Abstract. In this review, we discuss three broad areas which have been explored that may be responsible for the combination of altered lung fibroblasts, loss of alveolar epithelial cells, and excessive accumulation of ECM: inflammation and immune mechanisms, oxidative stress and oxidative signaling, and procoagulant mechanisms
Pulmonary fibrosis is a chronic progressive lung disease that steadily leads to lung architecture di...
Idiopathic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial pneumonia, is a...
Idiopathic pulmonary fibrosis is characterised by abnormal reepithelialisation and remodelling conse...
Idiopathic pulmonary fibrosis (IPF) is a devastating disease characterized by severe and progressive...
Pulmonary fibrosis is characterised by excessive scarring in the lung which leads to compromised lun...
Pulmonary fibrosis is the end stage of many diffuse parenchymal lung diseases. It is characterised b...
Fibrosis and structural remodeling of the lung tissue can significantly impair lung function, often ...
AbstractPulmonary fibrosis affects millions worldwide and, even though there has been a significant ...
Pulmonary fibrosis is the end-point of a numerous and heterogeneous group of disorders known as inte...
Recent data suggest that the separation of emphysema from fibrosis is not as clear-cut as it has app...
Pulmonary fibrosis (PF) encompasses a spectrum of chronic lung diseases that progressively impact th...
Background: Surgical manipulation of the intestine results in generation of oxygen free radicals lea...
Most chronic inflammatory illnesses include fibrosis as a pathogenic characteristic. Extracellular m...
The role of the immune system in idiopathic pulmonary fibrosis (IPF) pathogenesis has been debated, ...
Idiopathic pulmonary fibrosis (IPF) is a chronic disease characterized by fibroblasts activation, EC...
Pulmonary fibrosis is a chronic progressive lung disease that steadily leads to lung architecture di...
Idiopathic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial pneumonia, is a...
Idiopathic pulmonary fibrosis is characterised by abnormal reepithelialisation and remodelling conse...
Idiopathic pulmonary fibrosis (IPF) is a devastating disease characterized by severe and progressive...
Pulmonary fibrosis is characterised by excessive scarring in the lung which leads to compromised lun...
Pulmonary fibrosis is the end stage of many diffuse parenchymal lung diseases. It is characterised b...
Fibrosis and structural remodeling of the lung tissue can significantly impair lung function, often ...
AbstractPulmonary fibrosis affects millions worldwide and, even though there has been a significant ...
Pulmonary fibrosis is the end-point of a numerous and heterogeneous group of disorders known as inte...
Recent data suggest that the separation of emphysema from fibrosis is not as clear-cut as it has app...
Pulmonary fibrosis (PF) encompasses a spectrum of chronic lung diseases that progressively impact th...
Background: Surgical manipulation of the intestine results in generation of oxygen free radicals lea...
Most chronic inflammatory illnesses include fibrosis as a pathogenic characteristic. Extracellular m...
The role of the immune system in idiopathic pulmonary fibrosis (IPF) pathogenesis has been debated, ...
Idiopathic pulmonary fibrosis (IPF) is a chronic disease characterized by fibroblasts activation, EC...
Pulmonary fibrosis is a chronic progressive lung disease that steadily leads to lung architecture di...
Idiopathic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial pneumonia, is a...
Idiopathic pulmonary fibrosis is characterised by abnormal reepithelialisation and remodelling conse...