Click the Why column to see why an item matched the search.
| Match | Type | Why |
|---|
| Diagnosing idiopathic pulmonary fibrosis in 2018: bridging recommendations made by experts serving different societies. | Academic Article |
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| Grainyhead-like 2 (GRHL2) distribution reveals novel pathophysiological differences between human idiopathic pulmonary fibrosis and mouse models of pulmonary fibrosis. | Academic Article |
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| 2018 Clinical Practice Guideline Summary for Clinicians: Diagnosis of Idiopathic Pulmonary Fibrosis. | Academic Article |
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| Alveolar wall basement membranes in bleomycin-induced pulmonary fibrosis. | Academic Article |
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| Cyclosporin A upmodulates bleomycin-induced pulmonary fibrosis in BALB/c mice. | Academic Article |
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| Dermatomyositis and pulmonary fibrosis associated with anti-Jo-1 antibody. | Academic Article |
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| Functional role and species-specific contribution of arginases in pulmonary fibrosis. | Academic Article |
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| Functional Wnt signaling is increased in idiopathic pulmonary fibrosis. | Academic Article |
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| Gastroesophageal reflux disease and idiopathic pulmonary fibrosis. | Academic Article |
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| GDF15 is an epithelial-derived biomarker of idiopathic pulmonary fibrosis. | Academic Article |
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| IL-21 Promotes Pulmonary Fibrosis through the Induction of Profibrotic CD8+ T Cells. | Academic Article |
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| Increased Airway Wall Thickness in Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. | Academic Article |
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| Integrated Genomics Reveals Convergent Transcriptomic Networks Underlying Chronic Obstructive Pulmonary Disease and Idiopathic Pulmonary Fibrosis. | Academic Article |
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| miR-29 is a major regulator of genes associated with pulmonary fibrosis. | Academic Article |
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| Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition. | Academic Article |
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