Idiopathic pulmonary fibrosis (IPF) is a rare yet crucial persistent lung disorder that actuates
scarring of lung tissues, which makes breathing difficult. Smoking, environmental pollution …

Background: Idiopathic pulmonary fibrosis (IPF) is a life-threatening disease whose etiology
remains unknown. This study aims to explore diagnostic biomarkers and pathways involved …

Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease characterized by chronic
progressive pulmonary fibrosis and a poor prognosis. Genetic studies, including …

Idiopathic pulmonary fibrosis (IPF) is the most common and serious type of idiopathic
interstitial pneumonia, characterized by chronic, progressive, and low survival rates, while …

Idiopathic pulmonary fibrosis (IPF) remains a lethal disease with unknown etiology and
unmet medical need. The aim of this study was to perform an integrative analysis of multiple …

Molecular patterns and pathways in idiopathic pulmonary fibrosis (IPF) have been
extensively investigated, but few studies have assimilated multiomic platforms to provide an …

Background Idiopathic pulmonary fibrosis (IPF) is characterized by the accumulation of
extracellular matrix in the pulmonary interstitium and progressive functional decline. We …

Objective This study aimed to identify candidate gene biomarkers associated with immune
infiltration in idiopathic pulmonary fibrosis (IPF) based on machine learning algorithms …

Background: Idiopathic pulmonary fibrosis (IPF) is caused by aberrant repair because of
alveolar epithelial injury and can only be effectively treated with several compounds …

Idiopathic pulmonary fibrosis (IPF), characterized by irreversible scarring and progressive
destruction of the lung tissue, is one of the most common types of idiopathic interstitial …