Cited by 1,786Functional Brain Connectivity StudiesNeural dynamics and brain functionAdvanced Neuroimaging Techniques and Applications

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Intrinsic functional architecture in the anaesthetized monkey brain

Vincent, J. L., Patel, G. H., Fox, M. D., Snyder, A. Z., Baker, J. T., Van Essen, D. C., Zempel, J. M., Snyder, L. H., Corbetta, M., Raichle, M. E.·2007·Nature

DOI 10.1038/nature05758

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Abstract

The traditional approach to studying brain function is to measure physiological responses to controlled sensory, motor and cognitive paradigms. However, most of the brain's energy consumption is devoted to ongoing metabolic activity not clearly associated with any particular stimulus or behaviour. Functional magnetic resonance imaging studies in humans aimed at understanding this ongoing activity have shown that spontaneous fluctuations of the blood-oxygen-level-dependent signal occur continuously in the resting state. In humans, these fluctuations are temporally coherent within widely distributed cortical systems that recapitulate the functional architecture of responses evoked by experimentally administered tasks. Here, we show that the same phenomenon is present in anaesthetized monkeys even at anaesthetic levels known to induce profound loss of consciousness. We specifically demonstrate coherent spontaneous fluctuations within three well known systems (oculomotor, somatomotor and visual) and the 'default' system, a set of brain regions thought by some to support uniquely human capabilities. Our results indicate that coherent system fluctuations probably reflect an evolutionarily conserved aspect of brain functional organization that transcends levels of consciousness.

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Biostatistical Analysis
Baltosser, W. H., & Zar, J. H. (1996) · Ecology · doi:10.2307/2265725 · Cited by 35,166
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190
Self-citation
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Self-citation
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
Science
(2023) · doi:10.1126/science · Cited by 6,063
Signals from Chloroplasts Converge to Regulate Nuclear Gene Expression
Koussevitzky, S., Nott, A., Mockler, T. C., Hong, F., Sachetto‐Martins, G., Surpin, M. A., Lim, J. C.-S., Mittler, R., & Chory, J. (2007) · Science · doi:10.1126/science.1140516 · Cited by 5,765

Show all 46 references

Research works printed but not linked: 2

Brodmann, K. Localisation in the Cerebral Cortex (Smith-Gordon, London, 1994)
Lewis, J. W. & Van Essen, D. C. Mapping of architectonic subdivisions in the macaque monkey, with emphasis on parieto-occipital cortex. J. Comp. Neurol. 428, 79–111 (2000) · DOI

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Schmid, M. C., Panagiotaropoulos, T. I., Augath, M. A., Logothetis, N. K., & Smirnakis, S. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005527 · Cited by 82
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Smyser, C. D., Wheelock, M. D., Limbrick, D. D., & Neil, J. J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.07.057 · Cited by 87
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Yan, X., Kong, R., Xue, A., Yang, Q., Orbán, C., An, L., Holmes, A. J., Qian, X., Chen, J., Zuo, X., et al. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120010 · Cited by 86
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Baria, A. T., Mansour, A. R., Huang, L., Baliki, M. N., Cecchi, G., Mesulam, M. M., & Apkarian, A. V. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.01.072 · Cited by 84
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Meehan, T. P., & Bressler, S. L. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.08.002 · Cited by 84
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Buckner, R. L., & Margulies, D. S. (2019) · Nature Communications · doi:10.1038/s41467-019-09812-8 · Cited by 81
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Chan, A. W., Mohajerani, M. H., LeDue, J. M., Wang, Y. T., & Murphy, T. H. (2015) · Nature Communications · doi:10.1038/ncomms8738 · Cited by 79
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Abbott, L. F., Rajan, K., & Sompolinsky, H. (2011) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195393798.003.0004 · Cited by 79
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Ash, J. A., Lu, H., Taxier, L. R., Long, J. M., Yang, Y., Stein, E. A., & Rapp, P. R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1525309113 · Cited by 82
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Oler, J. A., Tromp, D., Fox, A. S., Kovner, R., Davidson, R. J., Alexander, A. L., McFarlin, D. R., Birn, R. M., Berg, B. E., deCampo, D. M., et al. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1198-9 · Cited by 82
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Nair, J., Klaassen, A.-L., Arato, J., Vyssotski, A. L., Harvey, M., & Rainer, G. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1712431115 · Cited by 77
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Brain activity is not only for thinking
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Self-citation
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Gros, C. (2009) · Cognitive Computation · doi:10.1007/s12559-008-9000-9 · Cited by 76
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Burton, H., Dixit, S., Litkowski, P., & Wingert, J. R. (2009) · Somatosensory & Motor Research · doi:10.3109/08990220903335742 · Cited by 81
Consciousness and cerebral baseline activity fluctuations
Boly, M., Phillips, C. L. M., Balteau, E., Schnakers, C., Degueldre, C., Moonen, G., Luxen, A., Peigneux, P., Faymonville, M.-É., Maquet, P., et al. (2008) · Human Brain Mapping · doi:10.1002/hbm.20602 · Cited by 82
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Gorges, M., Roselli, F., Müller, H.-P., Ludolph, A. C., Rasche, V., & Kassubek, J. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00200 · Cited by 76
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Chen, H., Zhang, T., Guo, L., Li, K., Yu, X., Li, L., Hu, X., Han, J., Hu, X. P., & Liu, T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs113 · Cited by 76
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Bellana, B., Liu, Z. ‐., Diamond, N. B., Grady, C. L., & Moscovitch, M. (2017) · Human Brain Mapping · doi:10.1002/hbm.23445 · Cited by 75
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Xu, A. G., Qian, M., Tian, F., Xu, B., Friedman, R. M., Wang, J., Song, X. M., Sun, Y., Chernov, M. M., Cayce, J. M., et al. (2019) · Science Advances · doi:10.1126/sciadv.aau7046 · Cited by 74
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Liégeois, R., Ziegler, E., Phillips, C. L. M., Geurts, P., Gómez, F. A., Bahri, M. A., Yeo, B. T. T., Soddu, A., Vanhaudenhuyse, A., Laureys, S., et al. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1083-y · Cited by 74
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Blautzik, J., Vetter, C., Peres, I., Gutyrchik, E., Keeser, D., Berman, A., Kirsch, V., Mueller, S., Pöppel, E., Reiser, M. F., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.010 · Cited by 77
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Self-citation
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Gargouri, F., Galléa, C., Mongin, M., Pyatigorskaya, N., Valabrègue, R., Ewenczyk, C., Sarazin, M., Yahia‐Cherif, L., Vidailhet, M., & Lehéricy, S. (2018) · Movement Disorders · doi:10.1002/mds.27561 · Cited by 72
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Garin, C. M., Hori, Y., Everling, S., Whitlow, C. T., Calabro, F. J., Luna, B., Froesel, M., Gacoin, M., Hamed, S. B., Dhénain, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110669 · Cited by 72
Primate comparative neuroscience using magnetic resonance imaging: promises and challenges
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Moeller, S., Nallasamy, N., Tsao, D. Y., & Freiwald, W. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0220-09.2009 · Cited by 76
A functional model of cortical gyri and sulci
Deng, F., Jiang, X., Zhu, D., Zhang, T., Li, K., Guo, L., & Liu, T. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0581-z · Cited by 73
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Festini, S. B., Bernard, J. A., Kwak, Y., Peltier, S., Bohnen, N. I., Müller, M. L. T. M., Dayalu, P., & Seidler, R. D. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00214 · Cited by 71
Infraslow EEG oscillations organize large-scale cortical–subcortical interactions during sleep: A combined EEG/fMRI study
Picchioni, D., Horovitz, S. G., Fukunaga, M., Carr, W. S., Meltzer, J. A., Balkin, T. J., Duyn, J. H., & Braun, A. R. (2010) · Brain Research · doi:10.1016/j.brainres.2010.12.035 · Cited by 71
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Dovern, A., Fink, G. R., Fromme, A. C. B., Wohlschläger, A. M., Weiss, P. H., & Riedl, V. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5401-11.2012 · Cited by 73
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Marrelec, G., & Fransson, P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0014788 · Cited by 70
The neural mechanisms of face processing: cells, areas, networks, and models
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Perl, Y. S., Pallavicini, C., Ipiña, I. P., Athena Demertzi, A., Bonhomme, V. L., Martial, C., Panda, R., Annen, J., Ibáñez, A. M., Kringelbach, M. L., et al. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009139 · Cited by 71
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Hutchison, R. M., Womelsdorf, T., Gati, J. S., Leung, L.-W. S., Menon, R. S., & Everling, S. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr181 · Cited by 72
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Sargolzaei, S., Cabrerizo, M., Goryawala, M., Eddin, A. S., & Adjouadi, M. (2014) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2014.10.018 · Cited by 69
Resting-state connectivity
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Gradual emergence of spontaneous correlated brain activity during fading of general anesthesia in rats: evidences from fMRI and local field potentials
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Chee, M. W. L., & Zhou, J. (2019) · Progress in brain research · doi:10.1016/bs.pbr.2019.02.009 · Cited by 68
Grand Challenges in Mapping the Human Brain: NSF Workshop Report
He, B., Coleman, T. P., Genin, G. M., Glover, G. H., Hu, X. P., Johnson, N., Liu, T., Makeig, S., Sajda, P., & Ye, K. (2013) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2013.2283970 · Cited by 69
Default Mode of Brain Activity Demonstrated by Positron Emission Tomography Imaging in Awake Monkeys: Higher Rest-Related than Working Memory-Related Activity in Medial Cortical Areas
Kojima, T., Onoe, H., Hikosaka, K., Tsutsui, K., Tsukada, H., & Watanabe, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1786-09.2009 · Cited by 68
The neuroscience of coaching.
Boyatzis, R. E., & Jack, A. I. (2018) · Consulting psychology journal · doi:10.1037/cpb0000095 · Cited by 75
Impaired Resting-State Functional Integrations within Default Mode Network of Generalized Tonic-Clonic Seizures Epilepsy
Song, M., Du, H., Wu, N., Hou, B., Wu, G.-C., Wang, J., Feng, H., & Jiang, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017294 · Cited by 68
Dynamic Connectivity Patterns in Conscious and Unconscious Brain
Ma, Y., Hamilton, C. M., & Zhang, N. (2016) · Brain Connectivity · doi:10.1089/brain.2016.0464 · Cited by 71
A role for the claustrum in cognitive controlPreprint
Madden, M. B., Stewart, B. W., White, M. G., Krimmel, S. R., Qadir, H., Barrett, F. S., Seminowicz, D. A., & Mathur, B. N. (2022) · PsyArXiv (OSF Preprints) · doi:10.1016/j.tics.2022.09.006 · Cited by 76
Evidence for coordinated functional activity within the extended amygdala of non-human and human primates
Oler, J. A., Birn, R. M., Patriat, R., Fox, A. S., Shelton, S. E., Burghy, C. A., Stodola, D. E., Essex, M. J., Davidson, R. J., & Kalin, N. H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.045 · Cited by 67
Amygdala–cingulate intrinsic connectivity is associated with degree of social inhibition
Blackford, J. U., Clauss, J. A., Avery, S. N., Cowan, R. L., Benningfield, M. M., & VanDerKlok, R. M. (2014) · Biological Psychology · doi:10.1016/j.biopsycho.2014.02.003 · Cited by 67
Long-term alterations in brain and behavior after postnatal Zika virus infection in infant macaques
Raper, J., Kovacs-Balint, Z., Mavigner, M., Gumber, S., Burke, M. W., Habib, J., Mattingly, C., Fair, D., Earl, E., Feczko, E., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16320-7 · Cited by 67
Multifaceted brain networks reconfiguration in disorders of consciousness uncovered by co‐activation patterns
Perri, C. D., Amico, E., Heine, L., Annen, J., Martial, C., Larroque, S. K., Soddu, A., Marinazzo, D., & Laureys, S. (2017) · Human Brain Mapping · doi:10.1002/hbm.23826 · Cited by 67
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Lv, Q., Yang, L., Li, G., Wang, Z., Shen, Z., Yu, W., Jiang, Q., Hou, B., Pu, J., Hu, H., et al. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.02.028 · Cited by 70
Default activity patterns at the neocortical microcircuit level
Luczak, A., & MacLean, J. N. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00030 · Cited by 69
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Grayson, D. S., Kroenke, C. D., Neuringer, M., & Fair, D. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3038-13.2014 · Cited by 68
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Fling, B. W., Peltier, S., Bo, J., Welsh, R. C., & Seidler, R. D. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00038 · Cited by 72
Correspondence Between Aberrant Intrinsic Network Connectivity and Gray-Matter Volume in the Ventral Brain of Preterm Born Adults
Bäuml, J., Daamen, M., Meng, C., Neitzel, J., Scheef, L., Jaekel, J., Busch, B., Baumann, N., Bartmann, P., Dieter Wolke, C., et al. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu133 · Cited by 74
Causal evidence of performance monitoring by neurons in posterior cingulate cortex during learning
Heilbronner, S. R., & Platt, M. L. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.028 · Cited by 66
Altered temporal variance and neural synchronization of spontaneous brain activity in anesthesia
Huang, Z., Wang, Z., Zhang, J., Dai, R., Wu, J., Li, Y., Liang, W., Mao, Y. Q., Yang, Z. H., Holland, G., et al. (2014) · Human Brain Mapping · doi:10.1002/hbm.22556 · Cited by 69
Resting state functional connectivity analysis for addiction medicine
Pariyadath, V., Gowin, J. L., & Stein, E. A. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.07.015 · Cited by 68
Orbitofrontal Connectivity with Resting-State Networks Is Associated with Midbrain Dopamine D3 Receptor Availability
Cole, D. M., Beckmann, C. F., Searle, G. E., Plisson, C., Tziortzi, A. C., Nichols, T. E., Gunn, R. N., Matthews, P. M., Rabiner, E. A., & Beaver, J. D. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr354 · Cited by 68
Indexing brain state-dependent pupil dynamics with simultaneous fMRI and optical fiber calcium recording
Pais‐Roldán, P., Takahashi, K., Sobczak, F., Chen, Y., Zhao, X., Zeng, H., Jiang, Y., & Yu, X. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1909937117 · Cited by 67
A Putative Multiple-Demand System in the Macaque Brain
Mitchell, D. J., Bell, A. H., Buckley, M. J., Mitchell, A. S., Sallet, J., & Duncan, J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0810-16.2016 · Cited by 65
Distributed Dynamical Computation in Neural Circuits with Propagating Coherent Activity Patterns
Gong, P., & van Leeuwen, C. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000611 · Cited by 66
Mapping functional connectivity based on synchronized CMRO2 fluctuations during the resting state
Wu, C. W., Gu, H., Lu, H., Stein, E. A., Chen, J., & Yang, Y. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.12.066 · Cited by 65

Authors: Vincent, J. L., Patel, G. H., Fox, M. D., Snyder, A. Z., Baker, J. T., Van Essen, D. C., Zempel, J. M., Snyder, L. H., Corbetta, M., & Raichle, M. E.
Affiliations: Washington University in St. Louis (US)
Corresponding author: Raichle, M. E.
ORCID: Patel, G. H.
Fox, M. D.
Snyder, A. Z.
Baker, J. T.
Zempel, J. M.
Snyder, L. H.
Corbetta, M.
Raichle, M. E.
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2007-05
Volume: 447
Issue: 7140
Pages: 83-86
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature05758
OpenAlex: W2027781650
Cited by: 1,786
References: 46
Citations by year: 2026: 25 · 2025: 34 · 2024: 58 · 2023: 61 · 2022: 67 · 2021: 65 · 2020: 81 · 2019: 81 · 2018: 107 · 2017: 100 · 2016: 111 · 2015: 132 · 2014: 125 · 2013: 150 · 2012: 120
FWCI: 51.95
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
RePEc: Research Papers in Economics (submittedVersion)
Padua Research Archive (University of Padova) (submittedVersion)
Funders: National Institutes of Health
National Institute of Neurological Disorders and Stroke (F31NS051972)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
Keywords: spontaneous neural fluctuations, resting-state brain activity, default mode network, oculomotor system, visual system, functional architecture, primate brain evolution, cross-species conservation, BOLD signal
MeSH terms: Anesthesia, Animals, Brain, Brain Mapping, Consciousness, Humans, Isoflurane, Macaca fascicularis, Macaca mulatta, Magnetic Resonance Imaging, Visual Cortex, Anesthetics, Inhalation

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Intrinsic functional architecture in the anaesthetized monkey brain

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