Galietta LJV - Search Results

1

Intrinsic Abnormalities of Cystic Fibrosis Airway Connective Tissue Revealed by an In Vitro 3D Stromal Model.

Mazio C, Scognamiglio LS, De Cegli R, Galietta LJV, Bernardo DD, Casale C, Urciuolo F, Imparato G, Netti PA. Mazio C, et al. Among authors: galietta ljv. Cells. 2020 Jun 1;9(6):1371. doi: 10.3390/cells9061371. Cells. 2020. PMID: 32492951 Free PMC article.

2

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

Tomati V, Caci E, Ferrera L, Pesce E, Sondo E, Cholon DM, Quinney NL, Boyles SE, Armirotti A, Ravazzolo R, Galietta LJ, Gentzsch M, Pedemonte N. Tomati V, et al. JCI Insight. 2018 Feb 8;3(3):e98699. doi: 10.1172/jci.insight.98699. eCollection 2018 Feb 8. JCI Insight. 2018. PMID: 29415893 Free PMC article.

3

Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells.

Scudieri P, Musante I, Venturini A, Guidone D, Genovese M, Cresta F, Caci E, Palleschi A, Poeta M, Santamaria F, Ciciriello F, Lucidi V, Galietta LJV. Scudieri P, et al. Among authors: galietta ljv. Cells. 2020 Sep 13;9(9):2090. doi: 10.3390/cells9092090. Cells. 2020. PMID: 32933106 Free PMC article.

4

Pharmacological approaches to cystic fibrosis.

Bandiera T, Galietta LJV. Bandiera T, et al. Among authors: galietta ljv. Eur J Med Chem. 2021 Apr 15;216:113240. doi: 10.1016/j.ejmech.2021.113240. Epub 2021 Jan 30. Eur J Med Chem. 2021. PMID: 33691259 No abstract available.

5

TMEM16A (ANO1) as a therapeutic target in cystic fibrosis.

Galietta LJV. Galietta LJV. Curr Opin Pharmacol. 2022 Jun;64:102206. doi: 10.1016/j.coph.2022.102206. Epub 2022 Mar 29. Curr Opin Pharmacol. 2022. PMID: 35364521 Review.

6

Airway surface hyperviscosity and defective mucociliary transport by IL-17/TNF-α are corrected by β-adrenergic stimulus.

Guidone D, Buccirossi M, Scudieri P, Genovese M, Sarnataro S, De Cegli R, Cresta F, Terlizzi V, Planelles G, Crambert G, Sermet I, Galietta LJ. Guidone D, et al. JCI Insight. 2022 Nov 22;7(22):e164944. doi: 10.1172/jci.insight.164944. JCI Insight. 2022. PMID: 36219481 Free PMC article.

7

Analysis of inhibitors of the anoctamin-1 chloride channel (transmembrane member 16A, TMEM16A) reveals indirect mechanisms involving alterations in calcium signalling.

Genovese M, Buccirossi M, Guidone D, De Cegli R, Sarnataro S, di Bernardo D, Galietta LJV. Genovese M, et al. Among authors: galietta ljv. Br J Pharmacol. 2023 Mar;180(6):775-785. doi: 10.1111/bph.15995. Epub 2022 Dec 18. Br J Pharmacol. 2023. PMID: 36444690 Free article.

8

Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.

Gianotti A, Melani R, Caci E, Sondo E, Ravazzolo R, Galietta LJ, Zegarra-Moran O. Gianotti A, et al. Am J Respir Cell Mol Biol. 2013 Sep;49(3):445-52. doi: 10.1165/rcmb.2012-0408OC. Am J Respir Cell Mol Biol. 2013. PMID: 23600628

9

Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel.

Pesce E, Gorrieri G, Sirci F, Napolitano F, Carrella D, Caci E, Tomati V, Zegarra-Moran O, di Bernardo D, Galietta LJ. Pesce E, et al. J Cyst Fibros. 2016 Jul;15(4):425-35. doi: 10.1016/j.jcf.2016.02.009. Epub 2016 Mar 10. J Cyst Fibros. 2016. PMID: 26971626 Free article.

10

High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel.

Tomati V, Pesce E, Caci E, Sondo E, Scudieri P, Marini M, Amato F, Castaldo G, Ravazzolo R, Galietta LJV, Pedemonte N. Tomati V, et al. Among authors: galietta ljv. J Biol Chem. 2018 Jan 26;293(4):1203-1217. doi: 10.1074/jbc.M117.816595. Epub 2017 Nov 20. J Biol Chem. 2018. PMID: 29158263 Free PMC article.

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