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PubMed 15958417 Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies. The Large(myd) mouse has a loss-of-function mutation in the putative glycosyltransferase gen 1.83 KB 2019-05-30 50 4
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PubMed 15987957 Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. Hereditary inclusion body myopathy (HI 1.7 KB 2018-03-09 54 10
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PubMed 16037488 Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia. Untreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] def 920 Bytes 2019-05-30 50 0
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PubMed 16037491 Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. Defects in the biosynthesis of N- and core 1 O-glycans may be found by isoele 1.88 KB 2019-05-30 68 1
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PubMed 16079417 Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts. Patients with Type I congenital disorders of glycosylation (CDG-I) make incom 1.92 KB 2019-05-30 50 8
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PubMed 16574813 Ganglioside GM3 modulates tumor suppressor PTEN-mediated cell cycle progression--transcriptional induction of p21(WAF1) and p27(kip1) by inhibition of PI-3K/AKT pathway. The simple ganglioside GM3 has 2.21 KB 2019-05-30 69 9
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PubMed 16192407 Phenotypic changes induced by expression of beta-galactoside alpha2,6 sialyltransferase I in the human colon cancer cell line SW948. Beta-galactoside alpha2,6 sialyltransferase (ST6Gal.I), the enzyme 1.83 KB 2019-05-30 53 12
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PubMed 16361247 Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement. Sialidosis and galactosialidosis are lysosomal storage 1.76 KB 2019-05-30 55 6
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PubMed 16377754 A defect in exodegradative pathways provides insight into endodegradation of heparan and dermatan sulfates. Within cells, dermatan sulfate (DS) and heparan sulfate (HS) are degraded in two steps. The 1.83 KB 2019-05-30 61 5
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PubMed 16428802 A specific detection of GlcNAcbeta1-6Manalpha1 branches in N-linked glycoproteins based on the specificity of N-acetylglucosaminyltransferase VI. Malignant transformation is often accompanied by an ab 1.6 KB 2019-05-30 54 3
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