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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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Dades bibliogràfiques
Publicat a:Front Pharmacol
Autors principals: Skibba, Melissa, Drelich, Adam, Poellmann, Michael, Hong, Seungpyo, Brasier, Allan R.
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7770469/
https://ncbi.nlm.nih.gov/pubmed/33384604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2020.607689
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