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Journal Abstract Search

80 related items for PubMed ID: 23022455

  • 1. Regional MeCP2 expression levels in the female MeCP2-deficient mouse brain correlate with specific behavioral impairments.
    Wither RG, Lang M, Zhang L, Eubanks JH.
    Exp Neurol; 2013 Jan; 239():49-59. PubMed ID: 23022455
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  • 2. Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice.
    D'Cruz JA, Wu C, Zahid T, El-Hayek Y, Zhang L, Eubanks JH.
    Neurobiol Dis; 2010 Apr; 38(1):8-16. PubMed ID: 20045053
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  • 3. 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
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  • 4. Selective preservation of MeCP2 in catecholaminergic cells is sufficient to improve the behavioral phenotype of male and female Mecp2-deficient mice.
    Lang M, Wither RG, Brotchie JM, Wu C, Zhang L, Eubanks JH.
    Hum Mol Genet; 2013 Jan 15; 22(2):358-71. PubMed ID: 23077217
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  • 7. 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
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  • 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
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  • 10. 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
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  • 13. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome.
    Asaka Y, Jugloff DG, Zhang L, Eubanks JH, Fitzsimonds RM.
    Neurobiol Dis; 2006 Jan 27; 21(1):217-27. PubMed ID: 16087343
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  • 14. 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 27; 66(2):117-23. PubMed ID: 17278996
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  • 16. A segment of the Mecp2 promoter is sufficient to drive expression in neurons.
    Adachi M, Keefer EW, Jones FS.
    Hum Mol Genet; 2005 Dec 01; 14(23):3709-22. PubMed ID: 16251199
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  • 17. 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
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  • 18. Synaptic plasticity deficits in an experimental model of rett syndrome: long-term potentiation saturation and its pharmacological reversal.
    Weng SM, McLeod F, Bailey ME, Cobb SR.
    Neuroscience; 2011 Apr 28; 180():314-21. PubMed ID: 21296130
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  • 19. Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.
    Medrihan L, Tantalaki E, Aramuni G, Sargsyan V, Dudanova I, Missler M, Zhang W.
    J Neurophysiol; 2008 Jan 28; 99(1):112-21. PubMed ID: 18032561
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  • 20. Breeding and maintenance of an Mecp2-deficient mouse model of Rett syndrome.
    Jugloff DG, Logan R, Eubanks JH.
    J Neurosci Methods; 2006 Jun 30; 154(1-2):89-95. PubMed ID: 16439027
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