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dc.contributor.authorSekar, Durairaj
dc.contributor.authorTusubira, Deusdedit
dc.contributor.authorRoss, Kehinde
dc.date.accessioned2023-08-22T08:48:37Z
dc.date.available2023-08-22T08:48:37Z
dc.date.issued2022
dc.identifier.citationSekar, D., Tusubira, D., & Ross, K. (2022). Corrigendum: TDP-43 and NEAT long non-coding RNA: Roles in neurodegenerative disease. Frontiers in Cellular Neuroscience, 16.en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/3086
dc.description.abstract“Understanding and ameliorating neurodegenerative diseases represents a key challenge for supporting the health span of the aging population. Diverse protein aggregates have been implicated in such neurodegenerative disorders, including amyloid-b, a-synuclein, tau, fused in sarcoma (FUS), and transactivation response element (TAR) DNA-binding protein 43 (TDP-43). Recent years have seen significant growth in our mechanistic knowledge of relationships between these proteins and some of the membrane-less nuclear structures that fulfill key roles in the cell function. These include the nucleolus, nuclear speckles, and paraspecklesen_US
dc.language.isoen_USen_US
dc.publisherFrontiers in Cellular Neuroscienceen_US
dc.subjectTDP-43en_US
dc.subjectLong non-coding RNAen_US
dc.subjectNEAT1en_US
dc.subjectNeuronsen_US
dc.subjectParaspecklesen_US
dc.subjectTAR DNA-binding protein 43en_US
dc.subjectNucleic acid therapiesen_US
dc.subjectSwimming microrobotsen_US
dc.titleCorrigendum: TDP-43 and NEAT long non-coding RNA: Roles in neurodegenerative diseaseen_US
dc.typeArticleen_US


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