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Results 1 - 10 of 86 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Abortion, Spontaneous 26109616 Altered ?1,6-GlcNAc and bisecting GlcNAc-branched N-glycan on integrin ?1 are associated with early spontaneous miscarriage in humans. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Adenocarcinoma 16136053 The Notch pathway in ovarian carcinomas and adenomas. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Adenocarcinoma 26279302 Lunatic Fringe is a potent tumor suppressor in Kras-initiated pancreatic cancer. causal interaction
ongoing research
unassigned
2
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Adenoma 16136053 The Notch pathway in ovarian carcinomas and adenomas. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Adenoma 30065304 Manic Fringe deficiency imposes Jagged1 addiction to intestinal tumor cells. causal interaction
ongoing research
therapeutic application
unassigned
3
3
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222alpha-1,6-mannosyl-glycoprotein 2-beta-n-acetylglucosaminyltransferase deficiency 7607254 Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS). unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Anemia 2953718 Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II. causal interaction
therapeutic application
unassigned
4
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Anemia, Dyserythropoietic, Congenital 2953718 Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II. causal interaction
therapeutic application
unassigned
4
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Brain Neoplasms 8536214 Glycosyltransferase activities in human meningiomas. Preliminary results. causal interaction
diagnostic usage
ongoing research
unassigned
1
3
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.222Breast Neoplasms 17537730 Inhibition of a specific N-glycosylation activity results in attenuation of breast carcinoma cell invasiveness-related phenotypes: inhibition of epidermal growth factor-induced dephosphorylation of focal adhesion kinase. causal interaction
diagnostic usage
ongoing research
therapeutic application
2
3
3
2
Results 1 - 10 of 86 > >>