(Q58134238)

English

The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster

article published in 2005

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scholarly article

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The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster (English)

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object named as

Angela Sparago

2

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object named as

Wolf Reik

10

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object named as

Andrea Riccio

11

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author name string

Flavia Cerrato

1

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Ines Di Matteo

3

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Xiangang Zou

4

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Wendy Dean

5

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Hiroyuki Sasaki

6

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Paul Smith

7

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Rita Genesio

8

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Marianne Bruggemann

9

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publication date

7 January 2005

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Human Molecular Genetics

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14

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503-511

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4

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Genomic imprinting: parental influence on the genome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Imprinting and the epigenetic asymmetry between parental genomes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

The non-coding Air RNA is required for silencing autosomal imprinted genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Genomic imprinting: intricacies of epigenetic regulation in clusters.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Dnmt3L and the establishment of maternal genomic imprints.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

The two-domain hypothesis in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Elucidation of the minimal sequence required to imprint H19 transgenes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Size matters: use of YACs, BACs and PACs in transgenic animals

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Essential role of Mash-2 in extraembryonic development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Genomic imprinting of Mash2, a mouse gene required for trophoblast development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Epigenetic reprogramming in mouse primordial germ cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Genomic imprinting in mammalian development: a parental tug-of-war

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Creation of mice expressing human antibody light chains by introduction of a yeast artificial chromosome containing the core region of the human immunoglobulin kappa locus.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

A Mup promoter-thymidine kinase reporter gene shows relaxed tissue-specific expression and confers male sterility upon transgenic mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI047

21 January 2018

Identifiers

10.1093/HMG/DDI047

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