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Journal Abstract Search

140 related items for PubMed ID: 16610957

  • 21. Association of monoamine-synthesizing genes with the depression tendency and personality in chronic fatigue syndrome patients.
    Fukuda S, Horiguchi M, Yamaguti K, Nakatomi Y, Kuratsune H, Ichinose H, Watanabe Y.
    Life Sci; 2013 Feb 27; 92(3):183-6. PubMed ID: 23246742
    [Abstract] [Full Text] [Related]

  • 22. Supervised selection of single nucleotide polymorphisms in chronic fatigue syndrome.
    Cifuentes RA, Barreto E.
    Biomedica; 2011 Feb 27; 31(4):613-21. PubMed ID: 22674373
    [Abstract] [Full Text] [Related]

  • 23. A functional polymorphism in the disrupted-in schizophrenia 1 gene is associated with chronic fatigue syndrome.
    Fukuda S, Hashimoto R, Ohi K, Yamaguti K, Nakatomi Y, Yasuda Y, Kamino K, Takeda M, Tajima S, Kuratsune H, Nishizawa Y, Watanabe Y.
    Life Sci; 2010 May 08; 86(19-20):722-5. PubMed ID: 20227423
    [Abstract] [Full Text] [Related]

  • 24. Allostatic load is associated with symptoms in chronic fatigue syndrome patients.
    Goertzel BN, Pennachin C, de Souza Coelho L, Maloney EM, Jones JF, Gurbaxani B.
    Pharmacogenomics; 2006 Apr 08; 7(3):485-94. PubMed ID: 16610958
    [Abstract] [Full Text] [Related]

  • 25. Single nucleotide polymorphisms and suicidal behaviour.
    Pregelj P.
    Psychiatr Danub; 2012 Sep 08; 24 Suppl 1():S61-4. PubMed ID: 22945190
    [Abstract] [Full Text] [Related]

  • 26. A systematic review of the association between fatigue and genetic polymorphisms.
    Wang T, Yin J, Miller AH, Xiao C.
    Brain Behav Immun; 2017 May 08; 62():230-244. PubMed ID: 28089639
    [Abstract] [Full Text] [Related]

  • 27. Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons.
    Lim JE, Pinsonneault J, Sadee W, Saffen D.
    Mol Psychiatry; 2007 May 08; 12(5):491-501. PubMed ID: 17453063
    [Abstract] [Full Text] [Related]

  • 28. 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 08; 7(1):61-9. PubMed ID: 17504246
    [Abstract] [Full Text] [Related]

  • 29. Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis.
    van Esch AA, de Vries E, Te Morsche RH, van Oijen MG, Jansen JB, Drenth JP.
    Neth J Med; 2011 Feb 08; 69(7):330-4. PubMed ID: 21934178
    [Abstract] [Full Text] [Related]

  • 30. Genetic variation in the beta-2 adrenergic receptor is associated with chronic musculoskeletal complaints in adolescents.
    Skouen JS, Smith AJ, Warrington NM, O' Sullivan PB, McKenzie L, Pennell CE, Straker LM.
    Eur J Pain; 2012 Oct 08; 16(9):1232-42. PubMed ID: 22416031
    [Abstract] [Full Text] [Related]

  • 31. Common genetic variations in human brain-specific tryptophan hydroxylase-2 and response to antidepressant treatment.
    Tzvetkov MV, Brockmöller J, Roots I, Kirchheiner J.
    Pharmacogenet Genomics; 2008 Jun 08; 18(6):495-506. PubMed ID: 18496129
    [Abstract] [Full Text] [Related]

  • 32. Polymorphisms of estrogen-related genes jointly confer susceptibility to human spermatogenic defect.
    Su MT, Chen CH, Kuo PH, Hsu CC, Lee IW, Pan HA, Chen YT, Kuo PL.
    Fertil Steril; 2010 Jan 08; 93(1):141-9. PubMed ID: 18980759
    [Abstract] [Full Text] [Related]

  • 33. 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 08; 28(8):1231-8. PubMed ID: 16837108
    [Abstract] [Full Text] [Related]

  • 34. Impact of five SNPs in dopamine-related genes on executive function.
    Mitaki S, Isomura M, Maniwa K, Yamasaki M, Nagai A, Nabika T, Yamaguchi S.
    Acta Neurol Scand; 2013 Jan 08; 127(1):70-6. PubMed ID: 22530780
    [Abstract] [Full Text] [Related]

  • 35. Association between tryptophan hydroxylase-2 gene and late-onset depression.
    Pereira Pde A, Romano-Silva MA, Bicalho MA, De Marco L, Correa H, de Campos SB, de Moraes EN, Torres KC, de Souza BR, de Miranda DM.
    Am J Geriatr Psychiatry; 2011 Sep 08; 19(9):825-9. PubMed ID: 21873838
    [Abstract] [Full Text] [Related]

  • 36. Impaired executive control is associated with a variation in the promoter region of the tryptophan hydroxylase 2 gene.
    Reuter M, Ott U, Vaitl D, Hennig J.
    J Cogn Neurosci; 2007 Mar 08; 19(3):401-8. PubMed ID: 17335389
    [Abstract] [Full Text] [Related]

  • 37. The effect of catechol-O-methyltransferase polymorphisms on pain is modified by depressive symptoms.
    Schwahn C, Grabe HJ, Meyer zu Schwabedissen H, Teumer A, Schmidt CO, Brinkman C, Kocher T, Nauck M, Völzke H, Biffar R, Bernhardt O.
    Eur J Pain; 2012 Jul 08; 16(6):878-89. PubMed ID: 22337325
    [Abstract] [Full Text] [Related]

  • 38. Somatization in major depression--clinical features and genetic associations.
    Klengel T, Heck A, Pfister H, Brückl T, Hennings JM, Menke A, Czamara D, Müller-Myhsok B, Ising M.
    Acta Psychiatr Scand; 2011 Oct 08; 124(4):317-28. PubMed ID: 21838737
    [Abstract] [Full Text] [Related]

  • 39. TPH2 -703G/T SNP may have important effect on susceptibility to suicidal behavior in major depression.
    Yoon HK, Kim YK.
    Prog Neuropsychopharmacol Biol Psychiatry; 2009 Apr 30; 33(3):403-9. PubMed ID: 19162119
    [Abstract] [Full Text] [Related]

  • 40. The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder.
    Fijal B, Perlis RH, Heinloth AN, Houston JP.
    J Pain; 2010 Sep 30; 11(9):910-5, 915.e1-9. PubMed ID: 20627703
    [Abstract] [Full Text] [Related]

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