Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 128

1.

Myristoylated Naked2 escorts transforming growth factor alpha to the basolateral plasma membrane of polarized epithelial cells.

Li C, Franklin JL, Graves-Deal R, Jerome WG, Cao Z, Coffey RJ.

Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5571-6. Epub 2004 Apr 2.

2.
3.

Myristoylated Naked2 antagonizes Wnt-beta-catenin activity by degrading Dishevelled-1 at the plasma membrane.

Hu T, Li C, Cao Z, Van Raay TJ, Smith JG, Willert K, Solnica-Krezel L, Coffey RJ.

J Biol Chem. 2010 Apr 30;285(18):13561-8. doi: 10.1074/jbc.M109.075945. Epub 2010 Feb 20.

6.

The proamphiregulin cytoplasmic domain is required for basolateral sorting, but is not essential for constitutive or stimulus-induced processing in polarized Madin-Darby canine kidney cells.

Brown CL, Coffey RJ, Dempsey PJ.

J Biol Chem. 2001 Aug 3;276(31):29538-49. Epub 2001 May 29. Erratum in: J Biol Chem 2001 Sep 28;276(39):36862.

7.
8.

Use of fluorescence-activated vesicle sorting for isolation of Naked2-associated, basolaterally targeted exocytic vesicles for proteomics analysis.

Cao Z, Li C, Higginbotham JN, Franklin JL, Tabb DL, Graves-Deal R, Hill S, Cheek K, Jerome WG, Lapierre LA, Goldenring JR, Ham AJ, Coffey RJ.

Mol Cell Proteomics. 2008 Sep;7(9):1651-67. doi: 10.1074/mcp.M700155-MCP200. Epub 2008 May 25.

9.

EGF receptor-independent action of TGF-alpha protects Naked2 from AO7-mediated ubiquitylation and proteasomal degradation.

Ding W, Li C, Hu T, Graves-Deal R, Fotia AB, Weissman AM, Coffey RJ.

Proc Natl Acad Sci U S A. 2008 Sep 9;105(36):13433-8. doi: 10.1073/pnas.0806298105. Epub 2008 Aug 29.

10.

Two different cytoplasmic tails direct isoforms of the membrane cofactor protein (CD46) to the basolateral surface of Madin-Darby canine kidney cells.

Maisner A, Liszewski MK, Atkinson JP, Schwartz-Albiez R, Herrler G.

J Biol Chem. 1996 Aug 2;271(31):18853-8.

11.

Contextual binding of p120ctn to E-cadherin at the basolateral plasma membrane in polarized epithelia.

Miranda KC, Joseph SR, Yap AS, Teasdale RD, Stow JL.

J Biol Chem. 2003 Oct 31;278(44):43480-8. Epub 2003 Aug 14.

12.

Sorting of rat liver and ileal sodium-dependent bile acid transporters in polarized epithelial cells.

Sun AQ, Ananthanarayanan M, Soroka CJ, Thevananther S, Shneider BL, Suchy FJ.

Am J Physiol. 1998 Nov;275(5 Pt 1):G1045-55.

13.

Involvement of a di-leucine motif in targeting of ABCC1 to the basolateral plasma membrane of polarized epithelial cells.

Emi Y, Harada Y, Sakaguchi M.

Biochem Biophys Res Commun. 2013 Nov 8;441(1):89-95. doi: 10.1016/j.bbrc.2013.10.013. Epub 2013 Oct 12.

PMID:
24129190
14.
15.
16.

The ammonium transporter RhBG: requirement of a tyrosine-based signal and ankyrin-G for basolateral targeting and membrane anchorage in polarized kidney epithelial cells.

Lopez C, Métral S, Eladari D, Drevensek S, Gane P, Chambrey R, Bennett V, Cartron JP, Le Van Kim C, Colin Y.

J Biol Chem. 2005 Mar 4;280(9):8221-8. Epub 2004 Dec 17.

17.

Differential trafficking of transforming growth factor-beta receptors and ligand in polarized epithelial cells.

Murphy SJ, Doré JJ, Edens M, Coffey RJ, Barnard JA, Mitchell H, Wilkes M, Leof EB.

Mol Biol Cell. 2004 Jun;15(6):2853-62. Epub 2004 Apr 9.

18.
19.
20.

Polarized transport of MHC class II molecules in Madin-Darby canine kidney cells is directed by a leucine-based signal in the cytoplasmic tail of the beta-chain.

Simonsen A, Pedersen KW, Nordeng TW, von der Lippe A, Stang E, Long EO, Bakke O.

J Immunol. 1999 Sep 1;163(5):2540-8.

Supplemental Content

Support Center