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Livres sur le sujet « Neural substrate »

Auteur : Grafiati

Publié le 9 mars 2023

Mis à jour le 10 mars 2023

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1

Iqbal, Azlan, Matej Guid, Simon Colton, Jana Krivec, Shazril Azman et Boshra Haghighi. The Digital Synaptic Neural Substrate. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28079-0.

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Call, Josep, Gordon M. Burghardt, Irene M. Pepperberg, Charles T. Snowdon et Thomas Zentall, dir. APA handbook of comparative psychology : Basic concepts, methods, neural substrate, and behavior. Washington : American Psychological Association, 2017. http://dx.doi.org/10.1037/0000011-000.

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3

Schmajuk, Nestor A. Latent Inhibition and Its Neural Substrates. Boston, MA : Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0841-0.

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4

Latent inhibition and its neural substrates. Boston : Kluwer Academic Pub., 2002.

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5

Schmajuk, Nestor A. Latent inhibition and its neural substrates. Boston : Kluwer Academic Pub., 2002.

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6

Loeb, C., et G. F. Poggio. Neural Substrates of Memory, Affective Functions, and Conscious Experience. Berlin, Heidelberg : Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-59432-8.

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7

Elizabeth, Hillis Argye, dir. New techniques for identifying the neural substrates of language. [Hove, East Sussex : Psychology Press, 2002.

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8

S, Lund Jennifer, Werner Gerhard 1921- et University of Pittsburgh. Center for Neuroscience., dir. Sensory processing in the mammalian brain : Neural substrates and experimental strategies. New York : Oxford University Press, 1989.

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9

Petrovici, Mihai Alexandru. Form Versus Function : Theory and Models for Neuronal Substrates. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39552-4.

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10

Colvin, Leigh Elizabeth. The Psychological Factors and Neural Substrates Associated with Metacognition among Community-Dwelling and Neurologic Cohorts of Older Adults. [New York, N.Y.?] : [publisher not identified], 2019.

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11

Hendrik, Gispen Willem, et Routtenberg Aryeh, dir. Protein kinase C and its brain substrates : Role in neuronal growth and plasticity : proceedings of the Third International Meeting on Brain Phosphoproteins, held at Zeist (The Netherlands) 24-26 August, 1990. Amsterdam : Elsevier, 1991.

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12

International Meeting on Brain Phosphoproteins (3rd 1990 Zeist, Netherlands). Protein kinaseC and its brain substrates : Role in neuronal growth and plasticity : proceedings of the Third International Meeting on Brain Phosphoproteins held at Zeist (The Netherlands), 24-26 August, 1990. Amsterdam : Elsevier, 1991.

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13

Iqbal, Azlan, Matej Guid, Jana Krivec, Shazril Azman et Simon Colton. Digital Synaptic Neural Substrate : A New Approach to Computational Creativity. Springer London, Limited, 2016.

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14

Iqbal, Azlan, Matej Guid, Jana Krivec, Shazril Azman et Simon Colton. Digital Synaptic Neural Substrate : A New Approach to Computational Creativity. Springer International Publishing AG, 2016.

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15

Garvey, Marjorie A. TMS : neurodevelopment and perinatal insults. Sous la direction de Charles M. Epstein, Eric M. Wassermann et Ulf Ziemann. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780198568926.013.0022.

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Neural substrate for changes in neuromotor skills of typically developing children involves the complex and organized maturation of underlying brain structures. This article gives an overview of the changes that occur in motor function, as children get older and those aspects of central nervous development which may form the neural substrates of motor function development. It describes those TMS evoked parameters, related to the motor system, that have been studied in both typically developing children and in those who have suffered perinatal insults to the central nervous system. TMS has its limitations and is especially useful when used in combination with other neurophysiological modalities. The focus for future studies should be on correlating TMS evoked parameters with behavioural measures in typically developing children and explanation of the neural substrates of the motor abnormalities in children with perinatal insults and developmental disabilities.

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16

APA Handbook of Comparative Psychology : Vol. 1 : Basic Concepts, Methods, Neural Substrate, and Behavior Vol. 2 : Perception, Learning, and Cognition. American Psychological Association, 2017.

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17

Dienel, Samuel J., et David A. Lewis. Cellular Mechanisms of Psychotic Disorders. Sous la direction de Dennis S. Charney, Eric J. Nestler, Pamela Sklar et Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0018.

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Cognitive dysfunction in schizophrenia, including disturbances in working memory, is a core feature of the illness and the best predictor of long-term functional outcome. Working memory relies on neural network oscillations in the prefrontal cortex. Gamma-aminobutyric acid (GABA) neurons in the prefrontal cortex, which are crucial for this oscillatory activity, exhibit a number of alterations in individuals diagnosed with schizophrenia. These GABA neuron disturbances may be secondary to upstream alterations in excitatory pyramidal cells in the prefrontal cortex. Together, these findings suggest both a neural substrate for working memory impairments in schizophrenia and therapeutic targets for improving functional outcomes in this patient population.

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18

Domhoff, G. William. The Neurocognitive Theory of Dreaming. The MIT Press, 2022. http://dx.doi.org/10.7551/mitpress/14679.001.0001.

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A comprehensive neurocognitive theory of dreaming based on the theories, methodologies, and findings of cognitive neuroscience and the psychological sciences. G. William Domhoff's neurocognitive theory of dreaming is the only theory of dreaming that makes full use of the new neuroimaging findings on all forms of spontaneous thought and shows how well they explain the results of rigorous quantitative studies of dream content. Domhoff identifies five separate issues—neural substrates, cognitive processes, the psychological meaning of dream content, evolutionarily adaptive functions, and historically invented cultural uses—and then explores how they are intertwined. He also discusses the degree to which there is symbolism in dreams, the development of dreaming in children, and the relative frequency of emotions in the dreams of children and adults. During dreaming, the neural substrates that support waking sensory input, task-oriented thinking, and movement are relatively deactivated. Domhoff presents the conditions that have to be fulfilled before dreaming can occur spontaneously. He describes the specific cognitive processes supported by the neural substrate of dreaming and then looks at dream reports of research participants. The “why” of dreaming, he says, may be the most counterintuitive outcome of empirical dream research. Though the question is usually framed in terms of adaptation, there is no positive evidence for an adaptive theory of dreaming. Research by anthropologists, historians, and comparative religion scholars, however, suggests that dreaming has psychological and cultural uses, with the most important of these found in religious ceremonies and healing practices. Finally, he offers suggestions for how future dream studies might take advantage of new technologies, including smart phones.

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19

Campagnola, Luke, et Paul Manis. Patch Clamp Recording in Brain Slices. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199939800.003.0001.

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Patch clamp recording in brain slices allows unparalleled access to neuronal membrane signals in a system that approximates the in-vivo neural substrate while affording greater control of experimental conditions. In this chapter we discuss the theory, methodology, and practical considerations of such experiments including the initial setup, techniques for preparing and handling viable brain slices, and patching and recording signals. A number of practical and technical issues faced by electrophysiologists are also considered, including maintaining slice viability, visualizing and identifying healthy cells, acquiring reliable patch seals, amplifier compensation features, hardware configuration, sources of electrical noise and table vibration, as well as basic data analysis issues and some troubleshooting tips.

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Adolphs, Ralph, et Elina Birmingham. Neural Substrates of Social Perception. Oxford University Press, 2011. http://dx.doi.org/10.1093/oxfordhb/9780199559053.013.0029.

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21

Raymont, Vanessa, et Robert D. Stevens. Cognitive Reserve. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199653461.003.0029.

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The cognitive reserve hypothesis suggests that the structure and function of an individual’s brain can modulate the clinical expression of brain damage and illness. This chapter describes passive and active models of reserve, their impact on neurological illness, and how these effects can be assessed. Passive models focus on the protective potential of anatomical features, such as brain size, neural density, and synaptic connectivity, while active models emphasize the connectivity and efficiency of neural networks and active compensation by alternative networks. It is likely that both models represent features of a common biological substrate and could help in the development of strategies to improve outcome following critical illness.

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22

Boraud, Thomas. How the Brain Makes Decisions. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780198824367.001.0001.

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The human decision-making process is tainted with irrationality. To address this issue, this book proposes a ‘bottom-up’ approach of the neural substrate of decision-making, starting from the fundamental question: What are the basic properties that a neural network of decision-making needs to possess? Combining data drawn from phylogeny and physiology, this book provides a general framework of the neurobiology of decision-making in vertebrates and explains how it evolved from the lamprey to the apes. It also addresses the consequences, examining how it impacts our capacity of reasoning and some aspects of the pathophysiology of high brain functions. To conclude, the text opens discussion to more philosophical concepts such as the question of free will.

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23

Schmajuk, Nestor. Latent Inhibition and Its Neural Substrates. Springer, 2002.

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24

Schmajuk, Nestor. Latent Inhibition and Its Neural Substrates. Springer, 2012.

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25

Schmajuk, Nestor. Latent Inhibition and Its Neural Substrates. Springer London, Limited, 2012.

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26

Rapp, Brenda. Dysgraphia : Cognitive Processes, Remediation, and Neural Substrates. Psychology Press, 2003.

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27

Domhoff, G. William. Dreaming Is an Intensified Form of Mind-Wandering, Based in an Augmented Portion of the Default Network. Sous la direction de Kalina Christoff et Kieran C. R. Fox. Oxford University Press, 2018. http://dx.doi.org/10.1093/oxfordhb/9780190464745.013.7.

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This chapter argues that dreaming is an intensified form of mind-wandering that makes use of embodied simulation. It further hypothesizes that the neural network that enables dreaming is very likely an augmented portion of the default network. This network is activated whenever there is (1) a mature and intact neural substrate that can support the cognitive process of dreaming; (2) an adequate level of cortical activation; (3) an occlusion of external stimuli; (4) a cognitively mature imagination system (a necessity indicated by the virtual lack of dreaming in preschoolers and its relative paucity until ages 8–9); and (5) the loss of conscious self-control, which may be neurologically mediated in the final step in a complex process by the decoupling of the dorsal attentional network from the anterior portions of the default network. If this testable theory proves to be correct, then dreaming may be the quintessential cognitive simulation.

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28

Domhoff, G. William. The Cognitive Neuroscience of Dreaming. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190673420.003.0006.

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The fifth chapter presents the evidence for the novel idea that the neural substrate that enables dreaming is based in subsystems within the waking default network. The evidence for this hypothesis includes neuroimaging studies of representative samples of children and adults as well as studies of neurological patients who report they have experienced alterations in their dreaming, or even lost the ability to dream, due to their injury or illness. Based on these relatively new findings from many research settings, some as recent as 2015 and 2016, both the developmental trajectory of dreaming and the nature of dream content can be explained by the neurocognitive theory of dreams.

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29

Domhoff, G. William. A Promising Agenda. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190673420.003.0010.

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The ninth and final chapter returns to the forward-looking orientation of the first five chapters by presenting an agenda for future dream research, which makes use of recent developments in both communications (such as smartphones) and neuroimaging. It suggests how new and better studies can be done of dream recall, dream content, and the development of dreaming in children. It presents a novel way in which the neural substrate that very likely supports dreaming could be studied in greater detail by detecting the brief episodes of dreaming that are now known to occur during extended periods of drifting waking thought (e.g., during mind-wandering and daydreaming).

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30

Calingasan, Noel Y. Neural substrates of metabolic controls of feeding behavior. 1992.

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31

Nutt, David J., et Liam J. Nestor. The glutamate system and addiction. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198797746.003.0009.

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Glutamate is the primary excitatory neurotransmitter in the brain. Glutamate is involved in synaptic plasticity, particularly within dopamine systems of the brain that are involved in reward. Glutamate-dependent plasticity is involved in the development of substance addiction through its actions at NMDA receptors during long-term potentiation (LTP) related learning and memory processes. This plasticity within brain circuitry involved in learning and memory is sustained during substance abstinence and may provide a neural substrate for a vulnerability to addiction relapse. Medications that possess the efficacy to reduce glutamate tone in certain brain circuits may reduce craving, and ultimately, relapse in substance dependence. Further research is required, however, to show that the modulation of glutamate transmission in the brain confers clinical benefits in substance addiction.

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32

Loeb, C., et G. F. Poggio. Neural Substrates of Memory, Affective Functions, and Conscious Experience. Springer London, Limited, 2012.

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33

Geary, David C., Daniel B. Berch et Kathleen Mann Koepke. Development of Mathematical Cognition : Neural Substrates and Genetic Influences. Elsevier Science & Technology Books, 2015.

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34

Geary, David C., Daniel B. Berch et Kathleen Mann Koepke. Development of Mathematical Cognition : Neural Substrates and Genetic Influences. Elsevier Science & Technology Books, 2015.

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35

Neural Substrates of Memory, Affective Functions, and Conscious Experience. Springer-Verlag, 2002.

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36

Weatherford, Sally Crinean. Neural substrates mediating glucagon-induced suppression of food intake. 1987.

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37

Westheimer, Gerald. The Shifted-Chessboard Pattern as Paradigm of the Exegesis of Geometrical-Optical Illusions. Oxford University Press, 2017. http://dx.doi.org/10.1093/acprof:oso/9780199794607.003.0036.

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The shifted chessboard or café wall illusion yields to analysis at the two poles of the practice of vision science: bottom-up, pursuing its course from the visual stimulus into the front end of the visual apparatus, and top-down, figuring how the rules governing perception might lead to it. Following the first approach, examination of the effects of light spread in the eye and of nonlinearity and center-surround antagonism in the retina has made some inroads and provided partial explanations; with respect to the second, principles of perspective and of continuity and smoothness of contours can be evoked, and arguments about perception as Bayesian inference can be joined. Insights from these two directions are helping neurophysiologists in their struggle to identify a neural substrate of the phenomenon Münsterberg described in 1897.

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Steriade, Mircea. Neuronal Substrates of Sleep and Epilepsy. Cambridge University Press, 2009.

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Steriade, Mircea. Neuronal Substrates of Sleep and Epilepsy. Cambridge University Press, 2005.

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Steriade, Mircea. Neuronal Substrates of Sleep and Epilepsy. Cambridge University Press, 2003.

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Steriade, Mircea. Neuronal Substrates of Sleep and Epilepsy. Cambridge University Press, 2003.

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Steriade, Mircea. Neuronal Substrates of Sleep and Epilepsy. Cambridge University Press, 2003.

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43

Berkowitz, Aaron L. The Cognitive Neuroscience of Improvisation. Sous la direction de George E. Lewis et Benjamin Piekut. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780195370935.013.004.

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Cognitive neuroscience research has begun to elucidate the neural substrates and cognitive processes that are involved in musical improvisation. In turn, the study of improvisation from the perspective of cognitive neuroscience has provided new insights about the brain and cognition. This chapter reviews brain imaging research studies of improvisation and explores the relevance of this work to musicians, musicologists, music educators, and cognitive neuroscientists with respect to the practice and pedagogy of improvisation, comparisons between music and language cognition, mirror neuron systems, and neural plasticity.

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44

Geva, Sharon. Inner Speech and Mental Imagery. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198796640.003.0005.

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Inner speech has been investigated using neuroscientific techniques since the beginning of the twentieth century. One of the most important finding is that inner and overt speech differ in many respects, not only in the absence/presence of articulatory movements. In addition, studies implicate the involvement of various brain regions in the production and processing of inner speech, including areas involved in phonology and semantics, as well as auditory and motor processing. By looking at parallels between inner speech and other domains of imagery, studies explore two major questions: Are there common types of representations that underlie all types of mental imagery? And, is there a neural substrate for imagery, above and beyond modality? While these questions cannot yet be fully answered, studies of the neuroscience of imagery are bringing us a step towards better understanding of inner speech.

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45

Jaeger, Thomas V. Dissociation of neural substrates underlying morphine's reinforcing and discriminative effects. 1995.

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46

Hillis, Argye. Aphasiology-New Techniques for Identifying the Neural Substrates of Language. Psychology Press, 2003.

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47

Erdem, Uğur Murat, Nicholas Roy, John J. Leonard et Michael E. Hasselmo. Spatial and episodic memory. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199674923.003.0029.

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The neuroscience of spatial memory is one of the most promising areas for developing biomimetic solutions to complex engineering challenges. Grid cells are neurons recorded in the medial entorhinal cortex that fire when rats are in an array of locations in the environment falling on the vertices of tightly packed equilateral triangles. Grid cells suggest an exciting new approach for enhancing robot simultaneous localization and mapping (SLAM) in changing environments and could provide a common map for situational awareness between human and robotic teammates. Current models of grid cells are well suited to robotics, as they utilize input from self-motion and sensory flow similar to inertial sensors and visual odometry in robots. Computational models, supported by in vivo neural activity data, demonstrate how grid cell representations could provide a substrate for goal-directed behavior using hierarchical forward planning that finds novel shortcut trajectories in changing environments.

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Chae, Younbyoung, Vitaly Napadow, Florian Beissner, Yi-Wen Lin et Richard E. Harris, dir. Neural Substrates of Acupuncture : from Peripheral to Central Nervous System Mechanisms. Frontiers Media SA, 2020. http://dx.doi.org/10.3389/978-2-88963-505-4.

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49

Lund, Jennifer S. Sensory Processing in the Mammalian Brain : Neural Substrates and Experimental Strategies. Oxford University Press, USA, 1988.

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50

Ladenheim, Ellen Elizabeth. Neural substrates involved in cholecystokinin- and bombesin- induced suppression of food intake. 1989.

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