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Biography and Research Information
OverviewAI-generated summary
Amanda L. Dragan's research focuses on host-pathogen interactions, particularly concerning the bacterium *Coxiella burnetii*, the causative agent of Q fever. Her work investigates how this pathogen invades host cells and elicits inflammatory responses. Dr. Dragan has explored the potential of targeting neurotransmitter systems with drugs to inhibit *Coxiella burnetii* growth in human cells, as well as examining distinct inflammatory reactions produced by different strains of the bacterium in human macrophages. She has also contributed to studies utilizing primary human lung tissue models to understand pathogen invasion. Her research interests extend to the development of novel antibacterial agents, including work on the late-stage functionalization of rifamycin derivatives through click chemistry. Dr. Dragan has published six papers and has an h-index of 5 with 158 citations. She collaborates with researchers at the University of Arkansas for Medical Sciences, including Daniel E. Voth and Anette Dragan.
Metrics
- h-index: 5
- Publications: 10
- Citations: 160
Selected Publications
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Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives (2026)
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Coxiella burnetii Strains Elicit Distinct Inflammatory Responses in Human Macrophages (2025)
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<i>Coxiella burnetii</i> strains elicit distinct inflammatory responses in human macrophages (2025)
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Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells (2021)
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Take my breath away: studying pathogen invasion of the human lung using primary tissue models (2021)
Collaboration Network
Top Collaborators
- Take my breath away: studying pathogen invasion of the human lung using primary tissue models
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
- Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives
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