Identification of key modules and hub genes associated with lung function in idiopathic pulmonary fibrosis

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive interstitial lung disease, characterized by a decline in lung function. To date, the pathophysiologic mechanisms associated with lung dysfunction remain unclear, and no effective therapy has been identified to improve lung...

Descripción completa

Detalles Bibliográficos
Autores principales: Xia, Yuechong, Lei, Cheng, Yang, Danhui, Luo, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Bioinformatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485506/
https://www.ncbi.nlm.nih.gov/pubmed/33194355
http://dx.doi.org/10.7717/peerj.9848

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485506/
https://www.ncbi.nlm.nih.gov/pubmed/33194355
http://dx.doi.org/10.7717/peerj.9848

Ejemplares similares