Imprinting: focusing on the center (Q34026945)

30 July 2017

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title

Imprinting: focusing on the center (English)

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30 July 2017

Ben-Porath I

1

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30 July 2017

Cedar H

series ordinal

2

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30 July 2017

publication date

1 October 2000

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Current Opinion in Genetics & Development

30 July 2017

published in

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30 July 2017

volume

10

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30 July 2017

issue

5

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30 July 2017

page(s)

550-554

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Imprinted expression of the Igf2r gene depends on an intronic CpG island.

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

An enhancer deletion affects both H19 and Igf2 expression

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Imprinting in Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Towards a molecular understanding of Prader-Willi and Angelman syndromes

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https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Imprinting-mutation mechanisms in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation

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https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

A mouse model for Prader-Willi syndrome imprinting-centre mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

The imprinting box of the mouse Igf2r gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

DNA methylation in early development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Chromatin conformation of the H19 epigenetic mark

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Inactive allele-specific methylation and chromatin structure of the imprinted gene U2af1-rs1 on mouse chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Transient inhibition of histone deacetylation alters the structural and functional imprint at fission yeast centromeres.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Allele-specific replication timing of imprinted gene regions

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Asynchronous replication of imprinted genes is established in the gametes and maintained during development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

The mouse H19 locus mediates a transition between imprinted and non-imprinted DNA replication patterns

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900126-X

7 January 2021

10.1016/S0959-437X(00)00126-X

Identifiers

DOI

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30 July 2017

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