Electrochemical measurement of membrane cholesterol correlates with CFTR function and is HDAC6-dependent
Age-Related differences in Dental Caries and Associated Risk Factors in Individuals with Cystic Fibrosis Ages 6-20 years: A Pilot Study
A Specialized Method of Sputum Collection and Processing for Therapeutic Interventions in Cystic Fibrosis
Characteristics and outcomes of oral antibiotic treated pulmonary exacerbations in children with cystic fibrosis.
RNA sequencing data from neutrophils of patients with cystic fibrosis reveals potential for developing biomarkers for pulmonary exacerbations
Combination potentiator ('co-potentiator') therapy for CF caused by CFTR mutants, including N1303K, that are poorly responsive to single potentiators.
Continuous glucose monitoring guided insulin therapy is associated with improved clinical outcomes in cystic fibrosis-related diabetes.
