oligonucleotide therapies for inherited childhood lung diseases
This study tested the utility of optical coherence tomography-based indentation to assess mechanical properties of respiratory tissues in disease
The study of the respiratory microbiota has revealed that the lungs of healthy and diseased individuals harbour distinct microbial communities. Imbal…
We identified numerous CpGs differentially methylated in relation to gestational age at birth that appear to reflect fetal developmental processes ac…
Non-invasive and sensitive clinical endpoints are needed to monitor onset and progression of early lung disease in children with cystic fibrosis (CF)…
Vitamin D deficiency exacerbates house dust mite-induced inflammation and alterations in lung structure and function
Idiopathic pulmonary fibrosis (IPF) is characterized by permanent scarring of lung tissue and declining lung function, and is an incurable disease wi…
PREDICT CF: Assessing the role of lung clearance index in predicting disease progression in children with
Surfactant, which was first identified in the 1920s, is pivotal to lower the surface tension in alveoli of the lungs and helps to lower the work of b…
Vitamin D deficiency affects lung growth and function