Zebrafish optomotor response to second-order motion illustrates that age-related changes in motion detection depend on the activated motion system
暂无分享,去创建一个
[1] D. Javitt,et al. Disruption of early visual processing in amyloid-positive healthy individuals and mild cognitive impairment , 2023, Alzheimer's Research & Therapy.
[2] M. Herzog,et al. No Common Factor Underlying Decline of Visual Abilities in Mild Cognitive Impairment , 2022, Experimental aging research.
[3] G. Sumbre,et al. Fourier Motion Processing in the Optic Tectum and Pretectum of the Zebrafish Larva , 2022, Frontiers in Neural Circuits.
[4] J. Wood,et al. Naturalistic Driving Techniques and Association of Visual Risk Factors With At-Fault Crashes and Near Crashes by Older Drivers With Vision Impairment. , 2021, JAMA ophthalmology.
[5] J. Wood,et al. Motion perception as a risk factor for motor vehicle collision involvement in drivers ≥ 70 years. , 2021, Accident; analysis and prevention.
[6] Utku Kaya,et al. The optomotor response of aging zebrafish reveals a complex relationship between visual motion characteristics and cholinergic system , 2020, Neurobiology of Aging.
[7] James E. Fitzgerald,et al. A Neural Representation of Naturalistic Motion-Guided Behavior in the Zebrafish Brain , 2020, Current Biology.
[8] Aristides B. Arrenberg,et al. Parallel Channels for Motion Feature Extraction in the Pretectum and Tectum of Larval Zebrafish. , 2020, Cell reports.
[9] Johann H. Bollmann,et al. The Zebrafish Visual System: From Circuits to Behavior. , 2019, Annual review of vision science.
[10] M. Herzog,et al. Associations between genetic variations and global motion perception , 2019, Experimental Brain Research.
[11] Aline F. Cretenoud,et al. No evidence for a common factor underlying visual abilities in healthy older people. , 2019, Developmental psychology.
[12] R. Hess,et al. Second-order visual sensitivity in the aging population , 2018, Aging Clinical and Experimental Research.
[13] K. Pilz,et al. Motion perception as a model for perceptual aging. , 2019, Journal of vision.
[14] Aristides B. Arrenberg,et al. Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum , 2019, BMC Biology.
[15] M. Adams,et al. Zebrafish—A Model Organism for Studying the Neurobiological Mechanisms Underlying Cognitive Brain Aging and Use of Potential Interventions , 2018, Front. Cell Dev. Biol..
[16] M. Adams,et al. Zebrafish Aging Models and Possible Interventions , 2018, Recent Advances in Zebrafish Researches.
[17] M. Adams,et al. Development of a novel zebrafish xenograft model in ache mutants using liver cancer cell lines , 2018, Scientific Reports.
[18] Markus Brauer,et al. Linear Mixed-Effects Models and the Analysis of Nonindependent Data: A Unified Framework to Analyze Categorical and Continuous Independent Variables that Vary Within-Subjects and/or Within-Items , 2017, Psychological methods.
[19] M. Mikl,et al. Changes in connectivity of the posterior default network node during visual processing in mild cognitive impairment: staged decline between normal aging and Alzheimer’s disease , 2017, Journal of Neural Transmission.
[20] M. Orger,et al. Zebrafish Behavior: Opportunities and Challenges. , 2017, Annual review of neuroscience.
[21] J. Faubert,et al. Cholinergic Potentiation Improves Perceptual-Cognitive Training of Healthy Young Adults in Three Dimensional Multiple Object Tracking , 2017, Front. Hum. Neurosci..
[22] Xi En Cheng,et al. Zebrafish tracking using convolutional neural networks , 2017, Scientific Reports.
[23] Haim Sompolinsky,et al. From Whole-Brain Data to Functional Circuit Models: The Zebrafish Optomotor Response , 2016, Cell.
[24] Cynthia Owsley,et al. Vision and Aging. , 2016, Annual review of vision science.
[25] M. Adams,et al. Short-term dietary restriction in old zebrafish changes cell senescence mechanisms , 2016, Neuroscience.
[26] S. Coombs,et al. Going with, then against the flow: evidence against the optomotor hypothesis of fish rheotaxis , 2015, Animal Behaviour.
[27] Valeria Anna Sovrano,et al. What can fish brains tell us about visual perception? , 2014, Front. Neural Circuits.
[28] Marco Dadda,et al. Do Fish Perceive Illusory Motion? , 2014, Scientific Reports.
[29] Yong Tang,et al. A normative framework for the study of second-order sensitivity in vision. , 2014, Journal of vision.
[30] J. Moshtaghian,et al. The effect of motion aftereffect on optomotor response in larva and adult zebrafish , 2014, Neuroscience Letters.
[31] R. Allard,et al. Feature tracking and aging , 2013, Front. Psychol..
[32] Ariel Rokem,et al. The benefits of cholinergic enhancement during perceptual learning are long-lasting , 2013, Front. Comput. Neurosci..
[33] Stephan C F Neuhauss,et al. Towards a comprehensive catalog of zebrafish behavior 1.0 and beyond. , 2013, Zebrafish.
[34] K. Hoffmann,et al. Contribution of Cholinergic and GABAergic Mechanisms to Direction Tuning, Discriminability, Response Reliability, and Neuronal Rate Correlations in Macaque Middle Temporal Area , 2012, The Journal of Neuroscience.
[35] Shin'ya Nishida,et al. Advancement of motion psychophysics: review 2001-2010. , 2011, Journal of vision.
[36] D. Braun,et al. Challenges to normal neural functioning provide insights into separability of motion processing mechanisms , 2011, Neuropsychologia.
[37] C. Owsley. Aging and vision , 2011, Vision Research.
[38] D. Burr,et al. Motion psychophysics: 1985–2010 , 2011, Vision Research.
[39] M. Silver,et al. Cholinergic Enhancement Augments Magnitude and Specificity of Visual Perceptual Learning in Healthy Humans , 2010, Current Biology.
[40] Ruth A. Carper,et al. Longitudinal Magnetic Resonance Imaging Study of Cortical Development through Early Childhood in Autism , 2010, The Journal of Neuroscience.
[41] J. Maunsell,et al. Attention improves performance primarily by reducing interneuronal correlations , 2009, Nature Neuroscience.
[42] Michael J. Goard,et al. Basal Forebrain Activation Enhances Cortical Coding of Natural Scenes , 2009, Nature Neuroscience.
[43] Yifeng Zhou,et al. Age-related decline of contrast sensitivity for second-order stimuli: earlier onset, but slower progression, than for first-order stimuli. , 2009, Journal of vision.
[44] Pieter R. Roelfsema,et al. Additive Effects of Attention and Stimulus Contrast in Primary Visual Cortex , 2009, Cerebral cortex.
[45] Dario L. Ringach,et al. Flies see second-order motion , 2008, Current Biology.
[46] K. Gegenfurtner,et al. Differential aging of motion processing mechanisms: Evidence against general perceptual decline , 2008, Vision Research.
[47] I. Zhdanova,et al. Aging of the circadian system in zebrafish and the effects of melatonin on sleep and cognitive performance , 2008, Brain Research Bulletin.
[48] M. Hawken,et al. Gain Modulation by Nicotine in Macaque V1 , 2007, Neuron.
[49] Valter Tucci,et al. Cognitive Aging in Zebrafish , 2006, PloS one.
[50] S. Neuhauss,et al. Genetic identification of AChE as a positive modulator of addiction to the psychostimulant D-amphetamine in zebrafish. , 2006, Journal of neurobiology.
[51] T. Ledgeway,et al. Sensitivity to spatial and temporal modulations of first-order and second-order motion , 2006, Vision Research.
[52] Herwig Baier,et al. Channeling of red and green cone inputs to the zebrafish optomotor response , 2005, Visual Neuroscience.
[53] C. Baker,et al. First- and second-order information in natural images: a filter-based approach to image statistics. , 2004, Journal of the Optical Society of America. A, Optics, image science, and vision.
[54] Junzo Uchiyama,et al. The zebrafish as a vertebrate model of functional aging and very gradual senescence , 2003, Experimental Gerontology.
[55] C. Neumeyer,et al. Wavelength dependence of the optomotor response in zebrafish (Danio rerio) , 2003, Vision Research.
[56] Herwig Baier,et al. Visuomotor Behaviors in Larval Zebrafish after GFP-Guided Laser Ablation of the Optic Tectum , 2003, The Journal of Neuroscience.
[57] Jocelyn Faubert,et al. Visual perception and aging. , 2002, Canadian journal of experimental psychology = Revue canadienne de psychologie experimentale.
[58] J. Vonesch,et al. Acetylcholinesterase is required for neuronal and muscular development in the zebrafish embryo , 2002, Nature Neuroscience.
[59] J M Zanker,et al. The optomotor response and spatial resolution of the visual system in male Xenos vesparum (Strepsiptera). , 2000, The Journal of experimental biology.
[60] Matthew C Smear,et al. Perception of Fourier and non-Fourier motion by larval zebrafish , 2000, Nature Neuroscience.
[61] A J Schofield,et al. What Does Second-Order Vision See in an Image? , 2000, Perception.
[62] Herwig Baier,et al. Zebrafish on the move: towards a behavior–genetic analysis of vertebrate vision , 2000, Current Opinion in Neurobiology.
[63] J. Faubert,et al. Larger effect of aging on the perception of higher-order stimuli , 2000, Vision Research.
[64] M. Georgeson,et al. Sensitivity to modulations of luminance and contrast in visual white noise: separate mechanisms with similar behaviour , 1999, Vision Research.
[65] C. Baker. Central neural mechanisms for detecting second-order motion , 1999, Current Opinion in Neurobiology.
[66] J. Hennig,et al. The Processing of First- and Second-Order Motion in Human Visual Cortex Assessed by Functional Magnetic Resonance Imaging (fMRI) , 1998, The Journal of Neuroscience.
[67] A. T. Smith,et al. Sensitivity to second-order motion as a function of temporal frequency and eccentricity , 1998, Vision Research.
[68] L. P. O'Keefe,et al. Processing of first- and second-order motion signals by neurons in area MT of the macaque monkey , 1998, Visual Neuroscience.
[69] Shin'ya Nishida,et al. Dual multiple-scale processing for motion in the human visual System , 1997, Vision Research.
[70] G. Sperling,et al. The functional architecture of human visual motion perception , 1995, Vision Research.
[71] Andrew T. Smith,et al. Evidence for separate motion-detecting mechanisms for first- and second-order motion in human vision , 1994, Vision Research.
[72] A. T. Smith,et al. Correspondence-based and energy-based detection of second-order motion in human vision. , 1994, Journal of the Optical Society of America. A, Optics, image science, and vision.
[73] G. Sperling,et al. Drift-balanced random stimuli: a general basis for studying non-Fourier motion perception. , 1988, Journal of the Optical Society of America. A, Optics and image science.
[74] Ken Nakayama,et al. Biological image motion processing: A review , 1985, Vision Research.
[75] Hironobu Osaki,et al. Cholinergic modulation of response gain in the primary visual cortex of the macaque. , 2012, Journal of neurophysiology.
[76] H. Maaswinkel,et al. Spatio-temporal frequency characteristics of the optomotor response in zebrafish , 2003, Vision Research.
[77] D G Pelli,et al. The VideoToolbox software for visual psychophysics: transforming numbers into movies. , 1997, Spatial vision.
[78] D H Brainard,et al. The Psychophysics Toolbox. , 1997, Spatial vision.
[79] M. Wullimann,et al. Functional anatomy of the zebrafish brain: a comparative evaluation , 1996 .
[80] P. Cavanagh,et al. Motion: the long and short of it. , 1989, Spatial vision.