Cryptochrome mediates light-dependent magnetosensitivity in Drosophila

Classical conditioning and retention in normal and mutantDrosophila melanogaster

Tully, T., & Quinn, W. G. (1985) · Journal of Comparative Physiology A · doi:10.1007/bf01350033 · Cited by 1,189 · see citing works

A Model for Photoreceptor-Based Magnetoreception in Birds

Ritz, T., Adem, S., & Schulten, K. (2000) · Biophysical Journal · doi:10.1016/s0006-3495(00)76629-x · Cited by 1,176 · see citing works

The cryb mutation identifies cryptochrome as a circadian photoreceptor in Drosophila

Stanewsky, R., Kaneko, M., Emery, P., Beretta, B., Wager-Smith, K., Kay, S. A., Rosbash, M., & Hall, J. C. (1998) · Cell · doi:10.1016/s0092-8674(00)81638-4 · Cited by 968 · see citing works

CRY, a Drosophila clock and light-regulated cryptochrome, is a major contributor to circadian rhythm resetting and photosensitivity

Emery, P., So, W. V., Kaneko, M., Hall, J. C., & Rosbash, M. (1998) · Cell · doi:10.1016/s0092-8674(00)81637-2 · Cited by 912 · see citing works

Magnetic orientation and magnetoreception in birds and other animals

Wiltschko, W., & Wiltschko, R. (2005) · Journal of Comparative Physiology A · doi:10.1007/s00359-005-0627-7 · Cited by 587 · see citing works

Chemical compass model of avian magnetoreception

Maeda, K., Henbest, K. B., Cintolesi, F., Kuprov, I., Rodgers, C. T., Liddell, P. A., Gust, D., Timmel, C. R., & Hore, P. J. (2008) · Nature · doi:10.1038/nature06834 · Cited by 496 · see citing works

A Biomagnetic Sensory Mechanism Based on Magnetic Field Modulated Coherent Electron Spin Motion

Schulten, K., Swenberg, C. E., & Weller, A. (1978) · Zeitschrift für Physikalische Chemie · doi:10.1524/zpch.1978.111.1.001 · Cited by 430 · see citing works

Biogenic magnetite as a basis for magnetic field detection in animals

Kirschvink, J. L., & Gould, J. L. (1981) · Biosystems · doi:10.1016/0303-2647(81)90060-5 · Cited by 415 · see citing works

The physics and neurobiology of magnetoreception

Johnsen, S., & Lohmann, K. J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1745 · Cited by 410 · see citing works

Magnetite-based magnetoreception

Kirschvink, J. L. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00235-x · Cited by 408 · see citing works

Insect Cryptochromes: Gene Duplication and Loss Define Diverse Ways to Construct Insect Circadian Clocks

Yuan, Q., Metterville, D. R., Briscoe, A. D., & Reppert, S. M. (2007) · Molecular Biology and Evolution · doi:10.1093/molbev/msm011 · Cited by 402 · see citing works

Uniform magnetic fields and double‐wrapped coil systems: Improved techniques for the design of bioelectromagnetic experiments

Kirschvink, J. L. (1992) · Bioelectromagnetics · doi:10.1002/bem.2250130507 · Cited by 360 · see citing works

Cryptochromes

Cashmore, A. R. (2003) · Cell · doi:10.1016/s0092-8674(03)00647-0 · Cited by 312 · see citing works

Magnetic maps in animals: nature's GPS

Lohmann, K. J., Lohmann, C. M. F., & Putman, N. F. (2007) · Journal of Experimental Biology · doi:10.1242/jeb.001313 · Cited by 271 · see citing works

The two CRYs of the butterfly

Zhu, H., Yuan, Q., Froy, O., Casselman, A., & Reppert, S. M. (2005) · Current Biology · doi:10.1016/j.cub.2005.11.030 · Cited by 238 · see citing works

The Extraretinal Eyelet ofDrosophila: Development, Ultrastructure, and Putative Circadian Function

Helfrich‐Förster, C., Edwards, T. N., Yasuyama, K., Wisotzki, B., Schneuwly, S., Stanewsky, R., Meinertzhagen, I. A., & Hofbauer, A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09255.2002 · Cited by 230 · see citing works

Genetic analysis of the circadian system in Drosophila melanogaster and mammals

Stanewsky, R. (2002) · Journal of Neurobiology · doi:10.1002/neu.10164 · Cited by 219 · see citing works

Behavioural evidence for use of a light-dependent magnetoreception mechanism by a vertebrate

Phillips, J. B., & Borland, S. C. (1992) · Nature · doi:10.1038/359142a0 · Cited by 218 · see citing works

A physicochemical mechanism for magnetic field detection by migratory birds and homing pigeons

Leask, M. J. M. (1977) · Nature · doi:10.1038/267144a0 · Cited by 206 · see citing works

Magnetoreception

Wiltschko, R., & Wiltschko, W. (2006) · BioEssays · doi:10.1002/bies.20363 · Cited by 185 · see citing works

Rhythm Defects Caused by Newly Engineered Null Mutations in Drosophila's cryptochrome Gene

Doleželová, E., Doležel, D., & Hall, J. C. (2007) · Genetics · doi:10.1534/genetics.107.076513 · Cited by 154 · see citing works

Marine Turtles Use Geomagnetic Cues during Open-Sea Homing

Luschi, P., Benhamou, S., Girard, C., Ciccione, S., Roos, D., Sudre, J., & Benvenuti, S. (2007) · Current Biology · doi:10.1016/j.cub.2006.11.062 · Cited by 139 · see citing works

Photochemistry and Photobiology of Cryptochrome Blue‐light Photopigments: The Search for a Photocycle

Partch, C. L., & Sancar, A. (2005) · Photochemistry and Photobiology · doi:10.1562/2005-07-08-ir-607 · Cited by 130 · see citing works

Animal Type 1 Cryptochromes

Öztürk, N., Song, S.-H., Selby, C. P., & Sancar, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m708612200 · Cited by 117 · see citing works

Wavelength-dependent effects of light on magnetic compass orientation in Drosophila melanogaster

Phillips, J. B., & Sayeed, O. (1993) · Journal of Comparative Physiology A · doi:10.1007/bf00216612 · Cited by 100 · see citing works

Shedding Light on Vertebrate Magnetoreception

Ritz, T., Dommer, D. H., & Phillips, J. B. (2002) · Neuron · doi:10.1016/s0896-6273(02)00707-9 · Cited by 87 · see citing works

Action Spectrum of Drosophila Cryptochrome

VanVickle-Chavez, S. J., & Gelder, R. N. V. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m609314200 · Cited by 69 · see citing works

A model for encoding of magnetic field intensity by magnetite-based magnetoreceptor cells

Walker, M. M. (2007) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2007.09.030 · Cited by 62 · see citing works

Perception of the geomagnetic field in the flyDrosophila melanogaster

Wehner, R., & Labhart, T. (1970) · Cellular and Molecular Life Sciences · doi:10.1007/bf02114135 · Cited by 46 · see citing works

Ectopic CRYPTOCHROME Renders TIM Light Sensitive in the Drosophila Ovary

Rush, B. L., Murad, A., Emery, P., & Giebultowicz, J. M. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406290416 · Cited by 37 · see citing works

The Radical-Pair Mechanism of Magnetoreception

Hore, P. J., & Mouritsen, H. (2016) · Annual Review of Biophysics · doi:10.1146/annurev-biophys-032116-094545 · Cited by 813 · see citing works

Chemical magnetoreception in birds: The radical pair mechanism

Rodgers, C. T., & Hore, P. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711968106 · Cited by 542 · see citing works

Long-distance navigation and magnetoreception in migratory animals

Mouritsen, H. (2018) · Nature · doi:10.1038/s41586-018-0176-1 · Cited by 536 · see citing works

Magnetic sensitivity of cryptochrome 4 from a migratory songbird

Xu, J., Jarocha, L. E., Zollitsch, T. M., Konowalczyk, M., Henbest, K. B., Richert, S., Golesworthy, M. J., Schmidt, J., Déjean, V., Sowood, D. J. C., et al. (2021) · Nature · doi:10.1038/s41586-021-03618-9 · Cited by 433 · see citing works

Sustained Quantum Coherence and Entanglement in the Avian Compass

Gauger, E. M., Rieper, E., Morton, J. J. L., Benjamin, S. C., & Vedral, V. (2011) · Physical Review Letters · doi:10.1103/physrevlett.106.040503 · Cited by 357 · see citing works

A magnetic protein biocompass

Qin, S., Yin, H. H., Yang, C., Dou, Y., Liu, Z., Zhang, P., He, Y. H., Huang, Y., Feng, J., Hao, J., et al. (2015) · Nature Materials · doi:10.1038/nmat4484 · Cited by 350 · see citing works

The Cryptochrome Blue Light Receptors

Yu, X., Liu, H., John Klejnot, B., & Lin, C. (2010) · The Arabidopsis Book · doi:10.1199/tab.0135 · Cited by 337 · see citing works

Magnetic Compass of Birds Is Based on a Molecule with Optimal Directional Sensitivity

Ritz, T., Wiltschko, R., Hore, P. J., Rodgers, C. T., Stapput, K., Thalau, P., Timmel, C. R., & Wiltschko, W. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2008.11.072 · Cited by 305 · see citing works

Animal cryptochromes mediate magnetoreception by an unconventional photochemical mechanism

Gegear, R. J., Foley, L. E., Casselman, A. L., & Reppert, S. M. (2010) · Nature · doi:10.1038/nature08719 · Cited by 289 · see citing works

Honeybees as a Model for the Study of Visually Guided Flight, Navigation, and Biologically Inspired Robotics

Srinivasan, M. V. (2011) · Physiological Reviews · doi:10.1152/physrev.00005.2010 · Cited by 282 · see citing works

The future of quantum biology

Marais, A., Adams, B., Ringsmuth, A. K., Ferretti, M., Gruber, J. M., Hendrikx, R., Schuld, M., Smith, S. L., Sinayskiy, I., Krüger, T. P. J., et al. (2018) · Journal of The Royal Society Interface · doi:10.1098/rsif.2018.0640 · Cited by 274 · see citing works

Cryptochrome Mediates Light-Dependent Magnetosensitivity of Drosophila's Circadian Clock

Yoshii, T., Ahmad, M., & Helfrich-Förster, C. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000086 · Cited by 232 · see citing works

Cryptochromes—a potential magnetoreceptor: what do we know and what do we want to know?

Liedvogel, M., & Mouritsen, H. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0411.focus · Cited by 231 · see citing works

Navigational mechanisms of migrating monarch butterflies

Reppert, S. M., Gegear, R. J., & Merlin, C. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.04.004 · Cited by 230 · see citing works

Human cryptochrome exhibits light-dependent magnetosensitivity

Foley, L. E., Gegear, R. J., & Reppert, S. M. (2011) · Nature Communications · doi:10.1038/ncomms1364 · Cited by 214 · see citing works

Structure and Function of Photolyase and in Vivo Enzymology: 50th Anniversary

Sancar, A. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.r800052200 · Cited by 204 · see citing works

CRYPTOCHROME Is a Blue-Light Sensor That Regulates Neuronal Firing Rate

Fogle, K. J., Parson, K. G., Dahm, N. A., & Holmes, T. C. (2011) · Science · doi:10.1126/science.1199702 · Cited by 197 · see citing works

Structures of Drosophila Cryptochrome and Mouse Cryptochrome1 Provide Insight into Circadian Function

Czarna, A., Berndt, A., Singh, H. R., Grudziecki, A., Ladurner, A. G., Timinszky, G., Kramer, A., & Wolf, E. (2013) · Cell · doi:10.1016/j.cell.2013.05.011 · Cited by 196 · see citing works

Light-activated Cryptochrome Reacts with Molecular Oxygen to Form a Flavin–Superoxide Radical Pair Consistent with Magnetoreception

Müller, P., & Ahmad, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.228940 · Cited by 190 · see citing works

Demystifying Monarch Butterfly Migration

Reppert, S. M., & de Roode, J. C. (2018) · Current Biology · doi:10.1016/j.cub.2018.02.067 · Cited by 185 · see citing works

Recognition and repair of UV lesions in loop structures of duplex DNA by DASH-type cryptochrome

Pokorny, R., Klar, T., Hennecke, U., Carell, T., Batschauer, A., & Essen, L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805830106 · Cited by 179 · see citing works

A magnetic compass aids monarch butterfly migration

Guerra, P. A., Gegear, R. J., & Reppert, S. M. (2014) · Nature Communications · doi:10.1038/ncomms5164 · Cited by 168 · see citing works

Chemical and structural analysis of a photoactive vertebrate cryptochrome from pigeon

Zoltowski, B. D., Chelliah, Y., Wickramaratne, A. C., Jarocha, L. E., Karki, N., Xu, W., Mouritsen, H., Hore, P. J., Hibbs, R. E., Green, C. B., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1907875116 · Cited by 164 · see citing works

Structure of full-length Drosophila cryptochrome

Zoltowski, B. D., Vaidya, A. T., Top, D., Widom, J. M., Young, M. W., & Crane, B. R. (2011) · Nature · doi:10.1038/nature10618 · Cited by 162 · see citing works

Magnetic-field perception

Lohmann, K. J. (2010) · Nature · doi:10.1038/4641140a · Cited by 160 · see citing works

The magnetic retina: light-dependent and trigeminal magnetoreception in migratory birds

Mouritsen, H., & Hore, P. J. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.01.005 · Cited by 154 · see citing works

Neurobiology of Monarch Butterfly Migration

Reppert, S. M., Guerra, P. A., & Merlin, C. (2015) · Annual Review of Entomology · doi:10.1146/annurev-ento-010814-020855 · Cited by 149 · see citing works

Photoexcited CRY1 and phyB interact directly with ARF6 and ARF8 to regulate their DNA‐binding activity and auxin‐induced hypocotyl elongation in Arabidopsis

Mao, Z., He, S., Xu, F., Wei, X., Jiang, L., Liu, Y., Wang, W., Li, T., Xu, P., Du, S., et al. (2019) · New Phytologist · doi:10.1111/nph.16194 · Cited by 141 · see citing works

Photoreceptor-based magnetoreception: optimal design of receptor molecules, cells, and neuronal processing

Ritz, T., Ahmad, M., Mouritsen, H., Wiltschko, R., & Wiltschko, W. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0456.focus · Cited by 135 · see citing works

Magnetoreception in eusocial insects: an update

Wajnberg, E., Acosta‐Avalos, D., Alves, O. C., de Oliveira, J. F., Srygley, R. B., & Esquivel, D. M. S. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0526.focus · Cited by 134 · see citing works

Multimodal interactions in insect navigation

Buehlmann, C., Mangan, M., & Graham, P. (2020) · Animal Cognition · doi:10.1007/s10071-020-01383-2 · Cited by 133 · see citing works

The magnetic map of hatchling loggerhead sea turtles

Lohmann, K. J., Putman, N. F., & Lohmann, C. M. F. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.11.005 · Cited by 131 · see citing works

A radical sense of direction: signalling and mechanism in cryptochrome magnetoreception

Dodson, C. A., Hore, P. J., & Wallace, M. I. (2013) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2013.07.002 · Cited by 129 · see citing works

Electron spin relaxation in cryptochrome-based magnetoreception

Kattnig, D. R., Solov’yov, I. A., & Hore, P. J. (2016) · Physical Chemistry Chemical Physics · doi:10.1039/c5cp06731f · Cited by 129 · see citing works

Interactive Features of Proteins Composing Eukaryotic Circadian Clocks

Crane, B. R., & Young, M. W. (2014) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060713-035644 · Cited by 125 · see citing works

Spectroscopy in sculpted fields

Yang, N., Tang, Y., & Cohen, A. E. (2009) · Nano Today · doi:10.1016/j.nantod.2009.05.001 · Cited by 125 · see citing works

Spin Biochemistry Modulates Reactive Oxygen Species (ROS) Production by Radio Frequency Magnetic Fields

Usselman, R. J., Hill, I., Singel, D. J., & Martino, C. F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093065 · Cited by 125 · see citing works

Extended Electron-Transfer in Animal Cryptochromes Mediated by a Tetrad of Aromatic Amino Acids

Nohr, D., Franz, S., Rodriguez, R., Paulus, B., Essen, L., Weber, S., & Schleicher, E. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.06.009 · Cited by 124 · see citing works

Functional motifs in the (6-4) photolyase crystal structure make a comparative framework for DNA repair photolyases and clock cryptochromes

Hitomi, K., DiTacchio, L., Arvai, A. S., Yamamoto, J., Kim, S., Todo, T., Tainer, J. A., Iwai, S., Panda, S., & Getzoff, E. D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809180106 · Cited by 123 · see citing works

Circadian Expression of Clock Genes in Two Mosquito Disease Vectors: cry2 Is Different

Gentile, C., Rivas, G. B. D. S., Meireles-Filho, A. C. A., Lima, J. B. P., & Peixoto, A. A. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409349169 · Cited by 116 · see citing works

Photolyase: Dynamics and electron-transfer mechanisms of DNA repair

Zhang, M., Wang, L., & Zhong, D. (2017) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2017.08.007 · Cited by 115 · see citing works

Animal Cryptochromes: Divergent Roles in Light Perception, Circadian Timekeeping and Beyond

Michael, A. K., Fribourgh, J. L., Gelder, R. N. V., & Partch, C. L. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12677 · Cited by 115 · see citing works

Chemical amplification of magnetic field effects relevant to avian magnetoreception

Kattnig, D. R., Evans, E. W., Déjean, V., Dodson, C. A., Wallace, M. I., Mackenzie, S. R., Timmel, C. R., & Hore, P. J. (2016) · Nature Chemistry · doi:10.1038/nchem.2447 · Cited by 114 · see citing works

Possible involvement of superoxide and dioxygen with cryptochrome in avian magnetoreception: Origin of Zeeman resonances observed by in vivo EPR spectroscopy

Hogben, H. J., Efimova, O., Wagner-Rundell, N., Timmel, C. R., & Hore, P. J. (2009) · Chemical Physics Letters · doi:10.1016/j.cplett.2009.08.051 · Cited by 114 · see citing works

An electromagnetic field disrupts negative geotaxis in Drosophila via a CRY-dependent pathway

Fedele, G., Green, E. W., Rosato, E., & Kyriacou, C. P. (2014) · Nature Communications · doi:10.1038/ncomms5391 · Cited by 113 · see citing works

Blue-light-receptive cryptochrome is expressed in a sponge eye lacking neurons and opsin

Rivera, A. S., Öztürk, N., Fahey, B., Plachetzki, D. C., Degnan, B. M., Sancar, A., & Oakley, T. H. (2012) · Journal of Experimental Biology · doi:10.1242/jeb.067140 · Cited by 112 · see citing works

Cryptochrome 2 mediates directional magnetoreception in cockroaches

Bazalová, O., Kvíčalová, M., Válková, T., Slabý, P., Bartoš, P., Netušil, R., Tomanová, K., Braeunig, P., Lee, H., Šauman, I., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1518622113 · Cited by 112 · see citing works

Light-dependent magnetic compass orientation in amphibians and insects: candidate receptors and candidate molecular mechanisms

Phillips, J. B., Jorge, P. E., & Muheim, R. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0459.focus · Cited by 110 · see citing works

Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies

Wan, G., Hayden, A. N., Iiams, S. E., & Merlin, C. (2021) · Nature Communications · doi:10.1038/s41467-021-21002-z · Cited by 110 · see citing works

Phylogenetic and Functional Classification of the Photolyase/Cryptochrome Family

Öztürk, N. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12676 · Cited by 109 · see citing works

Magnetic alignment in mammals and other animals

Begall, S., Malkemper, E. P., Červený, J., Němec, P., & Burda, H. (2012) · Mammalian Biology · doi:10.1016/j.mambio.2012.05.005 · Cited by 105 · see citing works

Chapter 3 Mapping and Manipulating Neural Circuits in the Fly Brain

Simpson, J. H. (2009) · Advances in genetics · doi:10.1016/s0065-2660(09)65003-3 · Cited by 103 · see citing works

Millitesla magnetic field effects on the photocycle of an animal cryptochrome

Sheppard, D. M. W., Li, J., Henbest, K. B., Neil, S. R. T., Maeda, K., Storey, J. G., Schleicher, E., Biskup, T., Rodriguez, R., Weber, S., et al. (2017) · Scientific Reports · doi:10.1038/srep42228 · Cited by 100 · see citing works

The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensor

Hochstoeger, T., Said, T. A., Maestre, D., Walter, F., Vilceanu, A., Pedron, M., Cushion, T. D., Snider, W., Nimpf, S., Nordmann, G. C., et al. (2020) · Science Advances · doi:10.1126/sciadv.abb9110 · Cited by 100 · see citing works

No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening

Edelman, N. B., Fritz, T. M., Nimpf, S., Pichler, P., Lauwers, M., Hickman, R. W., Papadaki-Anastasopoulou, A., Ushakova, L., Heuser, T., Resch, G. P., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1407915112 · Cited by 98 · see citing works

Genetic Analysis of Circadian Responses to Low Frequency Electromagnetic Fields in Drosophila melanogaster

Fedele, G., Edwards, M. D., Bhavnani, S., Hares, J. M., Murbach, M., Green, E. W., Dissel, S., Hastings, M. H., Rosato, E., & Kyriacou, C. P. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004804 · Cited by 98 · see citing works

Vertebrate Cryptochromes are Vestigial Flavoproteins

Kutta, R. J., Archipowa, N., Johannissen, L. O., Jones, A. R., & Scrutton, N. S. (2017) · Scientific Reports · doi:10.1038/srep44906 · Cited by 96 · see citing works

Solvent Driving Force Ensures Fast Formation of a Persistent and Well-Separated Radical Pair in Plant Cryptochrome

Lüdemann, G., Solov’yov, I. A., Kubař, T., & Elstner, M. (2014) · Journal of the American Chemical Society · doi:10.1021/ja510550g · Cited by 95 · see citing works

A behavioral perspective on the biophysics of the light-dependent magnetic compass: a link between directional and spatial perception?

Phillips, J. B., Muheim, R., & Jorge, P. E. (2010) · Journal of Experimental Biology · doi:10.1242/jeb.020792 · Cited by 94 · see citing works

Microsecond Light-Induced Proton Transfer to Flavin in the Blue Light Sensor Plant Cryptochrome

Langenbacher, T., Immeln, D., Dick, B., & Kottke, T. (2009) · Journal of the American Chemical Society · doi:10.1021/ja901628y · Cited by 93 · see citing works

Separation of photo-induced radical pair in cryptochrome to a functionally critical distance

Solov’yov, I. A., Domratcheva, T. M., & Schulten, K. J. (2014) · Scientific Reports · doi:10.1038/srep03845 · Cited by 90 · see citing works

Transient EPR

Weber, S. (2017) · Wiley eBooks · doi:10.1002/9780470034590.emrstm1509 · Cited by 89 · see citing works

FAD Regulates CRYPTOCHROME Protein Stability and Circadian Clock in Mice

Hirano, A., Braas, D., Fu, Y., & Ptáček, L. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.041 · Cited by 88 · see citing works

Primary Events in the Blue Light Sensor Plant Cryptochrome: Intraprotein Electron and Proton Transfer Revealed by Femtosecond Spectroscopy

Immeln, D., Weigel, A., Kottke, T., & Lustres, J. L. P. (2012) · Journal of the American Chemical Society · doi:10.1021/ja302121z · Cited by 87 · see citing works

Interactions between electromagnetic radiation and biological systems

Liu, L., Huang, B., Lu, Y., Zhao, Y., Tang, X., & Shi, Y. (2024) · iScience · doi:10.1016/j.isci.2024.109201 · Cited by 80 · see citing works

Radio frequency magnetic fields disrupt magnetoreception in American cockroach

Vácha, M., Půžová, T., & Kvíčalová, M. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.028670 · Cited by 79 · see citing works

Magnetic Strategies for Nervous System Control

Christiansen, M. G., Senko, A. W., & Anikeeva, P. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050241 · Cited by 76 · see citing works

Cryptochrome magnetoreception: four tryptophans could be better than three

Wong, S. Y., Wei, Y., Mouritsen, H., Solov’yov, I. A., & Hore, P. J. (2021) · Journal of The Royal Society Interface · doi:10.1098/rsif.2021.0601 · Cited by 76 · see citing works

Light-Induced Conformational Changes in Full-Length Arabidopsis thaliana Cryptochrome

Kondoh, M., Shiraishi, C., Müller, P., Ahmad, M., Hitomi, K., Getzoff, E. D., & Terazima, M. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.08.031 · Cited by 76 · see citing works

Expression patterns of cryptochrome genes in avian retina suggest involvement of Cry4 in light-dependent magnetoreception

Pinzon-Rodriguez, A., Bensch, S., & Muheim, R. (2018) · Journal of The Royal Society Interface · doi:10.1098/rsif.2018.0058 · Cited by 75 · see citing works

Reaction Kinetics and Mechanism of Magnetic Field Effects in Cryptochrome

Solov’yov, I. A., & Schulten, K. (2011) · The Journal of Physical Chemistry B · doi:10.1021/jp209508y · Cited by 75 · see citing works

Extremely Low Frequency Electromagnetic Fields impair the Cognitive and Motor Abilities of Honey Bees

Shepherd, S., Lima, M. A. P., de Oliveira, E. E., Sharkh, S. M., Jackson, C. W., & Newland, P. L. (2018) · Scientific Reports · doi:10.1038/s41598-018-26185-y · Cited by 75 · see citing works

Genetic and Molecular Characterization of a Cryptochrome from the Filamentous Fungus Neurospora crassa

Froehlich, A. C., Chen, C., Belden, W. J., Madeti, C., Roenneberg, T., Merrow, M. W., Loros, J., & Dunlap, J. (2010) · Eukaryotic Cell · doi:10.1128/ec.00380-09 · Cited by 74 · see citing works

The Circadian Clock in Lepidoptera

Brady, D. J., Saviane, A., Cappellozza, S., & Sandrelli, F. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.776826 · Cited by 73 · see citing works

Death Valley, Drosophila, and the Devonian Toolkit

Dickinson, M. H. (2013) · Annual Review of Entomology · doi:10.1146/annurev-ento-011613-162041 · Cited by 73 · see citing works

Cryptochrome-dependent magnetic field effect on seizure response in Drosophila larvae

Marley, R., Giachello, C. N., Scrutton, N. S., Baines, R., & Jones, A. R. (2014) · Scientific Reports · doi:10.1038/srep05799 · Cited by 73 · see citing works

Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila

Lamaze, A., Öztürk‐Çolak, A., Fischer, R., Peschel, N., Koh, K., & Jepson, J. E. C. (2017) · Scientific Reports · doi:10.1038/srep40304 · Cited by 73 · see citing works

DNA Repair in Mammalian Cells

Eker, A. P. M., Quayle, C., Chaves, I., & van der Horst, G. T. J. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-8735-0 · Cited by 72 · see citing works

Molecular evolution and functional divergence of zebrafish (Danio rerio) cryptochrome genes

Liu, C., Hu, J. M., Qu, C., Wang, L., Huang, G., Niu, P., Zhong, Z., Hong, F., Wang, G., Postlethwait, J. H., et al. (2015) · Scientific Reports · doi:10.1038/srep08113 · Cited by 71 · see citing works

Unraveling navigational strategies in migratory insects

Merlin, C., Heinze, S., & Reppert, S. M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.11.009 · Cited by 71 · see citing works

The sensitivity of a radical pair compass magnetoreceptor can be significantly amplified by radical scavengers

Kattnig, D. R., & Hore, P. J. (2017) · Scientific Reports · doi:10.1038/s41598-017-09914-7 · Cited by 70 · see citing works

A near-null magnetic field affects cryptochrome-related hypocotyl growth and flowering in Arabidopsis

Xu, C., Yin, X., Lv, Y., Wu, C., Zhang, Y., & Song, T. (2011) · Advances in Space Research · doi:10.1016/j.asr.2011.12.004 · Cited by 69 · see citing works

Magnetic field effects in flavoproteins and related systems

Evans, E. W., Dodson, C. A., Maeda, K., Biskup, T., Wedge, C. J., & Timmel, C. R. (2013) · Interface Focus · doi:10.1098/rsfs.2013.0037 · Cited by 69 · see citing works

Light-dependent Structural Change of Chicken Retinal Cryptochrome4

Watari, R., Chiaki, Y., Zemba, W., Kubo, Y., Okano, K., & Okano, T. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.395731 · Cited by 68 · see citing works

A Mechanosensory Pathway to the Drosophila Circadian Clock

Simoni, A., Wolfgang, W., Topping, M. P., Kavlie, R. G., Stanewsky, R., & Albert, J. T. (2014) · Science · doi:10.1126/science.1245710 · Cited by 68 · see citing works

Avian magnetite-based magnetoreception: a physiologist's perspective

Cadiou, H., & McNaughton, P. A. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0423.focus · Cited by 68 · see citing works

Essential elements of radical pair magnetosensitivity in Drosophila

Bradlaugh, A. A., Fedele, G., Munro, A. L., Hansen, C. N., Hares, J. M., Patel, S., Kyriacou, C. P., Jones, A. R., Rosato, E., & Baines, R. (2023) · Nature · doi:10.1038/s41586-023-05735-z · Cited by 67 · see citing works

Quantum effects in biology: Bird navigation

Ritz, T. (2011) · Procedia Chemistry · doi:10.1016/j.proche.2011.08.034 · Cited by 67 · see citing works

Essential Role of an Unusually Long-lived Tyrosyl Radical in the Response to Red Light of the Animal-like Cryptochrome aCRY

Oldemeyer, S., Franz, S., Wenzel, S., Essen, L., Mittag, M., & Kottke, T. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.726976 · Cited by 67 · see citing works

Effects of non-ionizing electromagnetic fields on flora and fauna, Part 2 impacts: how species interact with natural and man-made EMF

Levitt, B. B., Lai, H. C., & Manville, A. M. (2021) · Reviews on Environmental Health · doi:10.1515/reveh-2021-0050 · Cited by 65 · see citing works

Photoexcited CRYPTOCHROME 1 Interacts Directly with G-Protein β Subunit AGB1 to Regulate the DNA-Binding Activity of HY5 and Photomorphogenesis in Arabidopsis

Lian, H., Xu, P., He, S., Jun, W., Pan, J., Wang, W., Xu, F., Wang, S., Pan, J., Huang, J., et al. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.08.004 · Cited by 65 · see citing works

Microgravity simulation by diamagnetic levitation: effects of a strong gradient magnetic field on the transcriptional profile of Drosophila melanogaster

Herranz, R., Larkin, O. J., Dijkstra, C., Hill, R., Anthony, P., Davey, M. R., Eaves, L., van Loon, J. J. W. A., Medina, F. J., & Marco, R. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-52 · Cited by 64 · see citing works

Nanomagnetic Control of Intersystem Crossing

Cohen, A. E. (2009) · The Journal of Physical Chemistry A · doi:10.1021/jp907113p · Cited by 64 · see citing works

Photolyase: Dynamics and Mechanisms of Repair of Sun‐Induced DNA Damage

Zhang, M., Wang, L., & Zhong, D. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12695 · Cited by 64 · see citing works

BRAIN PHOTORECEPTOR PATHWAYS CONTRIBUTING TO CIRCADIAN RHYTHMICITY IN CRAYFISH

Sullivan, J. M., Genco, M. C., Marlow, E. D., Benton, J. L., Beltz, B. S., & Sandeman, D. C. (2009) · Chronobiology International · doi:10.1080/07420520903217960 · Cited by 63 · see citing works

Microsecond Deprotonation of Aspartic Acid and Response of the α/β Subdomain Precede C-Terminal Signaling in the Blue Light Sensor Plant Cryptochrome

Thöing, C., Oldemeyer, S., & Kottke, T. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b01404 · Cited by 62 · see citing works

Magnetocarcinogenesis: is there a mechanism for carcinogenic effects of weak magnetic fields?

Juutilainen, J., Herrala, M., Luukkonen, J., Naarala, J., & Hore, P. J. (2018) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2018.0590 · Cited by 62 · see citing works

Magnetic Sensing through the Abdomen of the Honey bee

Liang, C.-H., Chuang, C.-L., Jiang, J., & Yang, E. (2016) · Scientific Reports · doi:10.1038/srep23657 · Cited by 60 · see citing works

Electron–Electron Dipolar Interaction Poses a Challenge to the Radical Pair Mechanism of Magnetoreception

Babcock, N. S., & Kattnig, D. R. (2020) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.0c00370 · Cited by 59 · see citing works

Magnetic Fields Modulate Blue-Light-Dependent Regulation of Neuronal Firing by Cryptochrome

Giachello, C. N., Scrutton, N. S., Jones, A. R., & Baines, R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2140-16.2016 · Cited by 58 · see citing works

Animal cryptochromes mediate magnetoreception by an unconventional photochemical mechanism

Gegear, R. J., Foley, L. E., Casselman, A. L., & Reppert, S. M. (2010) · Nature · doi:10.1038/nature08719 · Cited by 289 · see citing works

A Cryptic Response?

Adler, E. M. (2008) · Science Signaling · doi:10.1126/scisignal.134ec299

Magnetic field effects on behaviour in Drosophila

Reppert, S. M. (2024) · Nature · doi:10.1038/s41586-024-07319-x · Cited by 8 · see citing works

Human cryptochrome exhibits light-dependent magnetosensitivity

Foley, L. E., Gegear, R. J., & Reppert, S. M. (2011) · Nature Communications · doi:10.1038/ncomms1364 · Cited by 214 · see citing works

Cryptochrome Mediates Light-Dependent Magnetosensitivity of Drosophila's Circadian Clock

Yoshii, T., Ahmad, M., & Helfrich-Förster, C. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000086 · Cited by 232 · see citing works