Area of research
Pulmonary and Respiratory Medicine · Physiology
Research interest
Research interests include Cystic Fibrosis Research Advances, Neonatal Respiratory Health Research, Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis, and Asthma and respiratory diseases.
Changes in sputum viscoelastic properties and airway inflammation in primary ciliary dyskinesia are comparable to cystic fibrosis on elexacaftor/tezacaftor/ivacaftor therapy
Reduction of systemic inflammation by elexacaftor/tezacaftor/ivacaftor correlates with lung function improvement in cystic fibrosis
Longitudinal effects of elexacaftor/tezacaftor/ivacaftor on sputum viscoelastic properties, airway infection and inflammation in patients with cystic fibrosis
Personalized CFTR Modulator Therapy for G85E and N1303K Homozygous Patients with Cystic Fibrosis
A novel thiol-saccharide mucolytic for the treatment of muco-obstructive lung diseases
Antibiotic use during pregnancy is linked to offspring gut microbial dysbiosis, barrier disruption, and altered immunity along the gut–lung axis
An optimized protocol for assessment of sputum macrorheology in health and muco-obstructive lung disease
Congenital Deletion of Nedd4-2 in Lung Epithelial Cells Causes Progressive Alveolitis and Pulmonary Fibrosis in Neonatal Mice
Linking Fibrotic Remodeling and Ultrastructural Alterations of Alveolar Epithelial Cells after Deletion of Nedd4-2
Conditional deletion of Nedd4-2 in lung epithelial cells causes progressive pulmonary fibrosis in adult mice
Development of pulmonary fibrosis in conditional Nedd4-2 deficient mice
Dephasing and diffusion on the alveolar surface
SLC26A9-mediated chloride secretion prevents mucus obstruction in airway inflammation