HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

glyoxylate reductase

the human 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; RefSeq NM_012203
Also Known As:
GRHPR protein, human; glyoxylate reductase/hydroxypyruvate reductase, human
Networked: 12 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Holmes, Ross P: 2 articles (10/2012 - 03/2012)
2. Knight, John: 2 articles (10/2012 - 03/2012)
3. Huang, Da: 1 article (01/2013)
4. Li, Feifei: 1 article (01/2013)
5. Huang, Xiaodong: 1 article (01/2013)
6. Zhang, Yixin: 1 article (01/2013)
7. Pan, Yinglian: 1 article (01/2013)
8. Lu, Cuihua: 1 article (01/2013)
9. Deng, Qingchun: 1 article (01/2013)
10. Chen, Buyou: 1 article (01/2013)

Related Diseases

1. Primary Hyperoxaluria (Oxaluria, Primary)
2. Hyperoxaluria
3. Renal Insufficiency (Renal Failure)
4. Rare Diseases (Rare Disease)
5. Nephrocalcinosis

Related Drugs and Biologics

1. Glycerate dehydrogenase
2. Hydroxypyruvate Reductase
3. Alanine-glyoxylate transaminase (alanine-glyoxylate aminotransferase)
4. Primary hyperoxaluria type 2
5. Oxidoreductases
6. Enzymes
7. 4-hydroxy-2-oxoglutarate aldolase
8. alpha-ketoisocaproic acid