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Results 1 - 10 of 233 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1Alzheimer Disease 33423317 Is SGSH heterozygosity a risk factor for early-onset neurodegenerative disease? unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1arylsulfatase (type i) deficiency 118467 Genetic complementation studies of multiple sulfatase deficiency. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1arylsulfatase (type i) deficiency 9880143 Pathologic findings of multiple sulfatase deficiency reflect the pattern of enzyme deficiencies. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1beta-glucuronidase deficiency 20084460 Storage correction in cells of patients suffering from mucopolysaccharidoses types IIIA and VII after treatment with genistein and other isoflavones. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1beta-Mannosidosis 1861455 Complementation studies in human and caprine beta-mannosidosis. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
2
1
1
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1Deficiency Diseases 116130 Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression? causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1Genetic Diseases, Inborn 25142140 High and prolonged sulfamidase secretion by the liver of MPS-IIIA mice following hydrodynamic tail vein delivery of antibiotic-free pFAR4 plasmid vector. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1Infections 26620043 Continual Low-Dose Infusion of Sulfamidase Is Superior to Intermittent High-Dose Delivery in Ameliorating Neuropathology in the MPS IIIA Mouse Brain. causal interaction
ongoing research
therapeutic application
unassigned
2
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1Intellectual Disability 31385193 Bioinformatics classification of mutations in patients with Mucopolysaccharidosis IIIA. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.10.1.1Leukemia 8930656 Correction of Sanfilippo A skin fibroblasts by retroviral vector-mediated gene transfer. ongoing research
unassigned
3
0
Results 1 - 10 of 233 > >>