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

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.10579openalex-snapshot
Ultrastructural analysis of a putative magnetoreceptor in the beak of homing pigeons
inferredcites →https://doi.org/10.1007/bf00216612openalex-snapshot
Wavelength-dependent effects of light on magnetic compass orientation in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00612020openalex-snapshot
The use of celestial and magnetic cues by orienting sockeye salmon smolts
inferredcites →https://doi.org/10.1007/s00114-004-0578-9openalex-snapshot
Retinal cryptochrome in a migratory passerine bird: a possible transducer for the avian magnetic compass
inferredcites →https://doi.org/10.1007/s00114-004-0595-8openalex-snapshot
Magnetic compass orientation of migratory birds in the presence of a 1.315�MHz oscillating field
inferredcites →https://doi.org/10.1007/s00114-006-0102-5openalex-snapshot
Avian magnetic compass: fast adjustment to intensities outside the normal functional window
inferredcites →https://doi.org/10.1007/s00114-007-0236-0openalex-snapshot
A novel concept of Fe-mineral-based magnetoreception: histological and physicochemical data from the upper beak of homing pigeons
inferredcites →https://doi.org/10.1007/s001140050422openalex-snapshot
A Magnetic Polarity Compass for Direction Finding in a Subterranean Mammal
inferredcites →https://doi.org/10.1007/s00359-005-0627-7openalex-snapshot
Magnetic orientation and magnetoreception in birds and other animals
inferredcites →https://doi.org/10.1007/s00425-006-0383-0openalex-snapshot
Magnetic intensity affects cryptochrome-dependent responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/0584-8539(95)90101-9openalex-snapshot
Electron paramagnetic resonance. Elementary theory and practical applications
inferredcites →https://doi.org/10.1016/j.cub.2005.07.037openalex-snapshot
Two Different Types of Light-Dependent Responses to Magnetic Fields in Birds
inferredcites →https://doi.org/10.1016/j.cub.2005.08.017openalex-snapshot
Chickens orient using a magnetic compass
inferredcites →https://doi.org/10.1016/s0006-3495(00)76629-xopenalex-snapshot
A Model for Photoreceptor-Based Magnetoreception in Birds
inferredcites →https://doi.org/10.1016/s0301-0104(03)00320-3openalex-snapshot
Anisotropic recombination of an immobilized photoinduced radical pair in a 50-μT magnetic field: a model avian photomagnetoreceptor
inferredcites →https://doi.org/10.1021/cr0204348openalex-snapshot
Structure and Function of DNA Photolyase and Cryptochrome Blue-Light Photoreceptors
inferredcites →https://doi.org/10.1021/ja048220qopenalex-snapshot
Radio Frequency Magnetic Field Effects on a Radical Recombination Reaction: A Diagnostic Test for the Radical Pair Mechanism
inferredcites →https://doi.org/10.1021/ja068209lopenalex-snapshot
Determination of Radical Re-encounter Probability Distributions from Magnetic Field Effects on Reaction Yields
inferredcites →https://doi.org/10.1038/35015128openalex-snapshot
Biological sensing of small field differences by magnetically sensitive chemical reactions
inferredcites →https://doi.org/10.1038/35018561openalex-snapshot
Magnetite defines a vertebrate magnetoreceptor
inferredcites →https://doi.org/10.1038/359142a0openalex-snapshot
Behavioural evidence for use of a light-dependent magnetoreception mechanism by a vertebrate
inferredcites →https://doi.org/10.1038/366162a0openalex-snapshot
HY4 gene of A. thaliana encodes a protein with characteristics of a blue-light photoreceptor
inferredcites →https://doi.org/10.1038/37057openalex-snapshot
Structure and function of the vertebrate magnetic sense
inferredcites →https://doi.org/10.1038/nature00958openalex-snapshot
Lateralization of magnetic compass orientation in a migratory bird
inferredcites →https://doi.org/10.1038/nature02534openalex-snapshot
Resonance effects indicate a radical-pair mechanism for avian magnetic compass
inferredcites →https://doi.org/10.1038/nature03077openalex-snapshot
Magnetoreception and its trigeminal mediation in the homing pigeon
inferredcites →https://doi.org/10.1038/nature06834openalex-snapshot
Chemical compass model of avian magnetoreception
inferredcites →https://doi.org/10.1038/nature07183openalex-snapshot
Cryptochrome mediates light-dependent magnetosensitivity in Drosophila
inferredcites →https://doi.org/10.1038/nsb933openalex-snapshot
Light-induced electron transfer in a cryptochrome blue-light photoreceptor
inferredcites →https://doi.org/10.1063/1.2808029openalex-snapshot
Electron Paramagnetic Resonance: Elementary Theory and Practical Applications
inferredcites →https://doi.org/10.1073/pnas.0405968101openalex-snapshot
Cryptochromes and neuronal-activity markers colocalize in the retina of migratory birds during magnetic orientation
inferredcites →https://doi.org/10.1073/pnas.0803620105openalex-snapshot
Magnetic-field effect on the photoactivation reaction of Escherichia coli DNA photolyase
inferredcites →https://doi.org/10.1074/jbc.m609842200openalex-snapshot
Cryptochrome Blue Light Photoreceptors Are Activated through Interconversion of Flavin Redox States
inferredcites →https://doi.org/10.1080/00268979809483134openalex-snapshot
Effects of weak magnetic fields on free radical recombination reactions
inferredcites →https://doi.org/10.1080/09553000050176270openalex-snapshot
The effects of weak magnetic fields on radical recombination reactions in micelles
inferredcites →https://doi.org/10.1088/1478-3975/3/3/007openalex-snapshot
On the use of magnets to disrupt the physiological compass of birds
inferredcites →https://doi.org/10.1097/00001756-200212030-00016openalex-snapshot
Dual regulation of cryptochrome 1 mRNA expression in chicken retina by light and circadian oscillators
inferredcites →https://doi.org/10.1098/rsif.2006.0130openalex-snapshot
The magnetic compass mechanisms of birds and rodents are based on different physical principles
inferredcites →https://doi.org/10.1098/rspb.2007.0904openalex-snapshot
Bats respond to polarity of a magnetic field
inferredcites →https://doi.org/10.1111/j.1439-0310.1968.tb00028.xopenalex-snapshot
Über den Einfluß statischer Magnetfelder auf die Zugorientierung der Rotkehlchen (Erithacus rubecula)
inferredcites →https://doi.org/10.1126/science.176.4030.62openalex-snapshot
Magnetic Compass of European Robins
inferredcites →https://doi.org/10.1126/science.3738508openalex-snapshot
Two Magnetoreception Pathways in a Migratory Salamander
inferredcites →https://doi.org/10.1186/1742-9994-4-5openalex-snapshot
Light-dependent magnetoreception in birds: increasing intensity of monochromatic light changes the nature of the response.
inferredcites →https://doi.org/10.1242/jeb.004853openalex-snapshot
The magnetic compass of domestic chickens,Gallus gallus
inferredcites →https://doi.org/10.1242/jeb.00874openalex-snapshot
Magnetic orientation in the mealworm beetle Tenebrio and the effect of light
inferredcites →https://doi.org/10.1242/jeb.020313openalex-snapshot
Light-dependent magnetoreception: orientation behaviour of migratory birds under dim red light
inferredcites →https://doi.org/10.1242/jeb.02573openalex-snapshot
Magnetic compass in the cornea: local anaesthesia impairs orientation in a mammal
inferredcites →https://doi.org/10.1242/jeb.155.1.37openalex-snapshot
Magnetic Orientation By Hatchling Loggerhead Sea Turtles (Caretta Caretta)
inferredcites →https://doi.org/10.1242/jeb.182.1.1openalex-snapshot
Geomagnetic Orientation of Loggerhead Sea Turtles: Evidence for an Inclination Compass
inferredcites →https://doi.org/10.1242/jeb.198.10.2041openalex-snapshot
Magnetic Orientation of Spiny Lobsters in the Ocean: Experiments with Undersea Coil Systems
inferredcites →https://doi.org/10.1242/jeb.199.5.1241openalex-snapshot
Does the Avian Ophthalmic Nerve Carry Magnetic Navigational Information?
inferredcites →https://doi.org/10.1242/jeb.204.19.3295openalex-snapshot
Light-dependent magnetoreception in birds: the behaviour of European robins,Erithacus rubecula, under monochromatic light of various wavelengths and intensities
inferredcites →https://doi.org/10.1242/jeb.205.24.3845openalex-snapshot
Magnetic compass orientation in European robins is dependent on both wavelength and intensity of light
inferredcites →https://doi.org/10.1371/journal.pone.0001106openalex-snapshot
Chemical Magnetoreception: Bird Cryptochrome 1a Is Excited by Blue Light and Forms Long-Lived Radical-Pairs
inferredcites →https://doi.org/10.1529/biophysj.106.097139openalex-snapshot
Magnetic Field Effects in Arabidopsis thaliana Cryptochrome-1
inferredcites →https://doi.org/10.1529/biophysj.107.105098openalex-snapshot
Theoretical Analysis of an Iron Mineral-Based Magnetoreceptor Model in Birds
inferredcites →https://doi.org/10.1529/biophysj.107.119362openalex-snapshot
Role of Exchange and Dipolar Interactions in the Radical Pair Model of the Avian Magnetic Compass
inferredcites →https://doi.org/10.2307/1267831openalex-snapshot
Circular Statistics in Biology
inferredcites →https://doi.org/10.2307/2530079openalex-snapshot
Circular Statistics in Biology
inferredcites →https://doi.org/10.2976/1.2714294openalex-snapshot
Magnetoreception in birds: Different physical processes for two types of directional responses

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Effect of Weak Magnetic Fields on Microbial Calcium Carbonate Precipitation: Potential Explanation for the Anti-Scaling Effect of Magnetic Treatment
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Biological Effects of Radiofrequency Energy as Related to Health and Safety
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Radical Enzymes
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EPR–ESR–EMR, an Ongoing Success Story
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Magnetoreception through Cryptochrome May Involve Superoxide
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Relativistic Interactions in the Radical Pair Model of Magnetic Field Sense in CRY-1 Protein of Arabidopsis thaliana
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Visual but not trigeminal mediation of magnetic compass information in a migratory bird
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Anthropogenic electromagnetic noise disrupts magnetic compass orientation in a migratory bird
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Radio waves zap the biomagnetic compass
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Quantum biology
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Magnetosensitivity of tightly bound radical pairs in cryptochrome is enabled by the quantum Zeno effect
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Long-distance navigation and magnetoreception in migratory animals
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Essential elements of radical pair magnetosensitivity in Drosophila
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Quantifying Magnetic Sensitivity of Radical Pair Based Compass by Quantum Fisher Information
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The sensitivity of a radical pair compass magnetoreceptor can be significantly amplified by radical scavengers
inferred← citeshttps://doi.org/10.1038/s41598-018-34007-4openalex-snapshot
An open quantum system approach to the radical pair mechanism
inferred← citeshttps://doi.org/10.1038/s41598-020-67165-5openalex-snapshot
Arabidopsis cryptochrome is responsive to Radiofrequency (RF) electromagnetic fields
inferred← citeshttps://doi.org/10.1038/s41598-020-72579-2openalex-snapshot
A novel isoform of cryptochrome 4 (Cry4b) is expressed in the retina of a night-migratory songbird
inferred← citeshttps://doi.org/10.1038/s41598-021-99753-4openalex-snapshot
Effects of an electric field on sleep quality and life span mediated by ultraviolet (UV)-A/blue light photoreceptor CRYPTOCHROME in Drosophila
inferred← citeshttps://doi.org/10.1038/s41598-022-12460-6openalex-snapshot
Human magnetic sense is mediated by a light and magnetic field resonance-dependent mechanism
inferred← citeshttps://doi.org/10.1038/s41598-023-46547-5openalex-snapshot
Effects of low-level RF fields reveal complex pattern of magnetic input to the avian magnetic compass
inferred← citeshttps://doi.org/10.1038/srep09917openalex-snapshot
Magnetoreception in the wood mouse (Apodemus sylvaticus): influence of weak frequency-modulated radio frequency fields
inferred← citeshttps://doi.org/10.1038/srep22417openalex-snapshot
Dark state population determines magnetic sensitivity in radical pair magnetoreception model
inferred← citeshttps://doi.org/10.1038/srep35443openalex-snapshot
Inhomogeneous ensembles of radical pairs in chemical compasses
inferred← citeshttps://doi.org/10.1038/srep36709openalex-snapshot
Multiscale description of avian migration: from chemical compass to behaviour modeling
inferred← citeshttps://doi.org/10.1039/c1pp05220aopenalex-snapshot
Firefly flashing under strong static magnetic field
inferred← citeshttps://doi.org/10.1039/c2cp23858fopenalex-snapshot
Experimental observation of preferential solvation on a radical ion pair using MARY spectroscopy
inferred← citeshttps://doi.org/10.1039/c3cp52019fopenalex-snapshot
Spin-locking in low-frequency reaction yield detected magnetic resonance
inferred← citeshttps://doi.org/10.1039/c4cp04095copenalex-snapshot
Probing a chemical compass: novel variants of low-frequency reaction yield detected magnetic resonance
inferred← citeshttps://doi.org/10.1039/c5cp06731fopenalex-snapshot
Electron spin relaxation in cryptochrome-based magnetoreception
inferred← citeshttps://doi.org/10.1039/c5sc01830gopenalex-snapshot
Synthesis and investigation of donor–porphyrin–acceptor triads with long-lived photo-induced charge-separate states
inferred← citeshttps://doi.org/10.1039/c9cp00782bopenalex-snapshot
Theoretical insights into the formation and stability of radical oxygen species in cryptochromes
inferred← citeshttps://doi.org/10.1039/c9fd00049fopenalex-snapshot
How quantum is radical pair magnetoreception?
inferred← citeshttps://doi.org/10.1039/c9pp00469fopenalex-snapshot
Cryptochrome mediated magnetic sensitivity in Arabidopsis occurs independently of light-induced electron transfer to the flavin
inferred← citeshttps://doi.org/10.1063/1.4891470openalex-snapshot
Multiple re-encounter approach to radical pair reactions and the role of nonlinear master equations
inferred← citeshttps://doi.org/10.1063/1.4958624openalex-snapshot
Spin relaxation of radicals in cryptochrome and its role in avian magnetoreception
inferred← citeshttps://doi.org/10.1063/1.4963793openalex-snapshot
Floquet theory of radical pairs in radiofrequency magnetic fields
inferred← citeshttps://doi.org/10.1063/1.5128128openalex-snapshot
The reference-probe model for a robust and optimal radical-pair-based magnetic compass sensor
inferred← citeshttps://doi.org/10.1063/1.5131557openalex-snapshot
Quantum control of radical pair reactions by local optimization theory
inferred← citeshttps://doi.org/10.1063/1.5133019openalex-snapshot
Electron transfer and spin dynamics of the radical-pair in the cryptochrome from Chlamydomonas reinhardtii by computational analysis
inferred← citeshttps://doi.org/10.1063/5.0038947openalex-snapshot
Nuclear polarization effects in cryptochrome-based magnetoreception
inferred← citeshttps://doi.org/10.1063/5.0078115openalex-snapshot
Anisotropic magnetic field effects in the re-oxidation of cryptochrome in the presence of scavenger radicals
inferred← citeshttps://doi.org/10.1063/5.0149644openalex-snapshot
On the anisotropic weak magnetic field effect in radical-pair reactions
inferred← citeshttps://doi.org/10.1063/5.0304559openalex-snapshot
Engineering the uncontrollable: Steering noisy spin-correlated radical-pairs with coherent and in coherent control
inferred← citeshttps://doi.org/10.1063/5.0314129openalex-snapshot
Introduction to modeling radical pair quantum spin dynamics with tensor networks
inferred← citeshttps://doi.org/10.1063/5.0348452openalex-snapshot
Microscopic dissection of chirality-induced spin selectivity in cryptochrome
inferred← citeshttps://doi.org/10.1070/rc2014v083n01abeh004335openalex-snapshot
Magnetic field-dependent molecular and chemical processes in biochemistry, genetics and medicine
inferred← citeshttps://doi.org/10.1073/pnas.0711968106openalex-snapshot
Chemical magnetoreception in birds: The radical pair mechanism
inferred← citeshttps://doi.org/10.1073/pnas.1120531109openalex-snapshot
Are biochemical reactions affected by weak magnetic fields?
inferred← citeshttps://doi.org/10.1073/pnas.1513391113openalex-snapshot
Polarized light modulates light-dependent magnetic compass orientation in birds
inferred← citeshttps://doi.org/10.1073/pnas.1600341113openalex-snapshot
The quantum needle of the avian magnetic compass
inferred← citeshttps://doi.org/10.1073/pnas.2301153120openalex-snapshot
Upper bound for broadband radiofrequency field disruption of magnetic compass orientation in night-migratory songbirds
inferred← citeshttps://doi.org/10.1074/jbc.m111.228940openalex-snapshot
Light-activated Cryptochrome Reacts with Molecular Oxygen to Form a Flavin–Superoxide Radical Pair Consistent with Magnetoreception
inferred← citeshttps://doi.org/10.1080/00268976.2016.1149631openalex-snapshot
Magnetic field effects in proteins
inferred← citeshttps://doi.org/10.1080/03949370.2020.1870571openalex-snapshot
Cryptochrome 1a localisation in light- and dark-adapted retinae of several migratory and non-migratory bird species: no signs of light-dependent activation
inferred← citeshttps://doi.org/10.1080/10643389.2013.781935openalex-snapshot
Environmental Impact of Radiofrequency Fields from Mobile Phone Base Stations
inferred← citeshttps://doi.org/10.1088/1361-6463/ac5554openalex-snapshot
A mechanism of compass-free migratory navigation
inferred← citeshttps://doi.org/10.1088/1367-2630/15/8/083024openalex-snapshot
Radical-pair model of magnetoreception with spin–orbit coupling
inferred← citeshttps://doi.org/10.1088/1367-2630/aad70fopenalex-snapshot
Molecular dynamics simulations disclose early stages of the photo-activation of cryptochrome 4
inferred← citeshttps://doi.org/10.1088/1367-2630/abed0bopenalex-snapshot
Chiral-induced spin selectivity in the formation and recombination of radical pairs: cryptochrome magnetoreception and EPR detection
inferred← citeshttps://doi.org/10.1088/2058-9565/ad48b4openalex-snapshot
On the optimality of the radical-pair quantum compass
inferred← citeshttps://doi.org/10.1088/2058-9565/ad68a1openalex-snapshot
Bang-bang optimal control in coherent spin dynamics of radical pairs in quantum biology
inferred← citeshttps://doi.org/10.1093/aob/mct052openalex-snapshot
Arabidopsis thaliana root elongation growth is sensitive to lunisolar tidal acceleration and may also be weakly correlated with geomagnetic variations
inferred← citeshttps://doi.org/10.1093/conphys/cov072openalex-snapshot
Conservation physiology of animal migration
inferred← citeshttps://doi.org/10.1093/czoolo/56.3.265openalex-snapshot
Avian magnetic compass: Its functional properties and physical basis
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190456757.013.16openalex-snapshot
Magnetoreception of Invertebrates
inferred← citeshttps://doi.org/10.1098/rsfs.2013.0037openalex-snapshot
Magnetic field effects in flavoproteins and related systems
inferred← citeshttps://doi.org/10.1098/rsif.2008.0519openalex-snapshot
Effect of magnetic fields on cryptochrome-dependent responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1098/rsif.2009.0367.focusopenalex-snapshot
Directional orientation of birds by the magnetic field under different light conditions
inferred← citeshttps://doi.org/10.1098/rsif.2009.0376.focusopenalex-snapshot
Night-migratory garden warblers can orient with their magnetic compass using the left, the right or both eyes
inferred← citeshttps://doi.org/10.1098/rsif.2009.0378.focusopenalex-snapshot
Can disordered radical pair systems provide a basis for a magnetic compass in animals?
inferred← citeshttps://doi.org/10.1098/rsif.2009.0399.focusopenalex-snapshot
Effects of disorder and motion in a radical pair magnetoreceptor
inferred← citeshttps://doi.org/10.1098/rsif.2009.0411.focusopenalex-snapshot
Cryptochromes—a potential magnetoreceptor: what do we know and what do we want to know?
inferred← citeshttps://doi.org/10.1098/rsif.2009.0456.focusopenalex-snapshot
Photoreceptor-based magnetoreception: optimal design of receptor molecules, cells, and neuronal processing
inferred← citeshttps://doi.org/10.1098/rsif.2009.0459.focusopenalex-snapshot
Light-dependent magnetic compass orientation in amphibians and insects: candidate receptors and candidate molecular mechanisms
inferred← citeshttps://doi.org/10.1098/rsif.2009.0491.focusopenalex-snapshot
Biophysics of magnetic orientation: strengthening the interface between theory and experimental design
inferred← citeshttps://doi.org/10.1098/rsif.2010.0159openalex-snapshot
Differential effects of magnetic pulses on the orientation of naturally migrating birds
inferred← citeshttps://doi.org/10.1098/rsif.2012.0374openalex-snapshot
Compass magnetoreception in birds arising from photo-induced radical pairs in rotationally disordered cryptochromes
inferred← citeshttps://doi.org/10.1098/rsif.2013.0638openalex-snapshot
Magnetoreception: activated cryptochrome 1a concurs with magnetic orientation in birds
inferred← citeshttps://doi.org/10.1098/rsif.2013.1063openalex-snapshot
Alternative radical pairs for cryptochrome-based magnetoreception
inferred← citeshttps://doi.org/10.1098/rsif.2014.0451openalex-snapshot
Magnetic orientation of garden warblers ( Sylvia borin ) under 1.4 MHz radiofrequency magnetic field
inferred← citeshttps://doi.org/10.1098/rsif.2014.0777openalex-snapshot
Magnetic field-driven induction of ZENK in the trigeminal system of pigeons ( Columba livia )
inferred← citeshttps://doi.org/10.1098/rsif.2014.1103openalex-snapshot
Magnetoreception in birds: the effect of radio-frequency fields
inferred← citeshttps://doi.org/10.1098/rsif.2015.1010openalex-snapshot
Light-dependent magnetoreception in birds: the crucial step occurs in the dark
inferred← citeshttps://doi.org/10.1098/rsif.2017.0364openalex-snapshot
Very weak oscillating magnetic field disrupts the magnetic compass of songbird migrants
inferred← citeshttps://doi.org/10.1098/rsif.2017.0405openalex-snapshot
A light-dependent magnetoreception mechanism insensitive to light intensity and polarization
inferred← citeshttps://doi.org/10.1098/rsif.2019.0285openalex-snapshot
Weak radiofrequency fields affect the insect circadian clock
inferred← citeshttps://doi.org/10.1098/rsif.2019.0295openalex-snapshot
Magnetoreception in birds
inferred← citeshttps://doi.org/10.1098/rsif.2019.0716openalex-snapshot
Electromagnetic 0.1–100 kHz noise does not disrupt orientation in a night-migrating songbird implying a spin coherence lifetime of less than 10 µs
inferred← citeshttps://doi.org/10.1098/rsif.2022.0325openalex-snapshot
Magnetic field effects in biology from the perspective of the radical pair mechanism
inferred← citeshttps://doi.org/10.1098/rsif.2024.0133openalex-snapshot
Orientation of birds in radiofrequency fields in the absence of the Earth’s magnetic field: a possible test for the radical pair mechanism of magnetoreception
inferred← citeshttps://doi.org/10.1098/rsif.2025.0225openalex-snapshot
Directionality range in Emlen funnels
inferred← citeshttps://doi.org/10.1098/rspa.2016.0822openalex-snapshot
Quantum effects in biology: golden rule in enzymes, olfaction, photosynthesis and magnetodetection
inferred← citeshttps://doi.org/10.1098/rspa.2020.0778openalex-snapshot
The avian compass can be sensitive even without sustained electron spin coherence
inferred← citeshttps://doi.org/10.1098/rspb.2013.0853openalex-snapshot
Avian magnetic compass can be tuned to anomalously low magnetic intensities
inferred← citeshttps://doi.org/10.1098/rspb.2018.0590openalex-snapshot
Magnetocarcinogenesis: is there a mechanism for carcinogenic effects of weak magnetic fields?
inferred← citeshttps://doi.org/10.1098/rsta.2011.0488openalex-snapshot
Decoherence in the chemical compass: the role of decoherence for avian magnetoreception
inferred← citeshttps://doi.org/10.1101/2021.10.29.466426openalex-snapshot
Essential elements of radical pair magnetosensitivity in Drosophila
inferred← citeshttps://doi.org/10.1101/2022.08.08.503164openalex-snapshot
Isotope effects on radical pair performance in cryptochrome: a new hypothesis for the evolution of animal migration
inferred← citeshttps://doi.org/10.1103/4l3h-b66copenalex-snapshot
Interradical motion can push magnetosensing precision toward quantum limits
inferred← citeshttps://doi.org/10.1103/physreva.85.040304openalex-snapshot
Quantum limits for the magnetic sensitivity of a chemical compass
inferred← citeshttps://doi.org/10.1103/physreva.94.062126openalex-snapshot
Temporal steering in four dimensions with applications to coupled qubits and magnetoreception
inferred← citeshttps://doi.org/10.1103/physrevb.85.245213openalex-snapshot
Effects of spin-spin interactions on magnetoresistance in disordered organic semiconductors
inferred← citeshttps://doi.org/10.1103/physreve.80.041919openalex-snapshot
Micromagnetic insight into a magnetoreceptor in birds: Existence of magnetic field amplifiers in the beak
inferred← citeshttps://doi.org/10.1103/physreve.88.032703openalex-snapshot
Estimating the hyperfine coupling parameters of the avian compass by comprehensively considering the available experimental results
inferred← citeshttps://doi.org/10.1103/physreve.90.042707openalex-snapshot
Sensitivity and entanglement in the avian chemical compass
inferred← citeshttps://doi.org/10.1103/physreve.90.042710openalex-snapshot
Quantum dynamics of the avian compass
inferred← citeshttps://doi.org/10.1103/physreve.90.042711openalex-snapshot
Effect of radio frequency fields on the radical pair magnetoreception model
inferred← citeshttps://doi.org/10.1103/physreve.91.042137openalex-snapshot
Statistical theory of designed quantum transport across disordered networks
inferred← citeshttps://doi.org/10.1103/physreve.91.052709openalex-snapshot
State transitions and decoherence in the avian compass
inferred← citeshttps://doi.org/10.1103/physreve.92.012720openalex-snapshot
Environment-induced anisotropy and sensitivity of the radical pair mechanism in the avian compass
inferred← citeshttps://doi.org/10.1103/physreve.95.052417openalex-snapshot
Functional window of the avian compass
inferred← citeshttps://doi.org/10.1103/physreve.96.042404openalex-snapshot
Biological cell as a soft magnetoelectric material: Elucidating the physical mechanisms underpinning the detection of magnetic fields by animals
inferred← citeshttps://doi.org/10.1103/physrevlett.104.220502openalex-snapshot
Quantum Control and Entanglement in a Chemical Compass
inferred← citeshttps://doi.org/10.1103/physrevlett.106.040503openalex-snapshot
Sustained Quantum Coherence and Entanglement in the Avian Compass
inferred← citeshttps://doi.org/10.1103/physrevlett.106.100501openalex-snapshot
Quantum Probe and Design for a Chemical Compass with Magnetic Nanostructures
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