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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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| Publicado no: | BMC Pulm Med |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | 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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