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Frontiers in Pharmacology|November 13, 2018
<i>In vitro</i> Methods for the Development and Analysis of Human Primary Airway EpitheliaAmbra Gianotti, Livia Delpiano, Emanuela CaciBiology|April 3, 2021
The Application of Bicarbonate Recovers the Chemical-Physical Properties of Airway Surface Liquid in Cystic Fibrosis Epithelia ModelsLoretta Ferrera, Valeria Capurro, Livia Delpiano, et al.Scientific Reports|December 9, 2016
Intermolecular Interactions in the TMEM16A Dimer Controlling Channel ActivityPaolo Scudieri, Ilaria Musante, Ambra Gianotti, et al.Biochimica Et Biophysica Acta|October 14, 2014
Functional analysis of acid-activated Cl⁻ channels: properties and mechanisms of regulationValeria Capurro, Ambra Gianotti, Emanuela Caci, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 19, 2015
Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucusAmbra Gianotti, Valeria Capurro, Paolo Scudieri, et al.American Journal of Respiratory Cell and Molecular Biology|April 23, 2013
Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosisAmbra Gianotti, Raffaella Melani, Emanuela Caci, et al.European Journal of Pharmacology|April 12, 2016
Pharmacological analysis of epithelial chloride secretion mechanisms in adult murine airwaysAmbra Gianotti, Loretta Ferrera, Amber R Philp, et al.JCI Insight|August 21, 2020
Lack of Kcnn4 improves mucociliary clearance in muco-obstructive lung diseaseGénesis Vega, Anita Guequén, Amber R Philp, et al.International Journal of Molecular Sciences|February 27, 2020
Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway EpitheliaAmbra Gianotti, Valeria Capurro, Livia Delpiano, et al.Physiological Genomics|June 6, 2022
KCa3.1 differentially regulates trachea and bronchi epithelial gene expression in a chronic-asthma mouse modelAmber R Philp, Fernando Miranda, Ambra Gianotti, et al.Pageof 2