(Q40747050)

23 September 2017

A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator (English)

1 reference

23 September 2017

5

1 reference

23 September 2017

Chandrasekhar Kanduri

1

1 reference

23 September 2017

Galina Fitzpatrick

2

1 reference

23 September 2017

Rituparna Mukhopadhyay

3

1 reference

23 September 2017

Meena Kanduri

4

1 reference

23 September 2017

Michael Higgins

6

1 reference

23 September 2017

Rolf Ohlsson

7

1 reference

23 September 2017

language of work or name

English

0 references

publication date

4 March 2002

1 reference

Journal of Biological Chemistry

23 September 2017

1 reference

23 September 2017

277

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23 September 2017

18106-18110

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23 September 2017

20

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Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

23 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

The 5' flank of mouse H19 in an unusual chromatin conformation unidirectionally blocks enhancer-promoter communication

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

CpG methylation regulates the Igf2/H19 insulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

Insulators and boundaries: versatile regulatory elements in the eukaryotic genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

Imprinting of mouse Kvlqt1 is developmentally regulated.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200031200

21 January 2018

Identifiers

DOI

10.1074/JBC.M200031200

1 reference

23 September 2017

1 reference