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“Huntingtin Holiday”: Progress toward an Antisense Therapy for Huntington’s Disease

Lowering mutant Huntingtin is a consensus therapeutic strategy for Huntington’s disease. In this issue of Neuron, Kordasiewicz et al. (2012) show the benefit of transient antisense oligonucleotide (ASO) therapy to degrade Huntingtin mRNA and elicit sustained therapeutic benefit in HD mice.

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Detalhes bibliográficos
Main Authors: Lu, Xiao-Hong, Yang, X. William
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3513277/
https://ncbi.nlm.nih.gov/pubmed/22726826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2012.06.001
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