EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.6.1.45 | Genetic Diseases, Inborn |
10400689 |
Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase. |
causal interaction
unassigned |
2
0 |
| 2.6.1.45 | Genetic Diseases, Inborn |
11717523 |
Crystallization and preliminary crystallographic analysis of human alanine:glyoxylate aminotransferase and its polymorphic variants. |
causal interaction
unassigned |
4
0 |
| 2.6.1.45 | Hamartoma |
8279626 |
Salivary gland anlage tumor ("congenital pleomorphic adenoma"). A clinicopathologic, immunohistochemical and ultrastructural study of nine cases. |
causal interaction
unassigned |
3
0 |
| 2.6.1.45 | Hamartoma |
30598408 |
Salivary gland anlage tumor: molecular profiling sheds light on a morphologic question. |
causal interaction
therapeutic application
unassigned |
4
4
0 |
| 2.6.1.45 | Hyperoxaluria |
7979103 |
Re-evaluation of conditions required for measurement of true alanine:glyoxylate aminotransferase activity in human liver: implications for the diagnosis of hyperoxaluria type I. |
diagnostic usage
ongoing research
unassigned |
2
4
0 |
| 2.6.1.45 | Hyperoxaluria |
8651256 |
Selective renal transplantation in primary hyperoxaluria type 1. |
causal interaction
unassigned |
3
0 |
| 2.6.1.45 | Hyperoxaluria |
8914045 |
Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria. |
therapeutic application
unassigned |
1
0 |
| 2.6.1.45 | Hyperoxaluria |
11158411 |
Combined liver-kidney transplantation for primary hyperoxaluria type 1 in young children. |
causal interaction
unassigned |
4
0 |
| 2.6.1.45 | Hyperoxaluria |
11708860 |
Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
3
1
0 |
| 2.6.1.45 | Hyperoxaluria |
15849466 |
Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria. |
causal interaction
unassigned |
3
0 |
