On the public citation graph

Dual-Reporter Mycobacteriophages (Φ 2 DRMs) Reveal Preexisting Mycobacterium tuberculosis Persistent Cells in Human Sputum

https://doi.org/10.1128/mbio.01023-16
0 signed · 134 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.279.12.943openalex-snapshot
Directly Observed Therapy for Treatment Completion of Pulmonary Tuberculosis Consensus Statement of the Public Health Tuberculosis Guidelines Panel
inferredcites →https://doi.org/10.1006/jmbi.2001.5331openalex-snapshot
Dimer formation and transcription activation in the sporulation response regulator Spo0A
inferredcites →https://doi.org/10.1016/j.tube.2003.08.003openalex-snapshot
M. tuberculosis persistence, latency, and drug tolerance
inferredcites →https://doi.org/10.1016/j.tube.2003.12.005openalex-snapshot
The use of microarray analysis to determine the gene expression profiles of Mycobacterium tuberculosis in response to anti-bacterial compounds
inferredcites →https://doi.org/10.1016/j.tube.2004.02.003openalex-snapshot
Mycobacterium tuberculosis gene expression during adaptation to stationary phase and low-oxygen dormancy
inferredcites →https://doi.org/10.1016/j.tube.2005.07.004openalex-snapshot
Exploring drug action on Mycobacterium tuberculosis using affymetrix oligonucleotide genechips
inferredcites →https://doi.org/10.1016/j.tube.2006.04.001openalex-snapshot
Understanding the action of INH on a highly INH-resistant Mycobacterium tuberculosis strain using Genechips
inferredcites →https://doi.org/10.1016/s0140-6736(00)74210-3openalex-snapshot
TREATMENT OF STAPHYLOCOCCAL INFECTIONS WITH PENICILLIN BY INTERMITTENT STERILISATION
inferredcites →https://doi.org/10.1038/nbt1037openalex-snapshot
Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein
inferredcites →https://doi.org/10.1038/ncomms2898openalex-snapshot
Mycobacterium tuberculosis is extraordinarily sensitive to killing by a vitamin C-induced Fenton reaction
inferredcites →https://doi.org/10.1038/nmeth.2764openalex-snapshot
Entering the era of single-cell transcriptomics in biology and medicine
inferredcites →https://doi.org/10.1038/nrmicro3491openalex-snapshot
A functional perspective on phenotypic heterogeneity in microorganisms
inferredcites →https://doi.org/10.1038/nrmicro749openalex-snapshot
Tuberculosis: a problem with persistence
inferredcites →https://doi.org/10.1039/c4lc00109eopenalex-snapshot
Dielectrophoresis-based purification of antibiotic-treated bacterial subpopulations
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.02779.xopenalex-snapshot
Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling
inferredcites →https://doi.org/10.1073/pnas.1414207111openalex-snapshot
Noncanonical SMC protein in Mycobacterium smegmatis restricts maintenance of Mycobacterium fortuitum plasmids
inferredcites →https://doi.org/10.1073/pnas.87.3.862openalex-snapshot
Phage shock protein, a stress protein of Escherichia coli.
inferredcites →https://doi.org/10.1073/pnas.90.17.8194openalex-snapshot
Beta-galactosidase activity in single differentiating bacterial cells.
inferredcites →https://doi.org/10.1073/pnas.95.16.9578openalex-snapshot
The 16-kDa α-crystallin (Acr) protein of Mycobacterium tuberculosis is required for growth in macrophages
inferredcites →https://doi.org/10.1073/pnas.96.22.12833openalex-snapshot
Exploring drug-induced alterations in gene expression in Mycobacterium tuberculosis by microarray hybridization
inferredcites →https://doi.org/10.1074/jbc.m406796200openalex-snapshot
The Transcriptional Responses of Mycobacterium tuberculosis to Inhibitors of Metabolism
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.123.3.445openalex-snapshot
MICROBIAL PERSISTENCE
inferredcites →https://doi.org/10.1084/jem.123.3.469openalex-snapshot
MICROBIAL PERSISTENCE
inferredcites →https://doi.org/10.1086/605605openalex-snapshot
Biphasic Kill Curve of Isoniazid Reveals the Presence of Drug‐Tolerant, Not Drug‐Resistant,Mycobacterium tuberculosisin the Guinea Pig
inferredcites →https://doi.org/10.1093/emboj/16.19.5914openalex-snapshot
Transcriptional silencing by the mycobacteriophage L5 repressor
inferredcites →https://doi.org/10.1099/00221287-148-10-3129openalex-snapshot
Dissection of the heat-shock response in Mycobacterium tuberculosis using mutants and microarrays a aA list of the 100 ORFs most highly induced by heat shock is provided as supplementary data with the online version of this paper (http://mic.sgmjournals.org).
inferredcites →https://doi.org/10.1099/mic.0.29281-0openalex-snapshot
Evidence for complex interactions of stress-associated regulons in an mprAB deletion mutant of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1111/j.1365-2958.1994.tb00496.xopenalex-snapshot
Gene expression in mycobacteria: transcriptional fusions based on xylE and analysis of the promoter region of the response regulator mtrA from Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04510.xopenalex-snapshot
The Mycobacterium tuberculosis iniA gene is essential for activity of an efflux pump that confers drug tolerance to both isoniazid and ethambutol
inferredcites →https://doi.org/10.1126/science.1229858openalex-snapshot
Dynamic Persistence of Antibiotic-Stressed Mycobacteria
inferredcites →https://doi.org/10.1128/aac.03016-15openalex-snapshot
Rapid Whole-Cell Assay of Antitubercular Drugs Using Second-Generation Fluoromycobacteriophages
inferredcites →https://doi.org/10.1128/aac.47.9.2903-2913.2003openalex-snapshot
Signature Gene Expression Profiles Discriminate between Isoniazid-, Thiolactomycin-, and Triclosan-Treated Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1128/jb.181.23.7373-7380.1999openalex-snapshot
Transcription Regulation of the Colicin K cka Gene Reveals Induction of Colicin Synthesis by Differential Responses to Environmental Signals
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
inferredcites →https://doi.org/10.1128/jb.185.2.654-659.2003openalex-snapshot
A cka-gfp Transcriptional Fusion Reveals that the Colicin K Activity Gene Is Induced in Only 3 Percent of the Population
inferredcites →https://doi.org/10.1128/jb.187.4.1357-1368.2005openalex-snapshot
High- and Low-Threshold Genes in the Spo0A Regulon of Bacillus subtilis
inferredcites →https://doi.org/10.1128/jcm.01175-08openalex-snapshot
Poor Performance of Universal Sample Processing Method for Diagnosis of Pulmonary Tuberculosis by Smear Microscopy and Culture in Uganda
inferredcites →https://doi.org/10.1128/jcm.03530-14openalex-snapshot
A Novel Reporter Phage To Detect Tuberculosis and Rifampin Resistance in a High-HIV-Burden Population
inferredcites →https://doi.org/10.1128/jcm.06192-11openalex-snapshot
ϕ 2 GFP10, a High-Intensity Fluorophage, Enables Detection and Rapid Drug Susceptibility Testing of Mycobacterium tuberculosis Directly from Sputum Samples
inferredcites →https://doi.org/10.1128/mbio.01245-14openalex-snapshot
Specialized Transduction Designed for Precise High-Throughput Unmarked Deletions in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1128/mbio.01275-14openalex-snapshot
A Mycobacterium tuberculosis Cytochrome bd Oxidase Mutant Is Hypersensitive to Bedaquiline
inferredcites →https://doi.org/10.1146/annurev.micro.61.111606.122346openalex-snapshot
The Mechanism of Isoniazid Killing: Clarity Through the Scope of Genetics
inferredcites →https://doi.org/10.1186/1471-2180-8-51openalex-snapshot
par genes in Mycobacterium bovis and Mycobacterium smegmatisare arranged in an operon transcribed from "SigGC" promoters
inferredcites →https://doi.org/10.1186/s12916-016-0609-3openalex-snapshot
Profiling persistent tubercule bacilli from patient sputa during therapy predicts early drug efficacy
inferredcites →https://doi.org/10.1371/journal.pone.0001502openalex-snapshot
The Enduring Hypoxic Response of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1371/journal.pone.0004870openalex-snapshot
Fluoromycobacteriophages for Rapid, Specific, and Sensitive Antibiotic Susceptibility Testing of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1371/journal.ppat.1000662openalex-snapshot
An Anaerobic-Type α-Ketoglutarate Ferredoxin Oxidoreductase Completes the Oxidative Tricarboxylic Acid Cycle of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1371/journal.ppat.1004510openalex-snapshot
Succinate Dehydrogenase is the Regulator of Respiration in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.3181/00379727-50-13772openalex-snapshot
Activity of Penicillin in vitro
inferredcites →https://doi.org/10.3181/00379727-50-13773openalex-snapshot
Observations on the Mechanism of Action of Penicillin.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3299435openalex-extracted
Characterization and Elimination of Stochastically Generated Persister Subpopulation in Mycobacteria
inferred← citeshttps://doi.org/10.2139/ssrn.4846396openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471266949.bmc298openalex-snapshot
Antitubercular Agents
inferred← citeshttps://doi.org/10.1002/cyto.a.24030openalex-snapshot
Recent Developments in the Application of Flow Cytometry to Advance our Understanding of Mycobacterium tuberculosis Physiology and Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-030-53024-2_5openalex-snapshot
Molecular and Systems Biology Approaches for Analyzing Drug-Tolerant Bacterial Persister Cells
inferred← citeshttps://doi.org/10.1007/978-3-031-65986-7_3openalex-snapshot
Deciphering Microbial Regulation of Heterogeneity and Drug Adaptation with Meta-transcriptomics and Other System-Level Tools
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2023.03.016openalex-snapshot
Phages for the treatment of Mycobacterium species
inferred← citeshttps://doi.org/10.1016/j.chembiol.2023.04.014openalex-snapshot
Chemical approaches to unraveling the biology of mycobacteria
inferred← citeshttps://doi.org/10.1016/j.chom.2024.04.015openalex-snapshot
Variability in cell division among anatomical sites shapes Escherichia coli antibiotic survival in a urinary tract infection mouse model
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.02.016openalex-snapshot
The Isoniazid Paradigm of Killing, Resistance, and Persistence in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.mib.2020.07.006openalex-snapshot
Impact of bacterial persisters on their host
inferred← citeshttps://doi.org/10.1016/j.tube.2019.01.002openalex-snapshot
Mycobacteriophage ZoeJ: A broad host-range close relative of mycobacteriophage TM4
inferred← citeshttps://doi.org/10.1016/j.tube.2022.102201openalex-snapshot
Differential expression of the Mycobacterium tuberculosis heat shock protein genes in response to drug-induced stress
inferred← citeshttps://doi.org/10.1021/acsinfecdis.7b00231openalex-snapshot
Targeting the Proteostasis Network for Mycobacterial Drug Discovery
inferred← citeshttps://doi.org/10.1038/nrmicro.2016.173openalex-snapshot
Shining a light on persisters
inferred← citeshttps://doi.org/10.1038/s41598-024-79389-wopenalex-snapshot
Assessing the propensity of TB clinical isolates to form viable but non-replicating subpopulations
inferred← citeshttps://doi.org/10.1039/9781839163401-00101openalex-snapshot
Screening Technologies
inferred← citeshttps://doi.org/10.1073/pnas.1704376114openalex-snapshot
Enhanced respiration prevents drug tolerance and drug resistance in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1073/pnas.1818009116openalex-snapshot
Chemical disarming of isoniazid resistance in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1073/pnas.1914741117openalex-snapshot
Loss of phenotypic inheritance associated with ydcI mutation leads to increased frequency of small, slow persisters in Escherichia coli
inferred← citeshttps://doi.org/10.1073/pnas.2405983121openalex-snapshot
Tracking the progeny of bacterial persisters using a CRISPR-based genomic recorder
inferred← citeshttps://doi.org/10.1089/phage.2024.0059openalex-snapshot
Preclinical Evidence for Phage Therapy to Treat Mycobacterial Infections: A Narrative Review
inferred← citeshttps://doi.org/10.1093/bioinformatics/btaa941openalex-snapshot
PathExt: a general framework for path-based mining of omics-integrated biological networks
inferred← citeshttps://doi.org/10.1093/femspd/fty017openalex-snapshot
Fluorescent Mycobacterium tuberculosis reporters: illuminating host–pathogen interactions
inferred← citeshttps://doi.org/10.1093/femsre/fuab042openalex-snapshot
Phenotypic heterogeneity in persisters: a novel ‘hunker’ theory of persistence
inferred← citeshttps://doi.org/10.1093/jambio/lxae286openalex-snapshot
A single upstream mutation of whiB7 underlies amikacin and clarithromycin resistance in Mycobacterium abscessus
inferred← citeshttps://doi.org/10.1098/rstb.2024.0536openalex-snapshot
Translational bacterial biomarkers and pharmacodynamic models in the treatment of tuberculosis
inferred← citeshttps://doi.org/10.1099/mic.0.001035openalex-snapshot
Ribosome hibernation: a new molecular framework for targeting nonreplicating persisters of mycobacteria
inferred← citeshttps://doi.org/10.1099/mic.0.001041openalex-snapshot
From infection niche to therapeutic target: the intracellular lifestyle of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1101/2024.01.10.574965openalex-snapshot
Gallein and isoniazid act synergistically to attenuate Mycobacterium tuberculosis growth in human macrophages
inferred← citeshttps://doi.org/10.1101/2025.10.17.683099openalex-snapshot
Mouse Models Uniformly Featuring Human-like Lesions Harboring Drug-tolerant Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1101/463232openalex-snapshot
PerSort facilitates characterization and elimination of persister subpopulation in mycobacteria
inferred← citeshttps://doi.org/10.1111/mmi.13952openalex-snapshot
RbpA and σB association regulates polyphosphate levels to modulate mycobacterial isoniazid‐tolerance
inferred← citeshttps://doi.org/10.1128/9781683670131.ch63openalex-snapshot
Mycobacteriophages
inferred← citeshttps://doi.org/10.1128/aac.00967-21openalex-snapshot
Assessing Antibiotic Tolerance of Staphylococcus aureus Derived Directly from Patients by the Replica Plating Tolerance Isolation System (REPTIS)
inferred← citeshttps://doi.org/10.1128/aac.01213-19openalex-snapshot
Adaptation of Mycobacterium tuberculosis to Biofilm Growth Is Genetically Linked to Drug Tolerance
inferred← citeshttps://doi.org/10.1128/aac.01703-20openalex-snapshot
The Promises and Limitations of N -Acetylcysteine as a Potentiator of First-Line and Second-Line Tuberculosis Drugs
inferred← citeshttps://doi.org/10.1128/aac.01834-18openalex-snapshot
Early Detection of Emergent Extensively Drug-Resistant Tuberculosis by Flow Cytometry-Based Phenotyping and Whole-Genome Sequencing
inferred← citeshttps://doi.org/10.1128/iai.00246-23openalex-snapshot
Delayed host mortality and immune response upon infection with P. aeruginosa persister cells
inferred← citeshttps://doi.org/10.1128/iai.00574-25openalex-snapshot
Mouse models of tuberculosis uniformly featuring hypoxic necrotic lesions and poor response to chemotherapy
inferred← citeshttps://doi.org/10.1128/jb.00411-20openalex-snapshot
Nanoluciferase Reporter Mycobacteriophage for Sensitive and Rapid Detection of Mycobacterium tuberculosis Drug Susceptibility
inferred← citeshttps://doi.org/10.1128/mbio.00374-24openalex-snapshot
Differential impacts of DNA repair machinery on fluoroquinolone persisters with different chromosome abundances
inferred← citeshttps://doi.org/10.1128/mbio.00938-18openalex-snapshot
Rational Design of Biosafety Level 2-Approved, Multidrug-Resistant Strains of Mycobacterium tuberculosis through Nutrient Auxotrophy
inferred← citeshttps://doi.org/10.1128/mbio.02101-17openalex-snapshot
Synergistic Lethality of a Binary Inhibitor of Mycobacterium tuberculosis KasA
inferred← citeshttps://doi.org/10.1128/mbio.02391-20openalex-snapshot
Sterilization by Adaptive Immunity of a Conditionally Persistent Mutant of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1128/mbio.02968-23openalex-snapshot
Inducing vulnerability to InhA inhibition restores isoniazid susceptibility in drug-resistant Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1128/microbiolspec.gpp3-0026-2018openalex-snapshot
Mycobacteriophages
inferred← citeshttps://doi.org/10.1128/msystems.00699-22openalex-snapshot
Mycobacterium tuberculosis Requires the Outer Membrane Lipid Phthiocerol Dimycocerosate for Starvation-Induced Antibiotic Tolerance
inferred← citeshttps://doi.org/10.1128/msystems.01127-20openalex-snapshot
PerSort Facilitates Characterization and Elimination of Persister Subpopulation in Mycobacteria
inferred← citeshttps://doi.org/10.1128/spectrum.02948-22openalex-snapshot
Noise in a Metabolic Pathway Leads to Persister Formation in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1134/s0026893318030020openalex-snapshot
Molecular Mechanisms of Drug Tolerance in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1139/cjm-2024-0116openalex-snapshot
Mechanisms and implications of phenotypic switching in bacterial pathogens
inferred← citeshttps://doi.org/10.1146/annurev-micro-020518-115650openalex-snapshot
Bacterial Persisters and Infection: Past, Present, and Progressing
inferred← citeshttps://doi.org/10.1146/annurev-virology-122019-070009openalex-snapshot
Actinobacteriophages: Genomics, Dynamics, and Applications
inferred← citeshttps://doi.org/10.1172/jci162688openalex-snapshot
A world without tuberculosis: moving from imagination to reality
inferred← citeshttps://doi.org/10.1172/jci173156openalex-snapshot
The Mycobacterium tuberculosis genome at 25 years: lessons and lingering questions
inferred← citeshttps://doi.org/10.1186/s12864-019-5782-2openalex-snapshot
Whole genome sequencing Mycobacterium tuberculosis directly from sputum identifies more genetic diversity than sequencing from culture
inferred← citeshttps://doi.org/10.1371/journal.pone.0338563openalex-snapshot
Rapid and efficient labeling by a selective organic fluorophore probe highlights heterogeneity of mycobacterial populations and persister resuscitation
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010459openalex-snapshot
Spatial relationships of intra-lesion heterogeneity in Mycobacterium tuberculosis microenvironment, replication status, and drug efficacy
inferred← citeshttps://doi.org/10.2147/idr.s419914openalex-snapshot
Mycobacterium tuberculosis Rv0494 Protein Contributes to Mycobacterial Persistence
inferred← citeshttps://doi.org/10.32604/biocell.2020.011713openalex-snapshot
Progresses of mycobacteriophage-based Mycobacterium tuberculosis detection
inferred← citeshttps://doi.org/10.3389/fcimb.2022.933458openalex-snapshot
Are all antibiotic persisters created equal?
inferred← citeshttps://doi.org/10.3389/fcimb.2022.956607openalex-snapshot
Phenotypic adaptation of Mycobacterium tuberculosis to host-associated stressors that induce persister formation
inferred← citeshttps://doi.org/10.3389/fcimb.2022.958555openalex-snapshot
Understanding the contribution of metabolism to Mycobacterium tuberculosis drug tolerance
inferred← citeshttps://doi.org/10.3389/fcimb.2022.981827openalex-snapshot
Persistence of Mycobacterium tuberculosis in response to infection burden and host-induced stressors
inferred← citeshttps://doi.org/10.3389/fcimb.2025.1589236openalex-snapshot
Rapid detection of drug resistance in Mycobacterium tuberculosis clinical isolates for first-line antitubercular drugs by using a novel reporter mycobacteriophage
inferred← citeshttps://doi.org/10.3389/fgene.2019.00477openalex-snapshot
Effects of Host, Sample, and in vitro Culture on Genomic Diversity of Pathogenic Mycobacteria
inferred← citeshttps://doi.org/10.3389/fmicb.2019.00249openalex-snapshot
Genome-Wide Transcriptional Responses of Mycobacterium to Antibiotics
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01924openalex-snapshot
Tolerance and Persistence to Drugs: A Main Challenge in the Fight Against Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.3389/fmicb.2020.618168openalex-snapshot
Early Drug Development and Evaluation of Putative Antitubercular Compounds in the -Omics Era
inferred← citeshttps://doi.org/10.3389/fmicb.2021.748121openalex-snapshot
Eradication of Porphyromonas gingivalis Persisters Through Colloidal Bismuth Subcitrate Synergistically Combined With Metronidazole
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1369763openalex-snapshot
Gallein potentiates isoniazid's ability to suppress Mycobacterium tuberculosis growth
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1415554openalex-snapshot
Regulatory role of Mycobacterium tuberculosis MtrA on dormancy/resuscitation revealed by a novel target gene-mining strategy
inferred← citeshttps://doi.org/10.3390/antibiotics10111323openalex-snapshot
The Mycobacterial DNA Methyltransferase HsdM Decreases Intrinsic Isoniazid Susceptibility
inferred← citeshttps://doi.org/10.3390/app10072278openalex-snapshot
Mycobacterial Cell Wall: A Source of Successful Targets for Old and New Drugs
inferred← citeshttps://doi.org/10.3390/biomedicines13112609openalex-snapshot
Promising Approaches Based on Bioimaging Reporters for Direct Rapid Detection of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.3390/ijms22020735openalex-snapshot
Mycobacteriophages as Potential Therapeutic Agents against Drug-Resistant Tuberculosis
inferred← citeshttps://doi.org/10.3390/ijms23105728openalex-snapshot
RNA Sequencing Reveals the Upregulation of FOXO Signaling Pathway in Porphyromonas gingivalis Persister-Treated Human Gingival Epithelial Cells
inferred← citeshttps://doi.org/10.3390/v12090944openalex-snapshot
Reporter Phage-Based Detection of Bacterial Pathogens: Design Guidelines and Recent Developments
inferred← citeshttps://doi.org/10.64898/2026.08.21.746198openalex-snapshot
Visualizing zinc-starved slow-replicating Mycobacterium tuberculosis in neutrophil-rich lung lesions
inferred← citeshttps://doi.org/10.70675/a814c67cz9630z40f6z8867z43d3267f3290openalex-snapshot
Single-cell screening for noise-modulating compounds : an unconventional strategy to tackle antibiotic persistence
inferred← citeshttps://doi.org/10.70675/d220d286z1b89z484fz9005z9223aaa1d9ccopenalex-snapshot
Analyse de la non-réponse aux antibiotiques in vivo, appliquée aux infections urinaires à Escherichia coli
inferred← citeshttps://doi.org/10.7554/elife.58542openalex-snapshot
Drivers and sites of diversity in the DNA adenine methylomes of 93 Mycobacterium tuberculosis complex clinical isolates
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.