Emerging cellular and molecular determinants of idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial pneumonia, is a progressive, irreversible, and typically lethal disease characterized by an abnormal fibrotic response involving vast areas of the lungs. Given the poor knowledge of the mechanisms underpinning IPF o...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Cell Mol Life Sci
Asıl Yazarlar: Phan, Thị Hằng Giang, Paliogiannis, Panagiotis, Nasrallah, Gheyath K., Giordo, Roberta, Eid, Ali Hussein, Fois, Alessandro Giuseppe, Zinellu, Angelo, Mangoni, Arduino Aleksander, Pintus, Gianfranco
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer International Publishing 2020
Konular:
Review
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7669490/
https://ncbi.nlm.nih.gov/pubmed/33201251
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-020-03693-7
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