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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.European Journal of Medicinal Chemistry|June 5, 2015
Synthesis and structure-activity relationship of aminoarylthiazole derivatives as correctors of the chloride transport defect in cystic fibrosisEmanuela Pesce, Marta Bellotti, Nara Liessi, 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.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.Scientific Reports|July 18, 2015
Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis MutationValeria Tomati, Elvira Sondo, Andrea Armirotti, 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.Journal of Medicinal Chemistry|September 18, 2020
Identification, Structure-Activity Relationship, and Biological Characterization of 2,3,4,5-Tetrahydro-1<i>H</i>-pyrido[4,3-<i>b</i>]indoles as a Novel Class of CFTR PotentiatorsNicoletta Brindani, Ambra Gianotti, Simone Giovani, et al.Science Translational Medicine|March 30, 2022
A PI3Kγ mimetic peptide triggers CFTR gating, bronchodilation, and reduced inflammation in obstructive airway diseasesAlessandra Ghigo, Alessandra Murabito, Valentina Sala, et al.Pageof 2