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641 related items for PubMed ID: 18287934

  • 1. A methyl-CpG-binding protein 2-enhanced green fluorescent protein reporter mouse model provides a new tool for studying the neuronal basis of Rett syndrome.
    Schmid RS, Tsujimoto N, Qu Q, Lei H, Li E, Chen T, Blaustein CS.
    Neuroreport; 2008 Mar 05; 19(4):393-8. PubMed ID: 18287934
    [Abstract] [Full Text] [Related]

  • 2. 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 05; 66(2):117-23. PubMed ID: 17278996
    [Abstract] [Full Text] [Related]

  • 3. The story of Rett syndrome: from clinic to neurobiology.
    Chahrour M, Zoghbi HY.
    Neuron; 2007 Nov 08; 56(3):422-37. PubMed ID: 17988628
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. MeCP2 dysfunction in Rett syndrome and related disorders.
    Moretti P, Zoghbi HY.
    Curr Opin Genet Dev; 2006 Jun 01; 16(3):276-81. PubMed ID: 16647848
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 99(1):112-21. PubMed ID: 18032561
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 21(1):217-27. PubMed ID: 16087343
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. MECP2 mutations in Serbian Rett syndrome patients.
    Djarmati A, Dobricić V, Kecmanović M, Marsh P, Jancić-Stefanović J, Klein C, Djurić M, Romac S.
    Acta Neurol Scand; 2007 Dec 01; 116(6):413-9. PubMed ID: 17986102
    [Abstract] [Full Text] [Related]

  • 10. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
    Hoffbuhr KC, Moses LM, Jerdonek MA, Naidu S, Hoffman EP.
    Ment Retard Dev Disabil Res Rev; 2002 Dec 01; 8(2):99-105. PubMed ID: 12112735
    [Abstract] [Full Text] [Related]

  • 11. MeCP2 in neurons: closing in on the causes of Rett syndrome.
    Caballero IM, Hendrich B.
    Hum Mol Genet; 2005 Apr 15; 14 Spec No 1():R19-26. PubMed ID: 15809268
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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 25; 27(12):3342-50. PubMed ID: 18557922
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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]

  • 17. Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.
    Santos M, Temudo T, Kay T, Carrilho I, Medeira A, Cabral H, Gomes R, Lourenço MT, Venâncio M, Calado E, Moreira A, Oliveira G, Maciel P.
    J Child Neurol; 2009 Jan 13; 24(1):49-55. PubMed ID: 19168818
    [Abstract] [Full Text] [Related]

  • 18. Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model.
    Viola A, Saywell V, Villard L, Cozzone PJ, Lutz NW.
    PLoS One; 2007 Jan 17; 2(1):e157. PubMed ID: 17237885
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution.
    Kaufmann WE, Johnston MV, Blue ME.
    Brain Dev; 2005 Nov 15; 27 Suppl 1():S77-S87. PubMed ID: 16182491
    [Abstract] [Full Text] [Related]

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