EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   7.2.1.3 | Adenocarcinoma |
18223212 |
Overexpression of cellular iron import proteins is associated with malignant progression of esophageal adenocarcinoma. |
causal interaction
unassigned |
3
0 |
| 7.2.1.3 | Anemia |
17087784 |
Immunolocalization of duodenal cytochrome B: a relationship with circulating markers of iron status. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
1
3
0 |
| 7.2.1.3 | Anemia |
26976781 |
Fermented Goat's Milk Consumption Improves Duodenal Expression of Iron Homeostasis Genes during Anemia Recovery. |
unassigned |
0 |
| 7.2.1.3 | Anemia |
28669019 |
Altered expression of intestinal duodenal cytochrome b and divalent metal transporter 1 might be associated with cardio-renal anemia syndrome. |
causal interaction
unassigned |
2
0 |
| 7.2.1.3 | Anemia, Hypochromic |
21104018 |
Overexpression of AtFRO6 in transgenic tobacco enhances ferric chelate reductase activity in leaves and increases tolerance to iron-deficiency chlorosis. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
1
2
0 |
| 7.2.1.3 | Anemia, Hypochromic |
26993237 |
CIPK23 is involved in iron acquisition of Arabidopsis by affecting ferric chelate reductase activity. |
diagnostic usage
unassigned |
1
0 |
| 7.2.1.3 | Anemia, Sideroblastic |
11673399 |
Recent advances in disorders of iron metabolism: mutations, mechanisms and modifiers. |
therapeutic application
unassigned |
1
0 |
| 7.2.1.3 | ascorbate ferrireductase (transmembrane) deficiency |
31822578 |
Congenital absence of norepinephrine due to CYB561 mutations. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
2
0 |
| 7.2.1.3 | Asthma |
34022066 |
Genome-wide association study identifies TNFSF15 associated with childhood asthma. |
causal interaction
diagnostic usage
unassigned |
1
1
0 |
| 7.2.1.3 | Brain Diseases |
30692144 |
Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities. |
unassigned |
0 |
