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# proj.
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# Ann.
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updated_at |
| PubMed |
11555618 |
Glycosidase active site mutations in human alpha-L-iduronidase.
Mucopolysaccharidosis type I (MPS I; McKusick 25280) results from a deficiency in alpha-L-iduronidase activity. Using a bioinformatics a |
1.75 KB |
2019-05-30 |
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55 |
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5 |
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| PubMed |
11588157 |
Galactosylation of N-linked oligosaccharides by human beta-1,4-galactosyltransferases I, II, III, IV, V, and VI expressed in Sf-9 cells.
Several studies showed that Sf-9 cells can synthesize the galac |
1.54 KB |
2019-05-30 |
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59 |
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8 |
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| PubMed |
11425801 |
Mouse ST6Gal sialyltransferase gene expression during mammary gland lactation.
The sialyltransferase ST6Gal mediates the biosynthetic addition of sialic acid, via an alpha2,6 linkage, to the nonreduci |
2.29 KB |
2019-05-30 |
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54 |
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5 |
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| PubMed |
11447138 |
Cell surface-expressed Thomsen-Friedenreich antigen in colon cancer is predominantly carried on high molecular weight splice variants of CD44.
Increased mucosal expression of TF, the Thomsen-Friedenre |
1.82 KB |
2019-05-30 |
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58 |
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7 |
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| PubMed |
12626384 |
A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.
Fabry disease is a lysosomal storage disease arising from deficiency of |
1.85 KB |
2019-05-30 |
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54 |
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1 |
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| PubMed |
12626422 |
The underglycosylation of plasma alpha 1-antitrypsin in congenital disorders of glycosylation type I is not random.
Conditions under which the glycosylation capacity of cells is limited provide an opp |
1.74 KB |
2019-05-30 |
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54 |
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2 |
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| PubMed |
12107080 |
Ectopic expression of a GlcNAc 6-O-sulfotransferase, GlcNAc6ST-2, in colonic mucinous adenocarcinoma.
The content of sulfated glycans having 6-O-sulfated GlcNAc residues alters in the course of coloni |
1.88 KB |
2019-05-30 |
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70 |
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1 |
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| PubMed |
12145188 |
Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb).
Recently, we reported a novel congenital disorder of glycosylation (CDG-IIb) caused by severe defi |
2.72 KB |
2019-08-21 |
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74 |
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3 |
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| PubMed |
12499404 |
Production in yeast of alpha-galactosidase A, a lysosomal enzyme applicable to enzyme replacement therapy for Fabry disease.
A mammalian-like sugar moiety was created in glycoprotein by Saccharomyces |
1.57 KB |
2019-05-30 |
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55 |
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4 |
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| PubMed |
10362839 |
Identification and characterization of a novel UDP-GalNAc:GlcAbeta-R alpha1,4-N-acetylgalactosaminyltransferase from a human sarcoma cell line.
We recently discovered a novel alpha-N-acetylgalactosami |
2.12 KB |
2018-03-09 |
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68 |
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4 |
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