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 1-20    21-32 
1.
Type II protein kinase a regulates CFTR in airway, parcreatic, and intestinal cells // Amer. J. Physiol., 1998. Vol. 274, N 3.-С.C819-C826

2.
The cystic fibrosis transmembrane regulator is present and functional in endosomes // J. Biol. Chem., 1992. Vol. 267, N 21.-С.14568-14572

3.
The cystic fibrosis transmembrane conductance regulator Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide // J. Biol. Chem., 1992. Vol. 267, N 9.-С.5727-5730

4.
Darling Katharine E.A. Role of the cystic fibrosis transmembrane conductance regulator in internalization of Pseudomonas aeruginosa // Cell. Microbiol., 2004. Vol. 6, N 6.-С.521-533

5.
Darling Katharine E.A. Role of the cystic fibrosis transmembrane conductance regulator in internalization of Pseudomonas aeruginosa // Cell. Microbiol., 2004. Vol. 6, N 6.-С.521-533

6.
Anderson Matthew P. Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains // Science, 1992. Vol. 257, N 5074.-С.1701-1704

7.
Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR) // Cell, 1992. Vol. 68, N 4.-С.809-818

8.
Proinflammatory effect of sodium 4-phenylbutyrate in 'ДЕЛЬТА'F508-cystic fibrosis transmembrane conductance regulator lung epithelial cells: Involvement of extracellular signal-regulated protein kinase 1/2 and c-Jun-NH[2]-terminal kinase signaling // J. Pharmacol. and Exp. Ther., 2008. Vol. 326, N 3.-С.949-956

9.
Preclinical evaluation of AAV vectors expressing the human CFTR cDNA // J. Cell. Biochem., 1995, Suppl. 21a.-С.364

10.
Tyrakowski T. Prawidlowa i zaburzona funkcia kanalu chlorkowego CFTR - biocheviczna analiza mukowiscydozy... // Post. Biochem., 1993. Vol. 39, N 1.-С.25-32

11.
Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung // Proc. Nat. Acad. Sci. USA, 2001. Vol. 98, N 24.-С.13972-13977

12.
Intermolecular interaction between CFTR and other proteins // Pediat. Pulmonol., 1999, Suppl. 19.-С.86-87

13.
Influence of salinity on the localization of Na{+}/K{+}-ATPase, Na{+}/K{+}/2Cl{-} contrasporter (NKCC) and CFTR anion channel in chloride cells of the Hawaiian goby (Stenogobius hawaiiensis) // J. Exp. Biol., 2003. Vol. 206, N 24.-С.4575-4583

14.
In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium // Cell, 1992. Vol. 68, N 1.-С.143-155

15.
Functional classification of mitochondrion-rich cells in euryhaline Mozambique tilapia (Oreochromis mossambicus) embryos, by means of triple immunofluorescence staining for N{+}/K{+}-ATPase, Na{+}/K{+}/2Cl{-} cotransporter and CFTR anion channel // J. Exp. Biol., 2005. Vol. 208, N 11.-С.2023-2036

16.
Dilda Functional characterization of CFTR in apical membranes purified from bovine tracheal epithelium // Pediat. Pulmonol., 1993, Suppl. N9.-С.228-229

17.
Loffing Exocytosis is not involved in activation of Cl{-} secretion via CFTR in Calu-3 airway epithelial cells // Amer. J. Physiol., 1998. Vol. 275, N 4.-С.C913-C920

18.
Defective CFTR increases synthesis and mass of sphingolipids that modulate membrane composition and lipid signaling // J. Lipid Res., 2009. Vol. 50, N 6.-С.1101-1108

19.
Cystic fibrosis transmembrane conductance regulator regulates luminal Cl{-}/CHO[3]{+} exchange in mouse submandibular and pancreatic ducts // J. Biol. Chem., 1999. Vol. 274, N 21.-С.14670-24677

20.
Cyclic AMP-dependent protein kinase activation of cystic fibrosis transmembrane conductance regulator chloride channelss in plannar lipid bilayers // J. Biol. Chem, 1992. Vol. 267, N 14.-С.9470-9473

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