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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yunguan, Yella, Jaswanth, Chen, Jing, McCormack, Francis X., Madala, Satish K., Jegga, Anil G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649521/
https://www.ncbi.nlm.nih.gov/pubmed/29058630
http://dx.doi.org/10.1186/s12890-017-0472-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649521/
https://www.ncbi.nlm.nih.gov/pubmed/29058630
http://dx.doi.org/10.1186/s12890-017-0472-9

Ejemplares similares