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534 related items for PubMed ID: 19249385

  • 1. Improvement in motor and exploratory behavior in Rett syndrome mice with restricted ketogenic and standard diets.
    Mantis JG, Fritz CL, Marsh J, Heinrichs SC, Seyfried TN.
    Epilepsy Behav; 2009 Jun; 15(2):133-41. PubMed ID: 19249385
    [Abstract] [Full Text] [Related]

  • 2. Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.
    Stearns NA, Schaevitz LR, Bowling H, Nag N, Berger UV, Berger-Sweeney J.
    Neuroscience; 2007 May 25; 146(3):907-21. PubMed ID: 17383101
    [Abstract] [Full Text] [Related]

  • 3. Evidence for abnormal early development in a mouse model of Rett syndrome.
    Santos M, Silva-Fernandes A, Oliveira P, Sousa N, Maciel P.
    Genes Brain Behav; 2007 Apr 25; 6(3):277-86. PubMed ID: 16848781
    [Abstract] [Full Text] [Related]

  • 4. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.
    Moretti P, Bouwknecht JA, Teague R, Paylor R, Zoghbi HY.
    Hum Mol Genet; 2005 Jan 15; 14(2):205-20. PubMed ID: 15548546
    [Abstract] [Full Text] [Related]

  • 5. Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome--Mecp2 gene dosage effects and BDNF expression.
    Kondo M, Gray LJ, Pelka GJ, Christodoulou J, Tam PP, Hannan AJ.
    Eur J Neurosci; 2008 Jun 15; 27(12):3342-50. PubMed ID: 18557922
    [Abstract] [Full Text] [Related]

  • 6. Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.
    Alvarez-Saavedra M, Sáez MA, Kang D, Zoghbi HY, Young JI.
    Hum Mol Genet; 2007 Oct 01; 16(19):2315-25. PubMed ID: 17635839
    [Abstract] [Full Text] [Related]

  • 7. Effects of postnatal dietary choline supplementation on motor regional brain volume and growth factor expression in a mouse model of Rett syndrome.
    Nag N, Mellott TJ, Berger-Sweeney JE.
    Brain Res; 2008 Oct 27; 1237():101-9. PubMed ID: 18778693
    [Abstract] [Full Text] [Related]

  • 8. Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome.
    De Filippis B, Ricceri L, Laviola G.
    Genes Brain Behav; 2010 Mar 01; 9(2):213-23. PubMed ID: 19958389
    [Abstract] [Full Text] [Related]

  • 9. Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp2 1lox mice.
    Nag N, Moriuchi JM, Peitzman CG, Ward BC, Kolodny NH, Berger-Sweeney JE.
    Behav Brain Res; 2009 Jan 03; 196(1):44-8. PubMed ID: 18687363
    [Abstract] [Full Text] [Related]

  • 10. Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
    Kaufmann WE, Tierney E, Rohde CA, Suarez-Pedraza MC, Clarke MA, Salorio CF, Bibat G, Bukelis I, Naram D, Lanham DC, Naidu S.
    J Intellect Disabil Res; 2012 Mar 03; 56(3):233-47. PubMed ID: 21385260
    [Abstract] [Full Text] [Related]

  • 11. Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice.
    Gemelli T, Berton O, Nelson ED, Perrotti LI, Jaenisch R, Monteggia LM.
    Biol Psychiatry; 2006 Mar 01; 59(5):468-76. PubMed ID: 16199017
    [Abstract] [Full Text] [Related]

  • 12. Targeted delivery of an Mecp2 transgene to forebrain neurons improves the behavior of female Mecp2-deficient mice.
    Jugloff DG, Vandamme K, Logan R, Visanji NP, Brotchie JM, Eubanks JH.
    Hum Mol Genet; 2008 May 15; 17(10):1386-96. PubMed ID: 18223199
    [Abstract] [Full Text] [Related]

  • 13. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG.
    Ment Retard Dev Disabil Res Rev; 2004 May 15; 10(2):154-8. PubMed ID: 15362175
    [Abstract] [Full Text] [Related]

  • 14. Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches.
    Ricceri L, De Filippis B, Laviola G.
    Behav Pharmacol; 2008 Sep 15; 19(5-6):501-17. PubMed ID: 18690105
    [Abstract] [Full Text] [Related]

  • 15. Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline.
    Ward BC, Agarwal S, Wang K, Berger-Sweeney J, Kolodny NH.
    Neurobiol Dis; 2008 Jul 15; 31(1):110-9. PubMed ID: 18571096
    [Abstract] [Full Text] [Related]

  • 16. Cognitive and social functions and growth factors in a mouse model of Rett syndrome.
    Schaevitz LR, Moriuchi JM, Nag N, Mellot TJ, Berger-Sweeney J.
    Physiol Behav; 2010 Jun 01; 100(3):255-63. PubMed ID: 20045424
    [Abstract] [Full Text] [Related]

  • 17. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks.
    Belichenko PV, Wright EE, Belichenko NP, Masliah E, Li HH, Mobley WC, Francke U.
    J Comp Neurol; 2009 May 20; 514(3):240-58. PubMed ID: 19296534
    [Abstract] [Full Text] [Related]

  • 18. MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.
    Schaevitz LR, Gómez NB, Zhen DP, Berger-Sweeney JE.
    Genes Brain Behav; 2013 Oct 20; 12(7):732-40. PubMed ID: 24283265
    [Abstract] [Full Text] [Related]

  • 19. Postnatal dietary choline supplementation alters behavior in a mouse model of Rett syndrome.
    Nag N, Berger-Sweeney JE.
    Neurobiol Dis; 2007 May 20; 26(2):473-80. PubMed ID: 17395475
    [Abstract] [Full Text] [Related]

  • 20. An altered neonatal behavioral phenotype in Mecp2 mutant mice.
    Picker JD, Yang R, Ricceri L, Berger-Sweeney J.
    Neuroreport; 2006 Apr 03; 17(5):541-4. PubMed ID: 16543822
    [Abstract] [Full Text] [Related]

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