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Nanoapproaches to Modifying Epigenetics of Epithelial Mesenchymal Transition for Treatment of Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis (IPF) is a chronically progressive interstitial lung that affects over 3 M people worldwide and rising in incidence. With a median survival of 2–3 years, IPF is consequently associated with high morbidity, mortality, and healthcare burden. Although two antifibrotic ther...

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Detalles Bibliográficos
Autores principales: Skibba, Melissa, Drelich, Adam, Poellmann, Michael, Hong, Seungpyo, Brasier, Allan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770469/
https://www.ncbi.nlm.nih.gov/pubmed/33384604
http://dx.doi.org/10.3389/fphar.2020.607689