EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level  |
|---|
    1.3.3.3 | Anemia |
15579372 |
Adherence modifies the regulation of gene expression induced by interleukin-10. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 1.3.3.3 | Anemia, Sideroblastic |
3992190 |
Coproporphyrinogen oxidase activity and porphyrin concentrations in peripheral red blood cells in hereditary sideroblastic anaemia. |
ongoing research
therapeutic application
unassigned |
4
1
0 |
| 1.3.3.3 | Brain Diseases |
29660996 |
A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). |
unassigned |
0 |
| 1.3.3.3 | Brain Neoplasms |
21824890 |
Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
3
1
0 |
| 1.3.3.3 | Brain Neoplasms |
23674837 |
Retraction of "Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence". Neuro-Oncology 13(11):1234-1243. |
unassigned |
0 |
| 1.3.3.3 | Carcinoma, Hepatocellular |
9674964 |
Effect of acute lead treatment on coproporphyrinogen oxidase activity in HepG2 cells. |
ongoing research
unassigned |
4
0 |
| 1.3.3.3 | Cataract |
23631845 |
Hereditary cataract of the Nakano mouse: Involvement of a hypomorphic mutation in the coproporphyrinogen oxidase gene. |
unassigned |
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
398301 |
The porphyrias. |
unassigned |
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
843348 |
Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria. |
unassigned |
0 |
| 1.3.3.3 | Coproporphyria, Hereditary |
3574346 |
Analysis of porphyrins and enzymes in porphyrin synthesis in Taenia solium cysticercus from man and pig. |
unassigned |
0 |
