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PUBMED FOR HANDHELDS

Journal Abstract Search


416 related items for PubMed ID: 21824415

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  • 4. Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.
    Pejhan S, Rastegar M.
    Biomolecules; 2021 Jan 08; 11(1):. PubMed ID: 33429932
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  • 5. FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.
    Deng V, Matagne V, Banine F, Frerking M, Ohliger P, Budden S, Pevsner J, Dissen GA, Sherman LS, Ojeda SR.
    Hum Mol Genet; 2007 Mar 15; 16(6):640-50. PubMed ID: 17309881
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  • 7. Evolving role of MeCP2 in Rett syndrome and autism.
    LaSalle JM, Yasui DH.
    Epigenomics; 2009 Oct 15; 1(1):119-30. PubMed ID: 20473347
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  • 13. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
    Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM.
    Hum Mol Genet; 2009 Feb 01; 18(3):525-34. PubMed ID: 19000991
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  • 17. Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.
    Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM.
    Proc Natl Acad Sci U S A; 2007 Dec 04; 104(49):19416-21. PubMed ID: 18042715
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  • 18. Regulation mechanism and research progress of MeCP2 in Rett syndrome.
    Yang W, Pan H.
    Yi Chuan; 2014 Jul 04; 36(7):625-30. PubMed ID: 25076025
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