275 related articles for article (PubMed ID: 16537452)
1. 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]
2. 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]
3. Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder.
Wu X; Steet RA; Bohorov O; Bakker J; Newell J; Krieger M; Spaapen L; Kornfeld S; Freeze HH
Nat Med; 2004 May; 10(5):518-23. PubMed ID: 15107842
[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. 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 RD; Cipollo JF; Costello CE; Loh E; Hong W; Freeze HH
Hum Mol Genet; 2007 Apr; 16(7):731-41. PubMed ID: 17331980
[TBL] [Abstract][Full Text] [Related]
6. Golgi function and dysfunction in the first COG4-deficient CDG type II patient.
Reynders E; Foulquier F; Leão Teles E; Quelhas D; Morelle W; Rabouille C; Annaert W; Matthijs G
Hum Mol Genet; 2009 Sep; 18(17):3244-56. PubMed ID: 19494034
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation.
Smith RD; Lupashin VV
Carbohydr Res; 2008 Aug; 343(12):2024-31. PubMed ID: 18353293
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. COG6-CDG: Novel variants and novel malformation.
Cirnigliaro L; Bianchi P; Sturiale L; Garozzo D; Mangili G; Keldermans L; Rizzo R; Matthijs G; Fiumara A; Jaeken J; Barone R
Birth Defects Res; 2022 Mar; 114(5-6):165-174. PubMed ID: 35068072
[TBL] [Abstract][Full Text] [Related]
13. Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder.
Spaapen LJ; Bakker JA; van der Meer SB; Sijstermans HJ; Steet RA; Wevers RA; Jaeken J
J Inherit Metab Dis; 2005; 28(5):707-14. PubMed ID: 16151902
[TBL] [Abstract][Full Text] [Related]
14. A rapid mass spectrometric strategy for the characterization of N- and O-glycan chains in the diagnosis of defects in glycan biosynthesis.
Faid V; Chirat F; Seta N; Foulquier F; Morelle W
Proteomics; 2007 Jun; 7(11):1800-13. PubMed ID: 17520685
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. More than just sugars: Conserved oligomeric Golgi complex deficiency causes glycosylation-independent cellular defects.
Blackburn JB; Kudlyk T; Pokrovskaya I; Lupashin VV
Traffic; 2018 Jun; 19(6):463-480. PubMed ID: 29573151
[TBL] [Abstract][Full Text] [Related]
17. Golgi inCOGnito: From vesicle tethering to human disease.
D'Souza Z; Taher FS; Lupashin VV
Biochim Biophys Acta Gen Subj; 2020 Nov; 1864(11):129694. PubMed ID: 32730773
[TBL] [Abstract][Full Text] [Related]
18. Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.
Hansske B; Thiel C; Lübke T; Hasilik M; Höning S; Peters V; Heidemann PH; Hoffmann GF; Berger EG; von Figura K; Körner C
J Clin Invest; 2002 Mar; 109(6):725-33. PubMed ID: 11901181
[TBL] [Abstract][Full Text] [Related]
19. 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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]