Хлопок одной ладонью - Николай Кукушкин

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Часть III. Откуда взялся я

ГЛАВА 9. МЫСЛЬ КАК АБСТРАКЦИЯ

1. Robinson, W. S. in The Routledge Handbook of Consciousness 51–63 (Routledge, 2018).

2. Travis, J. Glia: the brain's other cells. Science 266, 970–973 (1994).

3. Magistretti, P. J. Neuron-glia metabolic coupling and plasticity. J Exp Biol 209, 2304–2311, doi:10.1242/jeb.02208 (2006).

4. Panatier, A. et al. Glia-derived D-serine controls NMDA receptor activity and synaptic memory. Cell 125, 775–784, doi:10.1016/j.cell.2006.02.051 (2006).

5. Aloisi, F. Immune function of microglia. Glia 36, 165–179, doi:10.1002/glia.1106 (2001).

6. Graeber, M. B. Changing face of microglia. Science 330, 783–788, doi:10.1126/science.1190929 (2010).

7. Pardridge, W. M. Transport of nutrients and hormones through the blood-brain barrier. Diabetologia 20, 246–254 (1981).

8. Kandel, E. R. Principles of neural science (2013).

9. Meissner, H. P. & Schmelz, H. Membrane potential of beta-cells in pancreatic islets. Pflugers Arch 351, 195–206, doi:10.1007/bf00586918 (1974).

10. Wood, D. C. Action spectrum and electrophysiological responses correlated with the photophobic response of Stentor coeruleus. Photochemistry and photobiology 24, 261–266 (1976).

11. Wood, D. C. Electrophysiological studies of the protozoan, Stentor coeruleus. Journal of neurobiology 1, 363–377 (1969).

12. Nickel, M. Evolutionary emergence of synaptic nervous systems: what can we learn from the non-synaptic, nerveless Porifera? Invertebrate Biology 129, 1–16, doi:10.1111/j.1744–7410.2010.00193.x (2010).

13. Brenner, E. D. et al. Plant neurobiology: an integrated view of plant signaling. Trends in Plant Science 11, 413–419, doi:https://doi.org/10.1016/j.tplants.2006.06.009 (2006).

14. Satterlie, R. A. & Spencer, A. N. in Nervous systems in invertebrates 213–264 (Springer, 1987).

15. Hulbert, A. J. & Else, P. L. Comparison of the «mammal machine» and the «reptile machine»: energy use and thyroid activity. Am J Physiol 241, R350–356, doi:10.1152/ajpregu.1981.241.5. R350 (1981).

16. Dibrova, D. V., Galperin, M. Y., Koonin, E. V. & Mulkidjanian, A. Y. Ancient Systems of Sodium/Potassium Homeostasis as Predecessors of Membrane Bioenergetics. Biochemistry (Mosc) 80, 495–516, doi:10.1134/S0006297915050016 (2015).

17. Venkatesh, B. et al. Genetic basis of tetrodotoxin resistance in pufferfishes. Curr Biol 15, 2069–2072, doi:10.1016/j.cub.2005.10.068 (2005).

18. Soong, T. W. & Venkatesh, B. Adaptive evolution of tetrodotoxin resistance in animals. Trends Genet 22, 621–626, doi:10.1016/j.tig.2006.08.010 (2006).

19. Ballard, D. H. Brain computation as hierarchical abstraction (MIT Press, 2015).

20. Nickerson, R. S. & Adams, M. J. Long-term memory for a common object. Cognitive Psychology 11, 287–307, doi:https://doi.org/10.1016/0010–0285 (79) 90013–6 (1979).

21. Goldstein, A. G. & Chance, J. E. Visual recognition memory for complex configurations. Perception & Psychophysics 9, 237–241, doi:10.3758/BF03212641 (1971).

22. Miller, N. & Campbell, D. T. Recency and primacy in persuasion as a function of the timing of speeches and measurements. The Journal of Abnormal and Social Psychology 59, 1–9, doi:10.1037/h0049330 (1959).

23. Mackay, D. G. et al. Relations between emotion, memory, and attention: Evidence from taboo Stroop, lexical decision, and immediate memory tasks. Memory & Cognition 32, 474–488, doi:10.3758/BF03195840 (2004).

24. Simons, D. J. & Chabris, C. F. Gorillas in our midst: sustained inattentional blindness for dynamic events. Perception 28, 1059–1074, doi:10.1068/p281059 (1999).

25. Kukushkin, N. V. & Carew, T. J. Memory Takes Time. Neuron 95, 259–279, doi:10.1016/j.neuron.2017.05.029 (2017).

26. Kukushkin, N. V. Taking memory beyond the brain: Does tobacco dream of the mosaic virus? Neurobiol Learn Mem 153, 111–116, doi:10.1016/j.nlm.2018.01.003 (2018).

27. Denes, A. S. et al. Molecular architecture of annelid nerve cord supports common origin of nervous system centralization in bilateria. Cell 129, 277–288, doi:10.1016/j.cell.2007.02.040 (2007).

ГЛАВА 10. ОГОНЬ ИЗНУТРИ

1. Платон. Собр. соч. В 4 т. Т. 3. – М.: Мысль, 1994.

2. Siegel, R. E. Principles and Contradictions of Galen's Doctrine of Vision. Sudhoffs Archiv 54, 261–276 (1970).

3. Sabra, A. I. The Optics of Ibn Al-Haytham: Books I–III: on Direct Vision (Warburg Institute, University of London, 1989).

4. Gregg, V. R., Winer, G. A., Cottrell, J. E., Hedman, K. E. & Fournier, J. S. The persistence of a misconception about vision after educational interventions. Psychonomic Bulletin & Review 8, 622–626 (2001).

5. Thibodeau, P. Ancient Optics: Theories and Problems of Vision. A Companion to Science, Technology, and Medicine in Ancient Greece and Rome, 130–144, doi:10.1002/9781118373057.ch8 (2016).

6. Herwig, A. & Schneider, W. X. Predicting object features across saccades: Evidence from object recognition and visual search. Journal of Experimental Psychology: General 143, 1903–1922, doi:10.1037/a0036781 (2014).

7. Land, M. F. & Tatler, B. W. Looking and acting: Vision and eye movements in natural behaviour (Oxford University Press, 2009).

8. De Weerd, P., Gattass, R., Desimone, R. & Ungerleider, L. G. Responses of cells in monkey visual cortex during perceptual filling-in of an artificial scotoma. Nature 377, 731–734, doi:10.1038/377731a0 (1995).

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

10. Hill, V. M., O'Connor, R. M. & Shirasu-Hiza, M. Tired and stressed: Examining the need for sleep. Eur J Neurosci, doi:10.1111/ejn.14197 (2018).

11. Van Wylen, D. G., Park, T. S., Rubio, R. & Berne, R. M. Increases in cerebral interstitial fluid adenosine concentration during hypoxia, local potassium infusion, and ischemia. J Cereb Blood Flow Metab 6, 522–528, doi:10.1038/jcbfm.1986.97 (1986).

12. Kalinchuk, A. V. et al. Local energy depletion in the basal forebrain increases sleep. Eur J Neurosci 17, 863–869, doi:10.1046/j.1460–9568.2003.02532.x (2003).