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 |
2 |
  2.6.1.45 | Genetic Diseases, Inborn |
11717523 |
Crystallization and preliminary crystallographic analysis of human alanine:glyoxylate aminotransferase and its polymorphic variants. |
causal interaction |
4 |
  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. |
unassigned |
0 |
  2.6.1.45 | Genetic Diseases, Inborn |
11717523 |
Crystallization and preliminary crystallographic analysis of human alanine:glyoxylate aminotransferase and its polymorphic variants. |
unassigned |
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 |
3 |
  2.6.1.45 | Hamartoma |
30598408 |
Salivary gland anlage tumor: molecular profiling sheds light on a morphologic question. |
causal interaction |
4 |
  2.6.1.45 | Hamartoma |
30598408 |
Salivary gland anlage tumor: molecular profiling sheds light on a morphologic question. |
therapeutic application |
4 |
  2.6.1.45 | Hamartoma |
8279626 |
Salivary gland anlage tumor ("congenital pleomorphic adenoma"). A clinicopathologic, immunohistochemical and ultrastructural study of nine cases. |
unassigned |
0 |
  2.6.1.45 | Hamartoma |
30598408 |
Salivary gland anlage tumor: molecular profiling sheds light on a morphologic question. |
unassigned |
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 |
4 |