ZJ
Ziyi Jia
University of Minnesota System, Yale University, University of Minnesota
Research areas: Medicine · Infectious Diseases · Tuberculosis Research and Epidemiology · Computational Drug Discovery Methods · Microbial Natural Products and Biosynthesis
Employment
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University of Minnesota Research Support, Research Professional 22024 - 2026
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University of Minnesota Research Support, Researcher2024 - 2024
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University of Minnesota Research Support, Researcher2021 - 2024
Education
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Yale University PhD student2026 - 2032
Projects & Funding
Projects & funding information is unavailable.
Publications (15)
- Integrative computational approaches, molecular docking, and dynamic simulations reveal the antimycobacterial activity of fisetin as a potential inhibitor of Mycobacterium tuberculosis Save
- trans-Translation inhibitors that kill Mycobacterium tuberculosis and pathogenic non-tuberculous mycobacteria also disrupt metal homeostasis Save
- Metal–Ligand Interactions Save
- Essential role of MHC II in the antitubercular efficacy of pyrazinamide Save
- Essential role of MHC II in the antitubercular efficacy of pyrazinamide Save
- In vitro investigation of Datura innoxia phytocompounds against Mycobacterium tuberculosis H37Ra strain in association with in silico studies Save
- Essential Role of MHC II in the Antitubercular Efficacy of Pyrazinamide Save
- Discovery of antitubercular potential of trans-3-indoleacrylic acid and its derivatives targeting Mycobacterium tuberculosis Save
- Mechanism of the dual action self-potentiating antitubercular drug morphazinamide Save
- A trans-Translation Inhibitor is Potentiated by Zinc and Kills Mycobacterium tuberculosis and Nontuberculous Mycobacteria Save
- Identification of Datura innoxia as a potential source of antimycobacterial components Save
- Atrans-translation inhibitor is potentiated by zinc and killsMycobacterium tuberculosisand non-tuberculous mycobacteria Save
- Mechanism of the Dual Action Self-Potentiating Antitubercular Drug Morphazinamide Save
- A Nucleophilic Activity‐Based Probe Enables Profiling of PLP‐Dependent Enzymes Save
- Synthesis and biological evaluation of orally active prodrugs and analogs of para-aminosalicylic acid (PAS) Save