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Results 1 - 10 of 54 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Acanthosis Nigricans 30487246 De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. causal interaction
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Adrenoleukodystrophy 20166112 The role of ELOVL1 in very long-chain fatty acid homeostasis and X-linked adrenoleukodystrophy. causal interaction
ongoing research
therapeutic application
unassigned
4
1
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Adrenoleukodystrophy 22911730 Bezafibrate for x-linked adrenoleukodystrophy. causal interaction
therapeutic application
unassigned
2
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Adrenoleukodystrophy 25499606 Enzymatic characterization of ELOVL1, a key enzyme in very long-chain fatty acid synthesis. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
3
4
1
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Breast Neoplasms 21415164 Novel theranostic opportunities offered by characterization of altered membrane lipid metabolism in breast cancer progression. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Breast Neoplasms 27788154 Estrogen Enhances the Expression of the Polyunsaturated Fatty Acid Elongase Elovl2 via ER? in Breast Cancer Cells. ongoing research
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Corneal Opacity 29401594 Very long-chain tear film lipids produced by fatty acid elongase ELOVL1 prevent dry eye disease in mice. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Deafness 30487246 De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. causal interaction
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Deafness 32123819 Reduced chain length in myelin sphingolipids and poorer motor coordination in mice deficient in the fatty acid elongase Elovl1. causal interaction
ongoing research
therapeutic application
unassigned
3
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.199Demyelinating Diseases 20035504 Dicer ablation in oligodendrocytes provokes neuronal impairment in mice. causal interaction
therapeutic application
unassigned
3
1
0
Results 1 - 10 of 54 > >>