Results for 'Cortical Models'

994 found
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  1.  32
    Cortical models and the neurological gap.Bruce Bridgeman - 1998 - Consciousness and Cognition 7 (2):157-158.
  2.  14
    A biologically realistic cortical model of eye movement control in reading.Jakob Heinzle, Klaus Hepp & Kevan A. C. Martin - 2010 - Psychological Review 117 (3):808-830.
  3. A model for cortical 40-Hertz oscillations invokes inter-area interactions.Rodney M. J. Cotterill & C. Nielsen - 1991 - Neuroreport 2:289-92.
  4.  20
    A cortical edge-integration model of object-based lightness computation that explains effects of spatial context and individual differences.Michael E. Rudd - 2014 - Frontiers in Human Neuroscience 8.
  5.  99
    Statistical Models of Natural Images and Cortical Visual Representation.Aapo Hyvärinen - 2010 - Topics in Cognitive Science 2 (2):251-264.
    A fundamental question in visual neuroscience is: Why are the response properties of visual neurons as they are? A modern approach to this problem emphasizes the importance of adaptation to ecologically valid input, and it proceeds by modeling statistical regularities in ecologically valid visual input (natural images). A seminal model was linear sparse coding, which is equivalent to independent component analysis (ICA), and provided a very good description of the receptive fields of simple cells. Further models based on modeling (...)
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  6.  48
    Integrated cortical field model of consciousness.Marcel Kinsbourne - 1993 - Ciba Foundation Symposium 174 (43-50).
  7. Modelling global to local cortical interaction for scene analysis and perspective retrieval.N. Guyader, C. Massot & J. Hérault - 2004 - In Robert Schwartz (ed.), Perception. Malden Ma: Blackwell. pp. 71-71.
     
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  8.  14
    Trion model of cortical organization: Toward a theory of information processing and memory.G. Lo Shaw, D. J. Silverman & J. C. Pearson - 1986 - In G. Palm & A. Aertsen (eds.), Brain Theory. Springer. pp. 177--191.
  9.  22
    A spiking neuron model of cortical broadcast and competition.Murray Shanahan - 2008 - Consciousness and Cognition 17 (1):288-303.
    This paper presents a computer model of cortical broadcast and competition based on spiking neurons and inspired by the hypothesis of a global neuronal workspace underlying conscious information processing in the human brain. In the model, the hypothesised workspace is realised by a collection of recurrently inter-connected regions capable of sustaining and disseminating a reverberating spatial pattern of activation. At the same time, the workspace remains susceptible to new patterns arriving from outlying cortical populations. Competition among these (...) populations for influence on the workspace is effected by a combination of mutual inhibition and top-down amplification. (shrink)
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  10.  28
    Schizophrenia as a model of context-deficient cortical computation.Steven M. Silverstein & Lindsay S. Schenkel - 1997 - Behavioral and Brain Sciences 20 (4):696-697.
    Phillips & Singer's compelling presentation is weakest in its demonstration of commonalities between sensory plasticity and higher forms of learning and behavior. We propose that available data on schizophrenia can provide such evidence, because of the presence of impairments in a number of functions central to their model, and strong relationships between these dysfunctions and behavior.
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  11.  1
    Learned Overweight Internal Model Can Be Activated to Maintain Equilibrium When Tactile Cues Are Uncertain: Evidence From Cortical and Behavioral Approaches.Olivia Lhomond, Benjamin Juan, Theo Fornerone, Marion Cossin, Dany Paleressompoulle, François Prince & Laurence Mouchnino - 2021 - Frontiers in Human Neuroscience 15.
    Human adaptive behavior in sensorimotor control is aimed to increase the confidence in feedforward mechanisms when sensory afferents are uncertain. It is thought that these feedforward mechanisms rely on predictions from internal models. We investigate whether the brain uses an internal model of physical laws to help estimate body equilibrium when tactile inputs from the foot sole are depressed by carrying extra weight. As direct experimental evidence for such a model is limited, we used Judoka athletes thought to have (...)
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  12. A radical reversal in cortical information flow as the mechanism for human cognitive abilities: The frontal feedback model.R. A. Noack - 1995 - Journal of Mind and Behavior 16 (3):281-304.
    The paper argues that the rich cognitive abilities of humans are the result of a unique functional system in the human brain which is absent in the nonhuman brain. This "frontal feedback system" is suggested to have evolved in the transition from the great apes to humans and is a product of a reversal in the preferred direction of information flow in the human cortex due to the phylogenetic enlargement of the human frontal lobe. The frontal feedback system forms an (...)
     
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  13.  54
    Cortical connections and parallel processing: Structure and function.Dana H. Ballard - 1986 - Behavioral and Brain Sciences 9 (1):67-90.
    The cerebral cortex is a rich and diverse structure that is the basis of intelligent behavior. One of the deepest mysteries of the function of cortex is that neural processing times are only about one hundred times as fast as the fastest response times for complex behavior. At the very least, this would seem to indicate that the cortex does massive amounts of parallel computation.This paper explores the hypothesis that an important part of the cortex can be modeled as a (...)
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  14.  8
    Formulaic language in cortical and subcortical disease: Evidence of the dual process model.Bridges Kelly - 2014 - Frontiers in Psychology 5.
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  15.  52
    Six principles for biologically based computational models of cortical cognition.Randall C. O'Reilly - 1998 - Trends in Cognitive Sciences 2 (11):455-462.
  16. A cortical network for semantics: (de)constructing the N400.E. Lau, C. Phillips & D. Poeppel - 2008 - Nature Reviews Neuroscience 9:920-933.
    Measuring event-related potentials (ERPs) has been fundamental to our understanding of how language is encoded in the brain. One particular ERP response, the N400 response, has been especially influential as an index of lexical and semantic processing. However, there remains a lack of consensus on the interpretation of this component. Resolving this issue has important consequences for neural models of language comprehension. Here we show that evidence bearing on where the N400 response is generated provides key insights into what (...)
     
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  17.  5
    Transient Global Amnesia: An Electrophysiological Disorder Based on Cortical Spreading Depression—Transient Global Amnesia Model.Xuejiao Ding & Dantao Peng - 2020 - Frontiers in Human Neuroscience 14.
    Transient global amnesia is a benign memory disorder with etiologies that have been debated for a long time. The prevalence of stressful events before a TGA attack makes it hard to overlook these precipitating factors, given that stress has the potential to organically effect the brain. Cortical spreading depression was proposed as a possible cause decades ago. Being a regional phenomenon, CSD seems to affect every aspect of the micro-mechanism in maintaining the homeostasis of the central nervous system. Corresponding (...)
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  18.  54
    Cortical activity and the explanatory gap.John G. Taylor - 1998 - Consciousness and Cognition 7 (2):109-48.
    An exploration is given of neural network features now being uncovered in cortical processing which begins to go a little way to help bridge the ''Explanatory Gap'' between phenomenal consciousness and correlated brain activity. A survey of properties suggested as being possessed by phenomenal consciousness leads to a set of criteria to be required of the correlated neural activity. Various neural styles of processing are reviewed and those fitting the criteria are selected for further analysis. One particular processing style, (...)
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  19.  10
    Visual cortical γ−aminobutyric acid and perceptual suppression in amblyopia.Arjun Mukerji, Kelly N. Byrne, Eunice Yang, Dennis M. Levi & Michael A. Silver - 2022 - Frontiers in Human Neuroscience 16:949395.
    In amblyopia, abnormal visual experience during development leads to an enduring loss of visual acuity in adulthood. Physiological studies in animal models suggest that intracortical GABAergic inhibition may mediate visual deficits in amblyopia. To better understand the relationship between visual cortical γ-aminobutyric acid (GABA) and perceptual suppression in persons with amblyopia (PWA), we employed magnetic resonance spectroscopy (MRS) to quantify GABA levels in both PWA and normally-sighted persons (NSP). In the same individuals, we obtained psychophysical measures of perceptual (...)
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  20.  6
    Supplementary note on “A spiking neuron model of cortical broadcast and competition”.Murray Shanahan - 2008 - Consciousness and Cognition 17 (1):304-306.
  21. Conditions for Propagating Synchronous Spiking and Asynchronous Firing Rates in a Cortical Network Model.Arvind Kumar - unknown
    Isolated feedforward networks (FFNs) of spiking neurons have been studied extensively for their ability to propagate transient synchrony and asynchronous firing rates, in the presence of activity independent synaptic background noise (Diesmann et al., 1999; van Rossum et al., 2002). In a biologically realistic scenario, however, the FFN should be embedded in a recurrent network, such that the activity in the FFN and the network activity may dynamically interact. Previously, transient synchrony propagating in an FFN was found to destabilize the (...)
     
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  22. Of Bits and Logic: Cortical Columns in Learning and Memory.Robert Moss - 2006 - Journal of Mind and Behavior 27 (3-4).
    Despite the growing research and theoretical formulations tied to memory storage within the brain, the role of cortical columns has received relatively little attention. The current paper presents a theoretical formulation based on cortical columns as the binary units that contain all cortical information, and how memory and learning may occur based on the interaction patterns of columns. The described model is an extension of Lurian views, and suggests higher functions to result from the interaction of five (...)
     
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  23. Intuitive versus experimental approaches for modelling of visual cortical circuitry.Keisuke Toyama - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 366.
  24. Visual cortical processing: textural sensitivity and its implications for classical views.P. Hammond - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 326--333.
     
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  25. Inferring cortical organization from subjective visual patterns.M. A. Georgeson - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 223--232.
  26.  35
    Principles of cortical synchronization.Stephen Grossberg - 1997 - Behavioral and Brain Sciences 20 (4):689-690.
    Functional roles for cortical synchronization in self-organizing neural networks are described. These properties are best understood by models that link brain to behavior. Synchrony can express itself differently in cortical circuits that perform different behavioral tasks. Cortical temporal properties that seem inexplicable by synchrony are also mentioned.
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  27.  37
    Tensegrity behaviour of cortical and cytosolic cytoskeletal components in twisted living adherent cells.Valérie M. Laurent, Patrick Cañadas, Redouane Fodil, Emmanuelle Planus, Atef Asnacios, Sylvie Wendling & Daniel Isabey - 2002 - Acta Biotheoretica 50 (4):331-356.
    The present study is an attempt to relate the multicomponent response of the cytoskeleton (CSK), evaluated in twisted living adherent cells, to the heterogeneity of the cytoskeletal structure - evaluated both experimentally by means of 3D reconstructions, and theoretically considering the predictions given by two tensegrity models composed of (four and six) compressive elements and (respectively 12 and 24) tensile elements. Using magnetic twisting cytometry in which beads are attached to integrin receptors linked to the actin CSK of living (...)
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  28. Cortical circuitry underlying inhibitory processes in cat area 17.Peter Somogyi & K. A. C. Martin - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley.
     
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  29.  52
    Problems with a “cortical screen” for visual imagery.David Ingle - 2002 - Behavioral and Brain Sciences 25 (2):195-196.
    I support Pylyshyn's skepticism that visual imagery reflects a re-activation of the spatial layout of active neurons embedded within a topographical cortical map of visual space. The pickup of visual information via successive eye movements presents one problem and the two visual systems model poses another difficulty.
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  30. Properties of cortical color cells.Charles R. Michael - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 301.
     
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  31.  17
    Combining Gamma With Alpha and Beta Power Modulation for Enhanced Cortical Mapping in Patients With Focal Epilepsy.Mario E. Archila-Meléndez, Giancarlo Valente, Erik D. Gommer, João M. Correia, Sanne ten Oever, Judith C. Peters, Joel Reithler, Marc P. H. Hendriks, William Cornejo Ochoa, Olaf E. M. G. Schijns, Jim T. A. Dings, Danny M. W. Hilkman, Rob P. W. Rouhl, Bernadette M. Jansma, Vivianne H. J. M. van Kranen-Mastenbroek & Mark J. Roberts - 2020 - Frontiers in Human Neuroscience 14.
    About one third of patients with epilepsy have seizures refractory to the medical treatment. Electrical stimulation mapping is the gold standard for the identification of “eloquent” areas prior to resection of epileptogenic tissue. However, it is time-consuming and may cause undesired side effects. Broadband gamma activity recorded with extraoperative electrocorticography during cognitive tasks may be an alternative to ESM but until now has not proven of definitive clinical value. Considering their role in cognition, the alpha and beta bands could further (...)
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  32. Visual motion and cortical magnification.M. Wright & A. Johnston - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 233--241.
     
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  33. Coding with spike shapes and graded potentials in cortical networks.Mikko Juusola, Hugh P. C. Robinson & Gonzalo G. de Polavieja - 2007 - Bioessays 29 (2):178-187.
    In cortical neurones, analogue dendritic potentials are thought to be encoded into patterns of digital spikes. According to this view, neuronal codes and computations are based on the temporal patterns of spikes: spike times, bursts or spike rates. Recently, we proposed an ‘action potential waveform code’ for cortical pyramidal neurones in which the spike shape carries information. Broader somatic action potentials are reliably produced in response to higher conductance input, allowing for four times more information transfer than spike (...)
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  34.  32
    Aberrant Topological Patterns of Structural Cortical Networks in Psychogenic Erectile Dysfunction.Lu Zhao, Min Guan, Xiaobo Zhu, Sherif Karama, Budhachandra Khundrakpam, Meiyun Wang, Minghao Dong, Wei Qin, Jie Tian, Alan C. Evans & Dapeng Shi - 2015 - Frontiers in Human Neuroscience 9:166843.
    Male sexual arousal (SA) has been known as a multidimensional experience involving closely interrelated and coordinated neurobehavioral components that rely on widespread brain regions. Recent functional neuroimaging studies have shown relation between abnormal/altered dynamics in these circuits and male sexual dysfunction. However, alterations in the topological1 organization of structural brain networks in male sexual dysfunction are still unclear. Here, we used graph theory2 to investigate the topological properties of large-scale structural brain networks, which were constructed using inter-regional correlations of (...) thickness between 78 cortical regions (subcortical regions were not included due to the used cortical surface model) in 40 patients with psychogenic erectile dysfunction (pED) and 39 normal controls. Compared with normal controls, pED patients exhibited a less optimal global topological organization with reduced global and increased local efficiencies. Our results suggest disrupted neural integration among distant brain regions in pED patients, consistent with previous reports of impaired white matter structure and abnormal functional integrity in pED. Additionally, disrupted global network topology in pED was observed to be primarily relevant to altered subnetwork and nodal properties within the networks mediating the cognitive, motivational and inhibitory processes of male SA, possibly indicating disrupted integration of these networks in the whole brain networks and might account for pED patients’ abnormal cognitive, motivational and inhibitory processes for male SA. In total, our findings provide evidence for disrupted integrity in large-scale brain networks underlying the neurobehavioral processes of male SA in pED and provide new insights into the understanding of the pathophysiological mechanisms of pED. (shrink)
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  35.  9
    Levels, models, and brain activities: Neurodynamics is pluralistic.Péter Érdi - 1996 - Behavioral and Brain Sciences 19 (2):296-297.
    Some dichotomies related to modeling electrocortical activities are analyzed. Attractor neural networks versus biologically motivated models, near-equilibrium versus nonequilibrium processes, linear and nonlinear dynamics, stochastic and chaotic patterns, local and global scale simulation of cortical activities are discussed.
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  36. The role of accurate timing in human performance and the code for higher cortical function.L. Brothers & G. L. Shaw - 1989 - In Rodney M. J. Cotterill (ed.), Models of Brain Function. Cambridge University Press.
     
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  37.  7
    Simulation of Combined Stresses and Stress Concentration Factor Effects on a Femur Cortical Bones.Alex J. Velez-Cruz - 2022 - Minerva 3 (8):8-19.
    The purposes of this article were to obtain mechanical properties of the dry femur cortical bone samples through a tensile load and stress concentration factor approach and to provide simulations to predict experimental behaviors based on manipulations of certain properties and parameters of the biomaterial. Since bone samples have characteristics and geometries, the development of a mathematical model was necessary to describe the combination of stresses interacting in the bone when a tension load is applied. The samples have average (...)
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  38.  9
    Spatial-Temporal Functional Mapping Combined With Cortico-Cortical Evoked Potentials in Predicting Cortical Stimulation Results.Yujing Wang, Mark A. Hays, Christopher Coogan, Joon Y. Kang, Adeen Flinker, Ravindra Arya, Anna Korzeniewska & Nathan E. Crone - 2021 - Frontiers in Human Neuroscience 15.
    Functional human brain mapping is commonly performed during invasive monitoring with intracranial electroencephalographic electrodes prior to resective surgery for drug­ resistant epilepsy. The current gold standard, electrocortical stimulation mapping, is time ­consuming, sometimes elicits pain, and often induces after discharges or seizures. Moreover, there is a risk of overestimating eloquent areas due to propagation of the effects of stimulation to a broader network of language cortex. Passive iEEG spatial-temporal functional mapping has recently emerged as a potential alternative to ESM. However, (...)
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  39.  8
    Neuromodulation can significantly change the dynamical state of cortical networks.Hans Liljenström - 1996 - Behavioral and Brain Sciences 19 (2):303-304.
    We present simulation results of an olfactory cortex model complementing the results presented in Wright & Liley's target article. We show how the cortical dynamics as expressed in EEG can be regulated by neuromodulation and discuss how the system can attain global stability without cortical-subcortical interaction, as presumed necessary by Wright & Liley. Network structure is shown to be crucial.
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  40. The temporal dimension of thought: Cortical foundations of predicative representation.Markus Werning - 2005 - Synthese 146 (1-2):203-224.
    The paper argues that cognitive states of biological systems are inherently temporal. Three adequacy conditions for neuronal models of representation are vindicated: the compositionality of meaning, the compositionality of content, and the co-variation with content. Classicist and connectionist approaches are discussed and rejected. Based on recent neurobiological data, oscillatory networks are introduced as a third alternative. A mathematical description in a Hilbert space framework is developed. The states of this structure can be regarded as conceptual representations satisfying the three (...)
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  41. Why people see things that are not there: A novel perception and attention deficit model for recurrent complex visual hallucinations.Daniel Collerton, Elaine Perry & Ian McKeith - 2005 - Behavioral and Brain Sciences 28 (6):737-757.
    As many as two million people in the United Kingdom repeatedly see people, animals, and objects that have no objective reality. Hallucinations on the border of sleep, dementing illnesses, delirium, eye disease, and schizophrenia account for 90% of these. The remainder have rarer disorders. We review existing models of recurrent complex visual hallucinations (RCVH) in the awake person, including cortical irritation, cortical hyperexcitability and cortical release, top-down activation, misperception, dream intrusion, and interactive models. We provide (...)
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  42. A global workspace model for phenomenal and access consciousness.Antonino Raffone & Martina Pantani - 2010 - Consciousness and Cognition 19 (2):580-596.
    Both the global workspace theory and Block’s distinction between phenomenal and access consciousness, are central in the current debates about consciousness and the neural correlates of consciousness. In this article, a unifying global workspace model for phenomenal and access consciousness is proposed. In the model, recurrent neural interactions take place in distinct yet interacting access and phenomenal brain loops. The effectiveness of feedback signaling onto sensory cortical maps is emphasized for the neural correlates of phenomenal consciousness. Two forms of (...)
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  43.  34
    The Developmental Gap in Phenomenal Experience: A Comment on J. G. Taylor's “Cortical Activity and the Explanatory Gap”.Thomas C. Dalton - 1998 - Consciousness and Cognition 7 (2):159-164.
    J. G. Taylor advances an empirically testable local neural network model to understand the neural correlates of phenomenal experience. Taylor's model is better able to explain the presence and unity of phenomenal consciousness which support the idea that consciousness is coherent, undivided, and centered. However, Taylor fails to offer a satisfactory explanation of the nonlinear relationship between local and global neural systems. In addition, the ontological assumptions that PE is immediate, intrinsic, and incorrigible limit an understanding of the different experiential (...)
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  44.  19
    Neurolinguistic models and fossil reconstructions.Merlin Donald - 1995 - Behavioral and Brain Sciences 18 (1):188-189.
    Hominid-like morphology in habiline cranial endocasts does not necessarily imply the presence of language capacity. The cortical zone in question is not associated exclusively with language in humans, and its emergence in habilines might indicate the evolution of other cognitive functions special to humans that were preconditions for the later evolution of language.
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  45.  49
    Underconstrained thalamic activation + underconstrained top-down modulation of cortical input processing = underconstrained perceptions.Martin Sarter & Gary G. Berntson - 2004 - Behavioral and Brain Sciences 27 (6):803-804.
    Behrendt & Young's (B&Y's) theory offers a potentially important perspective on the neurobiology of schizophrenia, but it remains incomplete. In addition to bottom-up contributions, such as those associated with disturbances in sensory constraints on cognitive processes, a comprehensive model requires the integration of the consequences of abnormal top-down modulation of input processing for the evolution of “underconstrained” perceptions. Dysfunctional cholinergic modulation of input functions represents a necessary mechanism for the generation of false perceptions.
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  46.  46
    A neurocognitive model of meditation based on activation likelihood estimation (ALE) meta-analysis.Marco Sperduti, Pénélope Martinelli & Pascale Piolino - 2012 - Consciousness and Cognition 21 (1):269-276.
    Meditation comprises a series of practices mainly developed in eastern cultures aiming at controlling emotions and enhancing attentional processes. Several authors proposed to divide meditation techniques in focused attention and open monitoring techniques. Previous studies have reported differences in brain networks underlying FA and OM. On the other hand common activations across different meditative practices have been reported. Despite differences between forms of meditation and their underlying cognitive processes, we propose that all meditative techniques could share a central process that (...)
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  47.  53
    Learning Representations of Animated Motion Sequences—A Neural Model.Georg Layher, Martin A. Giese & Heiko Neumann - 2014 - Topics in Cognitive Science 6 (1):170-182.
    The detection and categorization of animate motions is a crucial task underlying social interaction and perceptual decision making. Neural representations of perceived animate objects are partially located in the primate cortical region STS, which is a region that receives convergent input from intermediate-level form and motion representations. Populations of STS cells exist which are selectively responsive to specific animated motion sequences, such as walkers. It is still unclear how and to what extent form and motion information contribute to the (...)
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  48. The developmental gap in phenomenal experience: A comment on J. G. Taylor's "cortical activity and the explanatory gap''. J:Consciousness and cognition 7 (2):159-164. [REVIEW]Thomas C. Dalton - 1998 - Consciousness and Cognition 7 (2):159-164.
    J. G. Taylor advances an empirically testable local neural network model to understand the neural correlates of phenomenal experience. Taylor's model is better able to explain the presence (i.e., persistence, latency, and seamlessness) and unity of phenomenal consciousness which support the idea that consciousness is coherent, undivided, and centered. However, Taylor fails to offer a satisfactory explanation of the nonlinear relationship between local and global neural systems. In addition, the ontological assumptions that PE is immediate, intrinsic, and incorrigible limit an (...)
     
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  49. Plant morphogenesis: A geometrical model for the ramification.Michel Ferré & Hervé Guyader - 1990 - Acta Biotheoretica 38 (3-4).
    A geometrical model is proposed that describes the emergence of a primordium at the shoot apex in Dicotyledons. It is based on recent fundamental results on plant morphogenesis, viz.: – the emergence is preceded by the reorganization of the microtubules of the cortical cytoskeleton, leading to a new orientation of the synthesis of the cell wall microfibrils; – the resulting global stress is related to the general orientation of the cell growth.
     
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  50. Geniculate orientation biases as Cartesian coordinates for cortical orientation detectors.T. R. Vidyasagar - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 390--395.
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