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Article

Integrative analyses of genes associated with idiopathic pulmonary fibrosis

2 Dec 2018

Abstract excerpt

Idiopathic pulmonary fibrosis (IPF), characterized by irreversible scarring and progressive destruction of the lung tissue, is one of the most common types of idiopathic interstitial pneumonia worldwide. However, there are no reliable candidates for curative therapies. Hence, elucidation of the mechanisms of IPF genesis and exploration of potential biomarkers and prognostic indicators are essential for accurate...

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Share to Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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PMID: 30506760
DOI: 10.1002/jcb.28153

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