I. Stancheva

发表

H19 lncRNA controls gene expression of the Imprinted Gene Network by recruiting MBD1

Julien Pontis, S. Ait-Si-Ali, P. Monnier, 2013, Proceedings of the National Academy of Sciences.

Methyl-CpG binding proteins: specialized transcriptional repressors or structural components of chromatin?

T. Clouaire, I. Stancheva, 2008, Cellular and Molecular Life Sciences.

A role for SUMO modification in transcriptional repression and activation.

M. J. Lyst, I. Stancheva, Matthew J. Lyst, 2007, Biochemical Society transactions.

Retraction: Regulation of MBD1‐mediated transcriptional repression by SUMO and PIAS proteins

X. Nan, M. J. Lyst, I. Stancheva, 2019, The EMBO journal.

The chromatin remodelling protein LSH/HELLS regulates the amount and distribution of DNA hydroxymethylation in the genome

B. Miotto, Laurence Colin, Martin Bachman, 2021, Epigenetics.

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.

H. Zoghbi, R. Meehan, I. Stancheva, 2003, Molecular cell.

Kaiso is a genome-wide repressor of transcription that is essential for amphibian development

R. Meehan, A. Ruzov, E. Prokhortchouk, 2004, Development.

DNA methylation and control of gene expression in vertebrate development.

R. Meehan, I. Stancheva, 2001, Essays in biochemistry.

Explorer Revisiting heterochromatin in embryonic stem cells

I. Stancheva, 2017 .

Revisiting Heterochromatin in Embryonic Stem Cells

I. Stancheva, 2011, PLoS genetics.

Retracted: Regulation of MBD1‐mediated transcriptional repression by SUMO and PIAS proteins

X. Nan, M. J. Lyst, I. Stancheva, 2006, The EMBO journal.

Chromatin structure and methylation of rat rRNA genes studied by formaldehyde fixation and psoralen cross-linking.

J. Sogo, T. Koller, I. Stancheva, 1997, Nucleic acids research.

Edinburgh Research Explorer Immortality, but not oncogenic transformation, of primary human cells leads to epigenetic reprogramming of DNA methylation and gene expression

T. Clouaire, I. Stancheva, Xun X. Bao, 2018 .

G9a/GLP Complex Maintains Imprinted DNA Methylation in Embryonic Stem Cells

B. Ramsahoye, J. Rappsilber, F. de lima Alves, 2016, Cell reports.

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.

H. Newbery, C. Abbott, L. Zimmerman, 2011, Biochemical and biophysical research communications.

Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome

G. Montana, N. Brockdorff, E. Heard, 2012, Developmental cell.

DNA methylation and chromatin structure

J. Zlatanova, I. Stancheva, P. Caiafa, 2004 .

The SNF2 family ATPase LSH promotes cell-autonomous de novo DNA methylation in somatic cells

B. Ramsahoye, Alastair R W Kerr, I. Stancheva, 2016, Nucleic acids research.

LSH and G9a/GLP complex are required for developmentally programmed DNA methylation.

Cara Merusi, I. Stancheva, J. Burrage, 2011, Genome research.

Targeting of De Novo DNA Methylation Throughout the Oct-4 Gene Regulatory Region in Differentiating Embryonic Stem Cells

A. Bird, R. Athanasiadou, Cara Merusi, 2010, PloS one.

LSH Cooperates with DNA Methyltransferases To Repress Transcription

I. Stancheva, K. Myant, 2007, Molecular and Cellular Biology.

Biological functions of methyl-CpG-binding proteins.

P. Defossez, I. Stancheva, 2011, Progress in molecular biology and translational science.

Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly.

Shireen A. Sarraf, I. Stancheva, 2004, Molecular cell.

Epigenetics . Eds. C. D. Allis, T. Jenuwein, D. Reinberg & M.-L. Caparros. Cold Spring Harbor Laboratory Press. 2007. 502 pages. ISBN 0 87969 724 5. Price $150. (hardback)

I. Stancheva, 2007 .

DNA binding selectivity of MeCP2 due to a requirement for A/T sequences adjacent to methyl-CpG.

A. Bird, R. Klose, Suzanne M. McDermott, 2005, Molecular cell.

DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos.

A. Niveleau, R. Meehan, O. el-Maarri, 2002, Developmental biology.

Caught in conspiracy: cooperation between DNA methylation and histone H3K9 methylation in the establishment and maintenance of heterochromatin.

I. Stancheva, 2005, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Retracted: Regulation of MBD1‐mediated transcriptional repression by SUMO and PIAS proteins

X. Nan, M. J. Lyst, I. Stancheva, 2006, The EMBO journal.

Transient depletion of xDnmt1 leads to premature gene activation in Xenopus embryos.

R. Meehan, I. Stancheva, Irina Stancheva, 2000, Genes & development.

Recruitment of MBD1 to target genes requires sequence-specific interaction of the MBD domain with methylated DNA

Cara Merusi, T. Clouaire, I. Stancheva, 2010, Nucleic acids research.

Lashings of DNA methylation, forkfuls of chromatin remodeling.

R. Meehan, I. Stancheva, S. Pennings, 2001, Genes & development.

Immortality, but not oncogenic transformation, of primary human cells leads to epigenetic reprogramming of DNA methylation and gene expression

Maria Xenophontos, K. Gordon, T. Clouaire, 2013, Nucleic acids research.

Nuclear envelope: connecting structural genome organization to regulation of gene expression.

E. C. Schirmer, I. Stancheva, 2014, Advances in experimental medicine and biology.

The SNF2 family ATPase LSH promotes phosphorylation of H2AX and efficient repair of DNA double-strand breaks in mammalian cells

K. Gordon, I. Stancheva, J. Burrage, 2012, Journal of Cell Science.

Loss of the maintenance methyltransferase, xDnmt1, induces apoptosis in Xenopus embryos

R. Meehan, C. Hensey, I. Stancheva, 2001, The EMBO journal.

Asymmetry of Dam remethylation on the leading and lagging arms of plasmid replicative intermediates

J. Sogo, T. Koller, I. Stancheva, 1999, The EMBO journal.

The chromatin remodeler LSH controls genome-wide cytosine hydroxymethylation

Chao Li, Laurence Colin, Martin Bachman, 2020, bioRxiv.

A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos.

H. Zoghbi, R. Meehan, I. Stancheva, 2016, Molecular cell.

Evolutionary importance of translation elongation factor eEF1A variant switching

H. Newbery, C. Abbott, I. Stancheva, 2013 .

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.

H. Zoghbi, R. Meehan, I. Stancheva, 2003, Molecules and Cells.

LSH and G9a/GLP complex are required for developmentally programmed DNA methylation.

Cara Merusi, I. Stancheva, K. Myant, 2011, Genome research.