the journal of infection

[1] Prevalence, sequence type, and quinolone resistance of Neisseria lactamica carried in children younger than 15 years in Shanghai, China.

[2] the inactivation of rnase g reduces the stenotrophomonas maltophilia susceptibility to quinolones by triggering the heat shock response.

[3] genetic background and expression of the new qepa4 gene variant recovered in clinical tem-1- and cmy-2-producing escherichia coli

[4] gyrA and parC associated with quinolone resistance in Vibrio anguillarum

[5] Quinolone resistance mechanisms among third-generation cephalosporin resistant isolates of Enterobacter spp. in a Bulgarian university hospital

[6] Investigation of six plasmid-mediated quinolone resistance genes among clinical isolates of pseudomonas: a genotypic study in Saudi Arabia

[7] The prevalence of plasmid-mediated quinolone resistance and ESBL-production in Enterobacteriaceae isolated from urinary tract infections

[8] Overview of the development of quinolone resistance in Salmonella species in China, 2005–2016

[9] Quinolone resistance mechanisms among third-generation cephalosporin resistant isolates of Enterobacter spp. in a Bulgarian university hospital

[10] Quinolone resistance mechanisms among third-generation cephalosporin resistant isolates of Enterobacter spp. in a Bulgarian university hospital

[11] Investigation of six plasmid-mediated quinolone resistance genes among clinical isolates of pseudomonas: a genotypic study in Saudi Arabia

[12] The prevalence of plasmid-mediated quinolone resistance and ESBL-production in Enterobacteriaceae isolated from urinary tract infections

[13] Overview of the development of quinolone resistance in Salmonella species in China, 2005–2016

[14] The occurrence of sulfonamide and quinolone resistance genes at the Fildes Peninsula in Antarctica.

[15] Prevalence, sequence type, and quinolone resistance of Neisseria lactamica carried in children younger than 15 years in Shanghai, China.

[16] The tcdA negative and tcdB positive Clostridium difficile ST81 clone exhibits high-level fluoroquinolone resistance: a multi-center study in Beijing, China.

[17] Factors influencing fluoroquinolone resistance

[18] carriage of quinolone resistance in faecal coliforms among healthy individuals: a study from northeast india

[19] fluoroquinolone prophylaxis against febrile neutropenia in areas with high fluoroquinolone resistance—an asian perspective

[20] mutations in the quinolone resistance-determining regions of gyra and parc in enterobacteriaceae isolates from brazil

[21] mutations in gyra & parc genes of shigella flexneri 2a determining the fluoroquinolone resistance

[22] incidence of fluoroquinolone resistance in pseudomonas aeruginosa from urinary tract infections

[23] investigation of plasmid-mediated quinolone resistance in pseudomonas aeruginosa clinical isolates

[24] fluoroquinolone resistance in non-multidrug-resistant tuberculosis—a surveillance study in new south wales, australia, and a review of global resistance rates

[25] characterization of vibrio fluvialis qnrvc5 gene in native and heterologous hosts: synergy of qnrvc5 with other determinants in conferring quinolone resistance

[26] Low-Level Fluoroquinolone Resistance among Campylobacter jejuni Isolates in Australia

[27] The emergence in Taiwan of fluoroquinolone resistance in Salmonella enterica serotype choleraesuis

[28] gyrA and parC associated with quinolone resistance in Vibrio anguillarum

[29] High prevalence of plasmid-mediated quinolone resistance genes qnr and aac(6′)-Ib-cr in clinical isolates of Enterobacteriaceae from nine teaching hospitals in China (Antimicrobial Agents and Chemotheraphy (2008) 52:12 (4268-4273))