DNA Damage Repair and Bacterial Pathogens

Immunity, Inflammation, and Cancer

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DNA Repair and Mutagenesis

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The DNA Damage Response: Making It Safe to Play with Knives

Ciccia, A., & Elledge, S. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.019 · Cited by 4,368

Intestinal inflammation targets cancer-inducing activity of the microbiota

Arthur, J. C., Perez-Chanona, E., Mühlbauer, M., Tomkovich, S., Uronis, J. M., Fan, T.-J., Campbell, B. J., Abujamel, T., Dogan, B., Rogers, A. B., et al. (2012) · Science · doi:10.1126/science.1224820 · Cited by 2,263

-H2AX in recognition and signaling of DNA double-strand breaks in the context of chromatin

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Escherichia coli Induces DNA Double-Strand Breaks in Eukaryotic Cells

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SOS response promotes horizontal dissemination of antibiotic resistance genes

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Helicobacter pylori: gastric cancer and beyond

Polk, D. B., & Peek, R. M. (2010) · Nature Reviews Cancer · doi:10.1038/nrc2857 · Cited by 1,158

Escherichia coli induces DNA damage in vivo and triggers genomic instability in mammalian cells

Cuevas-Ramos, G., Petit, C. R., Marcq, I., Boury, M., Oswald, E., & Nougayrède, J.-P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001261107 · Cited by 855

Ciprofloxacin Causes Persister Formation by Inducing the TisB toxin in Escherichia coli

Dörr, T., Vulić, M., & Lewis, K. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000317 · Cited by 781

Whole metagenome profiling reveals skin microbiome-dependent susceptibility to atopic dermatitis flare

Chng, K. R., Tay, A. S. L., Li, C., Ng, A. H. Q., Wang, J., Suri, B. K., Matta, S. A., McGovern, N., Janela, B., Wong, X. F. C. C., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.106 · Cited by 388

Bacterial Stress Responses as Potential Targets in Overcoming Antibiotic Resistance

Dawan, J., & Ahn, J. (2022) · Microorganisms · doi:10.3390/microorganisms10071385 · Cited by 230

TMEM173 Drives Lethal Coagulation in Sepsis

Zhang, H., Zeng, L., Xie, M., Liu, J., Zhou, B., Wu, R., Cao, L., Kroemer, G., Wang, H., Billiar, T. R., et al. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.02.004 · Cited by 203

Nickel Carcinogenesis Mechanism: DNA Damage

Guo, H., Liu, H., Wu, H., Cui, H., Fang, J. S., Zuo, Z., Deng, J., Li, Y., Wang, X., & Zhao, L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194690 · Cited by 191

Focus on UV-Induced DNA Damage and Repair—Disease Relevance and Protective Strategies

Kciuk, M., Marciniak, B., Mojzych, M., & Kontek, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197264 · Cited by 168

Resveratrol antibacterial activity against Escherichia coli is mediated by Z-ring formation inhibition via suppression of FtsZ expression

Hwang, D., & Lim, Y. (2015) · Scientific Reports · doi:10.1038/srep10029 · Cited by 165

DNA damage and innate immunity: links and trade-offs

Chatzinikolaou, G., Karakasilioti, I., & Garinis, G. A. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.06.003 · Cited by 145

Efflux Pump Induction by Quaternary Ammonium Compounds and Fluoroquinolone Resistance in Bacteria

Buffet‐Bataillon, S., Tattevin, P., Maillard, J., Bonnaure‐Mallet, M., & Jolivet‐Gougeon, A. (2015) · Future Microbiology · doi:10.2217/fmb.15.131 · Cited by 127

Lack of AcrB Efflux Function Confers Loss of Virulence on Salmonella enterica Serovar Typhimurium

Wang‐Kan, X., Blair, J. M. A., Chirullo, B., Betts, J. W., Ragione, R. M. L., Ivens, A. C., Ricci, V., Opperman, T. J., & Piddock, L. J. V. (2017) · mBio · doi:10.1128/mbio.00968-17 · Cited by 124

Targeting the Bacterial Division Protein FtsZ

Hurley, K. A., Santos, T. M. A., Nepomuceno, G. M., Huynh, V., Shaw, J. T., & Weibel, D. B. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5b01098 · Cited by 121

Bacterial DNA excision repair pathways

Wozniak, K. J., & Simmons, L. A. (2022) · Nature Reviews Microbiology · doi:10.1038/s41579-022-00694-0 · Cited by 107

Cellular stress promotes NOD1/2‐dependent inflammation via the endogenous metabolite sphingosine‐1‐phosphate

Pei, G., Żyła, J., He, L., Moura‐Alves, P., Steinle, H., Saikali, P., Lozza, L., Nieuwenhuizen, N. E., Weiner, J. M., Mollenkopf, H., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020106272 · Cited by 83

In Vitro Evaluation of the Potential Pharmacological Activity and Molecular Targets of New Benzimidazole-Based Schiff Base Metal Complexes

Aragón-Muriel, A., Liscano, Y., Upegui, Y., Robledo, S. M., Ramírez‐Apán, M. T., Morales‐Morales, D., Oñate-Garzón, J., & Polo‐Cerón, D. (2021) · Antibiotics · doi:10.3390/antibiotics10060728 · Cited by 83

The central role of the SOS DNA repair system in antibiotics resistance: A new target for a new infectious treatment strategy

Memar, M. Y., Yekani, M., Celenza, G., Poortahmasebi, V., Naghili, B., Bellio, P., & Baghi, H. B. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118562 · Cited by 77

Host Directed Therapy Against Infection by Boosting Innate Immunity

Bergman, P., Raqib, R., Rekha, R. S., Agerberth, B., & Gudmundsson, G. H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01209 · Cited by 72

White rot fungi and advanced combined biotechnology with nanomaterials: promising tools for endocrine-disrupting compounds biotransformation

Huang, D., Guo, X., Peng, Z., Zeng, G., Xu, P., Gong, X., Deng, R., Xue, W., Wang, R., Yi, H., et al. (2017) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2017.1386613 · Cited by 67

The problems of antibiotic resistance in cystic fibrosis and solutions

López-Causapé, C., Rojo‐Molinero, E., Macia, M. D., & Oliver, A. (2014) · Expert Review of Respiratory Medicine · doi:10.1586/17476348.2015.995640 · Cited by 72

The Dynamics of the Antimicrobial Resistance Mobilome of Salmonella enterica and Related Enteric Bacteria

Algarni, S., Ricke, S. C., Foley, S. L., & Han, J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.859854 · Cited by 69

DNA Damage: From Chronic Inflammation to Age-Related Deterioration

Ιωαννίδου, Ά., Goulielmaki, E., & Garinis, G. A. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00187 · Cited by 62

Oxidative stress-induced DNA damage and DNA repair mechanisms in mangrove bacteria exposed to climatic and heavy metal stressors

Rath, S., & Das, S. (2023) · Environmental Pollution · doi:10.1016/j.envpol.2023.122722 · Cited by 63

CRN 13 candidate effectors from plant and animal eukaryotic pathogens are DNA ‐binding proteins which trigger host DNA damage response

Ramirez‐Garcés, D., Camborde, L., Pel, M. J. C., Jauneau, A., Martinez, Y., Néant, I., Leclerc, C., Moreau, M., Dumas, B., & Gaulin, E. (2015) · New Phytologist · doi:10.1111/nph.13774 · Cited by 57

Molecular investigation of the radiation resistance of edible cyanobacterium Arthrospira sp. PCC 8005

Badri, H., Monsieurs, P., Coninx, I., Wattiez, R., & Leys, N. (2015) · MicrobiologyOpen · doi:10.1002/mbo3.229 · Cited by 56

The Secreted Protease PrtA Controls Cell Growth, Biofilm Formation and Pathogenicity in Xylella fastidiosa

Gouran, H., Gillespie, H. W., Nascimento, R., Chakraborty, S., Zaini, P. A., Jacobson, A., Phinney, B. S., Dolan, D., Durbin-Johnson, B. P., Antonova, E. S., et al. (2016) · Scientific Reports · doi:10.1038/srep31098 · Cited by 53

A Web Resource for Designing Subunit Vaccine Against Major Pathogenic Species of Bacteria

Nagpal, G., Usmani, S. S., & Raghava, G. P. S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02280 · Cited by 43

Transcriptomic and proteomic profiling response of methicillin-resistant Staphylococcus aureus (MRSA) to a novel bacteriocin, plantaricin GZ1-27 and its inhibition of biofilm formation

Du, H., Zhou, L., Lu, Z., Bie, X., Zhao, H., Niu, Y. D., & Lü, F. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10589-w · Cited by 43

Sensing Bacterial-Induced DNA Damaging Effects via Natural Killer Group 2 Member D Immune Receptor: From Dysbiosis to Autoimmunity and Carcinogenesis

Espinoza, J. L., & Minami, M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00052 · Cited by 45

Ciprofloxacin, amoxicillin, and aminoglycosides stimulate genetic and phenotypic changes in uropathogenic Escherichia coli strains

Adamus-Białek, W., Wawszczak-Kasza, M., Arabski, M., Majchrzak, M., Gulba, M., Jarych, D., Parniewski, P., & Głuszek, S. (2019) · Virulence · doi:10.1080/21505594.2019.1596507 · Cited by 40

Ciprofloxacin provokes SOS-dependent changes in respiration and membrane potential and causes alterations in the redox status of Escherichia coli

Smirnova, G. V., Tyulenev, A. V., Muzyka, N. G., Петерс, М. А., & Oktyabrsky, O. N. (2016) · Research in Microbiology · doi:10.1016/j.resmic.2016.07.008 · Cited by 39

Inactivation of Salmonella spp., pathogenic Escherichia coli , Staphylococcus spp., or Listeria monocytogenes in chicken purge or skin using a 405-nm LED array

Sommers, C. H., Gunther, N. W., IV, & Sheen, S. (2016) · Food Microbiology · doi:10.1016/j.fm.2016.12.011 · Cited by 39

CPX-351 exploits the gut microbiota to promote mucosal barrier function, colonization resistance, and immune homeostasis

Renga, G., Nunzi, E., Stincardini, C., Pariano, M., Puccetti, M., Pieraccini, G., Serio, C. D., Fraziano, M., Poerio, N., Oikonomou, V., et al. (2024) · Blood · doi:10.1182/blood.2023021380 · Cited by 44

Drivers of bacterial genomes plasticity and roles they play in pathogen virulence, persistence and drug resistance

Patel, S. V. (2016) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2016.08.030 · Cited by 37

The molecular mechanism and post-transcriptional regulation characteristic of Tetragenococcus halophilus acclimation to osmotic stress revealed by quantitative proteomics

Lin, J., Liang, H., Yan, J., & Luo, L. (2017) · Journal of Proteomics · doi:10.1016/j.jprot.2017.08.014 · Cited by 37

Proteome profiling of carbapenem-resistant K. pneumoniae clinical isolate (NDM-4): Exploring the mechanism of resistance and potential drug targets

Sharma, D., Garg, A., Kumar, M., & Khan, A. U. (2019) · Journal of Proteomics · doi:10.1016/j.jprot.2019.04.003 · Cited by 33

Factors and Mechanisms Influencing Conjugation In Vivo in the Gastrointestinal Tract Environment: A Review

Liu, W., Huang, Y., Zhang, H., Liu, Z., Huan, Q., Xiao, X., & Wang, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065919 · Cited by 33

Collateral sensitivity: An evolutionary trade‐off between antibiotic resistance mechanisms, attractive for dealing with drug‐resistance crisis

Yekani, M., Azargun, R., Sharifi, S., Nabizadeh, E., Nahand, J. S., Ansari, N. K., Memar, M. Y., & Sóki, J. (2023) · Health Science Reports · doi:10.1002/hsr2.1418 · Cited by 30

A Network Biology Approach to Decipher Stress Response in Bacteria Using Escherichia coli As a Model

Nagar, S. D., Aggarwal, B., Joon, S., Bhatnagar, R., & Bhatnagar, S. (2016) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2016.0028 · Cited by 30

Global transcriptome analysis of Halolamina sp. to decipher the salt tolerance in extremely halophilic archaea

Kurt‐Kızıldoğan, A., Abanoz-Seçgin, B., & Okay, S. (2016) · Gene · doi:10.1016/j.gene.2016.11.042 · Cited by 29

DNA double-strand breaks in the Toxoplasma gondii-infected cells by the action of reactive oxygen species

Zhuang, H., Yao, C., Zhao, X. F., Chen, X., Yang, Y., Huang, S., Pan, L., Du, A., & Yang, Y. (2020) · Parasites & Vectors · doi:10.1186/s13071-020-04324-7 · Cited by 25

Liquid Chromatography-Nanoelectrospray Ionization-High-Resolution Tandem Mass Spectrometry Analysis of Apurinic/Apyrimidinic Sites in Oral Cell DNA of Cigarette Smokers, e-Cigarette Users, and Nonsmokers

Guo, J., Ikuemonisan, J., Hatsukami, D. K., & Hecht, S. S. (2021) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.1c00308 · Cited by 25

Gene Network Analysis of Metallo Beta Lactamase Family Proteins Indicates the Role of Gene Partners in Antibiotic Resistance and Reveals Important Drug Targets

Anitha, P., Anbarasu, A., & Ramaiah, S. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25422 · Cited by 25

Exposure of cyanobacterium Nostoc sp. to the Mars-like stratosphere environment

Ye, T., Wang, B., Li, C., Bian, P., Chen, L., & Wang, G. (2021) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2021.112307 · Cited by 21

Evaluation of 1,4-naphthoquinone derivatives as antibacterial agents: activity and mechanistic studies

Liu, Z., Shen, Z., Xiang, S., Sun, Y., Cui, J., & Jia, J. (2022) · Frontiers of Environmental Science & Engineering · doi:10.1007/s11783-023-1631-2 · Cited by 23

The SOS Response Master Regulator LexA Regulates the Gene Transfer Agent of Rhodobacter capsulatus and Represses Transcription of the Signal Transduction Protein CckA

Kuchinski, K. S., Brimacombe, C. A., Westbye, A. B., Ding, H., & Beatty, J. T. (2016) · Journal of Bacteriology · doi:10.1128/jb.00839-15 · Cited by 23

Tightly controlled response to oxidative stress; an important factor in the tolerance of Bacteroides fragilis

Yekani, M., Baghi, H. B., Vahed, S. Z., Ghanbari, H., Hoseinpur, R., Azargun, R., Azimi, S., & Memar, M. Y. (2021) · Research in Microbiology · doi:10.1016/j.resmic.2021.103798 · Cited by 22

Improving the Editing Efficiency of CRISPR-Cas9 by Reducing the Generation of Escapers Based on the Surviving Mechanism

Li, Q., Sun, M., Lv, L., Zuo, Y., Zhang, S., Zhang, Y., & Yang, S. (2023) · ACS Synthetic Biology · doi:10.1021/acssynbio.2c00619 · Cited by 22

Multi-Organ Transcriptome Response of Lumpfish (Cyclopterus lumpus) to Aeromonas salmonicida Subspecies salmonicida Systemic Infection

Chakraborty, S., Hossain, A., Cao, T., Gnanagobal, H., Segovia, C., Hill, S., Monk, J., Porter, J., Boyce, D., Hall, J. R., et al. (2022) · Microorganisms · doi:10.3390/microorganisms10112113 · Cited by 22

Effects of dietary fat on androgen secretion and metabolism.

Gromadzka-Ostrowska, J. (2006) · PubMed · Cited by 21

Molecular processes underlying synergistic linuron mineralization in a triple‐species bacterial consortium biofilm revealed by differential transcriptomics

Albers, P., Weytjens, B., Mot, R. D., Kathleen Marchal, D., & Springael, D. (2018) · MicrobiologyOpen · doi:10.1002/mbo3.559 · Cited by 20

Auto-regulation of DNA degrading bacteriocins: molecular and ecological aspects

Ghazaryan, L., Soares, M. I. M., & Gillor, O. (2014) · Antonie van Leeuwenhoek · doi:10.1007/s10482-014-0136-1 · Cited by 18

Graphene Quantum Dots Nonmonotonically Influence the Horizontal Transfer of Extracellular Antibiotic Resistance Genes via Bacterial Transformation

Hu, X., Xu, Y., Liu, C., Gudda, F. O., Ling, W., Qin, C., & Gao, Y. (2023) · Small · doi:10.1002/smll.202301177 · Cited by 17

Contribution of SOS genes to H2O2-induced apoptosis-like death in Escherichia coli

Kim, H., & Lee, D. G. (2021) · Current Genetics · doi:10.1007/s00294-021-01204-0 · Cited by 17

Stresses in the food chain and their impact on antibiotic resistance of foodborne pathogens: A review

Yun, L., Wu, Y., Shao, J., Shi, J., Sun, L., Hong, Y., & Wang, X. (2025) · Food Microbiology · doi:10.1016/j.fm.2025.104741 · Cited by 16

Rescue of Escherichia coli cells from UV-induced death and filamentation by caspase-3 inhibitor

Wadhawan, S., & Gautam, S. (2019) · International Microbiology · doi:10.1007/s10123-019-00060-w · Cited by 15

Effect of low temperature on the resistance of Listeria monocytogenes and Escherichia coli O157:H7 to acid electrolyzed water

Yu, M., Jiang, C., Meng, Y., Wang, F., Qian, J., Fei, F., Zhenjie, Y., Zhao, W., Zhao, Y., & Liu, H. (2023) · Food Research International · doi:10.1016/j.foodres.2023.112776 · Cited by 15

Inactivation of Escherichia coli O157:H7, Salmonella Typhimurium, and Listeria monocytogenes on stainless steel by synergistic effects of tap water-based neutral electrolyzed water and lactic acid

Jee, D., & Ha, J. (2023) · Food Microbiology · doi:10.1016/j.fm.2023.104233 · Cited by 14

Computational methodology for predicting the landscape of the human–microbial interactome region level influence

Coelho, E. D., Santiago, A. M., Arrais, J. P., & Oliveira, J. L. (2015) · Journal of Bioinformatics and Computational Biology · doi:10.1142/s0219720015500237 · Cited by 14

Differences in the Transcriptomic Response of Campylobacter coli and Campylobacter lari to Heat Stress

Riedel, C., Förstner, K. U., Püning, C., Alter, T., Sharma, C. M., & Gölz, G. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00523 · Cited by 13

Alterations in amino acid metabolism during growth by Staphylococcus aureus following exposure to H2O2 – A multifactorial approach

Murphy, G. R., Dunstan, R. H., Macdonald, M. M., Gottfries, J., & Roberts, T. K. (2018) · Heliyon · doi:10.1016/j.heliyon.2018.e00620 · Cited by 12

DNA damage, inflammation and aging: Insights from mice

Arvanitaki, E. S., Stratigi, K., & Garinis, G. A. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.973781 · Cited by 14

Evolving Synergy Between Synthetic and Biotic Elements in Conjugated Polyelectrolyte/Bacteria Composite Improves Charge Transport and Mechanical Properties

McCuskey, S. R., Quek, G., Vázquez, R. J., Kundukad, B., Ismail, M. H., Astorga, S. E., Jiang, Y., & Bazan, G. C. (2024) · Advanced Science · doi:10.1002/advs.202405242 · Cited by 11

Evolutionary Stability of Salmonella Competition with the Gut Microbiota: How the Environment Fosters Heterogeneity in Exploitative and Interference Competition

Müller, J., Spriewald, S., Stecher, B., Stadler, E., & Fuchs, T. M. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.06.027 · Cited by 12

Focusing on DNA Repair and Damage Tolerance Mechanisms in Mycobacterium tuberculosis: An Emerging Therapeutic Theme

Mittal, P., Sinha, R., Kumar, A., Singh, P., Ngasainao, M. R., Singh, A. K., & Singh, I. K. (2020) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026620666200110114322 · Cited by 11

Identification of Small Molecule Inhibitors of the Pathogen Box against Vibrio cholerae

Kim, H., Burkinshaw, B. J., Lam, L. G., Manera, K., & Dong, T. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.00739-21 · Cited by 11

Photoinactivation and Photoablation of Porphyromonas gingivalis

Harris, D. M., & Sulewski, J. G. (2023) · Pathogens · doi:10.3390/pathogens12091160 · Cited by 10

Genomics and transcriptomics analyses provide insights into the cold adaptation strategies of an Antarctic bacterium, Cryobacterium sp. SO1

Teoh, C. P., Lavin, P. L., Lee, D. J. H., González‐Aravena, M., Najimudin, N., Lee, P. C., Cheah, Y. K., & Wong, C. (2021) · Polar Biology · doi:10.1007/s00300-021-02883-8 · Cited by 10

Metabolic switching and cell wall remodelling of Mycobacterium tuberculosis during bone tuberculosis

Kaur, K., Sharma, S., Abhishek, S., Kaur, P., Saini, U. C., Dhillon, M. S., Karakousis, P. C., & Verma, I. (2022) · Journal of Infection · doi:10.1016/j.jinf.2022.12.014 · Cited by 10

Designing a single-molecule biophysics tool for characterizing DNA damage for techniques that kill infectious pathogens through DNA damage effectsPreprint

Miller, H., Wollman, A. J. M., & Leake, M. C. (2016) · arXiv (Cornell University) · doi:10.48550/arxiv.1605.07789 · Cited by 9

Sunlight Inactivation of Enveloped Viruses in Clear Water

Anderson, C. E., & Boehm, A. B. B. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c06680 · Cited by 8

Hyperosmotic Adaptation of Pseudomonas protegens SN15-2 Helps Cells to Survive at Lethal Temperatures

Wang, X., Tang, D., & Wang, W. (2020) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-019-0430-x · Cited by 8

Genome-Wide Identification of Resveratrol Intrinsic Resistance Determinants in Staphylococcus aureus

Liu, L., Ingmer, H., & Vestergaard, M. R. (2021) · Antibiotics · doi:10.3390/antibiotics10010082 · Cited by 8

Potent intrinsic bactericidal activity of novel copper telluride nano-grape clusters with facile preparation

Zhou, Y., Lei, H., Wang, M., Shi, Y., & Wang, Z. (2023) · Biomaterials Science · doi:10.1039/d2bm01617f · Cited by 8

Emergence of Drug Resistance in Mycobacterium and Other Bacterial Pathogens: The Posttranslational Modification Perspective

Kandpal, M., Aggarwal, S., Jamwal, S. V., & Yadav, A. K. (2017) · Springer eBooks · doi:10.1007/978-3-319-48683-3_9 · Cited by 7

Synthetic temperature-inducible lethal gene circuits in Escherichia coli

Pearce, S. C., McWhinnie, R. L., & Nano, F. E. (2017) · Microbiology · doi:10.1099/mic.0.000446 · Cited by 7

Antibiotic-induced ROS-mediated Fur allosterism contributes to Helicobacter pylori resistance by inhibiting arsR activation of mutS and mutY

Xue, J., Li, W., Zhao, Y., Wang, L., Cheng, P., Zhang, L., Zheng, Y., Zhang, W., Bi, Y., Chen, Z., et al. (2024) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01679-23 · Cited by 6

The cis-encoded antisense RNA IsrA from Salmonella Typhimurium represses the expression of STM0294.1n (iasE), an SOS-induced gene coding for an endoribonuclease activity

Acuña, L. G., Barros, M. J., Núñez, P. C., Peñaloza, D., Montt, F., Pedraza-Delgado, D. A., Crossley, K., Gil, F., Fuentes, J. A., & Calderón, I. L. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.03.131 · Cited by 6

Regulation of maltocin synthesis in Stenotrophomonas maltophilia by positive and negative regulators

Sun, W. J., Liang, X., Zhu, C., Xu, Y. X., Ding, Y., & Huang, Y. (2022) · Research in Microbiology · doi:10.1016/j.resmic.2022.103956 · Cited by 6

Fast evolution of SOS-independent multi-drug resistance in bacteriaPreprint

Zhang, L., Guan, Y., Cheng, Y. Y., Cokcetin, N. N., Bottomley, A. L., Robinson, A., Harry, E. J., van Oijen, A. M., Su, Q. P., & Jin, D. (2024) · eLife · doi:10.7554/elife.95058 · Cited by 7

In vitro, in vivo, and cellular mechanisms of Astragalus onobrychis L. extract against protoscoleces and hydatid cysts of Echinococcus granulosus

Yadegari, J. G., Khalaf, A. K., Oladi, A., Shahbazi, A., & Mahmoudvand, H. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1531114 · Cited by 5

Signaling Pathways Sustaining Antibiotic Resistance

Etet, P. F. S., Kamdje, A. H. N., Vecchio, L., Farahna, M., & Mahomoodally, M. F. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803642-6.00003-4 · Cited by 5

Effects of ketamine in methicillin-resistant Staphylococcus aureus and in silico interaction with sortase A

Coutinho, T. D. N. P., Barroso, F. D. D., da Silva, C. R., da Silva, A. R., Cabral, V. P. D. F., Sá, L. G. D. A. V., Cândido, T. M., da Silva, L. J., Ferreira, T. L., da Silva, W. M. B., et al. (2021) · Canadian Journal of Microbiology · doi:10.1139/cjm-2021-0093 · Cited by 5

Large scale control and programming of gene expression using CRISPR

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The putative error prone polymerase REV1 mediates DNA damage and drug resistance in Candida albicans

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