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Journal Abstract Search

496 related items for PubMed ID: 14618678

  • 1. Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.
    Tunbridge E, Burnet PW, Sodhi MS, Harrison PJ.
    Synapse; 2004 Feb; 51(2):112-8. PubMed ID: 14618678
    [Abstract] [Full Text] [Related]

  • 2. Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
    Zinkstok J, Schmitz N, van Amelsvoort T, Moeton M, Baas F, Linszen D.
    Genes Brain Behav; 2008 Feb; 7(1):61-9. PubMed ID: 17504246
    [Abstract] [Full Text] [Related]

  • 3. A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val158Met genotype.
    Tunbridge EM, Weinberger DR, Harrison PJ.
    Mol Psychiatry; 2006 Feb; 11(2):116-7. PubMed ID: 16247488
    [No Abstract] [Full Text] [Related]

  • 4. Hyperprolinemia is a risk factor for schizoaffective disorder.
    Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, D'Amato T, Petit M, Thibaut F, Frébourg T, Campion D.
    Mol Psychiatry; 2005 May; 10(5):479-85. PubMed ID: 15494707
    [Abstract] [Full Text] [Related]

  • 5. Catechol-O-methyltransferase Val158Met genotype variation is associated with prefrontal-dependent task performance in schizotypal personality disorder patients and comparison groups.
    Minzenberg MJ, Xu K, Mitropoulou V, Harvey PD, Finch T, Flory JD, New AS, Goldman D, Siever LJ.
    Psychiatr Genet; 2006 Jun; 16(3):117-24. PubMed ID: 16691129
    [Abstract] [Full Text] [Related]

  • 6. Catechol-O-methyltransferase val108/158met genotype predicts working memory response to antipsychotic medications.
    Weickert TW, Goldberg TE, Mishara A, Apud JA, Kolachana BS, Egan MF, Weinberger DR.
    Biol Psychiatry; 2004 Nov 01; 56(9):677-82. PubMed ID: 15522252
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  • 8. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
    Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D.
    Hum Mol Genet; 2007 Jan 01; 16(1):83-91. PubMed ID: 17135275
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  • 10. Analysis of an association between the COMT polymorphism and clinical symptomatology in schizophrenia.
    Strous RD, Lapidus R, Viglin D, Kotler M, Lachman HM.
    Neurosci Lett; 2006 Jan 30; 393(2-3):170-3. PubMed ID: 16233957
    [Abstract] [Full Text] [Related]

  • 11. 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 06; 132(1):51-6. PubMed ID: 15548428
    [Abstract] [Full Text] [Related]

  • 12. The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia.
    Ohnishi T, Hashimoto R, Mori T, Nemoto K, Moriguchi Y, Iida H, Noguchi H, Nakabayashi T, Hori H, Ohmori M, Tsukue R, Anami K, Hirabayashi N, Harada S, Arima K, Saitoh O, Kunugi H.
    Brain; 2006 Feb 06; 129(Pt 2):399-410. PubMed ID: 16330500
    [Abstract] [Full Text] [Related]

  • 13. Catechol O-methyltransferase (COMT) mRNA expression in the dorsolateral prefrontal cortex of patients with schizophrenia.
    Matsumoto M, Weickert CS, Beltaifa S, Kolachana B, Chen J, Hyde TM, Herman MM, Weinberger DR, Kleinman JE.
    Neuropsychopharmacology; 2003 Aug 06; 28(8):1521-30. PubMed ID: 12799619
    [Abstract] [Full Text] [Related]

  • 14. Relationship of catechol-O-methyltransferase to schizophrenia and its correlates: evidence for associations and complex interactions.
    Lewandowski KE.
    Harv Rev Psychiatry; 2007 Aug 06; 15(5):233-44. PubMed ID: 17924258
    [Abstract] [Full Text] [Related]

  • 15. COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance.
    Burdick KE, Funke B, Goldberg JF, Bates JA, Jaeger J, Kucherlapati R, Malhotra AK.
    Bipolar Disord; 2007 Jun 06; 9(4):370-6. PubMed ID: 17547583
    [Abstract] [Full Text] [Related]

  • 16. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE, Howley S, Murphy KC.
    Dev Disabil Res Rev; 2008 Jun 06; 14(1):26-34. PubMed ID: 18636634
    [Abstract] [Full Text] [Related]

  • 17. Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy.
    Huuhka K, Anttila S, Huuhka M, Hietala J, Huhtala H, Mononen N, Lehtimäki T, Leinonen E.
    Neurosci Lett; 2008 Dec 19; 448(1):79-83. PubMed ID: 18929622
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 60(6):578-84. PubMed ID: 16730334
    [Abstract] [Full Text] [Related]

  • 19. The catechol-O-methyltransferase Val108/158Met polymorphism affects short-term treatment response to mirtazapine, but not to paroxetine in major depression.
    Szegedi A, Rujescu D, Tadic A, Müller MJ, Kohnen R, Stassen HH, Dahmen N.
    Pharmacogenomics J; 2005 Sep 15; 5(1):49-53. PubMed ID: 15520843
    [Abstract] [Full Text] [Related]

  • 20. Prefrontal cognition in schizophrenia and bipolar illness in relation to Val66Met polymorphism of the brain-derived neurotrophic factor gene.
    Rybakowski JK, Borkowska A, Skibinska M, Szczepankiewicz A, Kapelski P, Leszczynska-Rodziewicz A, Czerski PM, Hauser J.
    Psychiatry Clin Neurosci; 2006 Feb 15; 60(1):70-6. PubMed ID: 16472361
    [Abstract] [Full Text] [Related]

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