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An overview of the clinical application of antisense oligonucleotides for RNA-targeting therapies.
McClorey, Graham; Wood, Matthew J.
Afiliación
  • McClorey G; Department of Physiology, Anatomy and Genetics, University of Oxford, South Parks Road, OX1 3QX Oxford, UK.
  • Wood MJ; Department of Physiology, Anatomy and Genetics, University of Oxford, South Parks Road, OX1 3QX Oxford, UK. Electronic address: matthew.wood@dpag.ox.ac.uk.
Curr Opin Pharmacol ; 24: 52-8, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26277332
Despite the discovery more than two decades ago that antisense oligonucleotides (ASOs) could be used to modulate protein expression, there have been only two antisense drugs approved for clinical use till date. Despite this low success rate, the antisense field is undergoing resurgence due to the development of more potent and nuclease resistant chemistries, as well as nanoparticle delivery systems that enhance delivery to target tissues. In this review, we introduce the predominant therapeutic strategies in the antisense field whilst highlighting recent clinical findings that demonstrate the significant potential of these approaches for development of novel therapies in several diseases.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ARN / Oligonucleótidos Antisentido Límite: Animals / Humans Idioma: En Revista: Curr Opin Pharmacol Asunto de la revista: FARMACOLOGIA Año: 2015 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ARN / Oligonucleótidos Antisentido Límite: Animals / Humans Idioma: En Revista: Curr Opin Pharmacol Asunto de la revista: FARMACOLOGIA Año: 2015 Tipo del documento: Article