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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404506/
https://www.ncbi.nlm.nih.gov/pubmed/28440314
http://dx.doi.org/10.1038/srep46560

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404506/
https://www.ncbi.nlm.nih.gov/pubmed/28440314
http://dx.doi.org/10.1038/srep46560

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