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Journal Abstract Search

791 related items for PubMed ID: 18948693

  • 41. Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.
    Filosa S, Pecorelli A, D'Esposito M, Valacchi G, Hajek J.
    Free Radic Biol Med; 2015 Nov; 88(Pt A):81-90. PubMed ID: 25960047
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  • 44. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG.
    Ment Retard Dev Disabil Res Rev; 2004 Nov; 10(2):154-8. PubMed ID: 15362175
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  • 46. Novel mutations in the C-terminal region of the MECP2 gene in Tunisian Rett syndrome patients.
    Fendri-Kriaa N, Rouissi A, Ghorbel R, Mkaouar-Rebai E, Belguith N, Gouider-Khouja N, Fakhfakh F.
    J Child Neurol; 2012 May; 27(5):564-8. PubMed ID: 21940684
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  • 47. Deciphering Rett syndrome with mouse genetics, epigenomics, and human neurons.
    Tao J, Wu H, Sun YE.
    Int Rev Neurobiol; 2009 May; 89():147-60. PubMed ID: 19900619
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  • 53. 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; 12(7):732-40. PubMed ID: 24283265
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  • 54. MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics.
    Kleefstra T, Yntema HG, Nillesen WM, Oudakker AR, Mullaart RA, Geerdink N, van Bokhoven H, de Vries BB, Sistermans EA, Hamel BC.
    Eur J Hum Genet; 2004 Jan; 12(1):24-8. PubMed ID: 14560307
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  • 55. Germline mosaicism for a MECP2 mutation in a man with two Rett daughters.
    Evans JC, Archer HL, Whatley SD, Clarke A.
    Clin Genet; 2006 Oct; 70(4):336-8. PubMed ID: 16965328
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  • 56. Genetic basis of Rett syndrome.
    Van den Veyver IB, Zoghbi HY.
    Ment Retard Dev Disabil Res Rev; 2002 Oct; 8(2):82-6. PubMed ID: 12112732
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  • 57. Balanced X chromosome inactivation patterns in the Rett syndrome brain.
    Shahbazian MD, Sun Y, Zoghbi HY.
    Am J Med Genet; 2002 Aug 01; 111(2):164-8. PubMed ID: 12210344
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  • 58. 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
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  • 59. 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
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  • 60. Neural development of methyl-CpG-binding protein 2 null embryonic stem cells: a system for studying Rett syndrome.
    Okabe Y, Kusaga A, Takahashi T, Mitsumasu C, Murai Y, Tanaka E, Higashi H, Matsuishi T, Kosai K.
    Brain Res; 2010 Nov 11; 1360():17-27. PubMed ID: 20816763
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