Pub. Date : 2022 Jul 1
PMID : 35266883
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | PURPOSE OF REVIEW: Primary hyperoxaluria type 1 (PH1) is a rare genetic disorder that causes hepatic overproduction of oxalate and, often, nephrocalcinosis, nephrolithiasis, chronic kidney disease, and kidney failure. | Oxalates | alanine--glyoxylate and serine--pyruvate aminotransferase | Homo sapiens |
| 2 | SUMMARY: Novel treatments can reduce the plasma oxalate concentration and urinary oxalate excretion in PH1 patients. | Oxalates | alanine--glyoxylate and serine--pyruvate aminotransferase | Homo sapiens |