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Results 1 - 10 of 263 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Renal Insufficiency, Chronic 24125425 A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with chronic kidney disease. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Diabetes Mellitus, Type 2 22558392 A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with insulin sensitivity. causal interaction
therapeutic application
unassigned
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Insulin Resistance 22558392 A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with insulin sensitivity. causal interaction
therapeutic application
unassigned
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Coronary Artery Disease 31409409 A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients. causal interaction
diagnostic usage
unassigned
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Myocardial Infarction 31409409 A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients. causal interaction
diagnostic usage
unassigned
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Carcinoma, Hepatocellular 28741166 A new key player in VEGF-dependent angiogenesis in human hepatocellular carcinoma: dimethylarginine dimethylaminohydrolase 1. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Neoplasms 28741166 A new key player in VEGF-dependent angiogenesis in human hepatocellular carcinoma: dimethylarginine dimethylaminohydrolase 1. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Coronary Disease 20167924 A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease. causal interaction
ongoing research
therapeutic application
unassigned
4
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Stroke 20167924 A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease. causal interaction
ongoing research
therapeutic application
unassigned
4
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Thrombosis 20167924 A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease. causal interaction
ongoing research
therapeutic application
unassigned
4
4
1
0
Results 1 - 10 of 263 > >>