EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.1.1.26 | Carcinoma, Hepatocellular |
23486161 |
Glyoxylate Reductase/Hydroxypyruvate Reductase: A Novel Prognostic Marker for Hepatocellular Carcinoma Patients after Curative Resection. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
3
0 |
| 1.1.1.26 | Colitis |
26997491 |
Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
3
4
0 |
| 1.1.1.26 | Colorectal Neoplasms |
32370786 |
Downregulation of GLYR1 contributes to microsatellite instability colorectal cancer by targeting p21 via the p38MAPK and PI3K/AKT pathways. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
3
1
0 |
| 1.1.1.26 | Colorectal Neoplasms |
32624003 |
Correction to: Downregulation of GLYR1 contributes to microsatellite instability colorectal cancer by targeting p21 via the p38MAPK and PI3K/AKT pathways. |
unassigned |
0 |
| 1.1.1.26 | Crohn Disease |
26997491 |
Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
3
4
0 |
| 1.1.1.26 | Genetic Diseases, Inborn |
25410531 |
A mutation creating an out-of-frame alternative translation initiation site in the GRHPR 5'UTR causing primary hyperoxaluria type II. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 1.1.1.26 | glyoxylate reductase deficiency |
16597637 |
Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
2
1 |
| 1.1.1.26 | glyoxylate reductase deficiency |
19245173 |
[Primary hiperoxaluria: a new mutation in gen AGXT (R197Q) cause of neonatal convulsions] |
causal interaction
unassigned |
1
0 |
| 1.1.1.26 | glyoxylate reductase deficiency |
28569194 |
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
3
4
1 |
| 1.1.1.26 | glyoxylate reductase deficiency |
28681512 |
Combined Liver-Kidney Transplantation for Primary Hyperoxaluria Type 2: A Case Report. |
causal interaction
unassigned |
3
0 |
