EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.6.1.43 | Hyperoxaluria, 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 |
2.6.1.43 | Hyperoxaluria, 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 |
2.6.1.43 | Hyperoxaluria, Primary |
2045108 |
Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase. |
ongoing research unassigned |
1 0 |
2.6.1.43 | Hyperoxaluria, Primary |
2717533 |
Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1. |
causal interaction diagnostic usage unassigned |
2 2 0 |
2.6.1.43 | Hyperoxaluria, Primary |
2887776 |
Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation. |
ongoing research unassigned |
1 0 |
2.6.1.43 | Hyperoxaluria, 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 |
2.6.1.43 | Hyperoxaluria, 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 |
2.6.1.43 | Hyperoxaluria, 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 |
2.6.1.43 | Hyperoxaluria, 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 |
2.6.1.43 | Hyperoxaluria, 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 |