Results for '*Neural Pathways'

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  1. Reentrant neural pathways and the theory-ladenness of perception.Athanassios Raftopoulos - 2001 - Philosophy of Science 68 (3):S187-S199.
    In this paper I argue for the cognitive impenetrability of perception by undermining the argument from reentrant pathways. To do that I will adduce psychological and neuropsychological evidence showing that (a) early vision processing is not affected by our knowledge about specific objects and events, and (b) that the role of the descending pathways is to enable the early-vision processing modules to participate in higher-level visual or cognitive functions. My thesis is that a part of observation, which I (...)
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  2.  28
    Neural pathways mediating cross education of motor function.Kathy L. Ruddy & Richard G. Carson - 2013 - Frontiers in Human Neuroscience 7.
  3. Neural pathways associated with loss of consciousness caused by intracerebral microinjection of GABA-sub(A)-active anesthetics.I. Sukhotinsky, V. Zalkind, J. Lu, D. A. Hopkins, B. Saper & M. Devor - 2007 - European Journal of Neuroscience 25 (5):1417-1436.
     
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  4.  5
    Neural Pathways Involved in the Formation of an Image: the Biological Substrate.Julio J. Ramirez - 1988 - Bulletin of Science, Technology and Society 8 (3):318-322.
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  5.  23
    What neural pathways mediate express saccades?Marc A. Sommer, Peter H. Schiller & Robert M. McPeek - 1993 - Behavioral and Brain Sciences 16 (3):589-590.
  6. Neural pathways of social cognition.Tjeerd Jellema & Perrett & I. David - 2009 - In Robin Dunbar & Louise Barrett (eds.), Oxford Handbook of Evolutionary Psychology. Oxford University Press.
     
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  7.  17
    Pathway rewiring with neural transplantation.Piergiorgio Strata & Ferdinando Rossi - 1995 - Behavioral and Brain Sciences 18 (1):73-73.
    A lesion to the brain is not necessary for a successful neural transplantation. Embryonic Purkinje cells placed on the surface of an uninjured adult cerebellum can develop and migrate into the host molecular layer. Both the Purkinje cells that migrated into the host cerebellum and those that remained in the graft were innervated by collateral sprouting of adult intact climbing fibers.
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  8.  90
    The ventral visual pathway: an expanded neural framework for the processing of object quality.Dwight J. Kravitz, Kadharbatcha S. Saleem, Chris I. Baker, Leslie G. Ungerleider & Mortimer Mishkin - 2013 - Trends in Cognitive Sciences 17 (1):26-49.
  9.  16
    Parallel Excitatory and Inhibitory Neural Circuit Pathways Underlie Reward-Based Phasic Neural Responses.Huanyuan Zhou, KongFatt Wong-Lin & Da-Hui Wang - 2018 - Complexity 2018:1-20.
    Phasic activity of dopaminergic neurons in the ventral tegmental area or substantia nigra compacta has been suggested to encode reward-prediction error signal for reinforcement learning. Recent studies have shown that the lateral habenula neurons exhibit a similar response, but for nonrewarding or punishment signals. Hence, the transient signaling role of LHb neurons is opposite that of DA neurons and also that of several other brain nuclei such as the border region of the globus pallidus internal segment and the rostral medial (...)
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  10. Neural Correlates of Consciousness: Empirical and Conceptual Questions.Thomas Metzinger - 2000 - MIT Press. Edited by Thomas Metzinger.
  11. What is a neural correlate of consciousness?David J. Chalmers - 2000 - In Thomas Metzinger (ed.), Neural Correlates of Consciousness. MIT Press. pp. 17--39.
    The search for neural correlates of consciousness (or NCCs) is arguably the cornerstone in the recent resurgence of the science of consciousness. The search poses many difficult empirical problems, but it seems to be tractable in principle, and some ingenious studies in recent years have led to considerable progress. A number of proposals have been put forward concerning the nature and location of neural correlates of consciousness. A few of these include.
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  12.  33
    Evolution and ontogeny of neural circuits.Sven O. E. Ebbesson - 1984 - Behavioral and Brain Sciences 7 (3):321-331.
    Recent studies on neural pathways in a broad spectrum of vertebrates suggest that, in addition to migration and an increase in the number of certain select neurons, a significant aspect of neural evolution is a “parcellation” (segregation-isolation) process that involves the loss of selected connections by the new aggregates. A similar process occurs during ontogenetic development. These findings suggest that in many neuronal systems axons do not invade unknown territories during evolutionary or ontogenetic development but follow in their ancestors' (...)
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  13. The neural basis of predicate-argument structure.James R. Hurford - 2003 - Behavioral and Brain Sciences 26 (3):261-283.
    Neural correlates exist for a basic component of logical formulae, PREDICATE(x). Vision and audition research in primates and humans shows two independent neural pathways; one locates objects in body-centered space, the other attributes properties, such as colour, to objects. In vision these are the dorsal and ventral pathways. In audition, similarly separable “where” and “what” pathways exist. PREDICATE(x) is a schematic representation of the brain's integration of the two processes of delivery by the senses of the location (...)
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  14. Temporal binding and the neural correlates of sensory awareness.Andreas K. Engel & Wolf Singer - 2001 - Trends in Cognitive Sciences 5 (1):16-25.
    Theories of binding have recently come into the focus of the consciousness debate. In this review, we discuss the potential relevance of temporal binding mechanisms for sensory awareness. Specifically, we suggest that neural synchrony with a precision in the millisecond range may be crucial for conscious processing, and may be involved in arousal, perceptual integration, attentional selection and working memory. Recent evidence from both animal and human studies demonstrates that specific changes in neuronal synchrony occur during all of these processes (...)
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  15.  41
    Neural systems connecting interoceptive awareness and feelings.Olga Pollatos, Klaus Gramann & Rainer Schandry - 2007 - Human Brain Mapping 28 (1):9-18.
  16. Neural reuse: A fundamental organizational principle of the brain.Michael L. Anderson - 2010 - Behavioral and Brain Sciences 33 (4):245.
    An emerging class of theories concerning the functional structure of the brain takes the reuse of neural circuitry for various cognitive purposes to be a central organizational principle. According to these theories, it is quite common for neural circuits established for one purpose to be exapted (exploited, recycled, redeployed) during evolution or normal development, and be put to different uses, often without losing their original functions. Neural reuse theories thus differ from the usual understanding of the role of neural plasticity (...)
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  17.  13
    Neural Substrates of Consciousness: Implications for Clinical Psychiatry.Douglas F. Watt & David I. Pincus - 2004 - In Jaak Panksepp (ed.), Textbook of Biological Psychiatry. Wiley-Liss. pp. 75-110.
  18.  24
    Editorial: Multisensory integration as a pathway to neural specialization for print in typical and dyslexic readers across writing systems.Susana Araújo, Urs Maurer & Tânia Fernandes - 2022 - Frontiers in Psychology 13.
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  19.  75
    Overlapping neural systems mediating extinction, reversal and regulation of fear.Daniela Schiller & Mauricio R. Delgado - 2010 - Trends in Cognitive Sciences 14 (6):268-276.
  20. The representing brain: Neural correlates of motor intention and imagery.Marc Jeannerod - 1994 - Behavioral and Brain Sciences 17 (2):187-202.
    This paper concerns how motor actions are neurally represented and coded. Action planning and motor preparation can be studied using a specific type of representational activity, motor imagery. A close functional equivalence between motor imagery and motor preparation is suggested by the positive effects of imagining movements on motor learning, the similarity between the neural structures involved, and the similar physiological correlates observed in both imaging and preparing. The content of motor representations can be inferred from motor images at a (...)
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  21. Neural circuits for self-awareness: Evolutionary origins and implementation in the human brain.George I. Viamontes, Bernard D. Beitman, Claudia T. Viamontes & Jorge A. Viamontes - 2004 - In Bernard D. Beitman & Jyotsna Nair (eds.), Self-Awareness Deficits in Psychiatric Patients: Neurobiology, Assessment, and Treatment. W.W. Norton & Co. pp. 24-111.
  22.  13
    Multisensory neural integration of chemical and mechanical signals.Juan Antonio Sánchez-Alcañiz & Richard Benton - 2017 - Bioessays 39 (8):1700060.
    Chemosensation and mechanosensation cover an enormous spectrum of processes by which animals use information from the environment to adapt their behavior. For pragmatic reasons, these sensory modalities are commonly investigated independently. Recent advances, however, have revealed numerous situations in which they function together to control animals’ actions. Highlighting examples from diverse vertebrates and invertebrates, we first discuss sensory receptors and neurons that have dual roles in the detection of chemical and mechanical stimuli. Next we present cases where peripheral chemosensory and (...)
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  23.  2
    Neural cell adhesion molecule L1: relating disease to function.Reed A. Flickinger - 1998 - Bioessays 20 (8):668-675.
    Neural cell adhesion molecules of the immunoglobulin superfamily are important components of the network of guidance cues and receptors that govern axon growth and guidance during development. For neural cell adhesion molecule L1, the combined application of human genetics, knockout mouse technology, and cell biology is providing fundamental insight into the role of L1 in mediating neuronal differentiation. Disease-causing mutations as well as mouse models of L1 disruption can now be used to examine the relevance of L1 binding specificities and (...)
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  24. Temporal binding and the neural correlates of consciousness.Andreas K. Engel - 2003 - In Axel Cleeremans (ed.), The Unity of Consciousness. Oxford University Press.
  25.  7
    Neural cell adhesion molecule L1: relating disease to function.Sue Kenwrick & Patrick Doherty - 1998 - Bioessays 20 (8):668-675.
    Neural cell adhesion molecules of the immunoglobulin superfamily are important components of the network of guidance cues and receptors that govern axon growth and guidance during development. For neural cell adhesion molecule L1, the combined application of human genetics, knockout mouse technology, and cell biology is providing fundamental insight into the role of L1 in mediating neuronal differentiation. Disease-causing mutations as well as mouse models of L1 disruption can now be used to examine the relevance of L1 binding specificities and (...)
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  26. The Neural Correlates of Cued Reward Omission.Jessica A. Mollick, Luke J. Chang, Anjali Krishnan, Thomas E. Hazy, Kai A. Krueger, Guido K. W. Frank, Tor D. Wager & Randall C. O’Reilly - 2021 - Frontiers in Human Neuroscience 15.
    Compared to our understanding of positive prediction error signals occurring due to unexpected reward outcomes, less is known about the neural circuitry in humans that drives negative prediction errors during omission of expected rewards. While classical learning theories such as Rescorla–Wagner or temporal difference learning suggest that both types of prediction errors result from a simple subtraction, there has been recent evidence suggesting that different brain regions provide input to dopamine neurons which contributes to specific components of this prediction error (...)
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  27.  17
    Neural Basis and Motor Imagery Intervention Methodology Based on Neuroimaging Studies in Children With Developmental Coordination Disorders: A Review.Keisuke Irie, Amiri Matsumoto, Shuo Zhao, Toshihiro Kato & Nan Liang - 2021 - Frontiers in Human Neuroscience 15.
    Although the neural bases of the brain associated with movement disorders in children with developmental coordination disorder are becoming clearer, the information is not sufficient because of the lack of extensive brain function research. Therefore, it is controversial about effective intervention methods focusing on brain function. One of the rehabilitation techniques for movement disorders involves intervention using motor imagery. MI is often used for movement disorders, but most studies involve adults and healthy children, and the MI method for children with (...)
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  28.  10
    Combining Neural and Behavioral Measures Enhances Adaptive Training.Md Lutfor Rahman, Benjamin T. Files, Ashley H. Oiknine, Kimberly A. Pollard, Peter Khooshabeh, Chengyu Song & Antony D. Passaro - 2022 - Frontiers in Human Neuroscience 16.
    Adaptive training adjusts a training task with the goal of improving learning outcomes. Adaptive training has been shown to improve human performance in attention, working memory capacity, and motor control tasks. Additionally, correlations have been observed between neural EEG spectral features and the performance of some cognitive tasks. This relationship suggests some EEG features may be useful in adaptive training regimens. Here, we anticipated that adding a neural measure into a behavioral-based adaptive training system would improve human performance on a (...)
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  29. Reentry and the Dynamic Core: Neural Correlates of Conscious Experience.Gerald M. Edelman & Giulio Srinivasan Tononi - 2000 - In Thomas Metzinger (ed.), Neural Correlates of Consciousness. MIT Press.
  30.  51
    A solution to the tag-assignment problem for neural networks.Gary W. Strong & Bruce A. Whitehead - 1989 - Behavioral and Brain Sciences 12 (3):381-397.
    Purely parallel neural networks can model object recognition in brief displays – the same conditions under which illusory conjunctions have been demonstrated empirically. Correcting errors of illusory conjunction is the “tag-assignment” problem for a purely parallel processor: the problem of assigning a spatial tag to nonspatial features, feature combinations, and objects. This problem must be solved to model human object recognition over a longer time scale. Our model simulates both the parallel processes that may underlie illusory conjunctions and the serial (...)
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  31.  64
    Direct evidence for a parietal-frontal pathway subserving spatial awareness in humans.Michel T. de Schotten, Marika Urbanski, Hugues Duffau, Emmanuelle Volle, Richard Lévy, Bruno Dubois & Paolo Bartolomeo - 2005 - Science 309 (5744):2226-2228.
  32.  52
    The neural basis of chronic pain, its plasticity and modulation.Misha-Miroslav Backonja - 1997 - Behavioral and Brain Sciences 20 (3):435-437.
    Dysfunction or injury of pain-transmitting primary afferents' central pathways can result in pain. The organism as a whole responds to such injury and consequently many symptoms of neuropathic pain develop. The nervous system responds to painful events and injury with neuroplasticity. Both peripheral sensitization and central sensitization take place and are mediated by a number of biochemical factors, including genes and receptors. Correction of altered receptors activity is the logical way to intervene therapeutically. [berkley; blumberg et al.; coderre & (...)
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  33.  22
    Neural constructivism: How mammals make modules.Robert A. Barton - 1997 - Behavioral and Brain Sciences 20 (4):556-557.
    Although the developmental arguments in the Quartz & Sejnowski target article may have intrinsic merit, they do not warrant the authors' conclusion that innate modular architectures are absent or minimal, and that neocortical evolution is simply a progression toward more flexible representational structures. Modular architectures can develop and evolve in tandem with sub-cortical specialisation. I present comparative evidence for the co-evolution of specific thalamic and cortical visual pathways.
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  34.  37
    The acting subject: Toward the neural basis of social cognition.Vittorio Gallese - 2000 - In Thomas Metzinger (ed.), Neural Correlates of Consciousness. MIT Press. pp. 325--333.
  35.  7
    Mechanisms of neural crest cell migration.Marianne Bronner-Fraser - 1993 - Bioessays 15 (4):221-230.
    Neural crest cells are remarkable in their extensive and stereotypic patterns of migration. The pathways of neural crest migration have been documented by cell marking techniques, including interspecific neural tube grafts, immunocytochemistry and Dil‐labelling. In the trunk, neural crest cells migrate dorsally under the skin or ventrally through the somites, where they move in a segmental fashion through the rostral half of each sclerotome. The segmental migration of neural crest cells appears to be prescribed by the somites, perhaps by (...)
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  36.  23
    Opposing FGF and retinoid pathways: a signalling switch that controls differentiation and patterning onset in the extending vertebrate body axis.Ruth Diez del Corral & Kate G. Storey - 2004 - Bioessays 26 (8):857-869.
    Construction of the trunk/caudal region of the vertebrate embryo involves a set of distinct molecules and processes whose relationships are just coming into focus. In addition to the subdivision of the embryo into head and trunk domains, this “caudalisation” process requires the establishment and maintenance of a stem zone. This sequentially generates caudal tissues over a long period which then undergo differentiation and patterning in the extending body axis. Here we review recent studies that show that changes in the signalling (...)
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  37.  4
    Common and divergent pathways in alternative developmental processes of ascidians.Lucia Manni & Paolo Burighel - 2006 - Bioessays 28 (9):902-912.
    Colonial ascidians offer opportunities to investigate how developmental events are integrated to generate the animal form, since they can develop similar individuals (oozooids from eggs, blastozooids from pluripotent somatic cells) through very different reproductive processes, i.e. embryogenesis and blastogenesis. Moreover, thanks to their key phylogenetic position, they can help in the understanding of the molecular mechanisms of morphogenesis and their evolution in chordates. We review organogenesis of the ascidian neural complex comparing embryos and buds in terms of topology, developmental mechanisms (...)
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  38.  7
    Receptor tyrosine kinase‐dependent neural crest migration in response to differentially localized growth factors.Bernhard Wehrle-Haller & James A. Weston - 1997 - Bioessays 19 (4):337-345.
    How different neural crest derivatives differentiate in distinct embryonic locations in the vertebrate embryo is an intriguing issue. Many attempts have been made to understand the underlying mechanism of specific pathway choices made by migrating neural crest cells. In this speculative review we suggest a new mechanism for the regulation of neural crest cell migration patterns in avian and mammalian embryos, based on recent progress in understanding the expression and activity of receptor tyrosine kinases during embryogenesis. Distinct subpopulations of crest‐derived (...)
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  39. Space in the brain: Different neural substrates for allocentric and egocentric frames of reference.Melvyn A. Goodale & K. Murphy - 2000 - In Thomas Metzinger (ed.), Neural Correlates of Consciousness. MIT Press.
     
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  40. The role of frontocingulate pathways in the emotion-cognition interface: Emerging clues from depression.Diego A. Pizzagalli - 2005 - Behavioral and Brain Sciences 28 (2):214-215.
    By emphasizing nonlinear dynamics between appraisal and emotions, Lewis's model provides a valuable platform for integrating psychological and neural perspectives on the emotion-cognition interface. In this commentary, I discuss the role of neuroscience in shaping new conceptualizations of emotion and the putative role of theta oscillation within frontocingulate pathways in depression, a syndrome in which emotion-cognition relations are dysfunctional.
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  41.  2
    Mixed Neuropathologies, Neural Motor Resilience and Target Discovery for Therapies of Late-Life Motor Impairment.Aron S. Buchman & David A. Bennett - 2022 - Frontiers in Human Neuroscience 16.
    By age 85, most adults manifest some degree of motor impairment. However, in most individuals a specific etiology for motor decline and treatment to modify its inexorable progression cannot be identified. Recent clinical-pathologic studies provide evidence that mixed-brain pathologies are commonly associated with late-life motor impairment. Yet, while nearly all older adults show some degree of accumulation of Alzheimer’s disease and related dementias pathologies, the extent to which these pathologies contribute to motor decline varies widely from person to person. Slower (...)
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  42.  50
    Symbolic and nonsymbolic pathways of number processing.Tom Verguts & Wim Fias - 2008 - Philosophical Psychology 21 (4):539 – 554.
    Recent years have witnessed an enormous increase in behavioral and neuroimaging studies of numerical cognition. Particular interest has been devoted toward unraveling properties of the representational medium on which numbers are thought to be represented. We have argued that a correct inference concerning these properties requires distinguishing between different input modalities and different decision/output structures. To back up this claim, we have trained computational models with either symbolic or nonsymbolic input and with different task requirements, and showed that this allowed (...)
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  43.  18
    CREB signalling in neural stem/progenitor cells: Recent developments and the implications for brain tumour biology.Theo Mantamadiotis, Nikos Papalexis & Sebastian Dworkin - 2012 - Bioessays 34 (4):293-300.
    This paper discusses the evidence for the role of CREB in neural stem/progenitor cell (NSPC) function and oncogenesis and how these functions may be important for the development and growth of brain tumours. The cyclic‐AMP response element binding (CREB) protein has many roles in neurons, ranging from neuronal survival to higher order brain functions such as memory and drug addiction behaviours. Recent studies have revealed that CREB also has a role in NSPC survival, differentiation and proliferation. Recent work has shown (...)
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  44.  8
    The neurobiology of parenting: A neural circuit perspective.Johannes Kohl, Anita E. Autry & Catherine Dulac - 2017 - Bioessays 39 (1):e201600159.
    Social interactions are essential for animals to reproduce, defend their territory, and raise their young. The conserved nature of social behaviors across animal species suggests that the neural pathways underlying the motivation for, and the execution of, specific social responses are also maintained. Modern tools of neuroscience have offered new opportunities for dissecting the molecular and neural mechanisms controlling specific social responses. We will review here recent insights into the neural circuits underlying a particularly fascinating and important form of (...)
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  45.  39
    Hunger and Satiety Signaling: Modeling Two Hypothalamomedullary Pathways for Energy Homeostasis.Kazuhiro Nakamura & Yoshiko Nakamura - 2018 - Bioessays 40 (8):1700252.
    The recent discovery of the medullary circuit driving “hunger responses” – reduced thermogenesis and promoted feeding – has greatly expanded our knowledge on the central neural networks for energy homeostasis. However, how hypothalamic hunger and satiety signals generated under fasted and fed conditions, respectively, control the medullary autonomic and somatic motor mechanisms remains unknown. Here, in reviewing this field, we propose two hypothalamomedullary neural pathways for hunger and satiety signaling. To trigger hunger signaling, neuropeptide Y activates a group of (...)
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  46.  5
    The Multiple Pathways Model of Visual System. A Review.Matteo Baccarini - 2013 - Humana Mente 6 (24).
    Although seeing is commonly experienced as a unitary activity, the scientific description of vision resists such an intuitive account. Both psychologists and neuroscientists are in agreement with the idea that the elaboration of visual information is distributed across several different routes provided with different functions. Importantly, these routes can be mapped onto well-identified anatomical subdivision of the visual system. Crucially, although originally based on the assumption that different visual information are elaborated via different neural channels, such a model is nowadays (...)
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  47.  37
    Affective consciousness and the instinctual motor system: The neural sources of sadness and joy.Jaak Panksepp - 2000 - In Ralph D. Ellis & Natika Newton (eds.), The Caldron of Consciousness: Motivation, Affect and Self-Organization - an Anthology. Advances in Consciousness Research. John Benjamins. pp. 27-54.
  48.  21
    Self-, Social-, or Neural-Determination?Lawrence Cahoone - 2019 - Journal of Philosophical Investigations 13 (28):95-108.
    Human “free will” has been made problematic by several recent arguments against mental causation, the unity of the I or “self,” and the possibility that conscious decision-making could be temporally prior to action. This paper suggests a pathway through this thicket for free will or self-determination. Doing so requires an account of mind as an emergent process in the context of animal psychology and mental causation. Consciousness, a palpable but theoretically more obscure property of some minds, is likely to derive (...)
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  49.  23
    Associations between Socioeconomic Status, Cognition, and Brain Structure: Evaluating Potential Causal Pathways Through Mechanistic Models of Development.Michael S. C. Thomas & Selma Coecke - 2023 - Cognitive Science 47 (1):e13217.
    Differences in socioeconomic status (SES) correlate both with differences in cognitive development and in brain structure. Associations between SES and brain measures such as cortical surface area and cortical thickness mediate differences in cognitive skills such as executive function and language. However, causal accounts that link SES, brain, and behavior are challenging because SES is a multidimensional construct: correlated environmental factors, such as family income and parental education, are only distal markers for proximal causal pathways. Moreover, the causal accounts (...)
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  50.  84
    Three forms of binding and their neural substrates: Alternatives to temporal synchrony.R. C. O'Reilly, R. Busby & R. Soto - 2003 - In Axel Cleeremans (ed.), The Unity of Consciousness. Oxford University Press. pp. 168--192.
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