Idiopathic pulmonary fibrosis (IPF) is a lethal interstitial lung disease characterized by airway
remodeling, inflammation, alveolar destruction, and fibrosis. We utilized single-cell RNA …

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by progressive
decline in lung function, resulting in significant morbidity and mortality. Current concepts of …

Precision medicine is defined by the National Institute of Health's Precision Medicine
Initiative Working Group as an approach to disease treatment that takes into account …

Background and objective A common polymorphism in the MUC5B gene (rs35705950) is
associated with susceptibility to idiopathic pulmonary fibrosis (IPF) and familial interstitial …

Childhood interstitial lung disease (chILD) comprises a large and heterogeneous group of
rare disorders characterized by diffuse pulmonary infiltrates, restrictive lung physiology, and …

Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic interstitial lung pneumonia
associated with the histologic pattern of usual interstitial pneumonia (UIP). Although UIP is a …

The primary function of the lungs is gas exchange. Approximately 400 million years ago, the
Earth's atmosphere gained enough oxygen in the gas phase for the animals that emerged …

Objective Interstitial lung disease (ILD) is the most common pulmonary extra-articular
manifestations of rheumatoid arthritis (RA), but the pathogenesis of RA-ILD is unknown. The …

OBJECTIVE. Multidisciplinary discussion is essential in establishing the diagnosis of
idiopathic pulmonary fibrosis (IPF) and in determining prognosis. CONCLUSION. The CT …

OBJECTIVE. The CT findings of pulmonary fibrosis in patients with pulmonary alveolar
proteinosis (PAP) are not yet well defined. The objective of this study was to evaluate the CT …