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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Detalles Bibliográficos
Autores principales: Tian, Yaqiong, Li, Hui, Gao, Yujuan, Liu, Chuanmei, Qiu, Ting, Wu, Hongyan, Cao, Mengshu, Zhang, Yingwei, Ding, Hui, Chen, Jingyu, Cai, Hourong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6364390/
https://www.ncbi.nlm.nih.gov/pubmed/30774578
http://dx.doi.org/10.1186/s12014-019-9226-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6364390/
https://www.ncbi.nlm.nih.gov/pubmed/30774578
http://dx.doi.org/10.1186/s12014-019-9226-4

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