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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 1961759 Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 1996585 Combined hepatic and renal transplantation in primary hyperoxaluria type I: clinical report of nine cases. ongoing research
therapeutic application
unassigned
2
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 2045108 Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase. ongoing research
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 2717533 Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1. causal interaction
diagnostic usage
unassigned
2
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 2887776 Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation. ongoing research
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 3416563 Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1. diagnostic usage
ongoing research
unassigned
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 3418107 Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1. causal interaction
diagnostic usage
ongoing research
unassigned
3
4
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 11708860 Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria. causal interaction
ongoing research
therapeutic application
unassigned
4
3
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 12559847 The AGT gene in Africa: a distinctive minor allele haplotype, a polymorphism (V326I), and a novel PH1 mutation (A112D) in Black Africans. causal interaction
ongoing research
unassigned
3
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.43Hyperoxaluria, Primary 12777626 Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase. causal interaction
unassigned
3
0
Results 1 - 10 of 15 > >>