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Cloning and nucleotide sequence of the Campylobacter jejuni gyrA gene and characterization of quinolone resistance mutations.
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Bactericidal activities of single or multiple doses of various combinations of new antileprosy drugs and/or rifampin against M. leprae in mice.
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Mechanisms of resistance to quinolones.
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Nalidixic acid resistance: a second genetic character involved in DNA gyrase activity.
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Selection of a gyrA mutant of Mycobacterium tuberculosis resistant to fluoroquinolones during treatment with ofloxacin.
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Cloning and nucleotide sequence of Pseudomonas aeruginosa DNA gyrase gyrA gene from strain PAO1 and quinolone-resistant clinical isolates.
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Characterization of mutations in Mycobacterium smegmatis involved in resistance to fluoroquinolones.
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Cloning and characterization of a DNA gyrase A gene from Escherichia coli that confers clinical resistance to 4-quinolones.
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The division between fast- and slow-growing species corresponds to natural relationships among the mycobacteria.
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A rapid method for the detection of potentially viable Mycobacterium leprae in human biopsies: a novel application of PCR.
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Permeability barrier to hydrophilic solutes in Mycobacterium chelonei.
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Activities of ciprofloxacin and ofloxacin against rapidly growing mycobacteria with demonstration of acquired resistance following single-drug therapy.
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DNA cloning and organization of the Staphylococcus aureus gyrA and gyrB genes: close homology among gyrase proteins and implications for 4-quinolone action and resistance.
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Quinolone resistance-determining region in the DNA gyrase gyrA gene of Escherichia coli.
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DNA gyrase gyrA mutations in ciprofloxacin-resistant strains of Staphylococcus aureus: close similarity with quinolone resistance mutations in Escherichia coli.
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Differentiation of Mycobacterium species by direct sequencing of amplified DNA.
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Isolation and characterization of efficient plasmid transformation mutants of Mycobacterium smegmatis.
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Occurrence and stability of insertion sequences in Mycobacterium tuberculosis complex strains: evaluation of an insertion sequence-dependent DNA polymorphism as a tool in the epidemiology of tuberculosis.
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