Glyoxylate (BioDeep_00000897518)
代谢物信息卡片
Glyoxylate
化学式: C2HO3- (72.9925696)
中文名称: 乙醛酸
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(=O)C(=O)[O-]
InChI: InChI=1S/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)/p-1
相关代谢途径
Reactome(0)
BioCyc(32)
- creatinine degradation II
- allantoin degradation to glyoxylate III
- superpathway of glycol metabolism and degradation
- glycolate and glyoxylate degradation I
- glycolate and glyoxylate degradation II
- allantoin degradation to glyoxylate I
- allantoin degradation to ureidoglycolate I (urea producing)
- superpathway of allantoin degradation in yeast
- superpathway of allantoin degradation in plants
- superpathway of purines degradation in plants
- formaldehyde assimilation I (serine pathway)
- superpathway of pentose and pentitol degradation
- chitin degradation to ethanol
- superpathway of glycolysis, pyruvate dehydrogenase, TCA, and glyoxylate bypass
- TCA cycle I (prokaryotic)
- mixed acid fermentation
- superpathway of glyoxylate bypass and TCA
- caffeine degradation V (bacteria, via trimethylurate)
- 2,4-dichlorophenoxyacetate degradation
- photosynthetic 3-hydroxybutanoate biosynthesis (engineered)
- allantoin degradation to glyoxylate II
- ethylmalonyl-CoA pathway
- methylaspartate cycle
- crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
- TCA cycle V (2-oxoglutarate:ferredoxin oxidoreductase)
- nitrilotriacetate degradation
- L-valine biosynthesis
- trans-4-hydroxy-L-proline degradation I
- 2,4,5-trichlorophenoxyacetate degradation
- γ-coniciene and coniine biosynthesis
- pyruvate fermentation to isobutanol (engineered)
- butanol and isobutanol biosynthesis (engineered)
PlantCyc(7)
- superpathway of allantoin degradation in plants
- allantoin degradation to glyoxylate III
- allantoin degradation to glyoxylate I
- superpathway of purines degradation in plants
- Organic Nitrogen Assimilation
- superpathway of glyoxylate cycle and fatty acid degradation
- allantoin degradation to glyoxylate II
代谢反应
326 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(42)
- caffeine degradation V (bacteria, via trimethylurate):
1,6,8-trimethylallantoate + H2O ⟶ N,N'-dimethylurea + N-methylurea + glyoxylate - superpathway of glyoxylate bypass and TCA:
2-oxoglutarate + NAD+ + coenzyme A ⟶ CO2 + NADH + succinyl-CoA - TCA cycle variation I:
2-oxoglutarate + H+ ⟶ CO2 + succinate semialdehyde - glyoxylate cycle:
citrate ⟶ cis-aconitate + H2O - superpathway of glycolysis, pyruvate dehydrogenase, TCA, and glyoxylate bypass:
2-oxoglutarate + NAD+ + coenzyme A ⟶ CO2 + NADH + succinyl-CoA - superpathway of glyoxylate cycle:
O2 + a 2,3,4-saturated fatty acyl CoA ⟶ a trans-2-enoyl-CoA + hydrogen peroxide - glyoxylate cycle:
citrate ⟶ cis-aconitate + H2O - 2,4-dichlorophenoxyacetate degradation:
2,4-dichlorophenoxyacetate + 2-oxoglutarate + O2 ⟶ 2,4-dichlorophenol + CO2 + glyoxylate + succinate - allantoin degradation to glyoxylate III:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate III:
(S)-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate I:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - superpathway of allantoin degradation in yeast:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - superpathway of allantoin degradation in plants:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - superpathway of purines degradation in plants:
H2O + inosine ⟶ D-ribofuranose + hypoxanthine - allantoin degradation to glyoxylate I:
H2O + allantoate ⟶ (S)-ureidoglycolate + urea - superpathway of allantoin degradation in yeast:
H2O + allantoate ⟶ (S)-ureidoglycolate + urea - allantoin degradation to glyoxylate III:
S-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate I:
H2O + allantoate ⟶ (S)-ureidoglycolate + urea - superpathway of purines degradation in plants:
H2O + O2 + urate ⟶ 5-hydroxyisourate + hydrogen peroxide - superpathway of allantoin degradation in yeast:
S-ureidoglycolate ⟶ glyoxylate + urea - superpathway of allantoin degradation in plants:
H+ + H2O + urea ⟶ CO2 + ammonium - allantoin degradation to glyoxylate I:
S-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate III:
(S)-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate III:
S-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate III:
S-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate I:
S-(-)-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate III:
S-ureidoglycine + H2O ⟶ S-(-)-ureidoglycolate + H+ + ammonia - allantoin degradation to glyoxylate I:
H2O + allantoate ⟶ S-ureidoglycolate + urea - methylaspartate cycle:
ATP + hydrogencarbonate + propanoyl-CoA ⟶ (S)-methylmalonyl-CoA + ADP + H+ + phosphate - TCA cycle V (2-oxoglutarate:ferredoxin oxidoreductase):
D-threo-isocitrate + NADP+ ⟶ 2-oxoglutarate + CO2 + NADPH - TCA cycle V (2-oxoglutarate:ferredoxin oxidoreductase):
D-threo-isocitrate + NADP+ ⟶ 2-oxoglutarate + CO2 + NADPH - glyoxylate cycle:
D-threo-isocitrate ⟶ glyoxylate + succinate - butanol and isobutanol biosynthesis (engineered):
NAD+ + butan-1-ol ⟶ H+ + NADH + butan-1-al - glyphosate degradation II:
H2O + O2 + glyphosate ⟶ (aminomethyl)phosphonate + glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
NAD+ + gly + tetrahydrofolate ⟶ 5,10-methylenetetrahydrofolate + CO2 + H+ + NADH + ammonia - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
S-ureidoglycine + H2O ⟶ S-ureidoglycolate + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ S-ureidoglycine + CO2 + ammonium - 4-chloro-2-methylphenoxyacetate degradation:
2-methyl-4-chlorophenol + H+ + NADPH + O2 ⟶ 5-chloro-3-methylcatechol + H2O + NADP+
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(284)
- allantoin degradation to glyoxylate III:
(S)-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate I:
H2O + allantoate ⟶ (S)-ureidoglycolate + urea - allantoin degradation to glyoxylate I:
(S)-ureidoglycolate ⟶ glyoxylate + urea - allantoin degradation to glyoxylate III:
(S)-ureidoglycolate ⟶ glyoxylate + urea - superpathway of allantoin degradation in plants:
(S)-ureidoglycolate ⟶ glyoxylate + urea - superpathway of allantoin degradation in plants:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate III:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate I:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - superpathway of purines degradation in plants:
H2O + NAD+ + xanthine ⟶ H+ + NADH + urate - Organic Nitrogen Assimilation:
H2O + O2 + urate ⟶ CO2 + allantoin + hydrogen peroxide - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - allantoin degradation to glyoxylate III:
(S)-ureidoglycolate ⟶ glyoxylate + urea - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - allantoin degradation to glyoxylate III:
(S)-ureidoglycolate ⟶ glyoxylate + urea - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
H+ + H2O + adenine ⟶ ammonium + hypoxanthine - Organic Nitrogen Assimilation:
NAD+ + glu ⟶ 2-oxoglutarate + H+ + NADH + gln - 4-hydroxy-4-methyl-L-glutamate biosynthesis:
4-hydroxy-4-methyl-2-oxoglutarate ⟶ pyruvate - 4-hydroxy-4-methyl-L-glutamate biosynthesis:
4-hydroxy-4-methyl-2-oxoglutarate ⟶ pyruvate - 4-hydroxy-4-methyl-L-glutamate biosynthesis:
4-hydroxy-4-methyl-2-oxoglutarate ⟶ pyruvate - 4-hydroxy-4-methyl-L-glutamate biosynthesis:
4-hydroxy-4-methyl-2-oxoglutarate ⟶ pyruvate - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - photorespiration:
O2 + glycolate ⟶ glyoxylate + hydrogen peroxide - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - superpathway of allantoin degradation in plants:
H2O + allantoate ⟶ (S)-ureidoglycolate + urea - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - superpathway of allantoin degradation in plants:
H+ + H2O + urea ⟶ CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-ureidoglycolate + H+ + H2O ⟶ CO2 + ammonium + glyoxylate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - superpathway of allantoin degradation in plants:
H+ + H2O + urea ⟶ CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - superpathway of allantoin degradation in plants:
(S)-(+)-allantoin + H2O ⟶ H+ + allantoate - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium - allantoin degradation to glyoxylate II:
H+ + H2O + allantoate ⟶ (S)-ureidoglycine + CO2 + ammonium
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0 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
文献列表
- Ruth Belostotsky, Yaacov Frishberg. Catabolism of Hydroxyproline in Vertebrates: Physiology, Evolution, Genetic Diseases and New siRNA Approach for Treatment.
International journal of molecular sciences.
2022 Jan; 23(2):. doi:
10.3390/ijms23021005. [PMID: 35055190] - Bohan Wang, Jingchao Wei, Qi Huangfu, Fei Gao, Lanxin Qin, Jiao Zhong, Jiaming Wen, Zhangqun Ye, Xiaoqi Yang, Haoran Liu. Identification of Resolvin D1 and Protectin D1 as Potential Therapeutic Agents for Treating Kidney Stones.
Oxidative medicine and cellular longevity.
2022; 2022(?):4345037. doi:
10.1155/2022/4345037. [PMID: 35251472] - Shuo Zhao, Daniel Garcia, Yinglei Zhao, Danfeng Huang. Hydro-Electro Hybrid Priming Promotes Carrot (Daucus carota L.) Seed Germination by Activating Lipid Utilization and Respiratory Metabolism.
International journal of molecular sciences.
2021 Oct; 22(20):. doi:
10.3390/ijms222011090. [PMID: 34681749] - Qing-Lin Ye, Da-Ming Wang, Xin Wang, Zhi-Qiang Zhang, Qi-Xing Tian, Shi-Yao Feng, Zhi-Hui Zhang, De-Xin Yu, De-Mao Ding, Dong-Dong Xie. Sirt1 inhibits kidney stones formation by attenuating calcium oxalate-induced cell injury.
Chemico-biological interactions.
2021 Sep; 347(?):109605. doi:
10.1016/j.cbi.2021.109605. [PMID: 34333021] - Hiromasa Tanaka, Yugo Hosoi, Kenji Ishikawa, Jun Yoshitake, Takahiro Shibata, Koji Uchida, Hiroshi Hashizume, Masaaki Mizuno, Yasumasa Okazaki, Shinya Toyokuni, Kae Nakamura, Hiroaki Kajiyama, Fumitaka Kikkawa, Masaru Hori. Low temperature plasma irradiation products of sodium lactate solution that induce cell death on U251SP glioblastoma cells were identified.
Scientific reports.
2021 09; 11(1):18488. doi:
10.1038/s41598-021-98020-w. [PMID: 34531507] - Kathrin Gianmoena, Nina Gasparoni, Adelina Jashari, Philipp Gabrys, Katharina Grgas, Ahmed Ghallab, Karl Nordström, Gilles Gasparoni, Jörg Reinders, Karolina Edlund, Patricio Godoy, Alexander Schriewer, Heiko Hayen, Christian A Hudert, Georg Damm, Daniel Seehofer, Thomas S Weiss, Peter Boor, Hans-Joachim Anders, Manga Motrapu, Peter Jansen, Tobias S Schiergens, Maren Falk-Paulsen, Philip Rosenstiel, Clivia Lisowski, Eduardo Salido, Rosemarie Marchan, Jörn Walter, Jan G Hengstler, Cristina Cadenas. Epigenomic and transcriptional profiling identifies impaired glyoxylate detoxification in NAFLD as a risk factor for hyperoxaluria.
Cell reports.
2021 08; 36(8):109526. doi:
10.1016/j.celrep.2021.109526. [PMID: 34433051] - Hiba Baaziz, K Karl Compton, Sherry B Hildreth, Richard F Helm, Birgit E Scharf. McpT, a Broad-Range Carboxylate Chemoreceptor in Sinorhizobium meliloti.
Journal of bacteriology.
2021 08; 203(17):e0021621. doi:
10.1128/jb.00216-21. [PMID: 34124939] - Tao Ding, Tingting Zhao, Yinhui Li, Zhixiao Liu, Jiarong Ding, Boyao Ji, Yue Wang, Zhiyong Guo. Vitexin exerts protective effects against calcium oxalate crystal-induced kidney pyroptosis in vivo and in vitro.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2021 Jun; 86(?):153562. doi:
10.1016/j.phymed.2021.153562. [PMID: 33857849] - Khushboo Borah, Tom A Mendum, Nathaniel D Hawkins, Jane L Ward, Michael H Beale, Gerald Larrouy-Maumus, Apoorva Bhatt, Martine Moulin, Michael Haertlein, Gernot Strohmeier, Harald Pichler, V Trevor Forsyth, Stephan Noack, Celia W Goulding, Johnjoe McFadden, Dany J V Beste. Metabolic fluxes for nutritional flexibility of Mycobacterium tuberculosis.
Molecular systems biology.
2021 05; 17(5):e10280. doi:
10.15252/msb.202110280. [PMID: 33943004] - Long He, Peng Jin, Xuan Chen, Tian-Ye Zhang, Kai-Li Zhong, Peng Liu, Jian-Ping Chen, Jian Yang. Comparative proteomic analysis of Nicotiana benthamiana plants under Chinese wheat mosaic virus infection.
BMC plant biology.
2021 Jan; 21(1):51. doi:
10.1186/s12870-021-02826-9. [PMID: 33468046] - Xi Jin, Zhongyu Jian, Xiaoting Chen, Yucheng Ma, Hongwen Ma, Yu Liu, Lina Gong, Liyuan Xiang, Shiyu Zhu, Xiaoling Shu, Shiqian Qi, Hong Li, Kunjie Wang. Short Chain Fatty Acids Prevent Glyoxylate-Induced Calcium Oxalate Stones by GPR43-Dependent Immunomodulatory Mechanism.
Frontiers in immunology.
2021; 12(?):729382. doi:
10.3389/fimmu.2021.729382. [PMID: 34675921] - Mirco Dindo, Giorgia Mandrile, Carolina Conter, Rosa Montone, Daniela Giachino, Alessandra Pelle, Claudio Costantini, Barbara Cellini. The ILE56 mutation on different genetic backgrounds of alanine:glyoxylate aminotransferase: Clinical features and biochemical characterization.
Molecular genetics and metabolism.
2020 Sep; 131(1-2):171-180. doi:
10.1016/j.ymgme.2020.07.012. [PMID: 32792227] - Zhisheng Zhang, Xiu Liang, Lei Lu, Zheng Xu, Jiayu Huang, Han He, Xinxiang Peng. Two glyoxylate reductase isoforms are functionally redundant but required under high photorespiration conditions in rice.
BMC plant biology.
2020 Jul; 20(1):357. doi:
10.1186/s12870-020-02568-0. [PMID: 32727356] - Jasper Schierstaedt, Sven Jechalke, Joseph Nesme, Klaus Neuhaus, Søren J Sørensen, Rita Grosch, Kornelia Smalla, Adam Schikora. Salmonella persistence in soil depends on reciprocal interactions with indigenous microorganisms.
Environmental microbiology.
2020 07; 22(7):2639-2652. doi:
10.1111/1462-2920.14972. [PMID: 32128943] - M Luisa Hernández, Elena Lima-Cabello, Juan de D Alché, José M Martínez-Rivas, Antonio J Castro. Lipid Composition and Associated Gene Expression Patterns during Pollen Germination and Pollen Tube Growth in Olive (Olea europaea L.).
Plant & cell physiology.
2020 Jul; 61(7):1348-1364. doi:
10.1093/pcp/pcaa063. [PMID: 32384163] - Wan-Lin Wu, Yu-Yun Hsiao, Hsiang-Chia Lu, Chieh-Kai Liang, Chih-Hsiung Fu, Tian-Hsiang Huang, Ming-Hsiang Chuang, Li-Jun Chen, Zhong-Jian Liu, Wen-Chieh Tsai. Expression regulation of MALATE SYNTHASE involved in glyoxylate cycle during protocorm development in Phalaenopsis aphrodite (Orchidaceae).
Scientific reports.
2020 06; 10(1):10123. doi:
10.1038/s41598-020-66932-8. [PMID: 32572104] - Wei Zhou, Yanli Hong, Ailing Yin, Shijia Liu, Minmin Chen, Xifeng Lv, Xiaowei Nie, Ninghua Tan, Zhihao Zhang. Non-invasive urinary metabolomics reveals metabolic profiling of polycystic ovary syndrome and its subtypes.
Journal of pharmaceutical and biomedical analysis.
2020 Jun; 185(?):113262. doi:
10.1016/j.jpba.2020.113262. [PMID: 32222648] - Seanna L Hewitt, Rishikesh Ghogare, Amit Dhingra. Glyoxylic acid overcomes 1-MCP-induced blockage of fruit ripening in Pyrus communis L. var. 'D'Anjou'.
Scientific reports.
2020 04; 10(1):7084. doi:
10.1038/s41598-020-63642-z. [PMID: 32341384] - Vincenzo Cuomo, Cesare Gerardo Riccio, Salvatore Coppola. [Primary hyperoxaluria: case report and therapeutic perspectives].
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia.
2020 Feb; 37(1):. doi:
NULL. [PMID: 32068359] - Toshiaki Kozuka, Yuji Sawada, Hiroyuki Imai, Masatake Kanai, Masami Yokota Hirai, Shoji Mano, Matsuo Uemura, Mikio Nishimura, Makoto Kusaba, Akira Nagatani. Regulation of Sugar and Storage Oil Metabolism by Phytochrome during De-etiolation.
Plant physiology.
2020 02; 182(2):1114-1129. doi:
10.1104/pp.19.00535. [PMID: 31748417] - Dewi van Harskamp, Sander F Garrelfs, Michiel J S Oosterveld, Jaap W Groothoff, Johannes B van Goudoever, Henk Schierbeek. Development and Validation of a New Gas Chromatography-Tandem Mass Spectrometry Method for the Measurement of Enrichment of Glyoxylate Metabolism Analytes in Hyperoxaluria Patients Using a Stable Isotope Procedure.
Analytical chemistry.
2020 01; 92(2):1826-1832. doi:
10.1021/acs.analchem.9b03670. [PMID: 31867958] - Xiaoqi Yang, Haoran Liu, Tao Ye, Chen Duan, Peng Lv, Xiaoliang Wu, Jianhe Liu, Kehua Jiang, Hongyan Lu, Huan Yang, Ding Xia, Ejun Peng, Zhiqiang Chen, Kun Tang, Zhangqun Ye. AhR activation attenuates calcium oxalate nephrocalcinosis by diminishing M1 macrophage polarization and promoting M2 macrophage polarization.
Theranostics.
2020; 10(26):12011-12025. doi:
10.7150/thno.51144. [PMID: 33204326] - Jade Martins, Darina Czamara, Jennifer Lange, Frederik Dethloff, Elisabeth B Binder, Chris W Turck, Angelika Erhardt. Exposure-induced changes of plasma metabolome and gene expression in patients with panic disorder.
Depression and anxiety.
2019 12; 36(12):1173-1181. doi:
10.1002/da.22946. [PMID: 31374578] - Spencer M Heuchan, Bo Fan, Jessica J Kowalski, Elizabeth R Gillies, Hugh A L Henry. Development of Fertilizer Coatings from Polyglyoxylate-Polyester Blends Responsive to Root-Driven pH Change.
Journal of agricultural and food chemistry.
2019 Nov; 67(46):12720-12729. doi:
10.1021/acs.jafc.9b04717. [PMID: 31652059] - Yong Jia, Crista A Burbidge, Crystal Sweetman, Emi Schutz, Kathy Soole, Colin Jenkins, Robert D Hancock, John B Bruning, Christopher M Ford. An aldo-keto reductase with 2-keto-l-gulonate reductase activity functions in l-tartaric acid biosynthesis from vitamin C in Vitis vinifera.
The Journal of biological chemistry.
2019 11; 294(44):15932-15946. doi:
10.1074/jbc.ra119.010196. [PMID: 31488549] - Mingwei Wang, Hailiang Nie, Dandan Han, Xiaoqiang Qiao, Hongyuan Yan, Shigang Shen. Cauliflower-like resin microspheres with tuneable surface roughness as solid-phase extraction adsorbent for efficient extraction and determination of plant growth regulators in cucumbers.
Food chemistry.
2019 Oct; 295(?):259-266. doi:
10.1016/j.foodchem.2019.05.130. [PMID: 31174757] - Agnese Serafini, Lendl Tan, Stuart Horswell, Steven Howell, Daniel J Greenwood, Deborah M Hunt, Minh-Duy Phan, Mark Schembri, Mercedes Monteleone, Christine R Montague, Warwick Britton, Acely Garza-Garcia, Ambrosius P Snijders, Brian VanderVen, Maximiliano G Gutierrez, Nicholas P West, Luiz Pedro S de Carvalho. Mycobacterium tuberculosis requires glyoxylate shunt and reverse methylcitrate cycle for lactate and pyruvate metabolism.
Molecular microbiology.
2019 10; 112(4):1284-1307. doi:
10.1111/mmi.14362. [PMID: 31389636] - Lu Wang, Huaiyuan Zhang, Yao Zhang, Yuanda Song. 13C metabolic flux analysis on roles of malate transporter in lipid accumulation of Mucor circinelloides.
Microbial cell factories.
2019 Sep; 18(1):154. doi:
10.1186/s12934-019-1207-9. [PMID: 31506101] - Falicia Qi Yun Goh, Justin Jeyakani, Phornpimon Tipthara, Amaury Cazenave-Gassiot, Rajoshi Ghosh, Nicholas Bogard, Zhenxuan Yeo, Gane Ka-Shu Wong, Michael Melkonian, Markus R Wenk, Neil D Clarke. Gains and losses of metabolic function inferred from a phylotranscriptomic analysis of algae.
Scientific reports.
2019 07; 9(1):10482. doi:
10.1038/s41598-019-46869-3. [PMID: 31324835] - Junhua Xi, Yang Chen, Junfeng Jing, Yanbin Zhang, Chaozhao Liang, Zongyao Hao, Li Zhang. Sirtuin 3 suppresses the formation of renal calcium oxalate crystals through promoting M2 polarization of macrophages.
Journal of cellular physiology.
2019 07; 234(7):11463-11473. doi:
10.1002/jcp.27803. [PMID: 30588609] - Paola Faraoni, Elettra Sereni, Alessio Gnerucci, Francesca Cialdai, Monica Monici, Francesco Ranaldi. Glyoxylate cycle activity in Pinus pinea seeds during germination in altered gravity conditions.
Plant physiology and biochemistry : PPB.
2019 Jun; 139(?):389-394. doi:
10.1016/j.plaphy.2019.03.042. [PMID: 30959447] - Teruaki Sugino, Atsushi Okada, Kazumi Taguchi, Rei Unno, Shuzo Hamamoto, Ryosuke Ando, Tohru Mogami, Kenjiro Kohri, Hitoshi Yamashita, Takahiro Yasui. Brown adipocytes and β3-stimulant-induced brown-like adipocytes contribute to the prevention of renal crystal formation.
American journal of physiology. Renal physiology.
2019 06; 316(6):F1282-F1292. doi:
10.1152/ajprenal.00523.2018. [PMID: 30995115] - Yong Min, Wenjia Cao, Yun Xiong, Zhihao Si, Dawood Khan, Limei Chen. Formaldehyde assimilation through coordination of the glyoxylate pathway and the tricarboxylic acid cycle in broad bean roots.
Plant physiology and biochemistry : PPB.
2019 May; 138(?):65-79. doi:
10.1016/j.plaphy.2019.02.019. [PMID: 30852239] - Anjli Kukreja, Melissa Lasaro, Christian Cobaugh, Chris Forbes, Jian-Ping Tang, Xiang Gao, Cristina Martin-Higueras, Angel L Pey, Eduardo Salido, Susan Sobolov, Romesh R Subramanian. Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1.
Nucleic acid therapeutics.
2019 04; 29(2):104-113. doi:
10.1089/nat.2018.0740. [PMID: 30676254] - Mirco Dindo, Carolina Conter, Elisa Oppici, Veronica Ceccarelli, Lorella Marinucci, Barbara Cellini. Molecular basis of primary hyperoxaluria: clues to innovative treatments.
Urolithiasis.
2019 Feb; 47(1):67-78. doi:
10.1007/s00240-018-1089-z. [PMID: 30430197] - Masayuki Usami, Atsushi Okada, Kazumi Taguchi, Shuzo Hamamoto, Kenjiro Kohri, Takahiro Yasui. Genetic differences in C57BL/6 mouse substrains affect kidney crystal deposition.
Urolithiasis.
2018 Nov; 46(6):515-522. doi:
10.1007/s00240-018-1040-3. [PMID: 29362828] - Yufan Chao, Songyan Gao, Xuelei Wang, Na Li, Hongxia Zhao, Xiaofei Wen, Ziyang Lou, Xin Dong. Untargeted lipidomics based on UPLC-QTOF-MS/MS and structural characterization reveals dramatic compositional changes in serum and renal lipids in mice with glyoxylate-induced nephrolithiasis.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2018 Sep; 1095(?):258-266. doi:
10.1016/j.jchromb.2018.08.003. [PMID: 30099286] - Alexander T Eprintsev, Dmitry N Fedorin, Maria A Dobychina, Abir U Igamberdiev. Regulation of expression of the mitochondrial and peroxisomal forms of citrate synthase in maize during germination and in response to light.
Plant science : an international journal of experimental plant biology.
2018 Jul; 272(?):157-163. doi:
10.1016/j.plantsci.2018.04.017. [PMID: 29807587] - Manman Zhang, Chao Gao, Xiaoting Guo, Shiting Guo, Zhaoqi Kang, Dan Xiao, Jinxin Yan, Fei Tao, Wen Zhang, Wenyue Dong, Pan Liu, Chen Yang, Cuiqing Ma, Ping Xu. Increased glutarate production by blocking the glutaryl-CoA dehydrogenation pathway and a catabolic pathway involving L-2-hydroxyglutarate.
Nature communications.
2018 05; 9(1):2114. doi:
10.1038/s41467-018-04513-0. [PMID: 29844506] - Bei Yan, Yao Liu, Aixin Shi, Zhihong Wang, Jiye Aa, Xiaoping Huang, Yi Liu. Investigation of the Antifatigue Effects of Korean Ginseng on Professional Athletes by Gas Chromatography-Time-of-Flight-Mass Spectrometry-Based Metabolomics.
Journal of AOAC International.
2018 May; 101(3):701-707. doi:
10.5740/jaoacint.17-0220. [PMID: 28927488] - Mahmoud El-Maghrabey, Masaki Mine, Naoya Kishikawa, Kaname Ohyama, Naotaka Kuroda. A novel dual labeling approach enables converting fluorescence labeling reagents into fluorogenic ones via introduction of purification tags. Application to determination of glyoxylic acid in serum.
Talanta.
2018 Apr; 180(?):323-328. doi:
10.1016/j.talanta.2017.12.023. [PMID: 29332818] - Rui Zheng, Xiaoliang Fang, Lei He, Yanjiao Shao, Nana Guo, Liren Wang, Mingyao Liu, Dali Li, Hongquan Geng. Generation of a Primary Hyperoxaluria Type 1 Disease Model Via CRISPR/Cas9 System in Rats.
Current molecular medicine.
2018; 18(7):436-447. doi:
10.2174/1566524019666181212092440. [PMID: 30539697] - Jingbo Yu, Ling Kong, Aihua Zhang, Ying Han, Zhidong Liu, Hui Sun, Liang Liu, Xijun Wang. High-Throughput Metabolomics for Discovering Potential Metabolite Biomarkers and Metabolic Mechanism from the APPswe/PS1dE9 Transgenic Model of Alzheimer's Disease.
Journal of proteome research.
2017 09; 16(9):3219-3228. doi:
10.1021/acs.jproteome.7b00206. [PMID: 28753016] - Rosaria Campilongo, Rowena K Y Fung, Richard H Little, Lucia Grenga, Eleftheria Trampari, Simona Pepe, Govind Chandra, Clare E M Stevenson, Davide Roncarati, Jacob G Malone. One ligand, two regulators and three binding sites: How KDPG controls primary carbon metabolism in Pseudomonas.
PLoS genetics.
2017 Jun; 13(6):e1006839. doi:
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Nanomedicine : nanotechnology, biology, and medicine.
2017 04; 13(3):897-907. doi:
10.1016/j.nano.2016.12.011. [PMID: 27993722] - Kazuki Takahashi, Ryousuke Morimoto, Hiromitsu Tabeta, Mariko Asaoka, Masanori Ishida, Masayoshi Maeshima, Hirokazu Tsukaya, Ali Ferjani. Compensated Cell Enlargement in fugu5 is Specifically Triggered by Lowered Sucrose Production from Seed Storage Lipids.
Plant & cell physiology.
2017 04; 58(4):668-678. doi:
10.1093/pcp/pcx021. [PMID: 28201798] - Stéphanie Arrivault, Toshihiro Obata. Quantification of Photorespiratory Intermediates by Mass Spectrometry-Based Approaches.
Methods in molecular biology (Clifton, N.J.).
2017; 1653(?):97-104. doi:
10.1007/978-1-4939-7225-8_7. [PMID: 28822128] - Saoussen M'dimegh, Asma Omezzine, Mériam Ben Hamida-Rebai, Cécile Aquaviva-Bourdain, Ibtihel M'barek, Wissal Sahtout, Dorsaf Zellama, Geneviéve Souche, Abdellatif Achour, Saoussen Abroug, Ali Bouslama. Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure.
Transplant immunology.
2016 11; 39(?):60-65. doi:
10.1016/j.trim.2016.08.008. [PMID: 27568336] - Aleksandra Eckstein, Dominika Jagiełło-Flasińska, Aleksandra Lewandowska, Paweł Hermanowicz, Klaus-J Appenroth, Halina Gabryś. Mobilization of storage materials during light-induced germination of tomato (Solanum lycopersicum) seeds.
Plant physiology and biochemistry : PPB.
2016 Aug; 105(?):271-281. doi:
10.1016/j.plaphy.2016.05.008. [PMID: 27208503] - Zhenguo Ma, Frédéric Marsolais, Mark A Bernards, Mark W Sumarah, Natalia V Bykova, Abir U Igamberdiev. Glyoxylate cycle and metabolism of organic acids in the scutellum of barley seeds during germination.
Plant science : an international journal of experimental plant biology.
2016 Jul; 248(?):37-44. doi:
10.1016/j.plantsci.2016.04.007. [PMID: 27181945] - Younès Dellero, Mathieu Jossier, Jessica Schmitz, Veronica G Maurino, Michael Hodges. Photorespiratory glycolate-glyoxylate metabolism.
Journal of experimental botany.
2016 05; 67(10):3041-52. doi:
10.1093/jxb/erw090. [PMID: 26994478] - Cristina Martin-Higueras, Sergio Luis-Lima, Eduardo Salido. Glycolate Oxidase Is a Safe and Efficient Target for Substrate Reduction Therapy in a Mouse Model of Primary Hyperoxaluria Type I.
Molecular therapy : the journal of the American Society of Gene Therapy.
2016 Apr; 24(4):719-25. doi:
10.1038/mt.2015.224. [PMID: 26689264] - Chaitali Dutta, Nicole Avitahl-Curtis, Natalie Pursell, Marita Larsson Cohen, Benjamin Holmes, Rohan Diwanji, Wei Zhou, Luciano Apponi, Martin Koser, Bo Ying, Dongyu Chen, Xue Shui, Utsav Saxena, Wendy A Cyr, Anee Shah, Naim Nazef, Weimin Wang, Marc Abrams, Henryk Dudek, Eduardo Salido, Bob D Brown, Chengjung Lai. Inhibition of Glycolate Oxidase With Dicer-substrate siRNA Reduces Calcium Oxalate Deposition in a Mouse Model of Primary Hyperoxaluria Type 1.
Molecular therapy : the journal of the American Society of Gene Therapy.
2016 Apr; 24(4):770-8. doi:
10.1038/mt.2016.4. [PMID: 26758691] - Shivangi Rastogi, Pooja Agarwal, Manju Y Krishnan. Use of an adipocyte model to study the transcriptional adaptation of Mycobacterium tuberculosis to store and degrade host fat.
International journal of mycobacteriology.
2016 Mar; 5(1):92-8. doi:
10.1016/j.ijmyco.2015.10.003. [PMID: 26927997] - Pieter Giesbertz, Inken Padberg, Dietrich Rein, Josef Ecker, Anja S Höfle, Britta Spanier, Hannelore Daniel. Metabolite profiling in plasma and tissues of ob/ob and db/db mice identifies novel markers of obesity and type 2 diabetes.
Diabetologia.
2015 Sep; 58(9):2133-43. doi:
10.1007/s00125-015-3656-y. [PMID: 26058503] - Javier Sánchez-Martín, Jim Heald, Alison Kingston-Smith, Ana Winters, Diego Rubiales, Mariluz Sanz, Luis A J Mur, Elena Prats. A metabolomic study in oats (Avena sativa) highlights a drought tolerance mechanism based upon salicylate signalling pathways and the modulation of carbon, antioxidant and photo-oxidative metabolism.
Plant, cell & environment.
2015 Jul; 38(7):1434-52. doi:
10.1111/pce.12501. [PMID: 25533379] - Wenqiang Yang, Claudia Catalanotti, Tyler M Wittkopp, Matthew C Posewitz, Arthur R Grossman. Algae after dark: mechanisms to cope with anoxic/hypoxic conditions.
The Plant journal : for cell and molecular biology.
2015 May; 82(3):481-503. doi:
10.1111/tpj.12823. [PMID: 25752440] - Haiyan Hu, Wei Chen, Jiarong Ding, Meng Jia, Jingjing Yin, Zhiyong Guo. Fasudil prevents calcium oxalate crystal deposit and renal fibrogenesis in glyoxylate-induced nephrolithic mice.
Experimental and molecular pathology.
2015 Apr; 98(2):277-85. doi:
10.1016/j.yexmp.2015.02.006. [PMID: 25697583] - Alma Rosa Corrales Escobosa, Katarzyna Wrobel, Eunice Yanez Barrientos, Sarahi Jaramillo Ortiz, Alejandra Sarahi Ramirez Segovia, Kazimierz Wrobel. Effect of different glycation agents on Cu(II) binding to human serum albumin, studied by liquid chromatography, nitrogen microwave-plasma atomic-emission spectrometry, inductively-coupled-plasma mass spectrometry, and high-resolution molecular-mass spectrometry.
Analytical and bioanalytical chemistry.
2015 Feb; 407(4):1149-57. doi:
10.1007/s00216-014-8335-1. [PMID: 25428457] - Zhongjiang Peng, Wei Chen, Li Wang, Zhouheng Ye, Songyan Gao, Xuejun Sun, Zhiyong Guo. Inhalation of hydrogen gas ameliorates glyoxylate-induced calcium oxalate deposition and renal oxidative stress in mice.
International journal of clinical and experimental pathology.
2015; 8(3):2680-9. doi:
NULL. [PMID: 26045773] - Evan Barr-Beare, Vijay Saxena, Evann E Hilt, Krystal Thomas-White, Megan Schober, Birong Li, Brian Becknell, David S Hains, Alan J Wolfe, Andrew L Schwaderer. The Interaction between Enterobacteriaceae and Calcium Oxalate Deposits.
PloS one.
2015; 10(10):e0139575. doi:
10.1371/journal.pone.0139575. [PMID: 26448465] - Rita J M Volkers, L Basten Snoek, Harald J Ruijssenaars, Johannes H de Winde. Dynamic Response of Pseudomonas putida S12 to Sudden Addition of Toluene and the Potential Role of the Solvent Tolerance Gene trgI.
PloS one.
2015; 10(7):e0132416. doi:
10.1371/journal.pone.0132416. [PMID: 26181384] - Mark A Hooks, J William Allwood, Joanna K D Harrison, Joachim Kopka, Alexander Erban, Royston Goodacre, Janneke Balk. Selective induction and subcellular distribution of ACONITASE 3 reveal the importance of cytosolic citrate metabolism during lipid mobilization in Arabidopsis.
The Biochemical journal.
2014 Oct; 463(2):309-17. doi:
10.1042/bj20140430. [PMID: 25061985] - Yaacov Frishberg, Avraham Zeharia, Roman Lyakhovetsky, Ruth Bargal, Ruth Belostotsky. Mutations in HAO1 encoding glycolate oxidase cause isolated glycolic aciduria.
Journal of medical genetics.
2014 Aug; 51(8):526-9. doi:
10.1136/jmedgenet-2014-102529. [PMID: 24996905] - Laura Strittmatter, Yang Li, Nathan J Nakatsuka, Sarah E Calvo, Zenon Grabarek, Vamsi K Mootha. CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activity.
Human molecular genetics.
2014 May; 23(9):2313-23. doi:
10.1093/hmg/ddt624. [PMID: 24334609] - Inken Padberg, Erik Peter, Sandra González-Maldonado, Henning Witt, Matthias Mueller, Tanja Weis, Bianca Bethan, Volker Liebenberg, Jan Wiemer, Hugo A Katus, Dietrich Rein, Philipp Schatz. A new metabolomic signature in type-2 diabetes mellitus and its pathophysiology.
PloS one.
2014; 9(1):e85082. doi:
10.1371/journal.pone.0085082. [PMID: 24465478] - Victoria J Nikiforova, Pieter Giesbertz, Jan Wiemer, Bianca Bethan, Ralf Looser, Volker Liebenberg, Patricia Ruiz Noppinger, Hannelore Daniel, Dietrich Rein. Glyoxylate, a new marker metabolite of type 2 diabetes.
Journal of diabetes research.
2014; 2014(?):685204. doi:
10.1155/2014/685204. [PMID: 25525609] - Gordon J Hoover, René Jørgensen, Amanda Rochon, Vikramjit S Bajwa, A Rod Merrill, Barry J Shelp. Identification of catalytically important amino acid residues for enzymatic reduction of glyoxylate in plants.
Biochimica et biophysica acta.
2013 Dec; 1834(12):2663-71. doi:
10.1016/j.bbapap.2013.09.013. [PMID: 24076009] - Alessio Aprile, Lenka Havlickova, Riccardo Panna, Caterina Marè, Grazia M Borrelli, Daniela Marone, Carla Perrotta, Patrizia Rampino, Luigi De Bellis, Vladislav Curn, Anna M Mastrangelo, Fulvia Rizza, Luigi Cattivelli. Different stress responsive strategies to drought and heat in two durum wheat cultivars with contrasting water use efficiency.
BMC genomics.
2013 Nov; 14(?):821. doi:
10.1186/1471-2164-14-821. [PMID: 24267539] - Christian Blume, Christof Behrens, Holger Eubel, Hans-Peter Braun, Christoph Peterhansel. A possible role for the chloroplast pyruvate dehydrogenase complex in plant glycolate and glyoxylate metabolism.
Phytochemistry.
2013 Nov; 95(?):168-76. doi:
10.1016/j.phytochem.2013.07.009. [PMID: 23916564] - Mukesh K Dubey, Anders Broberg, Sanjeewani Sooriyaarachchi, Wimal Ubhayasekera, Dan Funck Jensen, Magnus Karlsson. The glyoxylate cycle is involved in pleotropic phenotypes, antagonism and induction of plant defence responses in the fungal biocontrol agent Trichoderma atroviride.
Fungal genetics and biology : FG & B.
2013 Sep; 58-59(?):33-41. doi:
10.1016/j.fgb.2013.06.008. [PMID: 23850601] - Wei Wei, Wenjun Zhu, Jiasen Cheng, Jiatao Xie, Bo Li, Daohong Jiang, Guoqing Li, Xianhong Yi, Yanping Fu. CmPEX6, a gene involved in peroxisome biogenesis, is essential for parasitism and conidiation by the sclerotial parasite Coniothyrium minitans.
Applied and environmental microbiology.
2013 Jun; 79(12):3658-66. doi:
10.1128/aem.00375-13. [PMID: 23563946] - Andrei Tintu, Ellen Rouwet, Henk Russcher. Interference of ethylene glycol with (L)-lactate measurement is assay-dependent.
Annals of clinical biochemistry.
2013 Jan; 50(Pt 1):70-2. doi:
10.1258/acb.2012.012052. [PMID: 23129723] - Yasuyuki Kubo. Function of peroxisomes in plant-pathogen interactions.
Sub-cellular biochemistry.
2013; 69(?):329-45. doi:
10.1007/978-94-007-6889-5_18. [PMID: 23821157] - Ruth Belostotsky, James Jonathon Pitt, Yaacov Frishberg. Primary hyperoxaluria type III--a model for studying perturbations in glyoxylate metabolism.
Journal of molecular medicine (Berlin, Germany).
2012 Dec; 90(12):1497-504. doi:
10.1007/s00109-012-0930-z. [PMID: 22729392] - Antonio Di Matteo, Adriana Sacco, Rosalba De Stefano, Luigi Frusciante, Amalia Barone. Comparative transcriptomic profiling of two tomato lines with different ascorbate content in the fruit.
Biochemical genetics.
2012 Dec; 50(11-12):908-21. doi:
10.1007/s10528-012-9531-3. [PMID: 22911514] - Kohki Chihara, Naoya Kishikawa, Kaname Ohyama, Kenichiro Nakashima, Naotaka Kuroda. Determination of glyoxylic acid in urine by liquid chromatography with fluorescence detection, using a novel derivatization procedure based on the Petasis reaction.
Analytical and bioanalytical chemistry.
2012 Jul; 403(9):2765-70. doi:
10.1007/s00216-012-6036-1. [PMID: 22580421] - Masahito Hirose, Keiichi Tozawa, Atsushi Okada, Shuzo Hamamoto, Yuji Higashibata, Bin Gao, Yutaro Hayashi, Hideo Shimizu, Yasue Kubota, Takahiro Yasui, Kenjiro Kohri. Role of osteopontin in early phase of renal crystal formation: immunohistochemical and microstructural comparisons with osteopontin knock-out mice.
Urological research.
2012 Apr; 40(2):121-9. doi:
10.1007/s00240-011-0400-z. [PMID: 21833789] - Leonardo Bianco de Carvalho, Pedro Luis da Costa Aguiar Alves, Fidel González-Torralva, Hugo Enrique Cruz-Hipolito, Antonia María Rojano-Delgado, Rafael De Prado, Javier Gil-Humanes, Francisco Barro, María Dolores Luque de Castro. Pool of resistance mechanisms to glyphosate in Digitaria insularis.
Journal of agricultural and food chemistry.
2012 Jan; 60(2):615-22. doi:
10.1021/jf204089d. [PMID: 22175446] - Vijai Bhadauria, Sabine Banniza, Albert Vandenberg, Gopalan Selvaraj, Yangdou Wei. Peroxisomal alanine: glyoxylate aminotransferase AGT1 is indispensable for appressorium function of the rice blast pathogen, Magnaporthe oryzae.
PloS one.
2012; 7(4):e36266. doi:
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BMC biotechnology.
2011 Nov; 11(?):111. doi:
10.1186/1472-6750-11-111. [PMID: 22104170] - Ibrahim F Ghalayini, Mohammed A Al-Ghazo, Mohammad N A Harfeil. Prophylaxis and therapeutic effects of raspberry (Rubus idaeus) on renal stone formation in Balb/c mice.
International braz j urol : official journal of the Brazilian Society of Urology.
2011 Mar; 37(2):259-66; discussion 267. doi:
10.1590/s1677-55382011000200013. [PMID: 21557843] - Bruno Stieger. Regulation of the expression of the hepatocellular sulfate-oxalate exchanger SAT-1 (SLC26A1) by glyoxylate: a metabolic link between liver and kidney?.
Journal of hepatology.
2011 Mar; 54(3):406-7. doi:
10.1016/j.jhep.2010.09.011. [PMID: 21084130] - Gaber M Abogadallah. Differential regulation of photorespiratory gene expression by moderate and severe salt and drought stress in relation to oxidative stress.
Plant science : an international journal of experimental plant biology.
2011 Mar; 180(3):540-7. doi:
10.1016/j.plantsci.2010.12.004. [PMID: 21421402] - Betty Wächtler, Duncan Wilson, Katja Haedicke, Frederic Dalle, Bernhard Hube. From attachment to damage: defined genes of Candida albicans mediate adhesion, invasion and damage during interaction with oral epithelial cells.
PloS one.
2011 Feb; 6(2):e17046. doi:
10.1371/journal.pone.0017046. [PMID: 21407800] - R A Corley, S A Saghir, M J Bartels, S C Hansen, J Creim, K E McMartin, W M Snellings. Extension of a PBPK model for ethylene glycol and glycolic acid to include the competitive formation and clearance of metabolites associated with kidney toxicity in rats and humans.
Toxicology and applied pharmacology.
2011 Feb; 250(3):229-44. doi:
10.1016/j.taap.2010.10.011. [PMID: 21074520] - Stefan Timm, Alexandra Florian, Kathrin Jahnke, Adriano Nunes-Nesi, Alisdair R Fernie, Hermann Bauwe. The hydroxypyruvate-reducing system in Arabidopsis: multiple enzymes for the same end.
Plant physiology.
2011 Feb; 155(2):694-705. doi:
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Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
2010 Dec; 25(12):2701-11. doi:
10.1002/jbmr.158. [PMID: 20577968] - A M Rojano-Delgado, F Priego-Capote, M D Luque de Castro, R De Prado. Screening and confirmatory analysis of glyoxylate: a biomarker of plants resistance against herbicides.
Talanta.
2010 Oct; 82(5):1757-62. doi:
10.1016/j.talanta.2010.07.068. [PMID: 20875573] - Saeed R Khan, Patricia A Glenton. Experimental induction of calcium oxalate nephrolithiasis in mice.
The Journal of urology.
2010 Sep; 184(3):1189-96. doi:
10.1016/j.juro.2010.04.065. [PMID: 20663521] - Melissa Li, James Galligan, Donna Wang, Gregory Fink. The effects of celiac ganglionectomy on sympathetic innervation to the splanchnic organs in the rat.
Autonomic neuroscience : basic & clinical.
2010 Apr; 154(1-2):66-73. doi:
10.1016/j.autneu.2009.11.009. [PMID: 20053590] - Antonia María Rojano-Delgado, José Ruiz-Jiménez, María Dolores Luque de Castro, Rafael De Prado. Determination of glyphosate and its metabolites in plant material by reversed-polarity CE with indirect absorptiometric detection.
Electrophoresis.
2010 Apr; 31(8):1423-30. doi:
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The American journal of forensic medicine and pathology.
2009 Sep; 30(3):273-5. doi:
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Plant physiology.
2009 Jun; 150(2):987-95. doi:
10.1104/pp.109.139394. [PMID: 19386803] - Liming Pei, Ronald M Evans. Retrofitting fat metabolism.
Cell metabolism.
2009 Jun; 9(6):483-4. doi:
10.1016/j.cmet.2009.05.006. [PMID: 19490901] - Gerhard Triebig, Philipp Werner, Holger Zimmer. A field study to determine the effectiveness of several respiratory protection masks on the styrene exposure during lamination activities.
Industrial health.
2009 Apr; 47(2):145-54. doi:
10.2486/indhealth.47.145. [PMID: 19367043] - Holger Fahnenstich, Telma E Scarpeci, Estela M Valle, Ulf-Ingo Flügge, Verónica G Maurino. Generation of hydrogen peroxide in chloroplasts of Arabidopsis overexpressing glycolate oxidase as an inducible system to study oxidative stress.
Plant physiology.
2008 Oct; 148(2):719-29. doi:
10.1104/pp.108.126789. [PMID: 18685041] - Ming Lin, David J Oliver. The role of acetyl-coenzyme a synthetase in Arabidopsis.
Plant physiology.
2008 Aug; 147(4):1822-9. doi:
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Urological research.
2008 Aug; 36(3-4):139-47. doi:
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