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Results 1 - 10 of 11 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Carcinoma 22049060 Loss of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) induces apoptotic processes in pancreatic carcinoma cells. causal interaction
diagnostic usage
ongoing research
unassigned
2
3
4
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Distal Myopathies 22855677 Novel Mutations of the GNE Gene in Distal Myopathy with Rimmed Vacuoles Presenting with Very Slow Progression. causal interaction
unassigned
2
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Distal Myopathies 24707269 A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation. causal interaction
unassigned
3
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Liver Cirrhosis, Biliary 9468341 Hexokinase isoenzymes in normal and cirrhotic human liver: suppression of glucokinase in cirrhosis. causal interaction
diagnostic usage
ongoing research
unassigned
1
3
3
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Liver Diseases, Alcoholic 9468341 Hexokinase isoenzymes in normal and cirrhotic human liver: suppression of glucokinase in cirrhosis. causal interaction
diagnostic usage
ongoing research
unassigned
1
3
3
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Muscular Diseases 15987957 Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. causal interaction
ongoing research
unassigned
1
3
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Muscular Diseases 22507750 Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations. causal interaction
unassigned
2
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Muscular Diseases 23127962 Respiratory dysfunction in patients severely affected by GNE myopathy (distal myopathy with rimmed vacuoles). causal interaction
diagnostic usage
unassigned
4
2
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Muscular Diseases 24707269 A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation. causal interaction
unassigned
3
0
Show all pathways known for 2.7.1.60Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.60Muscular Diseases 25002140 GNE myopathy: current update and future therapy. unassigned 0
Results 1 - 10 of 11 > >>