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Attention Decorrelates Sensory and Motor Signals in the Mouse Visual Cortex

https://doi.org/10.2139/ssrn.3762766
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What this work says

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

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Polyneuronal innervation of spiny stellate neurons in cat visual cortex
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New insights into action–perception coupling
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Suppression of the magnocellular pathway during saccades
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A Cortical Circuit for Gain Control by Behavioral State
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High-Yield Methods for Accurate Two-Alternative Visual Psychophysics in Head-Fixed Mice
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Effects of Arousal on Mouse Sensory Cortex Depend on Modality
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Sensory signals during active versus passive movement
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Visual perception and saccadic eye movements
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Brain state dependent activity in the cortex and thalamus
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Eye Movements: Keeping Vision Stable
inferredcites →https://doi.org/10.1016/j.cub.2013.04.012openalex-snapshot
Locomotion Controls Spatial Integration in Mouse Visual Cortex
inferredcites →https://doi.org/10.1016/j.cub.2015.05.028openalex-snapshot
Pattern and Component Motion Responses in Mouse Visual Cortical Areas
inferredcites →https://doi.org/10.1016/j.cub.2018.01.033openalex-snapshot
A New Perspective on Predictive Motor Signaling
inferredcites →https://doi.org/10.1016/j.cub.2018.01.038openalex-snapshot
Visual Selective Attention in Mice
inferredcites →https://doi.org/10.1016/j.cub.2019.03.065openalex-snapshot
Local and Global Influences of Visual Spatial Selection and Locomotion in Mouse Primary Visual Cortex
inferredcites →https://doi.org/10.1016/j.cub.2020.07.094openalex-snapshot
Brain States: Sensory Modulations All the Way Down
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Quantitative analysis of spontaneous saccade-like rapid eye movements in C57BL/6 mice
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The mouse posterior parietal cortex: Anatomy and functions
inferredcites →https://doi.org/10.1016/j.neuron.2007.06.018openalex-snapshot
Differential Attention-Dependent Response Modulation across Cell Classes in Macaque Visual Area V4
inferredcites →https://doi.org/10.1016/j.neuron.2009.01.002openalex-snapshot
The Normalization Model of Attention
inferredcites →https://doi.org/10.1016/j.neuron.2010.01.033openalex-snapshot
Modulation of Visual Responses by Behavioral State in Mouse Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2011.12.004openalex-snapshot
Functional Specialization of Seven Mouse Visual Cortical Areas
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.040openalex-snapshot
Sensorimotor Mismatch Signals in Primary Visual Cortex of the Behaving Mouse
inferredcites →https://doi.org/10.1016/j.neuron.2013.08.007openalex-snapshot
Subthreshold Mechanisms Underlying State-Dependent Modulation of Visual Responses
inferredcites →https://doi.org/10.1016/j.neuron.2014.06.031openalex-snapshot
Identification of a Brainstem Circuit Regulating Visual Cortical State in Parallel with Locomotion
inferredcites →https://doi.org/10.1016/j.neuron.2014.09.033openalex-snapshot
Pupil Fluctuations Track Fast Switching of Cortical States during Quiet Wakefulness
inferredcites →https://doi.org/10.1016/j.neuron.2015.03.028openalex-snapshot
Arousal and Locomotion Make Distinct Contributions to Cortical Activity Patterns and Visual Encoding
inferredcites →https://doi.org/10.1016/j.neuron.2015.05.038openalex-snapshot
Cortical Membrane Potential Signature of Optimal States for Sensory Signal Detection
inferredcites →https://doi.org/10.1016/j.neuron.2015.09.012openalex-snapshot
Waking State: Rapid Variations Modulate Neural and Behavioral Responses
inferredcites →https://doi.org/10.1016/j.neuron.2016.01.027openalex-snapshot
Cross-Modality Sharpening of Visual Cortical Processing through Layer-1-Mediated Inhibition and Disinhibition
inferredcites →https://doi.org/10.1016/j.neuron.2017.08.036openalex-snapshot
A Sensorimotor Circuit in Mouse Cortex for Visual Flow Predictions
inferredcites →https://doi.org/10.1016/j.neuron.2018.03.037openalex-snapshot
Vision and Locomotion Shape the Interactions between Neuron Types in Mouse Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2019.01.026openalex-snapshot
Cortical Areas Interact through a Communication Subspace
inferredcites →https://doi.org/10.1016/j.neuron.2019.08.025openalex-snapshot
Task-Dependent Changes in the Large-Scale Dynamics and Necessity of Cortical Regions
inferredcites →https://doi.org/10.1016/j.neuron.2019.09.045openalex-snapshot
Excitatory and Inhibitory Subnetworks Are Equally Selective during Decision-Making and Emerge Simultaneously during Learning
inferredcites →https://doi.org/10.1016/j.tins.2020.05.005openalex-snapshot
Movement-Related Signals in Sensory Areas: Roles in Natural Behavior
inferredcites →https://doi.org/10.1016/j.visres.2008.03.021openalex-snapshot
Neuronal mechanisms of visual stability
inferredcites →https://doi.org/10.1016/s0165-0173(01)00044-3openalex-snapshot
The cognitive neuroscience of sustained attention: where top-down meets bottom-up
inferredcites →https://doi.org/10.1016/s0166-2236(00)01685-4openalex-snapshot
Changes in visual perception at the time of saccades
inferredcites →https://doi.org/10.1016/s0896-6273(01)80034-9openalex-snapshot
Effects of Attention on the Reliability of Individual Neurons in Monkey Visual Cortex
inferredcites →https://doi.org/10.1016/s0896-6273(03)00286-1openalex-snapshot
New Paradigm for Optical Imaging
inferredcites →https://doi.org/10.1017/s0140525x00034361openalex-snapshot
A theory of visual stability across saccadic eye movements
inferredcites →https://doi.org/10.1038/21176openalex-snapshot
Feature-based attention influences motion processing gain in macaque visual cortex
inferredcites →https://doi.org/10.1038/nature11665openalex-snapshot
Inhibition dominates sensory responses in the awake cortex
inferredcites →https://doi.org/10.1038/nature13724openalex-snapshot
A synaptic and circuit basis for corollary discharge in the auditory cortex
inferredcites →https://doi.org/10.1038/nature17643openalex-snapshot
Robust neuronal dynamics in premotor cortex during motor planning
inferredcites →https://doi.org/10.1038/ncomms13289openalex-snapshot
Pupil fluctuations track rapid changes in adrenergic and cholinergic activity in cortex
inferredcites →https://doi.org/10.1038/ncomms9110openalex-snapshot
Saccadic modulation of stimulus processing in primary visual cortex
inferredcites →https://doi.org/10.1038/ncomms9114openalex-snapshot
V1 neurons respond differently to object motion versus motion from eye movements
inferredcites →https://doi.org/10.1038/nn.2501openalex-snapshot
Stimulus onset quenches neural variability: a widespread cortical phenomenon
inferredcites →https://doi.org/10.1038/nn.3552openalex-snapshot
Fast modulation of visual perception by basal forebrain cholinergic neurons
inferredcites →https://doi.org/10.1038/nn.3567openalex-snapshot
Integration of visual motion and locomotion in mouse visual cortex
inferredcites →https://doi.org/10.1038/nrc3398openalex-snapshot
Ceramide-orchestrated signalling in cancer cells
inferredcites →https://doi.org/10.1038/nrn2457openalex-snapshot
Corollary discharge across the animal kingdom
inferredcites →https://doi.org/10.1038/nrn3084openalex-snapshot
Cortical state and attention
inferredcites →https://doi.org/10.1038/nrn3136openalex-snapshot
Normalization as a canonical neural computation
inferredcites →https://doi.org/10.1038/s41467-017-01371-0openalex-snapshot
An automated platform for high-throughput mouse behavior and physiology with voluntary head-fixation
inferredcites →https://doi.org/10.1038/s41467-018-05012-yopenalex-snapshot
Task-dependent representations of stimulus and choice in mouse parietal cortex
inferredcites →https://doi.org/10.1038/s41583-019-0253-yopenalex-snapshot
Mechanisms underlying gain modulation in the cortex
inferredcites →https://doi.org/10.1038/s41593-018-0305-zopenalex-snapshot
Active control of arousal by a locus coeruleus GABAergic circuit
inferredcites →https://doi.org/10.1038/s41593-019-0502-4openalex-snapshot
Single-trial neural dynamics are dominated by richly varied movements
inferredcites →https://doi.org/10.1038/s41598-018-34966-8openalex-snapshot
The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of attention in head-fixed mice
inferredcites →https://doi.org/10.1073/pnas.0509557103openalex-snapshot
Microsaccades are triggered by low retinal image slip
inferredcites →https://doi.org/10.1093/acrefore/9780190264086.013.43openalex-snapshot
Normalization Principles in Computational Neuroscience
inferredcites →https://doi.org/10.1093/cercor/4.6.601openalex-snapshot
Analysis of Retinotopic Maps in Extrastriate Cortex
inferredcites →https://doi.org/10.1098/rstb.2010.0186openalex-snapshot
Neuronal mechanisms for visual stability: progress and problems
inferredcites →https://doi.org/10.1098/rstb.2015.0360openalex-snapshot
Wide-field optical mapping of neural activity and brain haemodynamics: considerations and novel approaches
inferredcites →https://doi.org/10.1101/533463openalex-snapshot
Distinct functional classes of excitatory neurons in mouse V1 are differentially modulated by learning and task engagement
inferredcites →https://doi.org/10.1101/819334openalex-snapshot
Application of the Hierarchical Bootstrap to Multi-Level Data in Neuroscience
inferredcites →https://doi.org/10.1109/tip.2015.2446948openalex-snapshot
Factorization-Based Texture Segmentation
inferredcites →https://doi.org/10.1109/tsmc.1979.4310076openalex-snapshot
A Threshold Selection Method from Gray-Level Histograms
inferredcites →https://doi.org/10.1126/science.1069590openalex-snapshot
A Pathway in Primate Brain for Internal Monitoring of Movements
inferredcites →https://doi.org/10.1126/science.1254126openalex-snapshot
Long-range and local circuits for top-down modulation of visual cortex processing
inferredcites →https://doi.org/10.1126/science.aag1420openalex-snapshot
Selective modulation of cortical state during spatial attention
inferredcites →https://doi.org/10.1126/science.aav3932openalex-snapshot
Thirst regulates motivated behavior through modulation of brainwide neural population dynamics
inferredcites →https://doi.org/10.1126/science.aav7893openalex-snapshot
Spontaneous behaviors drive multidimensional, brainwide activity
inferredcites →https://doi.org/10.1146/annurev-vision-091517-034317openalex-snapshot
Vision During Saccadic Eye Movements
inferredcites →https://doi.org/10.1146/annurev.neuro.28.061604.135709openalex-snapshot
AN INTEGRATIVE THEORY OF LOCUS COERULEUS-NOREPINEPHRINE FUNCTION: Adaptive Gain and Optimal Performance
inferredcites →https://doi.org/10.1146/annurev.neuro.31.060407.125627openalex-snapshot
Brain Circuits for the Internal Monitoring of Movements
inferredcites →https://doi.org/10.1152/jn.00188.2012openalex-snapshot
Cholinergic suppression of visual responses in primate V1 is mediated by GABAergic inhibition
inferredcites →https://doi.org/10.1152/jn.00290.2018openalex-snapshot
Pupil-linked arousal modulates behavior in rats performing a whisker deflection direction discrimination task
inferredcites →https://doi.org/10.1152/jn.01056.2015openalex-snapshot
Large-scale imaging of cortical dynamics during sensory perception and behavior
inferredcites →https://doi.org/10.1162/jocn_a_01251openalex-snapshot
Pupillary Correlates of Fluctuations in Sustained Attention
inferredcites →https://doi.org/10.1371/journal.pbio.3000387openalex-snapshot
Strategic deployment of feature-based attentional gain in primate visual cortex
inferredcites →https://doi.org/10.1371/journal.pcbi.1002219openalex-snapshot
Receptive Field Inference with Localized Priors
inferredcites →https://doi.org/10.1523/jneurosci.0430-16.2016openalex-snapshot
Enhanced Spatial Resolution During Locomotion and Heightened Attention in Mouse Primary Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.0835-07.2007openalex-snapshot
Responses of Neurons in Primary Visual Cortex to Transient Changes in Local Contrast and Luminance
inferredcites →https://doi.org/10.1523/jneurosci.1124-14.2014openalex-snapshot
Topography and Areal Organization of Mouse Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.1400-04.2004openalex-snapshot
A Quantitative Map of the Circuit of Cat Primary Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.1828-17.2017openalex-snapshot
Sensation during Active Behaviors
inferredcites →https://doi.org/10.1523/jneurosci.2054-15.2016openalex-snapshot
Saccadic Corollary Discharge Underlies Stable Visual Perception
inferredcites →https://doi.org/10.1523/jneurosci.2728-16.2017openalex-snapshot
Locomotion Enhances Neural Encoding of Visual Stimuli in Mouse V1
inferredcites →https://doi.org/10.3389/fnsys.2016.00109openalex-snapshot
Models of Neuronal Stimulus-Response Functions: Elaboration, Estimation, and Evaluation
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The psychometric function: I. Fitting, sampling, and goodness of fit
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Gaussian Processes for Machine Learning
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Mapping cortical mesoscopic networks of single spiking cortical or sub-cortical neurons

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.cell.2021.03.042openalex-snapshot
High-precision coding in visual cortex
inferred← citeshttps://doi.org/10.1016/j.neures.2023.05.002openalex-snapshot
Flexible information representation to stabilize sensory perception despite minor external input variations
inferred← citeshttps://doi.org/10.1038/s41467-020-20722-yopenalex-snapshot
Scaling of sensory information in large neural populations shows signatures of information-limiting correlations
inferred← citeshttps://doi.org/10.1038/s41593-023-01382-9openalex-snapshot
Organizing memories for generalization in complementary learning systems
inferred← citeshttps://doi.org/10.1073/pnas.2103952118openalex-snapshot
Probabilistic discrimination of relative stimulus features in mice
inferred← citeshttps://doi.org/10.1101/2021.03.02.433657openalex-snapshot
Distributed context-dependent choice information in mouse dorsal-parietal cortex
inferred← citeshttps://doi.org/10.1101/679324openalex-snapshot
High precision coding in visual cortex
inferred← citeshttps://doi.org/10.1162/opmi_a_00132openalex-snapshot
Bayesian Reinforcement Learning With Limited Cognitive Load
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