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<< < Results 11 - 20 of 263 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Bronchopulmonary Dysplasia 26663142 A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia. causal interaction
diagnostic usage
unassigned
4
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Hypertension, Pulmonary 26663142 A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia. causal interaction
diagnostic usage
unassigned
4
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Diabetes Mellitus 25701782 Accelerated onset of senescence of endothelial progenitor cells in patients with type 2 diabetes mellitus: Role of dimethylarginine dimethylaminohydrolase 2 and asymmetric dimethylarginine. causal interaction
diagnostic usage
ongoing research
unassigned
4
4
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Diabetes Mellitus, Type 2 25701782 Accelerated onset of senescence of endothelial progenitor cells in patients with type 2 diabetes mellitus: Role of dimethylarginine dimethylaminohydrolase 2 and asymmetric dimethylarginine. causal interaction
diagnostic usage
ongoing research
unassigned
4
4
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Glioma 21590769 Active site mutant dimethylarginine dimethylaminohydrolase 1 expression confers an intermediate tumour phenotype in C6 gliomas. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
1
2
3
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Neoplasms 21590769 Active site mutant dimethylarginine dimethylaminohydrolase 1 expression confers an intermediate tumour phenotype in C6 gliomas. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
1
2
3
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18nitric-oxide synthase (nadph) deficiency 19666122 ADMA and the role of the genes: Lessons from genetically modified animals and human gene polymorphisms. causal interaction
ongoing research
therapeutic application
unassigned
2
1
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Diabetic Nephropathies 31818438 ADMA elevation does not exacerbate development of diabetic nephropathy in mice with streptozotocin-induced diabetes mellitus. diagnostic usage
ongoing research
unassigned
1
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Diabetic Nephropathies 29096857 ADMA reduction does not protect mice with streptozotocin-induced diabetes mellitus from development of diabetic nephropathy. ongoing research
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.5.3.18Diabetic Nephropathies 23147199 ADMA, SDMA and L-arginine/ADMA Ratio but not DDAH Genetic Polymorphisms are Reliable Predictors of Diabetic Nephropathy Progression as Identified by Competing Risk Analysis. diagnostic usage
unassigned
3
0
<< < Results 11 - 20 of 263 > >>