State of the Art in Idiopathic Pulmonary Fibrosis

This reprint is a compilation of ten publications, including original-research and review articles, and the accompanying editorial within the scope of a Special Issue entitled: "State of the Art in Idiopathic Pulmonary Fibrosis" published in Cells.

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Bibliographische Detailangaben
Format:	Online
Sprache:	Englisch
Veröffentlicht:	MDPI - Multidisciplinary Digital Publishing Institute 2023
Schlagworte:	interstitial fibrosis lung alveolar fibroelastosis idiopathic pulmonary fibrosis pirfenidone nintedanib discontinuation body mass index adverse event antifibrotic treatment IPF alveolar epithelial cells intermediate epithelial cells transitional states LysoTracker flow cytometry lung transcriptomic profile CK5 NGFR CD24 epidermal growth factor epidermal growth factor receptor ErbB-signaling pulmonary fibrosis lung fibrosis tyrosine kinase inhibitor TGF-α TGF-β amphiregulin neuregulin 1 basal cells bronchial epithelium airway epithelium MUC5B single cell RNA sequencing epithelial populations antibody folding immunophilin interstitial lung disease ER stress tacrolimus FK506-binding protein peptidyl-prolyl isomerase 3D cultures IPF modelling drug screening idiopathic pulmonary fibrosis (IPF) histone deacetylase (HDAC) histone acetylation non-histone protein acetylation fibroblast-to-myofibroblast differentiation (FMD) type-II alveolar epithelial cell (AECII) bronchiolar basal cells bronchiolization Class I-HDAC-inhibitor (pan-)HDAC-inhibitor IGF1 IGF1R lung development bleomycin-induced pulmonary fibrosis bleomycin recombinant FGF10 alveolar epithelial progenitors AT2 cells n/a thema EDItEUR::M Medicine and Nursing
Online-Zugang:	ONIX_20230202_9783036563855_77
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State of the Art in Idiopathic Pulmonary Fibrosis

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