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Profile Publications (8)
XB-PERS-2796

Publications By Irina Stancheva

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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.   

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