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JCI Insight|October 19, 2018
Increased expression of ATP12A proton pump in cystic fibrosis airwaysPaolo Scudieri, Ilaria Musante, Emanuela Caci, et al.
The Journal of Physiology|September 19, 2012
Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasiaPaolo Scudieri, Emanuela Caci, Silvia Bruno, et al.
Frontiers in Pharmacology|January 9, 2019
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated MechanismEmanuela Pesce, Elvira Sondo, Loretta Ferrera, et al.
Plos One|June 30, 2015
Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial PyocyaninEmanuela Caci, Paolo Scudieri, Emma Di Carlo, 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.
Science Advances|March 5, 2020
Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channelNicoletta Pedemonte, Fabio Bertozzi, Emanuela Caci, et al.
International Journal of Molecular Sciences|February 13, 2026
Potential Link Between a Disruptive <i>CAPN6</i> Variant and Neurodevelopmental DisordersFrancesco Calì, Simone Treccarichi, Mirella Vinci, et al.
Human Mutation|March 10, 2019
Two CFTR mutations within codon 970 differently impact on the chloride channel functionalityFelice Amato, Paolo Scudieri, Ilaria Musante, et al.
Scientific Reports|May 10, 2023
Novel tricyclic pyrrolo-quinolines as pharmacological correctors of the mutant CFTR chloride channelMario Renda, Marilia Barreca, Anna Borrelli, et al.
Frontiers in Physiology|July 3, 2019
Normal Calcium-Activated Anion Secretion in a Mouse Selectively Lacking TMEM16A in Intestinal EpitheliumGénesis Vega, Anita Guequén, Malin E V Johansson, et al.
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