Библиография

1. 1. Арутюнян А.В., Милютина Ю.П., Залозняя И.В., Пустыгина А.В., Козина Л.С., Кореневский А.В. Использование различных экспериментальных моделей гипергомоцистеинемии в нейрохимических исследованиях. Нейрохимия. 2012. Т. 29. № 2. С. 83. (Arutjunyan A., Kozina L., Stvolinskiy S., Bulygina Y., Mashkina A., Khavinson V. 2012. Pinealon protects the rat offspring from prenatal hyperhomocysteinemia. Int. J. Clin. Exper. Med. 5(2). Р. 179).
2. 2. Белехова М. Г., Туманова Н. Л. Структурные основы слухо-соматического взаимодействия в мозгу черепахи Еmys orbicularis. Дендритный обмен между ядрами. Журнал эвол. биохим. и физиол. 1988. Т. 24. № 3. С. 326. (Belekhova M.G., Tumanova N.L. 1988. Structural bases of audio-somatic interactions in turtle Еmys orbicularis brain. Dendrite exchange between nuclei. J. Evol. Biochem. Physiol. (Russ.) V. 24. P. 326.)
3. 3. Борякова Е.Е., Гладышева О.С., Крылов В.Н. Возрастная динамика обонятельной чувствительности у самок лабораторных мышей и крыс к запаху изовалериановой кислоты. Сенсорные системы. 2007. Т. 21. № 4. С. 341. (Boryakova E.E., Gladysheva O.S., Krylov V.N. 2007. Age dynamics of olfactory sensitivity in female laboratory mice and rats to the smell of isovaleric acid. Sensory systems. V. 21. P. 341.)
4. 4. Мельник С.А., Гладышева О.С., Крылов В.Н. Возрастные изменения обонятельной чувствительности самцов мышей к запаху изовалериановой кислоты. Сенсорные системы. 2009. Т. 23. № 2. С. 151. (Mel’nik S.A., Gladysheva O.S., Krylov V.N. 2009. Age-related changes in the olfactory sensitivity of male mice to the smell of isovaleric acid. Sensory systems. V. 23. P. 151.)
5. 5. Мельник С.А., Гладышева О.С., Крылов В.Н. Влияние предварительного воздействия паров изовалериановой кислоты на обонятельную чувствительность самцов домовой мыши. Сенсорные системы. 2012. Т. 26. № 1. С. 52. (Mel’nik S.A., Gladysheva O.S., Krylov V.N. 2012. Influence of preliminary exposure to isovaleric acid vapors on the olfactory sensitivity of male house mice. V. 26 P. 52.)
6. 6. Allen T.A., Fortin N.J. 2013. The evolution of episodic memory. Proc. Natl. Acad. Sci. USA. V. 110. P. 10379.
7. 7. Berger T., Rubner P., Schautzer F., Egg R., Ulmer H., Mayringer I., Dilitz E., Deisenhammer F., Reindl M. 2003. Antimyelin antibodies as a predictor of clinically definite multiple sclerosis after a first demyelinating event. New England J. Med. V. 349. 139. doi:10.1056/NEJMoa022328
8. 8. Bergmann E., Zur G., Bershadsky G., Kahn I. 2016. The organization of mouse and human corticohippocampal networks estimated by intrinsic functional connectivity. Cereb. Cortex. 26. Р. 4497–4512. https://doi.org/10.1093/cercor/bhw327
9. 9. Buckner R.L., Krienen F.M. 2013. The evolution of distributed association networks in the human brain. Trends Cogn. Sci. V. 17. P. 648. https://doi.org/10.1016/j.tics.2013.09.017
10. 10. Dubrovskaya N.M., Vasilev D.S., Tumanova N.L., Alekseeva O.S., Nalivaeva N.N. 2022. Prenatal hypoxia impairs olfactory function in postnatal ontogeny in rats. Neurosci. Behav. Physiol. V. 52. P. 262. https://doi.org/10.1007/s11055-022-01233-3
11. 11. Gass N., Schwarz A.J., Sartorius A., Schenker E., Risterucci C., Spedding M., Zheng L., Meyer-Lindenberg A., Weber-Fahr W. 2014. Sub-anesthetic ketamine modulates intrinsic BOLD connectivity within the hippocampal-prefrontal circuit in the rat. Neuropsychopharmacol. V. 39. P. 895.
12. 12. Ketelslegers I.A., Van Pelt D.E., Bryde S., Neuteboom R.F., Catsman-Berrevoets C.E., Hamann D., Hintzen R.Q. 2015. Anti-MOG antibodies plead against MS diagnosis in an acquired demyelinating syndromes cohort. Multiple Sclerosis. V. 21. P. 1513. doi:10.1177/1352458514566666
13. 13. Kezuka T., Usui Y., Yamakawa N., Matsunaga Y., Matsuda R., Masuda M., Utsumi H., Tanaka K., Goto H. 2012. Relationship between NMO-antibody and anti-MOG antibody in optic neuritis. J. Neuro-Ophthalmol. V. 32. P. 107. doi:10.1097/WNO.0b013e31823c9b6c
14. 14. Kitley J., Woodhall M., Waters P., Leite M.I., Devenney E., Craig J., Palace J., Vincent A. 2012. Myelin-oligodendrocyte glycoprotein antibodies in adults with a neuromyelitis optica phenotype. Neurology. 79 (12). Р. 1273–1277. doi: 10.1212/WNL.0b013e31826aac4e
15. 15. Liska A., Galbusera A., Schwarz A.J., Gozzi A. 2015. Functional connectivity hubs of the mouse brain. Neuroimage. V. 115. P. 281. https://doi.org/10.1016/j.neuroimage.2015.04.033
16. 16. Lu J., Testa N., Jordan R., Elyan R., Kanekar S., Wang J., Eslinger P., Yang Q., Zhang B., Karunanayaka P. 2019. Functional connectivity between the resting-state olfactory network and the hippocampus in Alzheimer’s disease. Brain Sci. V. 9. P. 338. https://doi.org/10.3390/brainsci9120338
17. 17. Matsumoto-Oda A., Oda R., Hayashi Y., Murakami H., Maeda N., Kumazaki K., Shimizu K., Matsuzawa T. 2003. Vaginal fatty acids produced by chimpanzees during menstrual cycles. Folia Primatol (Basel). V. 74. P. 75. https://doi.org/10.1159/000070000
18. 18. Mechling A.E., Hübner N.S., Lee H-L., Hennig J., von Elverfeldt D., Harsan L-A. 2014. Fine-grained mapping of mouse brain functional connectivity with resting-state fMRI. Neuroimage. V. 96. P. 203. https://doi.org/10.1016/j.neuroimage.2014.03.078
19. 19. Müller-Schwarze D., Müller-Schwarze C., Singer A.G., Silverstein R.M. 1974. Mammalian pheromone: identification of active component in the subauricular scent of the male pronghorn. Science. V. 183. P. 860. https://doi.org/10.1126/science.183.4127.860
20. 20. Paxinos G., Watson C. 2007. The rat brain in stereotaxic coordinates. Elsevier: Amsterdam-Boston.
21. 21. Postnikova T.Y., Amakhin D.V., Trofimova A.M., Tumanova N.L., Dubrovskaya N.M., Kalinina D.S., Kovalenko A.A., Shcherbitskaia A.D., Vasilev D.S., Zaitsev A.V. 2022. Maternal Hyperhomocysteinemia Produces Memory Deficits Associated with Impairment of Long-Term Synaptic Plasticity in Young Rats. Cells. V. 12. P. 58. https://doi.org/10.3390/cells12010058
22. 22. Ribaut-Barassin C., Dupont J-L., Haeberlé a-M., Bombarde G., Huber G., Moussaoui S., Mariani J., Bailly Y. 2003. Alzheimer’s disease proteins in cerebellar and hippocampal synapses during postnatal development and aging of the rat. Neurosci. V. 120. P. 405. doi:10.1016/S0306-4522(03)00332-4
23. 23. Rice D., Barone S. 2000. Critical periods of vulnerability for the developing nervous system: Evidence from humans and animal models. Environ. Health Perspect. V. 108. P. 511. https://doi.org/10.1289/ehp.00108s3511
24. 24. Schwarz A.J., Gass N., Sartorius A., Zheng L., Spedding M., Schenker E., Risterucci C., Meyer-Lindenberg A., Weber-Fahr W. 2013. The low-frequency blood oxygenation level-dependent functional connectivity signature of the hippocampal-prefrontal network in the rat brain. Neurosci. V. 228. P. 243. https://doi.org/10.1016/j.neuroscience.2012.10.032
25. 25. Shcherbitskaia A.D., Vasilev D.S., Milyutina Y.P., Tumanova N.L., Mikhel A.V., Zalozniaia I.V., Arutjunyan A.V. 2021. Prenatal hyperhomocysteinemia induces glial activation and alters neuroinflammatory marker expression in infant rat hippocampus. Cells. V. 10. P. 1536. https://doi.org/10.3390/cells10061536
26. 26. Vasilev D.S., Shcherbitskaia A.D., Tumanova N.L., Mikhel A.V., Milyutina Y.P., Kovalenko A.A., Dubrovskaya N.M., Inozemtseva D.B., Zalozniaia I.V., Arutjunyan A.V. 2023. Maternal hyperhomocysteinemia disturbs the mechanisms of embryonic brain development and its maturation in early postnatal ontogenesis. Cells. V. 12. P. 189. https://doi.org/10.3390/cells12010189
27. 27. Zhou G., Olofsson J.K., Koubeissi M.Z., Menelaou G., Rosenow J., Schuele S.U., Xug P., Voss J.L., Lane G., Zelano C. 2021. Human hippocampal connectivity is stronger in olfaction than other sensory systems. Progress Neurobiol. V. 201. P. 102027. https://doi.org/10.1016/j.pneurobio.2021.102027