Quantitative proteomic characterization of lung tissue in idiopathic pulmonary fibrosis

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a progressive, eventually fatal disease. IPF is characterized by excessive accumulation of the extracellular matrix (ECM) in the alveolar parenchyma and progressive lung scarring. The pathogenesis of IPF and whether the ECM involved in the process r...

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Detalhes bibliográficos
Publicado no:Clin Proteomics
Main Authors: Tian, Yaqiong, Li, Hui, Gao, Yujuan, Liu, Chuanmei, Qiu, Ting, Wu, Hongyan, Cao, Mengshu, Zhang, Yingwei, Ding, Hui, Chen, Jingyu, Cai, Hourong
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6364390/
https://ncbi.nlm.nih.gov/pubmed/30774578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12014-019-9226-4
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