The porin and the permeating antibiotic: a selective diffusion barrier in Gram-negative bacteria

Molecular Basis of Bacterial Outer Membrane Permeability Revisited

Nikaido, H. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.4.593-656.2003 · Cited by 4,316

A Common Mechanism of Cellular Death Induced by Bactericidal Antibiotics

Kohanski, M. A., Dwyer, D. J., Hayete, B., Lawrence, C. A., & Collins, J. J. (2007) · Cell · doi:10.1016/j.cell.2007.06.049 · Cited by 2,982

Multidrug-resistance efflux pumps ? not just for resistance

Piddock, L. J. V. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1464 · Cited by 1,523

Crystal structures explain functional properties of two E. coli porins

Cowan, S. W., Schirmer, T., Rummel, G., Steiert, M., Ghosh, R., Pauptit, R. A., Jansonius, J. N., & Rosenbusch, J. P. (1992) · Nature · doi:10.1038/358727a0 · Cited by 1,521

Structure and function of bacterial outer membrane proteins: barrels in a nutshell

Koebnik, R., Locher, K. P., & Gelder, P. V. (2000) · Molecular Microbiology · doi:10.1046/j.1365-2958.2000.01983.x · Cited by 1,206

Efflux-mediated antimicrobial resistance

Poole, K. (2005) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dki171 · Cited by 1,082

Efflux-Mediated Drug Resistance in Bacteria

Li, X.-Z., & Nikaido, H. (2004) · Drugs · doi:10.2165/00003495-200464020-00004 · Cited by 803

Lack of development of new antimicrobial drugs: a potential serious threat to public health

Norrby, S. R., Nord, C. E., & Finch, R. (2005) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(05)01283-1 · Cited by 500

The structure of bacterial outer membrane proteins

Schulz, G. E. (2002) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(02)00577-1 · Cited by 488

Outer membrane barrier as a mechanism of antimicrobial resistance

Nikaido, H. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.11.1831 · Cited by 464

Emergence, evolution, and global dissemination of antimicrobial resistance: A One Health review

Ahmad, R., ullah, Z., Li, M., & Tong, Y. (2026) · Archives of Microbiology · doi:10.1007/s00203-026-04997-1 · Cited by 3

Conformational flexibility driving charge-selective substrate translocation across a bacterial transporter

Vikraman, D., Majumdar, B. B., Sharavanakkumar, S. K., Weichbrodt, C., Fertig, N., Winterhalter, M., Mondal, J., & Mahendran, K. R. (2024) · Chemical Science · doi:10.1039/d4sc00345d · Cited by 3

Components of Bacterial Cell Walls as Targets for Searching for New Antibacterial Compounds: Methods of Study

Chingizova, E. A., Novikova, O. D., Portnyagina, O. Y., & Aminin, D. L. (2025) · Molecular Biology · doi:10.1134/s0026893325700013 · Cited by 3

Systematic screen uncovers regulator contributions to chemical cues in Escherichia coli

Binsfeld, C., Olayo-Alarcón, R., Jiménez, L. P., Wartel, M., Stadler, M., Mateus, A., Müller, C. L., & Brochado, A. R. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003260 · Cited by 3

CRISPR-Cas9 targeting the blaKPC gene in a clinical isolate of Klebsiella michiganensis: Reduction of imipenem resistance and changes in genomic carbapenem resistance determinants

Tagliaferri, T. L., Krüttgen, A., Mendes, T. A. D. O., dos Santos, S. G., & Horz, H. (2025) · PLoS ONE · doi:10.1371/journal.pone.0328521 · Cited by 3

Differential proteomics of bacteria grown in vitro and in planta reveals functions used during growth on maize roots

Garrell, A.-K., Cheadle, J. B., Crook, N., Pal, G., Septer, A. N., Wagner, M. R., Beck, A. E., & Kleiner, M. (2026) · mSystems · doi:10.1128/msystems.00371-26 · Cited by 5

Bacterial RNAP Inhibitors: Synthesis and Evaluation of Prodrugs of Aryl‐ureidothiophene‐carboxylic acids

Ruthenbeck, A., Elgaher, W. A. M., Haupenthal, J., Hartmann, R. W., & Meier, C. (2017) · ChemistrySelect · doi:10.1002/slct.201702574 · Cited by 3

Global and Temporal Trends in the Use of Antibiotics and Spread of Antimicrobial Resistance

Sarfraz, I., Rasul, A., Hussain, G., Hussain, S. M., Samiullah, K., Rasool, B., Riaz, A., Asrar, M., & Selamoğlu, Z. (2020) · Emerging contaminants and associated treatment technologies · doi:10.1007/978-3-030-40422-2_4 · Cited by 3

Biological Activity of Lasiodiplodia pseudotheobromae IBRL OS- 64 Extracts, an Endophytic Fungus Isolated from Medicinal Herb, Ocimum sanctum Against Foodborne Diarrhea-Caused Bacteria

Taufiq, M. M. J., & Darah, D. (2020) · Pharmacognosy Journal · doi:10.5530/pj.2020.12.127 · Cited by 3

Evaluation of the rCIM for carbapenemase detection in Enterobacterales and Pseudomonas aeruginosa and description of the TSBrCIM, an optimized variant

Nockelmann, L., Cremanns, M., Gatermann, S. G., & Pfennigwerth, N. (2021) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2021.106345 · Cited by 3

Bacterial Porins

Aguilella, V. M., Queralt-Martín, M., & Alcaraz, A. (2015) · Springer series in biophysics · doi:10.1007/978-3-319-20149-8_5 · Cited by 3

The mechanism of an electrostatic nanofilter: overcoming entropy with electrostatics

Bodrenko, I. V., Ceccarelli, M., & Acosta‐Gutiérrez, S. (2023) · Physical Chemistry Chemical Physics · doi:10.1039/d3cp02895j · Cited by 3

Tracking the Activity and Position of Mitochondrial β-Barrel Proteins

Wang, S., & Nußberger, S. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3734-0_14 · Cited by 3

Quorum Sensing in Chromobacterium subtsugae ATCC 31532 (Formerly Chromobacterium violaceum ATCC 31532): Transcriptomic and Genomic Analyses

Deryabin, D. G., Инчагова, К. С., Nikonorova, E. R., Файзелгаянович, К. И., & Duskaev, G. K. (2025) · Microorganisms · doi:10.3390/microorganisms13051021 · Cited by 3

Mapping Ammonium Flux Across Bacterial Porins: A Novel Electrophysiological Assay with Antimicrobial Relevance

Ghai, I. (2025) · Applied Sciences · doi:10.3390/app15147677 · Cited by 3

The mesoscopic collective motion of self-propelling active particle suspension confined in two-dimensional micro-channel

Cai, S.-C., Shen, Y.-X., & Io, C. (2019) · Journal of Physics Condensed Matter · doi:10.1088/1361-648x/ab5772 · Cited by 3

An in vitro approach to combat multidrug resistance in Salmonella typhi and human colon cancer with Excoecaria agallocha L. extract

Sultana, T., Mitra, A. K., & Das, S. (2021) · Bulletin of the National Research Centre/Bulletin of the National Research Center · doi:10.1186/s42269-021-00668-x · Cited by 3

A Lead-Based Fragment Library Screening of the Glycosyltransferase WaaG from Escherichia coli

Riu, F., Ruda, A., Engström, O., Muheim, C., Mobarak, H., Ståhle, J., Kosma, P., Carta, A., Daley, D. O., & Widmalm, G. (2022) · Pharmaceuticals · doi:10.3390/ph15020209 · Cited by 4

The β-Lactam Antibiotics: Current Situation and Future Prospects in Manufacture and Therapy

Schmidt, F.-R. (2010) · Springer eBooks · doi:10.1007/978-3-642-11458-8_5 · Cited by 3

Principles of Antiinfective Therapy

Sykes, J. E., & Papich, M. G. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4377-0795-3.00006-5 · Cited by 3

Impact of defined cell envelope mutations in Escherichia coli on the in vitro antibacterial activity of avibactam/β-lactam combinations

McLeod, S. M., Patey, S. A., Huband, M. D., & Nichols, W. W. (2017) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2016.12.011 · Cited by 3

Hypericum roeperianum as a source of antibacterial agents

Guefack, M.-G. F., & Kuete, V. (2022) · Advances in botanical research · doi:10.1016/bs.abr.2022.08.016 · Cited by 3

Beta-lactamases in Enterobacteriaceae in broilers

Dierikx, C. M. (2013) · Utrecht University Repository (Utrecht University) · Cited by 3

Alterações da permeabilidade e expressão de bombas de efluxo em isolados clínicos de Pseudomonas aeruginosa resistente ao imipenem

Neves, P. (2012) · doi:10.11606/t.9.2012.tde-09022012-162542 · Cited by 3

Sensitizing Agents to Restore Antibiotic Resistance

Gadelii, A., Hassan, K., & Håkansson, A. (2019) · Wiley eBooks · doi:10.1002/9781119282549.ch17 · Cited by 3

Borrelia burgdorferi tolerates alteration to P66 porin function in a murine infectivity model

Fierros, C. H., Faucillion, M.-L., Hahn, B. L., Anderson, P. N., Bonde, M., Kessler, J. R., Surdel, M. C., Crawford, K. S., Gao, Y., Zhu, J., et al. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1528456 · Cited by 2

Enhancing activity and overcoming ciprofloxacin resistance via multifunctional nanostructured lipid carriers

Dlamini, S., Omolo, C. A., Elhassan, E., Ismail, E. A., Peters, X. Q., Kassam, S. Z. F., Gafar, M. A., Govender, J., Chemonges, C. C., & Govender, T. (2025) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2025.106933 · Cited by 2

Quantitative and chemical adaptation of exopolymeric substances formed by a river microbial consortium during exposure to the antibiotic trimethoprim

Duteil, T., Gorzsás, A., & Ramstedt, M. (2025) · Biofilm · doi:10.1016/j.bioflm.2025.100334 · Cited by 2

Amphiphilic Janus Nanoparticles Synergize with Antibiotics to Restore Susceptibility in Drug-Resistant Gram-Negative Bacteria

Zwama, M., Bhattacharyya, S., Sakurai, N., Nishino, K., & Yu, Y. (2025) · Nano Letters · doi:10.1021/acs.nanolett.5c05337 · Cited by 2

Circumnavigating Antibiotic Mechanisms of Action and Resistance Research

Priya, M., & de Carvalho, L. P. S. (2026) · Biochemistry · doi:10.1021/acs.biochem.5c00658 · Cited by 2

Microphysiological (“organ-on-a-chip”) models of pulmonary infections for developing novel anti-infectives

Rindchen, A., Schneider‐Daum, N., & Lehr, C. (2026) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2026.115917 · Cited by 2

OmpF, a nucleotide-sensing nanoprobe, computational evaluation of single channel activities

Abdolvahab, R. H., Mobasheri, H., Nikouee, A., & Ejtehadi, M. R. (2016) · Physica A Statistical Mechanics and its Applications · doi:10.1016/j.physa.2016.03.031 · Cited by 2

Subproteomic signature comparison of in vitro selected fluoroquinolone resistance and ciprofloxacin stress in Salmonella Typhimurium DT104B

Correia, S., Hébraud, M., Chafsey, I., Chambon, C., Viala, D., Torres, C., Caniça, M., Capelo, J. L., Poeta, P. A. C. Q. D., & Igrejas, G. (2017) · Expert Review of Proteomics · doi:10.1080/14789450.2017.1375856 · Cited by 2

Role of Natural Product in Modulation of Drug Transporters and New Delhi Metallo-β Lactamases

Chandar, B., & Bhattacharya, D. (2019) · Current Topics in Medicinal Chemistry · doi:10.2174/1871529x19666190415110724 · Cited by 2

IN VITRO ANTIMICROBIAL ACTIVITY OF SELECTED MEDICINAL PLANTS IN LOSHO, NAROK COUNTY KENYA

Duncan, C. M., Catherine, L., Saiffudin, D., & Joseph, N. (2015) · International Research Journal of Pharmacy · doi:10.7897/2230-8407.0612154 · Cited by 2

Microbial Resistance Mechanisms and Potential of Metal-Organic Framework in Mitigation Thereof

Polash, S. A., Váradi, L., & Shukla, R. (2022) · Nanotechnology in the life sciences · doi:10.1007/978-3-031-10220-2_7 · Cited by 2

Influence of Membrane Asymmetry on OmpF Insertion, Orientation and Function

Donoghue, A., Winterhalter, M., & Gutsmann, T. (2023) · Membranes · doi:10.3390/membranes13050517 · Cited by 2

Diagnostic low-dose X-ray radiation induces fluoroquinolone resistance in pathogenic bacteria

Cherif, J., Raddaoui, A., Trabelsi, M., & Souissi, N. (2023) · International Journal of Radiation Biology · doi:10.1080/09553002.2023.2232016 · Cited by 2

Molecular characterization and in-depth genomic analysis to unravel the pathogenic features of an environmental isolate Enterobacter sp. S-33

Kumari, K., Aggarwal, Y., & Singh, R. P. (2023) · International Microbiology · doi:10.1007/s10123-023-00461-y · Cited by 2

Molecular Model of Norfloxacin Translocation through Yersinia pseudotuberculosis Porin OmpF Channel: Electrophysiological and Molecular Modeling Study

Chistyulin, D. K., Zelepuga, E., Novikov, V. L., Balaneva, N. N., Glazunov, V. P., Chingizova, E. A., Хоменко, В. А., & Novikova, O. D. (2023) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747823070024 · Cited by 2

Synthesis of amino juglone derivatives with adjuvant activity against clinical isolated methicillin-resistant staphylococcus aureus strains

Majdi, C., Seghir, M., Wegrich, Y., Behilil, D., Bénimèlis, D., Dunyach‐Remy, C., Meffre, P. R., & Benfodda, Z. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107627 · Cited by 3

Towards understanding the molecular mechanism of cardiolipin transport in Salmonella typhimurium: interactions between an essential inner membrane protein YejM and its newly found ligand, YejL

Gabale, U., Qian, G., Roach, E., & Ressl, S. (2016) · F1000Research · doi:10.12688/f1000research.8647.1 · Cited by 1

Improving the clinical efficacy of drugs by liposomes against resistant bacteria (mdr bacteria) – an in vitro study

BOO, M. J., Gopukumar, S. T., & SEETHA, P. K. P. (2017) · International Journal of Pharma and Bio Sciences · doi:10.22376/ijpbs.2017.8.3.p42-57 · Cited by 2

High-grade mutant OmpF induces decreased bacterial survival rate.

Zhao, Z., Liu, T., Zhang, L., Luo, M., Nie, X., Li, Z.-X., & Pan, Y. (2014) · Acta Biochimica Polonica · doi:10.18388/abp.2014_1908 · Cited by 2

Le rôle des porines dans la résistance aux antibiotiques

Davin‐Regli, A., Masi, M., & Pagès, J. (2020) · Revue Francophone des Laboratoires · doi:10.1016/s1773-035x(20)30060-5 · Cited by 2

Acquired Antibiotic Resistance

Honceriu, I. (2022) · Journal of Experimental and Molecular Biology · doi:10.47743/jemb-2022-66 · Cited by 2

Antibiotics in the treatment of periodontal and peri-implant infections

Enersen, M., Hultin, M., Könönen, E., Poulsen, A. H., & Simm, R. (2019) · Den norske tannlegeforenings Tidende · doi:10.56373/2019-3-4 · Cited by 2

Mechanisms and Dynamics of Carbapenem Resistance in Escherichia coli

Adler, M. (2014) · Uppsala University Publications (Uppsala University) · Cited by 2

Antibiotic resistance transfer during food production and preservation

Meervenne, E. V. (2014) · Ghent University Academic Bibliography (Ghent University) · Cited by 2

Peptidoglycan recycling contributes to outer membrane integrity and carbapenem tolerance in Acinetobacter baumanniiPreprint

Islam, N., Kazi, M. I., Kang, K. N., Biboy, J., Gray, J., Ahmed, F., Schargel, R. D., Boutte, C. C., Dörr, T., Vollmer, W., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.23.469614 · Cited by 2

Genetic basis for in vivo piperacillin-tazobactam resistancePreprint

Gálvez-Benítez, L., de la Rosa, J. M. O., Rodríguez-Villodres, Á., Casimiro‐Soriguer, C. S., Panadero, I. M., Álvarez‐Marín, R., Bonnin, R. A., Naas, T., Pachón, J., Cisneros, J. M., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2752509/v1 · Cited by 2

Enhanced expression of recombinant proteins in Escherichia coli by co‐expression with Vibrio parahaemolyticus CsgG, a pore‐forming protein of the curli biogenesis pathway

Karan, S., Choudhury, D., & Dixit, A. (2020) · Journal of Applied Microbiology · doi:10.1111/jam.14886 · Cited by 1

Vaccination with OprB porin, and its epitopes offers protection against A. baumannii infections in mice

Raoufi, Z., & Abdollahi, S. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112972 · Cited by 1

Restoring tigecycline efficacy with lysine supplementation in tmexCD-toprJ-positive bacteria

Li, F., Xu, T., Fang, D., Wang, Z., & Liu, Y. (2025) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2025.107511 · Cited by 1

Structural Insights Into Papain‐Derived Synthetic Antibacterial Peptides for Targeting Klebsiella pneumoniae

Ferreira, M. A., Silva, P. S. E., Lacerda, A., Franco, P. D. M., da Silva, F. F. D., de Souza, T. F., Macedo, M. L. R., Migliolo, L., & de Oliveira, J. S. (2025) · Chemical Biology & Drug Design · doi:10.1111/cbdd.70130 · Cited by 1

Thermal treatment increases the antimicrobial activity of tepejilote rachis against Pseudomonas aeruginosa and Staphylococcus aureus

Bernardino‐Nicanor, A., Fernández-Avalos, S., & González-Cruz, L. (2025) · Natural Product Research · doi:10.1080/14786419.2025.2518418 · Cited by 1

Mechanism of the antifungal activity of the diterpenoid aldehyde traversianal against cucumber anthracnose fungus Colletotrichum orbiculare

Ino, M., Kihara, J., Ishihara, A., & Ueno, M. (2025) · Journal of General Plant Pathology · doi:10.1007/s10327-025-01249-w · Cited by 1

Porin‐Independent Uptake of Small Molecule Antibiotics Facilitated by Escherichia coli Outer Membrane Vesicles

Wu, M., Harrower, R. M., Li, Z., & Brown, A. C. (2025) · Biotechnology and Bioengineering · doi:10.1002/bit.70078 · Cited by 1

Understanding Drug Permeability in Pseudomonas aeruginosa

Ghai, I. (2025) · Life · doi:10.3390/life15111705 · Cited by 1

Controlling Nanopore Dynamics via Loop Stapling and Unstapling for Tunable Substrate Transport

Krishna, A., Puthumadathil, N., Sarkar, D. K., Majumdar, B. B., Vikraman, D., Mondal, J., & Mahendran, K. R. (2025) · ACS Nano · doi:10.1021/acsnano.5c16470 · Cited by 1

PPE64 is a mycomembrane channel protein that functions in heme iron uptake and moonlights in biofilm formation in Mycobacterium tuberculosis

Singh, P., Kaufman, C. B., Whitworth, L. C., Stubbendieck, R. M., Morgenstein, R. M., Wozniak, K. L., & Mitra, A. (2025) · mBio · doi:10.1128/mbio.03281-25 · Cited by 1

Various Bacillus and Paenibacillus Spp. Isolated From Soil Produce Compounds With Potent Antimicrobial Activity Against Clinically Relevant Pathogens

Moran, M., Turner, H., Yanchar, J., Preece, J., Ahlborn, G. J., & Robison, R. A. (2025) · MicrobiologyOpen · doi:10.1002/mbo3.70179 · Cited by 1

Xanthohumol restores the susceptibility of Escherichia coli to colistin

Han, N., Zhao, F., Li, Y., Xiong, W., Wan, P., & Zeng, Z. (2025) · One Health Advances · doi:10.1186/s44280-025-00096-w · Cited by 1

Activity of cefepime/enmetazobactam against highly multidrug-resistant bacterial isolates recovered from war-associated wounds in Ukraine

Boral, J., Toft, N., Baybes, A. E., Tellapragada, C., Nazarchuk, O. A., Fernandez, C., Giske, C. G., & Riesbeck, K. (2025) · JAC-Antimicrobial Resistance · doi:10.1093/jacamr/dlaf256 · Cited by 1

Ambler class C-type β-lactamases and porin alterations in Enterobacter cloacae complex and Klebsiella aerogenes in the Netherlands, 2012–2023

van Gorp, E., Lansu, S., Wielders, C. C. H., de Haan, A., Godeke, G.-J., Witteveen, S., Bos, J., Landman, F., Ouw, M., Wunderink, H. F., et al. (2026) · BMC Microbiology · doi:10.1186/s12866-026-04741-1 · Cited by 1

RNAi in the Postgenomic Era: Delivery, Drug Design, and Emerging Technologies

Saikia, S., Gogoi, I., Dey, D., Mili, K., Purkayastha, A., Mech, K. K., Bora, R., Neog, K., Chetia, P., & Puzari, M. (2026) · Springer eBooks · doi:10.1007/978-981-95-5378-5_10 · Cited by 1

Probiotics and Antibiotics: From Empirical Practice to a Biological Rationale for Targeted Choice During Antibiotic Therapy

Matera, M., Biagioli, V., Leo, S., & Drago, L. (2026) · Microorganisms · doi:10.3390/microorganisms14040763 · Cited by 2

Advances in BODIPY Derivatives for Antibacterial Phototherapy

Lv, L., Kim, H., Zhai, H., Ren, H., Wang, S., Sun, C., Wang, Y., Lee, H., Yoon, J., & Zhang, H. (2026) · Angewandte Chemie · doi:10.1002/ange.9448235 · Cited by 1

Phytogenic synthesis of cobalt oxide nanoparticles with Mallotus philippensis and their photocatalytic–antimicrobial efficiency

Kumar, S., Kumari, P., Kumar, M., & Kaushal, D. (2026) · Next research. · doi:10.1016/j.nexres.2026.102079 · Cited by 1

Microbicides - The Double-Edged Sword: Environmental Toxicity and Emerging Resistance

Pagès, J., Maillard, J., Davin‐Regli, A., & Springthorpe, S. (2012) · Wiley-Blackwell eBooks · doi:10.1002/9781118425831.ch11 · Cited by 1

The outer membrane protein CD is associated with resistance to penicillins in Moraxella catarrhalis

Saito, R., Miharu, Y., Matsuoka, S., Nonaka, S., Fujinami, Y., & Okamura, N. (2015) · Journal of Global Antimicrobial Resistance · doi:10.1016/j.jgar.2015.06.002 · Cited by 1

Computational and Biochemical Design of a Nanopore Cleavable by a Cancer‐Secreted Enzyme

Pittel, I., Alper, N., Yonai, S., Basch-Barzilay, S., Blum, L., Bachur, A., & Paas, Y. (2015) · ChemBioChem · doi:10.1002/cbic.201402378 · Cited by 1

Broad spectrum anti-microbial compounds producing bacteria from coast of Qingdao bays

Khan, M. N. (2015) · Pakistan Journal of Pharmaceutical Sciences · doi:10.36721/pjps/28/2/2015/2615/473-482 · Cited by 1

Role Of Two-Component Signal Transduction Systems In Antimicrobial Resistance Of Gram-Negative Pathogens

Raczkowska, A., Jaworska, K., Wyrożemski, Ł., & Brzostek, K. (2020) · Postępy Mikrobiologii - Advancements of Microbiology · doi:10.21307/pm-2020.59.3.19 · Cited by 1

Estudios en resistencia a los antibióticos beta-lactámicos en bacterias Gram negativas

Vivas, E. D. L. C., Bermúdez, A. M. C., Serrano, R. A. R., Restrepo, A. D. F., Arias, C. A. A., Alonso, G., & Verdugo, M. P. (2020) · Editorial Universidad Santiago de Cali eBooks · doi:10.35985/9789585583924 · Cited by 1

Clinical Impact of Bloodstream Infections – Characterization, Risk factors and Outcome

Holmbom, M. (2021) · Linköping University medical dissertations · doi:10.3384/diss.diva-181406 · Cited by 1

Resistance of Gram-negative Bacilli to Antimicrobials

Dean, C. R., Pascale, G. D., & Benton, B. M. (2018) · Springer eBooks · doi:10.1007/978-3-319-78538-7_4 · Cited by 1

How Mobility of Resistance Determinants Affects the Dissemination of Antimicrobial Resistance?

Adesola, R. O. (2022) · International Journal of Travel Medicine and Global Health · doi:10.34172/ijtmgh.2022.17 · Cited by 1

Limitations in predicting reduced susceptibility to third generation cephalosporins in Escherichia coli based on whole genome sequence data

Heydecke, A., Yin, H., Tano, E., & Sütterlin, S. (2023) · PLoS ONE · doi:10.1371/journal.pone.0295233 · Cited by 1

Role of ArcA in the regulation of antibiotic sensitivity in avian pathogenic Escherichia coli

Ma, K., Chinelo, O. R., Gu, M., Kong, F., Jiang, Y., Wang, H., & Xue, T. (2024) · Poultry Science · doi:10.1016/j.psj.2024.103686 · Cited by 1

Self-assembled lipophilic guanosine derivatives modulate membrane transport across lipid bilayers

Kumar, Y. P., Debnath, M., Das, T., Paul, R., & Dash, J. (2024) · Cell Reports Physical Science · doi:10.1016/j.xcrp.2024.102298 · Cited by 1

Crystallization and preliminary X-ray diffraction analysis of YejM from Salmonella typhimurium: an essential inner membrane protein involved in outer membrane directed cardiolipin transport

Gabale, U., Qian, G., Roach, E., & Ressl, S. (2017) · F1000Research · doi:10.12688/f1000research.8647.2 · Cited by 1

Dramatic change of the self-diffusions of colloidal ellipsoids by hydrodynamic interactions in narrow channels*

Li, H.-H., Zheng, Z., Xie, T., & Wang, Y. (2019) · Chinese Physics B · doi:10.1088/1674-1056/28/7/074701 · Cited by 1

Photocontrolled nanosystems for antibacterial drug delivery

Choi, S. K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817840-9.00011-4 · Cited by 1

Multidrug resistance in pathogenic microorganisms

Upmanyu, N., & Malviya, V. N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819001-2.00016-4 · Cited by 1

Design and Assembly of Transmembrane Helix Barrel

Mahendran, K. R. (2020) · The Journal of Membrane Biology · doi:10.1007/s00232-020-00145-y · Cited by 1

The role of coordinated regulation and aromatic metabolites in activating the mar/sox/rob regulon of Escherichia coli

Chubiz, L. M. (2011) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign) · Cited by 1

Antibiotic resistance in Gram-negative bacteria affecting children from León, Nicaragua

Amaya, E. (2010) · Figshare · Cited by 1

DETECTION OF CARBAPENEM-RESISTANT ENTEROBACTERIACEAE AMONGST NEONATES IN A REGIONAL HOSPITAL IN KWAZULU-NATAL: Screening for Carbapenemase Production and MIC Correlation

Govender, K. (2014) · ResearchSpace (University of KwaZulu-Natal) · Cited by 1

New functional identity of the essential inner membrane protein YejM: the cardiolipin translocator is also a metalloenzymePreprint

Gabale, U., Palomino, P. A. P., Kim, H., Chen, W., & Ressl, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.13.947838 · Cited by 1

Simulation-guided engineering of antibiotics for improved bacterial uptakePreprint

Ferreira, R. J., Aguilar, V., Giraldo, A. M. V., & Kasson, P. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.08.330332 · Cited by 1

Systematic Characterization of Transport Regulation in Escherichia coli across defined environmental cuesPreprint

Binsfeld, C., Olayo-Alarcón, R., Wartel, M., Stadler, M., Müller, C. L., & Brochado, A. R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.26.609649 · Cited by 1

Escherichia coli outer membrane vesicles encapsulating small molecule antibiotics improve drug function by facilitating transportPreprint

Wu, M., Harrower, R. M., Li, Z., & Brown, A. C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.08.631972 · Cited by 1

Elucidation of the Molecular Mechanisms That Contribute to Variation in Susceptibility Testing Show the Need for Alternative Detection Methods of KPC-producing Gram-negative Bacteria

Roth, A. L. (2012) · Creighton Digital Repository (CDR)

The biology of antibiotic resistance plasmids

Saw, H. T. H. (2015) · University of Birmingham Institutional Research Archive (University of Birmingham)

Antigenic relatedness defines Toll-like receptor 2 is crafted on ligand blueprint

Sinha, D., Ghosh, A. K., Mukherjee, S., Biswas, R., & Biswas, T. (2014) · Immunobiology · doi:10.1016/j.imbio.2014.06.007

Transmission And Evolution Of Salmonella

Soyer, Y. (2009) · eCommons (Cornell University)

Functional status of central circulatory system in experimental brain hypoxia -- contribution to development of brain edema.

Kapuściński, A. (1977) · PubMed

Evolution of Carbapenem-Resistance in Escherichia coli Extended Spectrum Beta-Lactamase-Encoding Plasmid Increases Carbapenem-Resistance

Adler, M. (2009)

EFFECTS OF PROTAMINE ON PSEUDOMONAS AERUGINOSA CELL ENVELOPE COMPONENTS: SURFACE REMODELLING

Mohan, M. (2010) · Library and Archives Canada (Government of Canada)

Exploring bacterial outer membrane barrier to combat bad bugs

Ghai, I., & Ghai, S. (2017) · Infection and Drug Resistance · doi:10.2147/idr.s144299 · Cited by 47

A Barrier to Entry: Examining the Bacterial Outer Membrane and Antibiotic Resistance

Ghai, I. (2023) · Applied Sciences · doi:10.3390/app13074238 · Cited by 54

Bacterial resistance to antibiotics as a function of outer membrane permeability

Nikaido, H. (1988) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/22.supplement_a.17 · Cited by 49

The Possible Role of Porins in Bacterial Antibiotic Resistance

Gutmann, L., Williamson, R., & Collatz, E. (1984) · Annals of Internal Medicine · doi:10.7326/0003-4819-101-4-554 · Cited by 13

Understanding antibiotic resistance via outer membrane permeability

Ghai, I., & Ghai, S. (2018) · Infection and Drug Resistance · doi:10.2147/idr.s156995 · Cited by 207