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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Detalles Bibliográficos
Autores principales: Lee, Jooyeon, Kim, Jung-Hyun, Hong, Seok-Ho, Yang, Se-Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Stem Cell Research 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904526/
https://www.ncbi.nlm.nih.gov/pubmed/33122472
http://dx.doi.org/10.15283/ijsc20093

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904526/
https://www.ncbi.nlm.nih.gov/pubmed/33122472
http://dx.doi.org/10.15283/ijsc20093

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