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MEG3 is increased in idiopathic pulmonary fibrosis and regulates epithelial cell differentiation
Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease causing fibrotic remodeling of the peripheral lung, leading to respiratory failure. Peripheral pulmonary epithelial cells lose normal alveolar epithelial gene expression patterns and variably express genes associated with div...
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| Опубликовано в: : | JCI Insight |
|---|---|
| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
American Society for Clinical Investigation
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6171798/ https://ncbi.nlm.nih.gov/pubmed/30185671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.122490 |
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