Cargando…
Detecting Splicing Variants in Idiopathic Pulmonary Fibrosis from Non-Differentially Expressed Genes
Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease of unknown cause that lacks a proven therapy for altering its high mortality rate. Microarrays have been employed to investigate the pathogenesis of IPF, but are presented mostly at the gene-expression level due to technologic limit...
Autores principales: | Deng, Nan, Sanchez, Cecilia G., Lasky, Joseph A., Zhu, Dongxiao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699530/ https://www.ncbi.nlm.nih.gov/pubmed/23844188 http://dx.doi.org/10.1371/journal.pone.0068352 |
Ejemplares similares
-
Safety, tolerability and appropriate use of nintedanib in idiopathic pulmonary fibrosis
por: Corte, Tamera, et al.
Publicado: (2015) -
Assessment of viral RNA in idiopathic pulmonary fibrosis using RNA-seq
por: Yin, Qinyan, et al.
Publicado: (2020) -
Idiopathic Pulmonary Fibrosis
por: Lynch, Joseph P., et al.
Publicado: (2011) -
Diagnosis of Idiopathic Pulmonary Fibrosis: Differential Diagnosis
por: Aburto, Myriam, et al.
Publicado: (2018) -
Differential telomerase expression in idiopathic pulmonary fibrosis and non-small cell lung cancer
por: ANTONIOU, K.M., et al.
Publicado: (2013)