261 related articles for article (PubMed ID: 15708848)
1. Analysis of glycosylation in CDG-Ia fibroblasts by fluorophore-assisted carbohydrate electrophoresis: implications for extracellular glucose and intracellular mannose 6-phosphate.
Gao N; Shang J; Lehrman MA
J Biol Chem; 2005 May; 280(18):17901-9. PubMed ID: 15708848
[TBL] [Abstract][Full Text] [Related]
2. Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection.
Orvisky E; Stubblefield B; Long RT; Martin BM; Sidransky E; Krasnewich D
Anal Biochem; 2003 Jun; 317(1):12-8. PubMed ID: 12729595
[TBL] [Abstract][Full Text] [Related]
3. Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts.
Eklund EA; Merbouh N; Ichikawa M; Nishikawa A; Clima JM; Dorman JA; Norberg T; Freeze HH
Glycobiology; 2005 Nov; 15(11):1084-93. PubMed ID: 16079417
[TBL] [Abstract][Full Text] [Related]
4. A zebrafish model of PMM2-CDG reveals altered neurogenesis and a substrate-accumulation mechanism for N-linked glycosylation deficiency.
Cline A; Gao N; Flanagan-Steet H; Sharma V; Rosa S; Sonon R; Azadi P; Sadler KC; Freeze HH; Lehrman MA; Steet R
Mol Biol Cell; 2012 Nov; 23(21):4175-87. PubMed ID: 22956764
[TBL] [Abstract][Full Text] [Related]
5. Increased biosynthesis of glycosphingolipids in congenital disorder of glycosylation Ia (CDG-Ia) fibroblasts.
Sala G; Dupré T; Seta N; Codogno P; Ghidoni R
Pediatr Res; 2002 Nov; 52(5):645-51. PubMed ID: 12409508
[TBL] [Abstract][Full Text] [Related]
6. Exogenous mannose does not raise steady state mannose-6-phosphate pools of normal or N-glycosylation-deficient human fibroblasts.
Higashidani A; Bode L; Nishikawa A; Freeze HH
Mol Genet Metab; 2009 Apr; 96(4):268-72. PubMed ID: 19157945
[TBL] [Abstract][Full Text] [Related]
7. Mannose supplementation corrects GDP-mannose deficiency in cultured fibroblasts from some patients with Congenital Disorders of Glycosylation (CDG).
Rush JS; Panneerselvam K; Waechter CJ; Freeze HH
Glycobiology; 2000 Aug; 10(8):829-35. PubMed ID: 10929009
[TBL] [Abstract][Full Text] [Related]
8. Mannose-6-phosphate regulates destruction of lipid-linked oligosaccharides.
Gao N; Shang J; Huynh D; Manthati VL; Arias C; Harding HP; Kaufman RJ; Mohr I; Ron D; Falck JR; Lehrman MA
Mol Biol Cell; 2011 Sep; 22(17):2994-3009. PubMed ID: 21737679
[TBL] [Abstract][Full Text] [Related]
9. Liposome-encapsulated mannose-1-phosphate therapy improves global N-glycosylation in different congenital disorders of glycosylation.
Budhraja R; Radenkovic S; Jain A; Muffels IJJ; Ismaili MHA; Kozicz T; Pandey A; Morava E
Mol Genet Metab; 2024 Jun; 142(2):108487. PubMed ID: 38733638
[TBL] [Abstract][Full Text] [Related]
10. Phosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblasts.
Sharma V; Ichikawa M; He P; Scott DA; Bravo Y; Dahl R; Ng BG; Cosford ND; Freeze HH
J Biol Chem; 2011 Nov; 286(45):39431-8. PubMed ID: 21949237
[TBL] [Abstract][Full Text] [Related]
11. The compartmentalisation of phosphorylated free oligosaccharides in cells from a CDG Ig patient reveals a novel ER-to-cytosol translocation process.
Peric D; Durrant-Arico C; Delenda C; Dupré T; De Lonlay P; de Baulny HO; Pelatan C; Bader-Meunier B; Danos O; Chantret I; Moore SE
PLoS One; 2010 Jul; 5(7):e11675. PubMed ID: 20652024
[TBL] [Abstract][Full Text] [Related]
12. Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations.
Dupré T; Vuillaumier-Barrot S; Chantret I; Sadou Yayé H; Le Bizec C; Afenjar A; Altuzarra C; Barnérias C; Burglen L; de Lonlay P; Feillet F; Napuri S; Seta N; Moore SE
J Med Genet; 2010 Nov; 47(11):729-35. PubMed ID: 20679665
[TBL] [Abstract][Full Text] [Related]
13. A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharide.
Burda P; Borsig L; de Rijk-van Andel J; Wevers R; Jaeken J; Carchon H; Berger EG; Aebi M
J Clin Invest; 1998 Aug; 102(4):647-52. PubMed ID: 9710431
[TBL] [Abstract][Full Text] [Related]
14. Abnormal synthesis of mannose 1-phosphate derived carbohydrates in carbohydrate-deficient glycoprotein syndrome type I fibroblasts with phosphomannomutase deficiency.
Körner C; Lehle L; von Figura K
Glycobiology; 1998 Feb; 8(2):165-71. PubMed ID: 9451026
[TBL] [Abstract][Full Text] [Related]
15. Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.
Freeze HH
Biochim Biophys Acta; 2009 Sep; 1792(9):835-40. PubMed ID: 19339218
[TBL] [Abstract][Full Text] [Related]
16. Neurological presentation of a congenital disorder of glycosylation CDG-Ia: implications for diagnosis and genetic counseling.
Drouin-Garraud V; Belgrand M; Grünewald S; Seta N; Dacher JN; Hénocq A; Matthijs G; Cormier-Daire V; Frébourg T; Saugier-Veber P
Am J Med Genet; 2001 Jun; 101(1):46-9. PubMed ID: 11343337
[TBL] [Abstract][Full Text] [Related]
17. Analyses of dolichol pyrophosphate-linked oligosaccharides in cell cultures and tissues by fluorophore-assisted carbohydrate electrophoresis.
Gao N; Lehrman MA
Glycobiology; 2002 May; 12(5):353-60. PubMed ID: 12070078
[TBL] [Abstract][Full Text] [Related]
18. Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia.
Dupré T; Barnier A; de Lonlay P; Cormier-Daire V; Durand G; Codogno P; Seta N
Glycobiology; 2000 Dec; 10(12):1277-81. PubMed ID: 11159919
[TBL] [Abstract][Full Text] [Related]
19. A Novel N-Tetrasaccharide in Patients with Congenital Disorders of Glycosylation, Including Asparagine-Linked Glycosylation Protein 1, Phosphomannomutase 2, and Mannose Phosphate Isomerase Deficiencies.
Zhang W; James PM; Ng BG; Li X; Xia B; Rong J; Asif G; Raymond K; Jones MA; Hegde M; Ju T; Cummings RD; Clarkson K; Wood T; Boerkoel CF; Freeze HH; He M
Clin Chem; 2016 Jan; 62(1):208-17. PubMed ID: 26430078
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij.
Wu X; Rush JS; Karaoglu D; Krasnewich D; Lubinsky MS; Waechter CJ; Gilmore R; Freeze HH
Hum Mutat; 2003 Aug; 22(2):144-50. PubMed ID: 12872255
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
