232 related articles for article (PubMed ID: 9658181)
1. Actin filaments and microtubules are involved in different membrane traffic pathways that transport sphingolipids to the apical surface of polarized HepG2 cells.
Zegers MM; Zaal KJ; van IJzendoorn SC; Klappe K; Hoekstra D
Mol Biol Cell; 1998 Jul; 9(7):1939-49. PubMed ID: 9658181
[TBL] [Abstract][Full Text] [Related]
2. Sphingolipid transport to the apical plasma membrane domain in human hepatoma cells is controlled by PKC and PKA activity: a correlation with cell polarity in HepG2 cells.
Zegers MM; Hoekstra D
J Cell Biol; 1997 Jul; 138(2):307-21. PubMed ID: 9230073
[TBL] [Abstract][Full Text] [Related]
3. Both microtubules and actin filaments are required for efficient postendocytotic traffic of the polymeric immunoglobulin receptor in polarized Madin-Darby canine kidney cells.
Maples CJ; Ruiz WG; Apodaca G
J Biol Chem; 1997 Mar; 272(10):6741-51. PubMed ID: 9045707
[TBL] [Abstract][Full Text] [Related]
4. (Glyco)sphingolipids are sorted in sub-apical compartments in HepG2 cells: a role for non-Golgi-related intracellular sites in the polarized distribution of (glyco)sphingolipids.
van IJzendoorn SC; Hoekstra D
J Cell Biol; 1998 Aug; 142(3):683-96. PubMed ID: 9700158
[TBL] [Abstract][Full Text] [Related]
5. Segregation of glucosylceramide and sphingomyelin occurs in the apical to basolateral transcytotic route in HepG2 cells.
van IJzendoorn SC; Zegers MM; Kok JW; Hoekstra D
J Cell Biol; 1997 Apr; 137(2):347-57. PubMed ID: 9128247
[TBL] [Abstract][Full Text] [Related]
6. Epithelial sphingolipid sorting is insensitive to reorganization of the Golgi by nocodazole, but is abolished by monensin in MDCK cells and by brefeldin A in Caco-2 cells.
van Meer G; van 't Hof W
J Cell Sci; 1993 Mar; 104 ( Pt 3)():833-42. PubMed ID: 8314877
[TBL] [Abstract][Full Text] [Related]
7. Cytoskeletal disruption in A6 kidney cells: impact on endo/exocytosis and NaCl transport regulation by antidiuretic hormone.
Verrey F; Groscurth P; Bolliger U
J Membr Biol; 1995 May; 145(2):193-204. PubMed ID: 7563021
[TBL] [Abstract][Full Text] [Related]
8. Polarized sphingolipid transport from the subapical compartment: evidence for distinct sphingolipid domains.
van IJzendoorn SC; Hoekstra D
Mol Biol Cell; 1999 Oct; 10(10):3449-61. PubMed ID: 10512879
[TBL] [Abstract][Full Text] [Related]
9. Efficient trafficking of MDR1/P-glycoprotein to apical canalicular plasma membranes in HepG2 cells requires PKA-RIIalpha anchoring and glucosylceramide.
Wojtal KA; de Vries E; Hoekstra D; van Ijzendoorn SC
Mol Biol Cell; 2006 Aug; 17(8):3638-50. PubMed ID: 16723498
[TBL] [Abstract][Full Text] [Related]
10. Microtubules and actin filaments are not critically involved in the biogenesis of epithelial cell surface polarity.
Salas PJ; Misek DE; Vega-Salas DE; Gundersen D; Cereijido M; Rodriguez-Boulan E
J Cell Biol; 1986 May; 102(5):1853-67. PubMed ID: 2871031
[TBL] [Abstract][Full Text] [Related]
11. Apical to basolateral transcytosis and apical recycling of immunoglobulin G in trophoblast-derived BeWo cells: effects of low temperature, nocodazole, and cytochalasin D.
Ellinger I; Rothe A; Grill M; Fuchs R
Exp Cell Res; 2001 Oct; 269(2):322-31. PubMed ID: 11570824
[TBL] [Abstract][Full Text] [Related]
12. Mechanisms and functional features of polarized membrane traffic in epithelial and hepatic cells.
Zegers MM; Hoekstra D
Biochem J; 1998 Dec; 336 ( Pt 2)(Pt 2):257-69. PubMed ID: 9820799
[TBL] [Abstract][Full Text] [Related]
13. The roles of actin cytoskeleton and microtubules for membrane recycling of a food vacuole in Tetrahymena thermophila.
Sugita M; Nakano K; Sato M; Toyooka K; Numata O
Cell Motil Cytoskeleton; 2009 Jul; 66(7):371-7. PubMed ID: 19418560
[TBL] [Abstract][Full Text] [Related]
14. Basolateral to apical transcytosis in polarized cells is indirect and involves BFA and trimeric G protein sensitive passage through the apical endosome.
Barroso M; Sztul ES
J Cell Biol; 1994 Jan; 124(1-2):83-100. PubMed ID: 7905002
[TBL] [Abstract][Full Text] [Related]
15. Trans-Golgi network and subapical compartment of HepG2 cells display different properties in sorting and exiting of sphingolipids.
Maier O; Hoekstra D
J Biol Chem; 2003 Jan; 278(1):164-73. PubMed ID: 12407103
[TBL] [Abstract][Full Text] [Related]
16. Endocytic traffic in polarized epithelial cells: role of the actin and microtubule cytoskeleton.
Apodaca G
Traffic; 2001 Mar; 2(3):149-59. PubMed ID: 11260520
[TBL] [Abstract][Full Text] [Related]
17. Intracellular sites involved in the biogenesis of bile canaliculi in hepatic cells.
Zaal KJ; Kok JW; Sormunen R; Eskelinen S; Hoekstra D
Eur J Cell Biol; 1994 Feb; 63(1):10-9. PubMed ID: 8005096
[TBL] [Abstract][Full Text] [Related]
18. Effect of calmodulin antagonists on endocytosis and intracellular transport of ricin in polarized MDCK cells.
Llorente A; Garred O; Holm PK; Eker P; Jacobsen J; van Deurs B; Sandvig K
Exp Cell Res; 1996 Sep; 227(2):298-308. PubMed ID: 8831568
[TBL] [Abstract][Full Text] [Related]
19. Actin microfilaments play a critical role in endocytosis at the apical but not the basolateral surface of polarized epithelial cells.
Gottlieb TA; Ivanov IE; Adesnik M; Sabatini DD
J Cell Biol; 1993 Feb; 120(3):695-710. PubMed ID: 8381123
[TBL] [Abstract][Full Text] [Related]
20. Hypertonicity-induced projections reflect cell polarity in mouse metaphase II oocytes: involvement of microtubules, microfilaments, and chromosomes.
Liu JL; Sung LY; Tian XC; Yang X
Biol Reprod; 2002 Dec; 67(6):1853-63. PubMed ID: 12444063
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
