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GRHPR encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. Additionally we are shipping Glyoxylate Reductase/hydroxypyruvate Reductase Proteins (11) and Glyoxylate Reductase/hydroxypyruvate Reductase Kits (2) and many more products for this protein.
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Human Polyclonal GRHPR Primary Antibody for IHC, WB - ABIN2783330
Takayama, Nagata, Ozono, Nonomura, Cramer: A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007
GRHPR was genotyped in Japanese patients with PH2 (show PhC2 Antibodies) and all GRHPR mutations described to date were reviewed in terms of geographic and ethnic association
Our findings suggest that the GRHPR defect in noncancerous tissues may represent an independent predictor of poor survival for hepatocellular carcinoma patients after curative resection
GRHPR directly interacts with SVCT1 (show SVCT1 Antibodies).
the GRHPR gene may have a role in primary hyperoxaluria type 2 in a Japanese patient [case report]
data indicate a species-specific regulation by PPARalpha (show PPARA Antibodies) of GRHPR, a key gene of the glyoxylate cycle
This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene.
glyoxylate reductase/hydroxypyruvate reductase
, Glyoxylate reductase/hydroxypyruvate reductase