ITGAV, a specific biomarker associated with the pathogenesis of idiopathic pulmonary fibrosis
Abstract Objective Idiopathic pulmonary fibrosis (IPF), which radiologically/pathologically manifests mainly as usual interstitial pneumonia (UIP), is easily confused with chronic hypersensitivity pneumonitis (CHP) and collagenous vascular disease in clinical settings, affecting the physician’s diag...
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| Main Authors: | Zhangyang Bi, Xiaodong Wang, Xue Liu, Xue Zhu, Guodong Zang, Li Tian, Wei Zhang |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-05-01
|
| Series: | Scientific Reports |
| Subjects: | |
| Online Access: | https://doi.org/10.1038/s41598-025-01459-4 |
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