Works matching AU Cullen, Kathleen
Results: 88
Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33819-3
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Age-Related Neurochemical Changes in the vestibular Nuclei.
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- Frontiers in Neurology, 2016, p. 1, doi. 10.3389/fneur.2016.00020
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Challenges to the Vestibular System in Space: How the Brain Responds and Adapts to Microgravity.
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- Frontiers in Neural Circuits, 2021, v. 15, p. 1, doi. 10.3389/fncir.2021.760313
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The neural encoding of self-generated and externally applied movement: implications for the perception of self-motion and spatial memory.
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- Frontiers in Integrative Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fnint.2013.00108
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Vestibular Contributions to Primate Neck Postural Muscle Activity during Natural Motion.
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- Journal of Neuroscience, 2023, v. 43, n. 13, p. 2326, doi. 10.1523/jneurosci.1831-22.2023
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The Neural Basis for Biased Behavioral Responses Evoked by Galvanic Vestibular Stimulation in Primates.
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- Journal of Neuroscience, 2023, v. 43, n. 11, p. 1905, doi. 10.1523/JNEUROSCI.0987-22.2023
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Neural Mechanisms Underlying High-Frequency Vestibulocollic Reflexes In Humans And Monkeys.
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- Journal of Neuroscience, 2020, v. 40, n. 9, p. 1874, doi. 10.1523/JNEUROSCI.1463-19.2020
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In vivo Conditions Induce Faithful Encoding of Stimuli by Reducing Nonlinear Synchronization in Vestibular Sensory Neurons.
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- PLoS Computational Biology, 2011, v. 7, n. 7, p. 1, doi. 10.1371/journal.pcbi.1002120
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Neural variability determines coding strategies for natural self-motion in macaque monkeys.
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- eLife, 2020, p. 1, doi. 10.7554/eLife.57484
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Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30348-x
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Context-independent encoding of passive and active self-motion in vestibular afferent fibers during locomotion in primates.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27753-z
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The Increased Sensitivity of Irregular Peripheral Canal and Otolith Vestibular Afferents Optimizes their Encoding of Natural Stimuli.
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- Journal of Neuroscience, 2015, v. 35, n. 14, p. 5522, doi. 10.1523/JNEUROSCI.3841-14.2015
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Local Population Synchrony and the Encoding of Eye Position in the Primate Neural Integrator.
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- Journal of Neuroscience, 2015, v. 35, n. 10, p. 4287, doi. 10.1523/JNEUROSCI.4253-14.2015
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Integration of Canal and Otolith Inputs by Central Vestibular Neurons Is Subadditive for Both Active and Passive Self-Motion: Implication for Perception.
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- Journal of Neuroscience, 2015, v. 35, n. 8, p. 3555, doi. 10.1523/JNEUROSCI.3540-14.2015
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Loss of a-Calcitonin Gene-Related Peptide (aCGRP) Reduces the Efficacy of the Vestibulo-ocular Reflex (VOR).
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- Journal of Neuroscience, 2014, v. 34, n. 31, p. 10453, doi. 10.1523/JNEUROSCI.3336-13.2014
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Statistics of the Vestibular Input Experienced during Natural Self-Motion: Implications for Neural Processing.
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- Journal of Neuroscience, 2014, v. 34, n. 24, p. 8347, doi. 10.1523/JNEUROSCI.0692-14.2014
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Multimodal Integration of Self-Motion Cues in the Vestibular System: Active versus Passive Translations.
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- Journal of Neuroscience, 2013, v. 33, n. 50, p. 19555, doi. 10.1523/JNEUROSCI.3051-13.2013
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Strong Correlations between Sensitivity and Variability Give Rise to Constant Discrimination Thresholds across the Otolith Afferent Population.
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- Journal of Neuroscience, 2013, v. 33, n. 27, p. 11302, doi. 10.1523/JNEUROSCI.0459-13.2013
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Vergence Neurons Identified in the Rostral Superior Colliculus Code Smooth Eye Movements in 3D Space.
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- Journal of Neuroscience, 2013, v. 33, n. 17, p. 7274, doi. 10.1523/JNEUROSCI.2268-12.2013
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Vestibular animal models: contributions to understanding physiology and disease.
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- Journal of Neurology, 2016, v. 263, p. 10, doi. 10.1007/s00415-015-7909-y
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Loss of peripheral vestibular input alters the statistics of head movement experienced during natural self‐motion.
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- Journal of Physiology, 2021, v. 599, n. 8, p. 2239, doi. 10.1113/JP281183
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The statistics of the vestibular input experienced during natural self-motion differ between rodents and primates.
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- Journal of Physiology, 2017, v. 595, n. 8, p. 2751, doi. 10.1113/JP273734
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Neuronal detection thresholds during vestibular compensation: contributions of response variability and sensory substitution.
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- Journal of Physiology, 2014, v. 592, n. 7, p. 1565, doi. 10.1113/jphysiol.2013.267534
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Loss of α-9 Nicotinic Acetylcholine Receptor Subunit Predominantly Results in Impaired Postural Stability Rather Than Gaze Stability.
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- Frontiers in Cellular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fncel.2021.799752
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Neural Variability, Detection Thresholds, and Information Transmission in the Vestibular System.
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- Journal of Neuroscience, 2007, v. 27, n. 4, p. 771, doi. 10.1523/JNEUROSCI.4690-06.2007
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Premotor Correlates of Integrated Feedback Control for Eye-Head Gaze Shifts.
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- Journal of Neuroscience, 2006, v. 26, n. 18, p. 4922, doi. 10.1523/JNEUROSCI.4099-05.2006
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Dissociating Self-Generated from Passively Applied Head Motion: Neural Mechanisms in the Vestibular Nuclei.
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- Journal of Neuroscience, 2004, v. 24, n. 9, p. 2102, doi. 10.1523/JNEUROSCI.3988-03.2004
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Passive Activation of Neck Proprioceptive Inputs Does Not Influence the Discharge Patterns of Vestibular Nuclei Neurons.
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- Annals of the New York Academy of Sciences, 2001, v. 942, n. 1, p. 486, doi. 10.1111/j.1749-6632.2001.tb03776.x
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Do Extraocular Motoneurons Encode Head Velocity during Head-Restrained versus Head-Unrestrained Saccadic and Smooth Pursuit Movements?
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- Annals of the New York Academy of Sciences, 2001, v. 942, n. 1, p. 497, doi. 10.1111/j.1749-6632.2001.tb03780.x
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Signal Processing by Vestibular Nuclei Neurons Is Dependent on the Current Behavioral Goal.
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- Annals of the New York Academy of Sciences, 2001, v. 942, n. 1, p. 345, doi. 10.1111/j.1749-6632.2001.tb03759.x
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Inhibitory Burst Neuron Activity Encodes Gaze, Not Eye, Metrics and Dynamics during Passive Head on Body Rotation.
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- Annals of the New York Academy of Sciences, 1996, v. 781, n. 1, p. 601, doi. 10.1111/j.1749-6632.1996.tb15735.x
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The Vestibular System Implements a Linear--Nonlinear Transformation In Order to Encode Self-Motion.
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- PLoS Biology, 2012, v. 10, n. 7, p. 1, doi. 10.1371/journal.pbio.1001365
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Brainstem processing of vestibular sensory exafference: implications for motion sickness etiology.
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- Experimental Brain Research, 2014, v. 232, n. 8, p. 2483, doi. 10.1007/s00221-014-3973-2
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Internal models of self-motion: computations that suppress vestibular reafference in early vestibular processing.
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- Experimental Brain Research, 2011, v. 210, n. 3/4, p. 377, doi. 10.1007/s00221-011-2555-9
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Cross-axis adaptation improves 3D vestibulo-ocular reflex alignment during chronic stimulation via a head-mounted multichannel vestibular prosthesis.
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- Experimental Brain Research, 2011, v. 210, n. 3/4, p. 595, doi. 10.1007/s00221-011-2591-5
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Vestibular control of the head: possible functions of the vestibulocollic reflex.
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- Experimental Brain Research, 2011, v. 210, n. 3/4, p. 331, doi. 10.1007/s00221-011-2611-5
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Different neural strategies for multimodal integration: comparison of two macaque monkey species.
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- Experimental Brain Research, 2009, v. 195, n. 1, p. 45, doi. 10.1007/s00221-009-1751-3
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Consensus Paper: The Role of the Cerebellum in Perceptual Processes.
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- Cerebellum, 2015, v. 14, n. 2, p. 197, doi. 10.1007/s12311-014-0627-7
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Neural Correlates of Sensory Prediction Errors in Monkeys: Evidence for Internal Models of Voluntary Self-Motion in the Cerebellum.
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- Cerebellum, 2015, v. 14, n. 1, p. 31, doi. 10.1007/s12311-014-0608-x
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A neural correlate for vestibulo-ocular reflex suppression during voluntary eye?head gaze shifts.
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- Nature Neuroscience, 1998, v. 1, n. 5, p. 404, doi. 10.1038/1619
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Self-motion evokes precise spike timing in the primate vestibular system.
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- Nature Communications, 2016, v. 7, n. 10, p. 13229, doi. 10.1038/ncomms13229
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Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo.
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- Nature Communications, 2016, v. 7, n. 5, p. 11238, doi. 10.1038/ncomms11238
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Envelope statistics of self-motion signals experienced by human subjects during everyday activities: Implications for vestibular processing.
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- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178664
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Rapid adaptation of multisensory integration in vestibular pathways.
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- Frontiers in Systems Neuroscience, 2015, v. 10, p. 1, doi. 10.3389/fnsys.2015.00059
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Dynamics of the horizontal vestibuloocular reflex after unilateral labyrinthectomy: response to high frequency, high acceleration, and high velocity rotations.
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- Experimental Brain Research, 2006, v. 175, n. 3, p. 471, doi. 10.1007/s00221-006-0567-7
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Temporal characteristics of neurons in the central mesencephalic reticular formation of head unrestrained monkeys.
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- Experimental Brain Research, 2006, v. 168, n. 4, p. 471, doi. 10.1007/s00221-005-0105-z
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Spatial characteristics of neurons in the central mesencephalic reticular formation (cMRF) of head-unrestrained monkeys.
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- Experimental Brain Research, 2006, v. 168, n. 4, p. 455, doi. 10.1007/s00221-005-0104-0
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A comparison of head-unrestrained and head-restrained pursuit: influence of eye position and target velocity on latency.
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- Experimental Brain Research, 2000, v. 133, n. 2, p. 139, doi. 10.1007/s002210000369
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Head movement kinematics are differentially altered for extended versus short duration gait exercises in individuals with vestibular loss.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-42441-2
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Aging Delays Completion of Head Rotation Cycles in Continuous Gaze Stabilization Exercises despite Putative Healthy Vestibular Function.
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- Gerontology, 2024, v. 70, n. 10, p. 1113, doi. 10.1159/000540230
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