The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Synchronized delta oscillations correlate with the resting-state functional MRI signal
Open accessAbstract
Synchronized low-frequency spontaneous fluctuations of the functional MRI (fMRI) signal have recently been applied to investigate large-scale neuronal networks of the brain in the absence of specific task instructions. However, the underlying neural mechanisms of these fluctuations remain largely unknown. To this end, electrophysiological recordings and resting-state fMRI measurements were conducted in α-chloralose-anesthetized rats. Using a seed-voxel analysis strategy, region-specific, anesthetic dose-dependent fMRI resting-state functional connectivity was detected in bilateral primary somatosensory cortex (S1FL) of the resting brain. Cortical electroencephalographic signals were also recorded from bilateral S1FL; a visual cortex locus served as a control site. Results demonstrate that, unlike the evoked fMRI response that correlates with power changes in the γ bands, the resting-state fMRI signal correlates with the power coherence in low-frequency bands, particularly the δ band. These data indicate that hemodynamic fMRI signal differentially registers specific electrical oscillatory frequency band activity, suggesting that fMRI may be able to distinguish the ongoing from the evoked activity of the brain.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913
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
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576
Neurophysiological investigation of the basis of the fMRI signal
Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,551
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
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 · Cited by 1,786
von Stein, A., & Sarnthein, J. (2000) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(00)00172-0 · Cited by 1,553
Breakdown of cortical effective connectivity during sleep
Massimini, M., Ferrarelli, F., Huber, R., Esser, S. K., Singh, H., & Tononi, G. (2005) · Science · doi:10.1126/science.1117256 · Cited by 1,534
Research works printed but not linked: 42
- 10.1073/pnas.0504136102 · DOI · Paper page
- 10.1148/radiol.2251011301 · DOI
- 10.1148/radiol.2241011005 · DOI · Paper page
- 10.1016/j.neuron.2007.02.013 · DOI
- 10.1038/jcbfm.1988.52 · DOI
- 10.1093/cercor/13.4.422 · DOI · Paper page
- RB Silberstein Event-Related Dynamics of Brain Oscillations, Progress in Brain Res, eds C Neuper, W Klimesch (Elsevier, Boston), pp. 63–76 (2006). · DOI
- 10.1523/JNEUROSCI.23-10-03972.2003 · DOI
- 10.1126/science.1110948 · DOI · Paper page
- 10.1016/S0306-4522(00)00353-5 · DOI · Paper page
- FH Lopes da Silva Event-Related Dynamics of Brain Oscillations, Progress in Brain Res, eds C Neuper, W Klimesch (Elsevier, Boston), pp. 3–17 (2006). · DOI
- H Lu, L Gitajn, W Rea, EA Stein, Y Yang Proc Intl Soc Magn Reson Med 14, 532 (2006).
- H Lu, H Gu, Y Zuo, CA Scholl, EA Stein, Y Yang Proc Intl Soc Magn Reson Med 15, 3212 (2007).
- 10.1002/mrm.20265 · DOI
- 10.1002/mrm.1910390415 · DOI · Paper page
- 10.1097/00000542-200311000-00019 · DOI
- 10.1002/(SICI)1522-2594(199903)41:3<469::AID-MRM7>3.0.CO;2-9 · DOI
- 10.1073/pnas.97.20.11026 · DOI
- 10.1016/S0079-6123(08)62182-2 · DOI
- 10.1097/00001756-200212200-00022 · DOI
- 10.1016/S1053-8119(03)00286-6 · DOI · Paper page
- 10.1103/PhysRevLett.59.381 · DOI
- 10.1097/00001756-200502280-00017 · DOI
- NE Crone Adv Neurol 84, 343–351 (2000).
- 10.1103/PhysRevB.13.556 · DOI
- 10.1007/BF00710911 · DOI
- 10.1038/jcbfm.1994.81 · DOI
- KM Garrett, J Gan J Pharmacol Exp 285, 680–686 (1998). · DOI
- 10.1016/S0013-4694(98)00051-0 · DOI · Paper page
- 10.1111/j.0953-816X.2004.03333.x · DOI
- A Fernandez, J Arrazola, F Maestu, C Amo, P Gil-Gregorio, C Wienbruch, T Ortiz Am J Neuroradiol 24, 481–487 (2003).
- 10.1139/y93-049 · DOI
- 10.1523/JNEUROSCI.21-12-04498.2001 · DOI
- S-J Li, F Luo, M Schulte, Hudetz Proc Intl Soc Magn Reson Med 14, 797 (2006).
- 10.1016/S0074-7742(08)60245-7 · DOI
- 10.1016/S0306-4522(96)00393-4 · DOI
- 10.1126/science.252.5009.1177 · DOI · Paper page
- 10.1152/jn.1999.82.6.3082 · DOI
- 10.1016/j.neuroscience.2003.12.018 · DOI
- MJ Lowe, P Rutecki, P Turski, A Woodard, J Sorenson NeuroImage 5, S194 (1997).
- 10.1002/hbm.1050 · DOI · Paper page
- 10.1016/j.neuroscience.2003.09.014 · DOI
Cited by
The brain's default mode network
Raichle, M. E. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014030 · Cited by 3,904
DPARSF: a MATLAB toolbox for “pipeline” data analysis of resting-state fMRI
Yan (2010) · Frontiers in System Neuroscience · doi:10.3389/fnsys.2010.00013 · Cited by 3,475
Dynamic functional connectivity: Promise, issues, and interpretations
Hutchison, R. M., Womelsdorf, T., Allen, E. A., Bandettini, P. A., Calhoun, V. D., Corbetta, M., Della Penna, S., Duyn, J. H., Glover, G. H., Gonzalez-Castillo, J., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.079 · Cited by 2,962
Default-mode brain dysfunction in mental disorders: A systematic review
Broyd, S. J., Demanuele, C., Debener, S., Helps, S. K., James, C. J., & Sonuga-Barke, E. J. S. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.09.002 · Cited by 1,675
Default Mode Network Activity and Connectivity in Psychopathology
Whitfield-Gabrieli, S., & Ford, J. M. (2012) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-032511-143049 · Cited by 1,465
Metadata
- Authors
- Lu, H., Zuo, Y., Gu, H., Waltz, J. A., Zhan, W., Scholl, C. A., Rea, W., Yang, Y., & Stein, E. A.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2007-11-13
- Volume
- 104
- Issue
- 46
- Pages
- 18265-18269
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2038427447
- Cited by
- 417
- References
- 8
- FWCI
- 9.44
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.