Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release by Gorrieri, Giulia, Scudieri, Paolo, Caci, Emanuela, Schiavon, Marco, Tomati, Valeria, Sirci, Francesco, Napolitano, Francesco, Carrella, Diego, Gianotti, Ambra, Musante, Ilaria, Favia, Maria, Casavola, Valeria, Guerra, Lorenzo, Rea, Federico, Ravazzolo, Roberto, Di Bernardo, Diego, Galietta, Luis J. V.

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SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung Disease by Gorrieri, Giulia, Zara, Federico, Scudieri, Paolo

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Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations by Gorrieri, Giulia, Tamburro, Serena, Baldassari, Simona, Guerrisi, Sara, Zara, Federico, Ricci, Emilia, Maria Cordelli, Duccio, Scudieri, Paolo, Musante, Ilaria

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ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory Diseases by Dębczyński, Michał, Gorrieri, Giulia, Mojsak, Damian, Guida, Floriana, Zara, Federico, Scudieri, Paolo

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Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation by Dębczyński, Michał, Mojsak, Damian, Tamburro, Serena, Baldassari, Simona, Musante, Ilaria, Casciaro, Rosaria, Ciciriello, Fabiana, Zara, Federico, Scudieri, Paolo, Gorrieri, Giulia

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Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel by Pesce, Emanuela, Gorrieri, Giulia, Sirci, Francesco, Napolitano, Francesco, Carrella, Diego, Caci, Emanuela, Tomati, Valeria, Zegarra-Moran, Olga, di Bernardo, Diego, Galietta, Luis J.V

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Microencapsulation of astaxanthin by ionic gelation: effect of different gelling polymers on the carotenoid load, stability and bioaccessibility by Vakarelova, Martina, Zanoni, Francesca, Donà, Giulia, Fierri, Ilaria, Chignola, Roberto, Gorrieri, Sara, Zoccatelli, Gianni

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