Quantum coherence in ion channels: resonances, transport and verification

The Structure of the Potassium Channel: Molecular Basis of K + Conduction and Selectivity

Doyle, D., Morais-Cabral, J. H., Pfuetzner, R. A., Kuo, A., Gulbis, J. M., Cohen, S. L., Chait, B. T., & MacKinnon, R. (1998) · Science · doi:10.1126/science.280.5360.69 · Cited by 6,816 · see citing works

Evidence for wavelike energy transfer through quantum coherence in photosynthetic systems

Engel, G. S., Calhoun, T. R., Read, E. L., Ahn, T.-K., Mančal, T., Cheng, Y.-C., Blankenship, R. E., & Fleming, G. R. (2007) · Nature · doi:10.1038/nature05678 · Cited by 3,315 · see citing works

Quantum Optics

Walls, D. F., & Milburn, G. J. (1994) · Springer eBooks · doi:10.1007/978-3-642-79504-6 · Cited by 2,197 · see citing works

X-ray structure of a ClC chloride channel at 3.0 Å reveals the molecular basis of anion selectivity

Dutzler, R., Campbell, E., Cadene, M., Chait, B., & MacKinnon, R. (2002) · Nature · doi:10.1038/415287a · Cited by 1,567 · see citing works

Biophysical and Molecular Mechanisms of Shaker Potassium Channel Inactivation

Hoshi, T., Zagotta, W. N., & Aldrich, R. W. (1990) · Science · doi:10.1126/science.2122519 · Cited by 1,527 · see citing works

Crystal structure and mechanism of a calcium-gated potassium channel

Jiang, Y., Lee, A., Chen, J., Cadène, M., Chait, B. T., & MacKinnon, R. (2002) · Nature · doi:10.1038/417515a · Cited by 1,332 · see citing works

Environment-assisted quantum walks in photosynthetic energy transfer

Mohseni, M., Rebentrost, P., Lloyd, S., & Aspuru-Guzik, A. (2008) · The Journal of Chemical Physics · doi:10.1063/1.3002335 · Cited by 1,189 · see citing works

ENERGY, QUANTA, AND VISION

Hecht, S., Shlaer, S., & Pirenne, M. H. (1942) · The Journal of General Physiology · doi:10.1085/jgp.25.6.819 · Cited by 1,125 · see citing works

Structure of the Amide I Band of Peptides Measured by Femtosecond Nonlinear-Infrared Spectroscopy

Hamm, P. M., Lim, M., & Hochstrasser, R. M. (1998) · The Journal of Physical Chemistry B · doi:10.1021/jp9813286 · Cited by 1,095 · see citing works

Principles of Selective Ion Transport in Channels and Pumps

Gouaux, E., & MacKinnon, R. (2005) · Science · doi:10.1126/science.1113666 · Cited by 1,060 · see citing works

Dephasing-assisted transport: quantum networks and biomolecules

Plenio, M. B., & Huelga, S. F. (2008) · New Journal of Physics · doi:10.1088/1367-2630/10/11/113019 · Cited by 1,002 · see citing works

Responses of retinal rods to single photons.

Baylor, D. A., Lamb, T. D., & Yau, K. W. (1979) · The Journal of Physiology · doi:10.1113/jphysiol.1979.sp012716 · Cited by 992 · see citing works

Dynamic localization of a charged particle moving under the influence of an electric field

Dunlap, D. H., & Kenkre, V. M. (1986) · Physical Review B · doi:10.1103/physrevb.34.3625 · Cited by 896 · see citing works

The First Step in Vision: Femtosecond Isomerization of Rhodopsin

Schoenlein, R. W., Peteanu, L. A., Mathies, R. A., & Shank, C. V. (1991) · Science · doi:10.1126/science.1925597 · Cited by 885 · see citing works

Energetic optimization of ion conduction rate by the K+ selectivity filter

Morais-Cabral, J. H., Zhou, Y., & MacKinnon, R. (2001) · Nature · doi:10.1038/35102000 · Cited by 860 · see citing works

Energetics of ion conduction through the K+ channel

Bernèche, S., & Roux, B. (2001) · Nature · doi:10.1038/35102067 · Cited by 804 · see citing works

Coherent Intrachain Energy Migration in a Conjugated Polymer at Room Temperature

Collini, E., & Scholes, G. D. (2009) · Science · doi:10.1126/science.1164016 · Cited by 790 · see citing works

Importance of quantum decoherence in brain processes

Tegmark, M. (2000) · Physical Review E · doi:10.1103/physreve.61.4194 · Cited by 776 · see citing works

Driven quantum transport on the nanoscale

Kohler, S., Lehmann, J., & Peter Hänggi, A. (2005) · Physics Reports · doi:10.1016/j.physrep.2004.11.002 · Cited by 739 · see citing works

The voltage-gated potassium channels and their relatives

Yellen, G. (2002) · Nature · doi:10.1038/nature00978 · Cited by 700 · see citing works

Highly efficient energy excitation transfer in light-harvesting complexes: The fundamental role of noise-assisted transport

Caruso, F., Chin, A. W., Datta, A., Huelga, S. F., & Plenio, M. B. (2009) · The Journal of Chemical Physics · doi:10.1063/1.3223548 · Cited by 655 · see citing works

Vibrationally Coherent Photochemistry in the Femtosecond Primary Event of Vision

Wang, Q., Schoenlein, R. W., Peteanu, L. A., Mathies, R. A., & Shank, C. V. (1994) · Science · doi:10.1126/science.7939680 · Cited by 636 · see citing works

Ion Channel Reconstitution

Miller, C. (1986) · Springer eBooks · doi:10.1007/978-1-4757-1361-9 · Cited by 605 · see citing works

Control of ion selectivity in potassium channels by electrostatic and dynamic properties of carbonyl ligands

Noskov, S. Y., Bernèche, S., & Roux, B. (2004) · Nature · doi:10.1038/nature02943 · Cited by 598 · see citing works

Structure of the gating domain of a Ca2+-activated K+ channel complexed with Ca2+/calmodulin

Schumacher, M. A., Rivard, A. F., Bächinger, H. P., & Adelman, J. P. (2001) · Nature · doi:10.1038/35074145 · Cited by 597 · see citing works

Noise-assisted energy transfer in quantum networks and light-harvesting complexes

Chin, A. W., Datta, A., Caruso, F., Huelga, S. F., & Plenio, M. B. (2010) · New Journal of Physics · doi:10.1088/1367-2630/12/6/065002 · Cited by 338 · see citing works

Efficiency of energy transfer in a light-harvesting system under quantum coherence

Olaya-Castro, A., Lee, C. F., Olsen, F. F., & Johnson, N. F. (2008) · Physical Review B · doi:10.1103/physrevb.78.085115 · Cited by 313 · see citing works

Two-dimensional spectroscopy at infrared and optical frequencies

Hochstrasser, R. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704079104 · Cited by 291 · see citing works

Optimization of Exciton Trapping in Energy Transfer Processes

Cao, J., & Silbey, R. (2009) · The Journal of Physical Chemistry A · doi:10.1021/jp9032589 · Cited by 269 · see citing works

Entanglement and entangling power of the dynamics in light-harvesting complexes

Caruso, F., Chin, A. W., Datta, A., Huelga, S. F., & Plenio, M. B. (2010) · Physical Review A · doi:10.1103/physreva.81.062346 · Cited by 223 · see citing works

Does quantum mechanics play a non-trivial role in life?

Davies, P. C. W. (2004) · Biosystems · doi:10.1016/j.biosystems.2004.07.001 · Cited by 187 · see citing works

Computational studies of membrane channels

Roux, B., & Schulten, K. (2004) · Structure · doi:10.1016/j.str.2004.06.013 · Cited by 145 · see citing works

Correlated Vibrational Dynamics Revealed by Two-Dimensional Infrared Spectroscopy

Demirdöven, N., Khalil, M., & Tokmakoff, A. (2002) · Physical Review Letters · doi:10.1103/physrevlett.89.237401 · Cited by 144 · see citing works

Three-Dimensional Structure of a Voltage-Gated Potassium Channel at 2.5 nm Resolution

Sokolova, O. S., Kolmakova-Partensky, L., & Grigorieff, N. (2001) · Structure · doi:10.1016/s0969-2126(01)00578-0 · Cited by 144 · see citing works

Ultrafast 2D–IR Spectroscopy of Transient Species

Bredenbeck, J., Helbing, J., Kolano, C., & Hamm, P. M. (2007) · ChemPhysChem · doi:10.1002/cphc.200700148 · Cited by 113 · see citing works

Signatures of vibrational interactions in coherent two-dimensional infrared spectroscopy

Khalil, M., & Tokmakoff, A. (2001) · Chemical Physics · doi:10.1016/s0301-0104(01)00230-0 · Cited by 100 · see citing works

Localization effects in ac-driven tight-binding lattices

Holthaus, M., & Hone, D. W. (1996) · Philosophical Magazine B · doi:10.1080/01418639608240331 · Cited by 99 · see citing works

Probing dynamics of complex molecular systems with ultrafast 2D IR vibrational echo spectroscopy

Finkelstein, I. J., Zheng, J., Ishikawa, H., Kim, S., Kwak, K., & Fayer, M. D. (2007) · Physical Chemistry Chemical Physics · doi:10.1039/b618158a · Cited by 95 · see citing works

Instantaneous Mapping of Coherently Coupled Electronic Transitions and Energy Transfers in a Photosynthetic Complex Using Angle-Resolved Coherent Optical Wave-Mixing

Mercer, I. P., El-Taha, Y. C., Kajumba, N., Marangos, J. P., Tisch, J. W. G., Gabrielsen, M., Cogdell, R. J., Springate, E., & Turcu, E. (2009) · Physical Review Letters · doi:10.1103/physrevlett.102.057402 · Cited by 90 · see citing works

Shining Light on the Rapidly Evolving Structure of Water

Tokmakoff, A. (2007) · Science · doi:10.1126/science.1144515 · Cited by 64 · see citing works

Efficient quantum state transfer in spin chains via adiabatic passage

Eckert, K., Romero‐Isart, O., & Sanpera, A. (2007) · New Journal of Physics · doi:10.1088/1367-2630/9/5/155 · Cited by 60 · see citing works

The Three-dimensional Structure of the Cardiac L-type Voltage-gated Calcium Channel

Wang, M.-C., Collins, R. F., Ford, R. C., Berrow, N. S., DOLPHIN, A. C., & Kitmitto, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m308057200 · Cited by 56 · see citing works

[3] Glass technology for patch clamp electrodes

Rae, J. L., & Levis, R. A. (1992) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(92)07005-9 · Cited by 46 · see citing works

Modeling Permeation Energetics in the KcsA Potassium Channel

Garofoli, S., & Jordan, P. C. (2003) · Biophysical Journal · doi:10.1016/s0006-3495(03)70011-3 · Cited by 46 · see citing works

Voltage-Gated Ion Channels as Drug Targets

(2006) · Methods and principles in medicinal chemistry · doi:10.1002/3527608141 · Cited by 41 · see citing works

Cooperative transport in a potassium ion channel

Gwan, J.-F., & Baumgaertner, A. (2007) · The Journal of Chemical Physics · doi:10.1063/1.2756531 · Cited by 34 · see citing works

Energy distribution and ion selectivity of the bacterial potassium channel

Av, D., Markov, I. V., Baryshnikov, V. G., & Tverdislov, V. A. (2006) · BIOPHYSICS · doi:10.1134/s0006350906040178 · Cited by 2 · see citing works

Vibrations, quanta and biology

Huelga, S. F., & Plenio, M. B. (2013) · Contemporary Physics · doi:10.1080/00405000.2013.829687 · Cited by 568 · see citing works

Dynamics of Excitons in Conjugated Molecules and Organic Semiconductor Systems

Dimitriev, O. P. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00648 · Cited by 275 · see citing works

A primary model of THz and far-infrared signal generation and conduction in neuron systems based on the hypothesis of the ordered phase of water molecules on the neuron surface I: signal characteristics

Xiang, Z., Tang, C., Chang, C., & Liu, G. (2019) · 中国科学通报：英文版 · doi:10.1016/j.scib.2019.12.004 · Cited by 198 · see citing works

Quantum Biology: An Update and Perspective

Kim, Y., Bertagna, F., D’Souza, E. M., Heyes, D. J., Johannissen, L. O., Nery, E. T., Pantelias, A., Jiménez, A. S.-P., Slocombe, L., Spencer, M. G., et al. (2021) · Quantum Reports · doi:10.3390/quantum3010006 · Cited by 178 · see citing works

Revisiting the Quantum Brain Hypothesis: Toward Quantum (Neuro)biology?

Jedlicka, P. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00366 · Cited by 97 · see citing works

Quantum effects in the brain: A review

Adams, B., & Petruccione, F. (2020) · AVS Quantum Science · doi:10.1116/1.5135170 · Cited by 80 · see citing works

Quantum effects in the understanding of consciousness

Hameroff, S. R., Craddock, T. J. A., & Tuszyński, J. A. (2014) · Journal of Integrative Neuroscience · doi:10.1142/s0219635214400093 · Cited by 68 · see citing works

Vibration-enhanced quantum transport

Semião, F. L., Furuya, K., & Milburn, G. J. (2010) · New Journal of Physics · doi:10.1088/1367-2630/12/8/083033 · Cited by 49 · see citing works

Quantum coherence in photosynthesis

Engel, G. S. (2011) · Procedia Chemistry · doi:10.1016/j.proche.2011.08.029 · Cited by 46 · see citing works

Microtubules as a potential platform for energy transfer in biological systems: a target for implementing individualized, dynamic variability patterns to improve organ function

Ilan, Y. (2022) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-022-04513-1 · Cited by 46 · see citing works

The significance of bioelectricity on all levels of organization of an organism. Part 1: From the subcellular level to cells

Funk, R. H. W., & Scholkmann, F. (2022) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2022.12.002 · Cited by 46 · see citing works

Arrays of waveguide-coupled optical cavities that interact strongly with atoms

Lepert, G., Trupke, M., Hartmann, M. J., Plenio, M. B., & Hinds, E. A. (2011) · New Journal of Physics · doi:10.1088/1367-2630/13/11/113002 · Cited by 45 · see citing works

Vibrational excitons in ionophores: experimental probes for quantum coherence-assisted ion transport and selectivity in ion channels

Ganim, Z., Tokmakoff, A., & Vaziri, A. (2011) · New Journal of Physics · doi:10.1088/1367-2630/13/11/113030 · Cited by 41 · see citing works

Plausibility of quantum coherent states in biological systems

Salari, V., Tuszyński, J. A., Rahnama, M., & Bernroider, G. (2011) · Journal of Physics Conference Series · doi:10.1088/1742-6596/306/1/012075 · Cited by 41 · see citing works

Observation of Floquet Raman Transition in a Driven Solid-State Spin System

Shu, Z., Liu, Y., Cao, Q., Yang, P., Zhang, S., Plenio, M. B., Jelezko, F., & Cai, J. (2018) · Physical Review Letters · doi:10.1103/physrevlett.121.210501 · Cited by 40 · see citing works

Quantum Interference and Selectivity through Biological Ion Channels

Salari, V., Naeij, H. R., & Shafiee, A. (2017) · Scientific Reports · doi:10.1038/srep41625 · Cited by 40 · see citing works

Future Potential of Quantum Computing and Simulations in Biological Science

Pal, S., Bhattacharya, M., Dash, S., Lee, S., & Chakraborty, C. (2023) · Molecular Biotechnology · doi:10.1007/s12033-023-00863-3 · Cited by 39 · see citing works

A new viewpoint and model of neural signal generation and transmission: Signal transmission on unmyelinated neurons

Xiang, Z., Tang, C., Chang, C., & Liu, G. (2020) · Nano Research · doi:10.1007/s12274-020-3016-1 · Cited by 37 · see citing works

From quantum chemistry to quantum biology: a path toward consciousness

Tuszyński, J. A. (2020) · Journal of Integrative Neuroscience · doi:10.31083/j.jin.2020.04.393 · Cited by 36 · see citing works

Selective ion binding and transport by membrane proteins – A computational perspective

Zhekova, H. R., Ngo, V. A., da Silva, M. C., Salahub, D. R., & Noskov, S. Y. (2017) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2017.03.019 · Cited by 35 · see citing works

Bacterial intelligence: imitation games, time-sharing, and long-range quantum coherence

Majumdar, S., & Pal, S. (2017) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-017-0394-6 · Cited by 35 · see citing works

Focus on quantum effects and noise in biomolecules

Fleming, G. R., Huelga, S. F., & Plenio, M. B. (2011) · New Journal of Physics · doi:10.1088/1367-2630/13/11/115002 · Cited by 35 · see citing works

Electroencephalographic field influence on calcium momentum waves

Ingber, L., Pappalepore, M., & Stesiak, R. R. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2013.11.002 · Cited by 34 · see citing works

Quantum superposition inspired spiking neural network

Sun, Y., Zeng, Y., & Zhang, T. (2021) · iScience · doi:10.1016/j.isci.2021.102880 · Cited by 35 · see citing works

Quantum information theoretic approach to the mind–brain problem

Georgiev, D. D. (2020) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2020.08.002 · Cited by 32 · see citing works

Relaxation of interacting open quantum systems

Shishkov, V. Y., Andrianov, E. S., Пухов, А. А., Vinogradov, A. P., & Lisyansky, A. A. (2019) · Physics-Uspekhi · doi:10.3367/ufne.2018.06.038359 · Cited by 31 · see citing works

The radical-pair mechanism as a paradigm for the emerging science of quantum biology

Kominis, I. K. (2015) · Modern Physics Letters B · doi:10.1142/s0217984915300136 · Cited by 31 · see citing works

Quantum decoherence time scales for ionic superposition states in ion channels

Salari, V., Moradi, N., Sajadi, M., Fazileh, F., & Shahbazi, F. (2015) · Physical Review E · doi:10.1103/physreve.91.032704 · Cited by 27 · see citing works

Information transmission in microbial and fungal communication: from classical to quantum

Majumdar, S., & Pal, S. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0462-6 · Cited by 25 · see citing works

A study of quantum mechanical probabilities in the classical Hodgkin–Huxley model

Moradi, N., Scholkmann, F., & Salari, V. (2014) · Journal of Integrative Neuroscience · doi:10.1142/s021963521550003x · Cited by 22 · see citing works

Linoleic acid: Is this the key that unlocks the quantum brain? Insights linking broken symmetries in molecular biology, mood disorders and personalistic emergentism

Cocchi, M., Minuto, C., Tonello, L., Gabrielli, F., Bernroider, G., Tuszyński, J. A., Cappello, F., & Rasenick, M. M. (2017) · BMC Neuroscience · doi:10.1186/s12868-017-0356-1 · Cited by 20 · see citing works

Quantum coherence on selectivity and transport of ion channels

Seifi, M., Soltanmanesh, A., & Shafiee, A. (2022) · Scientific Reports · doi:10.1038/s41598-022-13323-w · Cited by 24 · see citing works

Computing the Integrated Information of a Quantum Mechanism

Albantakis, L., Prentner, R., & Durham, I. T. (2023) · Entropy · doi:10.3390/e25030449 · Cited by 19 · see citing works

Quantum coherence-control of thermal energy transport: the V model as a case study

Ivander, F., Anto-Sztrikacs, N., & Segal, D. (2022) · New Journal of Physics · doi:10.1088/1367-2630/ac9498 · Cited by 18 · see citing works

Perturbation theory for Lindblad superoperators for interacting open quantum systems

Shishkov, V. Y., Andrianov, E. S., Пухов, А. А., Vinogradov, A. P., & Lisyansky, A. A. (2020) · Physical Review A · doi:10.1103/physreva.102.032207 · Cited by 18 · see citing works

Photons detected in the active nerve by photographic technique

Zangari, A., Micheli, D., Galeazzi, R., Tozzi, A., Balzano, V., Bellavia, G., & Caristo, M. E. (2021) · Scientific Reports · doi:10.1038/s41598-021-82622-5 · Cited by 18 · see citing works

Thinking as a quantum phenomenon

Melkikh, A. V. (2018) · Biosystems · doi:10.1016/j.biosystems.2018.12.007 · Cited by 16 · see citing works

A quantum–classical model of brain dynamics

Sergi, A., Messina, A., Vicario, C. M., & Martino, G. (2023) · Entropy · doi:10.3390/e25040592 · Cited by 16 · see citing works

Quantum Biological Channel Modeling and Capacity Calculation

Djordjević, I. B. (2012) · Life · doi:10.3390/life2040377 · Cited by 12 · see citing works

Quantum Electrochemical Equilibrium: Quantum Version of the Goldman–Hodgkin–Katz Equation

Qaswal, A. B. (2020) · Quantum Reports · doi:10.3390/quantum2020017 · Cited by 12 · see citing works

Quantum propensities in the brain cortex and free will

Georgiev, D. D. (2021) · Biosystems · doi:10.1016/j.biosystems.2021.104474 · Cited by 12 · see citing works

Mathematical Modeling of Ion Quantum Tunneling Reveals Novel Properties of Voltage-Gated Channels and Quantum Aspects of Their Pathophysiology in Excitability-Related Disorders

Qaswal, A. B., Ababneh, O. A., Khreesha, L. A., Al-Ani, A. T., Suleihat, A., & Abbad, M. (2021) · Pathophysiology · doi:10.3390/pathophysiology28010010 · Cited by 10 · see citing works

THz trapped ion model and THz spectroscopy detection of potassium channels

Wang, K., Wang, S., Yang, L., Wu, Z., Zeng, B., & Gong, Y. (2021) · Nano Research · doi:10.1007/s12274-021-3965-z · Cited by 10 · see citing works

Probing quantum coherence in qubit arrays

Almeida, J., de Groot, P. C., Huelga, S. F., Liguori-Schremp, A. M., & Plenio, M. B. (2013) · Journal of Physics B Atomic Molecular and Optical Physics · doi:10.1088/0953-4075/46/10/104002 · Cited by 10 · see citing works

On the classical vibrational coherence of carbonyl groups in the selectivity filter backbone of the KcsA ion channel

Salari, V., Sajadi, M., Bassereh, H., Rezania, V., Alaei, M., & Tuszyński, J. A. (2015) · Journal of Integrative Neuroscience · doi:10.1142/s0219635215500132 · Cited by 10 · see citing works

Quantum features of the transport through ion channels in the soft knock-on model

Polakowski, M., & Panfil, M. (2024) · Physical Biology · doi:10.1088/1478-3975/ad9cde · Cited by 9 · see citing works

Singular Value Decomposition Quantum Algorithm for Quantum Biology

Oh, E., Krogmeier, T. J., Schlimgen, A. W., & Head-Marsden, K. (2024) · ACS Physical Chemistry Au · doi:10.1021/acsphyschemau.4c00018 · Cited by 9 · see citing works

Quantum model for a periodically driven selectivity filter in a K + ion channel

Cifuentes, A. A., & Semião, F. L. (2014) · Journal of Physics B Atomic Molecular and Optical Physics · doi:10.1088/0953-4075/47/22/225503 · Cited by 9 · see citing works

Free Will and Nonlocality at Detection as Basic Principles of Quantum Physics

Suárez, A. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5212-6_5 · Cited by 9 · see citing works

The Myelin Sheath Maintains the Spatiotemporal Fidelity of Action Potentials by Eliminating the Effect of Quantum Tunneling of Potassium Ions through the Closed Channels of the Neuronal Membrane

Qaswal, A. B. (2019) · Quantum Reports · doi:10.3390/quantum1020026 · Cited by 9 · see citing works

Impact of Quantum Coherence on Inelastic Thermoelectric Devices: From Diode to Transistor

曹, B. 蓓. C., 韩, C. 崇. H., 郝, X. 翔. H., 王, C. 晨. W., & 陆, J. 金. L. (2024) · Chinese Physics Letters · doi:10.1088/0256-307x/41/7/077302 · Cited by 8 · see citing works

Quantum information theoretic approach to the hard problem of consciousness

Georgiev, D. D. (2025) · Biosystems · doi:10.1016/j.biosystems.2025.105458 · Cited by 7 · see citing works

Rotational dynamics of ATP synthase: mechanical constraints and energy dissipative channels

Matar, I. K., Fahimi, P., & Matta, C. F. (2025) · Pure and Applied Chemistry · doi:10.1515/pac-2025-0477 · Cited by 8 · see citing works

Quantum versus classical transport of energy in coupled two-level systems

Medina, I., Moreira, S. V., & Semião, F. L. (2021) · Physical Review A · doi:10.1103/physreva.103.052216 · Cited by 7 · see citing works

Coulomb interaction rules timescales in potassium ion channel tunneling

March, N. D., Prado, S. D., & Brunnet, L. G. (2018) · Journal of Physics Condensed Matter · doi:10.1088/1361-648x/aac40b · Cited by 8 · see citing works

Quantum state transfer through noisy quantum cellular automata

Avalle, M., Genoni, M., & Serafini, A. (2015) · UCL Discovery (University College London) · Cited by 6 · see citing works

Mimicking classical noise in ion channels by quantum decoherence

Seifi, M., Soltanmanesh, A., & Shafiee, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-67106-6 · Cited by 7 · see citing works

Directed excitation transfer in vibrating chains by external fields

Mülken, O., & Bauer, M. (2011) · Physical Review E · doi:10.1103/physreve.83.061123 · Cited by 6 · see citing works

Energy transport in the presence of entanglement

Cifuentes, A. A., & Semião, F. L. (2017) · Physical Review A · doi:10.1103/physreva.95.062302 · Cited by 6 · see citing works

Excitation energy transport with noise and disorder in a model of the selectivity filter of an ion channel

Jalalinejad, A., Bassereh, H., Salari, V., Ala-Nissilä, T., & Giacometti, A. (2018) · Journal of Physics Condensed Matter · doi:10.1088/1361-648x/aadeab · Cited by 6 · see citing works

Probing quantum coherence in qubit arraysPreprint

Almeida, J., de Groot, P. C., Huelga, S. F., Liguori, A. M., & Plenio, M. B. (2013) · Cited by 6 · see citing works

Conductance Channels in a Single-Entity Enzyme

Colombo, R. N. P., Nascimento, S. Q., & Crespilho, F. N. (2024) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.4c01796 · Cited by 5 · see citing works

Time-Irreversible Quantum-Classical Dynamics of Molecular Models in the Brain

Sergi, A., MESSINA, A., Saija, R., Martino, G., Caccamo, M. T., Kuo, M., & Nitsche, M. A. (2025) · Symmetry · doi:10.3390/sym17020285 · Cited by 5 · see citing works

Simulation of the sensing mechanism in quantum dot gas sensor by quantum light harvesting approach

Suntijitrungruang, O., Lakronwat, J., Uthailiang, T., Pongkitiwanichakul, P., & Boonchui, S. (2022) · Frontiers in Chemistry · doi:10.3389/fchem.2022.1036197 · Cited by 5 · see citing works

Influence of far-red light coherence on the functional state of plants

Budagovsky, A. V., Владимировна, С. Н., Budagovskaya, О. N., & Budagovsky, I. A. (2021) · Physical review. E · doi:10.1103/physreve.103.012411 · Cited by 5 · see citing works

Quantum tunneling time delay investigation of $${{\varvec{K}}}^{+}$$ ion in human telomeric G-quadruplex systems

Torabfam, G. Ç., Demir, G. K., & Demir, D. (2023) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-022-01982-z · Cited by 4 · see citing works

Transport threshold in a quantum model for the KscA ion channel

March, N. D., Prado, S. D., & Brunnet, L. G. (2021) · Journal of Physics Condensed Matter · doi:10.1088/1361-648x/ac2cf0 · Cited by 4 · see citing works

The Quest for Cognition in Purposive Action: From Cybernetics to Quantum Computing

Morasso, P. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2202039 · Cited by 4 · see citing works

A model of ion transport processes along and across the neuronal membrane

Xiang, Z., Liu, G. Z., Tang, C., & Yan, L. (2017) · Journal of Integrative Neuroscience · doi:10.3233/jin-160002 · Cited by 4 · see citing works

Quantum mechanisms in the brain: from conjectures and theories to experimental evidence

Craddock, T. J. A. (2025) · Quantum Effects and Measurement Techniques in Biology and Biophotonics · doi:10.1117/12.3043206 · Cited by 3 · see citing works

Relaxation of interacting open quantum systems

Shishkov, V. Y., Andrianov, E. S., Пухов, А. А., Vinogradov, A. P., & Lisyansky, A. A. (2018) · Uspekhi Fizicheskih Nauk · doi:10.3367/ufnr.2018.06.038359 · Cited by 4 · see citing works

Quantum state transfer through noisy quantum cellular automata

Avalle, M., Genoni, M. G., & Serafini, A. (2015) · Journal of Physics A Mathematical and Theoretical · doi:10.1088/1751-8113/48/19/195304 · Cited by 6 · see citing works

Quantum Effects in Biology and Their Applications to Light Harvesting and Sensing

Omar, Y., Plenio, M. B., Huelga, S. F., & Rasetti, M. (2011) · Procedia Computer Science · doi:10.1016/j.procs.2011.12.028 · Cited by 2 · see citing works

Quantum Effects in Biological Systems

Walschaers, M. (2018) · Springer theses · doi:10.1007/978-3-319-93151-7_6 · Cited by 3 · see citing works

Quantum effects in ion transport: A thermodynamic resource theory approach

Mohammadi, A. M., & Shafiee, A. (2025) · Biosystems · doi:10.1016/j.biosystems.2025.105412 · Cited by 1 · see citing works

Wave Mechanics of Ciliary Proteins: Quantum‐Enabled Sensing and Energy Transfer in the “Cellular Antenna”

Bilezikian, D. L., Davidoff, D., Caram, J. R., Fay, T. P., Kalra, A. P., & Weiss, P. S. (2026) · Aggregate · doi:10.1002/agt2.70354 · Cited by 1 · see citing works

The Electron-Conformational Model of Ryanodine Receptors of the Heart Cell

Moskvin, A. S. (2018) · Technical Physics · doi:10.1134/s1063784218090128 · Cited by 1 · see citing works

Quantum Information Theory and Quantum Mechanics-Based Biological Modeling and Biological Channel Capacity Calculation

Djordjević, I. B. (2015) · Springer eBooks · doi:10.1007/978-3-319-22816-7_4 · Cited by 1 · see citing works

The Role of Ion Transition from the Pore Cavity to the Selectivity Filter in the Mechanism of Selectivity and Rectification in the K v 1.2 Potassium Channel: Transfer of Ion Solvation from Cavity Water to the Protein and Water of the Selectivity FilterPreprint

Kariev, A. M., & Green, M. E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.16.994194 · Cited by 1 · see citing works

СВЕРХКРИТИЧЕСКИЙ МОЗГ ТЬЮРИНГА И УСИЛИТЕЛИ СВОБОДНЫХ БИТОВ: ХОРОША ЛИ ГИПОТЕЗА КВАНТОВОГО МОЗГА?

Vinnik, D. (2020) · Respublica literaria · doi:10.47850/s.2020.1.4

Similarities Between the AdS/CFT Correspondence and the Binding ProblemPreprint

Elliott, M. (2019) · doi:10.31234/osf.io/dgvyj

A quantum mechanical approach to random X chromosome inactivation

Lobato, R., & 159 rue Archambault, L. (2021) · AIMS Biophysics · doi:10.3934/biophy.2021026

Quantum biology: An overview

Lambert, N., & Nori, F. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-90800-9.00176-1

Correlated disorder as a tunable switch between trapping and conduction in quantum ion channels

Ramos, I. P. D. S., Lanzini, R. G., Brunnet, L. G., & Prado, S. D. (2025) · Frontiers in Quantum Science and Technology · doi:10.3389/frqst.2025.1725290

Entropic tunneling time sheds light on efficient potassium ion transition in KcsA channel

Torabfam, G. Ç., Demir, G. K., Demir, D., Pusuluk, O., & Mustafaoğlu, N. (2026) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2026.03.002

Quantum optical effects in neuronal microtubules: superradiance under structural disorder

Gassab, L., & Craddock, T. J. A. (2026) · Quantum Effects and Measurement Techniques in Biology and Biophotonics · doi:10.1117/12.3072614

Quantum Capacity of Continuously Observed Ion Channels

Trybek, P., & Dajka, J. (2026) · Entropy · doi:10.3390/e28050555

Research on Blocking Ion Channels in Cell Membranes Under the Action of Electromagnetic Field

Kundenko, M., Mardziavko, K., Mardziavko, V., & Rudenko, A. (2026) · International Conference on Electrical, Computer and Energy Technologies (ICECET) · doi:10.1109/icecet65726.2026.11632291

Quantum coherence on selectivity and transport of ion channels

Seifi, M., Soltanmanesh, A., & Shafiee, A. (2022) · Scientific Reports · doi:10.1038/s41598-022-13323-w · Cited by 24 · see citing works

Quantum Coherence in Ion Channels: An Alternating Electric Field Could Put the Idea to the Test

inquantio (2026) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.21468082

On the classical vibrational coherence of carbonyl groups in the selectivity filter backbone of the KcsA ion channel

Salari, V., Sajadi, M., Bassereh, H., Rezania, V., Alaei, M., & Tuszyński, J. A. (2015) · Journal of Integrative Neuroscience · doi:10.1142/s0219635215500132 · Cited by 10 · see citing works

On the Classical Vibrational Coherence of Carbonyl Groups in the Selectivity Filter Backbone of KcsA Ion ChannelPreprint

Salari, V., Sajadi, M., Bassereh, H., Rezania, V., Alaei, M., & Tuszyński, J. A. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1501.05605

A possible mechanisms for quantum coherence assisted ion transport in ion channels

Vaziri, A. (2011) · Bulletin of the American Physical Society