Turnover of type I and III collagen predicts progression of idiopathic pulmonary fibrosis

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is characterized by the accumulation of fibrillar collagens in the alveolar space resulting in reduced pulmonary function and a high mortality rate. Biomarkers measuring the turnover of type I and III collagen could provide valuable information for pro...

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Bibliografski detalji
Izdano u:Respir Res
Glavni autori: Jessen, H., Hoyer, N., Prior, T. S., Frederiksen, P., Karsdal, M. A., Leeming, D. J., Bendstrup, E., Sand, J. M. B., Shaker, S. B.
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2021
Teme:
Research
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8281632/
https://ncbi.nlm.nih.gov/pubmed/34261485
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-021-01801-0
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