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Journal Abstract Search

299 related items for PubMed ID: 15689435

  • 1. Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome.
    Meins M, Lehmann J, Gerresheim F, Herchenbach J, Hagedorn M, Hameister K, Epplen JT.
    J Med Genet; 2005 Feb; 42(2):e12. PubMed ID: 15689435
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  • 4. 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; 66(2):117-23. PubMed ID: 17278996
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  • 5. [Rett syndrome: clinical and molecular aspects].
    Záhoráková D, Zeman J, Martásek P.
    Cas Lek Cesk; 2007 Feb; 146(8):647-52. PubMed ID: 17874730
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  • 6. 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; 116(6):413-9. PubMed ID: 17986102
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  • 8. Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.
    Parmeggiani A, Tedde MR, Arbizzani A, Posar A, Scaduto MC, Santucci M, Sangiorgi S.
    J Child Neurol; 2009 Jun; 24(6):772-4. PubMed ID: 19189931
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  • 9. Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).
    Shi J, Shibayama A, Liu Q, Nguyen VQ, Feng J, Santos M, Temudo T, Maciel P, Sommer SS.
    Hum Mutat; 2005 May; 25(5):505. PubMed ID: 15841480
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  • 10. Rett syndrome: from the gene to the disease.
    Matijevic T, Knezevic J, Slavica M, Pavelic J.
    Eur Neurol; 2009 May; 61(1):3-10. PubMed ID: 18948693
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  • 11. De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features.
    Makrythanasis P, Moix I, Gimelli S, Fluss J, Aliferis K, Antonarakis SE, Morris MA, Béna F, Bottani A.
    Clin Genet; 2010 Aug; 78(2):175-80. PubMed ID: 20236124
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  • 13. Large genomic rearrangements in MECP2.
    Ravn K, Nielsen JB, Skjeldal OH, Kerr A, Hulten M, Schwartz M.
    Hum Mutat; 2005 Mar; 25(3):324. PubMed ID: 15712379
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  • 14. Identification of cis-regulatory elements for MECP2 expression.
    Liu J, Francke U.
    Hum Mol Genet; 2006 Jun 01; 15(11):1769-82. PubMed ID: 16613900
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  • 15. MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.
    Dayer AG, Bottani A, Bouchardy I, Fluss J, Antonarakis SE, Haenggeli CA, Morris MA.
    Brain Dev; 2007 Jan 01; 29(1):47-50. PubMed ID: 16844334
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