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Items: 1 to 20 of 101

1.

The deubiquitinating enzyme USP10 regulates the endocytic recycling of CFTR in airway epithelial cells.

Bomberger JM, Barnaby RL, Stanton BA.

Channels (Austin). 2010 May-Jun;4(3):150-4.

2.

The deubiquitinating enzyme USP10 regulates the post-endocytic sorting of cystic fibrosis transmembrane conductance regulator in airway epithelial cells.

Bomberger JM, Barnaby RL, Stanton BA.

J Biol Chem. 2009 Jul 10;284(28):18778-89. doi: 10.1074/jbc.M109.001685.

3.

Serum and glucocorticoid-inducible kinase1 increases plasma membrane wt-CFTR in human airway epithelial cells by inhibiting its endocytic retrieval.

Bomberger JM, Coutermarsh BA, Barnaby RL, Sato JD, Chapline MC, Stanton BA.

PLoS One. 2014 Feb 21;9(2):e89599. doi: 10.1371/journal.pone.0089599.

4.

c-Cbl facilitates endocytosis and lysosomal degradation of cystic fibrosis transmembrane conductance regulator in human airway epithelial cells.

Ye S, Cihil K, Stolz DB, Pilewski JM, Stanton BA, Swiatecka-Urban A.

J Biol Chem. 2010 Aug 27;285(35):27008-18. doi: 10.1074/jbc.M110.139881.

5.

Arsenic promotes ubiquitinylation and lysosomal degradation of cystic fibrosis transmembrane conductance regulator (CFTR) chloride channels in human airway epithelial cells.

Bomberger JM, Coutermarsh BA, Barnaby RL, Stanton BA.

J Biol Chem. 2012 May 18;287(21):17130-9. doi: 10.1074/jbc.M111.338855.

6.

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.

7.

Myosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes in polarized human airway epithelial cells.

Swiatecka-Urban A, Talebian L, Kanno E, Moreau-Marquis S, Coutermarsh B, Hansen K, Karlson KH, Barnaby R, Cheney RE, Langford GM, Fukuda M, Stanton BA.

J Biol Chem. 2007 Aug 10;282(32):23725-36.

8.

Nedd4-2 does not regulate wt-CFTR in human airway epithelial cells.

Koeppen K, Chapline C, Sato JD, Stanton BA.

Am J Physiol Lung Cell Mol Physiol. 2012 Oct 15;303(8):L720-7. doi: 10.1152/ajplung.00409.2011.

9.

Methods to monitor cell surface expression and endocytic trafficking of CFTR in polarized epithelial cells.

Bomberger JM, Guggino WB, Stanton BA.

Methods Mol Biol. 2011;741:271-83. doi: 10.1007/978-1-61779-117-8_18.

10.

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.

11.

Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures.

Cholon DM, O'Neal WK, Randell SH, Riordan JR, Gentzsch M.

Am J Physiol Lung Cell Mol Physiol. 2010 Mar;298(3):L304-14. doi: 10.1152/ajplung.00016.2009.

12.

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.

13.

Misfolding diverts CFTR from recycling to degradation: quality control at early endosomes.

Sharma M, Pampinella F, Nemes C, Benharouga M, So J, Du K, Bache KG, Papsin B, Zerangue N, Stenmark H, Lukacs GL.

J Cell Biol. 2004 Mar 15;164(6):923-33.

14.

ΔF508 CFTR surface stability is regulated by DAB2 and CHIP-mediated ubiquitination in post-endocytic compartments.

Fu L, Rab A, Tang Lp, Bebok Z, Rowe SM, Bartoszewski R, Collawn JF.

PLoS One. 2015 Apr 16;10(4):e0123131. doi: 10.1371/journal.pone.0123131.

15.

Disabled-2 protein facilitates assembly polypeptide-2-independent recruitment of cystic fibrosis transmembrane conductance regulator to endocytic vesicles in polarized human airway epithelial cells.

Cihil KM, Ellinger P, Fellows A, Stolz DB, Madden DR, Swiatecka-Urban A.

J Biol Chem. 2012 Apr 27;287(18):15087-99. doi: 10.1074/jbc.M112.341875.

16.

Syntaxin 16 binds to cystic fibrosis transmembrane conductance regulator and regulates its membrane trafficking in epithelial cells.

Gee HY, Tang BL, Kim KH, Lee MG.

J Biol Chem. 2010 Nov 12;285(46):35519-27. doi: 10.1074/jbc.M110.162438.

17.

N-glycans are direct determinants of CFTR folding and stability in secretory and endocytic membrane traffic.

Glozman R, Okiyoneda T, Mulvihill CM, Rini JM, Barriere H, Lukacs GL.

J Cell Biol. 2009 Mar 23;184(6):847-62. doi: 10.1083/jcb.200808124.

18.

Involvement of the Cdc42 pathway in CFTR post-translational turnover and in its plasma membrane stability in airway epithelial cells.

Ferru-Clément R, Fresquet F, Norez C, Métayé T, Becq F, Kitzis A, Thoreau V.

PLoS One. 2015 Mar 13;10(3):e0118943. doi: 10.1371/journal.pone.0118943.

19.

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.

20.

Na+/H+ exchanger regulatory factor 1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del cystic fibrosis transmembrane conductance regulator in human airway CFBE41o- cells.

Favia M, Guerra L, Fanelli T, Cardone RA, Monterisi S, Di Sole F, Castellani S, Chen M, Seidler U, Reshkin SJ, Conese M, Casavola V.

Mol Biol Cell. 2010 Jan 1;21(1):73-86. doi: 10.1091/mbc.E09-03-0185.

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