-
1
-
-
0034843704
-
Neutralization of pH in the Golgi apparatus causes redistribution of glycosyltransferases and changes in the O-glycosylation of mucins
-
Axelsson MA, Karlsson NG, Steel DM, Ouwendijk J, Nilsson T, Hansson GC. 2001. Neutralization of pH in the Golgi apparatus causes redistribution of glycosyltransferases and changes in the O-glycosylation of mucins. Glycobiology. 11:633-644. (Pubitemid 32785269)
-
(2001)
Glycobiology
, vol.11
, Issue.8
, pp. 633-644
-
-
Axelsson, M.A.B.1
Karlsson, N.G.2
Steel, D.M.3
Ouwendijk, J.4
Nilsson, T.5
Hansson, G.C.6
-
2
-
-
0013085340
-
Golgins in the structure and dynamics of the Golgi apparatus
-
DOI 10.1016/S0955-0674(03)00054-1
-
Barr FA, Short B. 2003. Golgins in the structure and dynamics of the Golgi apparatus. Curr Opin Cell Biol. 15:405-413. (Pubitemid 36928042)
-
(2003)
Current Opinion in Cell Biology
, vol.15
, Issue.4
, pp. 405-413
-
-
Barr, F.A.1
Short, B.2
-
3
-
-
0037167579
-
Regulation of ganglioside biosynthesis by enzyme complex formation of glycosyltransferases
-
Bieberich E, MacKinnon S, Silva J, Li DD, Tencomnao T, Irwin L, Kapitonov D, Yu RK. 2002. Regulation of ganglioside biosynthesis by enzyme complex formation of glycosyltransferases. Biochemistry. 41:11479-11487.
-
(2002)
Biochemistry.
, vol.41
, pp. 11479-11487
-
-
Bieberich, E.1
MacKinnon, S.2
Silva, J.3
Li, D.D.4
Tencomnao, T.5
Irwin, L.6
Kapitonov, D.7
Yu, R.K.8
-
4
-
-
0032417711
-
Procollagen traverses the Golgi stack without leaving the lumen of cisternae: Evidence for cisternal maturation
-
DOI 10.1016/S0092-8674(00)81723-7
-
Bonfanti L, Mironov AA, Jr, Martinez-Menarguez JA, Martella O, Fusella A, Baldassarre M, Buccione R, Geuze HJ, Mironov AA, Luini A. 1998. Procollagen traverses the Golgi stack without leaving the lumen of cister-nae: Evidence for cisternal maturation. Cell. 95:993-1003. (Pubitemid 29019051)
-
(1998)
Cell
, vol.95
, Issue.7
, pp. 993-1003
-
-
Bonfanti, L.1
Mironov Jr., A.A.2
Martinez-Menarguez, J.A.3
Martella, O.4
Fusella, A.5
Baldassarre, M.6
Buccione, R.7
Geuze, H.J.8
Mironov, A.A.9
Luini, A.10
-
5
-
-
33748313351
-
Retrograde transport from endosomes to the trans-Golgi network
-
DOI 10.1038/nrm1985, PII NRM1985
-
Bonifacino JS, Rojas R. 2006. Retrograde transport from endosomes to the trans-Golgi network. Nat Rev Mol Cell Biol. 7(8):568-579. (Pubitemid 44325348)
-
(2006)
Nature Reviews Molecular Cell Biology
, vol.7
, Issue.8
, pp. 568-579
-
-
Bonifacino, J.S.1
Rojas, R.2
-
6
-
-
0027892019
-
Cholesterol and the Golgi apparatus
-
Bretscher MS, Munro S. 1993. Cholesterol and the Golgi apparatus. Science. 261:1280-1281. (Pubitemid 24081166)
-
(1993)
Science
, vol.261
, Issue.5126
, pp. 1280-1281
-
-
Bretscher, M.S.1
Munro, S.2
-
7
-
-
34548169619
-
Structural analysis of conserved oligomeric Golgi complex subunit 2
-
DOI 10.1074/jbc.M703716200
-
Cavanaugh LF, Chen X, Richardson BC, Ungar D, Pelczer I, Rizo J, Hughson FM. 2007. Structural analysis of conserved oligomeric Golgi complex subunit 2. J Biol Chem. 282:23418-23426. (Pubitemid 47311945)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.32
, pp. 23418-23426
-
-
Cavanaugh, L.F.1
Chen, X.2
Richardson, B.C.3
Ungar, D.4
Pelczer, I.5
Rizo, J.6
Hughson, F.M.7
-
8
-
-
0031040995
-
Golgi localization of glycosyltransferases: More questions than answers
-
Colley KJ. 1997. Golgi localization of glycosyltransferases: More questions than answers. Glycobiology. 7:1-13. (Pubitemid 27091315)
-
(1997)
Glycobiology
, vol.7
, Issue.1
, pp. 1-13
-
-
Colley, K.J.1
-
9
-
-
0035659728
-
N-glycosylation of yeast, with emphasis on Candida albi-cans
-
Cutler JE. 2001. N-glycosylation of yeast, with emphasis on Candida albi-cans. Med Mycol. 39(Suppl. 1):75-86.
-
(2001)
Med Mycol
, vol.39
, Issue.SUPPL. 1
, pp. 75-86
-
-
Cutler, J.E.1
-
10
-
-
70349835304
-
GOLPH3 bridges phosphatidylinositol-4-phosphate and actomyosin to stretch and shape the Golgi to promote budding
-
Dippold HC, Ng MM, et al. 2009. GOLPH3 bridges phosphatidylinositol-4- phosphate and actomyosin to stretch and shape the Golgi to promote budding. Cell. 139(2):337-351.
-
(2009)
Cell
, vol.139
, Issue.2
, pp. 337-351
-
-
Dippold, H.C.1
Ng, M.M.2
-
11
-
-
0022385726
-
Compartmental organization of the Golgi stack
-
Dunphy WG, Rothman JE. 1985. Compartmental organization of the Golgi stack. Cell. 42:13-21. (Pubitemid 16237552)
-
(1985)
Cell
, vol.42
, Issue.1
, pp. 13-21
-
-
Dunphy, W.G.1
Rothman, J.E.2
-
12
-
-
0038050371
-
Cisternal maturation and vesicle transport: Join the band wagon!
-
DOI 10.1080/0968768031000114024
-
Elsner M, Hashimoto H, Nilsson T. 2003. Cisternal maturation and vesicle transport: Join the band wagon! (Review). Mol Membr Biol. 20:221-229. (Pubitemid 37046247)
-
(2003)
Molecular Membrane Biology
, vol.20
, Issue.3
, pp. 221-229
-
-
Elsner, M.1
Hashimoto, H.2
Nilsson, T.3
-
13
-
-
12244268655
-
The Drosophila Cog5 homologue is required for cytokinesis, cell elongation, and assembly of specialized golgi architecture during spermatogenesis
-
DOI 10.1091/mbc.E02-06-0343
-
Farkas RM, Giansanti MG, Gatti M, Fuller MT. 2003. The Drosophila Cog5 homologue is required for cytokinesis, cell elongation, and assembly of specialized Golgi architecture during spermatogenesis. Mol Biol Cell. 14:190-200. (Pubitemid 36106029)
-
(2003)
Molecular Biology of the Cell
, vol.14
, Issue.1
, pp. 190-200
-
-
Farkas, R.M.1
Giansanti, M.G.2
Gatti, M.3
Fuller, M.T.4
-
14
-
-
79958851815
-
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, Garcia-Silva MT, Briones P, Winchester B, Morelle W, Krieger M, et al. 2007. A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation. Hum Mol Genet. 12:12.
-
(2007)
Hum Mol Genet
, vol.12
, pp. 12
-
-
Foulquier, F.1
Ungar, D.2
Reynders, E.3
Zeevaert, R.4
Mills, P.5
Garcia-Silva, M.T.6
Briones, P.7
Winchester, B.8
Morelle, W.9
Krieger, M.10
-
15
-
-
33644853797
-
Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II
-
DOI 10.1073/pnas.0507685103
-
Foulquier F, Vasile E, Schollen E, Callewaert N, Raemaekers T, Quelhas D, Jaeken J, Mills P, Winchester B, Krieger M, et al. 2006. Conserved oligo-meric Golgi complex subunit 1 deficiency reveals a previously uncharacter-ized congenital disorder of glycosylation type II. Proc Natl Acad Sci USA. 103:3764-3769. (Pubitemid 43376629)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.10
, pp. 3764-3769
-
-
Foulquier, F.1
Vasile, E.2
Schollen, E.3
Callewaert, N.4
Raemaekers, T.5
Quelhas, D.6
Jaeken, J.7
Mills, P.8
Winchester, B.9
Krieger, M.10
Annaert, W.11
Matthijs, G.12
-
16
-
-
58149186651
-
Glycobiology in the cytosol: The bitter side of a sweet world
-
Funakoshi Y, Suzuki T. 2009. Glycobiology in the cytosol: The bitter side of a sweet world. Biochim Biophys Acta. 1790:81-94.
-
(2009)
Biochim Biophys Acta
, vol.1790
, pp. 81-94
-
-
Funakoshi, Y.1
Suzuki, T.2
-
18
-
-
0031809680
-
Targeting of proteins to the Golgi apparatus
-
DOI 10.1007/s004180050252
-
Gleeson PA. 1998. Targeting of proteins to the Golgi apparatus. Histochem Cell Biol. 109:517-532. (Pubitemid 28289227)
-
(1998)
Histochemistry and Cell Biology
, vol.109
, Issue.5-6
, pp. 517-532
-
-
Gleeson, P.A.1
-
19
-
-
0031559885
-
A cisternal maturation mechanism can explain the asymmetry of the Golgi stack
-
DOI 10.1016/S0014-5793(97)00984-8, PII S0014579397009848
-
Glick BS, Elston T, Oster G. 1997. A cisternal maturation mechanism can explain the asymmetry of the Golgi stack. FEBS Lett. 414:177-181. (Pubitemid 27389358)
-
(1997)
FEBS Letters
, vol.414
, Issue.2
, pp. 177-181
-
-
Glick, B.S.1
Elston, T.2
Oster, G.3
-
20
-
-
0036840817
-
Congenital disorders of glycosyla-tion: A review
-
Grunewald S, Matthijs G, Jaeken J. 2002. Congenital disorders of glycosyla-tion: A review. Pediatr Res. 52:618-624.
-
(2002)
Pediatr Res
, vol.52
, pp. 618-624
-
-
Grunewald, S.1
Matthijs, G.2
Jaeken, J.3
-
21
-
-
0027034140
-
Glycosylation
-
Hart GW. 1992. Glycosylation. Curr Opin Cell Biol. 4:1017-1023.
-
(1992)
Curr Opin Cell Biol
, vol.4
, pp. 1017-1023
-
-
Hart, G.W.1
-
23
-
-
0030006293
-
O-linked protein glycosylation structure and function
-
DOI 10.1007/BF01049675
-
Hounsell EF, Davies MJ, Renouf DV. 1996. O-linked protein glycosylation structure and function. Glycoconj J. 13:19-26. (Pubitemid 26074297)
-
(1996)
Glycoconjugate Journal
, vol.13
, Issue.1
, pp. 19-26
-
-
Hounsell, E.F.1
Davies, M.J.2
Renouf, D.V.3
-
24
-
-
0038042511
-
Congenital disorders of glycosylation (CDG): It's all in it!
-
Jaeken J. 2003. Congenital disorders of glycosylation (CDG): It's all in it! (Komrower Lecture). J Inherit Metab Dis. 26:99-118. (Pubitemid 36889736)
-
(2003)
Journal of Inherited Metabolic Disease
, vol.26
, Issue.2-3
, pp. 99-118
-
-
Jaeken, J.1
-
26
-
-
35548972537
-
Congenital disorders of glycosylation: A rapidly expanding disease family
-
Jaeken J, Matthijs G. 2007. Congenital disorders of glycosylation: A rapidly expanding disease family. Annu Rev Genomics Hum Genet. 8:261-278.
-
(2007)
Annu Rev Genomics Hum Genet
, vol.8
, pp. 261-278
-
-
Jaeken, J.1
Matthijs, G.2
-
27
-
-
0037051978
-
Abnormal glycosylation and altered Golgi structure in colorectal cancer: Dependence on intra-Golgi pH
-
DOI 10.1016/S0014-5793(02)02535-8, PII S0014579302025358
-
Kellokumpu S, Sormunen R, Kellokumpu I. 2002. Abnormal glycosylation and altered Golgi structure in colorectal cancer: Dependence on intra-Golgi pH. FEBS Lett. 516:217-224. (Pubitemid 34311965)
-
(2002)
FEBS Letters
, vol.516
, Issue.1-3
, pp. 217-224
-
-
Kellokumpu, S.1
Sormunen, R.2
Kellokumpu, I.3
-
28
-
-
0034768587
-
Sgf1p, a new component of the Sec34p/Sec35p complex
-
DOI 10.1034/j.1600-0854.2001.21111.x
-
Kim DW, Massey T, Sacher M, Pypaert M, Ferro-Novick S. 2001. Sgf1p, a new component of the Sec34p/Sec35p complex. Traf fic. 2:820-830. (Pubitemid 33040262)
-
(2001)
Traffic
, vol.2
, Issue.11
, pp. 820-830
-
-
Kim, D.-W.1
Massey, T.2
Sacher, M.3
Pypaert, M.4
Ferro-Novick, S.5
-
29
-
-
0022455528
-
Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-linked, O-linked, and lipid-linked carbohydrate chains
-
Kingsley DM, Kozarsky KF, Segal M, Krieger M. 1986. Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-linked, O-linked, and lipid-linked carbohydrate chains. J Cell Biol. 102:1576-1585. (Pubitemid 16078742)
-
(1986)
Journal of Cell Biology
, vol.102
, Issue.5
, pp. 1576-1585
-
-
Kingsley, D.M.1
Kozarsky, K.F.2
Segal, M.3
Krieger, M.4
-
30
-
-
0021126647
-
Receptor-mediated endocytosis of low density lipoprotein: Somatic cell mutants define multiple genes required for expression of surface-receptor activity
-
DOI 10.1073/pnas.81.17.5454
-
Kingsley DM, Krieger M. 1984. Receptor-mediated endocytosis of low density lipoprotein: Somatic cell mutants define multiple genes required for expression of surface-receptor activity. Proc Natl Acad Sci USA. 81:5454-5458. (Pubitemid 14000505)
-
(1984)
Proceedings of the National Academy of Sciences of the United States of America
, vol.81
, Issue.17
, pp. 5454-5458
-
-
Kingsley, D.M.1
Krieger, M.2
-
31
-
-
37549056201
-
Impaired glyco-sylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2
-
Kornak U, Reynders E, Dimopoulou A, van Reeuwijk J, Fischer B, Rajab A, Budde B, Nurnberg P, Foulquier F, Lefeber D, et al. 2008. Impaired glyco-sylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2. Nat Genet. 40:32-34.
-
(2008)
Nat Genet
, vol.40
, pp. 32-34
-
-
Kornak, U.1
Reynders, E.2
Dimopoulou, A.3
Van Reeuwijk, J.4
Fischer, B.5
Rajab, A.6
Budde, B.7
Nurnberg, P.8
Foulquier, F.9
Lefeber, D.10
-
32
-
-
0021891884
-
Assembly of asparagine-linked oligosacchar-ides
-
Kornfeld R, Kornfeld S. 1985. Assembly of asparagine-linked oligosacchar-ides. Annu Rev Biochem. 54:631-664.
-
(1985)
Annu Rev Biochem
, vol.54
, pp. 631-664
-
-
Kornfeld, R.1
Kornfeld, S.2
-
33
-
-
33847648364
-
Control systems for membrane fusion in the ancestral eukaryote; Evolution of tethering complexes and SM proteins
-
Koumandou VL, Dacks JB, Coulson RM, Field MC. 2007. Control systems for membrane fusion in the ancestral eukaryote; evolution of tethering complexes and SM proteins. BMC Evol Biol. 7:29.
-
(2007)
BMC Evol Biol
, vol.7
, pp. 29
-
-
Koumandou, V.L.1
Dacks, J.B.2
Coulson, R.M.3
Field, M.C.4
-
34
-
-
79958835211
-
COG8 deficiency causes new congenital disorder of glycosylation type IIh
-
Kranz C, Ng BG, Sun L, Sharma V, Eklund EA, Miura Y, Ungar D, Lupashin V, Winkel DR, Cipollo JF, et al. 2007. COG8 deficiency causes new congenital disorder of glycosylation type IIh. Hum Mol Genet. 1:1.
-
(2007)
Hum Mol Genet
, vol.1
, pp. 1
-
-
Kranz, C.1
Ng, B.G.2
Sun, L.3
Sharma, V.4
Eklund, E.A.5
Miura, Y.6
Ungar, D.7
Lupashin, V.8
Winkel, D.R.9
Cipollo, J.F.10
-
35
-
-
0019860247
-
Isolation of Chinese hamster cell mutants defective in the receptor-mediated endocytosis of low density lipoprotein
-
DOI 10.1016/0022-2836(81)90447-2
-
Krieger M, Brown MS, Goldstein JL. 1981. Isolation of Chinese hamster cell mutants defective in the receptor-mediated endocytosis of low density lipo-protein. J Mol Biol. 150:167-184. (Pubitemid 11023561)
-
(1981)
Journal of Molecular Biology
, vol.150
, Issue.2
, pp. 167-184
-
-
Krieger, M.1
Brown, M.S.2
Goldstein, J.L.3
-
36
-
-
79958831976
-
The conserved oligomeric Golgi complex acts in organ morphogenesis via glycosylation of an ADAM protease in C. elegans
-
Kubota Y, Sano M, Goda S, Suzuki N, Nishiwaki K. 2005. The conserved oligomeric Golgi complex acts in organ morphogenesis via glycosylation of an ADAM protease in C. elegans. Development. 14:14.
-
(2005)
Development
, vol.14
, pp. 14
-
-
Kubota, Y.1
Sano, M.2
Goda, S.3
Suzuki, N.4
Nishiwaki, K.5
-
37
-
-
32244443956
-
The conserved oligomeric Golgi complex acts in organ morphogenesis via glycosylation of an ADAM protease in C. elegans
-
DOI 10.1242/dev.02195
-
Kubota Y, Sano M, Goda S, Suzuki N, Nishiwaki K. 2006. The conserved oligomeric Golgi complex acts in organ morphogenesis via glycosylation of an ADAM protease in C. elegans. Development. 133:263-273. (Pubitemid 43210715)
-
(2006)
Development
, vol.133
, Issue.2
, pp. 263-273
-
-
Kubota, Y.1
Sano, M.2
Goda, S.3
Suzuki, N.4
Nishiwaki, K.5
-
38
-
-
49449087287
-
Glycosyltransferases: Structures, functions, and mechanisms
-
Lairson LL, Henrissat B, Davies GJ, Withers SG. 2008. Glycosyltransferases: Structures, functions, and mechanisms. Annu Rev Biochem. 77:521-555.
-
(2008)
Annu Rev Biochem
, vol.77
, pp. 521-555
-
-
Lairson, L.L.1
Henrissat, B.2
Davies, G.J.3
Withers, S.G.4
-
39
-
-
67651166603
-
Direct interaction between the COG complex and the SM protein, Sly1, is required for Golgi SNARE pairing
-
Laufman O, Kedan A, Hong W, Lev S. 2009. Direct interaction between the COG complex and the SM protein, Sly1, is required for Golgi SNARE pairing. EMBO J. 28:2006-2017.
-
(2009)
EMBO J
, vol.28
, pp. 2006-2017
-
-
Laufman, O.1
Kedan, A.2
Hong, W.3
Lev, S.4
-
40
-
-
78549285917
-
Molecular organization of the COG vesicle tethering complex
-
Lees JA, Yip CK, Walz T, Hughson FM. 2010. Molecular organization of the COG vesicle tethering complex. Nat Struct Mol Biol. 17 (11):1292-1297.
-
(2010)
Nat Struct Mol Biol.
, vol.17
, Issue.11
, pp. 1292-1297
-
-
Lees, J.A.1
Yip, C.K.2
Walz, T.3
Hughson, F.M.4
-
41
-
-
33645120423
-
Cell wall assembly in Saccharomyces cerevisiae
-
Lees JA, Yip CK, Walz T, Hughson FM. 2010. Cell wall assembly in Saccharomyces cerevisiae. Microbiol Mol Biol Rev. 70(2):317-343.
-
(2010)
Microbiol Mol Biol Rev
, vol.70
, Issue.2
, pp. 317-343
-
-
Lees, J.A.1
Yip, C.K.2
Walz, T.3
Hughson, F.M.4
-
43
-
-
77956096967
-
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. 2010. Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation. Hum Mol Genet. 19:3623-3633.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 3623-3633
-
-
Lübbehusen, J.1
Thiel, C.2
Rind, N.3
Ungar, D.4
Prinsen, B.H.5
De Koning, T.J.6
Van Hasselt, P.M.7
Körner, C.8
-
44
-
-
0035036072
-
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency
-
DOI 10.1038/88299
-
Lubke T, Marquardt T, Etzioni A, Hartmann E, von Figura K, Korner C. 2001. Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency. Nat Genet. 28:73-76. (Pubitemid 32405821)
-
(2001)
Nature Genetics
, vol.28
, Issue.1
, pp. 73-76
-
-
Lubke, T.1
Marquardt, T.2
Etzioni, A.3
Hartmann, E.4
Von Figura, K.5
Korner, C.6
-
45
-
-
0024409747
-
Mitotic Golgi fragments in HeLa cells and their role in the reassembly pathway
-
Lucocq JM, Berger EG, Warren G. 1989. Mitotic Golgi fragments in HeLa cells and their role in the reassembly pathway. J Cell Biol. 109:463-474. (Pubitemid 19197010)
-
(1989)
Journal of Cell Biology
, vol.109
, Issue.2
, pp. 463-474
-
-
Lucocq, J.1
Berger, E.G.2
Warren, G.3
-
46
-
-
38449104148
-
Glycosylation of glycolipids in the Golgi complex
-
Maccioni HJ. 2007. Glycosylation of glycolipids in the Golgi complex. J Neurochem. 103(Suppl. 1):81-90.
-
(2007)
J Neurochem
, vol.103
, Issue.SUPPL. 1
, pp. 81-90
-
-
MacCioni, H.J.1
-
49
-
-
15944399952
-
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter
-
DOI 10.1182/blood-2004-09-3509
-
Martinez-Duncker I, Dupre T, Piller V, Piller F, Candelier JJ, Trichet C, Tchernia G, Oriol R, Mollicone R. 2005. Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inac-tivation of the Golgi CMP-sialic acid transporter. Blood. 105:2671-2676. (Pubitemid 40446256)
-
(2005)
Blood
, vol.105
, Issue.7
, pp. 2671-2676
-
-
Martinez-Duncker, I.1
Dupre, T.2
Piller, V.3
Piller, F.4
Candelier, J.-J.5
Trichet, C.6
Tchernia, G.7
Oriol, R.8
Mollicone, R.9
-
50
-
-
0035945348
-
Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transport
-
DOI 10.1083/jcb.200108029
-
Martinez-Menárguez JA, Prekeris R, Oorschot VM, Scheller R, Slot JW, Geuze HJ, Klumperman J. 2001. Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transport. J Cell Biol. 155:1213-1224. (Pubitemid 34286271)
-
(2001)
Journal of Cell Biology
, vol.155
, Issue.7
, pp. 1213-1224
-
-
Martinez-Menarguez, J.A.1
Prekeris, R.2
Oorschot, V.M.J.3
Scheller, R.4
Slot, J.W.5
Geuze, H.J.6
Klumperman, J.7
-
51
-
-
0037155810
-
The cytoplasmic tail of α1,3-galactosyltransferase inhibits golgi localization of the full-length enzyme
-
DOI 10.1074/jbc.M111799200
-
Milland J, Russell SM, Dodson HC, McKenzie IF, Sandrin MS. 2002. The cytoplasmic tail of α1,3-galactosyltransferase inhibits Golgi localization of the full-length enzyme. J Biol Chem. 277:10374-10378. (Pubitemid 34968156)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.12
, pp. 10374-10378
-
-
Milland, J.1
Russell, S.M.2
Dodson, H.C.3
McKenzie, I.F.C.4
Sandrin, M.S.5
-
52
-
-
85066457486
-
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia
-
Morava E, Zeevaert R, Korsch E, Huijben K, Wopereis S, Matthijs G, Keymolen K, Lefeber DJ, De Meirleir L, Wevers RA. 2007. A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia. Eur J Hum Genet. 14:14.
-
(2007)
Eur J Hum Genet
, vol.14
, pp. 14
-
-
Morava, E.1
Zeevaert, R.2
Korsch, E.3
Huijben, K.4
Wopereis, S.5
Matthijs, G.6
Keymolen, K.7
Lefeber, D.J.8
De Meirleir, L.9
Wevers, R.A.10
-
53
-
-
0017570023
-
Dynamics of the Golgi apparatus: membrane differentiation and membrane flow
-
Morré DJ, Ovtracht L. 1977. Dynamics of the Golgi apparatus: Membrane differentiation and membrane flow. Int Rev Cytol Suppl. 5:61-188. (Pubitemid 8293134)
-
(1977)
International Review of Cytology
, Issue.SUPPL. 5
, pp. 61-188
-
-
Morre, D.J.1
Ovtracht, L.2
-
54
-
-
0029165107
-
An investigation of the role of transmembrane domains in Golgi protein retention
-
Munro S. 1995. An investigation of the role of transmembrane domains in Golgi protein retention. EMBO J. 14:4695-4704.
-
(1995)
EMBO J
, vol.14
, pp. 4695-4704
-
-
Munro, S.1
-
55
-
-
0035827374
-
What can yeast tell us about N-linked glycosylation in the Golgi apparatus?
-
DOI 10.1016/S0014-5793(01)02488-7, PII S0014579301024887
-
Munro S. 2001. What can yeast tell us about N-linked glycosylation in the Golgi apparatus? FEBS Lett. 498:223-227. (Pubitemid 32539208)
-
(2001)
FEBS Letters
, vol.498
, Issue.2-3
, pp. 223-227
-
-
Munro, S.1
-
56
-
-
0023911121
-
Purification, properties and cation activation of galactosyltransferase from lactating-rat mammary Golgi membranes
-
Navaratnam N, Ward S, Fisher C, Kuhn NJ, Keen JN, Findlay JB. 1988. Purification, properties and cation activation of galactosyltransferase from lactating-rat mammary Golgi membranes. Eur J Biochem. 171:623-629. (Pubitemid 18060914)
-
(1988)
European Journal of Biochemistry
, vol.171
, Issue.3
, pp. 623-629
-
-
Navaratnam, N.1
Ward, S.2
Fischer, C.3
Kuhn, N.J.4
Keen, J.N.5
Findlay, J.B.C.6
-
57
-
-
34248657552
-
Molecular and clinical characterization of a Moroccan Cog7 deficient patient
-
DOI 10.1016/j.ymgme.2007.02.011, PII S109671920700073X
-
Ng BG, Kranz C, Hagebeuk EE, Duran M, Abeling NG, Wuyts B, Ungar D, Lupashin V, Hartdorff CM, Poll-The BT, et al. 2007. Molecular and clinical characterization of a Moroccan Cog7 deficient patient. Mol Genet Metab. 91:201-204. (Pubitemid 46773022)
-
(2007)
Molecular Genetics and Metabolism
, vol.91
, Issue.2
, pp. 201-204
-
-
Ng, B.G.1
Kranz, C.2
Hagebeuk, E.E.O.3
Duran, M.4
Abeling, N.G.G.M.5
Wuyts, B.6
Ungar, D.7
Lupashin, V.8
Hartdorff, C.M.9
Poll-The, B.T.10
Freeze, H.H.11
-
58
-
-
0027978637
-
Retention and retrieval in the endoplasmic reticulum and the Golgi apparatus
-
DOI 10.1016/0955-0674(94)90070-1
-
Nilsson T, Warren G. 1994. Retention and retrieval in the endoplasmic reticu-lum and the Golgi apparatus. Curr Opin Cell Biol. 6:517-521. (Pubitemid 24241563)
-
(1994)
Current Opinion in Cell Biology
, vol.6
, Issue.4
, pp. 517-521
-
-
Nilsson, T.1
Warren, G.2
-
59
-
-
2342467375
-
The COG and COPI Complexes Interact to Control the Abundance of GEARs, a Subset of Golgi Integral Membrane Proteins
-
DOI 10.1091/mbc.E03-09-0699
-
Oka T, Ungar D, Hughson FM, Krieger M. 2004. The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins. Mol Biol Cell. 15:2423-2435. (Pubitemid 38580657)
-
(2004)
Molecular Biology of the Cell
, vol.15
, Issue.5
, pp. 2423-2435
-
-
Oka, T.1
Ungar, D.2
Hughson, F.M.3
Krieger, M.4
-
60
-
-
0034697118
-
Medial Golgi but not late golgi glycosyltransferases exist as high molecular weight complexes. Role of luminal domain in complex formation and localization
-
DOI 10.1074/jbc.275.16.11836
-
Opat AS, Houghton F, Gleeson PA. 2000. Medial Golgi but not late Golgi glycosyltransferases exist as high molecular weight complexes. Role of luminal domain in complex formation and localization. J Biol Chem. 275:11836-11845. (Pubitemid 30237751)
-
(2000)
Journal of Biological Chemistry
, vol.275
, Issue.16
, pp. 11836-11845
-
-
Opat, A.S.1
Houghton, F.2
Gleeson, P.A.3
-
61
-
-
0034623230
-
Structure/function of the human Ga1beta1,3-glucuronosyltransferase. Dimerization and functional activity are mediated by two crucial cysteine residues
-
Ouzzine M, Gulberti S, Netter P, Magdalou J, Fournel-Gigleux S. 2000. Structure/function of the human Ga1beta1,3-glucuronosyltransferase. Dimerization and functional activity are mediated by two crucial cysteine residues. J Biol Chem. 275:28254-28260.
-
(2000)
J Biol Chem
, vol.275
, pp. 28254-28260
-
-
Ouzzine, M.1
Gulberti, S.2
Netter, P.3
Magdalou, J.4
Fournel-Gigleux, S.5
-
62
-
-
70350690698
-
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. 2009. Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. Hum Mol Genet. 18 (22):4350-4356.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.22
, pp. 4350-4356
-
-
Paesold Burda, P.1
Maag, C.2
Troxler, H.3
Foulquier, F.4
Kleinert, P.5
Schnabel, S.6
Baumgartner, M.7
Hennet, T.8
-
63
-
-
39649119621
-
The pH of the secretory pathway: Measurement, determinants, and regulation
-
Paroutis P, Touret N, Grinstein S. 2004. The pH of the secretory pathway: Measurement, determinants, and regulation. Physiology (Bethesda). 19:207-215. (Pubitemid 39481936)
-
(2004)
Physiology
, Issue.4
, pp. 207-215
-
-
Paroutis, P.1
Touret, N.2
Grinstein, S.3
-
64
-
-
44849128559
-
Transport through the Golgi Apparatus by Rapid Partitioning within a Two-Phase Membrane System
-
DOI 10.1016/j.cell.2008.04.044, PII S0092867408006181
-
Patterson GH, Hirschberg K, Polishchuk RS, Gerlich D, Phair RD, Lippincott-Schwartz J. 2008. Transport through the Golgi apparatus by rapid partitioning within a two-phase membrane system. Cell. 133: 1055-1067. (Pubitemid 351795609)
-
(2008)
Cell
, vol.133
, Issue.6
, pp. 1055-1067
-
-
Patterson, G.H.1
Hirschberg, K.2
Polishchuk, R.S.3
Gerlich, D.4
Phair, R.D.5
Lippincott-Schwartz, J.6
-
65
-
-
0345687308
-
Mechanism of Constitutive Export from the Golgi: Bulk Flow via the Formation, Protrusion, and En Bloc Cleavage of large trans-Golgi Network Tubular Domains
-
DOI 10.1091/mbc.E03-01-0033
-
Polishchuk EV, Di Pentima A, Luini A, Polishchuk RS. 2003. Mechanism of constitutive export from the Golgi: Bulk flow via the formation, protrusion, and en bloc cleavage of large trans-Golgi network tubular domains. Mol Biol Cell. 14:4470-4485. (Pubitemid 37444649)
-
(2003)
Molecular Biology of the Cell
, vol.14
, Issue.11
, pp. 4470-4485
-
-
Polishchuk, E.V.1
Di Pentima, A.2
Luini, A.3
Polishchuk, R.S.4
-
66
-
-
22044452022
-
Subcompartmentalizing the Golgi apparatus
-
DOI 10.1016/j.ceb.2005.06.006, PII S0955067405000785, Membranes and Organelles
-
Puthenveedu MA, Linstedt AD. 2005. Subcompartmentalizing the Golgi apparatus. Curr Opin Cell Biol. 17:369-375. (Pubitemid 40968066)
-
(2005)
Current Opinion in Cell Biology
, vol.17
, Issue.4
, pp. 369-375
-
-
Puthenveedu, M.A.1
Linstedt, A.D.2
-
67
-
-
0035800822
-
Location and mechanism of α2,6-sialyltransferase dimer formation. Role of cysteine residues in enzyme dimerization, localization, activity, and processing
-
Qian R, Chen C, Colley KJ. 2001. Location and mechanism of α2,6-sialyltransferase dimer formation. Role of cysteine residues in enzyme dimerization, localization, activity, and processing. J Biol Chem. 276:28641-28649.
-
(2001)
J Biol Chem
, vol.276
, pp. 28641-28649
-
-
Qian, R.1
Chen, C.2
Colley, K.J.3
-
68
-
-
0028905820
-
Mapping the distribution of Golgi enzymes involved in the construction of complex oligosaccharides
-
Rabouille C, Hui N, Hunte F, Kieckbusch R, Berger EG, Warren G, Nilsson T. 1995. Mapping the distribution of Golgi enzymes involved in the construction of complex oligosaccharides. J Cell Sci. 108(Pt 4):1617-1627.
-
(1995)
J Cell Sci
, vol.108
, Issue.PART 4
, pp. 1617-1627
-
-
Rabouille, C.1
Hui, N.2
Hunte, F.3
Kieckbusch, R.4
Berger, E.G.5
Warren, G.6
Nilsson, T.7
-
69
-
-
0035999979
-
Identification of Sec36p, Sec37p, and Sec38p: Components of yeast complex that contains Sec34p and Sec35p
-
DOI 10.1091/mbc.01-10-0495
-
Ram RJ, Li B, Kaiser CA. 2002. Identification of Sec36p, Sec37p and Sec38p: Components of the yeast complex that contains Sec34p and Sec35p. Mol Biol Cell. 13:1484-1500. (Pubitemid 34522633)
-
(2002)
Molecular Biology of the Cell
, vol.13
, Issue.5
, pp. 1484-1500
-
-
Ram, R.J.1
Li, B.2
Kaiser, C.A.3
-
70
-
-
68749117665
-
Golgi function and dysfunction in the first COG4-deficient CDG type II patient
-
Reynders E, Foulquier F, Leao Teles E, Quelhas D, Morelle W, Rabouille C, Annaert W, Matthijs G. 2009. Golgi function and dysfunction in the first COG4-deficient CDG type II patient. Hum Mol Genet. 18:3244-3256.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3244-3256
-
-
Reynders, E.1
Foulquier, F.2
Leao Teles, E.3
Quelhas, D.4
Morelle, W.5
Rabouille, C.6
Annaert, W.7
Matthijs, G.8
-
71
-
-
69449100200
-
Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene
-
Richardson BC, Smith RD, Ungar D, Nakamura A, Jeffrey PD, Lupashin VV, Hughson FM. 2009. Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene. Proc Natl Acad Sci USA. 106:13329-13334.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 13329-13334
-
-
Richardson, B.C.1
Smith, R.D.2
Ungar, D.3
Nakamura, A.4
Jeffrey, P.D.5
Lupashin, V.V.6
Hughson, F.M.7
-
72
-
-
65549131351
-
Elevated Golgi pH impairs terminal N-glycosylation by inducing mislocali-zation of Golgi glycosyltransferases
-
Rivinoja A, Hassinen A, Kokkonen N, Kauppila A, Kellokumpu S. 2009. Elevated Golgi pH impairs terminal N-glycosylation by inducing mislocali-zation of Golgi glycosyltransferases. J Cell Physiol. 220:144-154.
-
(2009)
J Cell Physiol
, vol.220
, pp. 144-154
-
-
Rivinoja, A.1
Hassinen, A.2
Kokkonen, N.3
Kauppila, A.4
Kellokumpu, S.5
-
73
-
-
0020037889
-
Immunocytochemical localization of galactosyltransferase in HeLa cells: Codistribution with thiamine pyrophosphatase in trans-Golgi cisternae
-
DOI 10.1083/jcb.93.1.223
-
Roth J, Berger EG. 1982. Immunocytochemical localization of galactosyl-transferase in HeLa cells: Codistribution with thiamine pyrophosphatase in trans-Golgi cisternae. J Cell Biol. 93:223-229. (Pubitemid 12117060)
-
(1982)
Journal of Cell Biology
, vol.93
, Issue.1
, pp. 223-229
-
-
Roth, J.1
Berger, E.G.2
-
74
-
-
0022343674
-
Demonstration of an extensive trans-tubular network continuous with the Golgi apparatus stack that may function in glycosylation
-
Roth J, Taatjes DJ, Lucocq JM, Weinstein J, Paulson JC. 1985. Demonstration of an extensive trans-tubular network continuous with the Golgi apparatus stack that may function in glycosylation. Cell. 43:287-295. (Pubitemid 16199715)
-
(1985)
Cell
, vol.43
, Issue.1
, pp. 287-295
-
-
Roth, J.1
Taatjes, D.J.2
Lucocq, J.M.3
-
75
-
-
0021248658
-
Intercompartmental transport in the Golgi complex is a dissociative process: Facile transfer of membrane protein between two Golgi populations
-
Rothman JE, Miller RL, Urbani LJ. 1984. Intercompartmental transport in the Golgi complex is a dissociative process: Facile transfer of membrane protein between two Golgi populations. J Cell Biol. 99:260-271. (Pubitemid 14096890)
-
(1984)
Journal of Cell Biology
, vol.99
, Issue.1
, pp. 260-271
-
-
Rothman, J.E.1
Miller, R.L.2
Urbani, L.J.3
-
76
-
-
33845428100
-
Transition of galactosyltransferase 1 from trans-Golgi cisterna to the trans-Golgi network is signal mediated
-
DOI 10.1091/mbc.E06-08-0665
-
Schaub BE, Berger B, et al. 2006. Transition of galactosyltransferase 1 from trans-Golgi cisterna to the trans-Golgi network is signal mediated. Mol Biol Cell. 17(12):5153-5162. (Pubitemid 44907358)
-
(2006)
Molecular Biology of the Cell
, vol.17
, Issue.12
, pp. 5153-5162
-
-
Schaub, B.E.1
Berger, B.2
Berger, E.G.3
Rohrer, J.4
-
77
-
-
67749129161
-
Lysophosphatidic acid acyltransferase 3 regulates Golgi complex structure and function
-
Schmidt JA, Brown WJ. 2009. Lysophosphatidic acid acyltransferase 3 regulates Golgi complex structure and function. J Cell Biol. 186:211-218.
-
(2009)
J Cell Biol
, vol.186
, pp. 211-218
-
-
Schmidt, J.A.1
Brown, W.J.2
-
78
-
-
41649090365
-
Golgi Localization of Glycosyltransferases Requires a Vps74p Oligomer
-
DOI 10.1016/j.devcel.2008.02.016, PII S153458070800110X
-
Schmitz KR, Liu J, Li S, Setty TG, Wood CS, Burd CG, Ferguson KM. 2008. Golgi localization of glycosyltransferases requires a Vps74p oligo-mer. Dev Cell. 14:523-534. (Pubitemid 351479939)
-
(2008)
Developmental Cell
, vol.14
, Issue.4
, pp. 523-534
-
-
Schmitz, K.R.1
Liu, J.2
Li, S.3
Setty, T.G.4
Wood, C.S.5
Burd, C.G.6
Ferguson, K.M.7
-
79
-
-
37249008781
-
Interaction of the conserved oligomeric Golgi complex with t-SNARE Syntaxin5a/Sed5 enhances intra-Golgi SNARE complex stability
-
DOI 10.1083/jcb.200705145
-
Shestakova A, Suvorova E, Pavliv O, Khaidakova G, Lupashin V. 2007. Interaction of the conserved oligomeric Golgi complex with t-SNARE syn-taxin5a/Sed5 enhances intra-Golgi SNARE complex stability. J Cell Biol. 179:1179-1192. (Pubitemid 350277737)
-
(2007)
Journal of Cell Biology
, vol.179
, Issue.6
, pp. 1179-1192
-
-
Shestakova, A.1
Suvorova, E.2
Pavliv, O.3
Khaidakova, G.4
Lupashin, V.5
-
80
-
-
33645131266
-
COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation
-
Shestakova A, Zolov S, Lupashin V. 2006. COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation. Traffic. 7:191-204.
-
(2006)
Traffic
, vol.7
, pp. 191-204
-
-
Shestakova, A.1
Zolov, S.2
Lupashin, V.3
-
82
-
-
0030931796
-
Altered Golgi localization of core 2 β-1,6-N- acetylglucosaminyltransferase leads to decreased synthesis of branched O- glycans
-
DOI 10.1074/jbc.272.36.22695
-
Skrincosky D, Kain R, El-Battari A, Exner M, Kerjaschki D, Fukuda M. 1997. Altered Golgi localization of core 2 β-1,6-N- acetylglucosaminyltransferase leads to decreased synthesis of branched O-glycans. J Biol Chem. 272: 22695-22702. (Pubitemid 27386086)
-
(1997)
Journal of Biological Chemistry
, vol.272
, Issue.36
, pp. 22695-22702
-
-
Skrincosky, D.1
Kain, R.2
El-Battari, A.3
Exner, M.4
Kerjaschki, D.5
Fukuda, M.6
-
83
-
-
70350378203
-
The COG complex, Rab6 and COPI define a novel Golgi retrograde trafficking pathway that is exploited by SubAB toxin
-
Smith RD, Willett R, Kudlyk T, Pokrovskaya I, Paton AW, Paton JC, Lupashin VV. 2009. The COG complex, Rab6 and COPI define a novel Golgi retrograde trafficking pathway that is exploited by SubAB toxin. Traf fic. 10:1502-1517.
-
(2009)
Traf Fic
, vol.10
, pp. 1502-1517
-
-
Smith, R.D.1
Willett, R.2
Kudlyk, T.3
Pokrovskaya, I.4
Paton, A.W.5
Paton, J.C.6
Lupashin, V.V.7
-
84
-
-
34247482798
-
The interaction of two tethering factors, p115 and COG complex, is required for golgi integrity
-
DOI 10.1111/j.1600-0854.2006.00530.x
-
Sohda M, Misumi Y, Yoshimura S, Nakamura N, Fusano T, Ogata S, Sakisaka S, Ikehara Y. 2007. The interaction of two tethering factors, p115 and COG complex, is required for Golgi integrity. Traffic. 8:270-284. (Pubitemid 46656518)
-
(2007)
Traffic
, vol.8
, Issue.3
, pp. 270-284
-
-
Sohda, M.1
Misumi, Y.2
Yoshimura, S.-I.3
Nakamura, N.4
Fusano, T.5
Ogata, S.6
Sakisaka, S.7
Ikehara, Y.8
-
85
-
-
0036019907
-
Protein glycosylation: Nature, distribution, enzymatic formation, and disease implications of glycopeptide bonds
-
Spiro RG. 2002. Protein glycosylation: Nature, distribution, enzymatic formation, and disease implications of glycopeptide bonds. Glycobiology. 12:43R-56R. (Pubitemid 34760066)
-
(2002)
Glycobiology
, vol.12
, Issue.4
-
-
Spiro, R.G.1
-
86
-
-
0042970585
-
Association of the golgi UDP-galactose transporter with UDP-galactose:ceramide galactosyltransferase allows UDP-galactose import in the endoplasmic reticulum
-
DOI 10.1091/mbc.E03-03-0130
-
Sprong H, Degroote S, Nilsson T, Kawakita M, Ishida N, van der Sluijs P, van Meer G. 2003. Association of the Golgi UDP-galactose transporter with UDP-galactose:ceramide galactosyltransferase allows UDP-galactose import in the endoplasmic reticulum. Mol Biol Cell. 14:3482-3493. (Pubitemid 37013143)
-
(2003)
Molecular Biology of the Cell
, vol.14
, Issue.8
, pp. 3482-3493
-
-
Sprong, H.1
Degroote, S.2
Nilsson, T.3
Kawakita, M.4
Ishida, N.5
Van Der Sluijs, P.6
Van Meer, G.7
-
87
-
-
0032517823
-
Recycling of Golgi-resident glycosyltransferases through the ER reveals a novel pathway and provides an explanation for nocodazole-induced Golgi scattering
-
DOI 10.1083/jcb.143.6.1505
-
Storrie B, White J, et al. 1998. Recycling of Golgi-resident glycosyltrans-ferases through the ER reveals a novel pathway and provides an explanation for nocodazole-induced Golgi scattering. J Cell Biol. 143 (6):1505-1521. (Pubitemid 29006499)
-
(1998)
Journal of Cell Biology
, vol.143
, Issue.6
, pp. 1505-1521
-
-
Storrie, B.1
White, J.2
Rottger, S.3
Stelzer, E.H.K.4
Suganuma, T.5
Nilsson, T.6
-
88
-
-
0037071543
-
The Sec34/Sec35p complex, a Ypt1p effector required for retrograde intra-Golgi trafficking, interacts with Golgi SNAREs and COPI vesicle coat proteins
-
DOI 10.1083/jcb.200111081
-
Suvorova ES, Duden R, Lupashin VV. 2002. The Sec34/Sec35p complex, a Ypt1p effector required for retrograde intra-Golgi trafficking, interacts with Golgi SNAREs and COPI vesicle coat proteins. J Cell Biol. 157:631-643. (Pubitemid 34839791)
-
(2002)
Journal of Cell Biology
, vol.157
, Issue.4
, pp. 631-643
-
-
Suvorova, E.S.1
Duden, R.2
Lupashin, V.V.3
-
89
-
-
0026776288
-
The signal for Golgi retention of bovine β1,4-galactosyltransferase is in the transmembrane domain
-
Teasdale RD, D'Agostaro G, Gleeson PA. 1992. The signal for Golgi retention of bovine β1,4-galactosyltransferase is in the transmembrane domain. J Biol Chem. 267:13113.
-
(1992)
J Biol Chem
, vol.267
, pp. 13113
-
-
Teasdale, R.D.1
D'Agostaro, G.2
Gleeson, P.A.3
-
90
-
-
0022530474
-
Chloroquine and ammonium chloride prevent terminal glycosylation of immunoglobulins in plasma cells without affecting secretion
-
Thorens B, Vassalli P. 1986. Chloroquine and ammonium chloride prevent terminal glycosylation of immunoglobulins in plasma cells without affecting secretion. Nature. 321:618-620. (Pubitemid 16042215)
-
(1986)
Nature
, vol.321
, Issue.6070
, pp. 618-620
-
-
Thorens, B.1
Vassalli, P.2
-
91
-
-
0037193464
-
Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function
-
DOI 10.1083/jcb.200202016
-
Ungar D, Oka T, Brittle EE, Vasile E, Lupashin VV, Chatterton JE, Heuser JE, Krieger M, Waters MG. 2002. Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function. J Cell Biol. 157:405-415. Epub 2002 Apr 29. (Pubitemid 34839805)
-
(2002)
Journal of Cell Biology
, vol.157
, Issue.3
, pp. 405-415
-
-
Ungar, D.1
Oka, T.2
Brittle, E.E.3
Vasile, E.4
Lupashin, V.V.5
Chatterton, J.E.6
Heuser, J.E.7
Krieger, M.8
Gerard Waters, M.9
-
92
-
-
79958837615
-
Subunit architecture of the conserved oligomeric Golgi complex
-
Ungar D, Oka T, Vasile E, Krieger M, Hughson FM. 2005. Subunit architecture of the conserved oligomeric Golgi complex. J Biol Chem. 14:14.
-
(2005)
J Biol Chem
, vol.14
, pp. 14
-
-
Ungar, D.1
Oka, T.2
Vasile, E.3
Krieger, M.4
Hughson, F.M.5
-
93
-
-
0031858428
-
Concepts and principles of O-linked glycosylation
-
DOI 10.1080/10409239891204198
-
Van den Steen P, Rudd PM, Dwek RA, Opdenakker G. 1998. Concepts and principles of O-linked glycosylation. Crit Rev Biochem Mol Biol. 33:151-208. (Pubitemid 28334620)
-
(1998)
Critical Reviews in Biochemistry and Molecular Biology
, vol.33
, Issue.3
, pp. 151-208
-
-
Van Den Steen, P.1
Rudd, P.M.2
Dwek, R.A.3
Opdenakker, G.4
-
94
-
-
0033571293
-
Sec34p, a protein required for vesicle tethering to the yeast Golgi apparatus, is in a complex with Sec35p
-
VanRheenen SM, Cao X, Sapperstein SK, Chiang EC, Lupashin VV, Barlowe C, Waters MG. 1999. Sec34p, a protein required for vesicle tethering to the yeast Golgi apparatus, is in a complex with Sec35p. J Cell Biol. 147:729-742.
-
(1999)
J Cell Biol
, vol.147
, pp. 729-742
-
-
Vanrheenen, S.M.1
Cao, X.2
Sapperstein, S.K.3
Chiang, E.C.4
Lupashin, V.V.5
Barlowe, C.6
Waters, M.G.7
-
95
-
-
0031976097
-
Factors controlling the glycosylation potential of the Golgi apparatus
-
DOI 10.1016/S0962-8924(97)01198-7, PII S0962892497011987
-
Varki A. 1998. Factors controlling the glycosylation potential of the Golgi apparatus. Trends Cell Biol. 8:34-40. (Pubitemid 28040845)
-
(1998)
Trends in Cell Biology
, vol.8
, Issue.1
, pp. 34-40
-
-
Varki, A.1
-
97
-
-
0032491437
-
Purification and characterization of a novel 13 S hetero-oligomeric protein complex that stimulates in vitro Golgi transport
-
DOI 10.1074/jbc.273.45.29565
-
Walter DM, Paul KS, Waters MG. 1998. Purification and characterization of a novel 13 S hetero-oligomeric protein complex that stimulates in vitro Golgi transport. J Biol Chem. 273:29565-29576. (Pubitemid 28509964)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.45
, pp. 29565-29576
-
-
Walter, D.M.1
Paul, K.S.2
Waters, M.G.3
-
98
-
-
0038731763
-
Acidification and protein traffic
-
DOI 10.1016/S0074-7696(03)01005-2
-
Weisz OA. 2003. Acidification and protein traffic. Int Rev Cytol. 226:259-319. (Pubitemid 36959357)
-
(2003)
International Review of Cytology
, vol.226
, pp. 259-319
-
-
Weisz, O.A.1
-
99
-
-
0037524357
-
O-GlcNAc turns twenty: Functional implications for post-translational modification of nuclear and cytosolic proteins with a sugar
-
DOI 10.1016/S0014-5793(03)00641-0
-
Wells L, Hart GW. 2003. O-GlcNAc turns twenty: Functional implications for post-translational modification of nuclear and cytosolic proteins with a sugar. FEBS Lett. 546:154-158. (Pubitemid 36782297)
-
(2003)
FEBS Letters
, vol.546
, Issue.1
, pp. 154-158
-
-
Wells, L.1
Hart, G.W.2
-
100
-
-
0035489304
-
The Sec34/35 Golgi Transport Complex Is Related to the Exocyst, Defining a Family of Complexes Involved in Multiple Steps of Membrane Traffic
-
DOI 10.1016/S1534-5807(01)00063-6, PII S1534580701000636
-
Whyte JR, Munro S. 2001. The Sec34/35 Golgi transport complex is related to the exocyst, defining a family of complexes involved in multiple steps of membrane traffic. Dev Cell. 1:527-537. (Pubitemid 33586104)
-
(2001)
Developmental Cell
, vol.1
, Issue.4
, pp. 527-537
-
-
Whyte, J.R.C.1
Munro, S.2
-
101
-
-
76149142505
-
PtdIns4P recognition by Vps74/GOLPH3 links PtdIns 4-kinase signaling to retrograde Golgi trafficking
-
Wood CS, Schmitz KR, et al. 2009. PtdIns4P recognition by Vps74/GOLPH3 links PtdIns 4-kinase signaling to retrograde Golgi trafficking. J Cell Biol. 187(7):967-975.
-
(2009)
J Cell Biol
, vol.187
, Issue.7
, pp. 967-975
-
-
Wood, C.S.1
Schmitz, K.R.2
-
102
-
-
2442696341
-
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder
-
DOI 10.1038/nm1041
-
Wu X, Steet RA, Bohorov O, Bakker J, Newell J, Krieger M, Spaapen L, Kornfeld S, Freeze HH. 2004. Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder. Nat Med. 10:518-523. (Pubitemid 38667911)
-
(2004)
Nature Medicine
, vol.10
, Issue.5
, pp. 518-523
-
-
Wu, X.1
Steet, R.A.2
Bohorov, O.3
Bakker, J.4
Newell, J.5
Krieger, M.6
Spaapen, L.7
Kornfeld, S.8
Freeze, H.H.9
-
103
-
-
0030050828
-
New mutants of Saccharomyces cerevisiae affected in the transport of proteins from the endoplasmic reticulum to the Golgi complex
-
Wuestehube LJ, Duden R, Eun A, Hamamoto S, Korn P, Ram R, Schekman R. 1996. New mutants of Saccharomyces cerevisiae affected in the transport of proteins from the endoplasmic reticulum to the Golgi complex. Genetics. 142:393-406. (Pubitemid 26039210)
-
(1996)
Genetics
, vol.142
, Issue.2
, pp. 393-406
-
-
Wuestehube, L.J.1
Duden, R.2
Eun, A.3
Hamamoto, S.4
Korn, P.5
Ram, R.6
Schekman, R.7
-
104
-
-
0029067675
-
Golgi retention mechanism of β-1,4-galactosyltransferase. Membrane-spanning domain-dependent homodimerization and association with α- And β-tubulins
-
Yamaguchi N, Fukuda MN. 1995. Golgi retention mechanism of β-1,4-galactosyltransferase. Membrane-spanning domain-dependent homodimerization and association with α- and β-tubulins. J Biol Chem. 270:12170-12176.
-
(1995)
J Biol Chem
, vol.270
, pp. 12170-12176
-
-
Yamaguchi, N.1
Fukuda, M.N.2
-
105
-
-
69049088687
-
A new mutation in COG7 extends the spectrum of COG subunit deficiencies
-
Zeevaert R, Foulquier F, Cheillan D, Cloix I, Guffon N, Sturiale L, Garozzo D, Matthijs G, Jaeken J. 2009. A new mutation in COG7 extends the spectrum of COG subunit deficiencies. Eur J Med Genet. 52:303-305.
-
(2009)
Eur J Med Genet
, vol.52
, pp. 303-305
-
-
Zeevaert, R.1
Foulquier, F.2
Cheillan, D.3
Cloix, I.4
Guffon, N.5
Sturiale, L.6
Garozzo, D.7
Matthijs, G.8
Jaeken, J.9
-
106
-
-
58749088569
-
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. 2008. Cerebrocostomandibular-like syndrome and a mutation in the Conserved Oligomeric Golgi complex, subunit 1. Hum Mol Genet. 18:517-524.
-
(2008)
Hum Mol Genet
, vol.18
, pp. 517-524
-
-
Zeevaert, R.1
Foulquier, F.2
Dimitrov, B.3
Reynders, E.4
Van Damme-Lombaerts, R.5
Simeonov, E.6
Annaert, W.7
Matthijs, G.8
Jaeken, J.9
-
107
-
-
36849029786
-
Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation
-
DOI 10.1016/j.ymgme.2007.08.118, PII S109671920700371X
-
Zeevaert R, Foulquier F, Jaeken J, Matthijs G. 2008. Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation. Mol Genet Metab. 93:15-21. (Pubitemid 350236002)
-
(2008)
Molecular Genetics and Metabolism
, vol.93
, Issue.1
, pp. 15-21
-
-
Zeevaert, R.1
Foulquier, F.2
Jaeken, J.3
Matthijs, G.4
-
108
-
-
0036005794
-
The cystolic and transmembrane domains of the β1,6 N-acetylglucosaminyltransferase (C2GnT) function as a cis to medial/Golgi-targeting determinant
-
Zerfaoui M, Fukuda M, Langlet C, Mathieu S, Suzuki M, Lombardo D, El-Battari A. 2002. The cytosolic and transmembrane domains of the beta 1,6 N-acetylglucosaminyltransferase (C2GnT) function as a cis to medial/ Golgi-targeting determinant. Glycobiology. 12:15-24. (Pubitemid 34218315)
-
(2002)
Glycobiology
, vol.12
, Issue.1
, pp. 15-24
-
-
Zerfaoui, M.1
Fukuda, M.2
Langlet, C.3
Mathieu, S.4
Suzuki, M.5
Lombardo, D.6
El-Battari, A.7
-
109
-
-
14744272136
-
Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells
-
DOI 10.1083/jcb.200412003
-
Zolov SN, Lupashin VV. 2005. Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells. J Cell Biol. 168:747-759. (Pubitemid 40328159)
-
(2005)
Journal of Cell Biology
, vol.168
, Issue.5
, pp. 747-759
-
-
Zolov, S.N.1
Lupashin, V.V.2
|