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  1. The primary pharmacology of ceftazidime/avibactam: microbiology from clinical studies, and development of resistance during treatment
  2. The primary pharmacology of ceftazidime/avibactam: resistancein vitro
  3. The primary pharmacology of ceftazidime/avibactam: in vitro translational biology
  4. The primary pharmacology of ceftazidime/avibactam: in vivo translational biology and pharmacokinetics/pharmacodynamics (PK/PD)
  5. Evaluation of the post-antibiotic effect in vivo for the combination of a β-lactam antibiotic and a β-lactamase inhibitor: ceftazidime-avibactam in neutropenic mouse thigh and lung infections
  6. Selecting the dosage of ceftazidime–avibactam in the perfect storm of nosocomial pneumonia
  7. A model-based analysis of pharmacokinetic–pharmacodynamic (PK/PD) indices of avibactam against Pseudomonas aeruginosa
  8. Dose Selection and Validation for Ceftazidime-Avibactam in Adults with Complicated Intra-abdominal Infections, Complicated Urinary Tract Infections, and Nosocomial Pneumonia
  9. Loss of activity of ceftazidime-avibactam due to MexAB-OprM efflux and overproduction of AmpC cephalosporinase in Pseudomonas aeruginosa isolated from patients suffering from cystic fibrosis
  10. Selection of mutants with resistance or diminished susceptibility to ceftazidime/avibactam from ESBL- and AmpC-producing Enterobacteriaceae
  11. Ceftazidime-Avibactam Susceptibility Breakpoints againstEnterobacteriaceaeandPseudomonas aeruginosa
  12. Understanding the pharmacodynamics of a clinically-used β-lactamase inhibitor, avibactam
  13. A mathematical model-based analysis of the time–kill kinetics of ceftazidime/avibactam against Pseudomonas aeruginosa
  14. Ceftazidime-avibactam against a KPC-2 β-lactamase producing Klebsiella pneumoniae in vivo
  15. AmpC β-lactamase induction by avibactam and relebactam
  16. Understanding the penetration of potential novel antibiotics into bacteria
  17. The in vitro activity of ceftazidime–avibactam against 417 Gram-negative bacilli collected in 2014 and 2015 at a teaching hospital in São Paulo, Brazil
  18. Impact of defined cell envelope mutations in Escherichia coli on the in vitro antibacterial activity of avibactam/β-lactam combinations
  19. Pharmacodynamics of ceftazidime/avibactam against extracellular and intracellular forms ofPseudomonas aeruginosa
  20. Potentiation of ceftazidime by avibactam against β-lactam-resistantPseudomonas aeruginosain anin vitroinfection model
  21. Inhibitory activity of avibactam against selected β-lactamases expressed in an isogenic Escherichia coli strain
  22. The postantibiotic effect and post-β-lactamase-inhibitor effect of ceftazidime, ceftaroline and aztreonam in combination with avibactam against target Gram-negative bacteria
  23. Structural and sequence analysis of class A β-lactamases with respect to avibactam inhibition: impact of Ω-loop variations
  24. Role of the Outer Membrane and Porins in Susceptibility of β-Lactamase-Producing Enterobacteriaceae to Ceftazidime-Avibactam
  25. Activities of ceftazidime, ceftaroline, and aztreonam alone and combined with avibactam against isogenic Escherichia coli strains expressing selected single β-lactamases
  26. How teams of scientists work to discover new medically-useful antibacterial agents
  27. In VitroSusceptibility of Characterized β-Lactamase-Producing Strains Tested with Avibactam Combinations
  28. Efficacies of Ceftazidime-Avibactam and Ceftazidime against Pseudomonas aeruginosa in a Murine Lung Infection Model
  29. How foreign compounds like antibiotics get into bacteria
  30. Microbiology On-a-Chip
  31. Sequence analysis of the L1 metallo-β-lactamase from Xanthomonas maltophilia
  32. Outer membrane permeability and porin proteins of Yersinia enterocolitica
  33. The Penetration of Antibiotics into Aggregates of Mucoid and Non-mucoid Pseudomonas aeruginosa
  34. Sonication can reduce β-lactamase activity
  35. Inhibition of tobramycin diffusion by binding to alginate.
  36. Bioenergetics of dihydrostreptomycin transport byEscherichia coli
  37. On the mechanism of translocation of dihydrostreptomycin across the bacterial cytoplasmic membrane
  38. Respiration-dependent uptake of dihydrostreptomycin by Escherichia coli. Its irreversible nature and lack of evidence for a uniport process
  39. Irreversible uptake of dihydrostreptomycin by Escherichia coli K12
  40. THE PENETRATION OF ANTIBIOTICS THROUGH SODIUM ALGINATE AND THROUGH THE EXOPOLYSACCHARIDE OF A MUCOID STRAIN OF PSEUDOMONAS AERUGINOSA
  41. INHIBITORS OF FIREFLY LUCIFERASE IN CLINICAL URINE SPECIMENS
  42. The preparation of tightly coupled membrane vesicles from Paracoccus denitrificans