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- Title
Angelman Syndrome at the Synapse: Meeting Report of the Angelman Syndrome Foundation's 2009 Scientific Symposium.
- Authors
Williams, Charles; Franco, Lisa
- Abstract
Angelman syndrome is caused by disruption of the ubiquitin-protein ligase E3A gene (UBE3A). The gene encodes an ubiquitinating protein that is widely expressed in the body but has tissue-specific expression in brain neurons, resulting in transcription from only the maternal allele. The normal function of this protein is beginning to be delineated, but its protein targets and role in various cellular pathways remain elusive. Angelman syndrome mouse models lacking the protein in the brain provide insight into neuronal cell dysfunction, particularly in hippocampal neurons where dendritic structure and synaptic function become disturbed. The Angelman Syndrome Foundation's 2009 symposium theme was thus ''Angelman Syndrome at the Synapse,'' and the event enabled neuroscientists and other researchers and clinicians to present their current research on the syndrome.
- Subjects
ORLANDO (Fla.); FLORIDA; CONFERENCES &; conventions; ANGELMAN syndrome; HUMAN chromosome 15 abnormalities; DOPAMINE
- Publication
Journal of Child Neurology, 2010, Vol 25, Issue 2, p254
- ISSN
0883-0738
- Publication type
Proceeding
- DOI
10.1177/0883073809353450