Cargando…
IP-10 Is a Potential Biomarker of Cystic Fibrosis Acute Pulmonary Exacerbations
BACKGROUND: Cystic fibrosis (CF) is characterized by acute pulmonary exacerbations (APE). The CF nasal airway exhibits a similar ion transport defect as the lung, and colonization, infection, and inflammation within the nasal passages are common among CF patients. Nasal lavage fluid (NLF) is a minim...
Autores principales: | Solomon, George M., Frederick, Carla, Zhang, Shaoyan, Gaggar, Amit, Harris, Tom, Woodworth, Bradford A., Steele, Chad, Rowe, Steven M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745468/ https://www.ncbi.nlm.nih.gov/pubmed/23977293 http://dx.doi.org/10.1371/journal.pone.0072398 |
Ejemplares similares
-
Immunomodulation in Cystic Fibrosis: Why and How?
por: Giacalone, Vincent D., et al.
Publicado: (2020) -
Implementation of a successful eradication protocol for Burkholderia Cepacia complex in cystic fibrosis patients
por: Garcia, Bryan A., et al.
Publicado: (2018) -
Proline-Glycine-Proline (PGP) and High Mobility Group Box Protein-1 (HMGB1): Potential Mediators of Cystic Fibrosis Airway Inflammation
por: Gaggar, Amit, et al.
Publicado: (2010) -
Airway Inflammatory/Immune Responses in COPD and Cystic Fibrosis
por: De Rose, Virginia, et al.
Publicado: (2018) -
Acquired cystic fibrosis transmembrane conductance regulator dysfunction
por: Banks, Catherine, et al.
Publicado: (2018)