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ГЛАВА 10. ОГОНЬ ИЗНУТРИ

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9. Cirelli, C. & Tononi, G. Is sleep essential? PLoS Biol 6, e216, doi:10.1371/journal.pbio.0060216 (2008).

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15. Tononi, G. & Cirelli, C. Sleep and the price of plasticity: from synaptic and cellular homeostasis to memory consolidation and integration. Neuron 81, 12–34, doi:10.1016/j.neuron.2013.12.025 (2014).

16. Liu, Z.-W., Faraguna, U., Cirelli, C., Tononi, G. & Gao, X.-B. Direct evidence for wake-related increases and sleep-related decreases in synaptic strength in rodent cortex. Journal of Neuroscience 30, 8671–8675 (2010).

17. Babkoff, H., Sing, H. C., Thorne, D. R., Genser, S. G. & Hegge, F. W. Perceptual distortions and hallucinations reported during the course of sleep deprivation. Percept Mot Skills 68, 787–798, doi:10.2466/pms.1989.68.3.787 (1989).

18. Siegel, R. K. & West, L. J. Hallucinations: Behavior, experience, and theory (John Wiley & Sons, 1975).

19. West, L. J., Pierce, C. M. & Thomas, W. D. Lysergic Acid Diethylamide: Its Effects on a Male Asiatic Elephant. Science 138, 1100–1103, doi:10.1126/science.138.3545.1100 (1962).

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21. de Vivo, L. et al. Ultrastructural evidence for synaptic scaling across the wake/sleep cycle. Science 355, 507–510, doi:10.1126/science.aah5982 (2017).

22. Stickgold, R., Hobson, J. A., Fosse, R. & Fosse, M. Sleep, learning, and dreams: off-line memory reprocessing. Science 294, 1052–1057, doi:10.1126/science.1063530 (2001).

23. Siegel, J. M. The stuff dreams are made of: anatomical substrates of REM sleep. Nature neuroscience 9, 721 (2006).

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26. Penfield, W. The interpretive cortex; the stream of consciousness in the human brain can be electrically reactivated. Science 129, 1719–1725, doi:10.1126/science.129.3365.1719 (1959).

27. Bartolomei, F. et al. Cortical stimulation study of the role of rhinal cortex in deja vu and reminiscence of memories. Neurology 63, 858–864, doi:10.1212/01.wnl.0000137037.56916.3f (2004).

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29. Friston, K. A theory of cortical responses. Philos Trans R Soc Lond B Biol Sci 360, 815–836, doi:10.1098/rstb.2005.1622 (2005).

30. Harris, K. D. & Mrsic-Flogel, T. D. Cortical connectivity and sensory coding. Nature 503, 51–58, doi:10.1038/nature12654 (2013).

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33. Fiorani Junior, M., Rosa, M. G., Gattass, R. & Rocha-Miranda, C. E. Dynamic surrounds of receptive fields in primate striate cortex: a physiological basis for perceptual completion? Proc Natl Acad Sci USA 89, 8547–8551, doi:10.1073/pnas.89.18.8547 (1992).

34. Sirosh, J. & Miikkulainen, R. Cooperative self-organization of afferent and lateral connections in cortical maps. Biological Cybernetics 71, 65–78, doi:10.1007/BF00198912 (1994).

35. O'Reilly, R. C. & Rudy, J. W. Conjunctive representations in learning and memory: principles of cortical and hippocampal function. Psychol Rev 108, 311–345, doi:10.1037/0033-295x.108.2.311 (2001).

36. Isaacson, J. S. & Scanziani, M. How inhibition shapes cortical activity. Neuron 72, 231–243, doi:10.1016/j.neuron.2011.09.027 (2011).

37. Dorrn, A. L., Yuan, K., Barker, A. J., Schreiner, C. E. & Froemke, R. C. Developmental sensory experience balances cortical excitation and inhibition. Nature 465, 932–936, doi:10.1038/nature09119 (2010).

38. Benchenane, K., Tiesinga, P. H. & Battaglia, F. P. Oscillations in the prefrontal cortex: a gateway to memory and attention. Curr Opin Neurobiol 21, 475–485, doi:10.1016/j.conb.2011.01.004 (2011).

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40. Mumford, D. On the computational architecture of the neocortex. Biological cybernetics 65, 135–145 (1991).

41. Teyler, T. J. & DiScenna, P. The hippocampal memory indexing theory. Behavioral neuroscience 100, 147 (1986).

42. Tanaka, K. Z. et al. Cortical representations are reinstated by the hippocampus during memory retrieval. Neuron 84, 347–354 (2014).

43. Wallenstein, G. V., Hasselmo, M. E. & Eichenbaum, H. The hippocampus as an associator of discontiguous events. Trends in Neurosciences 21, 317–323, doi:https://doi.org/10.1016/S0166–2236 (97) 01220–4 (1998).

44. Bota, M., Sporns, O. & Swanson, L. W. Architecture of the cerebral cortical association connectome underlying cognition. Proc Natl Acad Sci USA 112, E2093–2101, doi:10.1073/pnas.1504394112 (2015).

45. van den Heuvel, M. P. & Sporns, O. Rich-club organization of the human connectome. J Neurosci 31, 15775–15786, doi:10.1523/JNEUROSCI.3539–11.2011 (2011).

46. Rebola, N., Carta, M. & Mulle, C. Operation and plasticity of hippocampal CA3 circuits: implications for memory encoding. Nat Rev Neurosci 18, 208–220, doi:10.1038/nrn.2017.10 (2017).

47. Sharon, T., Moscovitch, M. & Gilboa, A. Rapid neocortical acquisition of long-term arbitrary associations independent of the hippocampus. Proc Natl Acad Sci USA 108, 1146–1151, doi:10.1073/pnas.1005238108 (2011).

48. Morris, R. G. M., Garrud, P., Rawlins, J. N. P. a. & O'Keefe, J. Place navigation impaired in rats with hippocampal lesions. Nature 297, 681 (1982).

49. Rasch, B. & Born, J. Maintaining memories by reactivation. Curr Opin Neurobiol 17, 698–703, doi:10.1016/j.conb.2007.11.007 (2007).

50. Frankland, P. W. & Bontempi, B. The organization of recent and remote memories. Nat Rev Neurosci 6, 119–130, doi:10.1038/nrn1607 (2005).

51. Callaway, E. M. Feedforward, feedback and inhibitory connections in primate visual cortex. Neural Netw 17, 625–632, doi:10.1016/j.neunet.2004.04.004 (2004).

52. Kok, P., Bains, L. J., van Mourik, T., Norris, D. G. & de Lange, F. P. Selective Activation of the Deep Layers of the Human Primary Visual Cortex by Top-Down Feedback. Curr Biol 26, 371–376, doi:10.1016/j.cub.2015.12.038 (2016).

53. Elhilali, M. & Shamma, S. A. A cocktail party with a cortical twist: how cortical mechanisms contribute to sound segregation. J Acoust Soc Am 124, 3751–3771, doi:10.1121/1.3001672 (2008).

54. Kerlin, J. R., Shahin, A. J. & Miller, L. M. Attentional gain control of ongoing cortical speech representations in a «cocktail party». J Neurosci 30, 620–628, doi:10.1523/JNEUROSCI.3631–09.2010 (2010).

55. Northover, S. B., Pedersen, W. C., Cohen, A. B. & Andrews, P. W. Artificial surveillance cues do not increase generosity: two meta-analyses. Evolution and Human Behavior 38, 144–153, doi:https://doi.org/10.1016/j.evolhumbehav.2016.07.001 (2017).

56. Dear, K., Dutton, K. & Fox, E. Do 'watching eyes' influence antisocial behavior? A systematic review & meta-analysis. Evolution and Human Behavior 40, 269–280, doi:https://doi.org/10.1016/j.evolhumbehav.2019.01.006 (2019).

57. Nickerson, R. S. Confirmation bias: A ubiquitous phenomenon in many guises. Review of general psychology 2, 175–220 (1998).

58. Казанцева А. Кто бы мог подумать! Как мозг заставляет нас делать глупости. – М.: Corpus, 2014.

59. Shipp, S., Adams, R. A. & Friston, K. J. Reflections on agranular architecture: predictive coding in the motor cortex. Trends in neurosciences 36, 706–716 (2013).

60. Adams, R. A., Shipp, S. & Friston, K. J. Predictions not commands: active inference in the motor system. Brain Structure and Function 218, 611–643 (2013).

61. Thomson, E. E., Carra, R. & Nicolelis, M. A. Perceiving invisible light through a somatosensory cortical prosthesis. Nat Commun 4, 1482, doi:10.1038/ncomms2497 (2013).


ГЛАВА 9. МЫСЛЬ КАК АБСТРАКЦИЯ | Хлопок одной ладонью | ГЛАВА 11. СКОЛЬКО СТОИТ СЧАСТЬЕ