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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
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Article
Acesso em linha: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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