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 *

77 related articles for article (PubMed ID: 19491717)

  • 1. Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia.
    Andreou D; Saetre P; Lundmark P; Hansen T; Timm S; Melle I; Djurovic S; Andreassen OA; Werge T; Hall H; Agartz I; Terenius L; Jönsson EG
    Psychiatr Genet; 2009 Oct; 19(5):273-4. PubMed ID: 19491717
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women.
    Sazci A; Ergul E; Kucukali I; Kilic G; Kaya G; Kara I
    Brain Res Mol Brain Res; 2004 Dec; 132(1):51-6. PubMed ID: 15548428
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism in schizophrenia is associated with age at onset and symptoms.
    Numata S; Ueno S; Iga J; Yamauchi K; Hongwei S; Ohta K; Kinouchi S; Shibuya-Tayoshi S; Tayoshi S; Aono M; Kameoka N; Sumitani S; Tomotake M; Kaneda Y; Taniguchi T; Ishimoto Y; Ohmori T
    Neurosci Lett; 2006 Jun; 401(1-2):1-5. PubMed ID: 16533563
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association between the brain-derived neurotrophic factor Val66Met polymorphism and brain morphology in a Japanese sample of schizophrenia and healthy comparisons.
    Takahashi T; Suzuki M; Tsunoda M; Kawamura Y; Takahashi N; Tsuneki H; Kawasaki Y; Zhou SY; Kobayashi S; Sasaoka T; Seto H; Kurachi M; Ozaki N
    Neurosci Lett; 2008 Apr; 435(1):34-9. PubMed ID: 18325670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No association of the Val66Met polymorphism of the brain-derived neurotrophic factor with hippocampal volume in major depression.
    Jessen F; Schuhmacher A; von Widdern O; Guttenthaler V; Hofels S; Suliman H; Scheef L; Block W; Urbach H; Maier W; Zobel A
    Psychiatr Genet; 2009 Apr; 19(2):99-101. PubMed ID: 19668114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Systematic search for variations in the tyrosine hydroxylase gene and their associations with schizophrenia, affective disorders, and alcoholism.
    Ishiguro H; Arinami T; Saito T; Akazawa S; Enomoto M; Mitushio H; Fujishiro H; Tada K; Akimoto Y; Mifune H; Shiozuka S; Hamaguchi H; Toru M; Shibuya H
    Am J Med Genet; 1998 Sep; 81(5):388-96. PubMed ID: 9754624
    [TBL] [Abstract][Full Text] [Related]  

  • 8. COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia.
    Haraldsson HM; Ettinger U; Magnusdottir BB; Sigmundsson T; Sigurdsson E; Ingason A; Petursson H
    Psychiatry Res; 2009 Sep; 169(2):173-5. PubMed ID: 19647329
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The association of tyrosine hydroxylase gene polymorphism with mental disorder].
    Yu J; Pang H; Wang BJ
    Fa Yi Xue Za Zhi; 2008 Oct; 24(5):333-5. PubMed ID: 18979915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Influence of catechol-O-methyltransferase Val158Met polymorphism on neuropsychological and functional outcomes of classical rehabilitation and cognitive remediation in schizophrenia.
    Bosia M; Bechi M; Marino E; Anselmetti S; Poletti S; Cocchi F; Smeraldi E; Cavallaro R
    Neurosci Lett; 2007 May; 417(3):271-4. PubMed ID: 17383818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prefrontal electrophysiologic "noise" and catechol-O-methyltransferase genotype in schizophrenia.
    Winterer G; Egan MF; Kolachana BS; Goldberg TE; Coppola R; Weinberger DR
    Biol Psychiatry; 2006 Sep; 60(6):578-84. PubMed ID: 16730334
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington's disease.
    Kishikawa S; Li JL; Gillis T; Hakky MM; Warby S; Hayden M; MacDonald ME; Myers RH; Gusella JF
    Neurobiol Dis; 2006 Nov; 24(2):280-5. PubMed ID: 16962786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The association of DUSP6 gene with schizophrenia and bipolar disorder: its possible role in the development of bipolar disorder.
    Lee KY; Ahn YM; Joo EJ; Chang JS; Kim YS
    Mol Psychiatry; 2006 May; 11(5):425-6. PubMed ID: 16491131
    [No Abstract]   [Full Text] [Related]  

  • 15. No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease.
    Jennings CE; Owen CJ; Wilson V; Pearce SH
    Clin Endocrinol (Oxf); 2005 Mar; 62(3):362-5. PubMed ID: 15730420
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association between genetic polymorphism of XRCC1 Arg194Trp and risk of schizophrenia.
    Derakhshandeh S; Saadat I; Farrashbandi H; Saadat M
    Psychiatry Res; 2009 Sep; 169(2):186. PubMed ID: 19631990
    [No Abstract]   [Full Text] [Related]  

  • 17. Effect of catechol O-methyltransferase val(158)met polymorphism on the p50 gating endophenotype in schizophrenia.
    Lu BY; Martin KE; Edgar JC; Smith AK; Lewis SF; Escamilla MA; Miller GA; Cañive JM
    Biol Psychiatry; 2007 Oct; 62(7):822-5. PubMed ID: 17448448
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association study between kynurenine 3-monooxygenase gene and schizophrenia in the Japanese population.
    Aoyama N; Takahashi N; Saito S; Maeno N; Ishihara R; Ji X; Miura H; Ikeda M; Suzuki T; Kitajima T; Yamanouchi Y; Kinoshita Y; Yoshida K; Iwata N; Inada T; Ozaki N
    Genes Brain Behav; 2006 Jun; 5(4):364-8. PubMed ID: 16716206
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE).
    Djurovic S; Le Hellard S; Kähler AK; Jönsson EG; Agartz I; Steen VM; Hall H; Wang AG; Rasmussen HB; Melle I; Werge T; Andreassen OA
    Psychiatry Res; 2009 Aug; 168(3):256-8. PubMed ID: 19223264
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.
    Borroni B; Grassi M; Costanzi C; Zanetti M; Archetti S; Franzoni S; Caimi L; Padovani A
    Neurobiol Aging; 2007 Aug; 28(8):1231-8. PubMed ID: 16837108
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.