Idiopathic pulmonary fibrosis (IPF) is a chronic, rare progressive lung disease, characterized
by lung scarring and the irreversible loss of lung function. Two anti-fibrotic drugs, nintedanib …

Idiopathic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial
pneumonia (IIP), is characterized by irreversible scarring of the lung parenchyma and …

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and ultimately fatal disorder for
which there is no cure. While the disease is by definition idiopathic, accumulating evidence …

Recent advances in the genetics of idiopathic pulmonary fibr... : Current Opinion in Pulmonary
Medicine Recent advances in the genetics of idiopathic pulmonary fibrosis : Current Opinion …

Idiopathic pulmonary fibrosis (IPF) is a group of common and lethal forms of idiopathic
interstitial pulmonary disease. IPF is characterized by a progressive decline in lung function …

Background: Unraveling the genetic background in a significant proportion of patients with
both sporadic and familial IPF provided new insights into the pathogenic pathways of …

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease characterized by
progressive fibrosing interstitial pneumonia. The histological pattern, which displays dense …

Use of molecular research techniques in large populations of well-phenotyped patients is
leading to major advances in understanding of IPF. As new treatments for IPF emerge, it is to …

Idiopathic pulmonary fibrosis (IPF) is a complex, heterogeneous genetic disorder that is
associated with rare and common sequence variants in many genes (MUC5B, SFTPC …

A little more than 10 years ago, the completed sequencing of the human genome boldly
promised to usher in an era of enhanced understanding and accelerated development of …