Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene (Q28145754)

7 January 2021

Parental imprinting of the mouse H19 gene

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7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

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7 January 2021

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

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7 January 2021

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

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7 January 2021

The protein CTCF is required for the enhancer blocking activity of vertebrate insulators

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7 January 2021

A 5' element of the chicken beta-globin domain serves as an insulator in human erythroid cells and protects against position effect in Drosophila

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7 January 2021

Characterization of the chicken beta-globin insulator

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7 January 2021

A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development

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7 January 2021

Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene.

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7 January 2021

Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene

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7 January 2021

Chromatin conformation of the H19 epigenetic mark.

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7 January 2021

A potential imprint control element: identification of a conserved 42 bp sequence upstream of H19.

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7 January 2021

Role of a 461-bp G-rich repetitive element in H19 transgene imprinting.

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7 January 2021

Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus.

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7 January 2021

Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor.

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7 January 2021

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

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7 January 2021

Location of enhancers is essential for the imprinting of H19 and Igf2 genes

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7 January 2021

Enhancer competition between H19 and Igf2 does not mediate their imprinting

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7 January 2021

Disruption of imprinting caused by deletion of the H19 gene region in mice

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7 January 2021

Role for DNA methylation in genomic imprinting

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7 January 2021

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

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7 January 2021

Synthesis of microporous transition-metal-oxide molecular sieves by a supramolecular templating mechanism

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7 January 2021

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

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7 January 2021

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

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7 January 2021

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

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7 January 2021

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

1 reference

7 January 2021

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

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7 January 2021

Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

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7 January 2021

A novel cis-regulatory element, the PTS, mediates an anti-insulator activity in the Drosophila embryo

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7 January 2021