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5. Phenylalanine hydroxylase expression in liver of a fetus with phenylketonuria. Ledley FD; Koch R; Jew K; Beaudet A; O'Brien WE; Bartos DP; Woo SL J Pediatr; 1988 Sep; 113(3):463-8. PubMed ID: 2900886 [TBL] [Abstract][Full Text] [Related]
6. Quantification of phenylalanine hydroxylase activity by isotope-dilution liquid chromatography-electrospray ionization tandem mass spectrometry. Heintz C; Troxler H; Martinez A; Thöny B; Blau N Mol Genet Metab; 2012 Apr; 105(4):559-65. PubMed ID: 22300847 [TBL] [Abstract][Full Text] [Related]
7. Discussion: Phenylalanine hydroxylase in human kidney; relevance to Phenylketonuria. Ayling JE UCLA Forum Med Sci; 1975; (18):459-65. PubMed ID: 1239108 [No Abstract] [Full Text] [Related]
8. Phenylketonuria and its variants. Kaufman S; Milstien S Ann Clin Lab Sci; 1977; 7(2):178-85. PubMed ID: 557947 [TBL] [Abstract][Full Text] [Related]
9. Observations indicating the nature of the mutation in phenylketonuria. Choo KH; Cotton RG; Jennings IG; Danks DM J Inherit Metab Dis; 1980; 2(4):79-84. PubMed ID: 6796764 [TBL] [Abstract][Full Text] [Related]
10. Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population. Dobrowolski SF; Heintz C; Miller T; Ellingson C; Ellingson C; Ozer I; Gökçay G; Baykal T; Thöny B; Demirkol M; Blau N Mol Genet Metab; 2011 Feb; 102(2):116-21. PubMed ID: 21147011 [TBL] [Abstract][Full Text] [Related]
11. Expression of human phenylalanine hydroxylase activity in T lymphocytes of classical phenylketonuria children by retroviral-mediated gene transfer. Lin CM; Tan Y; Lee YM; Chang CC; Hsiao KJ J Inherit Metab Dis; 1997 Nov; 20(6):742-54. PubMed ID: 9427141 [TBL] [Abstract][Full Text] [Related]
12. Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria. Choo KH; Cotton RG; Danks DM; Jennings IG Biochem J; 1979 Aug; 181(2):285-94. PubMed ID: 496890 [TBL] [Abstract][Full Text] [Related]
13. Effect of glucagon on hepatic phenylalanine hydroxylase in vivo. Beirne E; Carty MP; Donlon J Biosci Rep; 1985 Jun; 5(6):463-7. PubMed ID: 4041562 [TBL] [Abstract][Full Text] [Related]
14. [Phenylalanine hydroxylase activity in the liver in children with the classic form of phenylketonuria]. Shaposhnikov AM; Barashnev IuI; Khal'chitskiĭ SE; Korneĭchuk VV; Okat'ev VS Vopr Okhr Materin Det; 1978 Jun; 23(6):42-7. PubMed ID: 676196 [No Abstract] [Full Text] [Related]
15. Control of liver and brain aromatic amino-acid metabolism by phenylalanine hydroxylase. Tourian A Vopr Biokhim Mozga; 1973; 8():211-9. PubMed ID: 4281155 [No Abstract] [Full Text] [Related]
16. Tetrahydrobiopterin protects phenylalanine hydroxylase activity in vivo: implications for tetrahydrobiopterin-responsive hyperphenylalaninemia. Thöny B; Ding Z; Martínez A FEBS Lett; 2004 Nov; 577(3):507-11. PubMed ID: 15556637 [TBL] [Abstract][Full Text] [Related]
17. Mutations in the regulatory domain of phenylalanine hydroxylase and response to tetrahydrobiopterin. Wang L; Surendran S; Michals-Matalon K; Bhatia G; Tanskley S; Koch R; Grady J; Tyring SK; Stevens RC; Guttler F; Matalon R Genet Test; 2007; 11(2):174-8. PubMed ID: 17627389 [TBL] [Abstract][Full Text] [Related]
18. Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylase. Bartholomé K; Dresel A J Inherit Metab Dis; 1982; 5(1):7-10. PubMed ID: 6820417 [TBL] [Abstract][Full Text] [Related]
19. Minimally invasive (13)C-breath test to examine phenylalanine metabolism in children with phenylketonuria. Turki A; Murthy G; Ueda K; Cheng B; Giezen A; Stockler-Ipsiroglu S; Elango R Mol Genet Metab; 2015; 115(2-3):78-83. PubMed ID: 25943030 [TBL] [Abstract][Full Text] [Related]
20. Glucagon stimulation of rat hepatic phenylalanine hydroxylase through phosphorylation in vivo. Donlon J; Kaufman S J Biol Chem; 1978 Oct; 253(19):6657-9. PubMed ID: 690116 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]