miRNA dysregulation in ischaemic stroke: Focus on diagnosis, prognosis, therapeutic and protective biomarkers

dc.contributor.authorVasudeva, K
dc.contributor.authorMunshi, A.
dc.date.accessioned2020-07-16T07:41:58Z
dc.date.accessioned2024-08-14T07:40:38Z
dc.date.available2020-07-16T07:41:58Z
dc.date.available2024-08-14T07:40:38Z
dc.date.issued2020
dc.description.abstractStroke is one of the leading causes of death and disability in both developing and developed countries. Biomarkers for stroke and its outcome can greatly facilitate early detection and management of the disease. miRNAs have been explored for their potential as biomarkers for diagnosis, prognosis and brain injury in ischaemic stroke. A substantial body of evidence suggests that miRNAs play key roles in numerous cellular changes following ischaemic stroke including mitochondrial dysfunction, energy failure, cytokine-mediated cytotoxicity, oxidative stress, activation of glial cells, increased intracellular calcium levels inflammatory responses and disruption of the blood�brain barrier (BBB). In addition, targeting specific miRNAs, therapeutic modulation of brain injury and apoptosis can also be achieved. Therefore, the current review has been compiled within an aim to give an overview of the developments exploiting miRNAs at different stages of stroke as prognostic, diagnostic, protective and therapeutic biomarkers. � 2020 Federation of European Neuroscience Societies and John Wiley & Sons Ltden_US
dc.identifier.doi10.1111/ejn.14695
dc.identifier.issn0953816X
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/2688
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/abs/10.1111/ejn.14695
dc.language.isoenen_US
dc.publisherBlackwell Publishing Ltden_US
dc.subjectbiomarkeren_US
dc.subjectbrain injuryen_US
dc.subjectmiRNAen_US
dc.subjectmRNAen_US
dc.subjectstrokeen_US
dc.titlemiRNA dysregulation in ischaemic stroke: Focus on diagnosis, prognosis, therapeutic and protective biomarkersen_US
dc.title.journalEuropean Journal of Neuroscienceen_US
dc.typeReviewen_US
dc.type.accesstypeClosed Accessen_US

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