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Modifications of Plasma Membrane Organization in Cancer Cells for Targeted Therapy

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Destabilization induced by electropermeabilization analyzed by atomic force microscopy

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DBS-relevant electric fields increase hydraulic conductivity ofin vitroendothelial monolayers

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Pulsed field ablation in medicine: irreversible electroporation and electropermeabilization theory and applications

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Single Cell Forces after Electroporation

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The Good and the Bad of Cell Membrane Electroporation

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Limb Sparing Treatment of Bleeding Melanoma Recurrence by Electrochemotherapy

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The latest research progress on minimally invasive treatments for hepatocellular carcinoma

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Electroporation of Brain Endothelial Cells on Chip toward Permeabilizing the Blood-Brain Barrier

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Non-Viral Transfection of Human T Lymphocytes

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Irreversible Electroporation: A Novel Ultrasound-guided Modality for Non-thermal Tumor Ablation

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High-Frequency Irreversible Electroporation (H-FIRE) Induced Blood–Brain Barrier Disruption Is Mediated by Cytoskeletal Remodeling and Changes in Tight Junction Protein Regulation

Partridge, B. R., Kani, Y., Lorenzo, M. F., Campelo, S. N., Allen, I. C., Hinckley, J., Hsu, F., Verbridge, S. S., Robertson, J. L., Davalos, R. V., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10061384 · Cited by 26 · see citing works

Modeling of Microvascular Permeability Changes after Electroporation

Čorović, S., Markelc, B., Dolinar, M., Čemažar, M., & Jarm, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121370 · Cited by 26 · see citing works

Irreversible electroporation of the liver: is there a safe limit to the ablation volume?

Sánchez‐Velázquez, P., Castellví, Q., Villanueva, A., Quesada, R., Pañella, C., Cáceres, M., Dorcaratto, D., Andaluz, A., Moll, X., Trujillo, M., et al. (2016) · Scientific Reports · doi:10.1038/srep23781 · Cited by 25 · see citing works

Combination of cold plasma and pulsed electric fields – A rationale for cancer patients in palliative care

Wolff, C. M., Steuer, A., Stoffels, I., von Woedtke, T., Weltmann, K., Bekeschus, S., & Kolb, J. F. (2019) · Clinical Plasma Medicine · doi:10.1016/j.cpme.2020.100096 · Cited by 24 · see citing works

Combining the single-walled carbon nanotubes with low voltage electrical stimulation to improve accumulation of nanomedicines in tumor for effective cancer therapy

Lee, P., Peng, C., & Shieh, M. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.01.038 · Cited by 23 · see citing works

AFM sensing cortical actin cytoskeleton destabilization during plasma membrane electropermeabilization

Chopinet, L., Dague, É., & Rols, M. (2014) · Cytoskeleton · doi:10.1002/cm.21194 · Cited by 22 · see citing works

A fundamental theoretical study on the different effect of electroporation on tumor blood vessels and normal blood vessels

Lv, Y., Feng, Z., Chen, S., Cheng, X. W., Zhang, J., & Yao, C. (2021) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2021.108010 · Cited by 21 · see citing works

Electroporation-induced changes in tumor vasculature and microenvironment can promote the delivery and increase the efficacy of sorafenib nanoparticles

Kodama, H., Shamay, Y., Kimura, Y., Shah, J., Solomon, S. B., Heller, D. A., & Srimathveeravalli, G. (2019) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2019.107328 · Cited by 19 · see citing works

Effects of Reversible and Irreversible Electroporation on Endothelial Cells and Tissue Blood Flow

Markelc, B., Čemažar, M., & Serša, G. (2017) · Springer eBooks · doi:10.1007/978-3-319-32886-7_70 · Cited by 18 · see citing works

The effects of point-source electroporation on the blood-brain barrier and brain vasculature in rats: An MRI and histology study

Sharabi, S., Last, D., Daniels, D., Zaltsman, S. L., & Mardor, Y. (2020) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2020.107521 · Cited by 18 · see citing works

Study of Astragalus mongholicus polysaccharides on endothelial cells permeability induced by HMGB1

Zheng, Y., Zhou, B., Song, Z.-F., Li, L., Wu, J., Zhang, R., & Tang, Y.-Q. (2012) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2012.08.001 · Cited by 17 · see citing works

Effects of Actin Cytoskeleton Disruption on Electroporation In Vitro

Kim, H. B., Lee, S., Chung, J. H., Kim, S. N., Sung, C. K., & Baik, K. Y. (2020) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-020-03271-4 · Cited by 17 · see citing works

Novel mechanism of gene transfection by low-energy shock wave

Ha, C. H., Lee, S. C., Kim, S., Chung, J., Bae, H., & Kwon, K. (2015) · Scientific Reports · doi:10.1038/srep12843 · Cited by 16 · see citing works

Hemorrhage Control of Liver Injury by Short Electrical Pulses

Mandel, Y., Malki, G., Adawi, E., Glassberg, E., Afek, A. B., Zagetzki, M., & Barnea, O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0049852 · Cited by 15 · see citing works

The use of cisplatin electrochemotherapy in nonmelanoma skin cancers: A single‐center study

GIORGI, V. D., Scarfì, F., Saqer, E., Gori, A., Tomassini, G. M., & Covarelli, P. (2020) · Dermatologic Therapy · doi:10.1111/dth.13547 · Cited by 14 · see citing works

Long-term effectiveness of irreversible electroporation in a murine model of colorectal liver metastasis

Sánchez‐Velázquez, P., Castellví, Q., Villanueva, A., Iglesias, M., Quesada, R., Pañella, C., Cáceres, M., Dorcaratto, D., Andaluz, A., Moll, X., et al. (2017) · Scientific Reports · doi:10.1038/srep44821 · Cited by 14 · see citing works

Redox-related Molecular Mechanism of Sensitizing Colon Cancer Cells to Camptothecin Analog SN38

Nikolova, B., Semkova, S., Tsoneva, I. C., Stoyanova, E., Lefterov, P., Lazarova, D., Zhelev, Z., Aoki, I., Higashi, T., & Bakalova, R. (2020) · Anticancer Research · doi:10.21873/anticanres.14519 · Cited by 13 · see citing works

A new spiral microelectrode assembly for electroporation and impedance measurements of adherent cell monolayers

García-Sánchez, T., Guitart, M., Rosell, J., Gómèz‐Foix, A. M., & Bragós, R. (2014) · Biomedical Microdevices · doi:10.1007/s10544-014-9860-6 · Cited by 12 · see citing works

Electrodes and Electric Field Distribution in Clinical Practice

Cindrič, H., Kos, B., & Damijan Miklavčič, A. (2021) · Springer eBooks · doi:10.1007/978-3-030-80668-2_2 · Cited by 11 · see citing works

Lab-on-chip microscope platform for electro-manipulation of a dense microtubules network

Havelka, D., Zhernov, I., Teplan, M., Lánský, Z., Chafai, D. E., & Cifra, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-06255-y · Cited by 11 · see citing works

Cytoskeletal Remodeling and Gap Junction Translocation Mediates Blood–Brain Barrier Disruption by Non-invasive Low-Voltage Pulsed Electric Fields

Rajagopalan, N. R., Vista, W.-R., Fujimori, M., Vroomen, L. G. P. H., Jiménez, J. M., Khadka, N., Bikson, M., & Srimathveeravalli, G. (2023) · Annals of Biomedical Engineering · doi:10.1007/s10439-023-03211-3 · Cited by 10 · see citing works

The Effect of High-Frequency Electric Pulses on Tumor Blood Flow In Vivo

Raeisi, E., Firoozabadi, M., Hajizadeh, S., Rajabi, H., & Hassan, Z. M. (2010) · The Journal of Membrane Biology · doi:10.1007/s00232-010-9288-8 · Cited by 8 · see citing works

Electric fields regulate cellular elasticity through intracellular Ca2+ concentrations

Han, S. J., Noh, M., Jang, J., Lee, J. B., & Kim, K. S. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30417 · Cited by 8 · see citing works

Acute Effects of Intratumor DNA Electrotransfer

Bhandary, M., Conniff, A. S., Miranda, K., & Heller, L. C. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14102097 · Cited by 8 · see citing works

Effects of Electroporation of Mammalian Cells on Cytoskeleton and Intercellular Connections

Čemažar, M., Božič, T., & Lisec, B. (2017) · Springer eBooks · doi:10.1007/978-3-319-26779-1_18-2 · Cited by 8 · see citing works

Dynamics of Engineered Artificial Membranes and Biosensors

Hoiles, W., Krishnamurthy, V., & Cornell, B. A. (2018) · Cambridge University Press eBooks · doi:10.1017/9781108526227 · Cited by 7 · see citing works

Transient Lymphatic Remodeling Follows Sub-Ablative High-Frequency Irreversible Electroporation Therapy in a 4T1 Murine Model

Esparza, S., Jacobs, E. J., Hammel, J. H., Michelhaugh, S. K., Alinezhadbalalami, N., Nagai-Singer, M. A., Imran, K. M., Davalos, R. V., Allen, I. C., Verbridge, S. S., et al. (2025) · Annals of Biomedical Engineering · doi:10.1007/s10439-024-03674-y · Cited by 6 · see citing works

DNA Electrotransfer Regulates Molecular Functions in Skeletal Muscle

Conniff, A. S., Tur, J., Kohena, K., Zhang, M., Gibbons, J., & Heller, L. C. (2023) · Bioelectricity · doi:10.1089/bioe.2022.0041 · Cited by 6 · see citing works

Characterization of two distinct immortalized endothelial cell lines, EA.hy926 and HMEC-1, for in vitro studies: exploring the impact of calcium electroporation, Ca2+ signaling and transcriptomic profiles

Lisec, B., Božič, T., Šantek, I., Markelc, B., Vrecl, M., Frangež, R., & Čemažar, M. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01503-2 · Cited by 6 · see citing works

Focused transhepatic electroporation mediated by hypersaline infusion through the portal vein in rat model. Preliminary results on differential conductivity

Pañella, C., Castellví, Q., Moll, X., Quesada, R., Villanueva, A., Iglesias, M., Naranjo, D., Sánchez‐Velázquez, P., Andaluz, A., Grande, L., et al. (2017) · Radiology and Oncology · doi:10.1515/raon-2017-0051 · Cited by 6 · see citing works

Blood Flow Modifying and Vascular-Disrupting Effects of Electroporation and Electrochemotherapy

Serša, G., Čemažar, M., & Markelc, B. (2017) · Springer eBooks · doi:10.1007/978-3-319-32886-7_165 · Cited by 5 · see citing works

Vascular-Disrupting Action of Electrochemotherapy: Mode of Action and Therapeutic Implications

Serša, G., & Čemažar, M. (2011) · Springer eBooks · doi:10.1007/978-1-4419-8363-3_7 · Cited by 5 · see citing works

The effects of external electric fields on proteins

Cifra, M., Pandey, S. K., Zakar, T., Poplová, M., Campoy, D. G. B., Průša, J., Havelka, D., Marracino, P., Liberti, M., Apollonio, F., et al. (2026) · Chemical Society Reviews · doi:10.1039/d3cs00244f · Cited by 4 · see citing works

Blood Flow Modifying and Vascular-Disrupting Effects of Electroporation and Electrochemotherapy

Serša, G., Čemažar, M., & Markelc, B. (2016) · Springer eBooks · doi:10.1007/978-3-319-26779-1_165-1 · Cited by 4 · see citing works

Effects of Reversible and Irreversible Electroporation on Endothelial Cells and Tissue Blood Flow

Markelc, B., Čemažar, M., & Serša, G. (2016) · Springer eBooks · doi:10.1007/978-3-319-26779-1_70-1 · Cited by 4 · see citing works

Biological Responses

Yano, K.-I., Rems, L., Kotnik, T., Damijan Miklavčič, A., Weaver, J. C., Smith, K. C., Son, R. S., Gowrishankar, T. R., Vernier, P. T., Levine, Z. A., et al. (2016) · Springer eBooks · doi:10.1007/978-4-431-56095-1_4 · Cited by 4 · see citing works

Fluorescent Imaging for Assessment of the Effect of Combined Application of Electroporation and Rifampicin on HaCaT Cells as a New Therapeutic Approach for Psoriasis

Nikolova, B., Kostadinova, A. S., Dimitrov, B., Zhelev, Z., Bakalova, R., Aoki, I., Saga, T., & Tsoneva, I. C. (2013) · Sensors · doi:10.3390/s130303625 · Cited by 4 · see citing works

The endothelial permeability increased by low voltage and high frequency electroporation.

Shankayi, Z., Firoozabadi, S. M. P., & Saraf, H. Z. (2013) · PubMed Central · Cited by 4 · see citing works

Benign Soft Tissue Lesions Responsible for Pain: When and How Should the IR Intervene

Filippiadis, D. K., Petsatodis, E., Charalampopoulos, G., Giannakis, A., Chlorogiannis, D., Velonakis, G., & Cornélis, F. (2025) · CardioVascular and Interventional Radiology · doi:10.1007/s00270-024-03940-5 · Cited by 3 · see citing works

Low-magnification image analysis of Giemsa stained, electroporation and bleomycin treated endothelial monolayers provides reliable monolayer integrity data

Meulenberg, C. J. W., & Čemažar, M. (2014) · Toxicology in Vitro · doi:10.1016/j.tiv.2013.12.020 · Cited by 2 · see citing works

Influence of Electroporation on HT29 Cell Proliferation, Spreading and Adhesion Properties

Mamman, H. B., Jamil, M. M. A., Rahman, N. A. A., Ambar, R., & Choon, C. C. (2020) · Lecture notes in electrical engineering · doi:10.1007/978-981-15-5281-6_55 · Cited by 1 · see citing works

1.4 nm gold nanoparticle-antibody conjugates for in situ gold immunolabelling after transduction into living human cells

Groysbeck, N., Haeberlé, A., Ory, S., Hanss, V., Eltsov, M., Schultz, P., & Zuber, G. (2023) · Comptes Rendus Chimie · doi:10.5802/crchim.251 · Cited by 1 · see citing works

Reversible electroporation triggers the release of microvesicles affecting viability, migration, and adhesion of melanoma cells

Szwedowicz, U., Dębicka, R., Pawlik, K. J., Przystupski, D., & Choromańska, A. (2026) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2026.119283 · Cited by 1 · see citing works

Changes in gap junction-mediated intercellular communication in a cell-monolayer after the exposure to nanosecond pulsed electric fields

Steuer, A., Zhuang, J., Daeschlein, G., & Kolb, J. F. (2013) · IEEE International Pulsed Power Conference (PPC) · doi:10.1109/ppc.2013.6627550 · Cited by 1 · see citing works

Optical Trapping Techniques Applied to the Study of Cell Membranes

Morss, A. (2012) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1 · see citing works

Endothelial Cell Isolation and Manipulation

Brostjan, C. (2019) · Learning materials in biosciences · doi:10.1007/978-3-030-12270-6_14 · Cited by 1 · see citing works

Effects of Electroporation of Mammalian Cells on Cytoskeleton and Intercellular Connections

Čemažar, M. (2016) · Springer eBooks · doi:10.1007/978-3-319-26779-1_18-1 · Cited by 1 · see citing works

Cardiomyocytes Permeabilization and Electrotransfection by Unipolar and Bipolar Asymmetric Electric Field Pulses

Kulbacka, J., Rembiałkowska, N., Radzevičiūtė-Valčiukė, E., Szewczyk, A., & Novickij, V. (2024) · Bioelectricity · doi:10.1089/bioe.2024.0001 · Cited by 1 · see citing works

Effects of Electrochemotherapy on Microcirculatory Vasomotion in Tumors

Jarm, T., Cugmas, B., & Čemažar, M. (2010) · World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany · doi:10.1007/978-3-642-13039-7_23 · Cited by 1 · see citing works

Differential Cellular Effects of Electroporation and Electrochemotherapy in Monolayers of Human Microvascular Endothelial Cells

Meulenberg, C. J. W., Todorović, V., & Čemažar, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052713 · Cited by 57 · see citing works

Effects of Electroporation of Mammalian Cells on Cytoskeleton and Intercellular Connections

Čemažar, M. (2016) · Springer eBooks · doi:10.1007/978-3-319-26779-1_18-1 · Cited by 1 · see citing works

Increased permeability of blood vessels after reversible electroporation is facilitated by alterations in endothelial cell-to-cell junctions

Markelc, B., Bellard, E., Serša, G., Jesenko, T., Pélofy, S., Teissié, J., Frangež, R., Rols, M., Čemažar, M., & Golzio, M. (2018) · Journal of Controlled Release · doi:10.1016/j.jconrel.2018.02.032 · Cited by 64 · see citing works

Intravital microscopy at the single vessel level brings new insights of vascular modification mechanisms induced by electropermeabilization

Bellard, E., Markelc, B., Pélofy, S., Guerroué, F. L., Serša, G., Teissié, J., Čemažar, M., & Golzio, M. (2012) · Journal of Controlled Release · doi:10.1016/j.jconrel.2012.09.010 · Cited by 72 · see citing works

Differential Mechanisms Associated with Vascular Disrupting Action of Electrochemotherapy: Intravital Microscopy on the Level of Single Normal and Tumor Blood Vessels

Markelc, B., Serša, G., & Čemažar, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059557 · Cited by 120 · see citing works