Antisense oligonucleotide treatment rescues UBE3A expression and multiple phenotypes of an Angelman syndrome mouse model
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Title
Antisense oligonucleotide treatment rescues UBE3A expression and multiple phenotypes of an Angelman syndrome mouse model
Authors
Keywords
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Journal
JCI Insight
Volume 6, Issue 15, Pages -
Publisher
American Society for Clinical Investigation
Online
2021-08-11
DOI
10.1172/jci.insight.145991
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Related references
Note: Only part of the references are listed.- Angelman Syndrome: From Mouse Models to Therapy
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- Cas9 gene therapy for Angelman syndrome traps Ube3a-ATS long non-coding RNA
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- (2020) Allison M. Bond et al. Brain Sciences
- Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes
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- Antisense oligonucleotides: the next frontier for treatment of neurological disorders
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- Truncation of Ube3a-ATS Unsilences Paternal Ube3a and Ameliorates Behavioral Defects in the Angelman Syndrome Mouse Model
- (2013) Linyan Meng et al. PLoS Genetics
- Comparative analysis of deutocerebral neuropils in Chilopoda (Myriapoda): implications for the evolution of the arthropod olfactory system and support for the Mandibulata concept
- (2012) Andy Sombke et al. BMC NEUROSCIENCE
- Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a
- (2012) Linyan Meng et al. HUMAN MOLECULAR GENETICS
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