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3-phenylpropionylglycine

Known as: Phenylpropionylglycine 
 
National Institutes of Health

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6 relations

Broader (1)

Glycine
Phenylpropionylglycine/Creatinine:MRto:24H:Urine:QnPhenylpropionylglycine/Creatinine:MRto:Pt:Urine:QnPhenylpropionylglycine/Creatinine:SRto:24H:Urine:QnPhenylpropionylglycine/Creatinine:SRto:Pt:Urine:Qn
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Papers overview

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2012
2012
Effect of ginseng polysaccharide on the urinary excretion of type 2 diabetic rats studied by liquid chromatography-mass spectrometry.
Ginseng polysaccharide is known to have anti-hyperglycemic and anti-hyperlipidemic effects in vivo and its precise mechanism of… Expand
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2012
2012
Abcb11 deficiency induces cholestasis coupled to impaired β-fatty acid oxidation in mice.
The bile salt export pump (BSEP) is an ATP-binding cassette transporter that serves as the primary system for removing bile salts… Expand
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2007
2007
Metabolomic and genetic analysis of biomarkers for peroxisome proliferator-activated receptor alpha expression and activation.
Peroxisome proliferator-activated receptor alpha (PPARalpha) is a nuclear receptor with manifold effects on intermediary… Expand
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2006
2006
Na+, K+ ATPase activity is markedly reduced by cis-4-decenoic acid in synaptic plasma membranes from cerebral cortex of rats
We have previously demonstrated that octanoic (OA) and decanoic acids (DA) inhibit Na+, K+ ATPase activity in synaptic plasma… Expand
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1995
1995
Common MCAD mutation in a healthy parent of two affected siblings
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is one of the most common metabolic disorders affecting Caucasians… Expand
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1993
1993
Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency.
Screening for medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency by urinary 3-phenylpropionylglycine may not be… Expand
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1990
1990
The Enzymatic Basis for the Dehydrogenation of 3-Phenylpropionic Acid: In Vitro Reaction of 3- Phenylpropionyl-CoA with Various Acyl-CoA Dehydrogenases
ABSTRACT: 3-Phenylpropionic acid is an end-product of the bacterial degradation of unabsorbed phenylalanine in the intestinal… Expand
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1990
1990
The detection of abnormal metabolites in MCAD deficiency: a new method
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (McKusick 20145) is an inborn error of fatty acid metabolism, first… Expand
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1989
1989
Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion…
We describe a gas chromatographic/mass spectrometric method for the accurate determination of n-hexanoylglycine, 3… Expand
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1988
1988
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, one of the most common inherited metabolic disorders, is often mistaken… Expand
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