EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
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 |
2.3.1.135 | Blindness |
32084365 |
Deletion of M-opsin prevents "M cone" degeneration in a mouse model of Leber congenital amaurosis. |
causal interaction unassigned |
2 0 |
2.3.1.135 | Carcinoma |
9989277 |
Reduced lecithin:retinol acyl transferase activity in cultured squamous cell carcinoma lines results in increased substrate-driven retinoic acid synthesis. |
ongoing research unassigned |
3 0 |
2.3.1.135 | Carcinoma, Squamous Cell |
9989277 |
Reduced lecithin:retinol acyl transferase activity in cultured squamous cell carcinoma lines results in increased substrate-driven retinoic acid synthesis. |
ongoing research unassigned |
3 0 |
2.3.1.135 | Hypercholesterolemia |
25906639 |
Asteroid hyalosis--current state of knowledge. |
unassigned |
0 |
2.3.1.135 | Hypertension |
25906639 |
Asteroid hyalosis--current state of knowledge. |
unassigned |
0 |