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source ID
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text
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# proj.
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# Ann.
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updated_at |
| PubMed |
10359825 |
A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-defic |
1.71 KB |
2018-12-10 |
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8 |
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9 |
2021-10-11
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| PubMed |
10536037 |
Cloning and expression of a human gene encoding an N-acetylgalactosamine-alpha2,6-sialyltransferase |
1.85 KB |
2019-05-30 |
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63 |
|
6 |
2021-10-11
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| PubMed |
10639137 |
The putative tumor suppressors EXT1 and EXT2 form a stable complex that accumulates in the Golgi app |
1.31 KB |
2015-11-15 |
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9 |
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17 |
2021-10-11
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| PubMed |
11115853 |
Neuronal expression of the fukutin gene.
Fukuyama-type congenital muscular dystrophy (FCMD), a relat |
1.74 KB |
2015-11-17 |
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6 |
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15 |
2021-10-11
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| PubMed |
11592034 |
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy w |
1.91 KB |
2015-11-17 |
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13 |
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13 |
2021-10-11
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| PubMed |
11741828 |
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a |
1.84 KB |
2015-11-17 |
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6 |
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16 |
2021-10-11
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| PubMed |
10187838 |
Molecular cloning and characterization of a human uronyl 2-sulfotransferase that sulfates iduronyl a |
1.71 KB |
2015-11-17 |
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41 |
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1 |
2021-10-11
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| PubMed |
11326279 |
The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.
Le |
1.54 KB |
2015-11-17 |
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5 |
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2 |
2021-10-11
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| PubMed |
11326280 |
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as |
1.76 KB |
2015-11-17 |
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5 |
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6 |
2021-10-11
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| PubMed |
11983712 |
Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7G |
1.57 KB |
2015-11-17 |
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28 |
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1 |
2021-10-11
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