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Self-duplexing CUG repeats selectively inhibit mutant huntingtin expression
Huntington’s disease (HD) is a neurodegenerative genetic disorder caused by the expansion of the CAG repeat in the translated sequence of the HTT gene. This expansion generates a mutant huntingtin protein that contains an abnormally elongated polyglutamine tract, which, together with mutant transcri...
Autores principales: | Fiszer, Agnieszka, Olejniczak, Marta, Galka-Marciniak, Paulina, Mykowska, Agnieszka, Krzyzosiak, Wlodzimierz J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905887/ https://www.ncbi.nlm.nih.gov/pubmed/24038471 http://dx.doi.org/10.1093/nar/gkt825 |
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