Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease involving pulmonary injury
associated with tissue repair, dysfunction and fibrosis. Recent studies indicate that some …

Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease involving pulmonary injury
associated with tissue repair, dysfunction and fibrosis. MicroRNAs (miRNAs), as gene …

Pulmonary fibrosis (PF) is a common, chronic and incurable lung disease, in which the lungs
become scarred over time. MicroRNAs (miRNAs/miRs) serve key roles in various biological …

Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial fibrotic lung disease with an
undefined etiology and no effective treatments. By binding to cell surface receptors …

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and usually lethal fibrotic lung
disease with largely unknown etiology and pathogenesis. Evidence suggests microRNAs …

Abstract Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive, and highly lethal
fibrotic lung disease with poor treatment and unknown etiology. Emerging evidence …

To identify microRNAs (miRNAs, miRs) with potential roles in lung fibrogenesis, we
performed genome-wide profiling of miRNA expression in lung tissues from a silica-induced …

Idiopathic pulmonary fibrosis (IPF) is a fatal disorder resulting from the progressive
remodeling of lungs, with no known effective treatment. Although transforming growth factor …

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and fatal fibrotic lung disease
characterized by profound changes in stem cell differentiation, epithelial cell phenotypes …

Aberrant proliferation and activation of lung fibroblasts contribute to the initiation and
progression of idiopathic pulmonary fibrosis (IPF). However, the mechanisms responsible for …