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Results 1 - 10 of 154 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Fabry Disease 209782 Reexpression of HPRT activity following cell fusion with polyethylene glycol. causal interaction
ongoing research
unassigned
1
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Congenital Disorders of Glycosylation 8808595 Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Liver Neoplasms 9661906 Progression of hepatic neoplasms is severely retarded in mice lacking the bisecting N-acetylglucosamine on N-glycans: evidence for a glycoprotein factor that facilitates hepatic tumor progression. ongoing research
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Neoplasms 9661906 Progression of hepatic neoplasms is severely retarded in mice lacking the bisecting N-acetylglucosamine on N-glycans: evidence for a glycoprotein factor that facilitates hepatic tumor progression. ongoing research
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Neoplasms 10866326 New evidence for an extra-hepatic role of N-acetylglucosaminyltransferase III in the progression of diethylnitrosamine-induced liver tumors in mice. causal interaction
ongoing research
therapeutic application
unassigned
1
2
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Neoplasms 11986323 Truncated, inactive N-acetylglucosaminyltransferase III (GlcNAc-TIII) induces neurological and other traits absent in mice that lack GlcNAc-TIII. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Congenital, Hereditary, and Neonatal Diseases and Abnormalities 12417412 Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa. ongoing research
therapeutic application
unassigned
4
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Obesity 12621063 MGAT2, a monoacylglycerol acyltransferase expressed in the small intestine. ongoing research
therapeutic application
unassigned
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Obesity 12730219 Properties of the mouse intestinal acyl-CoA:monoacylglycerol acyltransferase, MGAT2. therapeutic application
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.22Neoplasms 14633700 Reduced hepatocyte proliferation is the basis of retarded liver tumor progression and liver regeneration in mice lacking N-acetylglucosaminyltransferase III. causal interaction
ongoing research
unassigned
1
3
0
Results 1 - 10 of 154 > >>