Competitive edge at the imprinted Prader-Willi/Angelman region? (Q62075692)

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10 November 2019

title

Competitive edge at the imprinted Prader-Willi/Angelman region? (English)

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10 November 2019

2

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10 November 2019

author name string

Tilghman SM

series ordinal

1

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10 November 2019

Ingram RS

series ordinal

3

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10 November 2019

language of work or name

English

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publication date

1 March 1998

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10 November 2019

1 reference

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10 November 2019

volume

18

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10 November 2019

issue

3

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10 November 2019

page(s)

206-208

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https://scigraph.springernature.com/pub.10.1038/ng0398-206

10 November 2019

exact match

0 references

cites work

Competition--a common motif for the imprinting mechanism?

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

Parental imprinting and human disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

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/10.1038%2FNG0398-206

7 January 2021

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

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/10.1038%2FNG0398-206

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/10.1038%2FNG0398-206

7 January 2021

Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-206

7 January 2021