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Items: 1 to 20 of 602

1.

Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.

Li C, Naren AP.

Pharmacol Ther. 2005 Nov;108(2):208-23. Epub 2005 Jun 2. Review.

PMID:
15936089
2.

Analysis of CFTR interactome in the macromolecular complexes.

Li C, Naren AP.

Methods Mol Biol. 2011;741:255-70. doi: 10.1007/978-1-61779-117-8_17.

3.

The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane.

Moyer BD, Duhaime M, Shaw C, Denton J, Reynolds D, Karlson KH, Pfeiffer J, Wang S, Mickle JE, Milewski M, Cutting GR, Guggino WB, Li M, Stanton BA.

J Biol Chem. 2000 Sep 1;275(35):27069-74.

4.

Functional expression and apical localization of the cystic fibrosis transmembrane conductance regulator in MDCK I cells.

Mohamed A, Ferguson D, Seibert FS, Cai HM, Kartner N, Grinstein S, Riordan JR, Lukacs GL.

Biochem J. 1997 Feb 15;322 ( Pt 1):259-65.

5.

Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.

Stanton BA.

Wien Klin Wochenschr. 1997 Jun 27;109(12-13):457-64. Review.

PMID:
9261986
6.

Molecular studies of CFTR interacting proteins.

Wang S, Li M.

Pflugers Arch. 2001;443 Suppl 1:S62-4. Epub 2001 Sep 26. Review.

PMID:
11845305
7.
8.

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.

J Biol Chem. 2005 Dec 9;280(49):40925-33. Epub 2005 Oct 3.

9.

Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.

Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C.

Hepatology. 1999 Jun;29(6):1624-34.

PMID:
10347100
10.

What we know and what we do not know about cystic fibrosis transmembrane conductance regulator.

Ma J, Davis PB.

Clin Chest Med. 1998 Sep;19(3):459-71, v-vi. Review.

PMID:
9759549
11.

The role of the C terminus and Na+/H+ exchanger regulatory factor in the functional expression of cystic fibrosis transmembrane conductance regulator in nonpolarized cells and epithelia.

Benharouga M, Sharma M, So J, Haardt M, Drzymala L, Popov M, Schwapach B, Grinstein S, Du K, Lukacs GL.

J Biol Chem. 2003 Jun 13;278(24):22079-89. Epub 2003 Mar 21.

12.

The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions.

Vankeerberghen A, Cuppens H, Cassiman JJ.

J Cyst Fibros. 2002 Mar;1(1):13-29. Review.

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17.

PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator.

Swiatecka-Urban A, Duhaime M, Coutermarsh B, Karlson KH, Collawn J, Milewski M, Cutting GR, Guggino WB, Langford G, Stanton BA.

J Biol Chem. 2002 Oct 18;277(42):40099-105. Epub 2002 Aug 7.

18.

Interregulation of proton-gated Na(+) channel 3 and cystic fibrosis transmembrane conductance regulator.

Su X, Li Q, Shrestha K, Cormet-Boyaka E, Chen L, Smith PR, Sorscher EJ, Benos DJ, Matalon S, Ji HL.

J Biol Chem. 2006 Dec 1;281(48):36960-8. Epub 2006 Sep 29.

19.

Genetic disorders of membrane transport. II. Regulation of CFTR by small molecules including HCO3-.

Illek B, Fischer H, Machen TE.

Am J Physiol. 1998 Dec;275(6 Pt 1):G1221-6. Review.

PMID:
9843756
20.

CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.

Li C, Naren AP.

Integr Biol (Camb). 2010 Apr;2(4):161-77. doi: 10.1039/b924455g. Epub 2010 Mar 5. Review.

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