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Arthur Beaudet, MD

articles and announcements

Categories: Mouse Model

Arthur Beaudet, MD
January 23, 2020

A rigorous test in the mouse of whether increased DNA methylation can activate neuronal expression of the paternal Ube3a allele

$80,000 The mouse model provides an ideal way to evaluate therapeutic attempts to increase UBE3A function on the otherwise silenced paternally-derived mouse chromosome. Using novel genetic engineering methods, Dr. Beaudet and his lab were able to develop a engineered mouse […]

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January 23, 2020

Explore the therapeutic potential of levodopa to treat Angelman syndrome in mouse model

$50,000 There is a small amount of anecdotal experience and some neuroscience studies suggesting that levodopa might have therapeutic effect on the symptoms of AS. The Angelman mouse model is an ideal way to study this before developing any human […]

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January 23, 2020

Epigenetic regulation of Ube3a by a candidate Angelman syndrome drug (UNCilencer1)

$110,000 The ASF Joseph Wagstaff Postdoctoral Research Fellowship was granted to its first recipient.  Dr. King will do his postdoctoral research on a new drug UNCilencer1, which turns on the silenced paternal UBE3A gene in mouse neurons.  UNCilencer1 is a […]

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Dr. Ype Elgersma
January 15, 2020

To what extent are striatal deficits underlying clinical features of Angelman syndrome?

It remains unclear which brain areas (and hence which cellular changes) directly contribute to phenotypes of AS. Knowledge of the critically affected brain areas is important for two reasons: 1) it will help us to identify the most relevant mechanisms […]

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December 22, 2019

Role of the UBE3A Gene Product in Brain Protein Metabolism

$45,547 Dr. Wagstaff was one of the crucial investigators who discovered that UBE3A disruption was the cause of AS. With funds from this and other projects he was able to develop a mouse model for AS and this important development […]

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December 22, 2019

Dissecting the roles of Ube3a in synaptic plasticity by analyzing synaptic function at the single cell level and utilizing ‘Network Analysis Proteomics’ strategy

$56,000 This grant-funded research was to a premier AS researcher who was instrumental in developing a mouse model for AS and who demonstrated that an important enzyme associated with the synapse, CAMKII, was inhibited or partially inactivated in Angelman mice. […]

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December 22, 2019

Testing for Correction of the Angelman Syndrome Phenotype of UBE3A-Maternal-Deficient Mice by UBE3A Transgene

$47,000 This project was continued funding for an important AS investigator to enable his laboratory to work on studies of UBE3A in the mouse model in the hope of developing novel therapeutic initiatives. The experimental approach in this grant was […]

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December 22, 2019

Effects Of Premature Truncation Of The UBE3A Antisense transcript On UBE3A Imprinted Expression

$82,255 This grant continued ASF funding to one of the premier AS scientists, Dr. Joe Wagstaff, and his laboratory. The aim of this project was a bold attempt to create therapeutic effects in the mouse model by genetically engineering a […]

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