Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome

26 Apr 2010

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Epigenetics and DNA Methylation
Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 20423730
DOI: 10.1016/j.nbd.2010.04.012

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 10 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndromePMID 20423730Read ↗

Novel human pathological mutations. Gene symbol: UBE3A. Disease: Angelman Syndrome.Semantic proximity Read ↗

Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation.Semantic proximity Read ↗

UBE3A isoform-selective and non-selective contributions to Angelman syndrome phenotypes.Semantic proximity Read ↗

Angelman Syndrome causing UBE3A ligase displays predominantly synaptic ubiquitination activity in the mouse brainSemantic proximity Read ↗

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neuronsSemantic proximity Read ↗

Germline mosaicism of a novel UBE3A mutation in Angelman syndromeSemantic proximity Read ↗

SUBCELLULAR FUNCTIONS OF <i>UBE3A</i> ISOFORMS DRIVE SYNAPTIC DYSFUNCTION IN ANGELMAN SYNDROMESemantic proximity Read ↗

Abundance and localization of human UBE3A protein isoformsSemantic proximity Read ↗

Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes.Semantic proximity Read ↗

The spectrum of mutations in UBE3A causing Angelman syndrome.Semantic proximity Read ↗

Angelman Syndrome: From Mouse Models to Therapy.Semantic proximity Read ↗

Abundance and localization of human UBE3A protein isoforms.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.