CTCF maintains differential methylation at the Igf2/H19 locus

Schoenherr, Christopher J., Levorse, John M., Tilghman, Shirley M.·2003·Nature Genetics
DOI 10.1038/ng1057

Cited by (312)

Items 101–200 of 312

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  7. Modeling human epigenetic disorders in mice: Beckwith-Wiedemann Syndrome and Silver-Russell Syndrome
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  10. The Role of CCCTC-Binding Factor (CTCF) in Genomic Imprinting, Development, and Reproduction1
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  11. Genomic Imprinting of Dopa decarboxylase in Heart and Reciprocal Allelic Expression with Neighboring Grb10
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  12. YY1 as a controlling factor for the Peg3 and Gnas imprinted domains
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  13. Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus
    Judith Rixt Brouwer, Aline Huguet-Lachon, Annie Nicole, Arnold Münnich, Geneviève Gourdon · 2013 · Journal of Nucleic Acids
  14. The Transcriptional Status but Not the Imprinting Control Region Determines Allele-Specific Histone Modifications at the Imprinted H19 Locus
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  15. Structural impact of complete CpG methylation within target DNA on specific complex formation of the inducible transcription factor Egr‐1
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  17. Parental imprinting regulates insulin-like growth factor signaling: a Rosetta Stone for understanding the biology of pluripotent stem cells, aging and cancerogenesis
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  30. Potential role of estrogen in regulation of the Insulin-like growth factor2–H19 locus in the rat testis
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  41. Stability and Lability of Parental Methylation Imprints in Development and Disease
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  42. Hormonal regulation of H19 gene expression in prostate epithelial cells
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  44. Coordinated allele-specific histone acetylation at the differentially methylated regions of imprinted genes
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  46. Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles
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  49. A Randomly Integrated Transgenic H19 Imprinting Control Region Acquires Methylation Imprinting Independently of Its Establishment in Germ Cells
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  52. Imprinting Capacity of Gamete Lineages in Caenorhabditis elegans
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  53. Tissue-specific insulator function at H19/Igf2 revealed by deletions at the imprinting control region
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  54. A novel de novo point mutation of the OCT ‐binding site in the IGF2 / H19 ‐imprinting control region in a Beckwith–Wiedemann syndrome patient
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