Cargando…
Pulmonary fibrosis distal airway epithelia are dynamically and structurally dysfunctional
The airway epithelium serves as the interface between the host and external environment. In many chronic lung diseases, the airway is the site of substantial remodeling after injury. While, idiopathic pulmonary fibrosis (IPF) has traditionally been considered a disease of the alveolus and lung matri...
Autores principales: | Stancil, Ian T., Michalski, Jacob E., Davis-Hall, Duncan, Chu, Hong Wei, Park, Jin-Ah, Magin, Chelsea M., Yang, Ivana V., Smith, Bradford J., Dobrinskikh, Evgenia, Schwartz, David A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316442/ https://www.ncbi.nlm.nih.gov/pubmed/34315881 http://dx.doi.org/10.1038/s41467-021-24853-8 |
Ejemplares similares
-
Dysregulated Cell–Cell Communication Characterizes Pulmonary Fibrosis
por: Kurche, Jonathan S., et al.
Publicado: (2022) -
Airway Epithelia
por: Johnson, Larry G., et al.
Publicado: (2003) -
Polarized Signaling via Purinoceptors in Normal and Cystic Fibrosis Airway Epithelia
por: Paradiso, Anthony M., et al.
Publicado: (2001) -
CFTR dysfunction increases endoglin and TGF‐β signaling in airway epithelia
por: Nicola, Teodora, et al.
Publicado: (2019) -
Klotho Inhibits Interleukin-8 Secretion from Cystic Fibrosis Airway Epithelia
por: Krick, Stefanie, et al.
Publicado: (2017)