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1122 related items for PubMed ID: 16647848

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

  • 2. 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 Jun; 8(2):99-105. PubMed ID: 12112735
    [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. Rett syndrome: a prototypical neurodevelopmental disorder.
    Neul JL, Zoghbi HY.
    Neuroscientist; 2004 Apr 08; 10(2):118-28. PubMed ID: 15070486
    [Abstract] [Full Text] [Related]

  • 5. [Rett syndrome: clinical and molecular aspects].
    Záhoráková D, Zeman J, Martásek P.
    Cas Lek Cesk; 2007 Apr 08; 146(8):647-52. PubMed ID: 17874730
    [Abstract] [Full Text] [Related]

  • 6. 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 08; 66(2):117-23. PubMed ID: 17278996
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Rett syndrome: from the gene to the disease.
    Matijevic T, Knezevic J, Slavica M, Pavelic J.
    Eur Neurol; 2009 Mar 05; 61(1):3-10. PubMed ID: 18948693
    [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. Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.
    Raizis AM, Saleem M, MacKay R, George PM.
    N Z Med J; 2009 Jun 05; 122(1296):21-8. PubMed ID: 19652677
    [Abstract] [Full Text] [Related]

  • 11. Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders.
    Wong VC, Li SY.
    J Child Neurol; 2007 Dec 05; 22(12):1397-400. PubMed ID: 18174559
    [Abstract] [Full Text] [Related]

  • 12. 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 05; 24(1):49-55. PubMed ID: 19168818
    [Abstract] [Full Text] [Related]

  • 13. The ups and downs of BDNF in Rett syndrome.
    Sun YE, Wu H.
    Neuron; 2006 Feb 02; 49(3):321-3. PubMed ID: 16446133
    [Abstract] [Full Text] [Related]

  • 14. 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 02; 116(6):413-9. PubMed ID: 17986102
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene.
    Bartholdi D, Klein A, Weissert M, Koenig N, Baumer A, Boltshauser E, Schinzel A, Berger W, Mátyás G.
    Clin Genet; 2006 Apr 15; 69(4):319-26. PubMed ID: 16630165
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 21(1):217-27. PubMed ID: 16087343
    [Abstract] [Full Text] [Related]

  • 18. Rett syndrome.
    Ben Zeev Ghidoni B.
    Child Adolesc Psychiatr Clin N Am; 2007 Jul 15; 16(3):723-43. PubMed ID: 17562589
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. MeCP2 involvement in the regulation of neuronal alpha-tubulin production.
    Abuhatzira L, Shemer R, Razin A.
    Hum Mol Genet; 2009 Apr 15; 18(8):1415-23. PubMed ID: 19174478
    [Abstract] [Full Text] [Related]

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