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186 related items for PubMed ID: 19879900

  • 1. Schizophrenia-relevant behaviours in a genetic mouse model for Y2 deficiency.
    Karl T, Chesworth R, Duffy L, Herzog H.
    Behav Brain Res; 2010 Mar 05; 207(2):434-40. PubMed ID: 19879900
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  • 3. Behavioral profile of a heterozygous mutant mouse model for EGF-like domain neuregulin 1.
    Duffy L, Cappas E, Scimone A, Schofield PR, Karl T.
    Behav Neurosci; 2008 Aug 05; 122(4):748-59. PubMed ID: 18729627
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  • 4. Behavioural profile of a new mouse model for NPY deficiency.
    Karl T, Duffy L, Herzog H.
    Eur J Neurosci; 2008 Jul 05; 28(1):173-80. PubMed ID: 18616565
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  • 5. Schizophrenia-relevant behaviors in a genetic mouse model of constitutive Nurr1 deficiency.
    Vuillermot S, Joodmardi E, Perlmann T, Ove Ögren S, Feldon J, Meyer U.
    Genes Brain Behav; 2011 Jul 05; 10(5):589-603. PubMed ID: 21545404
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  • 7. Deficits in sensorimotor gating and tests of social behavior in a genetic model of reduced NMDA receptor function.
    Duncan GE, Moy SS, Perez A, Eddy DM, Zinzow WM, Lieberman JA, Snouwaert JN, Koller BH.
    Behav Brain Res; 2004 Aug 31; 153(2):507-19. PubMed ID: 15265649
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  • 10. Phencyclidine and genetic animal models of schizophrenia developed in relation to the glutamate hypothesis.
    Enomoto T, Noda Y, Nabeshima T.
    Methods Find Exp Clin Pharmacol; 2007 May 31; 29(4):291-301. PubMed ID: 17609743
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  • 11. Deficits in social behavior and sensorimotor gating in mice lacking phospholipase Cbeta1.
    Koh HY, Kim D, Lee J, Lee S, Shin HS.
    Genes Brain Behav; 2008 Feb 31; 7(1):120-8. PubMed ID: 17696993
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  • 12. Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol-O-methyltransferase.
    Babovic D, O'Tuathaigh CM, O'Connor AM, O'Sullivan GJ, Tighe O, Croke DT, Karayiorgou M, Gogos JA, Cotter D, Waddington JL.
    Neuroscience; 2008 Sep 09; 155(4):1021-9. PubMed ID: 18674597
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  • 13. Complexin2 null mutation requires a 'second hit' for induction of phenotypic changes relevant to schizophrenia.
    Radyushkin K, El-Kordi A, Boretius S, Castaneda S, Ronnenberg A, Reim K, Bickeböller H, Frahm J, Brose N, Ehrenreich H.
    Genes Brain Behav; 2010 Aug 09; 9(6):592-602. PubMed ID: 20412316
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  • 16. Neonatal perturbation of neurotrophic signaling results in abnormal sensorimotor gating and social interaction in adults: implication for epidermal growth factor in cognitive development.
    Futamura T, Kakita A, Tohmi M, Sotoyama H, Takahashi H, Nawa H.
    Mol Psychiatry; 2003 Jan 09; 8(1):19-29. PubMed ID: 12556905
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  • 17. Reduced attention and increased impulsivity in mice lacking NPY Y2 receptors: relation to anxiolytic-like phenotype.
    Greco B, Carli M.
    Behav Brain Res; 2006 May 15; 169(2):325-34. PubMed ID: 16529827
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  • 18. Behavioural, neural and cardiovascular adaptations in mice lacking the NPY Y1 receptor.
    Costoli T, Sgoifo A, Stilli D, Flugge G, Adriani W, Laviola G, Fuchs E, Pedrazzini T, Musso E.
    Neurosci Biobehav Rev; 2005 Feb 15; 29(1):113-23. PubMed ID: 15652259
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