150 related articles for article (PubMed ID: 8194602)
1. Vacuolar ATPase inactivation blocks recycling to the trans-Golgi network from the plasma membrane.
Reaves B; Banting G
FEBS Lett; 1994 May; 345(1):61-6. PubMed ID: 8194602
[TBL] [Abstract][Full Text] [Related]
2. TGN38/41 recycles between the cell surface and the TGN: brefeldin A affects its rate of return to the TGN.
Reaves B; Horn M; Banting G
Mol Biol Cell; 1993 Jan; 4(1):93-105. PubMed ID: 8443412
[TBL] [Abstract][Full Text] [Related]
3. Retrieval of TGN proteins from the cell surface requires endosomal acidification.
Chapman RE; Munro S
EMBO J; 1994 May; 13(10):2305-12. PubMed ID: 8194522
[TBL] [Abstract][Full Text] [Related]
4. Heterogeneous behavior of cells with respect to induction of retrograde transport from the trans-Golgi network to the Golgi upon inhibition of the vacuolar proton pump.
van Weert AW; Geuze HJ; Stoorvogel W
Eur J Cell Biol; 1997 Dec; 74(4):417-23. PubMed ID: 9438139
[TBL] [Abstract][Full Text] [Related]
5. Chimeric forms of furin and TGN38 are transported with the plasma membrane in the trans-Golgi network via distinct endosomal pathways.
Mallet WG; Maxfield FR
J Cell Biol; 1999 Jul; 146(2):345-59. PubMed ID: 10465644
[TBL] [Abstract][Full Text] [Related]
6. Transport from late endosomes to lysosomes, but not sorting of integral membrane proteins in endosomes, depends on the vacuolar proton pump.
van Weert AW; Dunn KW; Geuze HJ; Maxfield FR; Stoorvogel W
J Cell Biol; 1995 Aug; 130(4):821-34. PubMed ID: 7642700
[TBL] [Abstract][Full Text] [Related]
7. Active vacuolar H+ATPase is required for both endocytic and exocytic processes during viral infection of BHK-21 cells.
Palokangas H; Metsikkö K; Väänänen K
J Biol Chem; 1994 Jul; 269(26):17577-85. PubMed ID: 8021266
[TBL] [Abstract][Full Text] [Related]
8. The steady state distribution of humTGN46 is not significantly altered in cells defective in clathrin-mediated endocytosis.
Banting G; Maile R; Roquemore EP
J Cell Sci; 1998 Dec; 111 ( Pt 23)():3451-8. PubMed ID: 9811560
[TBL] [Abstract][Full Text] [Related]
9. Identification of different itineraries and retromer components for endosome-to-Golgi transport of TGN38 and Shiga toxin.
Lieu ZZ; Gleeson PA
Eur J Cell Biol; 2010 May; 89(5):379-93. PubMed ID: 20138391
[TBL] [Abstract][Full Text] [Related]
10. Vacuolar ATPase activity is required for endosomal carrier vesicle formation.
Clague MJ; Urbé S; Aniento F; Gruenberg J
J Biol Chem; 1994 Jan; 269(1):21-4. PubMed ID: 8276796
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 7865877
[TBL] [Abstract][Full Text] [Related]
12. Okadaic acid treatment leads to a fragmentation of the trans-Golgi network and an increase in expression of TGN38 at the cell surface.
Horn M; Banting G
Biochem J; 1994 Jul; 301 ( Pt 1)(Pt 1):69-73. PubMed ID: 8037693
[TBL] [Abstract][Full Text] [Related]
13. An electron microscopic study of TGN38/41 dynamics.
Ladinsky MS; Howell KE
J Cell Sci Suppl; 1993; 17():41-7. PubMed ID: 8144704
[TBL] [Abstract][Full Text] [Related]
14. Selective reentry of recycling cell surface glycoproteins to the biosynthetic pathway in human hepatocarcinoma HepG2 cells.
Volz B; Orberger G; Porwoll S; Hauri HP; Tauber R
J Cell Biol; 1995 Aug; 130(3):537-51. PubMed ID: 7622556
[TBL] [Abstract][Full Text] [Related]
15. A cytosolic complex of p62 and rab6 associates with TGN38/41 and is involved in budding of exocytic vesicles from the trans-Golgi network.
Jones SM; Crosby JR; Salamero J; Howell KE
J Cell Biol; 1993 Aug; 122(4):775-88. PubMed ID: 8349729
[TBL] [Abstract][Full Text] [Related]
16. The trans-Golgi network can be dissected structurally and functionally from the cisternae of the Golgi complex by brefeldin A.
Ladinsky MS; Howell KE
Eur J Cell Biol; 1992 Oct; 59(1):92-105. PubMed ID: 1468449
[TBL] [Abstract][Full Text] [Related]
17. Overexpression of TGN38/41 leads to mislocalisation of gamma-adaptin.
Reaves B; Banting G
FEBS Lett; 1994 Sep; 351(3):448-56. PubMed ID: 8082813
[TBL] [Abstract][Full Text] [Related]
18. TGN38-green fluorescent protein hybrid proteins expressed in stably transfected eukaryotic cells provide a tool for the real-time, in vivo study of membrane traffic pathways and suggest a possible role for ratTGN38.
Girotti M; Banting G
J Cell Sci; 1996 Dec; 109 ( Pt 12)():2915-26. PubMed ID: 9013339
[TBL] [Abstract][Full Text] [Related]
19. Perturbation of the morphology of the trans-Golgi network following Brefeldin A treatment: redistribution of a TGN-specific integral membrane protein, TGN38.
Reaves B; Banting G
J Cell Biol; 1992 Jan; 116(1):85-94. PubMed ID: 1730751
[TBL] [Abstract][Full Text] [Related]
20. Lumenal and transmembrane domains play a role in sorting type I membrane proteins on endocytic pathways.
Reaves BJ; Banting G; Luzio JP
Mol Biol Cell; 1998 May; 9(5):1107-22. PubMed ID: 9571243
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
