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A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos. , Stancheva I , Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR ., Mol Cell. July 7, 2016; 63 (1): 179.
Evolutionary importance of translation elongation factor eEF1A variant switching: eEF1A1 down-regulation in muscle is conserved in Xenopus but is controlled at a post-transcriptional level. , Newbery HJ, Stancheva I , Zimmerman LB , Abbott CM., Biochem Biophys Res Commun. July 22, 2011; 411 (1): 19-24.
Kaiso is a genome-wide repressor of transcription that is essential for amphibian development. , Ruzov A, Dunican DS, Prokhortchouk A, Pennings S, Stancheva I , Prokhortchouk E, Meehan RR ., Development. December 1, 2004; 131 (24): 6185-94.
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. , Stancheva I , Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR ., Mol Cell. August 1, 2003; 12 (2): 425-35.
DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos. , Stancheva I , El-Maarri O, Walter J, Niveleau A, Meehan RR ., Dev Biol. March 1, 2002; 243 (1): 155-65.
Loss of the maintenance methyltransferase, xDnmt1, induces apoptosis in Xenopus embryos. , Stancheva I , Hensey C, Meehan RR ., EMBO J. April 17, 2001; 20 (8): 1963-73.
DNA methylation and control of gene expression in vertebrate development. , Meehan RR , Stancheva I ., Essays Biochem. January 1, 2001; 37 59-70.
Transient depletion of xDnmt1 leads to premature gene activation in Xenopus embryos. , Stancheva I , Meehan RR ., Genes Dev. February 1, 2000; 14 (3): 313-27.