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Explore epigenetic therapy of using histone deacetylase inhibitors in the Angelman Syndrome mouse model
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Research

Explore epigenetic therapy of using histone deacetylase inhibitors in the Angelman Syndrome mouse model
  • About
    • What is Angelman syndrome?
    • Symptoms
    • Causes
    • Diagnosis & Tests
    • Treatment & Care
    • Angelman Syndrome Foundation
    • Our History
    • Board of Directors
    • Committees and Groups
  • Research
    • Angelman Syndrome Research
    • Types of Research
    • ASF Funded Research
    • Call for Proposals
    • Research Studies 101
    • Participate In A Study
    • Active Studies
    • For Industry
    • Published Articles
    • Clinical Trials 101
    • Treatments & Therapies
    • Phases & Therapeutic Pipeline
    • Find a Clinical Trial
  • Make an Impact
    • Ways to Donate
    • Donate Online
    • Join the ASF Cure Club
    • Text to Give
    • Send Sunshine
    • Start a Fundraiser
    • Programs & Events
    • Tips & Tools
    • Meet Fundraisers
    • Partner with us
    • Volunteer Opportunities
    • Join a Group Or Committee
    • Shop & Support
  • ASF Clinics
    • Find an ASF Clinic
    • Europe
    • North America
    • South America
    • The Middle East
    • For Families
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    • Clinic Patient Survey
    • FAQs
    • For Clinicians
    • Jacob Pritzker Fellowship
    • Clinical Care Toolkit
    • Angelman Publications
    • Join the Network
  • Find Resources
    • Resource Library
    • Newly Diagnosed
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    • Family Support
    • Search by Sub-Topic
      • Advocacy
      • Financial Planning & Support
      • Individualized Education Plan
    • ASF Podcast
  • Events
    • Event Calendar
    • Angelman Strong
    • Conferences and Symposia
    • Chicago Marathon
    • Tell Us About Your Event
  • News & Blog
  • Contact Us
  • 2026 Angelman Syndrome Foundation.
    All rights reserved.
  • 3015 E. New York Street, Suite A2 #285
    Aurora, IL 60504
  • (800) 432-6435
  • info@angelman.org

Archives: Funded Research

Explore epigenetic therapy of using histone deacetylase inhibitors in the Angelman Syndrome mouse model

Towards gene therapy for Angelman Syndrome using artificial transcription factors

Neuregulin-dependent alterations in glutamate receptor function and LTP in Angelman Syndrome model mice

Restoration of neocortial plasticity in a mouse model of Angelman Syndrome

Restoration of neocortial plasticity in a mouse model of Angelman Syndrome

A combined molecular and electrophysiological approach to understanding cerebellar defects in Angelman syndrome

The significance of EEG findings in Angelman Syndrome

Therapeutic effectiveness of levodopa in the treatment of seizures and motor defects using the Angelman Syndrome mouse model

The ubiquitin ligase E6-AP/UBE3A targets the polycomb repressive complex proteins Ring 1B and Bmi1 to ubiquitination and subsequent degradation: Structural and functional implications, and possible relationship to the pathogenesis of Angelman syndrome

Ube3a and altered neuronal trafficking in Angelman syndrome

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The mission of Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.

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  • 2026 Angelman Syndrome Foundation. All rights reserved.
  • 3015 E. New York Street, Suite A2 #285, Aurora, IL 60504
  • (800) 432-6435
  • info@angelman.org
  • 2026 Angelman Syndrome Foundation.
    All rights reserved.
  • 3015 E. New York Street, Suite A2 #285
    Aurora, IL 60504
  • (800) 432-6435
  • info@angelman.org