Mechanisms of vancomycin resistance in Staphylococcus aureus

Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility

Hiramatsu, K. (1997) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/40.1.135 · Cited by 1,984

Emergence of Vancomycin Resistance inStaphylococcus aureus

Smith, T. L., Pearson, M. L., Wilcox, K. R., Cruz, C., Lancaster, M. V., Robinson-Dunn, B., Tenover, F. C., Zervos, M., Band, J. D., White, E., et al. (1999) · New England Journal of Medicine · doi:10.1056/nejm199902183400701 · Cited by 1,086

Reduced Vancomycin Susceptibility in Staphylococcus aureus , Including Vancomycin-Intermediate and Heterogeneous Vancomycin-Intermediate Strains: Resistance Mechanisms, Laboratory Detection, and Clinical Implications

Howden, B. P., Davies, J. K., Johnson, P. D. R., Stinear, T. P., & Grayson, M. L. (2010) · Clinical Microbiology Reviews · doi:10.1128/cmr.00042-09 · Cited by 962

Vancomycin: A History

Levine, D. P. (2005) · Clinical Infectious Diseases · doi:10.1086/491709 · Cited by 883

Vancomycin-resistant Staphylococcus aureus: a new model of antibiotic resistance

Hiramatsu, K. (2001) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(01)00091-3 · Cited by 761

Genetics and mechanisms of glycopeptide resistance in enterococci

Arthur, M., & Courvalin, P. M. (1993) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.37.8.1563 · Cited by 692

The Development of Vancomycin Resistance in a Patient with Methicillin-ResistantStaphylococcus aureusInfection

Sieradzki, K., Roberts, R. B., Haber, S. W., & Tomasz, A. (1999) · New England Journal of Medicine · doi:10.1056/nejm199902183400704 · Cited by 638

Tracking the in vivo evolution of multidrug resistance in Staphylococcus aureus by whole-genome sequencing

Mwangi, M. M., Wu, S. W., Zhou, Y., Sieradzki, K., de LENCASTRE, H., Richardson, P., Bruce, D. G., Rubin, E. M., Myers, E. W., Siggia, E. D., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609839104 · Cited by 538

Reemergence of antibiotic-resistant Staphylococcus aureus in the genomics era

DeLeo, F. R., & Chambers, H. F. “. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38226 · Cited by 522

Two‐component system VraSR positively modulates the regulation of cell‐wall biosynthesis pathway in Staphylococcus aureus

Kuroda, M., Kuroda, H., Oshima, T., Takeuchi, F., Mori, H., & Hiramatsu, K. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03599.x · Cited by 515

Two-component signaling pathways modulate drug resistance of

Wu, S., Lin, K., Liu, Y., Zhang, H., & Lei, L. (2020) · Biomedical Reports · doi:10.3892/br.2020.1312 · Cited by 23

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Chen, X., Lou, W., Liu, J., Ding, B., Fan, W., & Hong, J. S. (2019) · Bioscience Reports · doi:10.1042/bsr20192354 · Cited by 22

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Gao, W., Han, X., Li, Y., Zhou, Z., Wang, J., Shi, R., Jiao, J., Qi, Y., Zhou, Y., & Zhao, J. (2022) · Journal of Applied Polymer Science · doi:10.1002/app.52847 · Cited by 22

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Kilian, R., Frasch, H.-J., Kulik, A., Wohlleben, W., & Stegmann, E. (2016) · Microbial Drug Resistance · doi:10.1089/mdr.2016.0128 · Cited by 22

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Laliwala, A., Pant, A., Svechkarev, D. A., Sadykov, M. R., & Mohs, A. M. (2024) · npj Biosensing · doi:10.1038/s44328-024-00016-9 · Cited by 22

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Tartor, Y. H., Enany, M. E., Ismail, N. I., El-Demerdash, A. S., Eidaroos, N. H., Algendy, R. M., Mahmmod, Y. S., & Elsohaby, I. (2024) · Scientific Reports · doi:10.1038/s41598-024-81516-6 · Cited by 21

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Chen, Y., Shi, Y., Zhu, W., You, J., Yang, J., Xie, Y., Zhao, H., Li, H., Fan, S., Li, L., et al. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.742040 · Cited by 21

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Agour, M. A., Hamed, A. A., Ghareeb, M. A., Abdel-Hamid, E. A. A., & Ibrahim, M. K. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-03092-5 · Cited by 21

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Mousavizadegan, M., Hosseini, M., Sheikholeslami, M. N., & Ganjali, M. R. (2024) · Microchimica Acta · doi:10.1007/s00604-024-06374-5 · Cited by 21

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Houri, H., Kazemian, H., Ebrahim‐Saraie, H. S., Taji, A., Tayebi, Z., & Heidari, H. (2017) · Journal of Global Antimicrobial Resistance · doi:10.1016/j.jgar.2017.06.002 · Cited by 21

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Suchý, T., Šupová, M., Sauerová, P., Kalbáčová, M. H., Klapková, E., Pokorný, M., Horný, L., Závora, J., Ballay, R., Denk, F., et al. (2019) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2019.04.021 · Cited by 21

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Alatorre-Fernández, P., Mayoral-Terán, C., Velázquez-Acosta, C., Rodríguez, C. F., Flores-Moreno, K., Cevallos, M. A., López‐Vidal, Y., & Volkow-Fernández, P. A. (2016) · American Journal of Infection Control · doi:10.1016/j.ajic.2016.10.002 · Cited by 20

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Xing, J., Wang, F., Cong, H., Wang, S., Shen, Y., & Yu, B. (2020) · The Analyst · doi:10.1039/d0an02018d · Cited by 20

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Khodair, A. I., Kassab, S. E., Kheder, N. A., & Fahim, A. M. (2022) · Carbohydrate Research · doi:10.1016/j.carres.2022.108546 · Cited by 21

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Abed, N. N., El-Enain, I. M. A., Helal, E. E.-H., & Yosri, M. (2022) · Journal of Taibah University Medical Sciences · doi:10.1016/j.jtumed.2022.10.006 · Cited by 20

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Joshi, A., & Patil, R. H. (2023) · Infectious Medicine · doi:10.1016/j.imj.2023.11.006 · Cited by 21

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Zheng, W., Cai, X., Li, S., & Li, Z. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00758 · Cited by 20

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Erriah, P., Puan, S. L., Normi, Y. M., Kamil, W. N. I. W. A., Nordin, S. A., Muhamad, A., & Sabri, S. (2024) · Journal of Applied Microbiology · doi:10.1093/jambio/lxae290 · Cited by 19

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Wei, J., Zhang, X., Sui, B., Ding, X., Li, Y., Liu, B., Wang, J., Lv, X., Zhang, Y., Jiang, X., et al. (2025) · ACS Nano · doi:10.1021/acsnano.4c14057 · Cited by 22

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Giulieri, S. G., Holmes, N. E., Stinear, T. P., & Howden, B. P. (2016) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2016.1233815 · Cited by 17

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Aguilera-Correa, J. J., Doadrio, A. L., Conde, A., Arenas, M. A., de Damborenea, J. J., Vallet‐Regí, M., & Esteban, J. (2018) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-018-6119-4 · Cited by 19

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Gatadi, S., Gour, J., Kaul, G., Shukla, M., Dasgupta, A., Akunuri, R., Tripathi, R., Yaddanapudi, V. M., Chopra, S., & Nanduri, S. (2018) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2018.08.012 · Cited by 19

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Park, J. W., Lee, H., Kim, J. W., & Kim, B. (2019) · Scientific Reports · doi:10.1038/s41598-019-42307-6 · Cited by 20

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Elsawy, S., Elsherif, W. M., & Hamed, R. A. A. (2021) · Pathogens and Global Health · doi:10.1080/20477724.2021.1914412 · Cited by 19

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Hong, S., Takahashi, H., Nadres, E. T., Mortazavian, H., Caputo, G. A., Younger, J. G., & Kuroda, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0169262 · Cited by 18

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Zeng, J., Hu, Y., Jia, T., Zhang, R., Su, T., Sun, J., Gao, H., Li, G., Cao, M., & Song, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199334 · Cited by 18

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Yamaguchi, T., Suzuki, S., Okamura, S., Miura, Y., Tsukimori, A., Nakamura, I., Ito, N., Masuya, A., Shiina, T., & Matsumoto, T. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05159-14 · Cited by 18

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Mihelič, M., Vlahoviček‐Kahlina, K., Renko, M., Mesnage, S., Doberšek, A., Taler‐Verčič, A., Jakas, A., & Türk, V. (2017) · IUCrJ · doi:10.1107/s2052252517000367 · Cited by 16

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Lu, C.-H., Shiau, C., Chang, Y.-C., Kung, H., Wu, J.-C., Lim, C.-H., Yeo, H., Chang, H.-C., Chien, H.-S., Huang, S.-H., et al. (2021) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkab114 · Cited by 17

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Zhang, F., Jun, M., Ledue, O., Herd, M., Malley, R., & Lu, Y. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.05.085 · Cited by 16

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Labibzadeh, M., Kaydani, G. A., Savari, M., & Ekrami, A. (2018) · Polish Journal of Microbiology · doi:10.21307/pjm-2018-043 · Cited by 16

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Al-Bdery, A. S. J., Mohammed, G. J., & Hussen, B. M. (2020) · Gene Reports · doi:10.1016/j.genrep.2020.100804 · Cited by 16

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Egyir, B., Bentum, J., Attram, N., Fox, A., Obeng‐Nkrumah, N., Labi, A.-K., Behene, E., Kumordjie, S., Yeboah, C., Agbodzi, B., et al. (2021) · Pathogens · doi:10.3390/pathogens10020196 · Cited by 17

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Rani, N. N. I. M., Hussein, Z. M., Mustapa, F., Azhari, H., Sekar, M., Chen, X. Y., & Amin, M. C. I. M. (2021) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2021.04.021 · Cited by 17

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Masim, M., Argimón, S., Espiritu, H. G., Magbanua, M., Lagrada, M. L., Olorosa, A. M., Cohen, V., Gayeta, J. M., Jeffrey, B., Abudahab, K., et al. (2021) · Western Pacific surveillance response journal · doi:10.5365/wpsar.2020.11.1.004 · Cited by 16

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Monteiro‐Neto, V., Neto, L. G. L., Abreu, A. G., & Monteiro, C. R. A. V. (2017) · InTech eBooks · doi:10.5772/intechopen.69430 · Cited by 16

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Olsufyeva, E., Shchekotikhin, A. E., Бычкова, Е. Н., Переверзева, Э. Р., Treshalin, I. D., Павловна, М. Е., Борисовна, И. Е., Chernobrovkin, M. G., Kozlov, R. S., Dekhnich, A. V., et al. (2018) · Drug Design Development and Therapy · doi:10.2147/dddt.s173923 · Cited by 16

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Onjai-uea, N., Paengkoum, S., Taethaisong, N., Thongpea, S., & Paengkoum, P. (2024) · Animals · doi:10.3390/ani14050811 · Cited by 19

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Wisal, A., Ullah, A., Anwar, W., Khan, Y., Basharat, Z., Irfan, M., Karim, A., Irfan, M., Imran, M., Morel, C. M., et al. (2024) · Molecular Genetics and Genomics · doi:10.1007/s00438-024-02115-8 · Cited by 15

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Hansen, T. A., Joshi, T., Larsen, A. R., Andersen, P. S., Harms, K., Mollerup, S., Willerslev, E., Fuursted, K., Nielsen, L. P., & Hansen, A. J. (2016) · Evolution Medicine and Public Health · doi:10.1093/emph/eow021 · Cited by 15

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Bornbusch, S. L., & Drea, C. M. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.704070 · Cited by 17

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Ren, Z., Yang, S., Han, J., Nie, C., Wang, C., Wang, J., Zheng, X., Yang, H., Zhang, Q., Jingjun, P., et al. (2022) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-022-04522-4 · Cited by 15

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Saraiva, F., de Araújo, A. C. C., de Araújo, A. É. V., & Senna, J. P. M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0225752 · Cited by 15

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Wang, X., Yang, T., & Wang, J. (2024) · Sensors & Diagnostics · doi:10.1039/d4sd00229f · Cited by 14

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Pinho, M. G., Götz, F., & Peschel, A. (2025) · Journal of Bacteriology · doi:10.1128/jb.00106-25 · Cited by 16

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Dhillon-LaBrooy, A., Braband, K. L., Tantawy, E., Rampoldi, F., Kao, Y.-S., Boukhallouk, F., Velásquez, L. N., Mamareli, P., Silva, L., Damasceno, L. E. A., et al. (2023) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2023.09.275 · Cited by 15

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She, P., Yang, Y., Li, L., Li, Y., Liu, S., Li, Z., Zhou, L., & Wu, Y. C. (2023) · mSystems · doi:10.1128/msystems.01026-23 · Cited by 15

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Wang, S., Jiang, Y., Che, L., Wang, R. H., & Li, S. C. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae515 · Cited by 15

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Zhang, Y., Zhang, Y.-Z., Kuang, Z., Xu, J.-Q., Li, C., Li, Y., Jiang, Y.-J., & Xie, J.-P. (2019) · Ground Water · doi:10.1111/gwat.12924 · Cited by 13

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Su, M., Davis, M. H., Peterson, J., Solís‐Lemus, C., Satola, S. W., & Read, T. D. (2021) · PeerJ · doi:10.7717/peerj.11764 · Cited by 14

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Pokhrel, R., Bhattarai, N., Baral, P., Gerstman, B. S., Park, J. H., Handfield, M., & Chapagain, P. P. (2021) · Journal of Chemical Theory and Computation · doi:10.1021/acs.jctc.1c00666 · Cited by 14

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Alby, K., & Miller, M. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-40181-4.00290-5 · Cited by 14

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Zhang, Y., Zhang, Y., Chen, C., Cheng, H., Deng, X., Li, D., Bai, B., Yu, Z., Deng, Q., Guo, J. Q., et al. (2022) · BMC Microbiology · doi:10.1186/s12866-022-02535-9 · Cited by 13

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Liu, X., Yuan, Q., Yang, Y., Li, K., Pang, N., Yang, M. H., Yang, M., Li, X., Guo, J., Liao, X., et al. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.161698 · Cited by 13

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Aros-Calt, S., Castelli, F. A., Lamourette, P., Gervasi, G., Junot, C., Muller, B. H., & Fenaille, F. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8814-3_18 · Cited by 13

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Vestö, K., Huseby, D. L., Snygg, I., Wang, H. H., Hughes, D., & Rhen, M. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02941 · Cited by 13

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Peng, H., Rao, Y., Yuan, W., Zheng, Y., Shang, W., Hu, Z., Yang, Y., Tan, L., Xiong, K., Li, S., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02955 · Cited by 13

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Rodríguez, F., Salinas, C., Fernández, S., Haim, M. S., Mollerach, M. E., Basualdo, W., Castro, H., †, B. Q., Arguello, R., Rodríguez, M., et al. (2020) · The Journal of Infection in Developing Countries · doi:10.3855/jidc.12108 · Cited by 13

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Abdul‐Mutakabbir, J. C., Kebriaei, R., Stamper, K. C., Sheikh, Z., Maassen, P. T., Lev, K. L., & Rybak, M. J. (2020) · Antibiotics · doi:10.3390/antibiotics9100696 · Cited by 13

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Munir, A., Waseem, H., Williams, M. R., Stedtfeld, R. D., Gülari, E., Tiedje, J. M., & Hashsham, S. A. (2017) · Microarrays · doi:10.3390/microarrays6020009 · Cited by 13

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Neto, N. A. S., Oliveira, J. T. A., Aguiar, T. K. B., Bezerra, L. P., Branco, L. A. C., Mesquita, F. P., Freitas, C. D. T., & Souza, P. F. N. (2022) · Pathogens · doi:10.3390/pathogens11090995 · Cited by 12

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Li, X., Cai, Y., Xia, Q., Liao, Y., & Qin, R. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1118793 · Cited by 13

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Liu, H., Bai, L., & Jiang, X. (2024) · Tetrahedron Letters · doi:10.1016/j.tetlet.2024.155314 · Cited by 12

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Karmakar, P. S., & Gaitonde, V. V. (2019) · Medicines · doi:10.3390/medicines6010021 · Cited by 13

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Tahmasebi, H., Dehbashi, S., & Arabestani, M. R. (2019) · BMC Research Notes · doi:10.1186/s13104-019-4166-7 · Cited by 12

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Tsai, C.-E., Yang, C., Chuang, Y., Wang, J., Sheng, W., Chen, Y., & Chang, S. (2022) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2022.05.057 · Cited by 12

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Olsufyeva, E. N., & Tevyashova, A. N. (2017) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026617666170130115957 · Cited by 12

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Teng, Z., Li, M., Shi, D., Deng, X., & Wang, J. (2018) · Journal of Global Antimicrobial Resistance · doi:10.1016/j.jgar.2018.05.013 · Cited by 12

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Kara, E. M., Bayrak, N., Yıldırım, H., Yıldız, M., Ataman, M., Çelık, B. Ö., & Tuyun, A. F. (2021) · Medicinal Chemistry Research · doi:10.1007/s00044-021-02772-z · Cited by 11

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Xia, W., Shan, J., Lutsenko, V., Cheng, Z., Liu, Y., Xu, J., Yu, S., Peng, Z., Yuan, H., & Hu, W. (2025) · Biomaterials Advances · doi:10.1016/j.bioadv.2025.214344 · Cited by 11

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mu, A. L. M. K. R., Abulikemu, M., Liang, Z., Abulikemu, A., & Tuxun, A. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s514978 · Cited by 14

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da Silva, P. B., Araújo, V. H. S., Fonseca‐Santos, B., Solcia, M. C., Ribeiro, C. M., da Silva, I. C., Alves, R. C., Pironi, A. M., Silva, A. C. L., Victorelli, F. D., et al. (2020) · Current Medicinal Chemistry · doi:10.2174/0929867327666200513080719 · Cited by 11

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Salam, L. B., Obayori, O. S., Ilori, M. O., & Amund, O. O. (2021) · Ecotoxicology · doi:10.1007/s10646-021-02422-5 · Cited by 12

A ‘time bomb’ in the human intestine—the multiple emergence and spread of antibiotic‐resistant bacteria

Zhang, Y., Xu, S., Yang, Y., Chou, S., & He, J. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15795 · Cited by 11

Antibody-Recruiting Small Molecules: Synthetic Constructs as Immunotherapeutics

McEnaney, P. J., Parker, C. G., & Zhang, A. X. (2017) · Annual reports in medicinal chemistry · doi:10.1016/bs.armc.2017.08.008 · Cited by 11

Antimicrobial peptides from Actinobacteria: Current status and future prospects

Joseph, J., Baskaran, A., Manigundan, K., Gopikrishnan, V., & Manikkam, R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820084-1.00009-0 · Cited by 11

Influence of the Polymer Architecture and Functionalization with Carboxylate Groups over the Release of Octenidine Hydrochloride from Poly(lactic acid)‐Based Nanoparticles

Maraldi, M., Guida, A., Sponchioni, M., & Moscatelli, D. (2020) · Macromolecular Materials and Engineering · doi:10.1002/mame.202000592 · Cited by 11

Antimicrobial peptides-An alternative candidates to antibiotics against Staphylococcus aureus and its antibiotic-resistant strains

Mazumdar, A., & Adam, V. (2021) · Journal of Molecular and Clinical Medicine · doi:10.31083/j.jmcm.2021.01.208 · Cited by 11

Evidence and Molecular Characterization of Multidrug Resistant Staphylococcus aureus Isolated From Equines in Pakistan

Anwaar, F., Ijaz, M. U., Rasheed, H., Shah, S. F. A., Haider, S. A. R., & Sabir, M. J. (2023) · Journal of Equine Veterinary Science · doi:10.1016/j.jevs.2023.104498 · Cited by 11

Vancomycin Use in Patients Discharged From the Emergency Department: A Retrospective Observational Cohort Study

Mueller, K. L., McCammon, C., Skrupky, L. P., & Fuller, B. M. (2015) · Journal of Emergency Medicine · doi:10.1016/j.jemermed.2015.01.001 · Cited by 11

Biocidal effects of stem bark extract of Chrysophyllum albidium G. Don on vancomycin-resistant Staphylococcus aureus

Akinpelu, D. A., Odewade, J. O., Aiyegoro, O. A., Ashafa, A. O. T., Akinpelu, O. F., & Agunbiade, M. O. (2016) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-016-1080-6 · Cited by 12

Taming Superbugs: Current Progress and Challenges in Combating ESKAPE Pathogens

Hetta, ‏. F., Khalaf, F. R., Kotb, A. A., Alatawi, M. N., Albalawi, A. S., Alharbi, A. A., Aljohani, M. K., Aljohani, S. S., Alatawi, M. S., Ellah, N. H. A., et al. (2025) · Pathogens · doi:10.3390/pathogens15010028 · Cited by 11

Vancomycin Use in Children and Neonates across Three Decades: A Bibliometric Analysis of the Top-Cited Articles

Minotti, C., Barbieri, E., Giaquinto, C., & Donà, D. (2021) · Pathogens · doi:10.3390/pathogens10101343 · Cited by 10

Using Protein Fingerprinting for Identifying and Discriminating Methicillin Resistant Staphylococcus aureus Isolates from Inpatient and Outpatient Clinics

Elbehiry, A., Marzouk, E., Moussa, I. M., Anagreyyah, S. A., AlGhamdi, A., Alqarni, A., Aljohani, A., Hemeg, H. A., Almuzaini, A. M., Alzaben, F. A., et al. (2023) · Diagnostics · doi:10.3390/diagnostics13172825 · Cited by 12

Antimicrobial activity of nature-inspired molecules against multidrug-resistant bacteria

Hamad, M., Al-Marzooq, F. I., Srinivasulu, V., Sulaiman, A., Menon, V., Ramadan, W. S. H., El‐Awady, R., & Al‐Tel, T. H. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1336856 · Cited by 12

Histone H1 kills MRSA

Marsman, G., Zheng, X., Čerina, D., Lacey, K. A., Liu, M., Humme, D., Goosmann, C., Brinkmann, V., Harbort, C. J., Torres, V. J., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114969 · Cited by 10

Pet dogs as reservoir of oxacillin and vancomycin-resistant Staphylococcus spp

dos Santos, I. C., Barbosa, L. N., da Silva, G. R., Otutumi, L. K., Zaniolo, M. M., dos Santos, M. C., Ferreira, L. R. D. P., Gonçalves, D. D., & Martins, L. D. A. (2021) · Research in Veterinary Science · doi:10.1016/j.rvsc.2021.12.005 · Cited by 10

Effects of intra-articular D-amino acids combined with systemic vancomycin on an experimental Staphylococcus aureus-induced periprosthetic joint infection

Li, Y., Wuermanbieke, S., Ren, J., Mu, W., Ma, H., Qi, F., Sun, X., Liu, Y., Amat, A., Zhang, X., et al. (2022) · Journal of Microbiology Immunology and Infection · doi:10.1016/j.jmii.2022.01.005 · Cited by 10

Bacterial Pyruvate Kinase: A New Potential Target to Combat Drug‐Resistant Staphylococcus aureus Infections

Akunuri, R., Unnissa, T., Vadakattu, M., Bujji, S., Ghouse, S. M., Yaddanapudi, V. M., Chopra, S., & Nanduri, S. (2022) · ChemistrySelect · doi:10.1002/slct.202201403 · Cited by 10

Rational Design of a Potent Antimicrobial Peptide Based on the Active Region of a Gecko Cathelicidin

Cai, Y., Wang, X., Zhang, T., An, Y., Luo, L., Li, C., Tian, G., Wu, Z., Wang, X., Shen, D., et al. (2024) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.3c00575 · Cited by 10

3D scaffolds coated with nanofibers displaying bactericidal activity for bone tissue applications

de Sá, K. D., Figueira, D. R., Miguel, S. P., Correia, T. R., Silva, A. P., & Correia, I. J. (2016) · International Journal of Polymeric Materials · doi:10.1080/00914037.2016.1236338 · Cited by 10

Health care-associated infections: Controlled delivery of cationic antiseptics from polymeric excipients

Maraldi, M., Lisi, M., Moretti, G., Sponchioni, M., & Moscatelli, D. (2021) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2021.120956 · Cited by 10

Phylogenetic Analysis of the Genes in D-Ala-D-Lactate Synthesizing Glycopeptide Resistance Operons: The Different Origins of Functional and Regulatory Genes

Kardos, G., Laczkó, L., Kaszab, E., Timmer, B., Szarka, K., Prépost, E., & Bànyai, K. (2024) · Antibiotics · doi:10.3390/antibiotics13070573 · Cited by 9

Imaging of Gut Bacterial Macroscopic Changes in Simulated Microgravity-Exposed Rats via In Vivo Metabolic Labeling

Wu, Z., Liu, H., Yan, L., Deng, Y., Tian, Z., Du, Y., Zhao, Y., Ma, H., Deng, Y., Li, Y., et al. (2024) · Analytical Chemistry · doi:10.1021/acs.analchem.4c05028 · Cited by 9

Staphylococcus aureus manipulates osteocytes to cause persistent chronic osteomyelitis and antibiotic resistance via pyroptosis pathway suppression

Cai, Y., Hu, H., Chen, Y., Li, J., Zhang, C., Yuan, X., Li, W., Huang, C., Lin, Y., Zhang, Z., et al. (2025) · Drug Resistance Updates · doi:10.1016/j.drup.2025.101295 · Cited by 9

Knockout of ykcB , a Putative Glycosyltransferase, Leads to Reduced Susceptibility to Vancomycin in Bacillus subtilis

Ishikawa, K., Shirakawa, R., Takano, D., Kosaki, T., Furuta, K., & Kaito, C. (2022) · Journal of Bacteriology · doi:10.1128/jb.00387-22 · Cited by 9

Dielectrophoresis microbial characterization and isolation of Staphylococcus aureus based on optimum crossover frequency

Rozaini, A. Z. A., Abdulhameed, A., Deivasigamani, R., Nadzreen, N., Zin, N. M., Kayani, A. B. A., & Buyong, M. R. (2023) · Electrophoresis · doi:10.1002/elps.202200276 · Cited by 9

New resorcylic acid derivatives of Lysimachia tengyuehensis against MRSA and VRE by interfering with bacterial metabolic imbalance

Shi, N., Wang, Z., Shi, Y.-Z., Jiang, L., Zhu, Y.-Y., He, X.-C., Zhou, Z.-S., Wei, M.-Z., Zhao, Y., & Luo, X. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.116714 · Cited by 9

Generation and Characterization of Murine Monoclonal Antibodies anti-PBP2a of Methicillin-resistant Staphylococcus aureus

Senna, J. P. M., Teixeira, M. D. G. M., Santiago, M. D. A., Batoreu, N. M., Valadares, N. F., & Galler, R. (2015) · Monoclonal Antibodies in Immunodiagnosis and Immunotherapy · doi:10.1089/mab.2015.0013 · Cited by 9

Genotyping of enterotoxigenic methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Staphylococcus aureus (VRSA) among commensal rodents in North Sinai, Egypt

Eidaroos, N. H., Youssef, A. I., El-Sebae, A. A., Enany, M. E., & Farid, D. S. (2021) · Journal of Applied Microbiology · doi:10.1111/jam.15226 · Cited by 9

The Escalating Challenge of Vancomycin Resistance in Staphylococcus aureus

Pfeltz, R. F., & Wilkinson, B. J. (2004) · Current Drug Targets - Infectious Disorders · doi:10.2174/1568005043340470 · Cited by 97

Molecular Mechanism of Resistance against Vancomycin in Staphylococcus aureus

(2026) · doi:10.47278/book.tl/2026.499

Staphylococcus aureus response and adaptation to vancomycin

Fait, A., Silva, S. F., Abrahamsson, J. Å. H., & Ingmer, H. (2024) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2024.04.006 · Cited by 19

Advances in Vancomycin Resistance: Research inStaphylococcus aureus

Hiramatsu, K., Kapi, M., Tajima, Y., Cui, L., Trakulsomboon, S., & Ito, T. (2014) · ASM Press eBooks · doi:10.1128/9781555817572.ch21 · Cited by 5

VanA-Type Vancomycin-ResistantStaphylococcus aureus

Périchon, B., & Courvalin, P. M. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00346-09 · Cited by 337