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Trimethylangelicin promotes the functional rescue of mutant F508del CFTR protein in cystic fibrosis airway cells.
Am J Physiol Lung Cell Mol Physiol. 2014 Jul 1;307(1):L48-61. doi: 10.1152/ajplung.00305.2013. Epub 2014 May 9.
Am J Physiol Lung Cell Mol Physiol. 2014.
PMID: 24816489
Free article.
Emerging relationship between CFTR, actin and tight junction organization in cystic fibrosis airway epithelium.
Castellani S, Favia M, Guerra L, Carbone A, Abbattiscianni AC, Di Gioia S, Casavola V, Conese M.
Castellani S, et al. Among authors: abbattiscianni ac.
Histol Histopathol. 2017 May;32(5):445-459. doi: 10.14670/HH-11-842. Epub 2016 Nov 11.
Histol Histopathol. 2017.
PMID: 27834058
Review.
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Correctors of mutant CFTR enhance subcortical cAMP-PKA signaling through modulating ezrin phosphorylation and cytoskeleton organization.
Abbattiscianni AC, Favia M, Mancini MT, Cardone RA, Guerra L, Monterisi S, Castellani S, Laselva O, Di Sole F, Conese M, Zaccolo M, Casavola V.
Abbattiscianni AC, et al.
J Cell Sci. 2016 Mar 15;129(6):1128-40. doi: 10.1242/jcs.177907. Epub 2016 Jan 28.
J Cell Sci. 2016.
PMID: 26823603
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