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Microsaccadic sampling of moving image information provides Drosophila hyperacute vision
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cne.10929openalex-snapshot
Chemical neuroanatomy of the fly's movement detection pathway
inferredcites →https://doi.org/10.1002/cne.903050206openalex-snapshot
Synaptic organization of columnar elements in the lamina of the wild type in Drosophila melanogaster
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05732.xopenalex-snapshot
Genetic and molecular identification of a Drosophila histidine decarboxylase gene required in photoreceptor transmitter synthesis.
inferredcites →https://doi.org/10.1007/978-1-4614-6675-8_333openalex-snapshot
Phototransduction Biophysics
inferredcites →https://doi.org/10.1007/978-3-642-10677-4_5openalex-snapshot
Data Modelling for Analysis of Adaptive Changes in Fly Photoreceptors
inferredcites →https://doi.org/10.1007/978-3-642-70408-6_1openalex-snapshot
Functional Organization of the Fly Retina
inferredcites →https://doi.org/10.1007/978-3-642-74082-4_3openalex-snapshot
Optics and Evolution of the Compound Eye
inferredcites →https://doi.org/10.1007/978-94-017-0619-3_3openalex-snapshot
Compound eye structure: Matching eye to environment
inferredcites →https://doi.org/10.1007/bf00188924openalex-snapshot
Theoretical predictions of spatiotemporal receptive fields of fly LMCs, and experimental validation
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Did neural pooling for night vision lead to the evolution of neural superposition eyes?
inferredcites →https://doi.org/10.1007/bf00203134openalex-snapshot
A theory of maximizing sensory information
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Genetic depletion of histamine from the nervous system of Drosophila eliminates specific visual and mechanosensory behavior
inferredcites →https://doi.org/10.1007/bf00213533openalex-snapshot
Linear and non-linear contrast coding in light-adapted blowfly photoreceptors
inferredcites →https://doi.org/10.1007/bf00213681openalex-snapshot
Three modes of spatiotemporal preprocessing by eyes
inferredcites →https://doi.org/10.1007/bf00213682openalex-snapshot
Fast and slow photoreceptors ? a comparative study of the functional diversity of coding and conductances in the Diptera
inferredcites →https://doi.org/10.1007/bf00214790openalex-snapshot
Rhabdom size and photoreceptor membrane turnover in a muscoid fly
inferredcites →https://doi.org/10.1007/bf00261833openalex-snapshot
Direct connections between the R7/8 and R1?6 photoreceptor subsystems in the dipteran visual system
inferredcites →https://doi.org/10.1007/bf00270828openalex-snapshot
Etude optique in vivo des éléments photorécepteurs dans l'œil composé de Drosophila
inferredcites →https://doi.org/10.1007/bf00270852openalex-snapshot
Das augenmuskelsystem der stubenfliege musca domestica
inferredcites →https://doi.org/10.1007/bf00272463openalex-snapshot
Development and application of white-noise modeling techniques for studies of insect visual nervous system
inferredcites →https://doi.org/10.1007/bf00288561openalex-snapshot
Optomotorische Untersuchung des visuellen systems einiger Augenmutanten der Fruchtfliege Drosophila
inferredcites →https://doi.org/10.1007/bf00288624openalex-snapshot
Ein Mechanismus zur Steuerung des Lichtflusses in den Rhabdomeren des Komplexauges von Musca
inferredcites →https://doi.org/10.1007/bf00299273openalex-snapshot
Visual field of single retinula cells and interommatidial inclination in the compound eye of the blowfly Calliphora erythrocephala
inferredcites →https://doi.org/10.1007/bf00303230openalex-snapshot
Lateral inhibition in an insect eye
inferredcites →https://doi.org/10.1007/bf00307446openalex-snapshot
Electrophysiological-histological studies on some functional properties of visual cells and second order neurons of an insect retina
inferredcites →https://doi.org/10.1007/bf00326704openalex-snapshot
Nonlinear dynamic transfer characteristics of cells in the peripheral visual pathway of flies
inferredcites →https://doi.org/10.1007/bf00331193openalex-snapshot
On the fine structure of the peripheral retina and lamina ganglionaris of the fly, Musca domestica
inferredcites →https://doi.org/10.1007/bf00337126openalex-snapshot
On optical crosstalk between fly rhabdomeres
inferredcites →https://doi.org/10.1007/bf00337254openalex-snapshot
A study of the response properties of retinula cells of flies using nonlinear identification theory
inferredcites →https://doi.org/10.1007/bf00344164openalex-snapshot
Le contr�le automatique du flux lumineux dans l'oeil compos� des Dipt�res
inferredcites →https://doi.org/10.1007/bf00360648openalex-snapshot
Elementary movement detectors in an insect visual system
inferredcites →https://doi.org/10.1007/bf00366593openalex-snapshot
Specific misalignments of rhabdomere visual axes in the neural superposition eye of dipteran flies
inferredcites →https://doi.org/10.1007/bf00604981openalex-snapshot
Properties of photoreceptors R7 and R8 in dorsal marginal ommatidia in the compound eyes ofMusca andCalliphora
inferredcites →https://doi.org/10.1007/bf00605029openalex-snapshot
Distribution and properties of sex-specific photoreceptors in the flyMusca domestica
inferredcites →https://doi.org/10.1007/bf00605031openalex-snapshot
Changes in the intensity-response function of an insect's photoreceptors due to light adaptation
inferredcites →https://doi.org/10.1007/bf00605384openalex-snapshot
Comparison of stimulus-response (V-log I) functions in five types of lepidopteran compound eyes (46 species)
inferredcites →https://doi.org/10.1007/bf00605401openalex-snapshot
Acuity of compound eyes: Physical limitations and design
inferredcites →https://doi.org/10.1007/bf00605402openalex-snapshot
Spatial information capacity of compound eyes
inferredcites →https://doi.org/10.1007/bf00609937openalex-snapshot
Receptive field patterns in photoreceptors of the fly
inferredcites →https://doi.org/10.1007/bf00610276openalex-snapshot
Visual movement detection under light- and dark-adaptation in the fly,Musca domestica
inferredcites →https://doi.org/10.1007/bf00610676openalex-snapshot
Waveguide theory applied to optically measured angular sensitivities of fly photoreceptors
inferredcites →https://doi.org/10.1007/bf00612641openalex-snapshot
Angular sensitivity of blowfly photoreceptors: intracellular measurements and wave-optical predictions
inferredcites →https://doi.org/10.1007/bf00612703openalex-snapshot
The spatial integration of signals in the retina and lamina of the fly compound eye under different conditions of luminance
inferredcites →https://doi.org/10.1007/bf00612784openalex-snapshot
The r�le of retinula cell types in visual behavior ofDrosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00613743openalex-snapshot
Spatial processing of visual information in the movement-detecting pathway of the fly
inferredcites →https://doi.org/10.1007/bf00615083openalex-snapshot
Angular sensitivity of blowfly photoreceptors: broadening by artificial electrical coupling
inferredcites →https://doi.org/10.1007/bf00631968openalex-snapshot
Angular sensitivity of light and dark adapted locust retinula cells
inferredcites →https://doi.org/10.1007/bf00657606openalex-snapshot
Common strategies for light adaptation in the peripheral visual systems of fly and dragonfly
inferredcites →https://doi.org/10.1007/bf00679908openalex-snapshot
Electrophysiological analysis of fly retina. I: Comparative properties of R1-6 and R 7 and 8
inferredcites →https://doi.org/10.1007/bf00698364openalex-snapshot
A regular net of reciprocal synapses in the visual system of the fly,Musca domestica
inferredcites →https://doi.org/10.1007/bf01324822openalex-snapshot
Electrical coupling of neuro-ommatidial photoreceptor cells in the blowfly
inferredcites →https://doi.org/10.1007/bf02163027openalex-snapshot
Singular value decomposition and least squares solutions
inferredcites →https://doi.org/10.1007/bf02215177openalex-snapshot
Les phénomènes de pseudopupille dans l'œil composé deDrosophila
inferredcites →https://doi.org/10.1007/bf02364581openalex-snapshot
Exact orthogonal kernel estimation from finite data records: Extending Wiener's identification of nonlinear systems
inferredcites →https://doi.org/10.1007/bf02368043openalex-snapshot
Applications of fast orthogonal search: Time-series analysis and resolution of signals in noise
inferredcites →https://doi.org/10.1007/s00359-002-0370-2openalex-snapshot
Angular and spectral sensitivity of fly photoreceptors. I. Integrated facet lens and rhabdomere optics
inferredcites →https://doi.org/10.1007/s00359-003-0390-6openalex-snapshot
Angular and spectral sensitivity of fly photoreceptors. II. Dependence on facet lens F-number and rhabdomere type in Drosophila
inferredcites →https://doi.org/10.1007/s00359-003-0477-0openalex-snapshot
Angular and spectral sensitivity of fly photoreceptors. III. Dependence on the pupil mechanism in the blowfly Calliphora
inferredcites →https://doi.org/10.1007/s00359-004-0541-4openalex-snapshot
Saccadic head and thorax movements in freely walking blowflies
inferredcites →https://doi.org/10.1007/s003590050393openalex-snapshot
Motion and vision: why animals move their eyes
inferredcites →https://doi.org/10.1007/s00441-005-0034-yopenalex-snapshot
A neural network to improve dim-light vision? Dendritic fields of first-order interneurons in the nocturnal bee Megalopta genalis
inferredcites →https://doi.org/10.1016/0042-6989(75)90029-2openalex-snapshot
The effect of motion on visual acuity of the compound eye: A theoretical analysis
inferredcites →https://doi.org/10.1016/0042-6989(82)90086-4openalex-snapshot
Spectral analysis of spatial sampling by photoreceptors: Topological disorder prevents aliasing
inferredcites →https://doi.org/10.1016/0042-6989(85)90210-xopenalex-snapshot
Shouldn't directional movement detection necessarily be “colour-blind”?
inferredcites →https://doi.org/10.1016/0042-6989(93)90163-qopenalex-snapshot
Spatiotemporal contrast sensitivity of early vision
inferredcites →https://doi.org/10.1016/0301-0082(93)90017-mopenalex-snapshot
Arthropod eye design and the physical limits to spatial resolving power
inferredcites →https://doi.org/10.1016/0896-6273(93)90268-vopenalex-snapshot
Spectral tuning of rhodopsin and metarhodopsin in vivo
inferredcites →https://doi.org/10.1016/j.cell.2016.05.031openalex-snapshot
Subcellular Imaging of Voltage and Calcium Signals Reveals Neural Processing In Vivo
inferredcites →https://doi.org/10.1016/j.conb.2015.01.008openalex-snapshot
Phototransduction in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2010.06.072openalex-snapshot
Walking Modulates Speed Sensitivity in Drosophila Motion Vision
inferredcites →https://doi.org/10.1016/j.cub.2011.10.022openalex-snapshot
Wiring Economy and Volume Exclusion Determine Neuronal Placement in the Drosophila Brain
inferredcites →https://doi.org/10.1016/j.cub.2011.11.028openalex-snapshot
Genetic Dissection Reveals Two Separate Retinal Substrates for Polarization Vision in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2012.01.050openalex-snapshot
Temporal Encoding of Spatial Information during Active Visual Fixation
inferredcites →https://doi.org/10.1016/j.cub.2012.05.047openalex-snapshot
Stochastic, Adaptive Sampling of Information by Microvilli in Fly Photoreceptors
inferredcites →https://doi.org/10.1016/j.cub.2013.07.007openalex-snapshot
Microscopic Eye Movements Compensate for Nonhomogeneous Vision within the Fovea
inferredcites →https://doi.org/10.1016/j.cub.2016.01.030openalex-snapshot
Neural Summation in the Hawkmoth Visual System Extends the Limits of Vision in Dim Light
inferredcites →https://doi.org/10.1016/j.neuron.2013.04.024openalex-snapshot
GABAergic Lateral Interactions Tune the Early Stages of Visual Processing in Drosophila
inferredcites →https://doi.org/10.1016/j.tcb.2006.11.006openalex-snapshot
Adherens junctions in Drosophila retinal morphogenesis
inferredcites →https://doi.org/10.1016/j.tins.2015.01.005openalex-snapshot
The unsteady eye: an information-processing stage, not a bug
inferredcites →https://doi.org/10.1016/j.visres.2006.11.024openalex-snapshot
Modelling the effect of microsaccades on retinal responses to stationary contrast patterns
inferredcites →https://doi.org/10.1016/j.visres.2012.06.011openalex-snapshot
Hyperacute motion detection by the lateral eyes of jumping spiders
inferredcites →https://doi.org/10.1016/s0006-3495(93)81116-0openalex-snapshot
The dynamic nonlinear behavior of fly photoreceptors evoked by a wide range of light intensities
inferredcites →https://doi.org/10.1016/s0042-6989(00)00067-5openalex-snapshot
Motion extrapolation is not responsible for the flash–lag effect
inferredcites →https://doi.org/10.1016/s0042-6989(97)00105-3openalex-snapshot
Processing of natural time series of intensities by the visual system of the blowfly
inferredcites →https://doi.org/10.1016/s0042-6989(98)00262-4openalex-snapshot
Seeing better at night: life style, eye design and the optimum strategy of spatial and temporal summation
inferredcites →https://doi.org/10.1016/s0042-6989(99)00171-6openalex-snapshot
Photoreceptor performance and the co-ordination of achromatic and chromatic inputs in the fly visual system
inferredcites →https://doi.org/10.1016/s0166-2236(00)01795-1openalex-snapshot
Neuronal latencies and the position of moving objects
inferredcites →https://doi.org/10.1016/s1364-6613(02)01963-0openalex-snapshot
Neural delays, visual motion and the flash-lag effect
inferredcites →https://doi.org/10.1017/cbo9781139174190openalex-snapshot
Introduction to Optics and Lasers in Engineering
inferredcites →https://doi.org/10.1017/s0952523800007495openalex-snapshot
Calcium homeostasis in photoreceptor cells ofDrosophilamutantsinaCandtrpstudied with the pupil mechanism
inferredcites →https://doi.org/10.1038/170036a0openalex-snapshot
Vision with a Stabilized Retinal Image
inferredcites →https://doi.org/10.1038/18678openalex-snapshot
Anticipation of moving stimuli by the retina
inferredcites →https://doi.org/10.1038/243299a0openalex-snapshot
Head Movement of Flies during Visually Guided Flight
inferredcites →https://doi.org/10.1038/255480a0openalex-snapshot
Retinal resistance barriers and electrical lateral inhibition
inferredcites →https://doi.org/10.1038/360068a0openalex-snapshot
Real and optimal neural images in early vision
inferredcites →https://doi.org/10.1038/379642a0openalex-snapshot
The rate of information transfer at graded-potential synapses
inferredcites →https://doi.org/10.1038/nature01384openalex-snapshot
The contribution of Shaker K+ channels to the information capacity of Drosophila photoreceptors
inferredcites →https://doi.org/10.1038/nature03066openalex-snapshot
TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells
inferredcites →https://doi.org/10.1038/nature05866openalex-snapshot
Miniature eye movements enhance fine spatial detail
inferredcites →https://doi.org/10.1038/nature09424openalex-snapshot
Functional connectivity in the retina at the resolution of photoreceptors
inferredcites →https://doi.org/10.1038/nature09545openalex-snapshot
ON and OFF pathways in Drosophila motion vision
inferredcites →https://doi.org/10.1038/nature10451openalex-snapshot
Feedback from rhodopsin controls rhodopsin exclusion in Drosophila photoreceptors
inferredcites →https://doi.org/10.1038/nature13427openalex-snapshot
Processing properties of ON and OFF pathways for Drosophila motion detection
inferredcites →https://doi.org/10.1038/nature14446openalex-snapshot
Neural dynamics for landmark orientation and angular path integration
inferredcites →https://doi.org/10.1038/nn.2269openalex-snapshot
Different receptive fields in axons and dendrites underlie robust coding in motion-sensitive neurons
inferredcites →https://doi.org/10.1038/nn.2492openalex-snapshot
Active flight increases the gain of visual motion processing in Drosophila
inferredcites →https://doi.org/10.1038/nn.3386openalex-snapshot
Object tracking in motion-blind flies
inferredcites →https://doi.org/10.1038/npre.2010.4325.1openalex-snapshot
Intrinsic Activity in the Fly Brain Gates Visual Information during Behavioral Choices
inferredcites →https://doi.org/10.1038/nrn3405openalex-snapshot
The impact of microsaccades on vision: towards a unified theory of saccadic function
inferredcites →https://doi.org/10.1068/v970196openalex-snapshot
Up-Down Asymmetries in Speed Perception
inferredcites →https://doi.org/10.1073/pnas.1005846107openalex-snapshot
Retina is structured to process an excess of darkness in natural scenes
inferredcites →https://doi.org/10.1073/pnas.1009381107openalex-snapshot
Central gating of fly optomotor response
inferredcites →https://doi.org/10.1073/pnas.1014438108openalex-snapshot
Compound eyes and retinal information processing in miniature dipteran species match their specific ecological demands
inferredcites →https://doi.org/10.1073/pnas.1310442111openalex-snapshot
Neuronal nonlinearity explains greater visual spatial resolution for darks than lights
inferredcites →https://doi.org/10.1073/pnas.1323297111openalex-snapshot
Selective attention in the honeybee optic lobes precedes behavioral choices
inferredcites →https://doi.org/10.1073/pnas.93.12.6079openalex-snapshot
Behavioral genetics of thermosensation and hygrosensation in Drosophila.
inferredcites →https://doi.org/10.1083/jcb.17.1.208openalex-snapshot
THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY
inferredcites →https://doi.org/10.1085/jgp.104.3.593openalex-snapshot
Contrast gain, signal-to-noise ratio, and linearity in light-adapted blowfly photoreceptors.
inferredcites →https://doi.org/10.1085/jgp.105.1.117openalex-snapshot
Transfer of graded potentials at the photoreceptor-interneuron synapse.
inferredcites →https://doi.org/10.1085/jgp.117.1.27openalex-snapshot
Light Adaptation in Drosophila Photoreceptors
inferredcites →https://doi.org/10.1085/jgp.117.1.3openalex-snapshot
Light Adaptation in Drosophila Photoreceptors
inferredcites →https://doi.org/10.1085/jgp.200308824openalex-snapshot
The Rate of Information Transfer of Naturalistic Stimulation by Graded Potentials
inferredcites →https://doi.org/10.1085/jgp.200509470openalex-snapshot
Feedback Network Controls Photoreceptor Output at the Layer of First Visual Synapses in Drosophila
inferredcites →https://doi.org/10.1085/jgp.79.6.1089openalex-snapshot
Adapting bump model for ventral photoreceptors of Limulus.
inferredcites →https://doi.org/10.1088/0954-898x_3_2_009openalex-snapshot
Could information theory provide an ecological theory of sensory processing?
inferredcites →https://doi.org/10.1098/rspb.1982.0085openalex-snapshot
Predictive coding: a fresh view of inhibition in the retina
inferredcites →https://doi.org/10.1098/rspb.1996.0222openalex-snapshot
Neural image enhancement allows honeybees to see at night
inferredcites →https://doi.org/10.1098/rspb.2000.1257openalex-snapshot
Sexual dimorphism matches photoreceptor performance to behavioural requirements
inferredcites →https://doi.org/10.1109/jsen.2010.2099112openalex-snapshot
A Multiaperture Bioinspired Sensor With Hyperacuity
inferredcites →https://doi.org/10.1109/tbme.2004.840187openalex-snapshot
Use of Meixner Functions in Estimation of Volterra Kernels of Nonlinear Systems With Delay
inferredcites →https://doi.org/10.1111/j.1469-7793.2000.00179.xopenalex-snapshot
Single photon responses in Drosophila photoreceptors and their regulation by Ca 2+
inferredcites →https://doi.org/10.1111/j.1475-1313.1992.tb00281.xopenalex-snapshot
Retinal information capacity and the function of the pupil
inferredcites →https://doi.org/10.1113/jp273645openalex-snapshot
How a fly photoreceptor samples light information in time
inferredcites →https://doi.org/10.1113/jphysiol.1981.sp013827openalex-snapshot
Single photon signals in fly photoreceptors and first order interneurones at behavioral threshold.
inferredcites →https://doi.org/10.1114/1.58openalex-snapshot
Two Methods for Calculating the Responses of Photoreceptors to Moving Objects
inferredcites →https://doi.org/10.1126/science.1058237openalex-snapshot
Choice Behavior of Drosophila Facing Contradictory Visual Cues
inferredcites →https://doi.org/10.1126/science.1081944openalex-snapshot
The Aerodynamics of Free-Flight Maneuvers in Drosophila
inferredcites →https://doi.org/10.1126/science.1099839openalex-snapshot
Visual Pattern Recognition in Drosophila Is Invariant for Retinal Position
inferredcites →https://doi.org/10.1126/science.1137931openalex-snapshot
Attention-Like Processes in Drosophila Require Short-Term Memory Genes
inferredcites →https://doi.org/10.1126/science.1215317openalex-snapshot
Multiple Spectral Inputs Improve Motion Discrimination in the Drosophila Visual System
inferredcites →https://doi.org/10.1126/science.1222376openalex-snapshot
Photomechanical Responses in Drosophila Photoreceptors
inferredcites →https://doi.org/10.1145/325165.325182openalex-snapshot
Antialiasing through stochastic sampling
inferredcites →https://doi.org/10.1146/annurev.bb.17.060188.000531openalex-snapshot
Mechanoelectrical Transduction by Hair Cells
inferredcites →https://doi.org/10.1146/annurev.ento.42.1.147openalex-snapshot
VISUAL ACUITY IN INSECTS
inferredcites →https://doi.org/10.1152/jn.00395.2003openalex-snapshot
ShakerK+Channels Contribute Early Nonlinear Amplification to the Light Response inDrosophilaPhotoreceptors
inferredcites →https://doi.org/10.1152/jn.01163.2003openalex-snapshot
Interactions Between Light-Induced Currents, Voltage-Gated Currents, and Input Signal Properties inDrosophilaPhotoreceptors
inferredcites →https://doi.org/10.1152/jn.1995.73.5.1782openalex-snapshot
Graded responses and spiking properties of identified first-order visual interneurons of the fly compound eye
inferredcites →https://doi.org/10.1152/jn.1995.74.6.2538openalex-snapshot
Nonlinear models of the first synapse in the light-adapted fly retina
inferredcites →https://doi.org/10.1152/jn.1997.77.3.1487openalex-snapshot
Visual Acuity for Moving Objects in First- and Second-Order Neurons of the Fly Compound Eye
inferredcites →https://doi.org/10.1152/jn.2001.86.2.950openalex-snapshot
Variations in Photoreceptor Response Dynamics Across the Fly Retina
inferredcites →https://doi.org/10.1167/8.11.8openalex-snapshot
Photoreceptor processing improves salience facilitating small target detection in cluttered scenes
inferredcites →https://doi.org/10.1167/9.4.18openalex-snapshot
Optimum spatiotemporal receptive fields for vision in dim light
inferredcites →https://doi.org/10.1201/9781351075060-1openalex-snapshot
Nonlinear Systems Analysis in Vision: Overview of Kernel Methods
inferredcites →https://doi.org/10.1201/9781351075060-15openalex-snapshot
The Trade-Off Between Resolution and Sensitivity in Compound Eyes
inferredcites →https://doi.org/10.1242/jeb.00600openalex-snapshot
Neural images of pursuit targets in the photoreceptor arrays of male and female housefliesMusca domestica
inferredcites →https://doi.org/10.1242/jeb.00949openalex-snapshot
Visual acuity of fly photoreceptors in natural conditions - dependence on UV sensitizing pigment and light-controlling pupil
inferredcites →https://doi.org/10.1242/jeb.080192openalex-snapshot
Figure-ground discrimination behavior in Drosophila. II. Visual influences on head movement
inferredcites →https://doi.org/10.1242/jeb.112.1.225openalex-snapshot
Early Visual Processing in Insects
inferredcites →https://doi.org/10.1242/jeb.112425openalex-snapshot
Cockroach optomotor responses below single photon level
inferredcites →https://doi.org/10.1242/jeb.146.1.39openalex-snapshot
The role of sensory adaptation in the retina
inferredcites →https://doi.org/10.1242/jeb.202.11.1481openalex-snapshot
Blowfly flight and optic flow : I. Thorax kinematics and flight dynamics
inferredcites →https://doi.org/10.1242/jeb.202.11.1491openalex-snapshot
Blowfly flight and optic flow: II. Head movements during flight
inferredcites →https://doi.org/10.1242/jeb.29.4.667openalex-snapshot
The Size of Ommatidia in Apposition Eyes
inferredcites →https://doi.org/10.1242/jeb.55.1.85openalex-snapshot
Separation of Receptor and Lamina Potentials in the Electroretinogram of Normal and Mutant Drosophila
inferredcites →https://doi.org/10.1364/josa.67.000696openalex-snapshot
Photoreceptor diameter and spacing for highest resolving power
inferredcites →https://doi.org/10.1364/josaa.4.002379openalex-snapshot
Relations between the statistics of natural images and the response properties of cortical cells
inferredcites →https://doi.org/10.1364/josab.1.000366openalex-snapshot
Role of primary excitation statistics in the generation of antibunched and sub-Poisson light
inferredcites →https://doi.org/10.1371/journal.pbio.0050116openalex-snapshot
Fly Photoreceptors Demonstrate Energy-Information Trade-Offs in Neural Coding
inferredcites →https://doi.org/10.1371/journal.pbio.1002115openalex-snapshot
Ih Channels Control Feedback Regulation from Amacrine Cells to Photoreceptors
inferredcites →https://doi.org/10.1371/journal.pone.0004306openalex-snapshot
Network Adaptation Improves Temporal Representation of Naturalistic Stimuli in Drosophila Eye: II Mechanisms
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Mathematical Theory of Communication
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Computational Foundations of Natural Intelligence
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Contrast sensitivity reveals an oculomotor strategy for temporally encoding space
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