These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 1297795)

  • 1. Novel aspects of metabolism and function of tetrahydrobiopterin.
    Kaufman S
    J Nutr Sci Vitaminol (Tokyo); 1992; Spec No():492-6. PubMed ID: 1297795
    [No Abstract]   [Full Text] [Related]  

  • 2. [The phenylalanine hydroxylase system].
    Dhondt JL; Farriaux JP
    Arch Fr Pediatr; 1983; 40 Suppl 1():219-21. PubMed ID: 6882139
    [No Abstract]   [Full Text] [Related]  

  • 3. [Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase].
    Rey F; Harpey JP; Leeming RJ; Blair JA; Aicardi J; Rey J
    Arch Fr Pediatr; 1977; 34(7 Suppl):CIX-CXX. PubMed ID: 931522
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
    Kure S; Hou DC; Ohura T; Iwamoto H; Suzuki S; Sugiyama N; Sakamoto O; Fujii K; Matsubara Y; Narisawa K
    J Pediatr; 1999 Sep; 135(3):375-8. PubMed ID: 10484807
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Atypical PKU with normal phenylalanine hydroxylase and dihydropteridine reductase activity in vitro.
    Leeming RJ; Smith I
    Arch Dis Child; 1979 Feb; 54(2):166-7. PubMed ID: 434898
    [No Abstract]   [Full Text] [Related]  

  • 6. Contrasting effects of N5-substituted tetrahydrobiopterin derivatives on phenylalanine hydroxylase, dihydropteridine reductase and nitric oxide synthase.
    Werner ER; Habisch HJ; Gorren AC; Schmidt K; Canevari L; Werner-Felmayer G; Mayer B
    Biochem J; 2000 Jun; 348 Pt 3(Pt 3):579-83. PubMed ID: 10839989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The mechanism of cofactor regeneration during phenylalanine hydroxylation.
    Bailey SW; Boerth SR; Dillard SB; Ayling JE
    Adv Exp Med Biol; 1993; 338():47-54. PubMed ID: 8304161
    [No Abstract]   [Full Text] [Related]  

  • 8. Hyperphenylalaninemia due to a deficiency of biopterin. A variant form of phenylketonuria.
    Kaufman S; Berlow S; Summer GK; Milstien S; Schulman JD; Orloff S; Spielberg S; Pueschel S
    N Engl J Med; 1978 Sep; 299(13):673-9. PubMed ID: 683251
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tetrahydrobiopterin for patients with phenylketonuria.
    Pey AL; Martinez A
    Lancet; 2007 Aug; 370(9586):462-3. PubMed ID: 17693159
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Physarum polycephalum expresses a dihydropteridine reductase with selectivity for pterin substrates with a 6-(1', 2'-dihydroxypropyl) substitution.
    Wild C; Golderer G; Gröbner P; Werner-Felmayer G; Werner ER
    Biol Chem; 2003 Jul; 384(7):1057-62. PubMed ID: 12956422
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Successful long term therapy of biopterin deficiency.
    Snyderman SE; Sansaricq C; Pulmones MT
    J Inherit Metab Dis; 1987; 10(3):260-6. PubMed ID: 3123784
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenylketonuria and its variants.
    Kaufman S
    Adv Hum Genet; 1983; 13():217-97. PubMed ID: 6362361
    [No Abstract]   [Full Text] [Related]  

  • 14. Tetrahydrobiopterin sensitivity in German patients with mild phenylalanine hydroxylase deficiency.
    Lindner M; Steinfeld R; Burgard P; Schulze A; Mayatepek E; Zschocke J
    Hum Mutat; 2003 Apr; 21(4):400. PubMed ID: 12655554
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Strategy for the screening of tetrahydrobiopterin deficiency among hyperphenylalaninaemic patients: 15-years experience.
    Dhondt JL
    J Inherit Metab Dis; 1991; 14(2):117-27. PubMed ID: 1886401
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blood spots on Guthrie cards can be used for inherited tetrahydrobiopterin deficiency screening in hyperphenylalaninaemic infants.
    Leeming RJ; Barford PA; Blair JA; Smith I
    Arch Dis Child; 1984 Jan; 59(1):58-61. PubMed ID: 6696496
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Comparative effects of different inhibitors of phenylalanine hydroxylase and dihydropteridine reductase. In vivo and in vitro study in rats].
    Charpentier C; Domange C; Wolf M; Barthon F; Laggoune B; Lemonnier A
    Arch Fr Pediatr; 1978 Dec; 35(10 Suppl):93-101. PubMed ID: 571268
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic disorders involving recycling and formation of tetrahydrobiopterin.
    Kaufman S
    Adv Pharmacol; 1998; 42():41-3. PubMed ID: 9327841
    [No Abstract]   [Full Text] [Related]  

  • 19. The enzymes of the hepatic phenylalanine hydroxylating system.
    Kaufman S
    J Inherit Metab Dis; 1978; 1(2):63-5. PubMed ID: 117244
    [No Abstract]   [Full Text] [Related]  

  • 20. The metabolic and molecular bases of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
    Blau N; Erlandsen H
    Mol Genet Metab; 2004 Jun; 82(2):101-11. PubMed ID: 15171997
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.