysosomal dysfunction caused by mutations in lysosomal genes results in lysosomal storage disorder (LSD), characterized by accumulation of damaged proteins and organelles in cells and functional abnormalities in major organs, including the heart, skeletal muscle, and liver. In LSD, autophagy is inhi...
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| Publicado no: | J Clin Invest |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7919732/ https://ncbi.nlm.nih.gov/pubmed/33373332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI143173 |
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