Proteomics

Dataset Information

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Human IPF and control lungs LC-MSMS


ABSTRACT: 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 in lung epithelial cells in adult mice produces chronic lung disease that shares key features with IPF including progressive fibrosis and bronchiolization with increased expression of Muc5b in peripheral airways, honeycombing and characteristic alterations in the lung proteome

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Lung

DISEASE(S): Pulmonary Fibrosis

SUBMITTER: Alexander Held  

LAB HEAD: Ursula Klingmüller

PROVIDER: PXD011116 | Pride | 2020-03-20

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
170228_2_MSz-DD_F8-2_TCL_1360.raw Raw
170228_4_MSz-DD_F8-2_TCL_1330.raw Raw
170228_6_MSz-DD_F8-2_TCL_762.raw Raw
170301_10_MSz-DD_F8-2_TCL_5250.raw Raw
170301_14_MSz-DD_F8-2_TCL_3655.raw Raw
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Publications


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]

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