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Unveiling the physiological mechanisms that drive the emergence of antibiotic resisters from antibiotic persister population of mycobacteria
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ejlt.200401054openalex-snapshot
An alternative spectrophotometric method for the determination of free glycerol in biodiesel
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SOS Repair Hypothesis: Phenomenology of an Inducible DNA Repair Which is Accompanied by Mutagenesis
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Growth ofMycobacterium smegmatis in minimal and complete media
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Asymmetric cell division in Mycobacterium tuberculosis and its unique features
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Epoxides: comparison of the induction of SOS repair in Escherichia coli PQ37 and the bacterial mutagenicity in the Ames test
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The variability of mycobacterium tuberculosis in patients with cavitary pulmonary tuberculosis in the course of chemotherapy
inferredcites →https://doi.org/10.1016/j.cell.2011.02.022openalex-snapshot
Drug Tolerance in Replicating Mycobacteria Mediated by a Macrophage-Induced Efflux Mechanism
inferredcites →https://doi.org/10.1016/j.cell.2013.04.006openalex-snapshot
Four-Dimensional Imaging of E. coli Nucleoid Organization and Dynamics in Living Cells
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Microbial Persistence and the Road to Drug Resistance
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Antidepressant fluoxetine induces multiple antibiotics resistance in Escherichia coli via ROS-mediated mutagenesis
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Electron microscopy analysis ofMycobacterium tuberculosiscell division
inferredcites →https://doi.org/10.1016/j.ijmyco.2014.04.002openalex-snapshot
Comparison of ambient air survival of Mycobacterium tuberculosis clinical strains associated with different epidemiological phenotypes
inferredcites →https://doi.org/10.1016/j.mib.2009.06.018openalex-snapshot
Role of reactive oxygen species in antibiotic action and resistance
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Guinea pig model of Mycobacterium tuberculosis latent/dormant infection
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Sublethal Antibiotic Treatment Leads to Multidrug Resistance via Radical-Induced Mutagenesis
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Unusual features of the cell cycle in mycobacteria: Polar-restricted growth and the snapping-model of cell division
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Bipolar Localization of the Replication Origin Regions of Chromosomes in Vegetative and Sporulating Cells of B. subtilis
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TREATMENT OF STAPHYLOCOCCAL INFECTIONS WITH PENICILLIN BY INTERMITTENT STERILISATION
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Comparative studies of bacteria with an atomic force microscopy operating in different modes
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Persister cells and tolerance to antimicrobials
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Inhibition of Salmonella intracellular proliferation by non-phagocytic eucaryotic cells
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SOS Mutator DNA Polymerase IV Functions in Adaptive Mutation and Not Adaptive Amplification
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Cell length, cell growth and cell division
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Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase
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Isocitrate lyase mediates broad antibiotic tolerance in Mycobacterium tuberculosis
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Division site selection linked to inherited cell surface wave troughs in mycobacteria
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Morphological plasticity as a bacterial survival strategy
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Tuberculosis: a problem with persistence
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DNA condensation in live E. coli provides evidence for transertion
inferredcites →https://doi.org/10.1042/bj0550416openalex-snapshot
The colorimetric estimation of formaldehyde by means of the Hantzsch reaction
inferredcites →https://doi.org/10.1042/bsr20140167openalex-snapshot
Sublethal vancomycin-induced ROS mediating antibiotic resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1073/pnas.0606329104openalex-snapshot
Filamentation by Escherichia coli subverts innate defenses during urinary tract infection
inferredcites →https://doi.org/10.1073/pnas.0609839104openalex-snapshot
Tracking the in vivo evolution of multidrug resistance in Staphylococcus aureus by whole-genome sequencing
inferredcites →https://doi.org/10.1073/pnas.0904741106openalex-snapshot
Macromolecular crowding induced elongation and compaction of single DNA molecules confined in a nanochannel
inferredcites →https://doi.org/10.1073/pnas.120161797openalex-snapshot
The SOS response regulates adaptive mutation
inferredcites →https://doi.org/10.1073/pnas.1203735109openalex-snapshot
Eradication of bacterial persisters with antibiotic-generated hydroxyl radicals
inferredcites →https://doi.org/10.1073/pnas.1213332109openalex-snapshot
BapE DNA endonuclease induces an apoptotic-like response to DNA damage in Caulobacter
inferredcites →https://doi.org/10.1073/pnas.1420702111openalex-snapshot
Emergence of antibiotic resistance from multinucleated bacterial filaments
inferredcites →https://doi.org/10.1073/pnas.72.8.2999openalex-snapshot
Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12.
inferredcites →https://doi.org/10.1073/pnas.94.9.4721openalex-snapshot
Bipolar localization of a chromosome partition protein in Bacillus subtilis
inferredcites →https://doi.org/10.1074/jbc.m110649200openalex-snapshot
Macrophages Inhibit Salmonella Typhimurium Replication through MEK/ERK Kinase and Phagocyte NADPH Oxidase Activities
inferredcites →https://doi.org/10.1074/jbc.m209264200openalex-snapshot
Development of Novel Fluorescence Probes That Can Reliably Detect Reactive Oxygen Species and Distinguish Specific Species
inferredcites →https://doi.org/10.1084/jem.104.5.737openalex-snapshot
FATE OF MYCOBACTERIUM TUBERCULOSIS IN MOUSE TISSUES AS DETERMINED BY THE MICROBIAL ENUMERATION TECHNIQUE
inferredcites →https://doi.org/10.1084/jem.104.5.763openalex-snapshot
THE FATE OF MYCOBACTERIUM TUBERCULOSIS IN MOUSE TISSUES AS DETERMINED BY THE MICROBIAL ENUMERATION TECHNIQUE
inferredcites →https://doi.org/10.1088/1367-2630/15/12/125016openalex-snapshot
Bacterial filamentation accelerates colonization of adhesive spots embedded in biopassive surfaces
inferredcites →https://doi.org/10.1093/clinchem/20.6.645openalex-snapshot
Characterization of the Periodate Oxidation of Glycerol and Related Compounds, and Application toward Determination of Serum Triglyceride Concentrations
inferredcites →https://doi.org/10.1093/infdis/jis601openalex-snapshot
Dynamic Population Changes in Mycobacterium tuberculosis During Acquisition and Fixation of Drug Resistance in Patients
inferredcites →https://doi.org/10.1093/mutage/9.3.245openalex-snapshot
Induction of the SOS response and mutations by reactive oxygen-generating compounds in various Escherichia coli mutants defective in the mutM, mutY or soxRS loci
inferredcites →https://doi.org/10.1097/00000441-192809000-00064openalex-snapshot
Tubercle Bacilli in Latent Tuberculous Lesions in Lung Tissue without Tuberculous Lesions
inferredcites →https://doi.org/10.1098/rstb.2004.1605openalex-snapshot
Diversity and redundancy in bacterial chromosome segregation mechanisms
inferredcites →https://doi.org/10.1099/00221287-129-7-2315openalex-snapshot
Electron Microscopic Observations of Cell Division in Mycobacterium vaccae V1
inferredcites →https://doi.org/10.1099/00221287-144-5-1309openalex-snapshot
Fused nucleoids resegregate faster than cell elongation in Escherichia coli pbpB(Ts) filaments after release from chloramphenicol inhibition
inferredcites →https://doi.org/10.1099/00221287-21-3-530openalex-snapshot
Bacterial Mutation in a Stationary Phase and the Question of Cell Turnover
inferredcites →https://doi.org/10.1099/mic.0.000264openalex-snapshot
The ploidy level of Synechocystis sp. PCC 6803 is highly variable and is influenced by growth phase and by chemical and physical external parameters
inferredcites →https://doi.org/10.1101/428961openalex-snapshot
The antioxidant drug N-acetylcysteine abolishes SOS-mediated mutagenesis produced by fluoroquinolones in bacteria
inferredcites →https://doi.org/10.1101/cshperspect.a012674openalex-snapshot
DNA Damage Responses in Prokaryotes: Regulating Gene Expression, Modulating Growth Patterns, and Manipulating Replication Forks
inferredcites →https://doi.org/10.1111/1574-6976.12077openalex-snapshot
SOS, the formidable strategy of bacteria against aggressions
inferredcites →https://doi.org/10.1111/j.1365-2443.2006.00982.xopenalex-snapshot
Impact of reactive oxygen species on spontaneous mutagenesis in Escherichia coli
inferredcites →https://doi.org/10.1111/j.1365-2958.1987.tb00529.xopenalex-snapshot
ParD: a new gene coding for a protein required for chromosome partitioning and septum localization in Escherichia coli
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Isolation and characterization of efficient plasmid transformation mutants of Mycobacterium smegmatis
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05333.xopenalex-snapshot
Interference of Mycobacterium tuberculosis cell division by Rv2719c, a cell wall hydrolase
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06750.xopenalex-snapshot
Novel role of Wag31 in protection of mycobacteria under oxidative stress
inferredcites →https://doi.org/10.1126/science.1079914openalex-snapshot
RacA, a Bacterial Protein That Anchors Chromosomes to the Cell Poles
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.1208747openalex-snapshot
Acceleration of Emergence of Bacterial Antibiotic Resistance in Connected Microenvironments
inferredcites →https://doi.org/10.1126/science.1229858openalex-snapshot
Dynamic Persistence of Antibiotic-Stressed Mycobacteria
inferredcites →https://doi.org/10.1128/aac.00276-07openalex-snapshot
Location of Persisting Mycobacteria in a Guinea Pig Model of Tuberculosis Revealed by R207910
inferredcites →https://doi.org/10.1128/aac.01343-16openalex-snapshot
De Novo Emergence of Genetically Resistant Mutants of Mycobacterium tuberculosis from the Persistence Phase Cells Formed against Antituberculosis Drugs In Vitro
inferredcites →https://doi.org/10.1128/aac.02354-17openalex-snapshot
Influence of Reactive Oxygen Species onDe NovoAcquisition of Resistance to Bactericidal Antibiotics
inferredcites →https://doi.org/10.1128/aac.02684-15openalex-snapshot
Effects of Stress, Reactive Oxygen Species, and the SOS Response on De Novo Acquisition of Antibiotic Resistance in Escherichia coli
inferredcites →https://doi.org/10.1128/aac.03169-14openalex-snapshot
Rifampin Induces Hydroxyl Radical Formation in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1128/aac.38.4.773openalex-snapshot
Cloning and nucleotide sequence of Mycobacterium tuberculosis gyrA and gyrB genes and detection of quinolone resistance mutations
inferredcites →https://doi.org/10.1128/aem.06774-11openalex-snapshot
Survival and Virulence of Salmonella enterica Serovar Enteritidis Filaments Induced by Reduced Water Activity
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Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.01285-09openalex-snapshot
The Three RelE Homologs of Mycobacterium tuberculosis Have Individual, Drug-Specific Effects on Bacterial Antibiotic Tolerance
inferredcites →https://doi.org/10.1128/jb.06184-11openalex-snapshot
Unveiling Unusual Features of Formation of Septal Partition and Constriction in Mycobacteria—an Ultrastructural Study
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Control of cell length in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.171.9.4633-4639.1989openalex-snapshot
Cell length, nucleoid separation, and cell division of rod-shaped and spherical cells of Escherichia coli
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spo0J is required for normal chromosome segregation as well as the initiation of sporulation in Bacillus subtilis
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Bacillus subtilis Cell Cycle as Studied by Fluorescence Microscopy: Constancy of Cell Length at Initiation of DNA Replication and Evidence for Active Nucleoid Partitioning
inferredcites →https://doi.org/10.1128/jb.181.1.270-283.1999openalex-snapshot
Adaptation of Mycobacterium smegmatis to Stationary Phase
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Localization of FtsI (PBP3) to the Septal Ring Requires Its Membrane Anchor, the Z Ring, FtsA, FtsQ, and FtsL
inferredcites →https://doi.org/10.1128/jb.182.22.6358-6365.2000openalex-snapshot
Detection of mRNA Transcripts and Active Transcription in Persistent Mycobacterium tuberculosis Induced by Exposure to Rifampin or Pyrazinamide
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FILAMENT FORMATION BY ESCHERICHIA COLI AT INCREASED HYDROSTATIC PRESSURES
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Comparative Cell Wall Analyses of Morphological Forms Within the Genus Actinomyces
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Giant Cells of Escherichia coli
inferredcites →https://doi.org/10.1128/jcm.40.12.4435-4438.2002openalex-snapshot
Characterization of rpoB Mutations in Rifampin-Resistant Clinical Isolates of Mycobacterium tuberculosis from Turkey by DNA Sequencing and Line Probe Assay
inferredcites →https://doi.org/10.1128/mbio.01127-19openalex-snapshot
The Landscape of Phenotypic and Transcriptional Responses to Ciprofloxacin in Acinetobacter baumannii: Acquired Resistance Alleles Modulate Drug-Induced SOS Response and Prophage Replication
inferredcites →https://doi.org/10.1134/s0026893317050077openalex-snapshot
Increase in Bacterial Resistance to Antibiotics after Cancer Therapy with Platinum-Based Drugs
inferredcites →https://doi.org/10.1159/000335791openalex-snapshot
Baicalein Suppresses the SOS Response System of Staphylococcus Aureus Induced by Ciprofloxacin
inferredcites →https://doi.org/10.1164/art.1952.66.1.36openalex-snapshot
A bacteriologic study of resected tuberculous lesions.
inferredcites →https://doi.org/10.1164/art.1952.66.1.44openalex-snapshot
A study of the tubercle bacillus in resected pulmonary lesions.
inferredcites →https://doi.org/10.1186/1756-0500-4-73openalex-snapshot
A modified agar pad method for mycobacterial live-cell imaging
inferredcites →https://doi.org/10.1371/journal.pone.0017550openalex-snapshot
Location of Intra- and Extracellular M. tuberculosis Populations in Lungs of Mice and Guinea Pigs during Disease Progression and after Drug Treatment
inferredcites →https://doi.org/10.1371/journal.pone.0034791openalex-snapshot
The Escherichia coli SOS Gene dinF Protects against Oxidative Stress and Bile Salts
inferredcites →https://doi.org/10.1371/journal.pone.0196300openalex-snapshot
Alternative ribosomal proteins are required for growth and morphogenesis of Mycobacterium smegmatis under zinc limiting conditions
inferredcites →https://doi.org/10.1371/journal.pone.0198058openalex-snapshot
Filamentation and restoration of normal growth in Escherichia coli using a combined CRISPRi sgRNA/antisense RNA approach
inferredcites →https://doi.org/10.1534/genetics.116.199471openalex-snapshot
The SOS and RpoS Regulons Contribute to Bacterial Cell Robustness to Genotoxic Stress by Synergistically Regulating DNA Polymerase Pol II
inferredcites →https://doi.org/10.1590/s1415-47572004000200026openalex-snapshot
Several pathways of hydrogen peroxide action that damage the E. coli genome
inferredcites →https://doi.org/10.2174/1874285801408010040openalex-snapshot
Highly Deviated Asymmetric Division in Very Low Proportion of Mycobacterial Mid-log Phase Cells
inferredcites →https://doi.org/10.2436/20.1501.01.159openalex-snapshot
Unique biological properties of Mycobacterium tuberculosis L-form variants: impact for survival under stress.
inferredcites →https://doi.org/10.3181/00379727-50-13773openalex-snapshot
Observations on the Mechanism of Action of Penicillin.
inferredcites →https://doi.org/10.3389/fcimb.2018.00410openalex-snapshot
Zinc Blockade of SOS Response Inhibits Horizontal Transfer of Antibiotic Resistance Genes in Enteric Bacteria
inferredcites →https://doi.org/10.3389/fmicb.2014.00274openalex-snapshot
Polyploidy in haloarchaea: advantages for growth and survival
inferredcites →https://doi.org/10.3389/fmicb.2016.00947openalex-snapshot
Mild Nutrient Starvation Triggers the Development of a Small-Cell Survival Morphotype in Mycobacteria
inferredcites →https://doi.org/10.3791/3145openalex-snapshot
Live Cell Imaging of Bacillus subtilis and Streptococcus pneumoniae using Automated Time-lapse Microscopy
inferredcites →https://doi.org/10.3978/j.issn.2305-5839.2015.12.09openalex-snapshot
SOS response and its regulation on the fluoroquinolone resistance.
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THE PERSISTENCE OF TUBERCULOUS INFECTIONS
inferredcites →https://doi.org/10.7150/ijbs.4.338openalex-snapshot
Inducible SOS Response System of DNA Repair and Mutagenesis in Escherichia coli
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1093/femsle/fnab090openalex-snapshot
A method for the enrichment, isolation and validation of Mycobacterium smegmatis population surviving in the presence of bactericidal concentrations of rifampicin and moxifloxacin
inferred← citeshttps://doi.org/10.1128/msphere.00994-20openalex-snapshot
Unique Mode of Cell Division by the Mycobacterial Genetic Resister Clones Emerging De Novo from the Antibiotic-Surviving Population
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