EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.3.1.155 | acetyl-coa c-myristoyltransferase deficiency |
9645074 |
[Peroxisomal 3-ketoacyl-CoA thiolase deficiency] |
causal interaction
unassigned |
4
0 |
| 2.3.1.155 | acetyl-coa c-myristoyltransferase deficiency |
11992265 |
Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein. |
causal interaction
unassigned |
4
0 |
| 2.3.1.155 | Adrenoleukodystrophy |
12054595 |
Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes. |
diagnostic usage
unassigned |
2
0 |
| 2.3.1.155 | Carcinoma, Hepatocellular |
15071170 |
trans-activation of PPARalpha and induction of PPARalpha target genes by perfluorooctane-based chemicals. |
therapeutic application
unassigned |
1
0 |
| 2.3.1.155 | Chondrodysplasia Punctata, Rhizomelic |
2181395 |
Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata. |
causal interaction
ongoing research
unassigned |
1
1
0 |
| 2.3.1.155 | Chondrodysplasia Punctata, Rhizomelic |
8295403 |
Peroxisomal 3-ketoacyl-CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata. |
causal interaction
ongoing research
unassigned |
3
1
0 |
| 2.3.1.155 | Zellweger Syndrome |
2181395 |
Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata. |
causal interaction
ongoing research
unassigned |
1
1
0 |
