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Journal Abstract Search

415 related items for PubMed ID: 14981523

  • 1. Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice.
    Frankland PW, Wang Y, Rosner B, Shimizu T, Balleine BW, Dykens EM, Ornitz EM, Silva AJ.
    Mol Psychiatry; 2004 Apr; 9(4):417-25. PubMed ID: 14981523
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  • 2. Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.
    Spencer CM, Serysheva E, Yuva-Paylor LA, Oostra BA, Nelson DL, Paylor R.
    Hum Mol Genet; 2006 Jun 15; 15(12):1984-94. PubMed ID: 16675531
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  • 5. Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium.
    Cell; 1994 Jul 15; 78(1):23-33. PubMed ID: 8033209
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  • 8. Transgenic mouse model for the fragile X syndrome.
    Kooy RF, D'Hooge R, Reyniers E, Bakker CE, Nagels G, De Boulle K, Storm K, Clincke G, De Deyn PP, Oostra BA, Willems PJ.
    Am J Med Genet; 1996 Aug 09; 64(2):241-5. PubMed ID: 8844056
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  • 9. Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.
    Koekkoek SK, Yamaguchi K, Milojkovic BA, Dortland BR, Ruigrok TJ, Maex R, De Graaf W, Smit AE, VanderWerf F, Bakker CE, Willemsen R, Ikeda T, Kakizawa S, Onodera K, Nelson DL, Mientjes E, Joosten M, De Schutter E, Oostra BA, Ito M, De Zeeuw CI.
    Neuron; 2005 Aug 04; 47(3):339-52. PubMed ID: 16055059
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  • 11. Reduction of BDNF expression in Fmr1 knockout mice worsens cognitive deficits but improves hyperactivity and sensorimotor deficits.
    Uutela M, Lindholm J, Louhivuori V, Wei H, Louhivuori LM, Pertovaara A, Akerman K, Castrén E, Castrén ML.
    Genes Brain Behav; 2012 Jul 04; 11(5):513-23. PubMed ID: 22435671
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  • 12. Selective breeding for deficient sensorimotor gating is accompanied by increased perseveration in rats.
    Freudenberg F, Dieckmann M, Winter S, Koch M, Schwabe K.
    Neuroscience; 2007 Sep 07; 148(3):612-22. PubMed ID: 17693035
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  • 14. The emerging fragile X premutation phenotype: evidence from the domain of social cognition.
    Cornish K, Kogan C, Turk J, Manly T, James N, Mills A, Dalton A.
    Brain Cogn; 2005 Feb 07; 57(1):53-60. PubMed ID: 15629215
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  • 15. Protective effects of melatonin against oxidative stress in Fmr1 knockout mice: a therapeutic research model for the fragile X syndrome.
    Romero-Zerbo Y, Decara J, el Bekay R, Sanchez-Salido L, Del Arco-Herrera I, de Fonseca FR, de Diego-Otero Y.
    J Pineal Res; 2009 Mar 07; 46(2):224-34. PubMed ID: 19141086
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  • 16. Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome.
    Spencer CM, Alekseyenko O, Serysheva E, Yuva-Paylor LA, Paylor R.
    Genes Brain Behav; 2005 Oct 07; 4(7):420-30. PubMed ID: 16176388
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  • 17. Genetic reduction of MMP-9 in the Fmr1 KO mouse partially rescues prepulse inhibition of acoustic startle response.
    Kokash J, Alderson EM, Reinhard SM, Crawford CA, Binder DK, Ethell IM, Razak KA.
    Brain Res; 2019 Sep 15; 1719():24-29. PubMed ID: 31128097
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  • 18. A neuropsychological investigation of male premutation carriers of fragile X syndrome.
    Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG.
    Neuropsychologia; 2004 Sep 15; 42(14):1934-47. PubMed ID: 15381024
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  • 19. The behavioral phenotype of FMR1 mutations.
    Boyle L, Kaufmann WE.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):469-76. PubMed ID: 20981777
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  • 20. Fragile X syndrome, the Fragile X related proteins, and animal models.
    Hoogeveen AT, Willemsen R, Oostra BA.
    Microsc Res Tech; 2002 May 01; 57(3):148-55. PubMed ID: 12112450
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