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Results 1 - 10 of 105 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Brain Diseases 29660996 A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). unassigned 0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 29660996 A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). unassigned 0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 14605502 A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells. causal interaction
unassigned
3
0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 7757079 A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria. unassigned 0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 9048920 A novel missense mutation in exon 4 of the human coproporphyrinogen oxidase gene in two patients with hereditary coproporphyria. causal interaction
ongoing research
therapeutic application
unassigned
3
2
1
0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 9747031 A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family. causal interaction
unassigned
3
0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Porphyrias, Hepatic 30385147 Acute hepatic porphyrias: Identification of 46 hydroxymethylbilane synthase, 11 coproporphyrinogen oxidase, and 20 protoporphyrinogen oxidase novel mutations. causal interaction
diagnostic usage
unassigned
1
1
0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Anemia 15579372 Adherence modifies the regulation of gene expression induced by interleukin-10. causal interaction
therapeutic application
unassigned
1
1
0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 913057 Alterations in the activity of enzymes of haem biosynthesis in lead poisoning and acute hepatic prophyria. causal interaction
unassigned
2
0
Show all pathways known for 1.3.3.3Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.3Coproporphyria, Hereditary 3574346 Analysis of porphyrins and enzymes in porphyrin synthesis in Taenia solium cysticercus from man and pig. unassigned 0
Results 1 - 10 of 105 > >>