Emanuela Caci

Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel.

Diego di Bernardo, Francesco Sirci, Diego Carrella, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening.

Kai Du, Nicoletta Pedemonte, A S Verkman, 2005, The Journal of clinical investigation.

TMEM16A, A Membrane Protein Associated with Calcium-Dependent Chloride Channel Activity

Roberto Ravazzolo, Ulrich Pfeffer, Nicoletta Pedemonte, 2008, Science.

Dual Activity of Aminoarylthiazoles on the Trafficking and Gating Defects of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Caused by Cystic Fibrosis Mutations*

Gianluca Damonte, Andrea Armirotti, Nicoletta Pedemonte, 2011, The Journal of Biological Chemistry.

Correction of G551D‐CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB‐07

C. Folli, L. Galietta, G. Cabrini, 2002, British journal of pharmacology.