EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
10196381 |
Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
2
4
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
15772093 |
Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency. |
unassigned |
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
17828604 |
Lack of adrenoleukodystrophy protein enhances oligodendrocyte disturbance and microglia activation in mice with combined Abcd1/Mag deficiency. |
causal interaction
ongoing research
unassigned |
4
2
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
18585430 |
Effect of dietary polyunsaturated fatty acids on the expression of peroxisomal ABC transporters. |
causal interaction
unassigned |
4
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
19406244 |
Induction of the adrenoleukodystrophy-related gene (ABCD2) by thyromimetics. |
causal interaction
unassigned |
4
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
22057157 |
Incidence of Abcd1 level on the induction of cell death and organelle dysfunctions triggered by very long chain fatty acids and TNF-? on oligodendrocytes and astrocytes. |
causal interaction
unassigned |
4
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
24239766 |
LXR antagonists induce ABCD2 expression. |
causal interaction
ongoing research
unassigned |
4
4
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
24363066 |
X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes. |
causal interaction
unassigned |
1
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
24480443 |
Regulation of the adrenoleukodystrophy-related gene (ABCD2): Focus on oxysterols and LXR antagonists. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 7.6.2.4 | abc-type fatty-acyl-coa transporter deficiency |
25255441 |
Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
2
3
0 |
