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Transcriptomics, metabolomics and lipidomics of chronically injured alveolar epithelial cells reveals similar features of IPF lung epithelium
View ORCID ProfileWilly Roque, Karina Cuevas-Mora, Dominic Sales, Wei Vivian Li, Ivan O. Rosas, Freddy Romero
doi: https://doi.org/10.1101/2020.05.08.084459
Willy Roque
1Department of Medicine, Rutgers – New Jersey Medical School, 185 S Orange Ave, Newark, NJ 07103, USA
Karina Cuevas-Mora
2Department of Medicine, Division of Pulmonary, Allergy and Critical Care and the Center for Translational Medicine; the Jane & Leonard Korman Respiratory Institute, Philadelphia, PA, US
Dominic Sales
2Department of Medicine, Division of Pulmonary, Allergy and Critical Care and the Center for Translational Medicine; the Jane & Leonard Korman Respiratory Institute, Philadelphia, PA, US
Wei Vivian Li
3Department of Biostatistics and Epidemiology, Rutgers School of Public Health, Piscataway 08854
Ivan O. Rosas
4Pulmonary, Critical Care and Sleep Medicine, Baylor College of Medicine
Freddy Romero
2Department of Medicine, Division of Pulmonary, Allergy and Critical Care and the Center for Translational Medicine; the Jane & Leonard Korman Respiratory Institute, Philadelphia, PA, US
Posted May 10, 2020.
Transcriptomics, metabolomics and lipidomics of chronically injured alveolar epithelial cells reveals similar features of IPF lung epithelium
Willy Roque, Karina Cuevas-Mora, Dominic Sales, Wei Vivian Li, Ivan O. Rosas, Freddy Romero
bioRxiv 2020.05.08.084459; doi: https://doi.org/10.1101/2020.05.08.084459
Transcriptomics, metabolomics and lipidomics of chronically injured alveolar epithelial cells reveals similar features of IPF lung epithelium
Willy Roque, Karina Cuevas-Mora, Dominic Sales, Wei Vivian Li, Ivan O. Rosas, Freddy Romero
bioRxiv 2020.05.08.084459; doi: https://doi.org/10.1101/2020.05.08.084459
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