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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Insulin Resistance 1460020 Molecular cloning, cDNA sequence, and bacterial expression of human glutamine:fructose-6-phosphate amidotransferase. causal interaction
unassigned
4
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Infections 26770025 Molecular docking based screening of G6PS with 1, 5 Benzothiazepine derivates for a potential inhibitor. therapeutic application
unassigned
1
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Diabetic Nephropathies 15308130 Molecular screening of the human glutamine-fructose-6-phosphate amidotransferase 1 (GFPT1) gene and association studies with diabetes and diabetic nephropathy. causal interaction
diagnostic usage
ongoing research
unassigned
3
1
2
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Insulin Resistance 15595739 Molecular therapeutic target for type-2 diabetes. therapeutic application
unassigned
1
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Starvation 30201609 mTORC2 modulates the amplitude and duration of GFAT1 Ser243 phosphorylation to maintain flux through the hexosamine pathway during starvation. therapeutic application
unassigned
1
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Myasthenic Syndromes, Congenital 22742743 Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates. causal interaction
unassigned
4
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Muscle Weakness 23569079 Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR. causal interaction
unassigned
3
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Myasthenic Syndromes, Congenital 23569079 Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR. causal interaction
unassigned
3
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Myasthenic Syndromes, Congenital 28712002 Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy. causal interaction
unassigned
1
0
Show all pathways known for 2.6.1.16Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.16Insulin Resistance 1743436 New insights into the metabolic regulation of insulin action and insulin resistance: role of glucose and amino acids. causal interaction
unassigned
1
0
<< < Results 91 - 100 of 125 > >>