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Journal Abstract Search

217 related items for PubMed ID: 15705354

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  • 2. Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.
    Ohtsuki T, Horiuchi Y, Koga M, Ishiguro H, Inada T, Iwata N, Ozaki N, Ujike H, Watanabe Y, Someya T, Arinami T.
    Neurosci Lett; 2008 Apr 25; 435(3):194-7. PubMed ID: 18384956
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  • 3. Case-control association study of human netrin G1 gene in Japanese schizophrenia.
    Fukasawa M, Aoki M, Yamada K, Iwayama-Shigeno Y, Takao H, Meerabux J, Toyota T, Nishikawa T, Yoshikawa T.
    J Med Dent Sci; 2004 Jun 25; 51(2):121-8. PubMed ID: 15508520
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  • 4. Genetic and expression analyses of FZD3 in schizophrenia.
    Ide M, Muratake T, Yamada K, Iwayama-Shigeno Y, Iwamoto K, Takao H, Toyota T, Kaneko N, Minabe Y, Nakamura K, Kato T, Mori N, Asada T, Someya T, Yoshikawa T.
    Biol Psychiatry; 2004 Sep 15; 56(6):462-5. PubMed ID: 15364045
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  • 6. Human netrin-G1 isoforms show evidence of differential expression.
    Meerabux JM, Ohba H, Fukasawa M, Suto Y, Aoki-Suzuki M, Nakashiba T, Nishimura S, Itohara S, Yoshikawa T.
    Genomics; 2005 Jul 15; 86(1):112-6. PubMed ID: 15901489
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  • 7. Decreased mRNA expression of netrin-G1 and netrin-G2 in the temporal lobe in schizophrenia and bipolar disorder.
    Eastwood SL, Harrison PJ.
    Neuropsychopharmacology; 2008 Mar 15; 33(4):933-45. PubMed ID: 17507910
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  • 9. Identification of a novel alternative splicing form of human netrin-4 and analyzing the expression patterns in adult rat brain.
    Zhang C, Meng F, Wang C, Guo H, Fan M, Liu S, Zhou R, He F.
    Brain Res Mol Brain Res; 2004 Nov 04; 130(1-2):68-80. PubMed ID: 15519678
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  • 10. Neurexin 3 polymorphisms are associated with alcohol dependence and altered expression of specific isoforms.
    Hishimoto A, Liu QR, Drgon T, Pletnikova O, Walther D, Zhu XG, Troncoso JC, Uhl GR.
    Hum Mol Genet; 2007 Dec 01; 16(23):2880-91. PubMed ID: 17804423
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  • 14. GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss.
    Addington AM, Gornick M, Duckworth J, Sporn A, Gogtay N, Bobb A, Greenstein D, Lenane M, Gochman P, Baker N, Balkissoon R, Vakkalanka RK, Weinberger DR, Rapoport JL, Straub RE.
    Mol Psychiatry; 2005 Jun 01; 10(6):581-8. PubMed ID: 15505639
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  • 15. Association of SOX10 with schizophrenia in the Japanese population.
    Maeno N, Takahashi N, Saito S, Ji X, Ishihara R, Aoyama N, Branko A, Miura H, Ikeda M, Suzuki T, Kitajima T, Yamanouchi Y, Kinoshita Y, Iwata N, Inada T, Ozaki N.
    Psychiatr Genet; 2007 Aug 01; 17(4):227-31. PubMed ID: 17621166
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  • 16. A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention.
    Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Ouyang WC, Chan HY, Chen JJ, Yang WC, Lin CY, Lee SF, Hwu HG.
    Biol Psychiatry; 2006 Sep 15; 60(6):554-62. PubMed ID: 16997000
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  • 17. Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain.
    Weickert CS, Straub RE, McClintock BW, Matsumoto M, Hashimoto R, Hyde TM, Herman MM, Weinberger DR, Kleinman JE.
    Arch Gen Psychiatry; 2004 Jun 15; 61(6):544-55. PubMed ID: 15184234
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  • 18. DTNBP1, NRG1, DAOA, DAO and GRM3 polymorphisms and schizophrenia: an association study.
    Jönsson EG, Saetre P, Vares M, Andreou D, Larsson K, Timm S, Rasmussen HB, Djurovic S, Melle I, Andreassen OA, Agartz I, Werge T, Hall H, Terenius L.
    Neuropsychobiology; 2009 Jun 15; 59(3):142-50. PubMed ID: 19439994
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  • 19. Tryptophan hydroxylase-1 gene variants associated with schizophrenia.
    Zaboli G, Jönsson EG, Gizatullin R, Asberg M, Leopardi R.
    Biol Psychiatry; 2006 Sep 15; 60(6):563-9. PubMed ID: 16806098
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