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Items: 1 to 20 of 163

1.

Mammalian homolog of Drosophila tumor suppressor lethal (2) giant larvae interacts with basolateral exocytic machinery in Madin-Darby canine kidney cells.

Müsch A, Cohen D, Yeaman C, Nelson WJ, Rodriguez-Boulan E, Brennwald PJ.

Mol Biol Cell. 2002 Jan;13(1):158-68.

2.

SNARE expression and localization in renal epithelial cells suggest mechanism for variability of trafficking phenotypes.

Li X, Low SH, Miura M, Weimbs T.

Am J Physiol Renal Physiol. 2002 Nov;283(5):F1111-22.

3.

Three-dimensional analysis of post-Golgi carrier exocytosis in epithelial cells.

Kreitzer G, Schmoranzer J, Low SH, Li X, Gan Y, Weimbs T, Simon SM, Rodriguez-Boulan E.

Nat Cell Biol. 2003 Feb;5(2):126-36.

PMID:
12545172
4.

SNARE protein trafficking in polarized MDCK cells.

Steegmaier M, Lee KC, Prekeris R, Scheller RH.

Traffic. 2000 Jul;1(7):553-60.

5.
6.

Differential localization of syntaxin isoforms in polarized Madin-Darby canine kidney cells.

Low SH, Chapin SJ, Weimbs T, Kömüves LG, Bennett MK, Mostov KE.

Mol Biol Cell. 1996 Dec;7(12):2007-18.

7.
8.

Basolateral sorting of syntaxin 4 is dependent on its N-terminal domain and the AP1B clathrin adaptor, and required for the epithelial cell polarity.

Reales E, Sharma N, Low SH, Fölsch H, Weimbs T.

PLoS One. 2011;6(6):e21181. doi: 10.1371/journal.pone.0021181. Epub 2011 Jun 15.

9.

Antigen retrieval reveals widespread basolateral expression of syntaxin 3 in renal epithelia.

Breton S, Inoue T, Knepper MA, Brown D.

Am J Physiol Renal Physiol. 2002 Mar;282(3):F523-9.

10.

Syntaxin 1A has a specific binding site in the H3 domain that is critical for targeting of H+-ATPase to apical membrane of renal epithelial cells.

Li G, Yang Q, Alexander EA, Schwartz JH.

Am J Physiol Cell Physiol. 2005 Sep;289(3):C665-72. Epub 2005 May 4.

11.

The Sec6/8 complex in mammalian cells: characterization of mammalian Sec3, subunit interactions, and expression of subunits in polarized cells.

Matern HT, Yeaman C, Nelson WJ, Scheller RH.

Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9648-53. Epub 2001 Aug 7.

12.
13.

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.

14.

Retinal pigment epithelial cells exhibit unique expression and localization of plasma membrane syntaxins which may contribute to their trafficking phenotype.

Low SH, Marmorstein LY, Miura M, Li X, Kudo N, Marmorstein AD, Weimbs T.

J Cell Sci. 2002 Dec 1;115(Pt 23):4545-53.

15.

Analysis of the Munc18b-syntaxin binding interface. Use of a mutant Munc18b to dissect the functions of syntaxins 2 and 3.

Kauppi M, Wohlfahrt G, Olkkonen VM.

J Biol Chem. 2002 Nov 15;277(46):43973-9. Epub 2002 Aug 26.

16.

Structurally conserved interaction of Lgl family with SNAREs is critical to their cellular function.

Gangar A, Rossi G, Andreeva A, Hales R, Brennwald P.

Curr Biol. 2005 Jun 21;15(12):1136-42.

17.

TGN38 recycles basolaterally in polarized Madin-Darby canine kidney cells.

Rajasekaran AK, Humphrey JS, Wagner M, Miesenböck G, Le Bivic A, Bonifacino JS, Rodriguez-Boulan E.

Mol Biol Cell. 1994 Oct;5(10):1093-103.

19.

Intracellular redirection of plasma membrane trafficking after loss of epithelial cell polarity.

Low SH, Miura M, Roche PA, Valdez AC, Mostov KE, Weimbs T.

Mol Biol Cell. 2000 Sep;11(9):3045-60.

20.

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

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