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  1. Surprisingly small subcortical structures are needed for the state of waking consciousness, while cortical projection areas seem to provide perceptual contents of consciousness.Bernard J. Baars - 1995 - Consciousness and Cognition 4 (2):159-62.
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  • The functional neuroanatomy of awareness: With a focus on the role of various anatomical systems in the control of intermodal attention.John Smythies - 1997 - Consciousness and Cognition 6 (4):455-81.
    This review considers a number of recent theories on the neural basis of consciousness, with particular attention to the theories of Bogen, Crick, Llinás, Newman, and Changeux. These theories allot different roles to various key brain areas, in particular the reticular and intralaminar nuclei of the thalamus and the cortex. Crick's hypothesis is that awareness is a function of reverberating corticothalamic loops and that the spotlight ofintramodalattention is controlled by the reticular nucleus of the thalamus. He also proposed different mechanisms (...)
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  • Neuronal assemblies: Necessity, signature, and detectability.Wolf Singer, Andreas K. Engel, A. Kreiter, M. Munk & P. R. Roelfsema - 1997 - Trends in Cognitive Sciences 1 (7):252-60.
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  • Thalamic contributions to attention and consciousness.James Newman - 1995 - Consciousness and Cognition 4 (2):172-93.
    A tacit assumption since the 19th Century has been that the neocortex serves as the "seat of consciousness." An unexpected challenge to that assumption arose in 1949 with the discovery that high-frequency EEG activation associated with an alert state requires the intactness of the brainstem reticular formation. This discovery became the impetus for nearly three decades of research on what came to be known as the reticular activating system. By the 1970s, however, methodological and philosophical controversies led to general abandonment (...)
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  • Neuroethology of releasing mechanisms: Prey-catching in toads.Jörg-Peter Ewert - 1987 - Behavioral and Brain Sciences 10 (3):337-368.
    Abstract“Sign stimuli” elicit specific patterns of behavior when an organism's motivation is appropriate. In the toad, visually released prey-catching involves orienting toward the prey, approaching, fixating, and snapping. For these action patterns to be selected and released, the prey must be recognized and localized in space. Toads discriminate prey from nonprey by certain spatiotemporal stimulus features. The stimulus-response relations are mediated by innate releasing mechanisms (RMs) with recognition properties partly modifiable by experience. Striato-pretecto-tectal connectivity determines the RM's recognition and localization (...)
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  • Temporal binding, binocular rivalry, and consciousness.Andreas K. Engel, Pascal Fries, Peter König, Michael Brecht & Wolf Singer - 1999 - Consciousness and Cognition 8 (2):128-51.
    Cognitive functions like perception, memory, language, or consciousness are based on highly parallel and distributed information processing by the brain. One of the major unresolved questions is how information can be integrated and how coherent representational states can be established in the distributed neuronal systems subserving these functions. It has been suggested that this so-called ''binding problem'' may be solved in the temporal domain. The hypothesis is that synchronization of neuronal discharges can serve for the integration of distributed neurons into (...)
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  • Separate visual pathways for perception and action.Melvyn A. Goodale & A. David Milner - 1992 - Trends in Neurosciences 15:20-25.
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  • Synchronization of oscillatory responses in visual cortex correlates with perception in interocular rivalry.Pascal Fries, Pieter R. Roelfsema, Andreas K. Engel & Wolf Singer - 1997 - Proceedings of the National Academy of Sciences Usa 94:12699-12704.
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  • Cerebral correlates of visual awareness.A. David Milner - 1995 - Neuropsychologia 33:1117-30.
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  • Some further ideas regarding the neuronal basis of awareness.Christof Koch & Francis Crick - 1994 - In Christof Koch & J. Davis (eds.), Large-Scale Neuronal Theories of the Brain. MIT Press. pp. 93.
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  • Consciousness and neuroscience.Francis Crick & Christof Koch - 1998 - Cerebral Cortex.
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  • Are we aware of neural activity in primary visual cortex.Francis Crick & Christof Koch - 1995 - Nature 375:121-23.
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  • Blindsight in man and monkey.Petra Stoerig & Alan Cowey - 1997 - Brain 120:535-59.
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  • Conscious visual perception without V.J. L. Barbur, J. D. G. Watson, R. D. G. Frackowiak & Semir Zeki - 1993 - Brain 116:1293-1302.
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  • Temporal coding in the visual cortex: New vistas on integration in the nervous system.Andreas K. Engel, P. Kreiter Konig & Schillen A. K. - 1992 - Trends in Neurosciences 15:218-26.
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  • Possible blindsight in infants lacking one cerebral hemisphere.O. Braddick, J. Atkinson, B. Hood & W. Harkness - 1992 - Nature 360:461-463.
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  • Some neurophysiologic aspects of consciousness.Joseph E. Bogen - 1997 - Seminars in Neurology 17:95-103.
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  • Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties.Charles M. Gray, P. Kreiter Konig, Andreas K. Engel & Wolf Singer - 1992 - Nature 338:334-7.
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  • The recognition potential and conscious awareness.A. P. Rudell & J. Hua - 1996 - Electroencephalography and Clinical Neurophysiology 98:309-318.
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  • Consciousness and the integration of information in the brain.Giulio Srinivasan Tononi & Gerald M. Edelman - 1998 - In H. Jasper, L. Descarries, V. Castellucci & S. Rossignol (eds.), Consciousness: At the Frontiers of Neuroscience. Lippincott-Raven.
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  • Blindsight: Conscious vs. unconscious aspects.Lawrence Weiskrantz - 1995 - In Joseph E. King & Karl H. Pribram (eds.), Scale in Conscious Experience. Lawrence Erlbaum. pp. 31-43.
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