BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 12210276)

  • 1. Aromatic amino acid hydroxylase genes and schizophrenia.
    Chao HM; Richardson MA
    Am J Med Genet; 2002 Aug; 114(6):626-30. PubMed ID: 12210276
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effect of pharmacological chaperones on brain tyrosine hydroxylase and tryptophan hydroxylase 2.
    Calvo AC; Scherer T; Pey AL; Ying M; Winge I; McKinney J; Haavik J; Thöny B; Martinez A
    J Neurochem; 2010 Aug; 114(3):853-63. PubMed ID: 20492352
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tryptophan hydroxylase-1 gene variants associated with schizophrenia.
    Zaboli G; Jönsson EG; Gizatullin R; Asberg M; Leopardi R
    Biol Psychiatry; 2006 Sep; 60(6):563-9. PubMed ID: 16806098
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Investigation of A218C tryptophan hydroxylase polymorphism: association with familial suicide behavior and proband's suicide attempt characteristics.
    Viana MM; De Marco LA; Boson WL; Romano-Silva MA; Corrêa H
    Genes Brain Behav; 2006 Jun; 5(4):340-5. PubMed ID: 16716203
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exon 3 of tyrosine hydroxylase gene: lack of association with Japanese schizophrenic patients.
    Ota M; Nakashima A; Ikemoto K; Nojima S; Tanaka M; Okuda M; Koga H; Mori K; Kaneko YS; Fujiwara K; Yamamoto H; Nagatsu T; Ota A
    Mol Psychiatry; 2001 May; 6(3):315-9. PubMed ID: 11326301
    [TBL] [Abstract][Full Text] [Related]  

  • 6. In vitro expression of 34 naturally occurring mutant variants of phenylalanine hydroxylase: correlation with metabolic phenotypes and susceptibility toward protein aggregation.
    Gjetting T; Petersen M; Guldberg P; Güttler F
    Mol Genet Metab; 2001 Feb; 72(2):132-43. PubMed ID: 11161839
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association study of structural mutations of the tyrosine hydroxylase gene with schizophrenia and Parkinson's disease.
    Kunugi H; Kawada Y; Hattori M; Ueki A; Otsuka M; Nanko S
    Am J Med Genet; 1998 Mar; 81(2):131-3. PubMed ID: 9613851
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structural interpretation of mutations in phenylalanine hydroxylase protein aids in identifying genotype-phenotype correlations in phenylketonuria.
    Jennings IG; Cotton RG; Kobe B
    Eur J Hum Genet; 2000 Sep; 8(9):683-96. PubMed ID: 10980574
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tetrahydrobiopterin binding to aromatic amino acid hydroxylases. Ligand recognition and specificity.
    Teigen K; Dao KK; McKinney JA; Gorren AC; Mayer B; Frøystein NA; Haavik J; Martínez A
    J Med Chem; 2004 Nov; 47(24):5962-71. PubMed ID: 15537351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria.
    Acosta A; Silva W; Carvalho T; Gomes M; Zago M
    Hum Mutat; 2001 Feb; 17(2):122-30. PubMed ID: 11180595
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The importance of arginine mutation for the evolutionary structure and function of phenylalanine hydroxylase gene.
    Lüleyap HU; Alptekin D; Pazarbaşi A; Kasap M; Kasap H; Demirhindi H; Mungan N; Ozer G; Froster UG
    Mutat Res; 2006 Oct; 601(1-2):39-45. PubMed ID: 16765994
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin.
    Dobrowolski SF; Borski K; Ellingson CC; Koch R; Levy HL; Naylor EW
    J Hum Genet; 2009 Jun; 54(6):335-9. PubMed ID: 19444284
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Intersubunit binding domains within tyrosine hydroxylase and tryptophan hydroxylase.
    Yohrling GJ; Jiang GC; Mockus SM; Vrana KE
    J Neurosci Res; 2000 Aug; 61(3):313-20. PubMed ID: 10900078
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the phenylalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles.
    Dobrowolski SF; Ellingson C; Coyne T; Grey J; Martin R; Naylor EW; Koch R; Levy HL
    Mol Genet Metab; 2007 Jul; 91(3):218-27. PubMed ID: 17502162
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Validation of PAH genotype-based predictions of metabolic phenylalanine hydroxylase deficiency phenotype: investigation of PKU/MHP patients from Lithuania.
    Kasnauskiene J; Cimbalistiene L; Kucinskas V
    Med Sci Monit; 2003 Mar; 9(3):CR142-6. PubMed ID: 12640344
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The tryptophan hydroxylase 1 (TPH1) gene and risk of schizophrenia: a moderate-scale case-control study and meta-analysis.
    Watanabe Y; Nunokawa A; Kaneko N; Someya T
    Neurosci Res; 2007 Nov; 59(3):322-6. PubMed ID: 17870198
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel association approach for determining the genetic predisposition to schizophrenia: case-control resource and testing of a candidate gene.
    Sobell JL; Heston LL; Sommer SS
    Am J Med Genet; 1993 May; 48(1):28-35. PubMed ID: 8357034
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pharmacological Chaperones that Protect Tetrahydrobiopterin Dependent Aromatic Amino Acid Hydroxylases Through Different Mechanisms.
    Hole M; Jorge-Finnigan A; Underhaug J; Teigen K; Martinez A
    Curr Drug Targets; 2016; 17(13):1515-26. PubMed ID: 26953246
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Different stabilities and denaturation pathways for structurally related aromatic amino acid hydroxylases.
    Kleppe R; Haavik J
    FEBS Lett; 2004 May; 565(1-3):155-9. PubMed ID: 15135070
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ten novel mutations in the phenylalanine hydroxylase gene (PAH) observed in Brazilian patients with phenylketonuria.
    Acosta AX; Silva WA; Carvalho TM; Zago MA
    Hum Mutat; 2001; 17(1):77. PubMed ID: 11139255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.