Show source-provided references
3. Metelmann, H.-R., Woedtke, T., and Weltmann, K.-D. (2018). Comprehensive Clinical Plasma Medicine: Cold Physical Plasma for Medical Application, Springer International Publishing.
10.1007/978-3-319-67627-2 ↗6. A first prospective randomized controlled trial to decrease bacterial load using cold atmospheric argon plasma on chronic wounds in patients
10.1111/j.1365-2133.2010.09744.x ↗8. Combined antibacterial effects of tissue-tolerable plasma and a modern conventional liquid antiseptic on chronic wound treatment
10.1002/jbio.201400007 ↗10. Cold atmospheric argon plasma treatment may accelerate wound healing in chronic wounds: Results of an open retrospective randomized controlled study in vivo
10.1016/j.cpme.2013.06.001 ↗11. Alleviation of chronic venous leg ulcers with a hand-held dielectric barrier discharge plasma generator (PlasmaDerm((R))VU-2010): Results of a monocentric, two-armed, open, prospective, randomized and controlled trial (NCT01415622)
10.1111/jdv.12490 ↗14. Scar formation of laser skin lesions after cold atmospheric pressure plasma (CAP) treatment: A clinical long term observation
10.1016/j.cpme.2012.12.001 ↗15. Laser scanning microscopy as a means to assess the augmentation of tissue repair by exposition of wounds to tissue tolerable plasma
10.1088/1612-2011/11/11/115701 ↗16. Randomized placebo-controlled human pilot study of cold atmospheric argon plasma on skin graft donor sites
10.1111/wrr.12078 ↗17. Effects and safety of atmospheric low-temperature plasma on bacterial reduction in chronic wounds and wound size reduction: A systematic review and meta-analysis
10.1111/iwj.12999 ↗20. Cold-plasma coagulation in the treatment of malignant pleural mesothelioma: Results of a combined approach
10.1510/icvts.2009.223768 ↗25. Actinic keratoses treated with cold atmospheric plasma
26. Privat-Maldonado, A., Bengtson, C., Razzokov, J., Smits, E., and Bogaerts, A. (2019). Modifying the Tumour Microenvironment: Challenges and Future Perspectives for Anticancer Plasma Treatments. Cancers, 11.
10.3390/cancers11121920 ↗28. The effect of the plasma needle on tumoral cell lines apoptosis
29. Reaction Chemistry Generated by Nanosecond Pulsed Dielectric Barrier Discharge Treatment is Responsible for the Tumor Eradication in the B16 Melanoma Mouse Model
10.1002/ppap.201500140 ↗32. Brullé, L., Vandamme, M., Riès, D., Martel, É., Robert, É., Lerondel, S., Trichet, V., Richard, S., Pouvesle, J.-M., and Le Pape, A. (2012). Effects of a Non Thermal Plasma Treatment Alone or in Combination with Gemcitabine in a MIA PaCa2-luc Orthotopic Pancreatic Carcinoma Model. PLoS ONE, 7.
10.1371/journal.pone.0052653 ↗33. Semmler, M.L., Bekeschus, S., Schäfer, M., Bernhardt, T., Fischer, T., Witzke, K., Seebauer, C., Rebl, H., Grambow, E., and Vollmar, B. (2020). Molecular Mechanisms of the Efficacy of Cold Atmospheric Pressure Plasma (CAP) in Cancer Treatment. Cancers, 12.
10.3390/cancers12020269 ↗37. High-voltage electrical stimulation for the management of Stage III and IV pressure ulcers among adults with spinal cord injury: Demonstration of its utility for recalcitrant wounds below the level of injury
10.1179/2045772311Y.0000000044 ↗38. Electrical Stimulation Therapy Increases Rate of Healing of Pressure Ulcers in Community-Dwelling People With Spinal Cord Injury
10.1016/j.apmr.2009.12.026 ↗40. Integrin-dependent human macrophage migration induced by oscillatory electrical stimulation
10.1114/1.263 ↗42. β4 Integrin and Epidermal Growth Factor Coordinately Regulate Electric Field-mediated Directional Migration via Rac1
10.1091/mbc.e06-05-0433 ↗43. Antibacterial activity of positive and negative polarity low-voltage pulsed current (LVPC) on six typical Gram-positive and Gram-negative bacterial pathogens of chronic wounds
10.1111/j.1524-475X.2007.00242.x ↗48. The emerging role of reactive oxygen and nitrogen species in redox biology and some implications for plasma applications to medicine and biology
10.1088/0022-3727/45/26/263001 ↗51. Role of nitric oxide, nitroxidative and oxidative stress in wound healing
58. Schmidt, A., and Bekeschus, S. (2018). Redox for Repair: Cold Physical Plasmas and Nrf2 Signaling Promoting Wound Healing. Antioxidants, 7.
10.3390/antiox7100146 ↗60. Arndt, S., Unger, P., Wacker, E., Shimizu, T., Heinlin, J., Li, Y.-F., Thomas, H.M., Morfill, G.E., Zimmermann, J.L., and Bosserhoff, A.-K. (2013). Cold Atmospheric Plasma (CAP) Changes Gene Expression of Key Molecules of the Wound Healing Machinery and Improves Wound Healing In Vitro and In Vivo. PLoS ONE, 8.
10.1371/journal.pone.0079325 ↗61. Arndt, S., Landthaler, M., Zimmermann, J.L., Unger, P., Wacker, E., Shimizu, T., Li, Y.-F., Morfill, G.E., Bosserhoff, A.-K., and Karrer, S. (2015). Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo. PLoS ONE, 10.
10.1371/journal.pone.0120041 ↗62. Cold atmospheric plasma modulates endothelial nitric oxide synthase signalling and enhances burn wound neovascularisation
10.1002/path.5323 ↗63. Cold atmospheric plasma (CAP) activates angiogenesis-related molecules in skin keratinocytes, fibroblasts and endothelial cells and improves wound angiogenesis in an autocrine and paracrine mode
10.1016/j.jdermsci.2017.11.008 ↗65. Endothelial Cell Proliferation is Enhanced by Low Dose Non-Thermal Plasma Through Fibroblast Growth Factor-2 Release
10.1007/s10439-009-9868-x ↗66. The HIPPO Transducer YAP and Its Targets CTGF and Cyr61 Drive a Paracrine Signalling in Cold Atmospheric Plasma-Mediated Wound Healing
10.1155/2020/4910280 ↗67. Non-thermal Plasma Activates Human Keratinocytes by Stimulation of Antioxidant and Phase II Pathways
10.1074/jbc.M114.603555 ↗69. Periodic Exposure of Keratinocytes to Cold Physical Plasma: An In Vitro Model for Redox-Related Diseases of the Skin
10.1155/2016/9816072 ↗70. A cold plasma jet accelerates wound healing in a murine model of full-thickness skin wounds
10.1111/exd.13156 ↗72. Bekeschus, S., Schmidt, A., Niessner, F., Gerling, T., Weltmann, K.-D., and Wende, K. (2017). Basic Research in Plasma Medicine—A Throughput Approach from Liquids to Cells. J. Vis. Exp., e56331.
10.3791/56331-v ↗74. Cellular mechanisms and physiological consequences of redox-dependent signalling
10.1038/nrm3801 ↗75. Nrf2 signaling and inflammation are key events in physical plasma-spurred wound healing
10.7150/thno.29754 ↗78. Overproduction of NOX-derived ROS in AML promotes proliferation and is associated with defective oxidative stress signaling
10.1182/blood-2013-04-491944 ↗80. Floating Electrode Dielectric Barrier Discharge Plasma in Air Promoting Apoptotic Behavior in Melanoma Skin Cancer Cell Lines
10.1007/s11090-007-9048-4 ↗81. Cold atmospheric plasma jet effects on V79-4 cells
82. Cellular Senescence: What, Why, and How
83. Cold atmospheric plasma, a new strategy to induce senescence in melanoma cells
10.1111/exd.12127 ↗86. Mitra, S., Nguyen, L.N., Akter, M., Park, G., Choi, E., and Choi, E. (2019). Impact of ROS Generated by Chemical, Physical, and Plasma Techniques on Cancer Attenuation. Cancers, 11.
10.3390/cancers11071030 ↗87. Matrix metalloproteinase-9 expression in post-hypoxic human brain capillary endothelial cells: H2O2 as a trigger and NF-κB as a signal transducer
10.1160/TH03-02-0070 ↗88. ROS-NFκΒ mediates TGF-β1-induced expression of urokinase-type plasminogen activator, matrix metalloproteinase-9 and cell invasion
10.1007/s11010-010-0418-5 ↗91. Promotion of Wound Healing by an Agonist of Adenosine A2A Receptor Is Dependent on Tissue Plasminogen Activator
10.1007/s10753-015-0184-3 ↗92. Mesenchymal Stem Cells Improve Wound Healing In Vivo via Early Activation of Matrix Metalloproteinase-9 and Vascular Endothelial Growth Factor
10.3346/jkms.2011.26.6.726 ↗95. Fine Tuning Cell Migration by a Disintegrin and Metalloproteinases
97. Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress† †Electronic supplementary information (ESI) available. See doi:10.1039/c5sc02311d Click here for additional data file
98. Wolff, C.M., Kolb, J.F., Weltmann, K.-D., Von Woedtke, T., and Bekeschus, S. (2020). Combination Treatment with Cold Physical Plasma and Pulsed Electric Fields Augments ROS Production and Cytotoxicity in Lymphoma. Cancers, 12.
10.3390/cancers12040845 ↗99. Schmidt, A., Von Woedtke, T., Stenzel, J., Lindner, T., Polei, S., Vollmar, B., and Bekeschus, S. (2017). One Year Follow-Up Risk Assessment in SKH-1 Mice and Wounds Treated with an Argon Plasma Jet. Int. J. Mol. Sci., 18.
10.3390/ijms18040868 ↗