Phenylalanine Metabolism Pathway

Known as: L-phenylalanine metabolic process, L-phenylalanine metabolism, Phenylalanine Metabolism 
The chemical reactions and pathways involving L-phenylalanine, the L-enantiomer of 2-amino-3-phenylpropanoic acid, i.e. (2S)-2-amino-3… (More)
National Institutes of Health

Papers overview

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2013
2013
During the life cycles of conifer trees, such as maritime pine (Pinus pinaster Ait.), large quantities of carbon skeletons are… (More)
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2012
2012
Metabolomics represents an emerging and powerful discipline that provides an accurate and dynamic picture of the phenotype of… (More)
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Review
2012
Review
2012
Phenylketonuria (PKU), an inborn error in phenylalanine metabolism, requires lifelong nutrition management with a low… (More)
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2011
2011
OBJECTIVES Alkaptonuria (AKU) is an orphan disease that has an estimated prevalence of 0.3/100,000. The disease is caused by the… (More)
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2006
2006
Bread spoilage is mainly due to the growth of filamentous fungi, and metabolites produced during sourdough fermentation by… (More)
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2004
2004
Summary: Phenylketonuria, an inborn error of phenylalanine metabolism, occurs with a frequency of about 1 in 10 000 births and is… (More)
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Review
2002
Review
2002
Tetrahydrobiopterin (BH4) deficiencies are disorders affecting phenylalanine metabolism in liver and neurotransmitters… (More)
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Highly Cited
1992
Highly Cited
1992
We report the clinical features, biochemical details, and treatment of the first detected cases of an inborn error of aromatic L… (More)
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1979
1979
Summary: Concentrations of phenylalanine in the plasma were markedly elevated in iron-deficient rats and appeared to vary… (More)
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1977
1977
A child with phenylketonuria had normal phenylalanine hydroxylase activity in vitro. In addition, all known components of the… (More)
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