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3-phenylpropionylglycine

Known as: Phenylpropionylglycine 
 
National Institutes of Health

Related topics

Related topics

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
2012
2012
Abcb11 Deficiency Induces Cholestasis Coupled to Impaired β-Fatty Acid Oxidation in Mice*
Background: Defective ABCB11 causes severe progressive cholestatic liver disease from early infancy. Results: Abcb11 knock-out… Expand
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Highly Cited
2007
Highly Cited
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
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
2006
2006
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
1991
1991
Screening Newborns for Multiple Organic Acidurias in Dried Filter Paper Urine Samples: Method Development
Screening urine for inherited and acquired organic acidurias in newborns has the potential of preventing severe disease, mental… 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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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
Highly Cited
1988
Highly Cited
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
1984
1984
Enzymatic evidence for a medium-chain acyl-CoA dehydrogenase deficiency in muscle of a patient with hypoketotic hypoglycemic dicarboxylic aciduria
A female patient came to our hospital at the age of 2 8/12 years with the clinical symptoms (vomitimg, diarrhea, hypoglycemia and… Expand
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