Giulia Prono
YOU?
Author Swipe
View article: CFTR Modulator Therapy for Rare CFTR Mutants
CFTR Modulator Therapy for Rare CFTR Mutants Open
Cystic fibrosis (CF), the most common genetic disease among the Caucasian population, is caused by mutations in the gene encoding for the CF transmembrane conductance regulator (CFTR), a chloride epithelial channel whose dysfunction result…
View article: Role of Protein Kinase A-Mediated Phosphorylation in CFTR Channel Activity Regulation
Role of Protein Kinase A-Mediated Phosphorylation in CFTR Channel Activity Regulation Open
Cystic fibrosis transmembrane conductance regulator (CFTR) is an anion channel expressed on the apical membrane of epithelial cells, where it plays a pivotal role in chloride transport and overall tissue homeostasis. CFTR constitutes a uni…
View article: Dysfunctional Inflammation in Cystic Fibrosis Airways: From Mechanisms to Novel Therapeutic Approaches
Dysfunctional Inflammation in Cystic Fibrosis Airways: From Mechanisms to Novel Therapeutic Approaches Open
Cystic fibrosis (CF) is an inherited disorder caused by mutations in the gene encoding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein, an ATP-gated chloride channel expressed on the apical surface of airway epit…