(Q54623728)

1 June 2018

title

Mouse imprinting defect mutations that model Angelman syndrome. (English)

1 reference

1 June 2018

author name string

Mei-Yi Wu

1

1 reference

1 June 2018

Ken-Shiung Chen

2

1 reference

1 June 2018

Jan Bressler

3

1 reference

1 June 2018

Aihua Hou

4

1 reference

1 June 2018

Ting-Fen Tsai

5

1 reference

1 June 2018

Arthur L Beaudet

6

1 reference

1 June 2018

publication date

1 January 2006

1 reference

1 June 2018

published in

Genesis

1 reference

1 June 2018

volume

44

1 reference

1 June 2018

issue

1

1 reference

1 June 2018

page(s)

12-22

1 reference

1 June 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

7 January 2021

Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

7 January 2021

Disruption of the bipartite imprinting center in a family with Angelman syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

A candidate model for Angelman syndrome in the mouse.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Targeted deletion of 5'HS2 of the murine beta-globin LCR reveals that it is not essential for proper regulation of the beta-globin locus.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Structure and function correlations at the imprinted mouse Snrpn locus.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

7 January 2021

Disruption of the mouse necdin gene results in early post-natal lethality

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

An imprinted, mammalian bicistronic transcript encodes two independent proteins

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Control elements within the PWS/AS imprinting box and their function in the imprinting process

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

7 January 2021

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Imprinting-mutation mechanisms in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Gene targeting in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Chromosome engineering in mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

7 January 2021

The imprinting box of the Prader-Willi/Angelman syndrome domain

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

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/10.1002%2FGENE.20179

7 January 2021

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20179

7 January 2021

Identifiers

DOI

10.1002/GENE.20179

1 reference

1 June 2018

PubMed ID

16397868

1 reference

1 June 2018