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glycine catabolic process

Known as: glycine breakdown, glycine catabolism, glycine degradation 
The chemical reactions and pathways resulting in the breakdown of glycine, aminoethanoic acid. [GOC:go_curators]
National Institutes of Health

Papers overview

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Review
2012
Review
2012
The glycine deportation system is an essential component of glycine catabolism in man whereby 400 to 800mg glycine per day are… Expand
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2012
2012
Clostridium acidurici is an anaerobic, homoacetogenic bacterium, which is able to use purines such as uric acid as sole carbon… Expand
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2006
2006
Glycine encephalopathy (GCE) is an autosomal recessive error of glycine degradation, resulting in a poor outcome with severe… Expand
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2002
2002
Non-ketotic hyperglycinemia (NKH), also termed glycine encephalopathy (MIM 605899), is an autosomal recessive inborn error of… Expand
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2000
2000
Nonketotic hyperglycinaemia (NKH) is an autosomal recessive disorder characterized by defective glycine degradation by the… Expand
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1996
1996
Nonketotic hyperglycinemia (NKH) is an inborn error of glycine degradation causing muscular hypotonia, seizures, apnea, and… Expand
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1989
1989
Glucagon stimulates 14CO2 production from [1-14C] glycine by isolated rat hepatocytes. Maximal stimulation (70%) of… Expand
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1984
1984
Glycine decarboxylation and serine synthesis were studied in pea (Pisum sativum L.) leaf discs, in metabolically active intact… Expand
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1981
1981
Nonketotic hyperglycinemia (NKH) is a rare disorder of glycine degradation with autosomal recessive inheritance. 1 There are… Expand
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1978
1978
At 25° C under aerobic conditions with or without gluamate 10% of the [1-14C]glycollate oxidised in spinach leaf peroxisomes was… Expand
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