3D In Vitro Models: Novel Insights into Idiopathic Pulmonary Fibrosis Pathophysiology and Drug Screening

Idiopathic pulmonary fibrosis (IPF) is a progressive and often lethal interstitial lung disease of unknown aetiology. IPF is characterised by myofibroblast activation, tissue stiffening, and alveolar epithelium injury. As current IPF treatments fail to halt disease progression or induce regeneration...

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Detalles Bibliográficos
Autores principales: Vazquez-Armendariz, Ana Ivonne, Barroso, Margarida Maria, El Agha, Elie, Herold, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099957/
https://www.ncbi.nlm.nih.gov/pubmed/35563831
http://dx.doi.org/10.3390/cells11091526

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099957/
https://www.ncbi.nlm.nih.gov/pubmed/35563831
http://dx.doi.org/10.3390/cells11091526

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