Towards the elimination of chronic obstructive pulmonary disease: a Lancet Commission

D Stolz, T Mkorombindo, DM Schumann, A Agusti… - The Lancet, 2022 - thelancet.com
Executive summary Despite substantial progress in reducing the global impact of many non-
communicable diseases, including heart disease and cancer, morbidity and mortality due to …

Hallmarks of the ageing lung

S Meiners, O Eickelberg… - European Respiratory …, 2015 - Eur Respiratory Soc
Ageing is the main risk factor for major non-communicable chronic lung diseases, including
chronic obstructive pulmonary disease, most forms of lung cancer and idiopathic pulmonary …

Airway mucin concentration as a marker of chronic bronchitis

M Kesimer, AA Ford, A Ceppe… - … England Journal of …, 2017 - Mass Medical Soc
Background Chronic obstructive pulmonary disease (COPD) is characterized by chronic
bronchitic and emphysematous components. In one biophysical model, the concentration of …

Ion channel modulators in cystic fibrosis

M Gentzsch, MA Mall - Chest, 2018 - Elsevier
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance
regulator (CFTR) gene and remains one of the most common life-shortening genetic …

CFTR: cystic fibrosis and beyond

MA Mall, D Hartl - 2014 - Eur Respiratory Soc
Cystic fibrosis (CF) remains the most common fatal hereditary lung disease. The discovery of
the cystic fibrosis transmembrane conductance regulator (CFTR) gene 25 years ago set the …

Optimization of Normal Human Bronchial Epithelial (NHBE) Cell 3D Cultures for in vitro Lung Model Studies

RE Rayner, P Makena, GL Prasad, E Cormet-Boyaka - Scientific reports, 2019 - nature.com
Robust in vitro lung models are required for risk assessment to measure key events leading
to respiratory diseases. Primary normal human bronchial epithelial cells (NHBE) represent a …

Airway mucus, inflammation and remodeling: emerging links in the pathogenesis of chronic lung diseases

Z Zhou-Suckow, J Duerr, M Hagner, R Agrawal… - Cell and tissue …, 2017 - Springer
Airway mucus obstruction is a hallmark of many chronic lung diseases including rare genetic
disorders such as cystic fibrosis (CF) and primary ciliary dyskinesia, as well as common lung …

At the root: defining and halting progression of early chronic obstructive pulmonary disease

FJ Martinez, MLK Han, JP Allinson, RG Barr… - American journal of …, 2018 - atsjournals.org
Chronic obstructive pulmonary disease (COPD) is a prevalent, heterogeneous disorder with
varying presentation and progression but with a limited number of disease-modifying …

Airway epithelium dysfunction in cystic fibrosis and COPD

V De Rose, K Molloy, S Gohy, C Pilette… - Mediators of …, 2018 - Wiley Online Library
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 …

Clinical issues of mucus accumulation in COPD

FL Ramos, JS Krahnke, V Kim - International journal of chronic …, 2014 - Taylor & Francis
Airway mucus is part of the lung's native immune function that traps particulates and
microorganisms, enabling their clearance from the lung by ciliary transport and cough …