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Results 1 - 8 of 8
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Brain Diseases 27066588 In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery. ongoing research
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Carcinogenesis 33148467 ACOT4 accumulation via AKT-mediated phosphorylation promotes pancreatic tumourigenesis. causal interaction
diagnostic usage
ongoing research
unassigned
3
1
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Carcinoma 31934097 The combined expressions of B7H4 and ACOT4 in cancer-associated fibroblasts are related to poor prognosis in patients with gastric carcinoma. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
4
3
1
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Fatty Liver 26546267 The direction of cross affects [corrected] obesity after puberty in male but not female offspring. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Ischemic Stroke 25961151 Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project. causal interaction
therapeutic application
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Neoplasms 31934097 The combined expressions of B7H4 and ACOT4 in cancer-associated fibroblasts are related to poor prognosis in patients with gastric carcinoma. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
4
3
1
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Neoplasms 33148467 ACOT4 accumulation via AKT-mediated phosphorylation promotes pancreatic tumourigenesis. causal interaction
diagnostic usage
ongoing research
unassigned
3
1
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.2.3Stroke 25961151 Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project. causal interaction
therapeutic application
unassigned
3
1
0
Results 1 - 8 of 8