2024; 23:s114.
. 208 Impact of diesel exhaust particles on cystic fibrosis lung disease. Journal of Cystic Fibrosis.2024; 23:s110.
. 198 Neutrophil extracellular traps increase Pseudomonal density in human bronchial epithelia. Journal of Cystic Fibrosis.2024; 97:76.
. HYPER-LOCALIZATION AND PREDICTIVE MODELING OF RAPID CYSTIC FIBROSIS DISEASE PROGRESSION. Annals of Epidemiology.2024; 23:s173-s174.
. 327 Comparison of human nasal and fisher rat thyroid cell-based theratyping results. Journal of Cystic Fibrosis.Quantifying abnormal alveolar microstructure in cystic fibrosis lung disease via hyperpolarized 129Xe diffusion MRI. Journal of Cystic Fibrosis. 2024; 23:926-935.
.A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptoms. Pediatric Pulmonology. 2024; 59:229-232.
.Taylor & Francis; Taylor & Francis; 2023.
. Upper Airway Disease in Cystic Fibrosis. Hodson and Geddes' Cystic Fibrosis. :2023; 22:s89.
. 168 Impact of TGF-β exposure on IL-6 secretion in cystic fibrosis airway epithelia. Journal of Cystic Fibrosis.2023; 22:s51.
. 98 Neutrophil extracellular traps disrupt bronchial epithelial junctional integrity and promote infection. Journal of Cystic Fibrosis.Gradual increase in sweat chloride concentration is associated with a higher risk of CRMS/CFSPID to CF reclassification. Pediatric Pulmonology. 2023; 58:1074-1084.
.Alpha-1 antitrypsin limits neutrophil extracellular trap disruption of airway epithelial barrier function. Frontiers in Immunology. 2023; 13:1023553.
.Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection. International Journal of Molecular Sciences. 2023; 24:1246.
.Novel Applications of Biomarkers and Personalized Medicine in Cystic Fibrosis. Clinics in Chest Medicine. 2022; 43:617-630.
.2022; 21:s336.
. 606 Focused clinical trials of modulator response for rare cystic fibrosis genotypes. Journal of Cystic Fibrosis.2022; 21:s223.
. 380 Neutrophil extracellular traps disrupt bronchial epithelial barrier function: Alpha-1 antitrypsin to the rescue. Journal of Cystic Fibrosis.2022; 21:s373.
. 683 Characteristics of cystic fibrosis transmembrane conductance regulator modulator response in nasal cell models derived from patients with rare cystic fibrosis transmembrane conductance regulator variants. Journal of Cystic Fibrosis.CRISPRi links COVID-19 GWAS loci to LZTFL1 and RAVER1. EBioMedicine. 2022; 75:103806.
.When CFSPID becomes CF. Journal of Cystic Fibrosis. 2022; 21:e23-e27.
.Rapid cystic fibrosis lung-function decline and in-vitro CFTR modulation. Journal of Cystic Fibrosis. 2021; 20:e69-e71.
.Pediatric flexible airway endoscopy training during a pandemic and beyond: Bending the curve. Pediatric Pulmonology. 2021; 56:1386-1388.
.Patient personalized translational tools in cystic fibrosis to transform data from bench to bed-side and back. American Journal of Physiology: Gastrointestinal and Liver Physiology. 2021; 320:G1123-G1130.
.Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis. International Journal of Molecular Sciences. 2021; 22:4448.
.Flexible Bronchoscopic Thrombus Cryoextraction in a Neonate on Extracorporeal Membrane Oxygenation. American Journal of Respiratory and Critical Care Medicine. 2021; 203:633-635.
.Neutrophil extracellular traps activate IL-8 and IL-1 expression in human bronchial epithelia. American Journal of Physiology: Lung Cellular and Molecular Physiology. 2020; 319:L137-L147.
.2020; 19:s113-s114.
. P203 Media impact on phenotype and function of an established airway epithelial cell line. Journal of Cystic Fibrosis.CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regions. NAR Genomics and Bioinformatics. 2020; 2:lqaa036.
.2020; 158:s-555.
. Su1243 BENCH TO BED-SIDE AND BACK TRANSLATION IN CF USING PATIENT-DERIVED STEM-CELL BASED MODEL SYSTEMS. Gastroenterology.