Airway Epithelium Dysfunction in Cystic Fibrosis and COPD
Cystic fibrosis is a genetic disease caused by mutations in the CFTR gene, whereas chronic obstructive pulmonary disease (COPD) is mainly caused by environmental factors (mostly cigarette smoking) on a genetically susceptible background. Although the etiology and pathogenesis of these diseases are d...
Main Authors: | Virginia De Rose, Kevin Molloy, Sophie Gohy, Charles Pilette, Catherine M. Greene |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2018-01-01
|
Series: | Mediators of Inflammation |
Online Access: | http://dx.doi.org/10.1155/2018/1309746 |
Similar Items
-
Airway Inflammatory/Immune Responses in COPD and Cystic Fibrosis
by: Virginia De Rose, et al.
Published: (2018-01-01) -
MicroRNA Expression in Cystic Fibrosis Airway Epithelium
by: Catherine M. Greene
Published: (2013-02-01) -
Dysfunctional Inflammation in Cystic Fibrosis Airways: From Mechanisms to Novel Therapeutic Approaches
by: Alessandra Ghigo, et al.
Published: (2021-02-01) -
Studies of Tight Junctions and Airway Surface Liquid in Airway Epithelium with Relevance to Cystic Fibrosis
by: Nilsson, Harriet
Published: (2009) -
cAMP triggers Na+ absorption by distal airway surface epithelium in cystic fibrosis swine
by: Xiaojie Luan, et al.
Published: (2021-10-01)