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Cellular metabolomics of pulmonary fibrosis, from amino acids to lipids
Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease of unknown etiology with limited treatment options. It is characterized by repetitive injury to alveolar epithelial cells and aberrant activation of numerous signaling pathways. Recent evidence suggests that metabolic repr...
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| Yayımlandı: | Am J Physiol Cell Physiol |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Physiological Society
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8163573/ https://ncbi.nlm.nih.gov/pubmed/33471621 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00586.2020 |
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