Pulmonary fibrosis requires cell-autonomous mesenchymal fibroblast growth factor (FGF) signaling

Idiopathic pulmonary fibrosis (IPF) is characterized by progressive pulmonary scarring, decline in lung function, and often results in death within 3–5 five years after diagnosis. Fibroblast growth factor (FGF) signaling has been implicated in the pathogenesis of IPF; however, the mechanism through...

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Dades bibliogràfiques
Publicat a:J Biol Chem
Autors principals: Guzy, Robert D., Li, Ling, Smith, Craig, Dorry, Samuel J., Koo, Hyun Young, Chen, Lin, Ornitz, David M.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Biochemistry and Molecular Biology 2017
Matèries:
Molecular Bases of Disease
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5481550/
https://ncbi.nlm.nih.gov/pubmed/28487375
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M117.791764
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