The peripheral blood proteome signature of idiopathic pulmonary fibrosis is distinct from normal and is associated with novel immunological processes

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal interstitial pneumonia. The disease pathophysiology is poorly understood and the etiology remains unclear. Recent advances have generated new therapies and improved knowledge of the natural history of IPF. These gains have been brokered...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: O’Dwyer, David N., Norman, Katy C., Xia, Meng, Huang, Yong, Gurczynski, Stephen J., Ashley, Shanna L., White, Eric S., Flaherty, Kevin R., Martinez, Fernando J., Murray, Susan, Noth, Imre, Arnold, Kelly B., Moore, Bethany B.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5404506/
https://ncbi.nlm.nih.gov/pubmed/28440314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep46560
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