Jordan T. Bird
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Instructor
Also affiliated: Arkansas Children's Hospital (2021–2025); Battelle (2024–2026); Knoxville College (2016); University of Tennessee at Knoxville (2015–2020)
Faculty Researcher
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Jordan T. Bird's research investigates host-pathogen interactions, focusing on the cellular and molecular mechanisms underlying infectious diseases. Recent work includes an in vivo transcriptional analysis of mice infected with *Leishmania major*, employing single-cell resolution to reveal cellular heterogeneity and altered transcriptomic profiles. Bird has also explored differences in cell death pathways related to nutrient depletion in cancer cells, specifically examining methionine dependence in melanoma. Further research interests encompass the development and application of computational tools for biological data analysis, such as the proteoDA package for quantitative proteomics. Bird's scholarly output is reflected in an h-index of 19 with over 1,930 citations across 56 publications. Key collaborators at the University of Arkansas for Medical Sciences include Stephanie D. Byrum, Tiffany Weinkopff, Hayden Roys, and Anne K. Bowlin, with whom Bird has co-authored multiple publications.
Metrics
- h-index: 19
- Publications: 56
- Citations: 1,959
Selected Publications
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Guanylate-binding proteins balance iNOS/Arg-1 in myeloid cells during <i>L. major</i> infection and promote host defense to infection (2026)
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Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis 4267 (2025)
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Phage Host Range Expansion Through Directed Evolution on Highly Phage-Resistant Strains of Klebsiella pneumoniae (2025)
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Guanylate-Binding Proteins Promote Host Defense Against <i>Leishmania major</i> by Balancing iNOS/Arg-1 in Myeloid Cells (2025)
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Enhanced Translational Activity Is Linked to Lymphatic Endothelial Cell Activation in Cutaneous Leishmaniasis (2025)
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HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection (2025)
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Complete genome sequences of three <i>Pseudomonas aeruginosa</i> jumbo bacteriophages discovered in Kenya (2024)
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HIF-α signaling regulates the macrophage inflammatory response during <i>Leishmania major</i> infection (2024)
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Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis (2024)
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Genome sequence of the <i>Klebsiella quasipneumoniae</i> bacteriophage EKq1 with activity against <i>Klebsiella pneumoniae</i> (2023)
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Characterization of methionine dependence in melanoma cells (2023)
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Complete genome sequence of the broad host range <i>Acinetobacter baumannii</i> phage EAb13 (2023)
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Genome Sequence of Staphylococcus aureus Phage ESa2 (2023)
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Both the Infection Status and Inflammatory Microenvironment Induce Transcriptional Remodeling in Macrophages in Murine Leishmanial Lesions (2023)
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Characterization of methionine dependence in melanoma cells (2023)
Collaboration Network
Top Collaborators
- Differences in cell death in methionine versus cysteine depletion
- In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- Deficiency of N-glycanase 1 perturbs neurogenesis and cerebral development modeled by human organoids
- Characterization of methionine dependence in melanoma cells
Showing 5 of 16 shared publications
- In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution
- Both the Infection Status and Inflammatory Microenvironment Induce Transcriptional Remodeling in Macrophages in Murine Leishmanial Lesions
- Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis
- In vivo reprogramming of murine host immune response genes following Leishmania major infection
- HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection
Showing 5 of 10 shared publications
- In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution
- Both the Infection Status and Inflammatory Microenvironment Induce Transcriptional Remodeling in Macrophages in Murine Leishmanial Lesions
- Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis
- In vivo reprogramming of murine host immune response genes following Leishmania major infection
- HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection
Showing 5 of 10 shared publications
- In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution
- Both the Infection Status and Inflammatory Microenvironment Induce Transcriptional Remodeling in Macrophages in Murine Leishmanial Lesions
- Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis
- In vivo reprogramming of murine host immune response genes following Leishmania major infection
- HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection
Showing 5 of 10 shared publications
- In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- PHF19 inhibition as a therapeutic target in multiple myeloma
- In vivo reprogramming of murine host immune response genes following Leishmania major infection
- HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection
Showing 5 of 8 shared publications
- In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution
- Both the Infection Status and Inflammatory Microenvironment Induce Transcriptional Remodeling in Macrophages in Murine Leishmanial Lesions
- Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis
- In vivo reprogramming of murine host immune response genes following Leishmania major infection
- HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection
Showing 5 of 8 shared publications
- Both the Infection Status and Inflammatory Microenvironment Induce Transcriptional Remodeling in Macrophages in Murine Leishmanial Lesions
- Enhanced translational activity is linked to lymphatic endothelial cell activation in cutaneous leishmaniasis
- HIF-α signaling regulates the macrophage inflammatory response during Leishmania major infection
- Enhanced Translational Activity Is Linked to Lymphatic Endothelial Cell Activation in Cutaneous Leishmaniasis
- HIF-α signaling regulates the macrophage inflammatory response during <i>Leishmania major</i> infection
Showing 5 of 8 shared publications
- Complete genome sequence of the broad host range <i>Acinetobacter baumannii</i> phage EAb13
- Genome sequence of the <i>Klebsiella quasipneumoniae</i> bacteriophage EKq1 with activity against <i>Klebsiella pneumoniae</i>
- Complete genome sequences of three <i>Pseudomonas aeruginosa</i> jumbo bacteriophages discovered in Kenya
- Genome Sequence of Staphylococcus aureus Phage ESa2
- Phage Host Range Expansion Through Directed Evolution on Highly Phage-Resistant Strains of Klebsiella pneumoniae
- Complete genome sequence of the broad host range <i>Acinetobacter baumannii</i> phage EAb13
- Genome sequence of the <i>Klebsiella quasipneumoniae</i> bacteriophage EKq1 with activity against <i>Klebsiella pneumoniae</i>
- Complete genome sequences of three <i>Pseudomonas aeruginosa</i> jumbo bacteriophages discovered in Kenya
- Genome Sequence of Staphylococcus aureus Phage ESa2
- Phage Host Range Expansion Through Directed Evolution on Highly Phage-Resistant Strains of Klebsiella pneumoniae
- Complete genome sequence of the broad host range <i>Acinetobacter baumannii</i> phage EAb13
- Genome sequence of the <i>Klebsiella quasipneumoniae</i> bacteriophage EKq1 with activity against <i>Klebsiella pneumoniae</i>
- Complete genome sequences of three <i>Pseudomonas aeruginosa</i> jumbo bacteriophages discovered in Kenya
- Genome Sequence of Staphylococcus aureus Phage ESa2
- Phage Host Range Expansion Through Directed Evolution on Highly Phage-Resistant Strains of Klebsiella pneumoniae
- Differences in cell death in methionine versus cysteine depletion
- Characterization of methionine dependence in melanoma cells
- Characterization of methionine dependence in melanoma cells
- Differences in cell death in methionine versus cysteine depletion
- Characterization of methionine dependence in melanoma cells
- Characterization of methionine dependence in melanoma cells
- Characterization of methionine dependence in melanoma cells
- PHF19 inhibition as a therapeutic target in multiple myeloma
- Characterization of methionine dependence in melanoma cells
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- Characterization of methionine dependence in melanoma cells
- Characterization of methionine dependence in melanoma cells
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- Characterization of methionine dependence in melanoma cells
- Characterization of methionine dependence in melanoma cells
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