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Journal Abstract Search

317 related items for PubMed ID: 17768266

  • 1. Association of functional polymorphisms of the human tryptophan hydroxylase 2 gene with risk for bipolar disorder in Han Chinese.
    Lin YM, Chao SC, Chen TM, Lai TJ, Chen JS, Sun HS.
    Arch Gen Psychiatry; 2007 Sep; 64(9):1015-24. PubMed ID: 17768266
    [Abstract] [Full Text] [Related]

  • 2. Polymorphism screening and haplotype analysis of the tryptophan hydroxylase gene (TPH1) and association with bipolar affective disorder in Taiwan.
    Lai TJ, Wu CY, Tsai HW, Lin YM, Sun HS.
    BMC Med Genet; 2005 Mar 31; 6():14. PubMed ID: 15799788
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  • 4. Association study of TPH2 polymorphisms and bipolar disorder in the Han Chinese population.
    Chen S, Huang X, Yu T, Li X, Cao Y, Li X, Xu F, Yang F, Jesse FF, Xu M, Li W, He L, He G.
    Prog Neuropsychopharmacol Biol Psychiatry; 2015 Jan 02; 56():97-100. PubMed ID: 25152196
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  • 5. SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression.
    Zill P, Baghai TC, Zwanzger P, Schüle C, Eser D, Rupprecht R, Möller HJ, Bondy B, Ackenheil M.
    Mol Psychiatry; 2004 Nov 02; 9(11):1030-6. PubMed ID: 15124006
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  • 6. Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations.
    Zhou Z, Roy A, Lipsky R, Kuchipudi K, Zhu G, Taubman J, Enoch MA, Virkkunen M, Goldman D.
    Arch Gen Psychiatry; 2005 Oct 02; 62(10):1109-18. PubMed ID: 16203956
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  • 7. Association of TPH1 with suicidal behaviour and psychiatric disorders in the Chinese population.
    Liu X, Li H, Qin W, He G, Li D, Shen Y, Shen J, Gu N, Feng G, He L.
    J Med Genet; 2006 Feb 02; 43(2):e4. PubMed ID: 16467214
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  • 8. Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura.
    Jung A, Huge A, Kuhlenbäumer G, Kempt S, Seehafer T, Evers S, Berger K, Marziniak M.
    J Neural Transm (Vienna); 2010 Nov 02; 117(11):1253-60. PubMed ID: 20740293
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  • 9. Tryptophan hydroxylase-1 gene variants associate with a group of suicidal borderline women.
    Zaboli G, Gizatullin R, Nilsonne A, Wilczek A, Jönsson EG, Ahnemark E, Asberg M, Leopardi R.
    Neuropsychopharmacology; 2006 Sep 02; 31(9):1982-90. PubMed ID: 16495936
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  • 11. Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population.
    Zheng P, Li E, Wang J, Cui X, Wang L.
    Behav Brain Funct; 2013 Jan 29; 9():6. PubMed ID: 23360517
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  • 12. Functional gene variants of the serotonin-synthesizing enzyme tryptophan hydroxylase 2 in migraine.
    Marziniak M, Kienzler C, Kuhlenbäumer G, Sommer C, Mössner R.
    J Neural Transm (Vienna); 2009 Jul 29; 116(7):815-9. PubMed ID: 19434366
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  • 13. Common variants in the TPH2 promoter confer susceptibility to paranoid schizophrenia.
    Yi Z, Zhang C, Lu W, Song L, Liu D, Xu Y, Fang Y.
    J Mol Neurosci; 2012 Jul 29; 47(3):465-9. PubMed ID: 22392150
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  • 14. TPH2 gene polymorphisms in the regulatory region are associated with paranoid schizophrenia in Northern Han Chinese.
    Xu XM, Ding M, Pang H, Wang BJ.
    Genet Mol Res; 2014 Mar 12; 13(1):1497-507. PubMed ID: 24668623
    [Abstract] [Full Text] [Related]

  • 15. Lack of association between TPH2 gene polymorphisms with major depressive disorder in multiethnic Malaysian population.
    Nazree NE, Loke AC, Zainal NZ, Mohamed Z.
    Asia Pac Psychiatry; 2015 Mar 12; 7(1):72-7. PubMed ID: 24376086
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  • 16. Association of tryptophan hydroxylase-2 polymorphisms with oppositional defiant disorder in a Chinese Han population.
    Wang CH, Liu C, Cong EZ, Xu GL, Lv TT, Zhang YL, Ning QF, Wang JK, Nie HY, Li Y.
    Behav Brain Funct; 2016 Nov 21; 12(1):30. PubMed ID: 27871272
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  • 17. The interaction between TPH2 promoter haplotypes and clinical-demographic risk factors in suicide victims with major psychoses.
    De Luca V, Hlousek D, Likhodi O, Van Tol HH, Kennedy JL, Wong AH.
    Genes Brain Behav; 2006 Feb 21; 5(1):107-10. PubMed ID: 16436194
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  • 18. Association between polymorphisms in the vesicle-associated membrane protein-associated protein A (VAPA) gene on chromosome 18p and bipolar disorder.
    Lohoff FW, Weller AE, Bloch PJ, Nall AH, Ferraro TN, Berrettini WH.
    J Neural Transm (Vienna); 2008 Sep 21; 115(9):1339-45. PubMed ID: 18665321
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