Biochemistry, Efflux, Genetics, Microbiology and Divalent are her primary areas of study. Protein structure, Multiple drug resistance, Transcription, Amino acid and Gene are subfields of Biochemistry in which her conducts study. Her Efflux study integrates concerns from other disciplines, such as Antiporters, Antiporter, Major facilitator superfamily, Repressor and Drug resistance.
Her Antiporters study also includes fields such as
Her scientific interests lie mostly in Microbiology, Biochemistry, Efflux, Staphylococcus aureus and Bacteria. Her Microbiology research includes themes of Gene and Virulence. Her Peptide sequence, Major facilitator superfamily, Transport protein, Protein structure and Transmembrane domain study are her primary interests in Biochemistry.
Her Efflux study combines topics from a wide range of disciplines, such as Multiple drug resistance, Membrane transport protein, Transporter and Escherichia coli. The Staphylococcus aureus study combines topics in areas such as Plasmid, Transcription factor, Cell membrane, Membrane fluidity and In silico. Her research in Bacteria intersects with topics in Antimicrobial, Gram-negative bacteria and Peptide.
Melissa H. Brown focuses on Microbiology, Acinetobacter baumannii, Efflux, Gene and Antibiotic resistance. Her Microbiology research is multidisciplinary, incorporating elements of Staphylococcus aureus, Bacteria and Virulence. Efflux is a subfield of Biochemistry that she studies.
Many of her research projects under Biochemistry are closely connected to Immunoassay and Cyclic nucleotide with Immunoassay and Cyclic nucleotide, tying the diverse disciplines of science together. Her work on Homology as part of general Gene research is frequently linked to Oral cavity, bridging the gap between disciplines. Her Antibiotic resistance research is multidisciplinary, incorporating perspectives in Multiple drug resistance, Isolation, Outbreak, Transmission and Staphylococcus.
Her primary scientific interests are in Microbiology, Acinetobacter baumannii, Efflux, Virulence and Ecology. Her Microbiology study frequently draws connections to other fields, such as Genetics. Her Efflux study is concerned with the larger field of Biochemistry.
Her work on Cell, Multiple drug resistance and Transporter as part of general Biochemistry study is frequently linked to Energy source, therefore connecting diverse disciplines of science. In the subject of general Ecology, her work in Ecosystem, Abundance, Phytoplankton and Salinity is often linked to Aquifer, thereby combining diverse domains of study. Her Membrane transport protein research integrates issues from Hypothetical protein and Escherichia coli.
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.
Proton-dependent multidrug efflux systems.
Ian T. Paulsen;Melissa H. Brown;Ronald A. Skurray.
Microbiological Research (1996)
Regulation of Bacterial Drug Export Systems
Steve Grkovic;Melissa H. Brown;Ronald A. Skurray.
Microbiology and Molecular Biology Reviews (2002)
The multidrug efflux protein NorM is a prototype of a new family of transporters
Melissa H. Brown;Ian T. Paulsen;Ronald A. Skurray.
Molecular Microbiology (1999)
Structural Mechanisms of QacR Induction and Multidrug Recognition
Maria A. Schumacher;Marshall C. Miller;Steve Grkovic;Melissa H. Brown.
Science (2001)
Cationic bactericidal peptides.
R.E.W. Hancock;T. Falla;M. Brown.
Advances in Microbial Physiology (1995)
Multidrug resistance proteins QacA and QacB from Staphylococcus aureus: membrane topology and identification of residues involved in substrate specificity.
I T Paulsen;M H Brown;T G Littlejohn;B A Mitchell.
Proceedings of the National Academy of Sciences of the United States of America (1996)
Recombinant DNA procedures for producing small antimicrobial cationic peptides in bacteria
Kevin L. Piers;Melissa H. Brown;Robert E.W. Hancock.
Gene (1993)
Structural basis for cooperative DNA binding by two dimers of the multidrug-binding protein QacR
Maria A. Schumacher;Marshall C. Miller;Steve Grkovic;Melissa H. Brown.
The EMBO Journal (2002)
QacR is a repressor protein that regulates expression of the Staphylococcus aureus multidrug efflux pump QacA.
Steve Grkovic;Melissa H. Brown;Natalie J. Roberts;Ian T. Paulsen.
Journal of Biological Chemistry (1998)
Investigation of the human pathogen Acinetobacter baumannii under iron limiting conditions
Bart A Eijkelkamp;Karl A Hassan;Ian T Paulsen;Melissa H Brown.
BMC Genomics (2011)
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