Biography and Research Information
OverviewAI-generated summary
Ananya Ranaraja's research focuses on the immune system's role in combating infectious diseases, particularly tuberculosis. Their work investigates how different types of immune cells, such as neutrophils and macrophages, respond to and influence the progression of Mycobacterium tuberculosis infections. Recent publications explore the metabolic activity of neutrophils as a potential niche for the bacteria and how monocyte-derived alveolar macrophages, induced by β-glucan, contribute to protection against infection. Additionally, their research examines the function of fatty acid oxidation in maintaining alveolar macrophage health and resistance to pathogens. Ranaraja has published three papers, accumulating 28 citations, and holds an h-index of 1. They have collaborated with researchers including J. Tucker Andrews and Lin‐Xi Li at the University of Arkansas for Medical Sciences.
Metrics
- h-index: 1
- Publications: 3
- Citations: 30
Selected Publications
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β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395 (2025)
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Fatty acid oxidation regulates alveolar macrophage homeostasis and resistance to infection 4350 (2025)
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Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis (2024)
Collaboration Network
Top Collaborators
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Fatty acid oxidation regulates alveolar macrophage homeostasis and resistance to infection 4350
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Fatty acid oxidation regulates alveolar macrophage homeostasis and resistance to infection 4350
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
- Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
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