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glyoxylate metabolic process

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

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Highly Cited
2012
Highly Cited
2012
Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the… Expand
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Review
2012
Review
2012
Glyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a highly reactive molecule, generated in… Expand
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2011
2011
BackgroundThe photorespiratory nitrogen cycle in C3 plants involves an extensive diversion of carbon and nitrogen away from the… Expand
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Highly Cited
2010
Highly Cited
2010
Oxalate is widely distributed in the plant kingdom. While excess oxalate in food crops is detrimental to animal and human health… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Primary hyperoxaluria type 1 (PH1) is an inborn error of glyoxylate metabolism with an extensive clinical and genetic… Expand
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Highly Cited
2003
Highly Cited
2003
Primary hyperoxaluria type 2, an inherited autosomal recessive disorder of endogenous oxalate overproduction, is caused by… Expand
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Review
2001
Review
2001
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepatic enzyme deficiencies result… Expand
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Highly Cited
1999
Highly Cited
1999
Growth experiments with Escherichia coli have shown that this organism is able to use allantoin as a sole nitrogen source but not… Expand
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Highly Cited
1973
Highly Cited
1973
Abstract Hyperoxaluria was found in 66 per cent of 18 patients with disease or resection of the ileum. Previous theories to… Expand
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Highly Cited
1969
Highly Cited
1969
The relative contributions of the dicarboxylic acid and the tricarboxylic acid cycles to the oxidative catabolism of glyoxylate… Expand
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