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State of the Art in Idiopathic Pulmonary Fibrosis

State of the Art in Idiopathic Pulmonary Fibrosis

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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.

This book is included in DOAB.

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Keywords

  • (pan-)HDAC-inhibitor
  • 3D cultures
  • adverse event
  • airway epithelium
  • alveolar epithelial cells
  • alveolar epithelial progenitors
  • alveolar fibroelastosis
  • amphiregulin
  • antibody folding
  • antifibrotic treatment
  • AT2 cells
  • basal cells
  • bleomycin
  • bleomycin-induced pulmonary fibrosis
  • body mass index
  • bronchial epithelium
  • bronchiolar basal cells
  • bronchiolization
  • CD24
  • CK5
  • Class I-HDAC-inhibitor
  • discontinuation
  • Drug Screening
  • epidermal growth factor
  • epidermal growth factor receptor
  • epithelial populations
  • ER stress
  • ErbB-signaling
  • fibroblast-to-myofibroblast differentiation (FMD)
  • FK506-binding protein
  • Flow Cytometry
  • histone acetylation
  • histone deacetylase (HDAC)
  • idiopathic pulmonary fibrosis
  • idiopathic pulmonary fibrosis (IPF)
  • IGF1
  • IGF1R
  • immunophilin
  • intermediate epithelial cells
  • interstitial fibrosis
  • interstitial lung disease
  • IPF
  • IPF modelling
  • Lung
  • lung development
  • lung fibrosis
  • lung transcriptomic profile
  • LysoTracker
  • medicine
  • MUC5B
  • n/a
  • neuregulin 1
  • NGFR
  • Nintedanib
  • non-histone protein acetylation
  • peptidyl-prolyl isomerase
  • pirfenidone
  • pulmonary fibrosis
  • recombinant FGF10
  • single cell RNA sequencing
  • tacrolimus
  • TGF-α
  • TGF-β
  • transitional states
  • type-II alveolar epithelial cell (AECII)
  • Tyrosine Kinase Inhibitor

Links

DOI: 10.3390/books978-3-0365-6384-8

Editions

edition cover

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