(Q35983002)

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Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains

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scholarly article

1 reference

Europe PubMed Central

11 August 2017

Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains (English)

1 reference

Europe PubMed Central

11 August 2017

author name string

Shiri Rabinovitz

1

1 reference

Europe PubMed Central

11 August 2017

Yotam Kaufman

2

1 reference

Europe PubMed Central

11 August 2017

Guy Ludwig

3

1 reference

Europe PubMed Central

11 August 2017

Aharon Razin

4

1 reference

Europe PubMed Central

11 August 2017

Ruth Shemer

5

1 reference

Europe PubMed Central

11 August 2017

language of work or name

0 references

publication date

23 April 2012

1 reference

Europe PubMed Central

11 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

11 August 2017

109

1 reference

Europe PubMed Central

11 August 2017

19

1 reference

Europe PubMed Central

11 August 2017

7403-7408

1 reference

Europe PubMed Central

11 August 2017

A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

Tissue-specific and imprinted epigenetic modifications of the human NDN gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

The imprinting mechanism of the Prader-Willi/Angelman regional control center

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

Capturing chromosome conformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

Imprinting-mutation mechanisms in Prader-Willi syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

2 October 2017

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358894

27 July 2018

Imprinting mechanisms in mammals.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1116661109

21 January 2018

Mechanisms of imprinting of the Prader-Willi/Angelman region.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1116661109

21 January 2018

Angelman syndrome 2005: updated consensus for diagnostic criteria.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1116661109

21 January 2018

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1116661109

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1116661109

21 January 2018

Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1116661109

21 January 2018

A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

1 reference

https://pubmed.ncbi.nlm.nih.gov/22529396

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue-specific methylation patterns and expression of the human apolipoprotein AI gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/22529396

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo

1 reference

https://pubmed.ncbi.nlm.nih.gov/22529396

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.1116661109

1 reference

Europe PubMed Central

11 August 2017

2012PNAS..109.7403R

0 references

1 reference

Europe PubMed Central

11 August 2017

1 reference

Europe PubMed Central

11 August 2017

ResearchGate publication ID

0 references

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