glyoxylate metabolic process

Known as: glyoxylate metabolism 
The chemical reactions and pathways involving glyoxylate, the anion of glyoxylic acid, HOC-COOH. [ISBN:0198506732]

Topic mentions per year

Topic mentions per year

1962-2017
0246819622017

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2012
2012
Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the… (More)
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2012
2012
The objective of present study was to offer insights into the metabolic responses of hepatocellular carcinoma (HCC) to surgical… (More)
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2012
2012
The groundwater contaminant 1,4-dioxane (dioxane) is transformed by several monooxygenase-expressing microorganisms, but only a… (More)
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2010
2010
Oxalate is widely distributed in the plant kingdom. While excess oxalate in food crops is detrimental to animal and human health… (More)
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2004
2004
Heterozygous mutants of barley (Hordeum vulgare L. cv. Maris Mink) with decreased activities of chloroplastic glutamine… (More)
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2003
2003
Primary hyperoxaluria type 2, an inherited autosomal recessive disorder of endogenous oxalate overproduction, is caused by… (More)
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1999
1999
Growth experiments with Escherichia coli have shown that this organism is able to use allantoin as a sole nitrogen source but not… (More)
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1997
1997
Primary hyperoxaluria type 1 (PH1) is a severe autosomal recessive inborn error of glyoxylate metabolism caused by deficiency of… (More)
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1988
1988
Primary hyperoxaluria type 1 (PH1) is an inherited disorder of glyoxylate metabolism caused by a deficiency of the hepatic… (More)
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1969
1969
The relative contributions of the dicarboxylic acid and the tricarboxylic acid cycles to the oxidative catabolism of glyoxylate… (More)
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