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Items: 1 to 20 of 101

1.

The role of regulated CFTR trafficking in epithelial secretion.

Bertrand CA, Frizzell RA.

Am J Physiol Cell Physiol. 2003 Jul;285(1):C1-18. Review.

2.

The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.

Swiatecka-Urban A, Brown A, Moreau-Marquis S, Renuka J, Coutermarsh B, Barnaby R, Karlson KH, Flotte TR, Fukuda M, Langford GM, Stanton BA.

J Biol Chem. 2005 Nov 4;280(44):36762-72. Epub 2005 Aug 30.

3.

Trafficking of GFP-tagged DeltaF508-CFTR to the plasma membrane in a polarized epithelial cell line.

Loffing-Cueni D, Loffing J, Shaw C, Taplin AM, Govindan M, Stanton CR, Stanton BA.

Am J Physiol Cell Physiol. 2001 Dec;281(6):C1889-97.

4.

Cysteine string protein interacts with and modulates the maturation of the cystic fibrosis transmembrane conductance regulator.

Zhang H, Peters KW, Sun F, Marino CR, Lang J, Burgoyne RD, Frizzell RA.

J Biol Chem. 2002 Aug 9;277(32):28948-58. Epub 2002 May 30.

5.

Intracellular CFTR: localization and function.

Bradbury NA.

Physiol Rev. 1999 Jan;79(1 Suppl):S175-91. Review.

6.

Non-conventional trafficking of the cystic fibrosis transmembrane conductance regulator through the early secretory pathway.

Yoo JS, Moyer BD, Bannykh S, Yoo HM, Riordan JR, Balch WE.

J Biol Chem. 2002 Mar 29;277(13):11401-9. Epub 2002 Jan 17.

7.

Regulated trafficking of the CFTR chloride channel.

Kleizen B, Braakman I, de Jonge HR.

Eur J Cell Biol. 2000 Aug;79(8):544-56. Review.

PMID:
11001491
8.

Endosomal SNARE proteins regulate CFTR activity and trafficking in epithelial cells.

Bilan F, Nacfer M, Fresquet F, Norez C, Melin P, Martin-Berge A, Costa de Beauregard MA, Becq F, Kitzis A, Thoreau V.

Exp Cell Res. 2008 Jul 1;314(11-12):2199-211. doi: 10.1016/j.yexcr.2008.04.012. Epub 2008 May 4.

PMID:
18570918
9.

The cystic fibrosis transmembrane conductance regulator and its function in epithelial transport.

Kunzelmann K.

Rev Physiol Biochem Pharmacol. 1999;137:1-70. Review.

PMID:
10207304
10.

A domain mimic increases DeltaF508 CFTR trafficking and restores cAMP-stimulated anion secretion in cystic fibrosis epithelia.

Clarke LL, Gawenis LR, Hwang TC, Walker NM, Gruis DB, Price EM.

Am J Physiol Cell Physiol. 2004 Jul;287(1):C192-9. Epub 2004 Mar 17.

11.

Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator.

Kunzelmann K, Nitschke R.

Exp Nephrol. 2000 Nov-Dec;8(6):332-42. Review.

PMID:
11014930
12.

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.

13.

Syntaxin 8 impairs trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) and inhibits its channel activity.

Bilan F, Thoreau V, Nacfer M, Dérand R, Norez C, Cantereau A, Garcia M, Becq F, Kitzis A.

J Cell Sci. 2004 Apr 15;117(Pt 10):1923-35. Epub 2004 Mar 23.

14.

TGFbeta down-regulation of the CFTR: a means to limit epithelial chloride secretion.

Howe KL, Wang A, Hunter MM, Stanton BA, McKay DM.

Exp Cell Res. 2004 Aug 15;298(2):473-84.

PMID:
15265695
15.

Pseudomonas aeruginosa inhibits endocytic recycling of CFTR in polarized human airway epithelial cells.

Swiatecka-Urban A, Moreau-Marquis S, Maceachran DP, Connolly JP, Stanton CR, Su JR, Barnaby R, O'toole GA, Stanton BA.

Am J Physiol Cell Physiol. 2006 Mar;290(3):C862-72. Epub 2005 Oct 19.

16.

Establishment and characterization of a novel polarized MDCK epithelial cellular model for CFTR studies.

Mendes F, Wakefield J, Bachhuber T, Barroso M, Bebok Z, Penque D, Kunzelmann K, Amaral MD.

Cell Physiol Biochem. 2005;16(4-6):281-90.

PMID:
16301828
17.

Efficient intracellular processing of the endogenous cystic fibrosis transmembrane conductance regulator in epithelial cell lines.

Varga K, Jurkuvenaite A, Wakefield J, Hong JS, Guimbellot JS, Venglarik CJ, Niraj A, Mazur M, Sorscher EJ, Collawn JF, Bebök Z.

J Biol Chem. 2004 May 21;279(21):22578-84. Epub 2004 Apr 1.

18.

Cystic fibrosis transmembrane conductance regulator trafficking is mediated by the COPI coat in epithelial cells.

Rennolds J, Tower C, Musgrove L, Fan L, Maloney K, Clancy JP, Kirk KL, Sztul E, Cormet-Boyaka E.

J Biol Chem. 2008 Jan 11;283(2):833-9. Epub 2007 Oct 10.

19.

Rab11b regulates the apical recycling of the cystic fibrosis transmembrane conductance regulator in polarized intestinal epithelial cells.

Silvis MR, Bertrand CA, Ameen N, Golin-Bisello F, Butterworth MB, Frizzell RA, Bradbury NA.

Mol Biol Cell. 2009 Apr;20(8):2337-50. doi: 10.1091/mbc.E08-01-0084. Epub 2009 Feb 25.

20.

Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI).

Yu Y, Platoshyn O, Safrina O, Tsigelny I, Yuan JX, Keller SH.

Biol Cell. 2007 Aug;99(8):433-44.

PMID:
17388782
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