Favia M - Search Results

1

Trimethylangelicin reduces IL-8 transcription and potentiates CFTR function.

Tamanini A, Borgatti M, Finotti A, Piccagli L, Bezzerri V, Favia M, Guerra L, Lampronti I, Bianchi N, Dall'Acqua F, Vedaldi D, Salvador A, Fabbri E, Mancini I, Nicolis E, Casavola V, Cabrini G, Gambari R. Tamanini A, et al. Among authors: favia m. Am J Physiol Lung Cell Mol Physiol. 2011 Mar;300(3):L380-90. doi: 10.1152/ajplung.00129.2010. Epub 2010 Dec 10. Am J Physiol Lung Cell Mol Physiol. 2011. PMID: 21148790 Free article.

2

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. 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.

3

CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity.

Monterisi S, Favia M, Guerra L, Cardone RA, Marzulli D, Reshkin SJ, Casavola V, Zaccolo M. Monterisi S, et al. Among authors: favia m. J Cell Sci. 2012 Mar 1;125(Pt 5):1106-17. doi: 10.1242/jcs.089086. Epub 2012 Feb 2. J Cell Sci. 2012. PMID: 22302988 Free PMC article.

4

NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: role of ezrin and the RhoA/ROCK pathway.

Castellani S, Guerra L, Favia M, Di Gioia S, Casavola V, Conese M. Castellani S, et al. Among authors: favia m. Lab Invest. 2012 Nov;92(11):1527-40. doi: 10.1038/labinvest.2012.123. Epub 2012 Sep 10. Lab Invest. 2012. PMID: 22964850 Free article.

5

Pseudomonas aeruginosa reduces the expression of CFTR via post-translational modification of NHERF1.

Rubino R, Bezzerri V, Favia M, Facchini M, Tebon M, Singh AK, Riederer B, Seidler U, Iannucci A, Bragonzi A, Cabrini G, Reshkin SJ, Tamanini A. Rubino R, et al. Among authors: favia m. Pflugers Arch. 2014 Dec;466(12):2269-78. doi: 10.1007/s00424-014-1474-6. Epub 2014 Mar 5. Pflugers Arch. 2014. PMID: 24595473

6

Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

Atlante A, Favia M, Bobba A, Guerra L, Casavola V, Reshkin SJ. Atlante A, et al. Among authors: favia m. J Bioenerg Biomembr. 2016 Jun;48(3):197-210. doi: 10.1007/s10863-016-9663-y. Epub 2016 May 5. J Bioenerg Biomembr. 2016. PMID: 27146408

7

Na+/H+ exchanger regulatory factor isoform 1 overexpression modulates cystic fibrosis transmembrane conductance regulator (CFTR) expression and activity in human airway 16HBE14o- cells and rescues DeltaF508 CFTR functional expression in cystic fibrosis cells.

Guerra L, Fanelli T, Favia M, Riccardi SM, Busco G, Cardone RA, Carrabino S, Weinman EJ, Reshkin SJ, Conese M, Casavola V. Guerra L, et al. Among authors: favia m. J Biol Chem. 2005 Dec 9;280(49):40925-33. doi: 10.1074/jbc.M505103200. Epub 2005 Oct 3. J Biol Chem. 2005. PMID: 16203733 Free article.

8

Beta-oestradiol rescues DeltaF508CFTR functional expression in human cystic fibrosis airway CFBE41o- cells through the up-regulation of NHERF1.

Fanelli T, Cardone RA, Favia M, Guerra L, Zaccolo M, Monterisi S, De Santis T, Riccardi SM, Reshkin SJ, Casavola V. Fanelli T, et al. Among authors: favia m. Biol Cell. 2008 Jul;100(7):399-412. doi: 10.1042/BC20070095. Biol Cell. 2008. PMID: 18184109

9

Na+/H+ exchanger regulatory factor 1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del cystic fibrosis transmembrane conductance regulator in human airway CFBE41o- cells.

Favia M, Guerra L, Fanelli T, Cardone RA, Monterisi S, Di Sole F, Castellani S, Chen M, Seidler U, Reshkin SJ, Conese M, Casavola V. Favia M, et al. Mol Biol Cell. 2010 Jan 1;21(1):73-86. doi: 10.1091/mbc.e09-03-0185. Epub 2009 Nov 4. Mol Biol Cell. 2010. PMID: 19889841 Free PMC article.

10

Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.

Carbone A, Castellani S, Favia M, Diana A, Paracchini V, Di Gioia S, Seia M, Casavola V, Colombo C, Conese M. Carbone A, et al. Among authors: favia m. J Cell Mol Med. 2014 Aug;18(8):1631-43. doi: 10.1111/jcmm.12303. Epub 2014 Jun 3. J Cell Mol Med. 2014. PMID: 24894806 Free PMC article.

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