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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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Detalhes bibliográficos
Publicado no:Am J Physiol Cell Physiol
Main Authors: Roque, Willy, Romero, Freddy
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2021
Assuntos:
Acesso em linha: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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