Φορτώνει......
Phosphorodiamidate morpholino oligomers suppress mutant huntingtin expression and attenuate neurotoxicity
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the huntingtin (HTT) gene. Disease pathogenesis derives, at least in part, from the long polyglutamine tract encoded by mutant HTT. Therefore, considerable effort has been dedicated to th...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Hum Mol Genet |
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| Κύριοι συγγραφείς: | , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Oxford University Press
2014
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4222366/ https://ncbi.nlm.nih.gov/pubmed/25035419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu349 |
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