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Journal Abstract Search

200 related items for PubMed ID: 17892388

  • 21. Tryptophan hydroxylase-2 gene variation influences personality traits and disorders related to emotional dysregulation.
    Gutknecht L, Jacob C, Strobel A, Kriegebaum C, Müller J, Zeng Y, Markert C, Escher A, Wendland J, Reif A, Mössner R, Gross C, Brocke B, Lesch KP.
    Int J Neuropsychopharmacol; 2007 Jun; 10(3):309-20. PubMed ID: 17176492
    [Abstract] [Full Text] [Related]

  • 22. Psychological vulnerability differences in students--carriers or not of the serotonin transporter promoter allele S: effect of adverse experiences.
    Veletza S, Samakouri M, Emmanouil G, Trypsianis G, Kourmouli N, Livaditis M.
    Synapse; 2009 Mar; 63(3):193-200. PubMed ID: 19086091
    [Abstract] [Full Text] [Related]

  • 23. Additive effects of serotonin transporter and tryptophan hydroxylase-2 gene variation on emotional processing.
    Herrmann MJ, Huter T, Müller F, Mühlberger A, Pauli P, Reif A, Renner T, Canli T, Fallgatter AJ, Lesch KP.
    Cereb Cortex; 2007 May; 17(5):1160-3. PubMed ID: 16801378
    [Abstract] [Full Text] [Related]

  • 24. Decision-making impairment is related to serotonin transporter promoter polymorphism in a sample of patients with obsessive-compulsive disorder.
    da Rocha FF, Malloy-Diniz L, Lage NV, Romano-Silva MA, de Marco LA, Correa H.
    Behav Brain Res; 2008 Dec 16; 195(1):159-63. PubMed ID: 18603313
    [Abstract] [Full Text] [Related]

  • 25. Effect of tryptophan hydroxylase-2 gene variants on amygdalar and hippocampal volumes.
    Inoue H, Yamasue H, Tochigi M, Takei K, Suga M, Abe O, Yamada H, Rogers MA, Aoki S, Sasaki T, Kasai K.
    Brain Res; 2010 May 17; 1331():51-7. PubMed ID: 20331984
    [Abstract] [Full Text] [Related]

  • 26. Effect of tryptophan hydroxylase-2 gene polymorphism G-703 T on personality in a population representative sample.
    Lehto K, Vaht M, Mäestu J, Veidebaum T, Harro J.
    Prog Neuropsychopharmacol Biol Psychiatry; 2015 Mar 03; 57():31-5. PubMed ID: 25455586
    [Abstract] [Full Text] [Related]

  • 27. Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics.
    Schuhmacher A, Becker T, Rujescu D, Quednow BB, Lennertz L, Wagner M, Benninghoff J, Rietschel M, Häfner H, Franke P, Wölwer W, Gaebel W, Maier W, Mössner R.
    J Psychiatr Res; 2012 Aug 03; 46(8):1073-80. PubMed ID: 22655589
    [Abstract] [Full Text] [Related]

  • 28. Serotonin transporter gene polymorphism (5-HTTLPR) in patients with recurrent aphthous stomatitis.
    Victoria JM, Correia-Silva Jde F, Pimenta FJ, Kalapothakis E, Gomez RS.
    J Oral Pathol Med; 2005 Sep 03; 34(8):494-7. PubMed ID: 16091117
    [Abstract] [Full Text] [Related]

  • 29. Low level of harm avoidance is associated with serotonin transporter functional haplotype in alcohol-dependent individuals.
    Koller G, Zill P, Skoruppa T, Bondy B, Preuss UW, Soyka M.
    Psychiatr Genet; 2008 Apr 03; 18(2):59-63. PubMed ID: 18349696
    [Abstract] [Full Text] [Related]

  • 30. Differential effects of 5-HTTLPR and DRD2/ANKK1 polymorphisms on electrocortical measures of error and feedback processing in children.
    Althaus M, Groen Y, Wijers AA, Mulder LJ, Minderaa RB, Kema IP, Dijck JD, Hartman CA, Hoekstra PJ.
    Clin Neurophysiol; 2009 Jan 03; 120(1):93-107. PubMed ID: 19046929
    [Abstract] [Full Text] [Related]

  • 31. Looking on the bright side of serotonin transporter gene variation.
    Homberg JR, Lesch KP.
    Biol Psychiatry; 2011 Mar 15; 69(6):513-9. PubMed ID: 21047622
    [Abstract] [Full Text] [Related]

  • 32. Serotonin transporter protein polymorphism and harm avoidance personality in migraine without aura.
    Park JW, Han SR, Yang DW, Kim YI, Lee KS.
    Headache; 2006 Jun 15; 46(6):991-6. PubMed ID: 16732845
    [Abstract] [Full Text] [Related]

  • 33. Tryptophan hydroxylase-2 (TPH2) in disorders of cognitive control and emotion regulation: a perspective.
    Waider J, Araragi N, Gutknecht L, Lesch KP.
    Psychoneuroendocrinology; 2011 Apr 15; 36(3):393-405. PubMed ID: 21257271
    [Abstract] [Full Text] [Related]

  • 34. Serotonin transporter, tryptophan hydroxylase, and monoamine oxidase A gene polymorphisms in premenstrual dysphoric disorder.
    Magnay JL, Ismail KM, Chapman G, Cioni L, Jones PW, O'Brien S.
    Am J Obstet Gynecol; 2006 Nov 15; 195(5):1254-9. PubMed ID: 17026953
    [Abstract] [Full Text] [Related]

  • 35. The association between serotonin-related gene polymorphisms and panic disorder.
    Yoon HK, Yang JC, Lee HJ, Kim YK.
    J Anxiety Disord; 2008 Dec 15; 22(8):1529-34. PubMed ID: 18436425
    [Abstract] [Full Text] [Related]

  • 36. Serotonin and early cognitive development: variation in the tryptophan hydroxylase 2 gene is associated with visual attention in 7-month-old infants.
    Leppänen JM, Peltola MJ, Puura K, Mäntymaa M, Mononen N, Lehtimäki T.
    J Child Psychol Psychiatry; 2011 Nov 15; 52(11):1144-52. PubMed ID: 21418063
    [Abstract] [Full Text] [Related]

  • 37. Genetic variation in serotonin transporter alters resting brain function in healthy individuals.
    Rao H, Gillihan SJ, Wang J, Korczykowski M, Sankoorikal GM, Kaercher KA, Brodkin ES, Detre JA, Farah MJ.
    Biol Psychiatry; 2007 Sep 15; 62(6):600-6. PubMed ID: 17481593
    [Abstract] [Full Text] [Related]

  • 38. Serotonin transporter genetic variation and biased attention for emotional word stimuli among psychiatric inpatients.
    Beevers CG, Gibb BE, McGeary JE, Miller IW.
    J Abnorm Psychol; 2007 Feb 15; 116(1):208-12. PubMed ID: 17324031
    [Abstract] [Full Text] [Related]

  • 39. Novel allelic variants in the human serotonin transporter gene linked polymorphism (5-HTTLPR) among depressed patients with suicide attempt.
    Segal J, Schenkel LC, Oliveira MH, Salum GA, Bau CH, Manfro GG, Leistner-Segal S.
    Neurosci Lett; 2009 Feb 13; 451(1):79-82. PubMed ID: 19103261
    [Abstract] [Full Text] [Related]

  • 40. Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.
    Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L.
    Genomics; 2008 Jun 13; 91(6):485-91. PubMed ID: 18387780
    [Abstract] [Full Text] [Related]

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