Turnover of type I and III collagen predicts progression of idiopathic pulmonary fibrosis
Abstract 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...
Main Authors: | H. Jessen, N. Hoyer, T. S. Prior, P. Frederiksen, M. A. Karsdal, D. J. Leeming, E. Bendstrup, J. M. B. Sand, S. B. Shaker |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-07-01
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Series: | Respiratory Research |
Online Access: | https://doi.org/10.1186/s12931-021-01801-0 |
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