Joseph Asante
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Postdoctoral Research Associate
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Joseph Asante Jnr's research investigates the intersection of drug transport mechanisms, specifically P-glycoprotein substrates, and their association with Alzheimer's disease risk. His work explores how these substrates may impact the transendothelial transport of amyloid-beta peptides, a key factor in Alzheimer's pathology. Asante Jnr has also examined the potential of ezetimibe in reducing Alzheimer's risk by inhibiting specific protein interactions involved in aggregation. His research extends to predictive modeling of viral protein mutations, with publications focusing on the structural and functional impacts of SARS-CoV-2 spike protein mutations. Collaborating with researchers at the University of Arkansas for Medical Sciences, including Steven W. Barger and Corey Nagel, Asante Jnr has contributed to studies on neurological disorders and disease mechanisms. His scholarship metrics include an h-index of 3, with 6 total publications and 26 citations.
Metrics
- h-index: 3
- Publications: 7
- Citations: 28
Positions
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Postdoctoral Research Associate 2024–presentUniversity of Arkansas for Medical Sciences Geriatrics ORCID
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Postdoctoral Research Associate publications 2024–2026University of Arkansas at Little Rock ORCID
Selected Publications
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Impact of P-glycoprotein substrates on transendothelial transport of amyloid-β peptide in an in vitro model (2026)
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Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics (2025)
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Impact of P-Glycoprotein Substrates on Transendothelial Transport of Amyloid-β Peptide (2025)
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Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics (2025)
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Prescription-based association of P-glycoprotein substrates with Alzheimer's disease risk: A nested case-control study (2025)
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P-glycoprotein and Alzheimer’s Disease: Threats and Opportunities (2025)
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Ezetimibe Lowers Risk of Alzheimer’s and Related Dementias over Sevenfold, Reducing Aggregation in Model Systems by Inhibiting 14-3-3G::Hexokinase Interaction (2024)
Collaboration Network
Top Collaborators
- P-glycoprotein and Alzheimer’s Disease: Threats and Opportunities
- Prescription-based association of P-glycoprotein substrates with Alzheimer's disease risk: A nested case-control study
- Impact of P-Glycoprotein Substrates on Transendothelial Transport of Amyloid-β Peptide
- Impact of P-glycoprotein substrates on transendothelial transport of amyloid-β peptide in an in vitro model
- Ezetimibe Lowers Risk of Alzheimer’s and Related Dementias over Sevenfold, Reducing Aggregation in Model Systems by Inhibiting 14-3-3G::Hexokinase Interaction
- Prescription-based association of P-glycoprotein substrates with Alzheimer's disease risk: A nested case-control study
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Correction: Structural and Functional Impacts of SARS-CoV-2 Spike Protein Mutations: Insights From Predictive Modeling and Analytics
- Ezetimibe Lowers Risk of Alzheimer’s and Related Dementias over Sevenfold, Reducing Aggregation in Model Systems by Inhibiting 14-3-3G::Hexokinase Interaction
- Ezetimibe Lowers Risk of Alzheimer’s and Related Dementias over Sevenfold, Reducing Aggregation in Model Systems by Inhibiting 14-3-3G::Hexokinase Interaction
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