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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Pubblicato in:Sci Rep
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2020
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7374599/
https://ncbi.nlm.nih.gov/pubmed/32694604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-67956-w
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