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Biomolecules|February 25, 2022
SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung DiseaseGiulia Gorrieri, Federico Zara, Paolo ScudieriBiomolecules|October 28, 2023
ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory DiseasesMichał Dębczyński, Giulia Gorrieri, Damian Mojsak, et al.Frontiers in Cell and Developmental Biology|February 16, 2026
Alternative splicing regulates PACC1 function and promotes acidosis-induced cytotoxicitySerena Tamburro, Giulia Gorrieri, Niccolò Callegari, et al.Stem Cell Research|February 13, 2024
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutationsGiulia Gorrieri, Serena Tamburro, Simona Baldassari, et al.Stem Cell Research|October 21, 2023
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutationMichał Dębczyński, Damian Mojsak, Serena Tamburro, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 15, 2016
Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channelEmanuela Pesce, Giulia Gorrieri, Francesco Sirci, et al.Neurobiology of Disease|December 1, 2025
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitorsIlaria Musante, Giulia Gorrieri, Serena Tamburro, et al.Scientific Reports|October 28, 2016
Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin ReleaseGiulia Gorrieri, Paolo Scudieri, Emanuela Caci, et al.Pageof 1