EC Number   |
Disease |
PubMed ID  |
Title of Publication |
Category |
Confidence Level |
|---|
   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 | Retinal Degeneration |
11133845 |
Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium. |
ongoing research
unassigned |
2
0 |
| 2.3.1.135 | Retinal Dystrophies |
11381255 |
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy. |
causal interaction
unassigned |
3
0 |
| 2.3.1.135 | Neoplasms |
12620121 |
Evolutionary history, structural features and biochemical diversity of the NlpC/P60 superfamily of enzymes. |
unassigned |
0 |
| 2.3.1.135 | 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 | 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 | 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 | Leber Congenital Amaurosis |
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 | Retinitis Pigmentosa |
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 |
