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Novel DNA Aptamers that Bind to Mutant Huntingtin and Modify Its Activity
The CAG repeat expansion that elongates the polyglutamine tract in huntingtin is the root genetic cause of Huntington’s disease (HD), a debilitating neurodegenerative disorder. This seemingly slight change to the primary amino acid sequence alters the physical structure of the mutant protein and alt...
Autores principales: | Shin, Baehyun, Jung, Roy, Oh, Hyejin, Owens, Gwen E., Lee, Hyeongseok, Kwak, Seung, Lee, Ramee, Cotman, Susan L., Lee, Jong-Min, MacDonald, Marcy E., Song, Ji-Joon, Vijayvargia, Ravi, Seong, Ihn Sik |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992459/ https://www.ncbi.nlm.nih.gov/pubmed/29858077 http://dx.doi.org/10.1016/j.omtn.2018.03.008 |
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