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Persistent neuronal Ube3a expression in the suprachiasmatic nucleus of Angelman syndrome model mice

Persistent neuronal Ube3a expression in the suprachiasmatic nucleus of Angelman syndrome model mice

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4910164

Persistent neuronal Ube3a expression in the suprachiasmatic nucleus of Angelman syndrome model mice

About this item

Full title

Persistent neuronal Ube3a expression in the suprachiasmatic nucleus of Angelman syndrome model mice

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2016-06, Vol.6 (1), p.28238, Article 28238

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Mutations or deletions of the maternal allele of the
UBE3A
gene cause Angelman syndrome (AS), a severe neurodevelopmental disorder. The paternal
UBE3A/Ube3a
allele becomes epigenetically silenced in most neurons during postnatal development in humans and mice; hence, loss of the maternal allele largely eliminates neuronal expression of...

Alternative Titles

Full title

Persistent neuronal Ube3a expression in the suprachiasmatic nucleus of Angelman syndrome model mice

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4910164

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4910164

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/srep28238

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