161 related articles for article (PubMed ID: 16769205)
1. Abnormal glycosylation with hypersialylated O-glycans in patients with Sialuria.
Wopereis S; Abd Hamid UM; Critchley A; Royle L; Dwek RA; Morava E; Leroy JG; Wilcken B; Lagerwerf AJ; Huijben KM; Lefeber DJ; Rudd PM; Wevers RA
Biochim Biophys Acta; 2006 Jun; 1762(6):598-607. PubMed ID: 16769205
[TBL] [Abstract][Full Text] [Related]
2. Sialic acid metabolism in sialuria fibroblasts.
Seppala R; Tietze F; Krasnewich D; Weiss P; Ashwell G; Barsh G; Thomas GH; Packman S; Gahl WA
J Biol Chem; 1991 Apr; 266(12):7456-61. PubMed ID: 2019577
[TBL] [Abstract][Full Text] [Related]
3. Reversible sialylation: synthesis of cytidine 5'-monophospho-N-acetylneuraminic acid from cytidine 5'-monophosphate with alpha2,3-sialyl O-glycan-, glycolipid-, and macromolecule-based donors yields diverse sialylated products.
Chandrasekaran EV; Xue J; Xia J; Locke RD; Matta KL; Neelamegham S
Biochemistry; 2008 Jan; 47(1):320-30. PubMed ID: 18067323
[TBL] [Abstract][Full Text] [Related]
4. Enhanced sialylation of recombinant human erythropoietin in Chinese hamster ovary cells by combinatorial engineering of selected genes.
Son YD; Jeong YT; Park SY; Kim JH
Glycobiology; 2011 Aug; 21(8):1019-28. PubMed ID: 21436238
[TBL] [Abstract][Full Text] [Related]
5. Apolipoprotein C-III isofocusing in the diagnosis of genetic defects in O-glycan biosynthesis.
Wopereis S; Grünewald S; Morava E; Penzien JM; Briones P; García-Silva MT; Demacker PN; Huijben KM; Wevers RA
Clin Chem; 2003 Nov; 49(11):1839-45. PubMed ID: 14578315
[TBL] [Abstract][Full Text] [Related]
6. Enhanced sialylation of EPO by overexpression of UDP-GlcNAc 2-epimerase/ManAc kinase containing a sialuria mutation in CHO cells.
Bork K; Reutter W; Weidemann W; Horstkorte R
FEBS Lett; 2007 Sep; 581(22):4195-8. PubMed ID: 17706199
[TBL] [Abstract][Full Text] [Related]
7. Clinical and biochemical studies in an American child with sialuria.
Krasnewich DM; Tietze F; Krause W; Pretzlaff R; Wenger DA; Diwadkar V; Gahl WA
Biochem Med Metab Biol; 1993 Feb; 49(1):90-6. PubMed ID: 8439453
[TBL] [Abstract][Full Text] [Related]
8. Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups.
Wopereis S; Morava E; Grünewald S; Adamowicz M; Huijben KM; Lefeber DJ; Wevers RA
Glycobiology; 2005 Dec; 15(12):1312-9. PubMed ID: 16037491
[TBL] [Abstract][Full Text] [Related]
9. Sialuria in a Portuguese girl: clinical, biochemical, and molecular characteristics.
Ferreira H; Seppala R; Pinto R; Huizing M; Martins E; Braga AC; Gomes L; Krasnewich DM; Sa Miranda MC; Gahl WA
Mol Genet Metab; 1999 Jun; 67(2):131-7. PubMed ID: 10356312
[TBL] [Abstract][Full Text] [Related]
10. Sialylated N-glycans in adult rat brain tissue--a widespread distribution of disialylated antennae in complex and hybrid structures.
Zamze S; Harvey DJ; Chen YJ; Guile GR; Dwek RA; Wing DR
Eur J Biochem; 1998 Nov; 258(1):243-70. PubMed ID: 9851715
[TBL] [Abstract][Full Text] [Related]
11. Enzymatic sialylation of IgA1 O-glycans: implications for studies of IgA nephropathy.
Takahashi K; Raska M; Stuchlova Horynova M; Hall SD; Poulsen K; Kilian M; Hiki Y; Yuzawa Y; Moldoveanu Z; Julian BA; Renfrow MB; Novak J
PLoS One; 2014; 9(2):e99026. PubMed ID: 24918438
[TBL] [Abstract][Full Text] [Related]
12. Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N- and O-glycan biosynthesis defects.
Wopereis S; Grünewald S; Huijben KM; Morava E; Mollicone R; van Engelen BG; Lefeber DJ; Wevers RA
Clin Chem; 2007 Feb; 53(2):180-7. PubMed ID: 17170056
[TBL] [Abstract][Full Text] [Related]
13. Transfer of synthetic sialic acid analogues to N- and O-linked glycoprotein glycans using four different mammalian sialyltransferases.
Gross HJ; Rose U; Krause JM; Paulson JC; Schmid K; Feeney RE; Brossmer R
Biochemistry; 1989 Sep; 28(18):7386-92. PubMed ID: 2510824
[TBL] [Abstract][Full Text] [Related]
14. Clinical course and biochemistry of sialuria.
Enns GM; Seppala R; Musci TJ; Weisiger K; Ferrell LD; Wenger DA; Gahl WA; Packman S
J Inherit Metab Dis; 2001 Jun; 24(3):328-36. PubMed ID: 11486897
[TBL] [Abstract][Full Text] [Related]
15. Increased alpha2,6 sialylation of N-glycans in a transgenic mouse model of hepatocellular carcinoma.
Pousset D; Piller V; Bureaud N; Monsigny M; Piller F
Cancer Res; 1997 Oct; 57(19):4249-56. PubMed ID: 9331085
[TBL] [Abstract][Full Text] [Related]
16. Sialylation of glycoprotein oligosaccharides with N-acetyl-, N-glycolyl-, and N-O-diacetylneuraminic acids.
Higa HH; Paulson JC
J Biol Chem; 1985 Jul; 260(15):8838-49. PubMed ID: 4019457
[TBL] [Abstract][Full Text] [Related]
17. Dominant inheritance of sialuria, an inborn error of feedback inhibition.
Leroy JG; Seppala R; Huizing M; Dacremont G; De Simpel H; Van Coster RN; Orvisky E; Krasnewich DM; Gahl WA
Am J Hum Genet; 2001 Jun; 68(6):1419-27. PubMed ID: 11326336
[TBL] [Abstract][Full Text] [Related]
18. Metabolic control of recombinant monoclonal antibody N-glycosylation in GS-NS0 cells.
Hills AE; Patel A; Boyd P; James DC
Biotechnol Bioeng; 2001 Oct; 75(2):239-51. PubMed ID: 11536148
[TBL] [Abstract][Full Text] [Related]
19. Mammalian sialyltransferase ST3Gal-II: its exchange sialylation catalytic properties allow labeling of sialyl residues in mucin-type sialylated glycoproteins and specific gangliosides.
Chandrasekaran EV; Xue J; Xia J; Locke RD; Patil SA; Neelamegham S; Matta KL
Biochemistry; 2011 Nov; 50(44):9475-87. PubMed ID: 21913655
[TBL] [Abstract][Full Text] [Related]
20. Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzyme.
Seppala R; Lehto VP; Gahl WA
Am J Hum Genet; 1999 Jun; 64(6):1563-9. PubMed ID: 10330343
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
