Oct4/Sox2 Binding Sites Contribute to Maintaining Hypomethylation of the Maternal Igf2/H19 Imprinting Control Region

Induction of DNA Demethylation Depending on Two Sets of Sox2 and Adjacent Oct3/4 Binding Sites (Sox-Oct Motifs) within the MouseH19/Insulin-like Growth Factor 2 (Igf2) Imprinted Control Region

(2012) Naohiro Hori et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Setting up and maintaining differential insulators and boundaries for genomic imprinting

(2011) Adele Murrell   Biochemistry and Cell Biology

Novel cis-regulatory function in ICR-mediated imprinted repression of H19

(2011) Folami Y. Ideraabdullah et al.   DEVELOPMENTAL BIOLOGY

Beckwith–Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1

(2011) Rebecca L Poole et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions

(2011) Simon Quenneville et al.   MOLECULAR CELL

De novo DNA methylation: a germ cell perspective

(2011) Sébastien A. Smallwood et al.   TRENDS IN GENETICS

BISMA - Fast and accurate bisulfite sequencing data analysis of individual clones from unique and repetitive sequences

(2010) Christian Rohde et al.   BMC BIOINFORMATICS

Genomic imprinting mechanisms in embryonic and extraembryonic mouse tissues

(2010) Q J Hudson et al.   HEREDITY

Sumoylation modulates a domain in CTCF that activates transcription and decondenses chromatin

(2010) Neal S. Kitchen et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

CTCF: Master Weaver of the Genome

(2009) Jennifer E. Phillips et al.   CELL

Beckwith–Wiedemann syndrome

(2009) Rosanna Weksberg et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders

(2009) Julie Demars et al.   HUMAN MOLECULAR GENETICS

Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain

(2009) Y. Kaufman et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Cohesin Is Required for Higher-Order Chromatin Conformation at the Imprinted IGF2-H19 Locus

(2009) Raffaella Nativio et al.   PLoS Genetics

Connecting microRNA Genes to the Core Transcriptional Regulatory Circuitry of Embryonic Stem Cells

(2008) Alexander Marson et al.   CELL

Three-dimensional conformation at the H19/Igf2 locus supports a model of enhancer tracking

(2008) N. Engel et al.   HUMAN MOLECULAR GENETICS

Dissecting direct reprogramming through integrative genomic analysis

(2008) Tarjei S. Mikkelsen et al.   NATURE

The Igf2/H19 imprinting control region exhibits sequence-specific and cell-type-dependent DNA methylation-mediated repression

(2008) Yinming Chen et al.   NUCLEIC ACIDS RESEARCH

Sexual dimorphism in parental imprint ontogeny and contribution to embryonic development

(2007) Déborah Bourc’his et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY