Identification of a unique temporal signature in blood and BAL associated with IPF progression

Idiopathic pulmonary fibrosis (IPF) is a progressive and heterogeneous interstitial lung disease of unknown origin with a low survival rate. There are few treatment options available due to the fact that mechanisms underlying disease progression are not well understood, likely because they arise fro...

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Detalles Bibliográficos
Autores principales: Norman, Katy C., O’Dwyer, David N., Salisbury, Margaret L., DiLillo, Katarina M., Lama, Vibha N., Xia, Meng, Gurczynski, Stephen J., White, Eric S., Flaherty, Kevin R., Martinez, Fernando J., Murray, Susan, Moore, Bethany B., Arnold, Kelly B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374599/
https://www.ncbi.nlm.nih.gov/pubmed/32694604
http://dx.doi.org/10.1038/s41598-020-67956-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374599/
https://www.ncbi.nlm.nih.gov/pubmed/32694604
http://dx.doi.org/10.1038/s41598-020-67956-w

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