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139 related items for PubMed ID: 17442488

  • 1. An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population.
    Zhang K, Gao J, An C, Gao X, Zheng Z, Li R, Huang S, Zhang F.
    Neurosci Lett; 2007 May 23; 419(1):83-7. PubMed ID: 17442488
    [Abstract] [Full Text] [Related]

  • 2. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
    Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I.
    Int Clin Psychopharmacol; 2010 Jul 23; 25(4):218-27. PubMed ID: 20531207
    [Abstract] [Full Text] [Related]

  • 3. Association between a functional COMT polymorphism, mental retardation and cognition in Qinba area children.
    Zhang KJ, Gao XC, Li RL, Chen C, Zheng ZJ, Huang SP, Zhang FC.
    Yi Chuan Xue Bao; 2006 Jun 23; 33(6):495-500. PubMed ID: 16800379
    [Abstract] [Full Text] [Related]

  • 4. Positive association of neuroligin-4 gene with nonspecific mental retardation in the Qinba Mountains Region of China.
    Qi H, Xing L, Zhang K, Gao X, Zheng Z, Huang S, Guo Y, Zhang F.
    Psychiatr Genet; 2009 Feb 23; 19(1):1-5. PubMed ID: 19125102
    [Abstract] [Full Text] [Related]

  • 5. 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 23; 28(8):1231-8. PubMed ID: 16837108
    [Abstract] [Full Text] [Related]

  • 6. Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families.
    Chen X, Wang X, O'Neill AF, Walsh D, Kendler KS.
    Mol Psychiatry; 2004 Oct 23; 9(10):962-7. PubMed ID: 15124004
    [Abstract] [Full Text] [Related]

  • 7. Clinical involvement of catechol-O-methyltransferase polymorphisms in schizophrenia spectrum disorders: influence on the severity of psychotic symptoms and on the response to neuroleptic treatment.
    Molero P, Ortuño F, Zalacain M, Patiño-García A.
    Pharmacogenomics J; 2007 Dec 23; 7(6):418-26. PubMed ID: 17363961
    [Abstract] [Full Text] [Related]

  • 8. Possible relationship between the COMT gene ValMet polymorphism and psychometric IQ in girls of the Qinba region in China.
    Zhang K, Zheng Z, Gao X, Li J, Zhang F.
    Neuropsychobiology; 2007 Dec 23; 56(2-3):98-103. PubMed ID: 18182829
    [Abstract] [Full Text] [Related]

  • 9. 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 23; 7(1):61-9. PubMed ID: 17504246
    [Abstract] [Full Text] [Related]

  • 10. Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia.
    Wang Y, Hu Y, Fang Y, Zhang K, Yang H, Ma J, Xu Q, Shen Y.
    Biol Psychiatry; 2009 Jun 15; 65(12):1048-54. PubMed ID: 19159868
    [Abstract] [Full Text] [Related]

  • 11. [Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene].
    Zhang XN, Ruan LM, Le YP, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug 15; 20(4):322-4. PubMed ID: 12903043
    [Abstract] [Full Text] [Related]

  • 12. Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk.
    Gellekink H, Muntjewerff JW, Vermeulen SH, Hermus AR, Blom HJ, den Heijer M.
    Thromb Haemost; 2007 Dec 15; 98(6):1226-31. PubMed ID: 18064318
    [Abstract] [Full Text] [Related]

  • 13. The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.
    Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Tan EK, Drozdzik M.
    Pharmacogenet Genomics; 2008 Sep 15; 18(9):815-21. PubMed ID: 18698234
    [Abstract] [Full Text] [Related]

  • 14. Positive association between POU1F1 and mental retardation in young females in the Chinese Han population.
    Sun Y, Zhang F, Gao J, Gao X, Guo T, Zhang K, Shi Y, Zheng Z, Tang W, Zheng Y, Li S, Li X, Feng G, Shen X, He L.
    Hum Mol Genet; 2006 Apr 01; 15(7):1237-43. PubMed ID: 16505001
    [Abstract] [Full Text] [Related]

  • 15. Study: the lack of significant association of the catechol-O-methyl transferase (COMT) gene polymorphism in violent offenders with mental retardation.
    Isir AB, Dai AI, Nacak M, Gorucu S.
    J Forensic Sci; 2010 Jan 01; 55(1):225-8. PubMed ID: 19895544
    [Abstract] [Full Text] [Related]

  • 16. [Polymorphism of catechol-O-methyltransferase gene in relation to the risk of endometrial cancer].
    Zhao XM, Xie MQ, Yang DZ, Wang LA, Li SJ, Zhuang YY, Tang XL.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Feb 01; 42(2):116-9. PubMed ID: 17442187
    [Abstract] [Full Text] [Related]

  • 17. COMT polymorphisms as predictors of cognitive dysfunction during manic and mixed episodes in bipolar I disorder.
    Soeiro-de-Souza MG, Machado-Vieira R, Soares Bio D, Do Prado CM, Moreno RA.
    Bipolar Disord; 2012 Aug 01; 14(5):554-64. PubMed ID: 22713126
    [Abstract] [Full Text] [Related]

  • 18. No evidence for association between DRD3 and COMT with schizophrenia in a Malay population.
    Tee SF, Tang PY, Loh HC.
    Genet Mol Res; 2011 Aug 26; 10(3):1850-5. PubMed ID: 21948748
    [Abstract] [Full Text] [Related]

  • 19. 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 26; 9(4):370-6. PubMed ID: 17547583
    [Abstract] [Full Text] [Related]

  • 20. Catechol-O-methyltransferase Val 108/158 Met polymorphism in premenopausal breast cancer patients.
    Sazci A, Ergul E, Utkan NZ, Canturk NZ, Kaya G.
    Toxicology; 2004 Nov 15; 204(2-3):197-202. PubMed ID: 15388245
    [Abstract] [Full Text] [Related]

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