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Items: 1 to 20 of 119

1.

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. Epub 2009 Apr 27.

2.

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.

3.

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. Epub 2010 Jun 4.

4.

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.

5.

Ubiquitin C-terminal hydrolase-L1 protects cystic fibrosis transmembrane conductance regulator from early stages of proteasomal degradation.

Henderson MJ, Vij N, Zeitlin PL.

J Biol Chem. 2010 Apr 9;285(15):11314-25. doi: 10.1074/jbc.M109.044057. Epub 2010 Feb 10.

6.

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. eCollection 2014 Feb 21.

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. Epub 2007 Apr 26.

8.

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. Epub 2012 Mar 30.

9.

Dab2 is a key regulator of endocytosis and post-endocytic trafficking of the cystic fibrosis transmembrane conductance regulator.

Fu L, Rab A, Tang LP, Rowe SM, Bebok Z, Collawn JF.

Biochem J. 2012 Jan 15;441(2):633-43. doi: 10.1042/BJ20111566.

10.

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.

11.

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. Epub 2004 Mar 8.

12.

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. Epub 2012 Aug 17.

13.

Myosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulator.

Swiatecka-Urban A, Boyd C, Coutermarsh B, Karlson KH, Barnaby R, Aschenbrenner L, Langford GM, Hasson T, Stanton BA.

J Biol Chem. 2004 Sep 3;279(36):38025-31. Epub 2004 Jul 9.

14.

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. Epub 2012 Mar 7.

15.

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.

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. Epub 2010 Sep 8.

17.

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. Epub 2009 Dec 11.

18.

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.

19.

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.

20.

The deubiquitinating enzyme UCH-L3 regulates the apical membrane recycling of the epithelial sodium channel.

Butterworth MB, Edinger RS, Ovaa H, Burg D, Johnson JP, Frizzell RA.

J Biol Chem. 2007 Dec 28;282(52):37885-93. Epub 2007 Oct 29.

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