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Influenza matrix protein 2 alters CFTR expression and function through its ion channel activity. , Londino JD., Am J Physiol Lung Cell Mol Physiol. May 1, 2013; 304 (9): L582-92.
F508del- CFTR increases intracellular Ca(2+) signaling that causes enhanced calcium-dependent Cl(-) conductance in cystic fibrosis. , Martins JR., Biochim Biophys Acta. November 1, 2011; 1812 (11): 1385-92.
ERp29 regulates DeltaF508 and wild-type cystic fibrosis transmembrane conductance regulator ( CFTR) trafficking to the plasma membrane in cystic fibrosis (CF) and non-CF epithelial cells. , Suaud L., J Biol Chem. June 17, 2011; 286 (24): 21239-53.
An energy-dependent maturation step is required for release of the cystic fibrosis transmembrane conductance regulator from early endoplasmic reticulum biosynthetic machinery. , Oberdorf J., J Biol Chem. November 18, 2005; 280 (46): 38193-202.
Synergic action of insulin and genistein on Na+/K+/2Cl- cotransporter in renal epithelium. , Ueda-Nishimura T., Biochem Biophys Res Commun. July 15, 2005; 332 (4): 1042-52.
Cysteine string protein interacts with and modulates the maturation of the cystic fibrosis transmembrane conductance regulator. , Zhang H ., J Biol Chem. August 9, 2002; 277 (32): 28948-58.
Control of cystic fibrosis transmembrane conductance regulator expression by BAP31. , Lambert G., J Biol Chem. June 8, 2001; 276 (23): 20340-5.
Structural cues involved in endoplasmic reticulum degradation of G85E and G91R mutant cystic fibrosis transmembrane conductance regulator. , Xiong X., J Clin Invest. September 1, 1997; 100 (5): 1079-88.