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Inhibition of Mutation and Combating the Evolution of Antibiotic Resistance
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Risk Factors for Fluoroquinolone Resistance in Nosocomial Escherichia coli and Klebsiella pneumoniae Infections
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Adaptive mutation: implications for evolution
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DNA Gyrase and Topoisomerase IV on the Bacterial Chromosome: Quinolone-induced DNA Cleavage
inferredcites →https://doi.org/10.1006/meth.1999.0901openalex-snapshot
Determining Mutation Rates in Bacterial Populations
inferredcites →https://doi.org/10.1007/s004380100541openalex-snapshot
Roles of chromosomal and episomal dinB genes encoding DNA pol IV in targeted and untargeted mutagenesis in Escherichia coli
inferredcites →https://doi.org/10.1016/0165-7992(92)90010-fopenalex-snapshot
The role of the excision and error-prone repair systems in mutagenesis by fluorinated quinolones in Salmonella typhimurium
inferredcites →https://doi.org/10.1016/j.tim.2004.04.004openalex-snapshot
Error-prone replication for better or worse
inferredcites →https://doi.org/10.1016/s0732-8893(02)00381-4openalex-snapshot
Emerging fluoroquinolone-resistance for common clinically important gram-negative bacteria in Taiwan
inferredcites →https://doi.org/10.1016/s0968-0004(00)01560-7openalex-snapshot
Replication fork arrest and DNA recombination
inferredcites →https://doi.org/10.1016/s1097-2765(02)00455-0openalex-snapshot
Direct Rescue of Stalled DNA Replication Forks via the Combined Action of PriA and RecG Helicase Activities
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Etoposide Metabolites Enhance DNA Topoisomerase II Cleavage near Leukemia-Associated MLL Translocation Breakpoints
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The importance of repairing stalled replication forks
inferredcites →https://doi.org/10.1038/35010020openalex-snapshot
Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis
inferredcites →https://doi.org/10.1038/35080556openalex-snapshot
Evolving responsively: adaptive mutation
inferredcites →https://doi.org/10.1038/sj.emboj.7600438openalex-snapshot
Defining the position of the switches between replicative and bypass DNA polymerases
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A class of gyrase mutants of Salmonella typhimurium show quinolone‐like lethality and require Rec functions for viability
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The processing of a Benzo(a)pyrene adduct into a frameshift or a base substitution mutation requires a different set of genes in Escherichia coli
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Replication restart in UV‐irradiated Escherichia coli involving pols II, III, V, PriA, RecA and RecFOR proteins
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03480.xopenalex-snapshot
Replication restart in gyrB Escherichia coli mutants
inferredcites →https://doi.org/10.1073/pnas.0401586101openalex-snapshot
Multiple pathways process stalled replication forks
inferredcites →https://doi.org/10.1073/pnas.092269199openalex-snapshot
SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness
inferredcites →https://doi.org/10.1073/pnas.111007198openalex-snapshot
Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli
inferredcites →https://doi.org/10.1073/pnas.111008698openalex-snapshot
Rescue of stalled replication forks by RecG: Simultaneous translocation on the leading and lagging strand templates supports an active DNA unwinding model of fork reversal and Holliday junction formation
inferredcites →https://doi.org/10.1073/pnas.121007798openalex-snapshot
Formation of Holliday junctions by regression of nascent DNA in intermediates containing stalled replication forks: RecG stimulates regression even when the DNA is negatively supercoiled
inferredcites →https://doi.org/10.1073/pnas.130192397openalex-snapshot
The RecD subunit of the Escherichia coli RecBCD enzyme inhibits RecA loading, homologous recombination, and DNA repair
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The tight linkage between DNA replication and double-strand break repair in bacteriophage T4
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Stationary-phase mutation in the bacterial chromosome: Recombination protein and DNA polymerase IV dependence
inferredcites →https://doi.org/10.1073/pnas.161004898openalex-snapshot
INTRODUCTION - Links between recombination and replication: Vital roles of recombination
inferredcites →https://doi.org/10.1073/pnas.220424697openalex-snapshot
SOS mutator activity: Unequal mutagenesis on leading and lagging strands
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Spontaneous and mutagen-induced deletions: mechanistic studies in Salmonella tester strain TA102.
inferredcites →https://doi.org/10.1073/pnas.81.5.1375openalex-snapshot
Autodigestion of lexA and phage lambda repressors.
inferredcites →https://doi.org/10.1073/pnas.83.11.3904openalex-snapshot
Role of RecA protein in untargeted UV mutagenesis of bacteriophage lambda: evidence for the requirement for the dinB gene.
inferredcites →https://doi.org/10.1073/pnas.94.25.13792openalex-snapshot
Multiple pathways for SOS-induced mutagenesis in Escherichia coli : An overexpression of dinB / dinP results in strongly enhancing mutagenesis in the absence of any exogenous treatment to damage DNA
inferredcites →https://doi.org/10.1073/pnas.96.16.8919openalex-snapshot
UmuD′ 2 C is an error-prone DNA polymerase, Escherichia coli pol V
inferredcites →https://doi.org/10.1073/pnas.96.7.3552openalex-snapshot
Replication fork assembly at recombination intermediates is required for bacterial growth
inferredcites →https://doi.org/10.1073/pnas.97.17.9419openalex-snapshot
Analysis of topoisomerase function in bacterial replication fork movement: Use of DNA microarrays
inferredcites →https://doi.org/10.1074/jbc.273.42.27668openalex-snapshot
The Mechanism of Inhibition of Topoisomerase IV by Quinolone Antibacterials
inferredcites →https://doi.org/10.1074/jbc.m304217200openalex-snapshot
The RuvAB Branch Migration Complex Can Displace Topoisomerase IV·Quinolone·DNA Ternary Complexes
inferredcites →https://doi.org/10.1074/jbc.m312184200openalex-snapshot
Situational Repair of Replication Forks
inferredcites →https://doi.org/10.1089/10766290152773347openalex-snapshot
Antibiotic Persistence: The Role of Spontaneous DNA Repair Response
inferredcites →https://doi.org/10.1093/emboj/16.11.3349openalex-snapshot
Mutation in Escherichia coli under starvation conditions: a new pathway leading to small deletions in strains defective in mismatch correction
inferredcites →https://doi.org/10.1093/emboj/16.2.430openalex-snapshot
DNA double‐strand breaks caused by replication arrest
inferredcites →https://doi.org/10.1093/emboj/19.22.6259openalex-snapshot
All three SOS‐inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis
inferredcites →https://doi.org/10.1093/genetics/134.4.1023openalex-snapshot
Mutants of Escherichia coli with increased fidelity of DNA replication.
inferredcites →https://doi.org/10.1093/genetics/159.4.1405openalex-snapshot
Growth-Dependent DNA Breakage and Cell Death in a Gyrase Mutant of Salmonella
inferredcites →https://doi.org/10.1093/infdis/158.4.831openalex-snapshot
Correlation of Antimicrobial Pharmacokinetic Parameters with Therapeutic Efficacy in an Animal Model
inferredcites →https://doi.org/10.1093/nar/20.24.6713openalex-snapshot
Bound Lac repressor protein differentially inhibits the unwinding reactions catalyzed by DNA helicases
inferredcites →https://doi.org/10.1101/gad.1009802openalex-snapshot
Translesion DNA synthesis in eukaryotes: A one- or two-polymerase affair
inferredcites →https://doi.org/10.1111/j.2042-7158.1993.tb05673.xopenalex-snapshot
Function of the SOS Process in Repair of DNA Damage Induced by Modern 4-Quinolones
inferredcites →https://doi.org/10.1126/science.1070236openalex-snapshot
Specialized DNA Polymerases, Cellular Survival, and the Genesis of Mutations
inferredcites →https://doi.org/10.1126/science.1101630openalex-snapshot
SOS Response Induction by ß-Lactams and Bacterial Defense Against Antibiotic Lethality
inferredcites →https://doi.org/10.1126/science.277.5331.1432openalex-snapshot
Laboratory Workhorse Decoded
inferredcites →https://doi.org/10.1126/science.277.5331.1453openalex-snapshot
The Complete Genome Sequence of Escherichia coli K-12
inferredcites →https://doi.org/10.1128/aac.34.6.1271openalex-snapshot
Quinolone resistance-determining region in the DNA gyrase gyrA gene of Escherichia coli
inferredcites →https://doi.org/10.1128/aac.35.8.1647openalex-snapshot
Quinolone resistance-determining region in the DNA gyrase gyrB gene of Escherichia coli
inferredcites →https://doi.org/10.1128/aac.39.2.520openalex-snapshot
Relationship between quinolone use and emergence of ciprofloxacin-resistant Escherichia coli in bloodstream infections
inferredcites →https://doi.org/10.1128/aac.41.9.2059openalex-snapshot
Adaptive mutations produce resistance to ciprofloxacin
inferredcites →https://doi.org/10.1128/aac.42.9.2375openalex-snapshot
In Vivo Activities of Amoxicillin and Amoxicillin-Clavulanate against Streptococcus pneumoniae : Application to Breakpoint Determinations
inferredcites →https://doi.org/10.1128/aac.47.10.3222-3232.2003openalex-snapshot
Mutation Rate and Evolution of Fluoroquinolone Resistance in Escherichia coli Isolates from Patients with Urinary Tract Infections
inferredcites →https://doi.org/10.1128/aac.47.2.804-808.2003openalex-snapshot
Molecular Epidemiology of Penicillin-Resistant and Ciprofloxacin-Resistant Streptococcus pneumoniae in Canada
inferredcites →https://doi.org/10.1128/jb.134.3.1195-1198.1978openalex-snapshot
Survival of recombination-deficient mutants of Escherichia coli during incubation with nalidixic acid
inferredcites →https://doi.org/10.1128/jb.140.2.424-435.1979openalex-snapshot
Escherichia coli Mutants Thermosensitive for Deoxyribonucleic Acid Gyrase Subunit A: Effects on Deoxyribonucleic Acid Replication, Transcription, and Bacteriophage Growth
inferredcites →https://doi.org/10.1128/jb.170.5.2163-2173.1988openalex-snapshot
Isolation and characterization of noncleavable (Ind-) mutants of the LexA repressor of Escherichia coli K-12
inferredcites →https://doi.org/10.1128/jb.181.9.2878-2882.1999openalex-snapshot
DNA Polymerase II ( polB ) Is Involved in a New DNA Repair Pathway for DNA Interstrand Cross-Links in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.182.1.9-13.2000openalex-snapshot
Role of PriA in Replication Fork Reactivation in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.184.24.6957-6965.2002openalex-snapshot
Different Spectra of Stationary-Phase Mutations in Early-Arising versus Late-Arising Mutants of Pseudomonas putida : Involvement of the DNA Repair Enzyme MutY and the Stationary-Phase Sigma Factor RpoS
inferredcites →https://doi.org/10.1128/jb.185.11.3469-3472.2003openalex-snapshot
Error-Prone Polymerase, DNA Polymerase IV, Is Responsible for Transient Hypermutation during Adaptive Mutation in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.186.4.1197-1199.2004openalex-snapshot
PriA Is Essential for Viability of the Escherichia coli Topoisomerase IV parE10 (Ts) Mutant
inferredcites →https://doi.org/10.1128/mmbr.54.1.18-51.1990openalex-snapshot
Nucleotide excision repair in Escherichia coli
inferredcites →https://doi.org/10.1128/mmbr.61.3.377-392.1997openalex-snapshot
DNA gyrase, topoisomerase IV, and the 4-quinolones
inferredcites →https://doi.org/10.1146/annurev.genet.32.1.379openalex-snapshot
RECOMBINATION AND RECOMBINATION-DEPENDENT DNA REPLICATION IN BACTERIOPHAGE T4
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Digital Quantification of DNA Replication and Chromosome Segregation Enables Determination of Antimicrobial Susceptibility after only 15 Minutes of Antibiotic Exposure
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The SOS system: A complex and tightly regulated response to DNA damage
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Changes in lipid distribution in E. coli strains in response to norfloxacin
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Defects in DNA double‐strand break repair resensitize antibiotic‐resistant Escherichia coli to multiple bactericidal antibiotics
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Evolutionary and genetic features of drug targets
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Comparative proteomic analysis of Staphylococcus aureus strains with differences in resistance to the cell wall‐targeting antibiotic vancomycin
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Fluoroquinolone Resistance: Mechanisms, Restrictive Dosing, and Anti-Mutant Screening Strategies for New Compounds
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Ordering up gene expression by slowing down transcription factor binding kinetics
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Single-molecule fluorescence microscopy reveals modulation of DNA polymerase IV-binding lifetimes by UmuD (K97A) and UmuD′
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Cross-talk between Pseudomonas aeruginosa and urinary tract infections
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Mathematical modelling of nonlinear dynamics generated from modular interconnections in cellular SOS response system
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Identification of a potent small-molecule inhibitor of bacterial DNA repair that potentiates quinolone antibiotic activity in methicillin-resistant Staphylococcus aureus
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Exploration of inhibitors of the bacterial LexA repressor-protease
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Total alkaloids of Sophora alopecuroides- and matrine-induced reactive oxygen species impair biofilm formation of Staphylococcus epidermidis and increase bacterial susceptibility to ciprofloxacin
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Bacterial SOS response: a food safety perspective
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Toward a quantitative understanding of antibiotic resistance evolution
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Optimizing dosage to prevent emergence of resistance – lessons from in vitro models
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Targeting evolution of antibiotic resistance by SOS response inhibition
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The Transcription Elongation Factor NusA Is Required for Stress-Induced Mutagenesis in Escherichia coli
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Antimicrobial resistance among invasive isolates of Streptococcus pneumoniae collected across Canada
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Roles of E. coli double-strand-break-repair proteins in stress-induced mutation
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RecQ-dependent death-by-recombination in cells lacking RecG and UvrD
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Specificity in suppression of SOS expression by recA4162 and uvrD303
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Insights into the complex levels of regulation imposed on Escherichia coli DNA polymerase V
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Effect of SOS-induced levels of imuABC on spontaneous and damage-induced mutagenesis in Caulobacter crescentus
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Fluorescent fusions of the N protein of phage Mu label DNA damage in living cells
inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.102693openalex-snapshot
R-loop-dependent replication and genomic instability in bacteria
inferred← citeshttps://doi.org/10.1016/j.drudis.2009.06.010openalex-snapshot
The impact of synthetic biology on drug discovery
inferred← citeshttps://doi.org/10.1016/j.drup.2012.03.005openalex-snapshot
Evolution of antibiotic resistance at non-lethal drug concentrations
inferred← citeshttps://doi.org/10.1016/j.envpol.2015.12.040openalex-snapshot
Initial hazard screening for genotoxicity of photo-transformation products of ciprofloxacin by applying a combination of experimental and in-silico testing
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.10.006openalex-snapshot
Fungicide-induced transposon movement in Monilinia fructicola
inferred← citeshttps://doi.org/10.1016/j.gene.2015.09.069openalex-snapshot
Overexpression of SOS genes in ciprofloxacin resistant Escherichia coli mutants
inferred← citeshttps://doi.org/10.1016/j.ijmm.2013.02.004openalex-snapshot
Antibiotics and antibiotic resistance: A bitter fight against evolution
inferred← citeshttps://doi.org/10.1016/j.ijpara.2021.02.007openalex-snapshot
Biochemical characterization of Recombinase A from Wolbachia endosymbiont of filarial nematode Brugia malayi (wBmRecA)
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108373openalex-snapshot
Reactive oxygen species accelerate de novo acquisition of antibiotic resistance in E. coli
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107650openalex-snapshot
Anti-mutagenic agent targeting LexA to combat antimicrobial resistance in mycobacteria
inferred← citeshttps://doi.org/10.1016/j.jgar.2017.04.008openalex-snapshot
Deficiency of quorum sensing system inhibits the resistance selection of Pseudomonas aeruginosa to ciprofloxacin and levofloxacin in vitro
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133849openalex-snapshot
Two synonymous single-nucleotide polymorphisms promoting fluoroquinolone resistance of Escherichia coli in the environment
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2006.06.003openalex-snapshot
Synthesis, characterization and DNA binding of magnesium–ciprofloxacin (cfH) complex [Mg(cf)2] · 2.5H2O
inferred← citeshttps://doi.org/10.1016/j.jprot.2013.03.008openalex-snapshot
A systematic quantitative proteomic examination of multidrug resistance in Acinetobacter baumannii
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.117116openalex-snapshot
Inhibition of the transcriptional repressor LexA: Withstanding drug resistance by inhibiting the bacterial mechanisms of adaptation to antimicrobials
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.118562openalex-snapshot
The central role of the SOS DNA repair system in antibiotics resistance: A new target for a new infectious treatment strategy
inferred← citeshttps://doi.org/10.1016/j.meegid.2008.09.007openalex-snapshot
Evolutionary epidemiology 20 years on: Challenges and prospects
inferred← citeshttps://doi.org/10.1016/j.mib.2009.06.018openalex-snapshot
Role of reactive oxygen species in antibiotic action and resistance
inferred← citeshttps://doi.org/10.1016/j.mib.2012.07.007openalex-snapshot
Antimicrobials as promoters of genetic variation
inferred← citeshttps://doi.org/10.1016/j.mib.2012.08.001openalex-snapshot
Induction of competence for genetic transformation by antibiotics: convergent evolution of stress responses in distant bacterial species lacking SOS?
inferred← citeshttps://doi.org/10.1016/j.mib.2023.102323openalex-snapshot
SOS-independent bacterial DNA damage responses: diverse mechanisms, unifying function
inferred← citeshttps://doi.org/10.1016/j.micinf.2005.12.025openalex-snapshot
Resistance to fluoroquinolones in Salmonella: emerging mechanisms and resistance prevention strategies
inferred← citeshttps://doi.org/10.1016/j.micinf.2010.04.009openalex-snapshot
SOS regulatory elements are essential for UPEC pathogenesis
inferred← citeshttps://doi.org/10.1016/j.micpath.2025.108060openalex-snapshot
Advance Helicobacter pylori eradication: Current therapeutic strategies and the potential of lipid-based nanocarriers for targeting receptors
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127711openalex-snapshot
Ferrous gluconate triggers ferroptosis in Escherichia coli: Implications of lipid peroxidation and DNA damage
inferred← citeshttps://doi.org/10.1016/j.micres.2025.128056openalex-snapshot
De novo evolution of antibiotic resistance to Oct-TriA1
inferred← citeshttps://doi.org/10.1016/j.mimet.2021.106315openalex-snapshot
Development of CRISPR-Cas9 knock-in tools for free fatty acid production using the fast-growing cyanobacterial strain Synechococcus elongatus UTEX 2973
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.01.003openalex-snapshot
Sublethal Antibiotic Treatment Leads to Multidrug Resistance via Radical-Induced Mutagenesis
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.10.015openalex-snapshot
Inhibiting the Evolution of Antibiotic Resistance
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.02.037openalex-snapshot
Gamblers: An Antibiotic-Induced Evolvable Cell Subpopulation Differentiated by Reactive-Oxygen-Induced General Stress Response
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.03.003openalex-snapshot
ppGpp and RNA-polymerase backtracking guide antibiotic-induced mutable gambler cells
inferred← citeshttps://doi.org/10.1016/j.molimm.2020.11.012openalex-snapshot
Immunomodulatory gene expression analysis in LPS-stimulated human polymorphonuclear leukocytes treated with antibiotics commonly used for multidrug-resistant strains
inferred← citeshttps://doi.org/10.1016/j.molmed.2007.04.004openalex-snapshot
New strategies for combating multidrug-resistant bacteria
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2023.111836openalex-snapshot
DinB (DNA polymerase IV), ImuBC and RpoS contribute to the generation of ciprofloxacin-resistance mutations in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.pep.2021.105967openalex-snapshot
Expression and Characterization of the Staphylococcus aureus RecA protein: A mapping of canonical functions
inferred← citeshttps://doi.org/10.1016/j.pt.2009.11.009openalex-snapshot
Darwinian interventions: taming pathogens through evolutionary ecology
inferred← citeshttps://doi.org/10.1016/j.resmic.2009.03.003openalex-snapshot
Subinhibitory fluoroquinolone exposure selects for reduced beta-lactam susceptibility in methicillin-resistant Staphylococcus aureus and alterations in the SOS-mediated response
inferred← citeshttps://doi.org/10.1016/j.resmic.2016.07.008openalex-snapshot
Ciprofloxacin provokes SOS-dependent changes in respiration and membrane potential and causes alterations in the redox status of Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2014.07.130openalex-snapshot
Ofloxacin sorption in soils after long-term tillage: The contribution of organic and mineral compositions
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.146503openalex-snapshot
Impact of antibiotic concentration gradients on nitrate reduction and antibiotic resistance in a microfluidic gradient chamber
inferred← citeshttps://doi.org/10.1016/j.str.2022.09.004openalex-snapshot
Nanobodies targeting LexA autocleavage disclose a novel suppression strategy of SOS-response pathway
inferred← citeshttps://doi.org/10.1016/j.str.2022.09.007openalex-snapshot
Pulling the wool over a pathogen’s eyes: Llama nanobody inhibitors of the bacterial SOS response
inferred← citeshttps://doi.org/10.1016/j.tim.2017.10.009openalex-snapshot
Not Just Antibiotics: Is Cancer Chemotherapy Driving Antimicrobial Resistance?
inferred← citeshttps://doi.org/10.1016/j.tim.2018.01.005openalex-snapshot
Evolutionary Mechanisms Shaping the Maintenance of Antibiotic Resistance
inferred← citeshttps://doi.org/10.1016/j.tips.2010.07.003openalex-snapshot
Evolutionary inspirations for drug discovery
inferred← citeshttps://doi.org/10.1016/j.tpb.2017.08.004openalex-snapshot
Evolutionary rescue of a parasite population by mutation rate evolution
inferred← citeshttps://doi.org/10.1016/j.vetmic.2009.04.020openalex-snapshot
Antimicrobial resistance and genetic characterization of fluoroquinolone-resistant Mannheimia haemolytica isolates from cattle with bovine pneumonia
inferred← citeshttps://doi.org/10.1016/s1359-6446(05)03616-0openalex-snapshot
Reversing the evolution of antibiotic resistance
inferred← citeshttps://doi.org/10.1016/s1773-2247(10)50072-8openalex-snapshot
Mechanisms of antibiotic resistance and delivery strategies to prevent its emergence
inferred← citeshttps://doi.org/10.1017/s146625230800159xopenalex-snapshot
Antimicrobial resistance: its emergence and transmission
inferred← citeshttps://doi.org/10.1021/acs.analchem.7b02809openalex-snapshot
Integrated Bacterial Identification and Antimicrobial Susceptibility Testing Using PCR and High-Resolution Melt
inferred← citeshttps://doi.org/10.1021/acs.biochem.2c00505openalex-snapshot
Engineered RecA Constructs Reveal the Minimal SOS Activation Complex
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b00109openalex-snapshot
Targets for Combating the Evolution of Acquired Antibiotic Resistance
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00877openalex-snapshot
Protein Cages: From Fundamentals to Advanced Applications
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.4c01074openalex-snapshot
An Antibiotic-Degrading Engineered Biofilm Platform to Combat Environmental Antibiotic Resistance
inferred← citeshttps://doi.org/10.1021/acscentsci.8b00447openalex-snapshot
A Rapid and Low-Cost Pathogen Detection Platform by Using a Molecular Agglutination Assay
inferred← citeshttps://doi.org/10.1021/acschembio.9b00886openalex-snapshot
The Kinetic and Molecular Basis for the Interaction of LexA and Activated RecA Revealed by a Fluorescent Amino Acid Probe
inferred← citeshttps://doi.org/10.1021/acsinfecdis.5c00467openalex-snapshot
Identification and Characterization of a Small-Molecule Inhibitor of the Pseudomonas aeruginosa SOS Response
inferred← citeshttps://doi.org/10.1021/acsinfecdis.7b00122openalex-snapshot
Inhibitors of LexA Autoproteolysis and the Bacterial SOS Response Discovered by an Academic–Industry Partnership
inferred← citeshttps://doi.org/10.1021/acssynbio.7b00108openalex-snapshot
A Small-Molecule Inducible Synthetic Circuit for Control of the SOS Gene Network without DNA Damage
inferred← citeshttps://doi.org/10.1021/acssynbio.7b00174openalex-snapshot
Managing the SOS Response for Enhanced CRISPR-Cas-Based Recombineering in E. coli through Transient Inhibition of Host RecA Activity
inferred← citeshttps://doi.org/10.1021/bi500026eopenalex-snapshot
Specificity Determinants for Autoproteolysis of LexA, a Key Regulator of Bacterial SOS Mutagenesis
inferred← citeshttps://doi.org/10.1021/bi800725qopenalex-snapshot
Domain Requirements for DNA Unwinding by Mycobacterial UvrD2, an Essential DNA Helicase
inferred← citeshttps://doi.org/10.1021/cb300018xopenalex-snapshot
Small-Molecule Inhibitors of Bacterial AddAB and RecBCD Helicase-Nuclease DNA Repair Enzymes
inferred← citeshttps://doi.org/10.1021/mp200274ropenalex-snapshot
The Goldilocks Principle and Antibiotic Resistance in Bacteria
inferred← citeshttps://doi.org/10.1021/pr070307yopenalex-snapshot
Identification and Antibody-Therapeutic Targeting of Chloramphenicol-Resistant Outer Membrane Proteins in Escherichia coli
inferred← citeshttps://doi.org/10.1021/pr800073copenalex-snapshot
Proteomic Analysis of Nalidixic Acid Resistance in Escherichia coli: Identification and Functional Characterization of OM Proteins
inferred← citeshttps://doi.org/10.1021/pr800310yopenalex-snapshot
Identification and Network of Outer Membrane Proteins Regulating Streptomysin Resistance in Escherichia coli
inferred← citeshttps://doi.org/10.1021/sb300101gopenalex-snapshot
Synthetic Biology of Antimicrobial Discovery
inferred← citeshttps://doi.org/10.1038/embor.2009.99openalex-snapshot
The SOS response promotes qnrB quinolone‐resistance determinant expression
inferred← citeshttps://doi.org/10.1038/nchembio.2007.27openalex-snapshot
Combating bacteria and drug resistance by inhibiting mechanisms of persistence and adaptation
inferred← citeshttps://doi.org/10.1038/ncomms3115openalex-snapshot
R-loops and nicks initiate DNA breakage and genome instability in non-growing Escherichia coli
inferred← citeshttps://doi.org/10.1038/nm0806-890openalex-snapshot
Side effects may include evolution
inferred← citeshttps://doi.org/10.1038/nrc3039openalex-snapshot
An analogy between the evolution of drug resistance in bacterial communities and malignant tissues
inferred← citeshttps://doi.org/10.1038/nrg2593openalex-snapshot
Mechanisms of change in gene copy number
inferred← citeshttps://doi.org/10.1038/nrg3415openalex-snapshot
Evaluating evolutionary models of stress-induced mutagenesis in bacteria
inferred← citeshttps://doi.org/10.1038/nrmicro1614openalex-snapshot
The antibiotic resistome: the nexus of chemical and genetic diversity
inferred← citeshttps://doi.org/10.1038/nrmicro1768openalex-snapshot
Bacterial DNA repair by non-homologous end joining
inferred← citeshttps://doi.org/10.1038/nrmicro2333openalex-snapshot
How antibiotics kill bacteria: from targets to networks
inferred← citeshttps://doi.org/10.1038/s41396-019-0344-9openalex-snapshot
Bacterial persistence promotes the evolution of antibiotic resistance by increasing survival and mutation rates
inferred← citeshttps://doi.org/10.1038/s41429-019-0160-5openalex-snapshot
High-throughput identification of the sensitivities of an Escherichia coli ΔrecA mutant strain to various chemical compounds
inferred← citeshttps://doi.org/10.1038/s41467-019-09058-4openalex-snapshot
Enhanced antibiotic resistance development from fluoroquinolone persisters after a single exposure to antibiotic
inferred← citeshttps://doi.org/10.1038/s41467-020-16932-zopenalex-snapshot
Highly parallel lab evolution reveals that epistasis can curb the evolution of antibiotic resistance
inferred← citeshttps://doi.org/10.1038/s41467-026-76025-1openalex-snapshot
Function-specific epistasis shapes evolutionary trajectories towards antibiotic resistance
inferred← citeshttps://doi.org/10.1038/s41564-022-01260-3openalex-snapshot
Enterotoxin tilimycin from gut-resident Klebsiella promotes mutational evolution and antibiotic resistance in mice
inferred← citeshttps://doi.org/10.1038/s41586-021-03440-3openalex-snapshot
Type III-A CRISPR immunity promotes mutagenesis of staphylococci
inferred← citeshttps://doi.org/10.1038/s41594-024-01317-3openalex-snapshot
The LexA–RecA* structure reveals a cryptic lock-and-key mechanism for SOS activation
inferred← citeshttps://doi.org/10.1038/s41598-018-27095-9openalex-snapshot
Phenotypic Switching Can Speed up Microbial Evolution
inferred← citeshttps://doi.org/10.1038/s41598-019-52832-zopenalex-snapshot
New insights on Pseudoalteromonas haloplanktis TAC125 genome organization and benchmarks of genome assembly applications using next and third generation sequencing technologies
inferred← citeshttps://doi.org/10.1038/s41598-024-59188-zopenalex-snapshot
A role for the stringent response in ciprofloxacin resistance in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/s42003-021-02783-xopenalex-snapshot
Potentiating antibiotic efficacy via perturbation of non-essential gene expression
inferred← citeshttps://doi.org/10.1038/s44259-024-00057-0openalex-snapshot
The putative error prone polymerase REV1 mediates DNA damage and drug resistance in Candida albicans
inferred← citeshttps://doi.org/10.1038/srep44150openalex-snapshot
Systems-level understanding of ethanol-induced stresses and adaptation in E. coli
inferred← citeshttps://doi.org/10.1039/b703159aopenalex-snapshot
Inhibition of Escherichia coli RecA by rationally redesigned N-terminal helix
inferred← citeshttps://doi.org/10.1039/b913490eopenalex-snapshot
Synthetic biology in the analysis and engineering of signaling processes
inferred← citeshttps://doi.org/10.1039/c2mb25090jopenalex-snapshot
Alterations of protein complexes and pathways in genetic information flow and response to stimulus contribute to Escherichia coli resistance to balofloxacin
inferred← citeshttps://doi.org/10.1039/d0cb00060dopenalex-snapshot
Antibacterial activity of a dual peptide targeting the Escherichia coli sliding clamp and the ribosome
inferred← citeshttps://doi.org/10.1039/d0sc01353fopenalex-snapshot
Microfluidic systems for rapid antibiotic susceptibility tests (ASTs) at the single-cell level
inferred← citeshttps://doi.org/10.1042/bst20170055openalex-snapshot
Single-molecule live-cell imaging of bacterial DNA repair and damage tolerance
inferred← citeshttps://doi.org/10.1042/bst20180178openalex-snapshot
Phage-based biocontrol strategies and their application in agriculture and aquaculture
inferred← citeshttps://doi.org/10.1042/bst20190364openalex-snapshot
Bacterial phenotypic heterogeneity in DNA repair and mutagenesis
inferred← citeshttps://doi.org/10.1051/e3sconf/202017501010openalex-snapshot
Extracts of medical plants suppress the SOS response and reduce mutagenesis in E. coli
inferred← citeshttps://doi.org/10.1051/medsci/2012282016openalex-snapshot
Antibiotiques et réponse SOS bactérienne
inferred← citeshttps://doi.org/10.1055/a-1890-5559openalex-snapshot
Herbal Products and Their Active Constituents Used Alone and in Combination with Antibiotics against Multidrug-Resistant Bacteria
inferred← citeshttps://doi.org/10.1063/1.3456057openalex-snapshot
Introduction to Focus Issue: Genetic Interactions
inferred← citeshttps://doi.org/10.1073/pnas.0610835104openalex-snapshot
An editing-defective aminoacyl-tRNA synthetase is mutagenic in aging bacteria via the SOS response
inferred← citeshttps://doi.org/10.1073/pnas.0800442106openalex-snapshot
Engineered bacteriophage targeting gene networks as adjuvants for antibiotic therapy
inferred← citeshttps://doi.org/10.1073/pnas.1104681108openalex-snapshot
Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli
inferred← citeshttps://doi.org/10.1073/pnas.1400093111openalex-snapshot
Enhanced killing of antibiotic-resistant bacteria enabled by massively parallel combinatorial genetics
inferred← citeshttps://doi.org/10.1073/pnas.1420702111openalex-snapshot
Emergence of antibiotic resistance from multinucleated bacterial filaments
inferred← citeshttps://doi.org/10.1073/pnas.1801101115openalex-snapshot
Real-time dynamics of mutagenesis reveal the chronology of DNA repair and damage tolerance responses in single cells
inferred← citeshttps://doi.org/10.1073/pnas.1901730116openalex-snapshot
Post-stress bacterial cell death mediated by reactive oxygen species
inferred← citeshttps://doi.org/10.1073/pnas.2001240117openalex-snapshot
Genetic dominance governs the evolution and spread of mobile genetic elements in bacteria
inferred← citeshttps://doi.org/10.1073/pnas.2407832121openalex-snapshot
The DNA damage response of Escherichia coli , revisited: Differential gene expression after replication inhibition
inferred← citeshttps://doi.org/10.1074/jbc.m109.005587openalex-snapshot
Dual Nuclease and Helicase Activities of Helicobacter pylori AddAB Are Required for DNA Repair, Recombination, and Mouse Infectivity
inferred← citeshttps://doi.org/10.1074/jbc.m110.152298openalex-snapshot
X-ray Crystal Structure of the Bacterial Conjugation Factor PsiB, a Negative Regulator of RecA
inferred← citeshttps://doi.org/10.1080/07448481.2021.1947842openalex-snapshot
Knowledge, attitudes, and practices related to antimicrobial resistance among undergraduate students at a large public university in 2020
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