EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
6.2.1.3 | Acidosis |
18806831 |
Promotion of glioma cell survival by acyl-CoA synthetase 5 under extracellular acidosis conditions. |
causal interaction diagnostic usage ongoing research therapeutic application |
4 3 4 4 |
6.2.1.3 | Acidosis |
30953950 |
Extracellular Acidosis Modulates the Expression of Epithelial-Mesenchymal Transition (EMT) Markers and Adhesion of Epithelial and Tumor Cells. |
causal interaction therapeutic application unassigned |
2 1 0 |
6.2.1.3 | Acquired Immunodeficiency Syndrome |
30909726 |
Preservation of Acyl Coenzyme A Attenuates Pathological and Metabolic Cardiac Remodeling Through Selective Lipid Trafficking. |
ongoing research therapeutic application unassigned |
1 1 0 |
6.2.1.3 | Adenocarcinoma |
16110457 |
Impaired expression of acyl-CoA synthetase 5 in sporadic colorectal adenocarcinomas. |
diagnostic usage ongoing research unassigned |
3 3 0 |
6.2.1.3 | Adenocarcinoma |
28153554 |
Low acyl-CoA synthetase 5 expression in colorectal carcinomas is prognostic for early tumour recurrence. |
causal interaction diagnostic usage ongoing research therapeutic application |
4 4 4 3 |
6.2.1.3 | Adenocarcinoma of Lung |
32347412 |
Roles of acyl-CoA synthetase long-chain family member 5 and colony stimulating factor 2 in inhibition of palmitic or stearic acids in lung cancer cell proliferation and metabolism. |
ongoing research unassigned |
2 0 |
6.2.1.3 | Adrenoleukodystrophy |
2309698 |
The red-green visual pigment gene region in adrenoleukodystrophy. |
causal interaction therapeutic application unassigned |
4 1 0 |
6.2.1.3 | Adrenoleukodystrophy |
2310609 |
Effect of clofibrate on peroxisomal lignoceroyl-CoA ligase activity. |
causal interaction unassigned |
1 0 |
6.2.1.3 | Adrenoleukodystrophy |
2705786 |
Adrenoleukodystrophy: impaired oxidation of fatty acids due to peroxisomal lignoceroyl-CoA ligase deficiency. |
ongoing research unassigned |
4 0 |
6.2.1.3 | Adrenoleukodystrophy |
3141702 |
X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts. |
causal interaction diagnostic usage ongoing research unassigned |
1 3 1 0 |