Unsupervised gene expression analyses identify IPF-severity correlated signatures, associated genes and biomarkers

BACKGROUND: Idiopathic Pulmonary Fibrosis (IPF) is a fatal fibrotic lung disease occurring predominantly in middle-aged and older adults. The traditional diagnostic classification of IPF is based on clinical, radiological, and histopathological features. However, the considerable heterogeneity in IP...

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Detaylı Bibliyografya
Yayımlandı:BMC Pulm Med
Asıl Yazarlar: Wang, Yunguan, Yella, Jaswanth, Chen, Jing, McCormack, Francis X., Madala, Satish K., Jegga, Anil G.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2017
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5649521/
https://ncbi.nlm.nih.gov/pubmed/29058630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12890-017-0472-9
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