EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.3.1.135 | Urinary Bladder Neoplasms |
15161698 |
Reduced lecithin: retinol acyltransferase expression correlates with increased pathologic tumor stage in bladder cancer. |
causal interaction diagnostic usage unassigned |
3 2 0 |
2.3.1.135 | Overweight |
30967641 |
The association of lecithin retinol acyltransferase and the 25(OH)D receptor with pediatric overweight and obesity. |
causal interaction diagnostic usage ongoing research unassigned |
3 3 3 0 |
2.3.1.135 | Melanoma |
24433184 |
Lecithin retinol acyltransferase as a potential prognostic marker for malignant melanoma. |
causal interaction diagnostic usage ongoing research therapeutic application |
1 4 2 4 |
2.3.1.135 | Neoplasm Metastasis |
24433184 |
Lecithin retinol acyltransferase as a potential prognostic marker for malignant melanoma. |
causal interaction diagnostic usage ongoing research therapeutic application |
1 4 2 4 |
2.3.1.135 | Nevus, Pigmented |
24433184 |
Lecithin retinol acyltransferase as a potential prognostic marker for malignant melanoma. |
causal interaction diagnostic usage ongoing research therapeutic application |
1 4 2 4 |
2.3.1.135 | Blindness |
17438524 |
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa. |
causal interaction ongoing research unassigned |
2 2 0 |
2.3.1.135 | Blindness |
21555576 |
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis. |
causal interaction unassigned |
2 0 |
2.3.1.135 | Blindness |
22531707 |
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis. |
unassigned |
0 |
2.3.1.135 | Blindness |
24664772 |
Pathophysilogical mechanism and treatment strategies for leber congenital amaurosis. |
causal interaction unassigned |
3 0 |
2.3.1.135 | Blindness |
25416279 |
Genetic deletion of S-opsin prevents rapid cone degeneration in a mouse model of Leber congenital amaurosis. |
causal interaction unassigned |
3 0 |