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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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Pubblicato in:Am J Physiol Cell Physiol
Autori principali: Roque, Willy, Romero, Freddy
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Physiological Society 2021
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Accesso online: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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