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Delivering a disease-modifying treatment for Huntington’s disease

dc.contributor.authorGodinho, Bruno M. C.
dc.contributor.authorMalhotra, Meenakshi
dc.contributor.authorO’Driscoll, Caitriona M.
dc.contributor.authorCryan, John F.
dc.date.accessioned2014-10-03T12:39:39Z
dc.date.available2014-10-03T12:39:39Z
dc.date.issued2015-01
dc.description.abstractHuntington's disease (HD) is an incurable genetic neurodegenerative disorder that leads to motor and cognitive decline. It is caused by an expanded polyglutamine tract within the Huntingtin (HTT) gene, which translates into a toxic mutant HTT protein. Although no cure has yet been discovered, novel therapeutic strategies, such as RNA interference (RNAi), antisense oligonucleotides (ASO), ribozymes, DNA enzymes, and genome-editing approaches, aimed at silencing or repairing the mutant HTT gene hold great promise. Indeed, several preclinical studies have demonstrated the utility of such strategies to improve HD neuropathology and symptoms. In this review, we critically summarise the main advances and limitations of each gene-silencing technology as an effective therapeutic tool for the treatment of HD.por
dc.identifier.citationGodinho BM, Malhotra M, O’Driscoll CM, Cryan JF. Delivering a disease-modifying treatment for Huntington’s disease. Drug Discov Today. 2015;20(1):50-64.por
dc.identifier.doi10.1016/j.drudis.2014.09.011
dc.identifier.urihttp://hdl.handle.net/10400.21/3848
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S1359644614003778#por
dc.subjectHuntington's diseasepor
dc.subjectNeurodegenerative disorderpor
dc.subjectHuntingtin genepor
dc.subjectRNA interferencepor
dc.subjectDNA enzymespor
dc.titleDelivering a disease-modifying treatment for Huntington’s diseasepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleDrug Discovery Todaypor
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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