His main research concerns Microbiology, Mycobacterium tuberculosis, Biochemistry, Dormancy and Mycobacterium bovis. His work deals with themes such as Bacilli, Bacteria, In vitro and Intracellular, which intersect with Microbiology. The concepts of his Mycobacterium tuberculosis study are interwoven with issues in Multiple drug resistance, Drug resistance, Virology, Immunology and Adenosine triphosphate.
His Immunology study incorporates themes from Clinical disease and Latent tuberculosis. His Biochemistry research includes elements of Nitric oxide and Respiration. His Mycobacterium bovis research is multidisciplinary, relying on both Response regulator, Downregulation and upregulation and Metronidazole.
Thomas Dick focuses on Mycobacterium tuberculosis, Biochemistry, Microbiology, Mutant and Enzyme. His Mycobacterium tuberculosis research incorporates elements of Drug resistance, Pharmacology, Drug discovery and Virology. His Pharmacology study integrates concerns from other disciplines, such as Potency and In vivo.
His Biochemistry study typically links adjacent topics like Mycobacterium. His research in Microbiology intersects with topics in Bacilli, Bacteria, Mycobacterium bovis and Mycobacterium abscessus. ATP synthase is the focus of his Enzyme research.
Thomas Dick mostly deals with Biochemistry, Mycobacterium tuberculosis, Mutant, ATP synthase and Mycobacterium abscessus. The study incorporates disciplines such as In vitro, Mechanism of action and Drug tolerance in addition to Mycobacterium tuberculosis. His Mutant study combines topics in areas such as Moiety, Docking, Recombinant DNA and Drug discovery.
He has researched ATP synthase in several fields, including ATP hydrolysis, Oxidative phosphorylation, Protein subunit, Cell biology and Bedaquiline. The various areas that he examines in his Mycobacterium abscessus study include Clarithromycin, Antibiotics, Rifabutin and Microbiology. When carried out as part of a general Microbiology research project, his work on Drug resistance and Multiple drug resistance is frequently linked to work in Genetic association, therefore connecting diverse disciplines of study.
Thomas Dick spends much of his time researching Mycobacterium tuberculosis, Biochemistry, ATP synthase, Binding site and Drug resistance. His Mycobacterium tuberculosis study combines topics from a wide range of disciplines, such as Mechanism of action, In vitro, Cytotoxicity, Drug tolerance and Coenzyme A. His research on In vitro often connects related topics like Microbiology.
His research in ATP synthase focuses on subjects like Protein subunit, which are connected to ATP hydrolysis, Mutagenesis, Amino acid, Protein Data Bank and Stereochemistry. His biological study spans a wide range of topics, including Allosteric regulation and Enzyme. His Drug resistance research also works with subjects such as
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The spectrum of latent tuberculosis: rethinking the biology and intervention strategies
Clifton E. Barry;Helena I. Boshoff;Véronique Dartois;Thomas Dick.
Nature Reviews Microbiology (2009)
The protonmotive force is required for maintaining ATP homeostasis and viability of hypoxic, nonreplicating Mycobacterium tuberculosis
Srinivasa P. S. Rao;Sylvie Alonso;Lucinda Rand;Lucinda Rand;Thomas Dick.
Proceedings of the National Academy of Sciences of the United States of America (2008)
Identification of a nitroimidazo-oxazine-specific protein involved in PA-824 resistance in Mycobacterium tuberculosis
Ujjini H. Manjunatha;Helena Boshoff;Cynthia S. Dowd;Liang Zhang.
Proceedings of the National Academy of Sciences of the United States of America (2006)
Mycobacterium bovis BCG Response Regulator Essential for Hypoxic Dormancy
Calvin Boon;Thomas Dick.
Journal of Bacteriology (2002)
A chemical genetic screen in Mycobacterium tuberculosis identifies carbon-source-dependent growth inhibitors devoid of in vivo efficacy
Kevin Pethe;Patricia C. Sequeira;Sanjay Agarwalla;Kyu Rhee.
Nature Communications (2010)
Nutrient-starved, non-replicating Mycobacterium tuberculosis requires respiration, ATP synthase and isocitrate lyase for maintenance of ATP homeostasis and viability.
Martin Gengenbacher;Srinivasa P. S. Rao;Kevin Pethe;Thomas Dick.
Cytoplasmic dynein (ddlc1) mutations cause morphogenetic defects and apoptotic cell death in Drosophila melanogaster.
Thomas Dick;Krishanu Ray;Helen K. Salz;William Chia.
Molecular and Cellular Biology (1996)
Oxygen depletion induced dormancy in Mycobacterium smegmatis
Thomas Dick;Boon Heng Lee;Bernadette Murugasu-Oei.
Fems Microbiology Letters (1998)
Comprehensive analysis of methods used for the evaluation of compounds against Mycobacterium tuberculosis
Scott G. Franzblau;Mary Ann DeGroote;Sang Hyun Cho;Koen Andries.
Para-aminosalicylic acid is a prodrug targeting dihydrofolate reductase in Mycobacterium tuberculosis
Jun Zheng;Eric J. Rubin;Pablo Bifani;Vanessa Mathys.
Journal of Biological Chemistry (2013)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: