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Researcher at Research Department
Ask questions about Kaiyue Zhao's research, publications, and ongoing work
Identified the implications of miR-148a-3p/p35/PTEN signaling in tau hyperphosphorylation and autoregulatory feedforward of Akt/CREB in Alzheimer’s disease, suggesting potential therapeutic targets.
Demonstrated that Tilianin improves cognitive function and reduces neuronal damage in a rat model of vascular dementia through p-CaMKII/ERK/CREB and ox-CaMKII-dependent MAPK/NF-κB pathways.
Showed that miR-30a-5p induces amyloid-beta (Aβ) production by inhibiting the nonamyloidogenic pathway in Alzheimer’s disease, contributing to the understanding of disease mechanisms.
Discovered that the miR-25802/KLF4/NF-κB signaling axis regulates microglia-mediated neuroinflammation in Alzheimer’s disease, highlighting a potential target for therapeutic intervention.
Revealed that Tilianin improves cognition in a vascular dementia rodent model by targeting miR-193b-3p/CaM- and miR-152-3p/CaMKIIα-mediated inflammatory and apoptotic pathways.
Explored the role of traditional Chinese medicine in ameliorating mitochondrial dysfunction via non-coding RNA signaling, with implications for treating neurodegenerative diseases.
Demonstrated that long noncoding RNA GAS5 acts as a competitive endogenous RNA to regulate GSK-3β and PTEN expression by sponging miR-23b-3p in Alzheimer’s disease.
Kaiyue Zhao investigates the roles of non-coding RNAs, particularly microRNAs and circular RNAs, in the pathogenesis of neurological diseases such as Alzheimer's disease and vascular dementia, seeking novel therapeutic targets. Her research explores molecular mechanisms and potential treatments using both in vitro and in vivo models.
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