"Phenylalanine Hydroxylase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An enzyme of the oxidoreductase class that catalyzes the formation of L-TYROSINE, dihydrobiopterin, and water from L-PHENYLALANINE, tetrahydrobiopterin, and oxygen. Deficiency of this enzyme may cause PHENYLKETONURIAS and PHENYLKETONURIA, MATERNAL. EC 184.108.40.206.
- Phenylalanine Hydroxylase
- Hydroxylase, Phenylalanine
- Phenylalanine 4-Hydroxylase
- 4-Hydroxylase, Phenylalanine
- Phenylalanine 4 Hydroxylase
- Phenylalanine 4-Monooxygenase
- 4-Monooxygenase, Phenylalanine
- Phenylalanine 4 Monooxygenase
Below are MeSH descriptors whose meaning is more general than "Phenylalanine Hydroxylase".
Below are MeSH descriptors whose meaning is more specific than "Phenylalanine Hydroxylase".
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Below are the most recent publications written about "Phenylalanine Hydroxylase" by people in Profiles.
A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editing. JCI Insight. 2020 10 15; 5(20).
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene. Hum Mutat. 2018 11; 39(11):1569-1580.
Kinetics of tetrahydrobiopterin synthesis by rabbit brain dihydrofolate reductase. Biochem J. 1978 Apr 01; 171(1):267-8.