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Results 1 - 10 of 32 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.164-hydroxy-2-oxoglutarate aldolase deficiency 22729392 Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism. causal interaction
unassigned
4
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.164-hydroxy-2-oxoglutarate aldolase deficiency 22781098 Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies. causal interaction
therapeutic application
unassigned
4
3
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria 22781098 Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies. causal interaction
therapeutic application
unassigned
4
3
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria 33350326 Mutations in HOGA1 do Not Confer a Dominant Phenotype Manifesting as Kidney Stone Disease. causal interaction
ongoing research
unassigned
4
3
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 20797690 Mutations in DHDPSL are responsible for primary hyperoxaluria type III. causal interaction
unassigned
3
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 21896830 Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. diagnostic usage
unassigned
3
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 21998747 Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria. diagnostic usage
ongoing research
unassigned
3
2
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 22115483 Re: Mutations in DHDPSL are Responsible for Primary Hyperoxaluria Type III. causal interaction
unassigned
4
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 22325509 Re: primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. diagnostic usage
therapeutic application
unassigned
3
1
0
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 22391140 The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3. causal interaction
diagnostic usage
ongoing research
unassigned
4
3
2
0
Results 1 - 10 of 32 > >>