Published in J Cell Biochem on February 01, 2011
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Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med Genet (2006) 1.08
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Hum Mol Genet (2008) 1.06
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Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2. Epigenetics (2007) 1.05
Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15. BMC Genet (2008) 1.04
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Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans. Nucleic Acids Res (2005) 0.97
MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation. Neurobiol Dis (2011) 0.95
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A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype. Hum Genet (2008) 0.90
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion. Hum Mol Genet (2013) 0.90
Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis. Epigenetics (2011) 0.90
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Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease. Hepatology (2013) 0.89
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Genomic organization and allelic expression of UBE3A in chicken. Gene (2006) 0.78
Prader-Willi syndrome, Snord115, and Htr2c editing. Neurogenetics (2009) 0.78
Inclusion of a matrix-attached region in a 7SK pol III vector increases the efficiency of shRNA-mediated gene silencing in embryonic carcinoma cells. Plasmid (2006) 0.75
Is urine the next source of stem cells? Regen Med (2013) 0.75
Epigenetic activation of the 5-hydroxytryptamine (serotonin) receptor 2C in embryonal carcinoma cells is DNA replication-dependent. Exp Cell Res (2004) 0.75