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656 related items for PubMed ID: 17383101

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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 01; 12(7):732-40. PubMed ID: 24283265
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 31(1):110-9. PubMed ID: 18571096
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 27(12):3342-50. PubMed ID: 18557922
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice.
    Pelka GJ, Watson CM, Radziewic T, Hayward M, Lahooti H, Christodoulou J, Tam PP.
    Brain; 2006 Apr 01; 129(Pt 4):887-98. PubMed ID: 16467389
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. 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 03; 15(2):133-41. PubMed ID: 19249385
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome.
    Belichenko NP, Belichenko PV, Li HH, Mobley WC, Francke U.
    J Comp Neurol; 2008 May 01; 508(1):184-95. PubMed ID: 18306326
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Postnatal changes in serotonergic innervation to the hippocampus of methyl-CpG-binding protein 2-null mice.
    Isoda K, Morimoto M, Matsui F, Hasegawa T, Tozawa T, Morioka S, Chiyonobu T, Nishimura A, Yoshimoto K, Hosoi H.
    Neuroscience; 2010 Feb 17; 165(4):1254-60. PubMed ID: 19932741
    [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. 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 01; 6(3):277-86. PubMed ID: 16848781
    [Abstract] [Full Text] [Related]

  • 18. Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains.
    Itoh M, Ide S, Takashima S, Kudo S, Nomura Y, Segawa M, Kubota T, Mori H, Tanaka S, Horie H, Tanabe Y, Goto Y.
    J Neuropathol Exp Neurol; 2007 Feb 01; 66(2):117-23. PubMed ID: 17278996
    [Abstract] [Full Text] [Related]

  • 19. Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome.
    Santos M, Summavielle T, Teixeira-Castro A, Silva-Fernandes A, Duarte-Silva S, Marques F, Martins L, Dierssen M, Oliveira P, Sousa N, Maciel P.
    Neuroscience; 2010 Oct 13; 170(2):453-67. PubMed ID: 20633611
    [Abstract] [Full Text] [Related]

  • 20. 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]

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