Ontology highlight
ABSTRACT:
INSTRUMENT(S): Q Exactive
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Lung
DISEASE(S): Idiopathic Pulmonary Fibrosis
SUBMITTER: Alexander Held
LAB HEAD: Ursula Klingmüller
PROVIDER: PXD011129 | Pride | 2020-03-20
REPOSITORIES: Pride
Items per page: 1 - 5 of 25 |
Nature communications 20200424 1
Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease characterized by patchy scarring of the distal lung with limited therapeutic options and poor prognosis. Here, we show that conditional deletion of the ubiquitin ligase Nedd4-2 (Nedd4l) in lung epithelial cells in adult mice produces chronic lung disease sharing key features with IPF including progressive fibrosis and bronchiolization with increased expression of Muc5b in peripheral airways, honeycombing and c ...[more]