237 related articles for article (PubMed ID: 16857184)
1. IntraGolgi distribution of the Conserved Oligomeric Golgi (COG) complex.
Vasile E; Oka T; Ericsson M; Nakamura N; Krieger M
Exp Cell Res; 2006 Oct; 312(16):3132-41. PubMed ID: 16857184
[TBL] [Abstract][Full Text] [Related]
2. Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells.
Zolov SN; Lupashin VV
J Cell Biol; 2005 Feb; 168(5):747-59. PubMed ID: 15728195
[TBL] [Abstract][Full Text] [Related]
3. COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation.
Shestakova A; Zolov S; Lupashin V
Traffic; 2006 Feb; 7(2):191-204. PubMed ID: 16420527
[TBL] [Abstract][Full Text] [Related]
4. Genetic analysis of the subunit organization and function of the conserved oligomeric golgi (COG) complex: studies of COG5- and COG7-deficient mammalian cells.
Oka T; Vasile E; Penman M; Novina CD; Dykxhoorn DM; Ungar D; Hughson FM; Krieger M
J Biol Chem; 2005 Sep; 280(38):32736-45. PubMed ID: 16051600
[TBL] [Abstract][Full Text] [Related]
5. Retrograde transport on the COG railway.
Ungar D; Oka T; Krieger M; Hughson FM
Trends Cell Biol; 2006 Feb; 16(2):113-20. PubMed ID: 16406524
[TBL] [Abstract][Full Text] [Related]
6. Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.
Paesold-Burda P; Maag C; Troxler H; Foulquier F; Kleinert P; Schnabel S; Baumgartner M; Hennet T
Hum Mol Genet; 2009 Nov; 18(22):4350-6. PubMed ID: 19690088
[TBL] [Abstract][Full Text] [Related]
7. Interaction of Golgin-84 with the COG complex mediates the intra-Golgi retrograde transport.
Sohda M; Misumi Y; Yamamoto A; Nakamura N; Ogata S; Sakisaka S; Hirose S; Ikehara Y; Oda K
Traffic; 2010 Dec; 11(12):1552-66. PubMed ID: 20874812
[TBL] [Abstract][Full Text] [Related]
8. A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation.
Foulquier F; Ungar D; Reynders E; Zeevaert R; Mills P; García-Silva MT; Briones P; Winchester B; Morelle W; Krieger M; Annaert W; Matthijs G
Hum Mol Genet; 2007 Apr; 16(7):717-30. PubMed ID: 17220172
[TBL] [Abstract][Full Text] [Related]
9. The interaction of two tethering factors, p115 and COG complex, is required for Golgi integrity.
Sohda M; Misumi Y; Yoshimura S; Nakamura N; Fusano T; Ogata S; Sakisaka S; Ikehara Y
Traffic; 2007 Mar; 8(3):270-84. PubMed ID: 17274799
[TBL] [Abstract][Full Text] [Related]
10. Deficiency of the Cog8 subunit in normal and CDG-derived cells impairs the assembly of the COG and Golgi SNARE complexes.
Laufman O; Freeze HH; Hong W; Lev S
Traffic; 2013 Oct; 14(10):1065-77. PubMed ID: 23865579
[TBL] [Abstract][Full Text] [Related]
11. Re'COG'nition at the Golgi.
Miller VJ; Ungar D
Traffic; 2012 Jul; 13(7):891-7. PubMed ID: 22300173
[TBL] [Abstract][Full Text] [Related]
12. C. elegans as a model system to study the function of the COG complex in animal development.
Kubota Y; Nishiwaki K
Biol Chem; 2006 Aug; 387(8):1031-5. PubMed ID: 16895472
[TBL] [Abstract][Full Text] [Related]
13. Differential effects of lobe A and lobe B of the Conserved Oligomeric Golgi complex on the stability of {beta}1,4-galactosyltransferase 1 and {alpha}2,6-sialyltransferase 1.
Peanne R; Legrand D; Duvet S; Mir AM; Matthijs G; Rohrer J; Foulquier F
Glycobiology; 2011 Jul; 21(7):864-76. PubMed ID: 21062782
[TBL] [Abstract][Full Text] [Related]
14. The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins.
Oka T; Ungar D; Hughson FM; Krieger M
Mol Biol Cell; 2004 May; 15(5):2423-35. PubMed ID: 15004235
[TBL] [Abstract][Full Text] [Related]
15. Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1.
Zeevaert R; Foulquier F; Dimitrov B; Reynders E; Van Damme-Lombaerts R; Simeonov E; Annaert W; Matthijs G; Jaeken J
Hum Mol Genet; 2009 Feb; 18(3):517-24. PubMed ID: 19008299
[TBL] [Abstract][Full Text] [Related]
16. Dynamic transport of SNARE proteins in the Golgi apparatus.
Cosson P; Ravazzola M; Varlamov O; Söllner TH; Di Liberto M; Volchuk A; Rothman JE; Orci L
Proc Natl Acad Sci U S A; 2005 Oct; 102(41):14647-52. PubMed ID: 16199514
[TBL] [Abstract][Full Text] [Related]
17. Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.
Foulquier F; Vasile E; Schollen E; Callewaert N; Raemaekers T; Quelhas D; Jaeken J; Mills P; Winchester B; Krieger M; Annaert W; Matthijs G
Proc Natl Acad Sci U S A; 2006 Mar; 103(10):3764-9. PubMed ID: 16537452
[TBL] [Abstract][Full Text] [Related]
18. Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation.
Zeevaert R; Foulquier F; Jaeken J; Matthijs G
Mol Genet Metab; 2008 Jan; 93(1):15-21. PubMed ID: 17904886
[TBL] [Abstract][Full Text] [Related]
19. Detailed Analysis of the Interaction of Yeast COG Complex.
Ishii M; Lupashin VV; Nakano A
Cell Struct Funct; 2018 Jul; 43(2):119-127. PubMed ID: 29899178
[TBL] [Abstract][Full Text] [Related]
20. Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.
Lübbehusen J; Thiel C; Rind N; Ungar D; Prinsen BH; de Koning TJ; van Hasselt PM; Körner C
Hum Mol Genet; 2010 Sep; 19(18):3623-33. PubMed ID: 20605848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
