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Heterogeneity of Fibroblasts and Myofibroblasts in Pulmonary Fibrosis
PURPOSE OF REVIEW: Idiopathic Pulmonary Fibrosis (IPF) is the most common form of interstitial lung diseases of unknown eathiopathogenesis, mean survival of 3-5 years and limited therapeutics. Characterized by a loss of alveolar type II epithelial cells and aberrant activation of stromal cells, cons...
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| Publicado en: | Curr Pathobiol Rep |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5654579/ https://ncbi.nlm.nih.gov/pubmed/29082111 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40139-017-0134-x |
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