GORRIERI, GIULIA
GORRIERI, GIULIA
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory Diseases
2023-01-01 Debczynski, M.; Gorrieri, G.; Mojsak, D.; Guida, F.; Zara, F.; Scudieri, P.
Evaluation of a systems biology approach to identify pharmacological correctors of the mutant {CFTR} chloride channel
2016-01-01 Pesce, Emanuela; Gorrieri, Giulia; Sirci, Francesco; Napolitano, Francesco; Carrella, Diego; Caci, Emanuela; Tomati, Valeria; Zegarra-Moran, Olga; di Bernardo, Diego; Galietta, Luis J. V.
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation
2023-01-01 Debczynski, M.; Mojsak, D.; Tamburro, S.; Baldassari, S.; Musante, I.; Casciaro, R.; Ciciriello, F.; Zara, F.; Scudieri, P.; Gorrieri, G.
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations
2024-01-01 Gorrieri, Giulia; Tamburro, Serena; Baldassari, Simona; Guerrisi, Sara; Zara, Federico; Ricci, Emilia; Maria Cordelli, Duccio; Scudieri, Paolo; Musante, Ilaria
Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release
2016-01-01 Gorrieri, G; Scudieri, Paolo; Caci, E; Schiavon, M; Tomati, V; Sirci, F; Napolitano, F; Carrella, D; Gianotti, Ambra; Musante, Ilaria; Favia, M; Casavola, V; Guerra, L; Rea, F; Ravazzolo, Roberto; Di Bernardo, D; Galietta, LUIS JUAN VICENTE
SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung Disease
2022-01-01 Gorrieri, G.; Zara, F.; Scudieri, P.
TARGETING THE ATP12A PROTON PUMP PROVIDES NEW THERAPEUTIC OPPORTUNITIES FOR CYSTIC FIBROSIS
2025-05-23 Gorrieri, Giulia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory Diseases | 1-gen-2023 | Debczynski, M.; Gorrieri, G.; Mojsak, D.; Guida, F.; Zara, F.; Scudieri, P. | |
| Evaluation of a systems biology approach to identify pharmacological correctors of the mutant {CFTR} chloride channel | 1-gen-2016 | Pesce, Emanuela; Gorrieri, Giulia; Sirci, Francesco; Napolitano, Francesco; Carrella, Diego; Caci, Emanuela; Tomati, Valeria; Zegarra-Moran, Olga; di Bernardo, Diego; Galietta, Luis J. V. | |
| Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation | 1-gen-2023 | Debczynski, M.; Mojsak, D.; Tamburro, S.; Baldassari, S.; Musante, I.; Casciaro, R.; Ciciriello, F.; Zara, F.; Scudieri, P.; Gorrieri, G. | |
| Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations | 1-gen-2024 | Gorrieri, Giulia; Tamburro, Serena; Baldassari, Simona; Guerrisi, Sara; Zara, Federico; Ricci, Emilia; Maria Cordelli, Duccio; Scudieri, Paolo; Musante, Ilaria | |
| Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release | 1-gen-2016 | Gorrieri, G; Scudieri, Paolo; Caci, E; Schiavon, M; Tomati, V; Sirci, F; Napolitano, F; Carrella, D; Gianotti, Ambra; Musante, Ilaria; Favia, M; Casavola, V; Guerra, L; Rea, F; Ravazzolo, Roberto; Di Bernardo, D; Galietta, LUIS JUAN VICENTE | |
| SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung Disease | 1-gen-2022 | Gorrieri, G.; Zara, F.; Scudieri, P. | |
| TARGETING THE ATP12A PROTON PUMP PROVIDES NEW THERAPEUTIC OPPORTUNITIES FOR CYSTIC FIBROSIS | 23-mag-2025 | Gorrieri, Giulia |