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Emerging relationship between CFTR, actin and tight junction organization in cystic fibrosis airway epithelium.
Histol Histopathol. 2017 May;32(5):445-459. doi: 10.14670/HH-11-842. Epub 2016 Nov 11.
Histol Histopathol. 2017.
PMID: 27834058
Review.
Trimethylangelicin promotes the functional rescue of mutant F508del CFTR protein in cystic fibrosis airway cells.
Favia M, Mancini MT, Bezzerri V, Guerra L, Laselva O, Abbattiscianni AC, Debellis L, Reshkin SJ, Gambari R, Cabrini G, Casavola V.
Favia M, et al. Among authors: abbattiscianni ac.
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.
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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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