Tanya Parish

Professor

Washington University School of Medicine

United States

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Tanya Parish is a Professor at the University of Washington School of Medicine, USA. Her research primarily focuses on Mycobacterium tuberculosis, particularly in the development of novel therapeutic agents targeting various bacterial mechanisms. She has published extensively on inhibitors of MmpL3, DNA Gyrase, and other pathways pertinent to tuberculosis treatment.

Tanya Parish

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Articles (19)

Thienopyrimidine amide analogs target MmpL3 in Mycobacterium tuberculosis

Common Biological Properties of Mycobacterium tuberculosis MmpL3 Inhibitors

Structure–Activity Relationship Study of Benzamides as Mycobacterium tuberculosis QcrB Inhibitors

New Triazolopyrimidines with Improved Activity against Mycobacterium tuberculosis

Novel 3-Aminothieno[2,3-b]pyridine-2-carboxamides with Activity against Mycobacterium tuberculosis

Deep learning–driven bacterial cytological profiling to determine antimicrobial mechanisms in Mycobacterium tuberculosis

Structural Aspects of Mycobacterium tuberculosis DNA Gyrase Targeted by Novel Bacterial Topoisomerase Inhibitors

An arylsulfonamide that targets cell wall biosynthesis in Mycobacterium tuberculosis

8-Hydroxyquinoline Series Exerts Bactericidal Activity against Mycobacterium tuberculosis Via Copper-Mediated Toxicity

Benzene Amide Ether Scaffold is Active against Non-replicating and Intracellular Mycobacterium tuberculosis

Inoculum-dependent bactericidal activity of a Mycobacterium tuberculosis MmpL3 inhibitor

Identification of 2-Amino Benzothiazoles with Bactericidal Activity against Mycobacterium tuberculosis

Rv0233 is not essential for the survival of Mycobacterium tuberculosis in stress conditions

Evaluation of 3-Deoxy-D-Arabino-Heptulosonate 7-Phosphate Synthase (DAHPS) as a Vulnerable Target in Mycobacterium tuberculosis

Correction for Shelton et al., “Deletion of Rv2571c Confers Resistance to Arylamide Compounds in Mycobacterium tuberculosis”

The driving force for mycolic acid export by mycobacterial MmpL3 is proton translocation

Chemical Exploration of a Highly Selective Scaffold with Activity against Intracellular Mycobacterium tuberculosis

Triazolopyrimidines Target Aerobic Respiration in Mycobacterium tuberculosis

Novel C-3-(N-alkyl-aryl)-aminomethyl rifamycin SV derivatives exhibit activity against rifampicin-resistant Mycobacterium tuberculosis RpoBS522L strain and display a different binding mode at the RNAP β-subunit site compared to rifampicin

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Jo-Ann Jee

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