Area of research
Pulmonary and Respiratory Medicine · Otorhinolaryngology
Research interest
Research interests include Cystic fibrosis, Medicine, Cystic fibrosis transmembrane conductance regulator, Pseudomonas aeruginosa, Mucociliary clearance, and Ivacaftor.
Hypoxia‐induced cystic fibrosis transmembrane conductance regulator dysfunction is a universal mechanism underlying reduced mucociliary transport in sinusitis
LPS decreases CFTR open probability and mucociliary transport through generation of reactive oxygen species
Improvement cues of lesion absorption using the adjuvant therapy of traditional Chinese medicine Qinbudan tablet for retreatment pulmonary tuberculosis with standard anti-tuberculosis regimen
Contribution of Short Chain Fatty Acids to the Growth of Pseudomonas aeruginosa in Rhinosinusitis
The impact of <i>Lactococcus lactis</i> (probiotic nasal rinse) co‐culture on growth of patient‐derived strains of <i>Pseudomonas aeruginosa</i>
<i>In‐vitro</i> evaluation of a ciprofloxacin and azithromycin sinus stent for <i>Pseudomonas aeruginosa</i> biofilms
Herbal dry extract BNO 1011 improves clinical and mucociliary parameters in a rabbit model of chronic rhinosinusitis
In‐vitro evaluation of a ciprofloxacin‐ and ivacaftor‐coated sinus stent against <i>Pseudomonas aeruginosa</i> biofilms
Controlled delivery of ciprofloxacin and ivacaftor via sinus stent in a preclinical model of <i>Pseudomonas</i> sinusitis
Ivacaftor, a Cystic Fibrosis Transmembrane Conductance Regulator Potentiator, Enhances Ciprofloxacin Activity Against <i>Pseudomonas aeruginosa</i>
Resveratrol and ivacaftor are additive G551D CFTR‐channel potentiators: therapeutic implications for cystic fibrosis sinus disease
<scp>l</scp>‐Methionine anti‐biofilm activity against <i>Pseudomonas aeruginosa</i> is enhanced by the cystic fibrosis transmembrane conductance regulator potentiator, ivacaftor
Submucosal gland mucus strand velocity is decreased in chronic rhinosinusitis
Characterization of primary rat nasal epithelial cultures in CFTR knockout rats as a model for CF sinus disease
Chlorogenic Acid Activates CFTR‐Mediated Cl<sup>–</sup> Secretion in Mice and Humans
Cystic fibrosis transmembrane conductance regulator activation by the solvent ethanol: implications for topical drug delivery
Porcine nasal epithelial cultures for studies of cystic fibrosis sinusitis
Comparison of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Ciliary Beat Frequency Activation by the CFTR Modulators Genistein, VRT-532, and UC<sub>CF</sub>-152 in Primary Sinonasal Epithelial Cultures
IP-10 Is a Potential Biomarker of Cystic Fibrosis Acute Pulmonary Exacerbations