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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 4.1.3.16Hyperoxaluria, 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 22771891 4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition. diagnostic usage
unassigned
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 32003182 [Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder]. diagnostic usage
unassigned
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
Show all pathways known for 4.1.3.16Display the word mapDisplay the reaction diagram Show all sequences 4.1.3.16Hyperoxaluria, Primary 22851625 The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type III. 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 31123811 Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children. causal interaction
ongoing research
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 31696211 Regulation of human 4-hydroxy-2-oxoglutarate aldolase by pyruvate and ?-ketoglutarate: implications for primary hyperoxaluria type-3. ongoing research
therapeutic application
unassigned
2
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 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 33948853 Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variants. ongoing research
unassigned
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 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
Results 1 - 10 of 32 > >>