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GGDB-2020
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PubMed
10206952
Molecular cloning of a novel alpha2,3-sialyltransferase (ST3Gal VI) that sialylates type II lactosamine structures on glycoproteins and glycolipids. A novel member of the human CMP-NeuAc:beta-galactos
1.34 KB
2015-11-17
42
15
2021-12-17
PubMed
12217961
ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg. In the endoplasmic reticulum (ER) of eukaryotes, N-linked glycans are first assembled on the lipid carrier dolichyl py
1.73 KB
2015-11-17
14
9
2021-12-17
PubMed
12369018
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Walker-Warburg syndrome (WWS) is an autosomal recessive developmental dis
1.81 KB
2015-11-17
5
12
2021-12-17
PubMed
12480927
A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation. The underlying causes of type I congenital dis
1.69 KB
2015-11-17
27
0
2021-12-17
PubMed
10318803
The tumor suppressor EXT-like gene EXTL2 encodes an alpha1, 4-N-acetylhexosaminyltransferase that transfers N-acetylgalactosamine and N-acetylglucosamine to the common glycosaminoglycan-protein linkag
1.95 KB
2015-11-18
42
8
2021-12-17
PubMed
10366449
Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1. We have isolated a human
1.55 KB
2015-11-18
4
10
2021-12-17
PubMed
15620693
A novel beta1,3-N-acetylglucosaminyltransferase (beta3Gn-T8), which synthesizes poly-N-acetyllactosamine, is dramatically upregulated in colon cancer. A new member of the UDP-N-acetylglucosamine: beta
1.15 KB
2015-11-18
6
7
2021-12-17
PubMed
15148656
Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. Defects of lipid-linked oligosaccharide assembly lead to alterati
1.46 KB
2018-12-10
6
8
2021-12-17
PubMed
10049591
CHST1 and CHST2 sulfotransferases expressed by human vascular endothelial cells: cDNA cloning, expression, and chromosomal localization. Sulfation is essential for the generation of functional vascula
1001 Bytes
2015-11-20
4
19
2021-12-17
PubMed
10082676
Molecular cloning and expression of a second glucuronyltransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope. A cDNA encoding a novel glucuronyltransferase was cloned from a rat b
1.14 KB
2015-11-20
4
0
2021-12-17
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