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Organoid Model in Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive- fibrosing disease characterized by extensive deposition of extracellular matrix (ECM), scarring of the lung parenchyma. Despite increased awareness of IPF, etiology and physiological mechanism of IPF are unclear. Therefore, preclinical m...
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| Publié dans: | Int J Stem Cells |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Korean Society for Stem Cell Research
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7904526/ https://ncbi.nlm.nih.gov/pubmed/33122472 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15283/ijsc20093 |
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