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Regulation of Transforming Growth Factor-β1–driven Lung Fibrosis by Galectin-3
Rationale: Idiopathic pulmonary fibrosis (IPF) is a chronic dysregulated response to alveolar epithelial injury with differentiation of epithelial cells and fibroblasts into matrix-secreting myofibroblasts resulting in lung scaring. The prognosis is poor and there are no effective therapies or relia...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
American Thoracic Society
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3410728/ https://ncbi.nlm.nih.gov/pubmed/22095546 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201106-0965OC |
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