There is increasing evidence from preclinical studies. There is growing evidence from preclinical studies in cell cultures and small organisms that exposure to Electromagnetic Fields (EMFs) produces beneficial biological effects. However, controversy persists due to the absence of a clearly defined mechanism. Classical physics, constrained by the non-ionizing nature of these exposures, cannot account for these effects, which do not involve the breaking of chemical bonds to induce conformational changes in proteins. Emerging studies suggest that these effects are mediated through quantum mechanical phenomena—specifically, quantum tunneling and particle-wave duality—acting on the water surrounding proteins at their interfaces. Furthermore, we present evidence of EMF-induced conformational changes in Intrinsically Disordered Proteins (IDPs), including beta-amyloid, tau, alpha-synuclein, and Heat Shock Factor 1 (HSF1). These findings offer a new framework for understanding EMF bioeffects and open promising avenues for research in biophysics and quantum biology. In this context, we address the challenge of reproducibility by examining how variables such as frequency, intensity, Specific Absorption Rate (SAR), and exposure time windows interact, along with how parameters like polarization, phase, pulse modulation, and scheduling influence outcomes. Experimental data identify specific RF frequencies and SAR levels that activate proteostasis and autophagy in cell cultures and small animal models, with potential applications in human treatments that remain consistent with safety thresholds established by regulatory agencies.
Kinsey, L.J., Beane, W.S. and Tseng, K.A. (2024) Accelerating an Integrative View of Quantum Biology. Frontiers in Physiology , 14, Article ID: 1349013. https://doi.org/10.3389/fphys.2023.1349013
Patwa, H., Babcock, N.S. and Kurian, P. (2024) Quantum-Enhanced Photoprotection in Neuroprotein Architectures Emerges from Collective Light-Matter Interactions. Frontiers in Physics , 12, Article ID: 1387271. https://doi.org/10.3389/fphy.2024.1387271
Otten, M., et al . (2024) Quantum Resources Required for Binding Affinity Calculations of Amyloid Beta.
Messori, C., Prinzera, S.V. and di Bardone, F.B. (2019) Deep into the Water: Exploring the Hydro-Electromagnetic and Quantum-Electrodynamic Properties of Interfacial Water in Living Systems. Open Access Library Journal , 6, 1-50. https://doi.org/10.4236/oalib.1105435
Chen, L., Zhang, S., Liu, X. and Ge, X. (2023) Recent Advances in Water-Mediated Multiphase Catalysis. Current Opinion in Colloid & Interface Science , 65, Article ID: 101691. https://doi.org/10.1016/j.cocis.2023.101691
Reid, K.M., Singh, A.K., Bikash, C.R., Wei, J., Tal-Gan, Y., Vinh, N.Q., et al . (2022) The Origin and Impact of Bound Water around Intrinsically Disordered Proteins. Biophysical Journal , 121, 540-551. https://doi.org/10.1016/j.bpj.2022.01.011
Assaker, K., Carteret, C., Lebeau, B., Marichal, C., Vidal, L., Stébé, M., et al . (2013) Water-Catalyzed Low-Temperature Transformation from Amorphous to Semi-Crystalline Phase of Ordered Mesoporous Titania Framework. ACS Sustainable Chemistry & Engineering , 2, 120-125. https://doi.org/10.1021/sc400323w
Giudice, E.D., Tedeschi, A., Vitiello, G. and Voeikov, V. (2013) Coherent Structures in Liquid Water Close to Hydrophilic Surfaces. Journal of Physics : Conference Series , 442, Article ID: 012028. https://doi.org/10.1088/1742-6596/442/1/012028
Peng, Z., Yan, J., Fan, X., Mizianty, M.J., Xue, B., Wang, K., et al . (2014) Exceptionally Abundant Exceptions: Comprehensive Characterization of Intrinsic Disorder in All Domains of Life. Cellular and Molecular Life Sciences , 72, 137-151. https://doi.org/10.1007/s00018-014-1661-9
Stavropoulos, I., Khaldi, N., Davey, N.E., O’Brien, K., Martin, F. and Shields, D.C. (2012) Protein Disorder and Short Conserved Motifs in Disordered Regions Are Enriched near the Cytoplasmic Side of Single-Pass Transmembrane Proteins. PLOS ONE , 7, e44389. https://doi.org/10.1371/journal.pone.0044389
Uversky, V.N. (2009) Intrinsically Disordered Proteins and Their Environment: Effects of Strong Denaturants, Temperature, pH, Counter Ions, Membranes, Binding Partners, Osmolytes, and Macromolecular Crowding. The Protein Journal , 28, 305-325. https://doi.org/10.1007/s10930-009-9201-4
Uversky, V.N. (2011) Intrinsically Disordered Proteins from a to Z. The International Journal of Biochemistry & Cell Biology , 43, 1090-1103. https://doi.org/10.1016/j.biocel.2011.04.001
Uversky, V.N., Li, J. and Fink, A.L. (2001) Evidence for a Partially Folded Intermediate in α -Synuclein Fibril Formation. Journal of Biological Chemistry , 276, 10737-10744. https://doi.org/10.1074/jbc.m010907200
Ruff, K.M., Roberts, S., Chilkoti, A. and Pappu, R.V. (2018) Advances in Understanding Stimulus-Responsive Phase Behavior of Intrinsically Disordered Protein Polymers. Journal of Molecular Biology , 430, 4619-4635. https://doi.org/10.1016/j.jmb.2018.06.031
Fonin, A.V., Darling, A.L., Kuznetsova, I.M., Turoverov, K.K. and Uversky, V.N. (2018) Intrinsically Disordered Proteins in Crowded Milieu: When Chaos Prevails within the Cellular Gumbo. Cellular and Molecular Life Sciences , 75, 3907-3929. https://doi.org/10.1007/s00018-018-2894-9
Turoverov, K.K., Kuznetsova, I.M. and Uversky, V.N. (2010) The Protein Kingdom Extended: Ordered and Intrinsically Disordered Proteins, Their Folding, Supramolecular Complex Formation, and Aggregation. Progress in Biophysics and Molecular Biology , 102, 73-84. https://doi.org/10.1016/j.pbiomolbio.2010.01.003
Dogan, J., Gianni, S. and Jemth, P. (2014) The Binding Mechanisms of Intrinsically Disordered Proteins. Physical Chemistry Chemical Physics , 16, 6323-6331. https://doi.org/10.1039/c3cp54226b
Wright, P.E. and Dyson, H.J. (2014) Intrinsically Disordered Proteins in Cellular Signalling and Regulation. Nature Reviews Molecular Cell Biology , 16, 18-29. https://doi.org/10.1038/nrm3920
Fisher, C.K. and Stultz, C.M. (2011) Constructing Ensembles for Intrinsically Disordered Proteins. Current Opinion in Structural Biology , 21, 426-431. https://doi.org/10.1016/j.sbi.2011.04.001
Uversky, V.N. (2013) Unusual Biophysics of Intrinsically Disordered Proteins. Biochimica et Biophysica Acta (BBA) — Proteins and Proteomics , 1834, 932-951. https://doi.org/10.1016/j.bbapap.2012.12.008
van der Lee, R., Buljan, M., Lang, B., Weatheritt, R.J., Daughdrill, G.W., Dunker, A.K., et al . (2014) Classification of Intrinsically Disordered Regions and Proteins. Chemical Reviews , 114, 6589-6631. https://doi.org/10.1021/cr400525m
Darling, A.L. and Uversky, V.N. (2018) Intrinsic Disorder and Posttranslational Modifications: The Darker Side of the Biological Dark Matter. Frontiers in Genetics , 9, Article No. 158. https://doi.org/10.3389/fgene.2018.00158
Mann, M. and Jensen, O.N. (2003) Proteomic Analysis of Post-Translational Modifications. Nature Biotechnology , 21, 255-261. https://doi.org/10.1038/nbt0303-255
Youle, R.J. and Strasser, A. (2008) The BCL-2 Protein Family: Opposing Activities That Mediate Cell Death. Nature Reviews Molecular Cell Biology , 9, 47-59. https://doi.org/10.1038/nrm2308
Jungblut, P.R., Holzhütter, H.G., Apweiler, R. and Schlüter, H. (2008) The Speciation of the Proteome. Chemistry Central Journal , 2, 1-10. https://doi.org/10.1186/1752-153x-2-16
Kulkarni, P., Jolly, M.K., Jia, D., Mooney, S.M., Bhargava, A., Kagohara, L.T., et al . (2017) Phosphorylation-Induced Conformational Dynamics in an Intrinsically Disordered Protein and Potential Role in Phenotypic Heterogeneity. Proceedings of the National Academy of Sciences , 114, E2644-E2653. https://doi.org/10.1073/pnas.1700082114
Saito, M., Hess, D., Eglinger, J., Fritsch, A.W., Kreysing, M., Weinert, B.T., et al . (2018) Acetylation of Intrinsically Disordered Regions Regulates Phase Separation. Nature Chemical Biology , 15, 51-61. https://doi.org/10.1038/s41589-018-0180-7
Rahman, M.M., Zamakhaeva, S., Rush, J.S., Chaton, C.T., Kenner, C.W., Hla, Y.M., et al . (2025) Glycosylation of Serine/Threonine-Rich Intrinsically Disordered Regions of Membrane-Associated Proteins in Streptococci. Nature Communications , 16, Article No. 4011. https://doi.org/10.1038/s41467-025-58692-8
Zhang, Z., Ji, J., Hossain, M.S., Bailey, B., Nangia, S. and Mozhdehi, D. (2024) Lipidation Alters the Phase-Separation of Resilin-Like Polypeptides. Soft Matter , 20, 4007-4014. https://doi.org/10.1039/d4sm00358f
Bauer, V., Schmidtgall, B., Gógl, G., Dolenc, J., Osz, J., Nominé, Y., et al . (2021) Conformational Editing of Intrinsically Disordered Protein by α -Methylation. Chemical Science , 12, 1080-1089. https://doi.org/10.1039/d0sc04482b
Uversky, V.N., Yamin, G., Munishkina, L.A., Karymov, M.A., Millett, I.S., Doniach, S., et al . (2005) Effects of Nitration on the Structure and Aggregation of α -Synuclein. Molecular Brain Research , 134, 84-102. https://doi.org/10.1016/j.molbrainres.2004.11.014
Geist, L., Henen, M.A., Haiderer, S., Schwarz, T.C., Kurzbach, D., Zawadzka-Kazimierczuk, A., et al . (2013) Protonation-Dependent Conformational Variability of Intrinsically Disordered Proteins. Protein Science , 22, 1196-1205. https://doi.org/10.1002/pro.2304
Feng, J., She, Y., Li, C. and Shen, L. (2023) Metal Ion Mediated Aggregation of Alzheimer’s Disease Peptides and Proteins in Solutions and at Surfaces. Advances in Colloid and Interface Science , 320, Article ID: 103009. https://doi.org/10.1016/j.cis.2023.103009
Wise-Scira, O., Dunn, A., Aloglu, A.K., Sakallioglu, I.T. and Coskuner, O. (2013) Structures of the E46K Mutant-Type α -Synuclein Protein and Impact of E46K Mutation on the Structures of the Wild-Type α -Synuclein Protein. ACS Chemical Neuroscience , 4, 498-508. https://doi.org/10.1021/cn3002027
Levine, Z.A., Larini, L., LaPointe, N.E., Feinstein, S.C. and Shea, J. (2015) Regulation and Aggregation of Intrinsically Disordered Peptides. Proceedings of the National Academy of Sciences , 112, 2758-2763. https://doi.org/10.1073/pnas.1418155112
Kjaergaard, M., Nørholm, A., Hendus‒Altenburger, R., Pedersen, S.F., Poulsen, F.M. and Kragelund, B.B. (2010) Temperature-Dependent Structural Changes in Intrinsically Disordered Proteins: Formation of α -Helices or Loss of Polyproline II? Protein Science , 19, 1555-1564. https://doi.org/10.1002/pro.435
Vidović, M. and Komić Milić, S. (2021) Regulation of Proteolysis of Intrinsically Disordered Proteins: Physiological Consequences. A Closer Look at Proteolysis. 1-46.
Uversky, V.N., Oldfield, C.J. and Dunker, A.K. (2008) Intrinsically Disordered Proteins in Human Diseases: Introducing the D 2 Concept. Annual Review of Biophysics , 37, 215-246. https://doi.org/10.1146/annurev.biophys.37.032807.125924
Tanaka, M., Morita, S. and Hayashi, T. (2021) Role of Interfacial Water in Determining the Interactions of Proteins and Cells with Hydrated Materials. Colloids and Surfaces B : Biointerfaces , 198, Article ID: 111449. https://doi.org/10.1016/j.colsurfb.2020.111449
Seneff, S. and Kyriakopoulos, A.M. (2025) Taurine Prevents Mitochondrial Dysfunction and Protects Mitochondria from Reactive Oxygen Species and Deuterium Toxicity. Amino Acids , 57, Article No. 6. https://doi.org/10.1007/s00726-024-03440-3
Figueroa, X.A. and Pollack, G.H. (2011) Exclusion-Zone Formation from Discontinuous Nafion Surfaces. International Journal of Design & Nature and Ecodynamics , 6, 286-296. https://doi.org/10.2495/dne-v6-n4-286-296
Elton, D.C., Spencer, P.D., Riches, J.D. and Williams, E.D. (2020) Exclusion Zone Phenomena in Water—A Critical Review of Experimental Findings and Theories. International Journal of Molecular Sciences , 21, Article No. 5041. https://doi.org/10.3390/ijms21145041
Lin, L., Jiang, W., Xu, X. and Xu, P. (2020) A Critical Review of the Application of Electromagnetic Fields for Scaling Control in Water Systems: Mechanisms, Characterization, and Operation. NPJ Clean Water , 3, Article No. 25. https://doi.org/10.1038/s41545-020-0071-9
Chai, B., Mahtani, A.G. and Pollack, G.H. (2012) Unexpected Presence of Solute-Free Zones at Metal-Water Interfaces. Contemporary Materials , 3, 1-12. https://doi.org/10.7251/com1201001c
Chai, B., Yoo, H. and Pollack, G.H. (2009) Effect of Radiant Energy on Near-Surface Water. The Journal of Physical Chemistry B , 113, 13953-13958. https://doi.org/10.1021/jp908163w
Rad, I., Stahlberg, R., Kung, K. and Pollack, G.H. (2021) Low Frequency Weak Electric Fields Can Induce Structural Changes in Water. PLOS ONE , 16, e0260967. https://doi.org/10.1371/journal.pone.0260967
Del Giudice, E., Preparata, G. and Vitiello, G. (1988) Water as a Free Electric Dipole Laser. Physical Review Letters , 61, 1085-1088. https://doi.org/10.1103/physrevlett.61.1085
De Ninno, A., Del Giudice, E., Gamberale, L. and Castellano, A.C. (2013) The Structure of Liquid Water Emerging from the Vibrational Spectroscopy: Interpretation with QED Theory.
Pollack, G.H. (2019) The Fourth Phase of Water. Tantor Audio.
Taschin, A., Bartolini, P., Eramo, R., Righini, R. and Torre, R. (2013) Evidence of Two Distinct Local Structures of Water from Ambient to Supercooled Conditions. Nature Communications , 4, Article No. 2401. https://doi.org/10.1038/ncomms3401
Geesink, H.J., Jerman, I. and Meijer, D.K. (2020) Water, the Cradle of Life via Its Coherent Quantum Frequencies. Water , 11, 78-108.
Ho, M. (2015) Illuminating Water and Life: Emilio Del Giudice. Electromagnetic Biology and Medicine , 34, 113-122. https://doi.org/10.3109/15368378.2015.1036079
Otting, G., Liepinsh, E. and Wüthrich, K. (1991) Protein Hydration in Aqueous Solution. Science , 254, 974-980. https://doi.org/10.1126/science.1948083
Moilanen, D.E., Piletic, I.R. and Fayer, M.D. (2007) Water Dynamics in Nafion Fuel Cell Membranes: The Effects of Confinement and Structural Changes on the Hydrogen Bond Network. The Journal of Physical Chemistry C , 111, 8884-8891. https://doi.org/10.1021/jp067460k
Mentré, P. (2004) Interfacial Water: A Modulator of Biological Activity. Journal of Biological Physics and Chemistry , 4, 115-123. https://doi.org/10.4024/10me04r.jbpc.04.02
Arunan, E., Desiraju, G.R., Klein, R.A., Sadlej, J., Scheiner, S., Alkorta, I., et al . (2011) Defining the Hydrogen Bond: An Account (IUPAC Technical Report). Pure and Applied Chemistry , 83, 1619-1636. https://doi.org/10.1351/pac-rep-10-01-01
Ball, P. (2007) Water as an Active Constituent in Cell Biology. Chemical Reviews , 108, 74-108. https://doi.org/10.1021/cr068037a
Pal, S.K. and Zewail, A.H. (2004) Dynamics of Water in Biological Recognition. Chemical Reviews , 104, 2099-2124. https://doi.org/10.1021/cr020689l
Nguyen, T.H., Zhang, C., Weichselbaum, E., Knyazev, D.G., Pohl, P. and Carloni, P. (2018) Interfacial Water Molecules at Biological Membranes: Structural Features and Role for Lateral Proton Diffusion. PLOS ONE , 13, e0193454. https://doi.org/10.1371/journal.pone.0193454
Bothma, J.P., Gilmore, J.B. and McKenzie, R.H. (2010) The Role of Quantum Effects in Proton Transfer Reactions in Enzymes: Quantum Tunneling in a Noisy Environment? New Journal of Physics , 12, Article ID: 055002. https://doi.org/10.1088/1367-2630/12/5/055002
Meng, X., Guo, J., Peng, J., Chen, J., Wang, Z., Shi, J., et al . (2015) Direct Visualization of Concerted Proton Tunnelling in a Water Nanocluster. Nature Physics , 11, 235-239. https://doi.org/10.1038/nphys3225
Allemann, R.K. and Scrutton, N.S. (2009) Quantum Tunnelling in Enzyme-Catalysed Reactions. Royal Society of Chemistry.
del Giudice, E., Doglia, S., Milani, M. and Vitiello, G. (1986) Electromagnetic Field and Spontaneous Symmetry Breaking in Biological Matter. Nuclear Physics B , 275, 185-199. https://doi.org/10.1016/0550-3213(86)90595-x
Fichou, Y., Schirò, G., Gallat, F., Laguri, C., Moulin, M., Combet, J., et al . (2015) Hydration Water Mobility Is Enhanced around Tau Amyloid Fibers. Proceedings of the National Academy of Sciences , 112, 6365-6370. https://doi.org/10.1073/pnas.1422824112
Camino, J.D., Gracia, P. and Cremades, N. (2021) The Role of Water in the Primary Nucleation of Protein Amyloid Aggregation. Biophysical Chemistry , 269, Article ID: 106520. https://doi.org/10.1016/j.bpc.2020.106520
Bellissent-Funel, M., Hassanali, A., Havenith, M., Henchman, R., Pohl, P., Sterpone, F., et al . (2016) Water Determines the Structure and Dynamics of Proteins. Chemical Reviews , 116, 7673-7697. https://doi.org/10.1021/acs.chemrev.5b00664
Elgabarty, H., Kaliannan, N.K. and Kühne, T.D. (2019) Enhancement of the Local Asymmetry in the Hydrogen Bond Network of Liquid Water by an Ultrafast Electric Field Pulse. Scientific Reports , 9, Article No. 10002. https://doi.org/10.1038/s41598-019-46449-5
Zhao, H., Tan, Y., Zhang, L., Zhang, R., Shalaby, M., Zhang, C., et al . (2020) Ultrafast Hydrogen Bond Dynamics of Liquid Water Revealed by Terahertz-Induced Transient Birefringence. Light : Science & Applications , 9, 1-10. https://doi.org/10.1038/s41377-020-00370-z
Faupin, J., Fröhlich, J. and Schubnel, B. (2015) On the Probabilistic Nature of Quantum Mechanics and the Notion of Closed Systems. Annales Henri Poincaré , 17, 689-731. https://doi.org/10.1007/s00023-015-0416-y
Day, T.J.F., Schmitt, U.W. and Voth, G.A. (2000) The Mechanism of Hydrated Proton Transport in Water. Journal of the American Chemical Society , 122, 12027-12028. https://doi.org/10.1021/ja002506n
Siwick, B.J. and Bakker, H.J. (2007) On the Role of Water in Intermolecular Proton-Transfer Reactions. Journal of the American Chemical Society , 129, 13412-13420. https://doi.org/10.1021/ja069265p
Odutola, J.A., Hu, T.A., Prinslow, D., O’dell, S.E. and Dyke, T.R. (1988) Water Dimer Tunneling States with k = 0. The Journal of Chemical Physics , 88, 5352-5361. https://doi.org/10.1063/1.454595
Rao, M.L., Sedlmayr, S.R., Roy, R. and Kanzius, J. (2010) Polarized Microwave and RF Radiation Effects on the Structure and Stability of Liquid Water. Current Science , 98, 1500-1504.
Vallée, P., Lafait, J., Legrand, L., Mentré, P., Monod, M. and Thomas, Y. (2005) Effects of Pulsed Low-Frequency Electromagnetic Fields on Water Characterized by Light Scattering Techniques: Role of Bubbles. Langmuir , 21, 2293-2299. https://doi.org/10.1021/la047916u
Calabrò, E. and Magazù, S. (2017) Response of Hydrogen Bonding to Low-Intensity 50 Hz Electromagnetic Field in Typical Proteins in Bi-Distilled Water Solution. Spectroscopy Letters , 50, 330-335. https://doi.org/10.1080/00387010.2017.1328444
James, D. and Armishaw, R. (1975) Structure of Aqueous Solutions: Infrared Spectra of the Water Librational Mode in Solutions of Monovalent Halides. Australian Journal of Chemistry , 28, 1179-1186. https://doi.org/10.1071/ch9751179
English, N.J. and MacElroy, J.M.D. (2003) Molecular Dynamics Simulations of Microwave Heating of Water. The Journal of Chemical Physics , 118, 1589-1592. https://doi.org/10.1063/1.1538595
Panagopoulos, D.J., Messini, N., Karabarbounis, A., Philippetis, A.L. and Margaritis, L.H. (2000) A Mechanism for Action of Oscillating Electric Fields on Cells. Biochemical and Biophysical Research Communications , 272, 634-640. https://doi.org/10.1006/bbrc.2000.2746
Panagopoulos, D.J., Johansson, O. and Carlo, G.L. (2015) Polarization: A Key Difference between Man-Made and Natural Electromagnetic Fields, in Regard to Biological Activity. Scientific Reports , 5, Article No. 14914. https://doi.org/10.1038/srep14914
Philbin, T.G. (2012) Quantum Dynamics of the Damped Harmonic Oscillator. New Journal of Physics , 14, Article ID: 083043. https://doi.org/10.1088/1367-2630/14/8/083043
Pikovsky, A., Rosenblum, M. and Kurths, J. (2001) Synchronization: A Unified Approach to Nonlinear Science. Cambridge University Press. https://doi.org/10.1017/cbo9780511755743
Samdal, S. (1994) The Effect of Large Amplitude Motion on the Comparison of Bond Distances from Ab Initio Calculations and Experimentally Determined Bond Distances, and on Root-Mean-Square Amplitudes of Vibration, Shrinkage, Asymmetry Constants, Symmetry Constraints, and Inclusion of Rotational Constants Using the Electron Diffraction Method. Journal of Molecular Structure , 318, 133-141. https://doi.org/10.1016/0022-2860(93)07897-6
Kirillova, S. and Carugo, O. (2011) Hydration Sites of Unpaired RNA Bases: A Statistical Analysis of the PDB Structures. BMC Structural Biology , 11, Article No. 41. https://doi.org/10.1186/1472-6807-11-41
Grifoni, M. and Hänggi, P. (1998) Driven Quantum Tunneling. Physics Reports , 304, 229-354. https://doi.org/10.1016/s0370-1573(98)00022-2
Shi, S., Zhang, Q., Zhang, L., Wang, R., Zhu, Z., Jiang, G., et al . (2011) Geometrical Structures, Vibrational Frequencies, Force Constants and Dissociation Energies of Isotopic Water Molecules (H 2 O, HDO, D 2 O, HTO, DTO, and T 2 O) under Dipole Electric Field. Chinese Physics B , 20, Article ID: 063102. https://doi.org/10.1088/1674-1056/20/6/063102
Baranyai, A., Bartók, A. and Chialvo, A.A. (2005) Computer Simulation of the 13 Crystalline Phases of Ice. The Journal of Chemical Physics , 123, Article ID: 054502. https://doi.org/10.1063/1.1989313
Laage, D. and Hynes, J.T. (2006) A Molecular Jump Mechanism of Water Reorientation. Science , 311, 832-835. https://doi.org/10.1126/science.1122154
Marx, D., Tuckerman, M.E., Hutter, J. and Parrinello, M. (1999) The Nature of the Hydrated Excess Proton in Water. Nature , 397, 601-604. https://doi.org/10.1038/17579
Bagchi, B. (2005) Water Dynamics in the Hydration Layer around Proteins and Micelles. Chemical Reviews , 105, 3197-3219. https://doi.org/10.1021/cr020661+
Schönichen, A., Webb, B.A., Jacobson, M.P. and Barber, D.L. (2013) Considering Protonation as a Posttranslational Modification Regulating Protein Structure and Function. Annual Review of Biophysics , 42, 289-314. https://doi.org/10.1146/annurev-biophys-050511-102349
Fossat, M.J. (2025) MEDOC: A Fast, Scalable, and Mathematically Exact Algorithm for the Site-Specific Prediction of the Protonation Degree in Large Disordered Proteins. Journal of Chemical Information and Modeling , 65, 873-881. https://doi.org/10.1021/acs.jcim.4c01860
Pelton, J.G., Torchia, D.A., Meadow, N.D. and Roseman, S. (1993) Tautomeric States of the Active-Site Histidines of Phosphorylated and Unphosphorylated III glc , a Signal-Transducing Protein from Escherichia coli , Using Two-dimensional Heteronuclear NMR Techniques. Protein Science , 2, 543-558. https://doi.org/10.1002/pro.5560020406
Cerón-Carrasco, J.P. and Jacquemin, D. (2013) Electric-Field Induced Mutation of DNA: A Theoretical Investigation of the GC Base Pair. Physical Chemistry Chemical Physics , 15, 4548-4553. https://doi.org/10.1039/c2cp44066k
Cerón-Carrasco, J.P. and Jacquemin, D. (2013) Electric Field Induced DNA Damage: An Open Door for Selective Mutations. Chemical Communications , 49, 7578-7580. https://doi.org/10.1039/c3cc42593b
Cerón-Carrasco, J.P., Cerezo, J. and Jacquemin, D. (2014) How DNA Is Damaged by External Electric Fields: Selective Mutation vs. Random Degradation. Physical Chemistry Chemical Physics , 16, 8243-8246. https://doi.org/10.1039/c3cp54518k
Antonov, L. (2016) Tautomerism: Concepts and Applications in Science and Technology. John Wiley & Sons.
Singh, V., Fedeles, B.I. and Essigmann, J.M. (2014) Role of Tautomerism in RNA Biochemistry. RNA , 21, 1-13. https://doi.org/10.1261/rna.048371.114
Abou-Zied, O.K., Jimenez, R. and Romesberg, F.E. (2001) Tautomerization Dynamics of a Model Base Pair in DNA. Journal of the American Chemical Society , 123, 4613-4614. https://doi.org/10.1021/ja003647s
Peng, C.S., Jones, K.C. and Tokmakoff, A. (2011) Anharmonic Vibrational Modes of Nucleic Acid Bases Revealed by 2D IR Spectroscopy. Journal of the American Chemical Society , 133, 15650-15660. https://doi.org/10.1021/ja205636h
Aggarwal, L. and Biswas, P. (2018) Hydration Water Distribution around Intrinsically Disordered Proteins. The Journal of Physical Chemistry B , 122, 4206-4218. https://doi.org/10.1021/acs.jpcb.7b11091
Grubmüller, H., Heller, H., Windemuth, A. and Schulten, K. (1991) Generalized Verlet Algorithm for Efficient Molecular Dynamics Simulations with Long-Range Interactions. Molecular Simulation , 6, 121-142. https://doi.org/10.1080/08927029108022142
Maity, H., Baidya, L. and Reddy, G. (2022) Salt-Induced Transitions in the Conformational Ensembles of Intrinsically Disordered Proteins. The Journal of Physical Chemistry B , 126, 5959-5971. https://doi.org/10.1021/acs.jpcb.2c03476
Kulkarni, P., Bhattacharya, S., Achuthan, S., Behal, A., Jolly, M.K., Kotnala, S., et al . (2022) Intrinsically Disordered Proteins: Critical Components of the Wetware. Chemical Reviews , 122, 6614-6633. https://doi.org/10.1021/acs.chemrev.1c00848
Zhang, T., Faraggi, E., Li, Z. and Zhou, Y. (2013) Intrinsically Semi-Disordered State and Its Role in Induced Folding and Protein Aggregation. Cell Biochemistry and Biophysics , 67, 1193-1205. https://doi.org/10.1007/s12013-013-9638-0
Nandi, P.K., Futera, Z. and English, N.J. (2016) Perturbation of Hydration Layer in Solvated Proteins by External Electric and Electromagnetic Fields: Insights from Non-Equilibrium Molecular Dynamics. The Journal of Chemical Physics , 145, Article ID: 205101. https://doi.org/10.1063/1.4967774
Upadhyay, A. and Ekenna, C. (2023) A New Tool to Study the Binding Behavior of Intrinsically Disordered Proteins. International Journal of Molecular Sciences , 24, Article No. 11785. https://doi.org/10.3390/ijms241411785
Abyzov, A., Blackledge, M. and Zweckstetter, M. (2022) Conformational Dynamics of Intrinsically Disordered Proteins Regulate Biomolecular Condensate Chemistry. Chemical Reviews , 122, 6719-6748. https://doi.org/10.1021/acs.chemrev.1c00774
Kolesnikov, A.I., Reiter, G.F., Choudhury, N., Prisk, T.R., Mamontov, E., Podlesnyak, A., et al . (2016) Quantum Tunneling of Water in Beryl: A New State of the Water Molecule. Physical Review Letters , 116, Article ID: 167802. https://doi.org/10.1103/physrevlett.116.167802
Mao, A.H., Lyle, N. and Pappu, R.V. (2012) Describing Sequence-Ensemble Relationships for Intrinsically Disordered Proteins. Biochemical Journal , 449, 307-318. https://doi.org/10.1042/bj20121346
Mitrea, D.M. and Kriwacki, R.W. (2016) Phase Separation in Biology; Functional Organization of a Higher Order. Cell Communication and Signaling , 14, 1-20. https://doi.org/10.1186/s12964-015-0125-7
Kato, M., Han, T.W., Xie, S., Shi, K., Du, X., Wu, L.C., et al . (2012) Cell-Free Formation of RNA Granules: Low Complexity Sequence Domains Form Dynamic Fibers within Hydrogels. Cell , 149, 753-767. https://doi.org/10.1016/j.cell.2012.04.017
Dormann, D. and Lemke, E.A. (2024) Adding Intrinsically Disordered Proteins to Biological Ageing Clocks. Nature Cell Biology , 26, 851-858. https://doi.org/10.1038/s41556-024-01423-w
Manyilov, V.D., Ilyinsky, N.S., Nesterov, S.V., Saqr, B.M.G.A., Dayhoff, G.W., Zinovev, E.V., et al . (2023) Chaotic Aging: Intrinsically Disordered Proteins in Aging-Related Processes. Cellular and Molecular Life Sciences , 80, Article No. 269. https://doi.org/10.1007/s00018-023-04897-3
López-Otín, C., Blasco, M.A., Partridge, L., Serrano, M. and Kroemer, G. (2023) Hallmarks of Aging: An Expanding Universe. Cell , 186, 243-278. https://doi.org/10.1016/j.cell.2022.11.001
Martinelli, A.H.S., Lopes, F.C., John, E.B.O., Carlini, C.R. and Ligabue-Braun, R. (2019) Modulation of Disordered Proteins with a Focus on Neurodegenerative Diseases and Other Pathologies. International Journal of Molecular Sciences , 20, Article No. 1322. https://doi.org/10.3390/ijms20061322
Anbo, H., Sato, M., Okoshi, A. and Fukuchi, S. (2019) Functional Segments on Intrinsically Disordered Regions in Disease-Related Proteins. Biomolecules , 9, Article No. 88. https://doi.org/10.3390/biom9030088
Scholes, G.D., et al . (2017) Using Coherence to Enhance Function in Chemical and Biophysical Systems. Nature (London ), 543, 647-656. https://doi.org/10.1038/nature21425
Bennett, C.H. and DiVincenzo, D.P. (2000) Quantum Information and Computation. Nature , 404, 247-255. https://doi.org/10.1038/35005001
Cavanagh, J., Fairbrother, W.J., Palmer, A.G., Rance, M. and Skelton, N.J. (2007) Heteronuclear NMR Experiments. In: Cavanagh, J., Fairbrother, W.J., Palmer, A.G., Rance, M. and Skelton, N.J., Eds., Protein NMR Spectroscopy , Elsevier, 533-678. https://doi.org/10.1016/b978-012164491-8/50009-9
Kragelj, J., Ozenne, V., Blackledge, M. and Jensen, M.R. (2013) Conformational Propensities of Intrinsically Disordered Proteins from NMR Chemical Shifts. ChemPhysChem , 14, 3034-3045. https://doi.org/10.1002/cphc.201300387
Narth, C., Gillet, N., Cailliez, F., Lévy, B. and de la Lande, A. (2015) Electron Transfer, Decoherence, and Protein Dynamics: Insights from Atomistic Simulations. Accounts of Chemical Research , 48, 1090-1097. https://doi.org/10.1021/ar5002796
Tenenbaum, A. (2021) Kinetic Coherence Underlies the Dynamics of Disordered Proteins. RSC Advances , 11, 36242-36249. https://doi.org/10.1039/d1ra06823g
Rather, S.R., Scholes, G.D. and Chen, L.X. (2024) From Coherence to Function: Exploring the Connection in Chemical Systems. Accounts of Chemical Research , 57, 2620-2630. https://doi.org/10.1021/acs.accounts.4c00312
Binolfi, A., Theillet, F. and Selenko, P. (2012) Bacterial In-Cell NMR of Human Α-Synuclein: A Disordered Monomer by Nature? Biochemical Society Transactions , 40, 950-954. https://doi.org/10.1042/bst20120096
Usselman, R.J., Chavarriaga, C., Castello, P.R., Procopio, M., Ritz, T., Dratz, E.A., et al . (2016) The Quantum Biology of Reactive Oxygen Species Partitioning Impacts Cellular Bioenergetics. Scientific Reports , 6, Article No. 38543. https://doi.org/10.1038/srep38543
Pesce, F., Bremer, A., Tesei, G., Hopkins, J.B., Grace, C.R., Mittag, T., et al . (2024) Design of Intrinsically Disordered Protein Variants with Diverse Structural Properties. Science Advances , 10, eadm9926. https://doi.org/10.1126/sciadv.adm9926
Gehi, B.R., Gadhave, K., Uversky, V.N. and Giri, R. (2022) Intrinsic Disorder in Proteins Associated with Oxidative Stress-Induced JNK Signaling. Cellular and Molecular Life Sciences , 79, Article No. 202. https://doi.org/10.1007/s00018-022-04230-4
Leterrier, J. (2001) Water and the Cytoskeleton. Cellular and Molecular Bi ology ( Noisy - le - Grand , France ), 47, 901-923.
Westerheide, S.D. and Morimoto, R.I. (2005) Heat Shock Response Modulators as Therapeutic Tools for Diseases of Protein Conformation. Journal of Biological Chemistry , 280, 33097-33100. https://doi.org/10.1074/jbc.r500010200
Gomez-Pastor, R., Burchfiel, E.T. and Thiele, D.J. (2017) Regulation of Heat Shock Transcription Factors and Their Roles in Physiology and Disease. Nature Reviews Molecular Cell Biology , 19, 4-19. https://doi.org/10.1038/nrm.2017.73
Sengupta, U. and Kayed, R. (2022) Amyloid Β, Tau, and α -Synuclein Aggregates in the Pathogenesis, Prognosis, and Therapeutics for Neurodegenerative Diseases. Progress in Neurobiology , 214, Article ID: 102270. https://doi.org/10.1016/j.pneurobio.2022.102270
Firman, T. and Ghosh, K. (2017) Sequence Charge Decoration Dictates Coil-Globule Transition in Intrinsically Disordered Proteins. The Journal of Chemical Physics , 148, Article ID: 123305. https://doi.org/10.1063/1.5005821
Theillet, F., Binolfi, A., Frembgen-Kesner, T., Hingorani, K., Sarkar, M., Kyne, C., et al . (2014) Physicochemical Properties of Cells and Their Effects on Intrinsically Disordered Proteins (IDPs). Chemical Reviews , 114, 6661-6714. https://doi.org/10.1021/cr400695p
Gao, J. and Xu, D. (2012) Correlation between Posttranslational Modification and Intrinsic Disorder in Protein. Pacific Symposium on Biocomputing , 94-103. https://doi.org/10.1142/9789814366496_0010
Khoury, G.A., Baliban, R.C. and Floudas, C.A. (2011) Proteome-Wide Post-Translational Modification Statistics: Frequency Analysis and Curation of the Swiss-Prot Database. Scientific Reports , 1, Article No. 90. https://doi.org/10.1038/srep00090
Zhao, B., Katuwawala, A., Oldfield, C.J., Hu, G., Wu, Z., Uversky, V.N., et al . (2021) Intrinsic Disorder in Human RNA-Binding Proteins. Journal of Molecular Biology , 433, Article ID: 167229. https://doi.org/10.1016/j.jmb.2021.167229
Liu, A.Y., Minetti, C.A., Remeta, D.P., Breslauer, K.J. and Chen, K.Y. (2022) HSF1, Aging, and Neurodegeneration. In: Turksen, K., Ed., Cell Biology and Translational Medicine , Volume 18: Tissue Differentiation , Repair in Health and Disease , Springer, 23-49. https://doi.org/10.1007/5584_2022_733
Ren, Q., et al . (2025) The Molecular Mechanism of Temperature-Dependent Phase Separation of Heat Shock Factor 1. Nature Chemical Biology , 21, 831-842.
Shamovsky, I., Ivannikov, M., Kandel, E.S., Gershon, D. and Nudler, E. (2006) RNA-Mediated Response to Heat Shock in Mammalian Cells. Nature , 440, 556-560. https://doi.org/10.1038/nature04518
Zhang, H., Shao, S., Zeng, Y., Wang, X., Qin, Y., Ren, Q., et al . (2022) Reversible Phase Separation of HSF1 Is Required for an Acute Transcriptional Response during Heat Shock. Nature Cell Biology , 24, 340-352. https://doi.org/10.1038/s41556-022-00846-7
Anckar, J. and Sistonen, L. (2011) Regulation of HSF1 Function in the Heat Stress Response: Implications in Aging and Disease. Annual Review of Biochemistry , 80, 1089-1115. https://doi.org/10.1146/annurev-biochem-060809-095203
Huang, C., Wu, J., Xu, L., Wang, J., Chen, Z. and Yang, R. (2018) Regulation of HSF1 Protein Stabilization: An Updated Review. European Journal of Pharmacology , 822, 69-77. https://doi.org/10.1016/j.ejphar.2018.01.005
Westerheide, S.D., Anckar, J., Stevens, S.M., Sistonen, L. and Morimoto, R.I. (2009) Stress-Inducible Regulation of Heat Shock Factor 1 by the Deacetylase Sirt1. Science , 323, 1063-1066. https://doi.org/10.1126/science.1165946
Raynes, R., Brunquell, J. and Westerheide, S.D. (2013) Stress Inducibility of SIRT1 and Its Role in Cytoprotection and Cancer. Genes & Cancer , 4, 172-182. https://doi.org/10.1177/1947601913484497
Ma, X., Xu, L., Alberobello, A.T., Gavrilova, O., Bagattin, A., Skarulis, M., et al . (2015) Celastrol Protects against Obesity and Metabolic Dysfunction through Activation of a HSF1-PGC1 α Transcriptional Axis. Cell Metabolism , 22, 695-708. https://doi.org/10.1016/j.cmet.2015.08.005
Zelin, E. and Freeman, B.C. (2015) Lysine Deacetylases Regulate the Heat Shock Response Including the Age-Associated Impairment of Hsf1. Journal of Molecular Biology , 427, 1644-1654. https://doi.org/10.1016/j.jmb.2015.02.010
Dasdag, O., Adalier, N. and Dasdag, S. (2020) Electromagnetic Radiation and Alzheimer’s Disease. Biotechnology & Biotechnological Equipment , 34, 1087-1094. https://doi.org/10.1080/13102818.2020.1820378
Perez, F.P., Bandeira, J.P., Perez Chumbiauca, C.N., Lahiri, D.K., Morisaki, J. and Rizkalla, M. (2022) Multidimensional Insights into the Repeated Electromagnetic Field Stimulation and Biosystems Interaction in Aging and Age-Related Diseases. Journal of Biomedical Science , 29, 1-22. https://doi.org/10.1186/s12929-022-00825-y
International Commission on Non-Ionizing Radiation Protection (ICNIRP) (2020) Guidelines for Limiting Exposure to Electromagnetic Fields (100 kHz to 300 GHz). Health Physics , 118, 483-524.
Marchesi, N., Osera, C., Fassina, L., Amadio, M., Angeletti, F., Morini, M., et al . (2014) Autophagy Is Modulated in Human Neuroblastoma Cells through Direct Exposition to Low Frequency Electromagnetic Fields. Journal of Cellular Physiology , 229, 1776-1786. https://doi.org/10.1002/jcp.24631
Hirai, T., Taniura, H., Goto, Y., Ogura, M., Sng, J.C.G. and Yoneda, Y. (2006) Stimulation of Ubiquitin-Proteasome Pathway through the Expression of Amidohydrolase for N-Terminal Asparagine (ntan1) in Cultured Rat Hippocampal Neurons Exposed to Static Magnetism. Journal of Neurochemistry , 96, 1519-1530. https://doi.org/10.1111/j.1471-4159.2006.03655.x
Park, J., Kwon, J.H., Kim, N. and Song, K. (2017) Effects of 1950 MHz Radiofrequency Electromagnetic Fields on A β Processing in Human Neuroblastoma and Mouse Hippocampal Neuronal Cells. Journal of Radiation R esearch , 59, 18-26. https://doi.org/10.1093/jrr/rrx045
Jeong, Y., Kang, G., Kwon, J., Choi, H., Pack, J., Kim, N., et al . (2015) 1950 MHz Electromagnetic Fields Ameliorate A β Pathology in Alzheimer’s Disease Mice. Current Alzheimer Research , 12, 481-492. https://doi.org/10.2174/156720501205150526114448
Rao, R.R., Halper, J. and Kisaalita, W.S. (2002) Effects of 60 Hz Electromagnetic Field Exposure on APP695 Transcription Levels in Differentiating Human Neuroblastoma Cells. Bioelectrochemistry , 57, 9-15. https://doi.org/10.1016/s1567-5394(02)00004-x
Antonini, R.A., Benfante, R., Gotti, C., Moretti, M., Kuster, N., Schuderer, J., et al . (2006) Extremely Low-Frequency Electromagnetic Field (ELF-EMF) Does Not Affect the Expression of α 3, α 5 and α 7 Nicotinic Receptor Subunit Genes in SH-SY5Y Neuroblastoma Cell Line. Toxicology Letters , 164, 268-277. https://doi.org/10.1016/j.toxlet.2006.01.006
Del Giudice, E., Facchinetti, F., Nofrate, V., Boccaccio, P., Minelli, T., Dam, M., et al . (2007) Fifty Hertz Electromagnetic Field Exposure Stimulates Secretion of β -Amyloid Peptide in Cultured Human Neuroglioma. Neuroscience Letters , 418, 9-12. https://doi.org/10.1016/j.neulet.2007.02.057
He, G., Luo, Z., Shen, T., Li, P., Yang, J., Luo, X., et al . (2016) Inhibition of STAT3-and MAPK-Dependent PGE2 Synthesis Ameliorates Phagocytosis of Fibrillar β -Amyloid Peptide (1-42) via EP2 Receptor in EMF-Stimulated N9 Microglial Cells. Journal of Neuroinflammation , 13, Article No. 296. https://doi.org/10.1186/s12974-016-0762-9
Newton, T.M., Duce, J.A. and Bayle, E.D. (2019) The Proteostasis Network Provides Targets for Neurodegeneration. British Journal of Pharmacology , 176, 3508-3514. https://doi.org/10.1111/bph.14643
Kovács, D., Sigmond, T., Hotzi, B., Bohár, B., Fazekas, D., Deák, V., et al . (2019) HSF1Base: A Comprehensive Database of HSF1 (Heat Shock Factor 1) Target Genes. International Journal of Molecular Sciences , 20, Article No. 5815. https://doi.org/10.3390/ijms20225815
Perez, F.P., Zhou, X., Morisaki, J. and Jurivich, D. (2008) Electromagnetic Field Therapy Delays Cellular Senescence and Death by Enhancement of the Heat Shock Response. Experimental Gerontology , 43, 307-316. https://doi.org/10.1016/j.exger.2008.01.004
Manai, F., et al . (2014) A Low-Frequency Electromagnetic (LF-EMF) Exposure Scheme Induces Autophagy Activation to Counteract in Vitro A β -Amyloid Neurotoxicity. Atti del, 7.
Trivedi, R., Knopf, B., Rakoczy, S., Manocha, G.D., Brown-Borg, H. and Jurivich, D.A. (2023) Disrupted HSF1 Regulation in Normal and Exceptional Brain Aging. Biogerontology , 25, 147-160. https://doi.org/10.1007/s10522-023-10063-w
Watanabe, Y., Taguchi, K. and Tanaka, M. (2023) Roles of Stress Response in Autophagy Processes and Aging-Related Diseases. International Journal of Molecular Sciences , 24, Article No. 13804. https://doi.org/10.3390/ijms241813804
Perez, P., Moinuddin, F.S., ul ain Shamim, S., Joseph, Q.J., Morisaki, D.J. and Zhou, X. (2012) Longevity Pathways: HSF1 and Foxo Pathways, a New Therapeutic Target to Prevent Age-Related Diseases. Current Aging Science , 5, 87-95. https://doi.org/10.2174/1874609811205020087
Perez, F.P., Zhou, X., Morisaki, J., Ilie, J., James, T. and Jurivich, D.A. (2008) Engineered Repeated Electromagnetic Field Shock Therapy for Cellular Senescence and Age-Related Diseases. Rejuvenation Research , 11, 1049-1058. https://doi.org/10.1089/rej.2008.0793
Chou, C.K., Bassen, H., Osepchuk, J., Balzano, Q., Petersen, R., Meltz, M., et al . (1996) Radio Frequency Electromagnetic Exposure: Tutorial Review on Experimental Dosimetry. Bioelectromagnetics , 17, 195-208. https://doi.org/10.1002/(sici)1521-186x(1996)17:3<195::aid-bem5>3.0.co;2-z
Baldi, E. and Bucherelli, C. (2005) The Inverted “u-Shaped” Dose-Effect Relationships in Learning and Memory: Modulation of Arousal and Consolidation. Nonlinearity in Biology , Toxicology , Medicine , 3, 9-21. https://doi.org/10.2201/nonlin.003.01.002
Ahmad, R.H.M.A., Fakhoury, M. and Lawand, N. (2021) Electromagnetic Field in Alzheimer’s Disease: A Literature Review of Recent Preclinical and Clinical Studies. Current Alzheimer Research , 17, 1001-1012. https://doi.org/10.2174/1567205017666201130085853
Shirbandi, K., et al . (2023) Exposure to Low Levels of Radiofrequency Electromagnetic Fields Emitted from Cell-Phones as a Promising Treatment of Alzheimer’s Disease: A Scoping Review Study. Journal of Biomedical Physics & Engineering , 13, 3.
BioInitiative (2012) A Rationale for Biologically-Based Exposure Standards for Low-Intensity Electromagnetic Radiation. 2022 Updated Research Summaries.
Perez, F.P., Maloney, B., Chopra, N., Morisaki, J.J. and Lahiri, D.K. (2021) Repeated Electromagnetic Field Stimulation Lowers Amyloid- β Peptide Levels in Primary Human Mixed Brain Tissue Cultures. Scientific Reports , 11, Article No. 621. https://doi.org/10.1038/s41598-020-77808-2
Tsoy, A., Saliev, T., Abzhanova, E., Turgambayeva, A., Kaiyrlykyzy, A., Akishev, M., et al . (2019) The Effects of Mobile Phone Radiofrequency Electromagnetic Fields on β -Amyloid-Induced Oxidative Stress in Human and Rat Primary Astrocytes. Neuroscience , 408, 46-57. https://doi.org/10.1016/j.neuroscience.2019.03.058
Wang, C., Zhu, X., Chen, R., Zhang, X. and Lian, N. (2023) Upregulation of UBR1 m6A Methylation by METTL14 Inhibits Autophagy in Spinal Cord Injury. eneuro , 10, ENEURO.0338-22.2023. https://doi.org/10.1523/eneuro.0338-22.2023
Osera, C., Amadio, M., Falone, S., Fassina, L., Magenes, G., Amicarelli, F., et al . (2015) Pre-Exposure of Neuroblastoma Cell Line to Pulsed Electromagnetic Field Prevents H 2 O 2 -Induced ROS Production by Increasing MnSOD Activity. Bioelectromagnetics , 36, 219-232. https://doi.org/10.1002/bem.21900
Osera, C., Fassina, L., Amadio, M., Venturini, L., Buoso, E., Magenes, G., et al . (2011) Cytoprotective Response Induced by Electromagnetic Stimulation on SH-SY5Y Human Neuroblastoma Cell Line. Tissue Engineering Part A , 17, 2573-2582. https://doi.org/10.1089/ten.tea.2011.0071
Leszczynski, D., Joenväärä, S., Reivinen, J. and Kuokka, R. (2002) Non-Thermal Activation of the hsp27/p38MAPK Stress Pathway by Mobile Phone Radiation in Human Endothelial Cells: Molecular Mechanism for Cancer-and Blood-Brain Barrier-Related Effects. Differentiation , 70, 120-129. https://doi.org/10.1046/j.1432-0436.2002.700207.x
Arendash, G.W., Mori, T., Dorsey, M., Gonzalez, R., Tajiri, N. and Borlongan, C. (2012) Electromagnetic Treatment to Old Alzheimer’s Mice Reverses β -Amyloid Deposition, Modifies Cerebral Blood Flow, and Provides Selected Cognitive Benefit. PLOS ONE , 7, e35751. https://doi.org/10.1371/journal.pone.0035751
Arendash, G.W. (2012) Transcranial Electromagnetic Treatment against Alzheimer’s Disease: Why It Has the Potential to Trump Alzheimer’s Disease Drug Development. Journal of Alzheimer ’ s Disease , 32, 243-266. https://doi.org/10.3233/jad-2012-120943
Dragicevic, N., Bradshaw, P.C., Mamcarz, M., Lin, X., Wang, L., Cao, C., et al . (2011) Long-Term Electromagnetic Field Treatment Enhances Brain Mitochondrial Function of Both Alzheimer’s Transgenic Mice and Normal Mice: A Mechanism for Electromagnetic Field-Induced Cognitive Benefit? Neuroscience , 185, 135-149. https://doi.org/10.1016/j.neuroscience.2011.04.012
Arendash, G.W., Sanchez-Ramos, J., Mori, T., Mamcarz, M., Lin, X., Runfeldt, M., et al . (2010) Electromagnetic Field Treatment Protects against and Reverses Cognitive Impairment in Alzheimer’s Disease Mice. Journal of Alzheimer ’ s Disease , 19, 191-210. https://doi.org/10.3233/jad-2010-1228
Jeong, H., Andersson, J., Hess, A. and Jezzard, P. (2023) Effect of Subject-Specific Head Morphometry on Specific Absorption Rate Estimates in Parallel-Transmit MRI at 7 T. Magnetic Resonance in Medicine , 89, 2376-2390. https://doi.org/10.1002/mrm.29589
Banaceur, S., Banasr, S., Sakly, M. and Abdelmelek, H. (2013) Whole Body Exposure to 2.4 GHz WIFI Signals: Effects on Cognitive Impairment in Adult Triple Transgenic Mouse Models of Alzheimer’s Disease (3xTg-AD). Behavioural Brain Research , 240, 197-201. https://doi.org/10.1016/j.bbr.2012.11.021
Jeong, Y.J., Son, Y., Choi, H., Kim, N., Lee, Y., Ko, Y., et al . (2020) Behavioral Changes and Gene Profile Alterations after Chronic 1,950-MHz Radiofrequency Exposure: An Observation in C57BL/6 Mice. Brain and Behavior , 10, e01815. https://doi.org/10.1002/brb3.1815
Kumlin, T., Iivonen, H., Miettinen, P., Juvonen, A., van Groen, T., Puranen, L., et al . (2007) Mobile Phone Radiation and the Developing Brain: Behavioral and Morphological Effects in Juvenile Rats. Radiation Research , 168, 471-479. https://doi.org/10.1667/rr1002.1
Wang, K., Lu, J., Xing, Z., Zhao, Q., Hu, L., Xue, L., et al . (2017) Effect of 1.8 GHz Radiofrequency Electromagnetic Radiation on Novel Object Associative Recognition Memory in Mice. Scientific Reports , 7, Article No. 44521. https://doi.org/10.1038/srep44521
Son, Y., Kim, J.S., Jeong, Y.J., Jeong, Y.K., Kwon, J.H., Choi, H., et al . (2018) Long-Term RF Exposure on Behavior and Cerebral Glucose Metabolism in 5xFAD Mice. Neuroscience Letters , 666, 64-69. https://doi.org/10.1016/j.neulet.2017.12.042
Hu, Y., Lai, J., Wan, B., Liu, X., Zhang, Y., Zhang, J., et al . (2016) Long-Term Exposure to ELF-MF Ameliorates Cognitive Deficits and Attenuates Tau Hyperphosphorylation in 3xTg AD Mice. NeuroToxicology , 53, 290-300. https://doi.org/10.1016/j.neuro.2016.02.012
Liu, X., Zuo, H., Wang, D., Peng, R., Song, T., Wang, S., et al . (2015) Improvement of Spatial Memory Disorder and Hippocampal Damage by Exposure to Electromagnetic Fields in an Alzheimer’s Disease Rat Model. PLOS ONE , 10, e0126963. https://doi.org/10.1371/journal.pone.0126963
Akbarnejad, Z., Esmaeilpour, K., Shabani, M., Asadi-Shekaari, M., Saeedi goraghani, M. and Ahmadi-Zeidabadi, M. (2017) Spatial Memory Recovery in Alzheimer’s Rat Model by Electromagnetic Field Exposure. International Journal of Neuroscience , 128, 691-696. https://doi.org/10.1080/00207454.2017.1411353
de Pomerai, D., Daniells, C., David, H., Allan, J., Duce, I., Mutwakil, M., et al . (2000) Non-Thermal Heat-Shock Response to Microwaves. Nature , 405, 417-418. https://doi.org/10.1038/35013144
Shallom, J.M., Di Carlo, A.L., Ko, D., Penafiel, L.M., Nakai, A. and Litovitz, T.A. (2002) Microwave Exposure Induces Hsp70 and Confers Protection against Hypoxia in Chick Embryos. Journal of Cellular Biochemistry , 86, 490-496. https://doi.org/10.1002/jcb.10243
Weisbrot, D., Lin, H., Ye, L., Blank, M. and Goodman, R. (2003) Effects of Mobile Phone Radiation on Reproduction and Development in drosophila Melanogaster . Journal of Cellular Biochemistry , 89, 48-55. https://doi.org/10.1002/jcb.10480
Arendash, G., Cao, C., Abulaban, H., Baranowski, R., Wisniewski, G., Becerra, L., et al . (2019) A Clinical Trial of Transcranial Electromagnetic Treatment in Alzheimer’s Disease: Cognitive Enhancement and Associated Changes in Cerebrospinal Fluid, Blood, and Brain Imaging. Journal of Alzheimer ’ s Disease , 71, 57-82. https://doi.org/10.3233/jad-190367
Arendash, G., Abulaban, H., Steen, S., Andel, R., Wang, Y., Bai, Y., et al . (2022) Transcranial Electromagnetic Treatment Stops Alzheimer’s Disease Cognitive Decline over a 2½-Year Period: A Pilot Study. Medicines , 9, Article No. 42. https://doi.org/10.3390/medicines9080042
Cao, C., Abulaban, H., Baranowski, R., Wang, Y., Bai, Y., Lin, X., et al . (2022) Transcranial Electromagnetic Treatment “Rebalances” Blood and Brain Cytokine Levels in Alzheimer’s Patients: A New Mechanism for Reversal of Their Cognitive Impairment. Frontiers in Aging Neuroscience , 14, Article ID: 829049. https://doi.org/10.3389/fnagi.2022.829049
Söderqvist, F., Hardell, L., Carlberg, M. and Mild, K.H. (2010) Radiofrequency Fields, Transthyretin, and Alzheimer’s Disease. Journal of Alzheimer ’ s Disease , 20, 599-606. https://doi.org/10.3233/jad-2010-1395
Sandyk, R. (1994) Alzheimer’s Disease: Improvement of Visual Memory and Visuoconstructive Performance by Treatment with Picotesla Range Magnetic Fields. International Journal of Neuroscience , 76, 185-225. https://doi.org/10.3109/00207459408986003
He, G.-L., Liu, Y., Li, M., Chen, C.-H., Gao, P., Yu, Z.-P. and Yang, X.-S. (2014) The Amelioration of Phagocytic Ability in Microglial Cells by Curcumin through the Inhibition of EMF-Induced Pro-Inflammatory Responses. Journal of Neuroinflammation , 11, Article No. 49. https://doi.org/10.1186/1742-2094-11-49
Barthélémy, A., Mouchard, A. and Villégier, A. (2016) Glial Markers and Emotional Memory in Rats Following Cerebral Radiofrequency Exposures. 2016 IEEE Radio and Antenna Days of the Indian Ocean ( RADIO ), Reunion, 10-13 October 2016, 1-2. https://doi.org/10.1109/radio.2016.7772023
Jiang, D., Li, J., Zhang, J., Xu, S., Kuang, F., Lang, H., et al . (2013) Electromagnetic Pulse Exposure Induces Overexpression of Beta Amyloid Protein in Rats. Archives of Medical Research , 44, 178-184. https://doi.org/10.1016/j.arcmed.2013.03.005
Akbarnejad, Z., Esmaeilpour, K., Shabani, M., Asadi-Shekaari, M., Saeedi Goraghani, M. and Ahmadi-Zeidabadi, M. (2018) Spatial Memory Recovery in Alzheimer’s Rat Model by Electromagnetic Field Exposure. International Journal of Neuroscience , 128, 691-696. https://doi.org/10.1080/00207454.2017.1411353
Qiao, S., Peng, R., Yan, H., Gao, Y., Wang, C., Wang, S., et al . (2014) Reduction of Phosphorylated Synapsin I (ser-553) Leads to Spatial Memory Impairment by Attenuating GABA Release after Microwave Exposure in Wistar Rats. PLOS ONE , 9, e95503. https://doi.org/10.1371/journal.pone.0095503
Prochnow, N., Gebing, T., Ladage, K., Krause-Finkeldey, D., El Ouardi, A., Bitz, A., et al . (2011) Electromagnetic Field Effect or Simply Stress? Effects of UMTS Exposure on Hippocampal Longterm Plasticity in the Context of Procedure Related Hormone Release. PLOS ONE , 6, e19437. https://doi.org/10.1371/journal.pone.0019437
Wang, H., Peng, R., Zhou, H., Wang, S., Gao, Y., Wang, L., et al . (2013) Impairment of Long-Term Potentiation Induction Is Essential for the Disruption of Spatial Memory after Microwave Exposure. International Journal of Radiation Biology , 89, 1100-1107. https://doi.org/10.3109/09553002.2013.817701
Wang, H., Peng, R., Zhao, L., Wang, S., Gao, Y., Wang, L., et al . (2015) The Relationship between NMDA Receptors and Microwave-Induced Learning and Memory Impairment: A Long-Term Observation on Wistar Rats. International Journal of Radiation Biology , 91, 262-269. https://doi.org/10.3109/09553002.2014.988893
Wang, H., Tan, S., Xu, X., Zhao, L., Zhang, J., Yao, B., et al . (2017) Long Term Impairment of Cognitive Functions and Alterations of NMDAR Subunits after Continuous Microwave Exposure. Physiology & Behavior , 181, 1-9. https://doi.org/10.1016/j.physbeh.2017.08.022
Foroozandeh, E., Naeini, M.S., Ahadi, H. and Foroozandeh, J. (2011) Effects of 90min Exposure to 8mT Electromagnetic Fields on Memory in Mice. Journal of American Science , 7, 58-61.
Yang, X., He, G., Hao, Y., Chen, C., Li, M., Wang, Y., et al . (2010) The Role of the JAK2-STAT3 Pathway in Pro-Inflammatory Responses of EMF-Stimulated N9 Microglial Cells. Journal of Neuroinflammation , 7, Article No. 54. https://doi.org/10.1186/1742-2094-7-54
Cleary, S.F., Cao, G., Liu, L., Egle, P.M. and Shelton, K.R. (1997) Stress Proteins Are Not Induced in Mammalian Cells Exposed to Radiofrequency or Microwave Radiation. Bioelectromagnetics , 18, 499-505. https://doi.org/10.1002/(sici)1521-186x(1997)18:7<499::aid-bem5>3.0.co;2-y
Regel, S.J., Tinguely, G., Schuderer, J., Adam, M., Kuster, N., Landolt, H., et al . (2007) Pulsed Radio-Frequency Electromagnetic Fields: Dose-Dependent Effects on Sleep, the Sleep EEG and Cognitive Performance. Journal of Sleep Research , 16, 253-258. https://doi.org/10.1111/j.1365-2869.2007.00603.x
Regel, S.J., Gottselig, J.M., Schuderer, J., Tinguely, G., Rétey, J.V., Kuster, N., et al . (2007) Pulsed Radio Frequency Radiation Affects Cognitive Performance and the Waking Electroencephalogram. NeuroReport , 18, 803-807. https://doi.org/10.1097/wnr.0b013e3280d9435e
Kim, J.H., Yu, D., Huh, Y.H., Lee, E.H., Kim, H. and Kim, H.R. (2017) Long-Term Exposure to 835 MHz RF-EMF Induces Hyperactivity, Autophagy and Demyelination in the Cortical Neurons of Mice. Scientific Reports , 7, Article No. 41129. https://doi.org/10.1038/srep41129
I.S. C95.1 (2019) Safety Levels with Respect to Human Exposure to Electric, Magnetic, and Electromagnetic Fields, 0 Hz to 300 GHz.
Lanni, I., Chiacchierini, G., Papagno, C., Santangelo, V. and Campolongo, P. (2024) Treating Alzheimer’s Disease with Brain Stimulation: From Preclinical Models to Non-Invasive Stimulation in Humans. Neuroscience & Biobehavioral Reviews , 165, Article ID: 105831. https://doi.org/10.1016/j.neubiorev.2024.105831
Ribeiro, F.M., Camargos, E.R.d.S., Souza, L.C.d. and Teixeira, A.L. (2013) Animal Models of Neurodegenerative Diseases. Revista Brasileira de Psiquiatria , 35, S82-S91. https://doi.org/10.1590/1516-4446-2013-1157
Guerriero, F., Botarelli, E., Mele, G., Polo, L., Zoncu, D., Renati, P., et al . (2015) An Innovative Intervention for the Treatment of Cognitive Impairment-Emisymmetric Bilateral Stimulation Improves Cognitive Functions in Alzheimer’s Disease and Mild Cognitive Impairment: An Open-Label Study. Neuropsychiatric Disease and Treatment , 11, 2391-2404. https://doi.org/10.2147/ndt.s90966
Son, Y., Park, H., Jeong, Y.J., Choi, H., Kim, N. and Lee, H. (2023) Long-Term Radiofrequency Electromagnetic Fields Exposure Attenuates Cognitive Dysfunction in 5×FAD Mice by Regulating Microglial Function. Neural Regeneration Research , 18, 2497-2503. https://doi.org/10.4103/1673-5374.371379
Zhi, W., Zou, Y., Ma, L., He, S., Guo, Z., Zhao, X., et al . (2023) 900 MHz Electromagnetic Field Exposure Relieved AD-Like Symptoms on APP/PS1 Mice: A Potential Non-Invasive Strategy for AD Treatment. Biochemical and Biophysical Research Communications , 658, 97-106. https://doi.org/10.1016/j.bbrc.2023.03.083
Komaki, A., Salehi, I., Keymoradzadeh, A., Taheri Azandaryani, M. and Golipoor, Z. (2021) Effect of Long-Term Exposure to Extremely Low-Frequency Electromagnetic Fields on β -Amyloid Deposition and Microglia Cells in an Alzheimer Model in Rats. Journal of Guilan University of Medical Sciences , 30, 218-229. https://doi.org/10.32598/jgums.30.3.1609.2
Zhang, S., et al . (2024) Effects of 2.4 GHz Radiofrequency Electromagnetic Field Exposure on Hippocampal Proteins in APP/PS1 Mice.
Teranishi, M., Ito, M., Huang, Z., Nishiyama, Y., Masuda, A., Mino, H., et al . (2024) Extremely Low-Frequency Electromagnetic Field (ELF-EMF) Increases Mitochondrial Electron Transport Chain Activities and Ameliorates Depressive Behaviors in Mice. International Journal of Molecular Sciences , 25, Article No. 11315. https://doi.org/10.3390/ijms252011315
Kim, J.H., Yu, D., Kim, H., Huh, Y.H., Cho, S., Lee, J., et al . (2017) Exposure to 835 MHz Radiofrequency Electromagnetic Field Induces Autophagy in Hippocampus but Not in Brain Stem of Mice. Toxicology and Industrial Health , 34, 23-35. https://doi.org/10.1177/0748233717740066
Guo, R.-W., et al . (2024) Rotating Magnetic Field Inhibits A β Protein Aggregation and Alleviates Cognitive Impairment in Alzheimer’s Disease Mice. Zoological Research , 45, 924.
Zhang, J., Chen, Y., Zhao, Y., Wang, P., Ding, H., Liu, C., et al . (2023) Terahertz Irradiation Improves Cognitive Impairments and Attenuates Alzheimer’s Neuropathology in the APPSWE/PS1DE9 Mouse: A Novel Therapeutic Intervention for Alzheimer’s Disease. Neuroscience Bulletin , 40, 857-871. https://doi.org/10.1007/s12264-023-01145-3
Moya-Gómez, A., Font, L.P., Burlacu, A., Alpizar, Y.A., Cardonne, M.M., Brône, B., et al . (2023) Extremely Low-Frequency Electromagnetic Stimulation (ELF-EMS) Improves Neurological Outcome and Reduces Microglial Reactivity in a Rodent Model of Global Transient Stroke. International Journal of Molecular Sciences , 24, Article No. 11117. https://doi.org/10.3390/ijms241311117
Abkhezr, H., Mohaddes, G., Nikniaz, Z., Abbasalizad Farhangi, M., Heydari, H. and Nikniaz, L. (2023) The Effect of Extremely Low Frequency Electromagnetic Field on Spatial Memory of Mice and Rats: A Systematic Review. Learning and Motivation , 81, Article ID: 101873. https://doi.org/10.1016/j.lmot.2023.101873
Eskandani, R. and Zibaii, M.I. (2023) Unveiling the Biological Effects of Radio-Frequency and Extremely-Low Frequency Electromagnetic Fields on the Central Nervous System Performance. BioImpacts , 14, Article No. 30064. https://doi.org/10.34172/bi.2023.30064
Perez, F.P., Morisaki, J., Kanakri, H. and Rizkalla, M. (2024) Electromagnetic Field Stimulation Therapy for Alzheimer’s Disease. Neurology ( Chic ), 3, 1020.
Jiang, D., Li, J., Zhang, J., Xu, S., Kuang, F., Lang, H., et al . (2016) Long-Term Electromagnetic Pulse Exposure Induces Abeta Deposition and Cognitive Dysfunction through Oxidative Stress and Overexpression of APP and BACE1. Brain Research , 1642, 10-19. https://doi.org/10.1016/j.brainres.2016.02.053
Zhang, Y., Liu, X., Zhang, J. and Li, N. (2014) Short-Term Effects of Extremely Low Frequency Electromagnetic Fields Exposure on Alzheimer’s Disease in Rats. International Journal of Radiation Biology , 91, 28-34. https://doi.org/10.3109/09553002.2014.954058
Bouji, M., Lecomte, A., Gamez, C., Blazy, K. and Villégier, A. (2019) Impact of Cerebral Radiofrequency Exposures on Oxidative Stress and Corticosterone in a Rat Model of Alzheimer’s Disease. Journal of Alzheimer ’ s Disease , 73, 467-476. https://doi.org/10.3233/jad-190593
Son, Y., Jeong, Y.J., Kwon, J.H., Choi, H., Pack, J., Kim, N., et al . (2016) 1950 MHz Radiofrequency Electromagnetic Fields Do Not Aggravate Memory Deficits in 5xFAD Mice. Bioelectromagnetics , 37, 391-399. https://doi.org/10.1002/bem.21992
Perez, F.P., Walker, B., Morisaki, J., Kanakri, H. and Rizkalla, M. (2025) Neurostimulation Devices to Treat Alzheimer’s Disease. Exploration of Neuroscience , 4, Article ID: 100674. https://doi.org/10.37349/en.2025.100674
Messori, C., Prinzera, S.V. and Di Bardone, F.B. (2019) The Super-Coherent State of Biological Water. Open Access Library Journal , 6, 1-5. https://doi.org/10.4236/oalib.1105236
Madl, P. and Renati, P. (2023) Quantum Electrodynamics Coherence and Hormesis: Foundations of Quantum Biology. International Journal of Molecular Sciences , 24, Article No. 14003. https://doi.org/10.3390/ijms241814003
Huang, Z., Ito, M., Zhang, S., Toda, T., Takeda, J., Ogi, T., et al . (2023) Extremely Low-Frequency Electromagnetic Field Induces Acetylation of Heat Shock Proteins and Enhances Protein Folding. Ecotoxicology and Environmental Safety , 264, Article ID: 115482. https://doi.org/10.1016/j.ecoenv.2023.115482
Morotomi-Yano, K., Oyadomari, S., Akiyama, H. and Yano, K. (2012) Nanosecond Pulsed Electric Fields Act as a Novel Cellular Stress That Induces Translational Suppression Accompanied by eIF2 α Phosphorylation and 4E-BP1 Dephosphorylation. Experimental Cell Research , 318, 1733-1744. https://doi.org/10.1016/j.yexcr.2012.04.016
Kim, K., Lee, Y.S., Kim, N., Choi, H. and Lim, K. (2022) 5G Electromagnetic Radiation Attenuates Skin Melanogenesis in Vitro by Suppressing ROS Generation. Antioxidants , 11, Article No. 1449. https://doi.org/10.3390/antiox11081449
Lang, B.J., Guerrero, M.E., Prince, T.L., Okusha, Y., Bonorino, C. and Calderwood, S.K. (2021) The Functions and Regulation of Heat Shock Proteins; Key Orchestrators of Proteostasis and the Heat Shock Response. Archives of Toxicology , 95, 1943-1970. https://doi.org/10.1007/s00204-021-03070-8
Usselman, R.J., Hill, I., Singel, D.J. and Martino, C.F. (2014) Spin Biochemistry Modulates Reactive Oxygen Species (ROS) Production by Radio Frequency Magnetic Fields. PLOS ONE , 9, e93065. https://doi.org/10.1371/journal.pone.0093065
Zeng, Y., Shen, Y., Hong, L., Chen, Y., Shi, X., Zeng, Q., et al . (2017) Effects of Single and Repeated Exposure to a 50-Hz 2-Mt Electromagnetic Field on Primary Cultured Hippocampal Neurons. Neuroscience Bulletin , 33, 299-306. https://doi.org/10.1007/s12264-017-0113-6
Benassi, B., Filomeni, G., Montagna, C., Merla, C., Lopresto, V., Pinto, R., et al . (2015) Extremely Low Frequency Magnetic Field (ELF-MF) Exposure Sensitizes SH-SY5Y Cells to the Pro-Parkinson’s Disease Toxin MPP+. Molecular Neurobiology , 53, 4247-4260. https://doi.org/10.1007/s12035-015-9354-4
Schuermann, D. and Mevissen, M. (2021) Manmade Electromagnetic Fields and Oxidative Stress—Biological Effects and Consequences for Health. International Journal of Molecular Sciences , 22, Article No. 3772. https://doi.org/10.3390/ijms22073772
Kang, K.A., Lee, H.C., et al . (2013) Effects of Combined Radiofrequency Radiation Exposure on Levels of Reactive Oxygen Species in Neuronal Cells. Journal of Radiation Research , 55, 265-276. https://doi.org/10.1093/jrr/rrt116
de Gannes, F.P., Haro, E., Hurtier, A., Taxile, M., Ruffié, G., Billaudel, B., et al . (2011) Effect of Exposure to the Edge Signal on Oxidative Stress in Brain Cell Models. Radiation Research , 175, 225-230. https://doi.org/10.1667/rr2320.1
Alejandro, M., Herlinda, B., Aparicio-Bautista, D.I., Siddhartha, M., Overduin, M. and Basurto-Islas, G. (2025) Molecular Mechanisms Associated with the Interaction of External Electromagnetic Fields in Protein Dynamics and Aggregation: A Focus on Amyloid- β Peptide. Progress in Biomedical Engineering , 7, Article ID: 032010. https://doi.org/10.1088/2516-1091/adea02
Saikia, J., Pandey, G., Sasidharan, S., Antony, F., Nemade, H.B., Kumar, S., et al . (2019) Electric Field Disruption of Amyloid Aggregation: Potential Noninvasive Therapy for Alzheimer’s Disease. ACS Chemical Neuroscience , 10, 2250-2262. https://doi.org/10.1021/acschemneuro.8b00490
Bhattacharjee, S., Choi, J., Park, S., Shim, K., Baek, C., Han, H., et al . (2025) In Vitro Treatment of Alzheimer’s Disease by Disintegrating Amyloid- β Using Electromagnetic Waves. IEEE Transactions on Antennas and Propagation , 73, 6788-6799. https://doi.org/10.1109/tap.2025.3568638
Muscat, S., Stojceski, F. and Danani, A. (2020) Elucidating the Effect of Static Electric Field on Amyloid Beta 1-42 Supramolecular Assembly. Journal of Molecular Graphics and Modelling , 96, Article ID: 107535. https://doi.org/10.1016/j.jmgm.2020.107535
Vargas-Rosales, P.A., D’Addio, A., Zhang, Y. and Caflisch, A. (2023) Disrupting Dimeric β -Amyloid by Electric Fields. ACS Physical Chemistry Au , 3, 456-466. https://doi.org/10.1021/acsphyschemau.3c00021
Salehi, N., Lohrasebi, A. and Bordbar, A.K. (2023) Preventing the Amyloid-Beta Peptides Accumulation on the Cell Membrane by Applying GHz Electric Fields: A Molecular Dynamic Simulation. Journal of Molecular Graphics and Modelling , 123, Article ID: 108516. https://doi.org/10.1016/j.jmgm.2023.108516
Allen, R.M., Scanlan, J.M. and Gama-Chonlon, L. (2023) Bilateral Rtms Shows No Advantage in Depression nor in Comorbid Depression and Anxiety: A Naturalistic Study. Psychiatric Quarterly , 95, 107-120. https://doi.org/10.1007/s11126-023-10062-7
Yang, Y., Hsieh, S., Chang, H., Sung, J., Chuu, C., Yen, C., et al . (2022) Gamma Frequency Inhibits the Secretion and Aggregation of Amyloid- β and Decreases the Phosphorylation of mTOR and Tau Proteins in Vitro . Journal of Alzheimer ’ s Disease , 90, 917-928. https://doi.org/10.3233/jad-220307
Lobyntseva, A., Ganaiem, M., Ivashko-Pachima, Y., Barnstable, C.J., Weisinger, B., Parabucki, A., et al . (2025) Extremely Low-Frequency and Low-Intensity Electromagnetic Field Technology (ELF-EMF) Sculpts Microtubules. European Journal of Neuroscience , 61, e70023. https://doi.org/10.1111/ejn.70023
Todorova, N., Bentvelzen, A. and Yarovsky, I. (2020) Electromagnetic Field Modulates Aggregation Propensity of Amyloid Peptides. The Journal of Chemical Physics , 152, Article ID: 035104. https://doi.org/10.1063/1.5126367
Toschi, F., Lugli, F., Biscarini, F. and Zerbetto, F. (2008) Effects of Electric Field Stress on a β -Amyloid Peptide. The Journal of Physical Chemistry B , 113, 369-376. https://doi.org/10.1021/jp807896g
Lin, J.C. (2012) Electromagnetic Fields in Biological Systems. Taylor & Francis.
Lambert, N., Chen, Y., Cheng, Y., Li, C., Chen, G. and Nori, F. (2012) Quantum Biology. Nature Physics , 9, 10-18. https://doi.org/10.1038/nphys2474
Marino, A.A. and Becker, R.O. (1977) Biological Effects of Extremely Low Frequency Electric and Magnetic Fields: A Review. Physiological Chemistry and Physics , 9, 131-147.
Semchenko, I.V., Mikhalka, I.S., Khakhomov, S.A., Samofalov, A.L. and Balmakou, A.P. (2022) DNA-Like Helices as Nanosized Polarizers of Electromagnetic Waves. Frontiers in Nanotechnology , 4, Article ID: 794213. https://doi.org/10.3389/fnano.2022.794213
Li, M., Liu, M. and Sha, Y. (2021) Induced and Inversed Circularly Polarized Luminescence of Achiral Thioflavin T Assembled on Peptide Fibril. Small , 18, Article ID: 2106130. https://doi.org/10.1002/smll.202106130
Zhang, Z., Fan, F., Shi, W., Zhang, T. and Chang, S. (2021) Terahertz Circular Polarization Sensing for Protein Denaturation Based on a Twisted Dual-Layer Metasurface. Biomedical Optics Express , 13, 209-221. https://doi.org/10.1364/boe.443473
Perez, F., Morisaki, J., Kanakri, H., Rizkalla, M. and Abdalla, A. (2025) A Novel Design of a Portable Birdcage via Meander Line Antenna (MLA) to Lower Beta Amyloid (a β ) in Alzheimer’s Disease. IEEE Journal of Translational Engineering in Health and Medicine , 13, 158-173. https://doi.org/10.1109/jtehm.2025.3559693
Wyszkowska, J., Jankowska, M. and Gas, P. (2019) Electromagnetic Fields and Neurodegenerative Diseases. Przegląd Elektrotechniczny , 95, 131-135. https://doi.org/10.15199/48.2019.01.33
Fymat, A.L. (2020) Electromagnetic Therapy for Neurological and Neurodegenerative Diseases: II. Deep Brain Stimulation. Open Access Journal of Neurology & Neurosurgery , 13, Article No. 555855. https://doi.org/10.19080/oajnn.2020.13.555855