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Cystic Fibrosis Defective Response to Infection Involves Autophagy and Lipid Metabolism
Cystic fibrosis (CF) is a hereditary disease, with 70% of patients developing a proteinopathy related to the deletion of phenylalanine 508. CF is associated with multiple organ dysfunction, chronic inflammation, and recurrent lung infections. CF is characterized by defective autophagy, lipid metabol...
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| Publicado no: | Cells |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7463682/ https://ncbi.nlm.nih.gov/pubmed/32781626 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9081845 |
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