ITGAV, a specific biomarker associated with the pathogenesis of idiopathic pulmonary fibrosis

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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Bibliographic Details
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:
Machine learning
ITGAV
IPF
Immune cells
UIP
Online Access:https://doi.org/10.1038/s41598-025-01459-4
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https://doi.org/10.1038/s41598-025-01459-4

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