Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Teresa Fanelli"'
Autor:
Stefania Maria Riccardi, Stephan J. Reshkin, Rosa Angela Cardone, Valeria Casavola, Manuela Zaccolo, Maria Favia, Teresa De Santis, Stefania Monterisi, Teresa Fanelli, Lorenzo Guerra
Publikováno v:
Biology of the Cell. 100:399-412
BACKGROUND INFORMATION: CF (cystic fibrosis) is a disease caused by mutations within the CFTR (CF transmembrane conductance regulator) gene. The most common mutation, DeltaF508 (deletion of Phe-508), results in a protein that is defective in folding
Autor:
Stephan J. Reshkin, Salvatore Carrabino, Valeria Casavola, Stefania Maria Riccardi, Rosa Angela Cardone, Giovanni Busco, Edward J. Weinman, Maria Favia, Massimo Conese, Teresa Fanelli, Lorenzo Guerra
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2005, 280 (49), pp.40925-40933. ⟨10.1074/jbc.M505103200⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2005, 280 (49), pp.40925-40933. ⟨10.1074/jbc.M505103200⟩
There is evidence that cystic fibrosis transmembrane conductance regulator (CFTR) interacting proteins play critical roles in the proper expression and function of CFTR. The Na(+)/H(+) exchanger regulatory factor isoform 1 (NHERF1) was the first iden
Autor:
Stephan J. Reshkin, Lorenzo Guerra, Heini Murer, Valeria Casavola, Rosa Angela Cardone, Serge M. Gisler, Anna Bagorda, Teresa Fanelli, Francesca Di Sole, Corinna Hemle-Kolb
Publikováno v:
Journal of Biological Chemistry. 277:21480-21488
Although Cystic fibrosis transmembrane conductance regulator (CFTR) has been shown to regulate the activity of NHE3, the potential reciprocal interaction of NHE3 to modulate the protein kinase A (PKA)-dependent regulation of CFTR in epithelial cells
Autor:
Stefania Monterisi, Francesca Di Sole, Rosa Angela Cardone, Maria Favia, Stephan J. Reshkin, Ursula Seidler, Valeria Casavola, Massimo Conese, Teresa Fanelli, Stefano Castellani, Mingmin Chen, Lorenzo Guerra
Publikováno v:
Molecular Biology of the Cell
NHERF1 overexpression increases functional apical expression of F508del CFTR in CFBE41o- cells. Here, we show that this occurs via the formation of the multiprotein complex NHERF1-phosphoezrin-actin, which provides a regulated linkage between F508del
Autor:
Sj Reshkin, Manuela Zaccolo, Teresa Fanelli, Maria Favia, S. Monterisi, Lorenzo Guerra, Valeria Casavola, Massimo Conese
Publikováno v:
Journal of Cystic Fibrosis. 7
Autor:
P. G. Suh, F. Di Sole, Teresa Fanelli, Maria Favia, Anna Bagorda, Stephan J. Reshkin, Valeria Casavola, Lorenzo Guerra
Publikováno v:
Biochemical and biophysical research communications. 347(2)
It has been shown that when CFTR and NHE3 are co-expressed on the apical membrane of the A6-NHE3 cell monolayers, the two transporters interact via a shared regulatory complex composed of NHERF2, ezrin, and PKA. We observe here that co-expression of
Autor:
Anna Bagorda, Stephan J. Reshkin, Valeria Casavola, Maria Svelto, K. A. Jacobson, Teresa Fanelli, Giuseppe Calamita, Maria Favia, Lorenzo Guerra
Publikováno v:
Pflugers Archiv : European journal of physiology. 449(1)
Nucleotide binding to purinergic P2Y receptors contributes to the regulation of a variety of physiological functions in renal epithelial cells. Here, we investigate the regulatory mechanism of the P2Y1 receptor agonist 2-methylthioadenosine diphospha
Autor:
R.A. Cardone, Sj Reshkin, Teresa Fanelli, S.M. Riccardi, Maria Favia, Massimo Conese, Valeria Casavola, Lorenzo Guerra
Publikováno v:
Journal of Cystic Fibrosis. 7:S18-S19
Autor:
Lorenzo Guerra, R.A. Cardone, S.M. Riccardi, G. Busco, Maria Favia, S. Carrabino, Massimo Conese, Teresa Fanelli, Valeria Casavola, Sj Reshkin
Publikováno v:
Journal of Cystic Fibrosis. 6:S7
Autor:
Teresa Fanelli, Rosa Angela Cardone, Maria Favia, Lorenzo Guerra, Manuela Zaccolo, Stefania Monterisi, Teresa De santis, Stefania Maria Riccardi, Stephan Joel Reshkin, Valeria Casavola
Publikováno v:
Biology of the Cell (Wiley-Blackwell); 2008, Vol. 100 Issue 7, p399-412, 14p