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The metabolism of phenylalanine.
1966The metabolism of phenylalanine-C14 was studied in three different groups of rats: normal animals, phenylalanine-deficient animals and rats which had been maintained on a high (5 and 7%) phenylalanine diet from 21 days of age and considered to be "experimentally phenylketonuric".
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Modulation of auxin formation by the cytosolic phenylalanine biosynthetic pathway
Nature Chemical Biology, 2020J. Lynch +10 more
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The availability of D-phenylalanine and DL-phenylalanine
American Journal of Psychiatry, 1985J G Lofft, R H Bridenbaugh
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Developmental Medicine & Child Neurology, 1970 Effects of phenylalanine on phenylalanine hydroxylase separation and stability
Biochemical Medicine, 1985Ennis C. Layne +2 more
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Thermal profiling reveals phenylalanine hydroxylase as an off-target of panobinostat.
Nature Chemical Biology, 2016Isabelle Becher +12 more
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Phenylketonuria: Phenylalanine Neurotoxicity
2015Phenylketonuria (PKU) was the first inherited metabolic disease identified by newborn screening and treated with diet to prevent the development of intellectual disability. Classification of the severity of phenylketonuria is based on the genetic mutation, dietary phenylalanine tolerance, and pretreatment blood phenylalanine concentrations ...
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