 Phenylalanine Hydroxylase
"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 1.14.16.1.
| Descriptor ID |
D010651
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| MeSH Number(s) |
D08.811.682.690.708.601
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| Concept/Terms |
Phenylalanine Hydroxylase- Phenylalanine Hydroxylase
- Hydroxylase, Phenylalanine
- Phenylalanine 4-Hydroxylase
- 4-Hydroxylase, Phenylalanine
- Phenylalanine 4 Hydroxylase
- Phenylalanine 4-Monooxygenase
- 4-Monooxygenase, Phenylalanine
- Phenylalanine 4 Monooxygenase
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Below are MeSH descriptors whose meaning is more general than "Phenylalanine Hydroxylase".
Below are MeSH descriptors whose meaning is more specific than "Phenylalanine Hydroxylase".
This graph shows the total number of publications written about "Phenylalanine Hydroxylase" by people in this website by year, and whether "Phenylalanine Hydroxylase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
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Below are the most recent publications written about "Phenylalanine Hydroxylase" by people in Profiles.
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Kidd JR, Pakstis AJ, Zhao H, Lu RB, Okonofua FE, Odunsi A, Grigorenko E, Tamir BB, Friedlaender J, Schulz LO, Parnas J, Kidd KK. Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations. Am J Hum Genet. 2000 Jun; 66(6):1882-99.
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