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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Detalles Bibliográficos
Autores principales: Jessen, H., Hoyer, N., Prior, T. S., Frederiksen, P., Karsdal, M. A., Leeming, D. J., Bendstrup, E., Sand, J. M. B., Shaker, S. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281632/
https://www.ncbi.nlm.nih.gov/pubmed/34261485
http://dx.doi.org/10.1186/s12931-021-01801-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281632/
https://www.ncbi.nlm.nih.gov/pubmed/34261485
http://dx.doi.org/10.1186/s12931-021-01801-0

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