Background Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung
disease. Many studies suggest that autophagy may be related to disease progression and …

Idiopathic pulmonary fibrosis (IPF) is a progressive, eventually fatal disease characterized
by fibrosis of the lung parenchyma and loss of lung function. IPF is believed to be caused by …

COPD (chronic obstructive pulmonary disease) and ILD (interstitial lung disease) are two
common respiratory diseases. They share similar clinical traits but require different …

Idiopathic pulmonary fibrosis (IPF) is a serious interstitial pneumonia leading to
considerable morbidity and mortality. The unavailability of prompt biomarkers for IPF has …

Rationale: Idiopathic pulmonary fibrosis (IPF) is one of the most aggressive forms of
idiopathic interstitial pneumonia. Some miRNAs may be associated with IPF and may affect …

Background. Idiopathic Pulmonary Fibrosis (IPF) is one of the most common idiopathic
interstitial pneumonia, which can occur all over the world. The median survival time of …

Background Idiopathic pulmonary fibrosis (IPF) is increasingly recognized as a chronic,
progressive and fatal lung disease with an unknown etiology. Current studies focus on …

Idiopathic pulmonary fibrosis (IPF), the most frequent form of irreversible interstitial
pneumonia with unknown etiology, is characterized by massive remodeling of lung …

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal lung disease that poses a
significant challenge to medical professionals due to its increasing incidence and …

Unfolded protein response (UPR) signaling and endoplasmic reticulum (ER) stress have
been linked to pulmonary fibrosis. However, the relationship between UPR status and …