On the public citation graph
Network analysis reveals differential metabolic functionality in antibiotic-resistant Pseudomonas aeruginosa
0 signed · 67 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.arcmed.2005.06.009openalex-snapshot
Resistance to Antibiotics: Are We in the Post-Antibiotic Era?
inferredcites →https://doi.org/10.1016/j.cell.2018.01.037openalex-snapshot
Targeting Antibiotic Tolerance, Pathogen by Pathogen
inferredcites →https://doi.org/10.1016/j.chembiol.2016.12.015openalex-snapshot
Carbon Sources Tune Antibiotic Susceptibility in Pseudomonas aeruginosa via Tricarboxylic Acid Cycle Control
inferredcites →https://doi.org/10.1016/j.chom.2015.07.006openalex-snapshot
Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis Lungs
inferredcites →https://doi.org/10.1016/j.cmet.2015.01.008openalex-snapshot
Exogenous Alanine and/or Glucose plus Kanamycin Kills Antibiotic-Resistant Bacteria
inferredcites →https://doi.org/10.1016/j.copbio.2017.11.014openalex-snapshot
Biomedical applications of genome-scale metabolic network reconstructions of human pathogens
inferredcites →https://doi.org/10.1016/j.copbio.2018.01.026openalex-snapshot
Toward prediction and control of antibiotic-resistance evolution
inferredcites →https://doi.org/10.1016/j.ijantimicag.2006.12.012openalex-snapshot
Pandrug-resistant Gram-negative bacteria: the dawn of the post-antibiotic era?
inferredcites →https://doi.org/10.1038/ismej.2014.45openalex-snapshot
Microbiome of prebiotic-treated mice reveals novel targets involved in host response during obesity
inferredcites →https://doi.org/10.1038/msb.2009.77openalex-snapshot
Applications of genome‐scale metabolic reconstructions
inferredcites →https://doi.org/10.1038/msb.2013.57openalex-snapshot
Bacterial evolution of antibiotic hypersensitivity
inferredcites →https://doi.org/10.1038/nbt.3956openalex-snapshot
iML1515, a knowledgebase that computes Escherichia coli traits
inferredcites →https://doi.org/10.1038/ncomms14631openalex-snapshot
Reconstruction of the metabolic network of Pseudomonas aeruginosa to interrogate virulence factor synthesis
inferredcites →https://doi.org/10.1038/ncomms6792openalex-snapshot
Prediction of antibiotic resistance by gene expression profiles
inferredcites →https://doi.org/10.1038/ng.1034openalex-snapshot
Evolutionary paths to antibiotic resistance under dynamically sustained drug selection
inferredcites →https://doi.org/10.1038/nprot.2011.308openalex-snapshot
Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox v2.0
inferredcites →https://doi.org/10.1038/nrg3351openalex-snapshot
Understanding, predicting and manipulating the genotypic evolution of antibiotic resistance
inferredcites →https://doi.org/10.1038/nrg3643openalex-snapshot
Constraint-based models predict metabolic and associated cellular functions
inferredcites →https://doi.org/10.1038/nrg3744openalex-snapshot
Empirical fitness landscapes and the predictability of evolution
inferredcites →https://doi.org/10.1073/pnas.0511100103openalex-snapshot
An ordered, nonredundant library of Pseudomonas aeruginosa strain PA14 transposon insertion mutants
inferredcites →https://doi.org/10.1073/pnas.1311217110openalex-snapshot
Genome-wide fitness profiling reveals adaptations required by Haemophilus in coinfection with influenza A virus in the murine lung
inferredcites →https://doi.org/10.1073/pnas.1509743112openalex-snapshot
Antibiotic efficacy is linked to bacterial cellular respiration
inferredcites →https://doi.org/10.1086/338782openalex-snapshot
Multiple Mechanisms of Antimicrobial Resistance in Pseudomonas aeruginosa: Our Worst Nightmare?
inferredcites →https://doi.org/10.1093/nar/gkv1227openalex-snapshot
Enhanced annotations and features for comparing thousands of Pseudomonas genomes in the Pseudomonas genome database
inferredcites →https://doi.org/10.1096/fasebj.3.14.2556311openalex-snapshot
Bacterial adaptation to oxidative stress: implications for pathogenesis and interaction with phagocytic cells
inferredcites →https://doi.org/10.1099/mic.0.2007/014506-0openalex-snapshot
Virulence determinants from a cystic fibrosis isolate of Pseudomonas aeruginosa include isocitrate lyase
inferredcites →https://doi.org/10.1101/gr.3832305openalex-snapshot
Parallel adaptive evolution cultures ofEscherichia colilead to convergent growth phenotypes with different gene expression states
inferredcites →https://doi.org/10.1111/1462-2920.13336openalex-snapshot
Pyomelanin‐producing Pseudomonas aeruginosa selected during chronic infections have a large chromosomal deletion which confers resistance to pyocins
inferredcites →https://doi.org/10.1111/eva.12196openalex-snapshot
The fitness costs of antibiotic resistance mutations
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02211.xopenalex-snapshot
Early adaptive developments of Pseudomonas aeruginosa after the transition from life in the environment to persistent colonization in the airways of human cystic fibrosis hosts
inferredcites →https://doi.org/10.1111/j.1574-6976.2008.00146.xopenalex-snapshot
Genome-scale models of bacterial metabolism: reconstruction and applications
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00282.xopenalex-snapshot
Metabolic regulation of antibiotic resistance
inferredcites →https://doi.org/10.1126/science.287.5457.1479openalex-snapshot
Effects of Environment on Compensatory Mutations to Ameliorate Costs of Antibiotic Resistance
inferredcites →https://doi.org/10.1126/science.aag0822openalex-snapshot
Spatiotemporal microbial evolution on antibiotic landscapes
inferredcites →https://doi.org/10.1126/scitranslmed.3006609openalex-snapshot
Use of Collateral Sensitivity Networks to Design Drug Cycling Protocols That Avoid Resistance Development
inferredcites →https://doi.org/10.1128/aac.00507-08openalex-snapshot
Novel Genetic Determinants of Low-Level Aminoglycoside Resistance in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/aac.00704-06openalex-snapshot
Cumulative Effects of Several Nonenzymatic Mechanisms on the Resistance of Pseudomonas aeruginosa to Aminoglycosides
inferredcites →https://doi.org/10.1128/aac.01203-10openalex-snapshot
Nitric Oxide Protects Bacteria from Aminoglycosides by Blocking the Energy-Dependent Phases of Drug Uptake
inferredcites →https://doi.org/10.1128/aac.44.5.1223-1228.2000openalex-snapshot
Evidence for Active Efflux as the Primary Mechanism of Resistance to Ciprofloxacin in Salmonella enterica Serovar Typhimurium
inferredcites →https://doi.org/10.1128/aac.46.5.1204-1211.2002openalex-snapshot
Fitness Cost of Chromosomal Drug Resistance-Conferring Mutations
inferredcites →https://doi.org/10.1128/aem.72.3.2070-2079.2006openalex-snapshot
The atu and liu Clusters Are Involved in the Catabolic Pathways for Acyclic Monoterpenes and Leucine in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/cmr.00040-09openalex-snapshot
Antibacterial-Resistant Pseudomonas aeruginosa : Clinical Impact and Complex Regulation of Chromosomally Encoded Resistance Mechanisms
inferredcites →https://doi.org/10.1128/iai.01199-10openalex-snapshot
Genotype and Phenotypes of an Intestine-Adapted Escherichia coli K-12 Mutant Selected by Animal Passage for Superior Colonization
inferredcites →https://doi.org/10.1128/iai.74.2.1091-1096.2006openalex-snapshot
Virulence of Staphylococcus aureus Small Colony Variants in the Caenorhabditis elegans Infection Model
inferredcites →https://doi.org/10.1128/jb.00555-07openalex-snapshot
Oxidative Stress Evokes a Metabolic Adaptation That Favors Increased NADPH Synthesis and Decreased NADH Production in Pseudomonas fluorescens
inferredcites →https://doi.org/10.1128/jb.00740-06openalex-snapshot
Experimental and Computational Assessment of Conditionally Essential Genes inEscherichia coli
inferredcites →https://doi.org/10.1128/jb.01138-07openalex-snapshot
Nutritional Cues Control Pseudomonas aeruginosa Multicellular Behavior in Cystic Fibrosis Sputum
inferredcites →https://doi.org/10.1128/jb.01175-10openalex-snapshot
Pseudomonas aeruginosa Enhances Production of an Antimicrobial in Response to N -Acetylglucosamine and Peptidoglycan
inferredcites →https://doi.org/10.1128/jb.02127-14openalex-snapshot
The Staphylococcus aureus NuoL-Like Protein MpsA Contributes to the Generation of Membrane Potential
inferredcites →https://doi.org/10.1128/jb.187.14.4908-4920.2005openalex-snapshot
A Cystic Fibrosis Epidemic Strain of Pseudomonas aeruginosa Displays Enhanced Virulence and Antimicrobial Resistance
inferredcites →https://doi.org/10.1128/mbio.00078-15openalex-snapshot
Genetic Basis of Persister Tolerance to Aminoglycosides in Escherichia coli
inferredcites →https://doi.org/10.1128/mr.51.4.439-457.1987openalex-snapshot
Bacterial uptake of aminoglycoside antibiotics
inferredcites →https://doi.org/10.1186/1475-2859-12-64openalex-snapshot
Adaptive laboratory evolution – principles and applications for biotechnology
inferredcites →https://doi.org/10.1186/gb-2003-4-9-r54openalex-snapshot
An expanded genome-scale model of Escherichia coli K-12 (iJR904 GSM/GPR)
inferredcites →https://doi.org/10.1186/s12864-017-3905-1openalex-snapshot
Novel Plasmodium falciparum metabolic network reconstruction identifies shifts associated with clinical antimalarial resistance
inferredcites →https://doi.org/10.1186/s12866-015-0563-9openalex-snapshot
Within-host microevolution of Pseudomonas aeruginosa in Italian cystic fibrosis patients
inferredcites →https://doi.org/10.1186/s12918-017-0427-zopenalex-snapshot
A scalable metabolite supplementation strategy against antibiotic resistant pathogen Chromobacterium violaceum induced by NAD+/NADH+ imbalance
inferredcites →https://doi.org/10.1371/journal.pbio.2001586openalex-snapshot
History of antibiotic adaptation influences microbial evolutionary dynamics during subsequent treatment
inferredcites →https://doi.org/10.1371/journal.ppat.1000541openalex-snapshot
Interplay in the Selection of Fluoroquinolone Resistance and Bacterial Fitness
inferredcites →https://doi.org/10.1371/journal.ppat.1000712openalex-snapshot
Nutrient Availability as a Mechanism for Selection of Antibiotic Tolerant Pseudomonas aeruginosa within the CF Airway
inferredcites →https://doi.org/10.1371/journal.ppat.1004947openalex-snapshot
N-acetylglucosamine Regulates Virulence Properties in Microbial Pathogens
inferredcites →https://doi.org/10.15252/msb.20167028openalex-snapshot
Metabolic constraints on the evolution of antibiotic resistance
inferredcites →https://doi.org/10.3389/fmicb.2017.00816openalex-snapshot
Adaptive Laboratory Evolution of Antibiotic Resistance Using Different Selection Regimes Lead to Similar Phenotypes and Genotypes
inferredcites →https://doi.org/10.3389/fphys.2012.00299openalex-snapshot
Integration of expression data in genome-scale metabolic network reconstructions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1371/journal.pone.0210008openalex-snapshot
Constraints-based analysis identifies NAD+ recycling through metabolic reprogramming in antibiotic resistant Chromobacterium violaceum
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.