scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1051372330 |
P356 | DOI | 10.1186/1471-2180-9-69 |
P932 | PMC publication ID | 2670838 |
P698 | PubMed publication ID | 19364397 |
P5875 | ResearchGate publication ID | 24275663 |
P50 | author | Rebeca Santiso | Q60608102 |
Jaime María de Berenguer de Santiago | Q64590457 | ||
José L Fernández | Q42454842 | ||
German Bou | Q42555605 | ||
P2093 | author name string | Jaime Gosalvez | |
María Tamayo | |||
P2860 | cites work | Lethal fragmentation of bacterial chromosomes mediated by DNA gyrase and quinolones. | Q54462457 |
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Genetic analysis of the requirements for SOS induction by nalidixic acid in Escherichia coli | Q33218546 | ||
Cell division in Escherichia coli cultures monitored at single cell resolution | Q33330202 | ||
Incision of DNA-protein crosslinks by UvrABC nuclease suggests a potential repair pathway involving nucleotide excision repair | Q34011521 | ||
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Quorum sensing and multidrug transporters in Escherichia coli | Q34478849 | ||
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Structure, molecular mechanisms, and evolutionary relationships in DNA topoisomerases | Q35771555 | ||
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Quinolone-mediated bacterial death. | Q36921143 | ||
Bactericidal activities of five quinolones for Escherichia coli strains with mutations in genes encoding the SOS response or cell division | Q39871693 | ||
DNA gyrase on the bacterial chromosome: DNA cleavage induced by oxolinic acid | Q40260992 | ||
Transcription regulates oxolinic acid-induced DNA gyrase cleavage at specific sites on the E. coli chromosome | Q40527610 | ||
Fundamental structural units of the Escherichia coli nucleoid revealed by atomic force microscopy | Q40773408 | ||
Repair of DNA double-strand breaks in Escherichia coli, which requires recA function and the presence of a duplicate genome | Q40840136 | ||
Mycobacterial nonhomologous end joining mediates mutagenic repair of chromosomal double-strand DNA breaks | Q42078607 | ||
DNA fragmentation in microorganisms assessed in situ. | Q42134359 | ||
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Fluoroquinolone-modifying enzyme: a new adaptation of a common aminoglycoside acetyltransferase | Q46862305 | ||
Nucleotide excision repair and homologous recombination systems commit differentially to the repair of DNA-protein crosslinks. | Q46950735 | ||
Quinolone resistance from a transferable plasmid. | Q54143628 | ||
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 69 | |
P577 | publication date | 2009-04-13 | |
P1433 | published in | BMC Microbiology | Q15759430 |
P1476 | title | Rapid assessment of the effect of ciprofloxacin on chromosomal DNA from Escherichia coli using an in situ DNA fragmentation assay | |
P478 | volume | 9 |
Q34002949 | A rapid in situ procedure for determination of bacterial susceptibility or resistance to antibiotics that inhibit peptidoglycan biosynthesis |
Q50545461 | Bacteriostatic versus bactericidal activity of ciprofloxacin in Escherichia coli assessed by flow cytometry using a novel far-red dye. |
Q57657398 | Cell wall active antibiotics reduce chromosomal DNA fragmentation by peptidoglycan hydrolysis in Staphylococcus aureus |
Q34604406 | Comparative transcription analysis and toxin production of two fluoroquinolone-resistant mutants of Clostridium perfringens |
Q38682369 | Escherichia coli DNA ligase B may mitigate damage from oxidative stress. |
Q41580320 | Fast assessment of resistance to carbapenems and ciprofloxacin of clinical strains of Acinetobacter baumannii |
Q90455912 | Genome-wide assessment of antimicrobial tolerance in Yersinia pseudotuberculosis under ciprofloxacin stress |
Q33797306 | Gyramides prevent bacterial growth by inhibiting DNA gyrase and altering chromosome topology |
Q90114640 | Microbial Metabolism Modulates Antibiotic Susceptibility within the Murine Gut Microbiome |
Q54237618 | Our Evolving Understanding of the Mechanism of Quinolones. |
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Q21144990 | SOS response induces persistence to fluoroquinolones in Escherichia coli |
Q90029135 | Stochastic Gene Expression Influences the Selection of Antibiotic Resistance Mutations |
Q92430058 | Watching DNA Replication Inhibitors in Action: Exploiting Time-Lapse Microfluidic Microscopy as a Tool for Target-Drug Interaction Studies in Mycobacterium |
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