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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… 
National Institutes of Health

Related topics

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9 relations
Cytoplasmic Aspartate AminotransferaseDDC protein, humanDDC wt AlleleMAOA protein, human

Papers overview

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2011
2011
LEVANTAMENTO EPIDEMIOLÓGICO DA FENILCETONÚRIA NO ESTADO DE GOIÁS
Phenylketonuria is a genetic disease resultant of deficiencies in phenylalanine metabolism. The accumulation of the phenylalanine… 
2008
2008
Influence of anabolic hormones on phenylalanine metabolism. I. Studies on chronic phenylketonuric patients.
2008
2008
Influence of anabolic hormones on phenylalanine metabolism. II. Studies in animals.
Review
1992
Review
1992
Nurses' role in preventing birth defects in offspring of women with phenylketonuria.
Most women who began nutrition support as neonates for a diagnosis of phenylketonuria, an inherited defect in phenylalanine… 
1991
1991
[Inherited metabolic aberration of phenylalanine in the family members of patients with essential hypertension and stroke].
L-2H-Leu, L-2H-Val, L-2H-Ile, L-2H-Phe, 14N-Lys were chosen for comparing their metabolic kinetic variables among those with… 
1990
1990
Genetic analysis of treated and untreated phenylketonuria in one family.
We describe a family in which four subjects in two generations have a disorder of phenylalanine metabolism. Two first cousins had… 
1979
1979
Effects of alpha-aminooxy-beta-phenylpropionic acid on phenylalanine metabolism in p-fluorophenylalanine sensitive and resistant tobacco cells.
A p-fluorophenylalanine (PFP) resistant cell line with high phenylalanine ammonia lyase (PAL) activity and wild type cells with… 
1979
1979
[A program of EEG supervision for monitoring patients with anomalies in phenylalanine metabolism].
Review
1973
Review
1973
[Congenital disorders of phenylalanine metabolism].
1970
1970
[Screening program for early detection of phenylketonuria and other disorders of phenylalanine metabolism in the newborn in Israel].