EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.2.1.49 | Adenocarcinoma |
1997178 |
Induction of alpha-N-acetylgalactosamine-O-serine/threonine (Tn) antigen-mediated cellular immune response for active immunotherapy in mice. |
unassigned |
0 |
| 3.2.1.49 | Adenocarcinoma |
14767536 |
Effect of salivary gland adenocarcinoma cell-derived alpha-N-acetylgalactosaminidase on the bioactivity of macrophage activating factor. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
4
1
0 |
| 3.2.1.49 | alpha-galactosidase deficiency |
12091494 |
Defects in degradation of blood group A and B glycosphingolipids in Schindler and Fabry diseases. |
ongoing research
unassigned |
4
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
1418679 |
An investigation into the glycolipid metabolism of alpha-N-acetylgalactosaminidase-deficient fibroblasts using native and artificial glycolipids. |
causal interaction
diagnostic usage
unassigned |
4
1
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
1907616 |
Lysosomal alpha-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
2025241 |
Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiency. |
ongoing research
unassigned |
4
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
2122119 |
Disorders of glycoprotein degradation. |
causal interaction
unassigned |
2
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
2122121 |
Schindler disease: an inherited neuroaxonal dystrophy due to alpha-N-acetylgalactosaminidase deficiency. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
2160280 |
Relationship of the multiple forms of human alpha-D-galactosidase and alpha-D-fucosidase in the normal and in Fabry's disease. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 3.2.1.49 | alpha-n-acetylgalactosaminidase deficiency |
2208741 |
A method for the rapid detection of urinary glycopeptides in alpha-N-acetylgalactosaminidase deficiency and other lysosomal storage diseases. |
causal interaction
diagnostic usage
unassigned |
3
3
0 |
