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Characterization and structure-activity relationships of indenoisoquinoline-derived topoisomerase I inhibitors in unsilencing the dormant Ube3a gene associated with Angelman syndrome

BACKGROUND: Angelman syndrome (AS) is a severe neurodevelopmental disorder lacking effective therapies. AS is caused by mutations in ubiquitin protein ligase E3A (UBE3A), which is genomically imprinted such that only the maternally inherited copy is expressed in neurons. We previously demonstrated t...

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Detalhes bibliográficos
Publicado no:Mol Autism
Main Authors: Lee, Hyeong-Min, Clark, Ellen P., Kuijer, M. Bram, Cushman, Mark, Pommier, Yves, Philpot, Benjamin D.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6098585/
https://ncbi.nlm.nih.gov/pubmed/30140420
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-018-0228-2
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