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Cerebellar-Recipient Motor Thalamus Drives Behavioral Context-Specific Movement Initiation
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19960429)368:2<215::aid-cne4>3.0.co;2-6openalex-snapshot
Comparison of cerebellothalamic and pallidothalamic projections in the monkey (Macaca fuscata): A double anterograde labeling study
inferredcites →https://doi.org/10.1002/ana.410380608openalex-snapshot
Cerebellar outflow lesions: A comparison of movement deficits resulting from lesions at the levels of the cerebellum and thalamus
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Topographic organization in the corticocortical connections of medial agranular cortex in rats
inferredcites →https://doi.org/10.1007/bf00238606openalex-snapshot
Motor command in the ventrolateral thalamic nucleus: Neuronal variability can be overcome by ensemble average
inferredcites →https://doi.org/10.1007/bf00239355openalex-snapshot
Cerebellar nuclear topography of simple and synergistic movements in the alert baboon (Papio papio)
inferredcites →https://doi.org/10.1007/bf00255233openalex-snapshot
Converging cerebellofugal inputs to the thalamus
inferredcites →https://doi.org/10.1007/bf01208592openalex-snapshot
Parallel pathways for movement initiation in monkeys
inferredcites →https://doi.org/10.1007/s12311-013-0506-7openalex-snapshot
Does the Cerebellum Initiate Movement?
inferredcites →https://doi.org/10.1016/0006-8993(75)90387-xopenalex-snapshot
Timing of activity in cerebellar dentate nucleus and cerebral motor cortex during prompt volitional movement
inferredcites →https://doi.org/10.1016/0091-3057(87)90532-6openalex-snapshot
Motivational vs. motor effects of striatal and pallidal gabergic projections to subthalamic and entopenduncular nuclei, ventromedial thalamus, and ventral globus pallidus
inferredcites →https://doi.org/10.1016/0301-0082(95)00002-dopenalex-snapshot
The role of the cerebello-thalamo-cortical pathway in skilled movement
inferredcites →https://doi.org/10.1016/0304-3940(90)90360-lopenalex-snapshot
A comparison of preparation-related neuronal activity changes in the prefrontal, premotor, primary motor and posterior parietal areas of the monkey cortex: preliminary results
inferredcites →https://doi.org/10.1016/0306-4522(86)90182-xopenalex-snapshot
Fastigial nucleus projections in the midbrain and thalamus in dogs
inferredcites →https://doi.org/10.1016/j.cell.2016.09.051openalex-snapshot
Distinct Hippocampal Pathways Mediate Dissociable Roles of Context in Memory Retrieval
inferredcites →https://doi.org/10.1016/j.celrep.2015.04.042openalex-snapshot
Cellular Mechanisms Underlying Behavioral State-Dependent Bidirectional Modulation of Motor Cortex Output
inferredcites →https://doi.org/10.1016/j.conb.2016.02.005openalex-snapshot
The basal ganglia: from motor commands to the control of vigor
inferredcites →https://doi.org/10.1016/j.jneumeth.2017.07.031openalex-snapshot
NoRMCorre: An online algorithm for piecewise rigid motion correction of calcium imaging data
inferredcites →https://doi.org/10.1016/j.neuron.2010.09.015openalex-snapshot
Cortical Preparatory Activity: Representation of Movement or First Cog in a Dynamical Machine?
inferredcites →https://doi.org/10.1016/j.neuron.2013.10.020openalex-snapshot
Flow of Cortical Activity Underlying a Tactile Decision in Mice
inferredcites →https://doi.org/10.1016/j.neuron.2017.07.039openalex-snapshot
The Basal Ganglia Do Not Select Reach Targets but Control the Urgency of Commitment
inferredcites →https://doi.org/10.1016/j.neuron.2018.01.004openalex-snapshot
Motor Cortex Embeds Muscle-like Commands in an Untangled Population Response
inferredcites →https://doi.org/10.1016/j.neuron.2018.08.016openalex-snapshot
Thalamocortical Axonal Activity in Motor Cortex Exhibits Layer-Specific Dynamics during Motor Learning
inferredcites →https://doi.org/10.1016/j.neuron.2019.05.022openalex-snapshot
Cerebellar Contribution to Preparatory Activity in Motor Neocortex
inferredcites →https://doi.org/10.1016/s0896-6273(02)00698-0openalex-snapshot
Complex Movements Evoked by Microstimulation of Precentral Cortex
inferredcites →https://doi.org/10.1038/nature14178openalex-snapshot
A motor cortex circuit for motor planning and movement
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nmeth999openalex-snapshot
Retrograde neuronal tracing with a deletion-mutant rabies virus
inferredcites →https://doi.org/10.1038/nn.3643openalex-snapshot
Cortical activity in the null space: permitting preparation without movement
inferredcites →https://doi.org/10.1038/nprot.2009.248openalex-snapshot
Production of glycoprotein-deleted rabies viruses for monosynaptic tracing and high-level gene expression in neurons
inferredcites →https://doi.org/10.1038/s41586-018-0633-xopenalex-snapshot
A cortico-cerebellar loop for motor planning
inferredcites →https://doi.org/10.1038/s41593-018-0209-yopenalex-snapshot
DeepLabCut: markerless pose estimation of user-defined body parts with deep learning
inferredcites →https://doi.org/10.1038/s41598-018-21640-2openalex-snapshot
FISSA: A neuropil decontamination toolbox for calcium imaging signals
inferredcites →https://doi.org/10.1093/cercor/bhn231openalex-snapshot
Two Types of Thalamocortical Projections from the Motor Thalamic Nuclei of the Rat: A Single Neuron-Tracing Study Using Viral Vectors
inferredcites →https://doi.org/10.1101/266320openalex-snapshot
Motor cortex is an input-driven dynamical system controlling dexterous movement
inferredcites →https://doi.org/10.1109/cic.2003.1291140openalex-snapshot
An open-source algorithm to detect onset of arterial blood pressure pulses
inferredcites →https://doi.org/10.1109/tbme.2004.839800openalex-snapshot
Spike Detection Using the Continuous Wavelet Transform
inferredcites →https://doi.org/10.1113/jphysiol.1979.sp013057openalex-snapshot
Discharges of intracerebellar nuclear cells in monkeys.
inferredcites →https://doi.org/10.1113/jphysiol.1985.sp015565openalex-snapshot
Magnocellular red nucleus activity during different types of limb movement in the macaque monkey.
inferredcites →https://doi.org/10.1113/jphysiol.1992.sp018910openalex-snapshot
The activity of monkey thalamic and motor cortical neurones in a skilled, ballistic movement.
inferredcites →https://doi.org/10.1146/annurev-neuro-072116-031033openalex-snapshot
What, If, and When to Move: Basal Ganglia Circuits and Self-Paced Action Initiation
inferredcites →https://doi.org/10.1152/jn.00307.2006openalex-snapshot
Preparatory Activity in Premotor and Motor Cortex Reflects the Speed of the Upcoming Reach
inferredcites →https://doi.org/10.1152/jn.01034.2004openalex-snapshot
Activity Properties and Location of Neurons in the Motor Thalamus That Project to the Cortical Motor Areas in Monkeys
inferredcites →https://doi.org/10.1152/jn.1976.39.5.1032openalex-snapshot
Activity of ventrolateral thalamic neurons during arm movement
inferredcites →https://doi.org/10.1152/jn.1977.40.5.1038openalex-snapshot
Cerebellar participation in generation of prompt arm movements
inferredcites →https://doi.org/10.1152/jn.1978.41.3.654openalex-snapshot
Correlation of neural discharge with pattern and force of muscular activity, joint position, and direction of intended next movement in motor cortex and cerebellum
inferredcites →https://doi.org/10.1152/jn.1983.50.6.1359openalex-snapshot
Fast ballistic arm movements triggered by visual, auditory, and somesthetic stimuli in the monkey. II. Effects of unilateral dentate lesion on discharge of precentral cortical neurons and reaction time
inferredcites →https://doi.org/10.1152/jn.1989.62.1.198openalex-snapshot
Cerebellar neuronal activity related to whole-arm reaching movements in the monkey
inferredcites →https://doi.org/10.1152/jn.1991.65.2.301openalex-snapshot
Basal ganglia motor control. II. Late pallidal timing relative to movement onset and inconsistent pallidal coding of movement parameters
inferredcites →https://doi.org/10.1152/jn.1993.70.6.2660openalex-snapshot
Preferential activity of dentate neurons during limb movements guided by vision
inferredcites →https://doi.org/10.1152/jn.1996.75.3.1087openalex-snapshot
Changes in the control of arm position, movement, and thalamic discharge during local inactivation in the globus pallidus of the monkey
inferredcites →https://doi.org/10.1152/jn.1997.78.2.939openalex-snapshot
Effects of Inactivating Individual Cerebellar Nuclei on the Performance and Retention of an Operantly Conditioned Forelimb Movement
inferredcites →https://doi.org/10.1152/jn.2000.83.5.2780openalex-snapshot
Temporary Inactivation in the Primate Motor Thalamus During Visually Triggered and Internally Generated Limb Movements
inferredcites →https://doi.org/10.1162/jocn.1989.1.2.136openalex-snapshot
Timing Functions of The Cerebellum
inferredcites →https://doi.org/10.1523/jneurosci.0893-14.2014openalex-snapshot
Reduced Reach-Related Modulation of Motor Thalamus Neural Activity in a Rat Model of Parkinson's Disease
inferredcites →https://doi.org/10.1523/jneurosci.2221-16.2017openalex-snapshot
Cerebellar Roles in Self-Timing for Sub- and Supra-Second Intervals
inferredcites →https://doi.org/10.1523/jneurosci.3762-05.2006openalex-snapshot
Neural Variability in Premotor Cortex Provides a Signature of Motor Preparation
inferredcites →https://doi.org/10.1523/jneurosci.4338-12.2013openalex-snapshot
Organization of Cortical and Thalamic Input to Pyramidal Neurons in Mouse Motor Cortex
inferredcites →https://doi.org/10.7554/elife.31826openalex-snapshot
Conservation of preparatory neural events in monkey motor cortex regardless of how movement is initiated
inferredcites →https://doi.org/10.7554/elife.58848openalex-snapshot
Neural population dynamics in motor cortex are different for reach and grasp
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.2022.02.006openalex-snapshot
A midbrain-thalamus-cortex circuit reorganizes cortical dynamics to initiate movement
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109090openalex-snapshot
Thalamic control of cortical dynamics in a model of flexible motor sequencing
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2020.06.046openalex-snapshot
The Cerebellar Nuclei and Dexterous Limb Movements
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2020.101951openalex-snapshot
The thalamus integrates the macrosystems of the brain to facilitate complex, adaptive brain network dynamics
inferred← citeshttps://doi.org/10.1038/s41593-021-00798-5openalex-snapshot
Independent generation of sequence elements by motor cortex
inferred← citeshttps://doi.org/10.1073/pnas.2012658118openalex-snapshot
Area-specific thalamocortical synchronization underlies the transition from motor planning to execution
inferred← citeshttps://doi.org/10.1101/2020.06.09.143040openalex-snapshot
Generation of Rapid Sequences by Motor Cortex
inferred← citeshttps://doi.org/10.1101/2020.10.27.357087openalex-snapshot
Spatiotemporal organization of movement-invariant and movement-specific signaling in the output layer of motor cortex
inferred← citeshttps://doi.org/10.1101/2021.03.26.437236openalex-snapshot
Purkinje Cell Activity in Medial and Lateral Cerebellum During Suppression of Voluntary Eye Movements in Rhesus Macaques
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