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3-phenylpropionylglycine
Known as:
Phenylpropionylglycine
National Institutes of Health
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Related topics
Related topics
6 relations
Broader (1)
Glycine
Phenylpropionylglycine/Creatinine:MRto:24H:Urine:Qn
Phenylpropionylglycine/Creatinine:MRto:Pt:Urine:Qn
Phenylpropionylglycine/Creatinine:SRto:24H:Urine:Qn
Phenylpropionylglycine/Creatinine:SRto:Pt:Urine:Qn
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Urinary metabolomic profiling in rats exposed to dietary di(2-ethylhexyl) phthalate (DEHP) using ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF…
Xinwen Dong
,
Yunbo Zhang
,
+6 authors
Cheng Wang
Environmental science and pollution research…
2017
Corpus ID: 21220103
Di(2-ethylhexyl) phthalate (DEHP) is an omnipresent environmental chemical with widespread nonoccupational human exposure through…
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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.
Jun Niu
,
Zifeng Pi
,
H. Yue
,
Yang Wang
,
Qing Yu
,
Shuying Liu
Journal of chromatography. B, Analytical…
2012
Corpus ID: 25774033
Highly Cited
2012
Highly Cited
2012
Abcb11 Deficiency Induces Cholestasis Coupled to Impaired β-Fatty Acid Oxidation in Mice*
Yuanyuan Zhang
,
Fei Li
,
+9 authors
J. Schuetz
Journal of Biological Chemistry
2012
Corpus ID: 34123032
Background: Defective ABCB11 causes severe progressive cholestatic liver disease from early infancy. Results: Abcb11 knock-out…
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Review
2012
Review
2012
Development of an isotope labeling ultra-high performance liquid chromatography mass spectrometric method for quantification of acylglycines in human urine.
A. Stanislaus
,
Kevin Guo
,
Liang Li
Analytica Chimica Acta
2012
Corpus ID: 205211542
Highly Cited
2010
Highly Cited
2010
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
P. Rinaldo
,
J. O’Shea
,
P. Coates
,
D. Hale
,
C. Stanley
,
K. Tanaka
New England Journal of Medicine
2010
Corpus ID: 23836494
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, one of the most common inherited metabolic disorders, is often mistaken…
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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.
Yueying Zhen
,
K. Krausz
,
Chi Chen
,
J. Idle
,
F. Gonzalez
Molecular Endocrinology
2007
Corpus ID: 13780272
Peroxisome proliferator-activated receptor alpha (PPARalpha) is a nuclear receptor with manifold effects on intermediary…
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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
D. R. Assis
,
R. Maria
,
+6 authors
M. Wajner
Experimental Neurology
2006
Corpus ID: 2350674
1991
1991
Screening Newborns for Multiple Organic Acidurias in Dried Filter Paper Urine Samples: Method Development
M. Tuchman
,
M. McCann
,
P. E. Johnson
,
B. Lemieux
Pediatric Research
1991
Corpus ID: 2734738
Screening urine for inherited and acquired organic acidurias in newborns has the potential of preventing severe disease, mental…
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1990
1990
Abnormal urinary excretion of unsaturated dicarboxylic acids in patients with medium-chain acyl-CoA dehydrogenase deficiency.
K. Tserng
,
S. Jin
,
D. Kerr
,
C. Hoppel
Journal of Lipid Research
1990
Corpus ID: 34513721
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…
P. Rinaldo
,
J. O’Shea
,
R. D. Welch
,
K. Tanaka
Biomedical & environmental mass spectrometry
1989
Corpus ID: 46581953
We describe a gas chromatographic/mass spectrometric method for the accurate determination of n-hexanoylglycine, 3…
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