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Huntington disease: update on ongoing therapeutic developments and a look toward the future

dc.contributor.authorSampaio, Cristina
dc.date.accessioned2024-06-21T11:12:18Z
dc.date.available2024-06-21T11:12:18Z
dc.date.issued2024
dc.description© 2024 Published by Elsevier Ltd.pt_PT
dc.description.abstractHuntington’s disease (HD) is a genetic condition inherited in an autosomal dominant pattern characterized by neurodegeneration. The root cause of HD is a CAG tract expansion occurring in exon 1 of the huntingtin (HTT) gene. This mutation sets in motion a series of detrimental events that progressively lead to neuronal death and structural changes, mainly within the central nervous system but also affecting other organs. Currently, no disease-modifying treatments for HD exist, but an active research effort focuses on potential therapies, with several programs in various stages of development. This review provides an overview of the HD targets that have genetic and mechanistic validation and the clinical programs that are pursuing such targets at the time of writing. Programs that are completed or terminated will not be extensively covered. Other therapeutic approaches under development target downstream processes and have potential applicability across various neurodegenerative diseases; a detailed discussion of these therapies is beyond the scope of this review. Cell-based therapies will not be reviewed due to the specificity of the topic. However, there are active programs in the preclinical stage.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationParkinsonism Relat Disord. 2024 May:122:106049pt_PT
dc.identifier.doi10.1016/j.parkreldis.2024.106049pt_PT
dc.identifier.eissn1873-5126
dc.identifier.issn1353-8020
dc.identifier.urihttp://hdl.handle.net/10451/65083
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/journal/parkinsonism-and-related-disorderspt_PT
dc.titleHuntington disease: update on ongoing therapeutic developments and a look toward the futurept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleParkinsonism & Related Disorderspt_PT
oaire.citation.volume122pt_PT
person.familyNameSampaio
person.givenNameCristina
person.identifier.orcid0000-0002-7052-9079
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationcb8e1445-bca9-4565-be74-e23dd4f191c1
relation.isAuthorOfPublication.latestForDiscoverycb8e1445-bca9-4565-be74-e23dd4f191c1

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