Fanet H, Capuron L, Castanon N, Calon F, Vancassel S
Curr Neuropharmacol. 2020; 19(5):591-609.
PMID: 32744952
PMC: 8573752.
DOI: 10.2174/1570159X18666200729103529.
Latremoliere A, Costigan M
Neurosci Bull. 2017; 34(1):143-155.
PMID: 28667479
PMC: 5799129.
DOI: 10.1007/s12264-017-0152-z.
Latremoliere A, Costigan M
Curr Pharm Biotechnol. 2011; 12(10):1728-41.
PMID: 21466440
PMC: 4469332.
DOI: 10.2174/138920111798357393.
Kenney F, KRETCHMER N
J Clin Invest. 1959; 38:2189-96.
PMID: 14408533
PMC: 293310.
DOI: 10.1172/JCI103998.
TISCHLER B, McGeer E
Can Med Assoc J. 1962; 87:1331-2.
PMID: 13985151
PMC: 1920846.
Phenylalanine metabolism and folic acid antagonists.
Goodfriend T, Kaufman S
J Clin Invest. 1961; 40:1743-50.
PMID: 13707008
PMC: 290868.
DOI: 10.1172/JCI104397.
Non-heme iron enzymes: contrasts to heme catalysis.
Solomon E, Decker A, Lehnert N
Proc Natl Acad Sci U S A. 2003; 100(7):3589-94.
PMID: 12598659
PMC: 152966.
DOI: 10.1073/pnas.0336792100.
Phenylketonuric Tetrahymena: phenylalanine hydroxylase mutants and other tyrosine auxotrophs.
Sanford Y, Orias E
Proc Natl Acad Sci U S A. 1981; 78(12):7614-8.
PMID: 6950403
PMC: 349319.
DOI: 10.1073/pnas.78.12.7614.
Metabolism of phenylalanine in mice homozygous for the gene 'dilute lethal'.
WOOLF L, JAKUBOVIC A, Woolf F, Bory P
Biochem J. 1970; 119(5):895-903.
PMID: 5531182
PMC: 1179490.
DOI: 10.1042/bj1190895.
Atypical phenylketonuria. An approach to diagnosis and management.
Yu J, Stuckey S, OHalloran M
Arch Dis Child. 1970; 45(242):561-5.
PMID: 5506944
PMC: 1647635.
DOI: 10.1136/adc.45.242.561.
Effect of phenylalanine on protein synthesis in the developing rat brain.
Agrawal H, Bone A, Davison A
Biochem J. 1970; 117(2):325-31.
PMID: 5463265
PMC: 1178865.
DOI: 10.1042/bj1170325.
Detection of hepatic phenylalanine 4-hydroxylase in classical phenylketonuria.
Friedman P, Fisher D, Kang E, Kaufman S
Proc Natl Acad Sci U S A. 1973; 70(2):552-6.
PMID: 4405625
PMC: 433304.
DOI: 10.1073/pnas.70.2.552.
Enzymes involved in phenylalanine metabolism in the human foetus and child.
McLean A, Marwick M, Clayton B
J Clin Pathol. 1973; 26(9):678-83.
PMID: 4148075
PMC: 477849.
DOI: 10.1136/jcp.26.9.678.
Hyperphenylalaninaemia caused by defects in biopterin metabolism.
Kaufman S
J Inherit Metab Dis. 1985; 8 Suppl 1:20-7.
PMID: 3930837
DOI: 10.1007/BF01800655.
Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase.
McDonald J, Bode V, Dove W, Shedlovsky A
Proc Natl Acad Sci U S A. 1990; 87(5):1965-7.
PMID: 2308957
PMC: 53605.
DOI: 10.1073/pnas.87.5.1965.
Conversion of 6-substituted tetrahydropterins to 7-isomers via phenylalanine hydroxylase-generated intermediates.
Davis M, Kaufman S, Milstien S
Proc Natl Acad Sci U S A. 1991; 88(2):385-9.
PMID: 1988938
PMC: 50815.
DOI: 10.1073/pnas.88.2.385.
Some metabolic relationships between biopterin and folate: implications for the "methyl trap hypothesis".
Kaufman S
Neurochem Res. 1991; 16(9):1031-6.
PMID: 1784330
DOI: 10.1007/BF00965847.
The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.
Konecki D, Lichter-Konecki U
Hum Genet. 1991; 87(4):377-88.
PMID: 1679029
DOI: 10.1007/BF00197152.
"7-tetrahydrobiopterin," a naturally occurring analogue of tetrahydrobiopterin, is a cofactor for and a potential inhibitor of the aromatic amino acid hydroxylases.
Davis M, Ribeiro P, Tipper J, Kaufman S
Proc Natl Acad Sci U S A. 1992; 89(21):10109-13.
PMID: 1359535
PMC: 50287.
DOI: 10.1073/pnas.89.21.10109.
Abnormal amino acid metabolism and brain protein synthesis during neural development.
Hughes J, Johnson T
Neurochem Res. 1978; 3(4):381-99.
PMID: 34113
DOI: 10.1007/BF00966321.
