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 *

124 related articles for article (PubMed ID: 942423)

  • 21. Sensitive in vivo assay of the phenylalanine hydroxylating system with a small intravenous dose of heptadeutero L-phenylalanine using high pressure liquid chromatography and capillary gas chromatography/mass fragmentography.
    Trefz FK; Erlenmaier T; Hunneman DH; Bartholomé K; Lutz P
    Clin Chim Acta; 1979 Dec; 99(3):211-30. PubMed ID: 519859
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular basis for the heterogeneity of phenylketonuria].
    Bartholomé K
    Naturwissenschaften; 1980 Oct; 67(10):495-8. PubMed ID: 7432543
    [TBL] [Abstract][Full Text] [Related]  

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

  • 24. The isoenzymes of phenylalanine hydroxylase in humans.
    Parker CE; Barranger J; Newhouse R; Bessman S
    Ann Clin Biochem; 1977 May; 14(3):122-3. PubMed ID: 869487
    [No Abstract]   [Full Text] [Related]  

  • 25. Cataractogenesis in infant rats with model phenylketonuria.
    Gunter R; Brown WJ; Schalock R
    Percept Mot Skills; 1972 Aug; 35(1):47-9. PubMed ID: 4262342
    [No Abstract]   [Full Text] [Related]  

  • 26. Penylalanine hydroxylation in phenylketonuria.
    Hoffbauer RW; Schrempf G; Mönch E
    Lancet; 1976 Nov; 2(7993):1031. PubMed ID: 62257
    [No Abstract]   [Full Text] [Related]  

  • 27. Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia.
    Bartholomé K; Lutz P; Bickel H
    Pediatr Res; 1975 Dec; 9(12):899-903. PubMed ID: 1196708
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. [Advances in the studies of molecular heredity of phenylketonuria].
    Zhang Z; He YS
    Yi Chuan; 2004 Sep; 26(5):729-34. PubMed ID: 15640093
    [TBL] [Abstract][Full Text] [Related]  

  • 30. In vitro expression analysis of R68G and R68S mutations in phenylalanine hydroxylase gene.
    Zekanowsk C; Perez B; Desviat LR; Wiszniewski W; Ugarte M
    Acta Biochim Pol; 2000; 47(2):365-9. PubMed ID: 11051201
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Degradation rates differ between mutant and wild-type forms of phenylalanine hydroxylase expressed in vitro.
    Waters PJ; Scriver CR; Parniak MA
    Biochem Soc Trans; 1998 Aug; 26(3):S276. PubMed ID: 9765995
    [No Abstract]   [Full Text] [Related]  

  • 32. Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: a mechanism underlying phenylketonuria.
    Waters PJ; Parniak MA; Akerman BR; Jones AO; Scriver CR
    J Inherit Metab Dis; 1999 May; 22(3):208-12. PubMed ID: 10384369
    [No Abstract]   [Full Text] [Related]  

  • 33. Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria.
    Bénit P; Rey F; Melle D; Munnich A; Rey J
    Hum Mutat; 1994; 4(3):229-31. PubMed ID: 7833954
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. [Determination of phenylalanine hydroxylase in patients with phenylketonuria and hyperphenylalaninemia].
    Bartholomé K; Lutz P
    Monatsschr Kinderheilkd (1902); 1976 May; 124(5):421-2. PubMed ID: 934137
    [No Abstract]   [Full Text] [Related]  

  • 36. In vivo inhibition of rat liver phenylalanine hydroxylase by p-chlorophenylalanine and Esculin. Experimental model of phenylketonuria.
    Valdivieso F; Gimenez C; Mayor F
    Biochem Med; 1975 Jan; 12(1):72-8. PubMed ID: 124571
    [No Abstract]   [Full Text] [Related]  

  • 37. Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism.
    Eichinger A; Danecka MK; Möglich T; Borsch J; Woidy M; Büttner L; Muntau AC; Gersting SW
    Hum Mol Genet; 2018 May; 27(10):1732-1742. PubMed ID: 29514280
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Phenylalanine hydroxylase activity in the livers of patients with phenylketonuria].
    Shaposhnikov AM; Skachkov MM
    Vopr Med Khim; 1974; 20(6):656-60. PubMed ID: 4450535
    [No Abstract]   [Full Text] [Related]  

  • 39. In vitro residual activities in 20 variants of phenylalanine hydroxylase and genotype-phenotype correlation in phenylketonuria patients.
    Zhang X; Ye J; Shen N; Tao Y; Han L; Qiu W; Zhang H; Liang L; Fan Y; Wang J; Gong Z; Wang Y; You G; Fu Q; Mo X; Gu X; Yu Y
    Gene; 2019 Jul; 707():239-245. PubMed ID: 31102715
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Focus on the molecular genetics of phenylketonuria.
    Zschocke J
    Hum Mutat; 2003 Apr; 21(4):331-2. PubMed ID: 12655542
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.