Modulation of Brain Resting-State Networks by Sad Mood Induction
There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neu...
Saved in:
Published in | PloS one Vol. 3; no. 3; p. e1794 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
19.03.2008
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning.
In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (approximately 0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'.
These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. |
---|---|
AbstractList | There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning. In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (~0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'. These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. Background There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these ‘resting-state networks’ may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning. Methodology/Principal Findings In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (∼0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the ‘default mode network’. Conclusions/Significance These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. Background There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning. Methodology/Principal Findings In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (~0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'. Conclusions/Significance These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning. In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (approximately 0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'. These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. Background There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these ‘resting-state networks’ may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning. Methodology/Principal Findings In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (∼0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the ‘default mode network’. Conclusions/Significance These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. BACKGROUND: There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (approximately 0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'. CONCLUSIONS/SIGNIFICANCE: These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning.BACKGROUNDThere is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies. In humans, these slow BOLD variations are thought to reflect an underlying or intrinsic form of brain functional connectivity in discrete neuroanatomical systems. While these 'resting-state networks' may be relatively enduring phenomena, other evidence suggest that dynamic changes in their functional connectivity may also emerge depending on the brain state of subjects during scanning.In this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (approximately 0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'.METHODOLOGY/PRINCIPAL FINDINGSIn this study, we examined healthy subjects (n = 24) with a mood induction paradigm during two continuous fMRI recordings to assess the effects of a change in self-generated mood state (neutral to sad) on the functional connectivity of these resting-state networks (n = 24). Using independent component analysis, we identified five networks that were common to both experimental states, each showing dominant signal fluctuations in the very low frequency domain (approximately 0.04 Hz). Between the two states, we observed apparent increases and decreases in the overall functional connectivity of these networks. Primary findings included increased connectivity strength of a paralimbic network involving the dorsal anterior cingulate and anterior insula cortices with subjects' increasing sadness and decreased functional connectivity of the 'default mode network'.These findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood.CONCLUSIONS/SIGNIFICANCEThese findings support recent studies that suggest the functional connectivity of certain resting-state networks may, in part, reflect a dynamic image of the current brain state. In our study, this was linked to changes in subjective mood. |
Audience | Academic |
Author | Ortiz, Hector Pantelis, Christos Yücel, Murat Harrison, Ben J. Fornito, Alex Pujol, Jesus |
AuthorAffiliation | 1 Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Melbourne Health, Victoria, Australia Harvard Medical School, United States of America 3 ORYGEN Research Centre, Melbourne, Victoria, Australia 4 Howard Florey Institute, The University of Melbourne, Victoria, Australia 2 Institut d'Alta Tecnologia-PRBB, CRC Corporació Sanitària, Barcelona, Spain |
AuthorAffiliation_xml | – name: 2 Institut d'Alta Tecnologia-PRBB, CRC Corporació Sanitària, Barcelona, Spain – name: 4 Howard Florey Institute, The University of Melbourne, Victoria, Australia – name: Harvard Medical School, United States of America – name: 1 Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Melbourne Health, Victoria, Australia – name: 3 ORYGEN Research Centre, Melbourne, Victoria, Australia |
Author_xml | – sequence: 1 givenname: Ben J. surname: Harrison fullname: Harrison, Ben J. – sequence: 2 givenname: Jesus surname: Pujol fullname: Pujol, Jesus – sequence: 3 givenname: Hector surname: Ortiz fullname: Ortiz, Hector – sequence: 4 givenname: Alex surname: Fornito fullname: Fornito, Alex – sequence: 5 givenname: Christos surname: Pantelis fullname: Pantelis, Christos – sequence: 6 givenname: Murat surname: Yücel fullname: Yücel, Murat |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18350136$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkl1v0zAYhSM0xD7gHyCIhDSJixZ_xU64QIyJj0obk1bg1npjO62HGxfbAfbvcdduaieEUC4SvXnOsd-jc1js9b43RfEUozGmAr-68kPowY2XeTxGCGHRsAfFAW4oGXGC6N7W935xGOMVQhWtOX9U7OOaVghTflC8Pfd6cJCs70vfle8C2L68NDHZfjaaJkim_GzSLx--x7K9Lqegy3PvdTnp9aBWqsfFww5cNE8276Pi64f3X04_jc4uPk5OT85GSpA6jbAhjNWMAYeqbeoGdao1ICqiqAFKNSIK14I3XFcdBsKrljYd1iCwamuENT0qnq99l85HuVk-SkwxIXXNBc_EZE1oD1dyGewCwrX0YOXNwIeZhJCsckZ2jDdgUMcoFoxx0xoBjKPG5Ku1WrTZ683mtKFdGK1MnwK4HdPdP72dy5n_KQnhFNM6GxxvDIL_MeQ85cJGZZyD3vghSoEYQUjgDL64B_59t_GamkG-vu07n09V-dFmYVVuQGfz_ISJnBzHeCV4uSPITDK_0wyGGOVkevn_7MW3XfZ4i50bcGkevRtWVYi74LPtBO-iu61eBl6vARV8jMF0Utl0U8S8mnUSI7nq-W0cctVzuel5FrN74jv_f8n-AMF6AL4 |
CitedBy_id | crossref_primary_10_1073_pnas_1204185109 crossref_primary_10_1177_0305735620928578 crossref_primary_10_1002_hbm_25037 crossref_primary_10_1073_pnas_0905314106 crossref_primary_10_1007_s11682_014_9318_8 crossref_primary_10_1093_cercor_bhx290 crossref_primary_10_1002_hbm_25277 crossref_primary_10_1016_j_bandc_2017_09_003 crossref_primary_10_1111_head_12944 crossref_primary_10_1016_j_neuroimage_2017_03_064 crossref_primary_10_1097_j_pain_0000000000000708 crossref_primary_10_1162_jocn_a_01449 crossref_primary_10_1371_journal_pone_0022912 crossref_primary_10_3758_s13415_024_01216_6 crossref_primary_10_1089_brain_2012_0101 crossref_primary_10_1097_j_pain_0000000000001599 crossref_primary_10_1016_j_msard_2022_104170 crossref_primary_10_1016_j_nicl_2013_11_009 crossref_primary_10_1093_scan_nst185 crossref_primary_10_1109_TNSRE_2012_2221480 crossref_primary_10_1016_j_biopsych_2010_01_014 crossref_primary_10_1080_20023294_2017_1357412 crossref_primary_10_1007_s11682_019_00076_w crossref_primary_10_31887_DCNS_2016_18_3_efinn crossref_primary_10_1186_s13229_016_0096_6 crossref_primary_10_1016_j_neuroimage_2022_119359 crossref_primary_10_1016_j_brs_2020_04_013 crossref_primary_10_1155_2016_9504642 crossref_primary_10_1016_j_neuroimage_2011_12_090 crossref_primary_10_1109_ACCESS_2019_2936434 crossref_primary_10_2967_jnumed_119_234930 crossref_primary_10_1016_j_ynstr_2021_100418 crossref_primary_10_1016_j_pscychresns_2010_01_005 crossref_primary_10_1093_cercor_bhn256 crossref_primary_10_1186_1744_859X_7_9 crossref_primary_10_1007_s11571_020_09633_2 crossref_primary_10_1002_erv_2259 crossref_primary_10_1016_j_neuroimage_2020_117292 crossref_primary_10_1016_j_neubiorev_2013_01_017 crossref_primary_10_1093_scan_nst058 crossref_primary_10_1089_brain_2021_0125 crossref_primary_10_1089_brain_2011_0030 crossref_primary_10_3389_fpsyt_2019_00924 crossref_primary_10_1177_0333102410365164 crossref_primary_10_1016_j_ijpsycho_2021_01_016 crossref_primary_10_1007_s00429_010_0265_x crossref_primary_10_1093_cercor_bhr099 crossref_primary_10_1007_s11065_014_9252_y crossref_primary_10_1016_j_bja_2018_03_023 crossref_primary_10_1016_j_cortex_2020_06_017 crossref_primary_10_1016_j_neubiorev_2020_01_006 crossref_primary_10_22172_cogbio_2015_27_2_008 crossref_primary_10_1089_brain_2013_0166 crossref_primary_10_1016_j_neuroimage_2021_118377 crossref_primary_10_1093_scan_nst041 crossref_primary_10_1371_journal_pone_0093098 crossref_primary_10_1016_j_cortex_2011_02_011 crossref_primary_10_1016_j_neulet_2011_01_012 crossref_primary_10_1093_scan_nsv068 crossref_primary_10_1016_j_neuroimage_2015_08_031 crossref_primary_10_1002_brb3_377 crossref_primary_10_1152_jn_00411_2021 crossref_primary_10_1007_s11065_021_09512_5 crossref_primary_10_1016_j_neuroimage_2010_10_021 crossref_primary_10_1016_j_biopsych_2011_03_040 crossref_primary_10_1016_j_concog_2017_01_006 crossref_primary_10_1111_psyp_14630 crossref_primary_10_1016_j_neuroimage_2020_116738 crossref_primary_10_3758_s13415_012_0134_6 crossref_primary_10_1016_j_neuroimage_2010_01_002 crossref_primary_10_1016_j_brainres_2017_03_027 crossref_primary_10_1016_j_brainresbull_2009_02_002 crossref_primary_10_1016_j_jad_2009_05_029 crossref_primary_10_1017_S0033291715002615 crossref_primary_10_1002_hbm_25677 crossref_primary_10_1002_hbm_21513 crossref_primary_10_3389_fnhum_2018_00168 crossref_primary_10_3758_s13415_013_0216_0 crossref_primary_10_1002_hbm_21270 crossref_primary_10_1523_ENEURO_0083_18_2018 crossref_primary_10_1371_journal_pone_0103492 crossref_primary_10_1016_j_brainres_2015_11_001 crossref_primary_10_1097_j_pain_0000000000000746 crossref_primary_10_3389_fnbeh_2017_00252 crossref_primary_10_1007_s10334_010_0212_0 crossref_primary_10_1016_j_brainresbull_2015_12_001 crossref_primary_10_1016_j_bbr_2011_01_008 crossref_primary_10_1016_j_neuroimage_2012_03_027 crossref_primary_10_1007_s10334_010_0228_5 crossref_primary_10_1093_scan_nsr003 crossref_primary_10_1038_npp_2017_35 crossref_primary_10_1016_j_jneumeth_2010_07_028 crossref_primary_10_1016_j_jneumeth_2009_11_010 crossref_primary_10_1017_S0033291712000323 crossref_primary_10_1002_hbm_25225 crossref_primary_10_1371_journal_pone_0017081 crossref_primary_10_1016_j_ifacol_2021_04_077 crossref_primary_10_1177_2167702616683506 crossref_primary_10_1016_j_nicl_2022_102977 crossref_primary_10_1093_cercor_bhs352 crossref_primary_10_1111_cns_12431 crossref_primary_10_1016_j_neuroimage_2011_03_033 crossref_primary_10_1093_schbul_sbac159 crossref_primary_10_1016_j_neulet_2008_07_050 crossref_primary_10_3389_fnhum_2017_00280 crossref_primary_10_1038_s41598_017_07063_5 crossref_primary_10_1016_j_neuroimage_2021_118800 crossref_primary_10_1371_journal_pone_0021976 crossref_primary_10_1186_s12883_020_01772_7 crossref_primary_10_1016_j_biopsych_2024_03_012 crossref_primary_10_1016_j_neuroimage_2014_04_053 crossref_primary_10_1002_hipo_22480 crossref_primary_10_1111_nyas_13338 crossref_primary_10_1016_j_jad_2016_10_022 crossref_primary_10_1093_scan_nsz065 crossref_primary_10_3389_fnhum_2015_00142 crossref_primary_10_1016_j_neubiorev_2009_01_002 crossref_primary_10_1016_j_neuroimage_2016_03_004 crossref_primary_10_1111_nyas_12882 crossref_primary_10_1016_j_neuroimage_2014_09_027 crossref_primary_10_1016_j_pscychresns_2011_10_008 crossref_primary_10_1016_j_neuroimage_2013_05_099 crossref_primary_10_1016_j_biopsych_2017_11_010 crossref_primary_10_1016_j_neuroimage_2014_11_037 crossref_primary_10_1016_j_tics_2012_02_001 crossref_primary_10_1016_j_jad_2017_01_013 crossref_primary_10_1097_YCO_0b013e328337d78d crossref_primary_10_1371_journal_pone_0036356 crossref_primary_10_1002_hbm_24559 crossref_primary_10_1002_hbm_22250 crossref_primary_10_1002_jnr_24364 crossref_primary_10_2967_jnumed_116_185835 crossref_primary_10_1016_j_brainres_2012_01_064 crossref_primary_10_1371_journal_pone_0028196 crossref_primary_10_1016_j_neuroimage_2009_07_056 crossref_primary_10_1177_11795735211015076 crossref_primary_10_1111_epi_12400 crossref_primary_10_1371_journal_pbio_3002797 crossref_primary_10_1371_journal_pone_0024271 crossref_primary_10_1016_j_neuroimage_2013_11_006 crossref_primary_10_1134_S0362119722010030 crossref_primary_10_1016_j_neuroimage_2019_04_014 crossref_primary_10_1007_s00213_011_2221_8 crossref_primary_10_1073_pnas_0911855107 crossref_primary_10_1093_cercor_bhr313 crossref_primary_10_1002_hbm_26604 crossref_primary_10_1002_hbm_22129 crossref_primary_10_1002_hbm_22403 crossref_primary_10_1016_j_psyneuen_2020_105096 crossref_primary_10_1523_JNEUROSCI_4141_12_2013 crossref_primary_10_1016_j_neuroimage_2014_06_065 |
Cites_doi | 10.1073/pnas.0601417103 10.1073/pnas.0704380104 10.1109/TMI.2003.822821 10.1001/archpsyc.64.8.946 10.1002/(SICI)1097-0193(1999)8:2/3<151::AID-HBM13>3.0.CO;2-5 10.1016/0272-7358(90)90075-L 10.1016/j.neuropsychologia.2006.06.017 10.1523/JNEUROSCI.5587-06.2007 10.1006/nimg.1997.0315 10.1016/j.schres.2006.12.027 10.1006/nimg.2002.1087 10.1016/j.neuroimage.2005.08.035 10.1109/MEMB.2006.1607672 10.1017/S0033291797004856 10.1016/S0079-6123(06)56005-4 10.1016/j.mri.2004.09.004 10.1016/j.neuropsychologia.2006.05.023 10.1016/j.braindev.2006.07.002 10.1073/pnas.0504136102 10.1002/hbm.10022 10.1523/JNEUROSCI.2250-06.2006 10.1016/j.neuroimage.2006.02.048 10.1002/cne.20752 10.1002/hbm.20294 10.1016/j.neuroimage.2004.11.053 10.1073/pnas.0135058100 10.1098/rstb.2005.1634 10.1002/cne.20749 10.1016/j.mri.2006.09.032 10.1073/pnas.0308627101 10.1126/science.288.5472.1769 10.1073/pnas.0604187103 10.1037/0022-3514.48.6.1595 10.1016/j.mri.2005.02.009 10.1016/j.mri.2003.09.007 10.1002/(SICI)1097-0193(1998)6:3<160::AID-HBM5>3.0.CO;2-1 10.1038/79871 10.1006/nimg.2000.0654 10.1002/hbm.1048 10.1073/pnas.0600674103 10.1523/JNEUROSCI.3874-05.2006 10.1002/mrm.1910340409 10.1002/hbm.20069 10.1016/S0006-3223(00)00874-X 10.1038/sj.npp.1300543 10.1097/01.wnr.0000129997.95055.15 10.1038/nrn894 10.1016/j.brainresbull.2006.06.012 10.1073/pnas.071043098 10.1176/ajp.2007.164.3.450 10.1038/jcbfm.1993.4 10.1073/pnas.0700668104 10.1162/neco.1995.7.6.1129 10.1146/annurev.neuro.29.051605.112819 10.1038/nature05758 10.1016/j.neuroimage.2005.12.040 10.1109/MEMB.2006.1607674 10.1038/nrn2201 10.1073/pnas.87.24.9868 10.1073/pnas.98.2.676 10.1162/089892903321593117 10.1016/j.mri.2006.04.018 10.1001/archpsyc.63.7.749 10.1038/nn1176 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2008 Public Library of Science 2008 Harrison et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Harrison et al. 2008 |
Copyright_xml | – notice: COPYRIGHT 2008 Public Library of Science – notice: 2008 Harrison et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: Harrison et al. 2008 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM IOV ISR 3V. 7QG 7QL 7QO 7RV 7SN 7SS 7T5 7TG 7TM 7U9 7X2 7X7 7XB 88E 8AO 8C1 8FD 8FE 8FG 8FH 8FI 8FJ 8FK ABJCF ABUWG AEUYN AFKRA ARAPS ATCPS AZQEC BBNVY BENPR BGLVJ BHPHI C1K CCPQU D1I DWQXO FR3 FYUFA GHDGH GNUQQ H94 HCIFZ K9. KB. KB0 KL. L6V LK8 M0K M0S M1P M7N M7P M7S NAPCQ P5Z P62 P64 PATMY PDBOC PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS PTHSS PYCSY RC3 7X8 5PM DOA |
DOI | 10.1371/journal.pone.0001794 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Gale In Context: Opposing Viewpoints Gale In Context: Science ProQuest Central (Corporate) Animal Behavior Abstracts Bacteriology Abstracts (Microbiology B) Biotechnology Research Abstracts Nursing & Allied Health Database Ecology Abstracts Entomology Abstracts (Full archive) Immunology Abstracts Meteorological & Geoastrophysical Abstracts Nucleic Acids Abstracts Virology and AIDS Abstracts Agricultural Science Collection Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) ProQuest Pharma Collection Public Health Database Technology Research Database ProQuest SciTech Collection ProQuest Technology Collection ProQuest Natural Science Journals Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) Materials Science & Engineering Collection ProQuest Central (Alumni) ProQuest One Sustainability ProQuest Central UK/Ireland Advanced Technologies & Aerospace Collection Agricultural & Environmental Science Collection ProQuest Central Essentials Biological Science Collection ProQuest Central (New) Technology Collection Natural Science Collection Environmental Sciences and Pollution Management ProQuest One ProQuest Materials Science Collection ProQuest Central Korea Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student AIDS and Cancer Research Abstracts SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Materials Science Database Nursing & Allied Health Database (Alumni Edition) Meteorological & Geoastrophysical Abstracts - Academic ProQuest Engineering Collection ProQuest Biological Science Collection Agricultural Science Database ProQuest Health & Medical Collection Medical Database Algology Mycology and Protozoology Abstracts (Microbiology C) Biological Science Database Engineering Database Nursing & Allied Health Premium Advanced Technologies & Aerospace Database ProQuest Advanced Technologies & Aerospace Collection Biotechnology and BioEngineering Abstracts Environmental Science Database Materials Science Collection ProQuest Central Premium ProQuest One Academic (New) Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China Engineering Collection Environmental Science Collection Genetics Abstracts MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Agricultural Science Database Publicly Available Content Database ProQuest Central Student ProQuest Advanced Technologies & Aerospace Collection ProQuest Central Essentials Nucleic Acids Abstracts SciTech Premium Collection ProQuest Central China Environmental Sciences and Pollution Management ProQuest One Applied & Life Sciences ProQuest One Sustainability Health Research Premium Collection Meteorological & Geoastrophysical Abstracts Natural Science Collection Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) Engineering Collection Advanced Technologies & Aerospace Collection Engineering Database Virology and AIDS Abstracts ProQuest Biological Science Collection ProQuest One Academic Eastern Edition Agricultural Science Collection ProQuest Hospital Collection ProQuest Technology Collection Health Research Premium Collection (Alumni) Biological Science Database Ecology Abstracts ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts Environmental Science Collection Entomology Abstracts Nursing & Allied Health Premium ProQuest Health & Medical Complete ProQuest One Academic UKI Edition Environmental Science Database ProQuest Nursing & Allied Health Source (Alumni) Engineering Research Database ProQuest One Academic Meteorological & Geoastrophysical Abstracts - Academic ProQuest One Academic (New) Technology Collection Technology Research Database ProQuest One Academic Middle East (New) Materials Science Collection ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central ProQuest Health & Medical Research Collection Genetics Abstracts ProQuest Engineering Collection Biotechnology Research Abstracts Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Bacteriology Abstracts (Microbiology B) Algology Mycology and Protozoology Abstracts (Microbiology C) Agricultural & Environmental Science Collection AIDS and Cancer Research Abstracts Materials Science Database ProQuest Materials Science Collection ProQuest Public Health ProQuest Nursing & Allied Health Source ProQuest SciTech Collection Advanced Technologies & Aerospace Database ProQuest Medical Library Animal Behavior Abstracts Materials Science & Engineering Collection Immunology Abstracts ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE Agricultural Science Database MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 4 dbid: 8FG name: ProQuest Technology Collection url: https://search.proquest.com/technologycollection1 sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Sciences (General) |
DocumentTitleAlternate | Brain Resting-State Networks |
EISSN | 1932-6203 |
ExternalDocumentID | 1312288676 oai_doaj_org_article_f469ae0f4317446ebe7a4609eb98bd7b PMC2263138 2900685101 A472656116 18350136 10_1371_journal_pone_0001794 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GeographicLocations | Australia Victoria Australia |
GeographicLocations_xml | – name: Victoria Australia – name: Australia |
GroupedDBID | --- 123 29O 2WC 53G 5VS 7RV 7X2 7X7 7XC 88E 8AO 8C1 8CJ 8FE 8FG 8FH 8FI 8FJ A8Z AAFWJ AAUCC AAWOE AAYXX ABDBF ABIVO ABJCF ABUWG ACGFO ACIHN ACIWK ACPRK ACUHS ADBBV ADRAZ AEAQA AENEX AEUYN AFKRA AFPKN AFRAH AHMBA ALIPV ALMA_UNASSIGNED_HOLDINGS AOIJS APEBS ARAPS ATCPS BAWUL BBNVY BCNDV BENPR BGLVJ BHPHI BKEYQ BPHCQ BVXVI BWKFM CCPQU CITATION CS3 D1I D1J D1K DIK DU5 E3Z EAP EAS EBD EMOBN ESX EX3 F5P FPL FYUFA GROUPED_DOAJ GX1 HCIFZ HH5 HMCUK HYE IAO IEA IGS IHR IHW INH INR IOV IPY ISE ISR ITC K6- KB. KQ8 L6V LK5 LK8 M0K M1P M48 M7P M7R M7S M~E NAPCQ O5R O5S OK1 OVT P2P P62 PATMY PDBOC PHGZM PHGZT PIMPY PQQKQ PROAC PSQYO PTHSS PYCSY RNS RPM SV3 TR2 UKHRP WOQ WOW ~02 ~KM CGR CUY CVF ECM EIF NPM PJZUB PPXIY PQGLB BBORY PMFND 3V. 7QG 7QL 7QO 7SN 7SS 7T5 7TG 7TM 7U9 7XB 8FD 8FK AZQEC C1K DWQXO FR3 GNUQQ H94 K9. KL. M7N P64 PKEHL PQEST PQUKI PRINS RC3 7X8 5PM PUEGO - 02 AAPBV ABPTK ADACO BBAFP KM |
ID | FETCH-LOGICAL-c728t-1e244844a6a5b9890fcbea752c3ea33d02c187696d5f1a265b39f1da71cb801d3 |
IEDL.DBID | M48 |
ISSN | 1932-6203 |
IngestDate | Fri Nov 26 17:13:30 EST 2021 Wed Aug 27 01:19:24 EDT 2025 Thu Aug 21 18:43:00 EDT 2025 Thu Jul 10 17:14:08 EDT 2025 Fri Jul 25 10:14:55 EDT 2025 Tue Jun 10 21:31:20 EDT 2025 Fri Jun 27 03:58:30 EDT 2025 Fri Jun 27 04:02:19 EDT 2025 Thu May 22 20:58:01 EDT 2025 Mon Jul 21 06:05:22 EDT 2025 Tue Jul 01 03:30:51 EDT 2025 Thu Apr 24 23:06:15 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 3 |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. Creative Commons Attribution License |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c728t-1e244844a6a5b9890fcbea752c3ea33d02c187696d5f1a265b39f1da71cb801d3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: BH AF CP MY. Performed the experiments: BH AF CP MY. Analyzed the data: BH JP HO. Wrote the paper: BH. |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.1371/journal.pone.0001794 |
PMID | 18350136 |
PQID | 1312288676 |
PQPubID | 1436336 |
PageCount | e1794 |
ParticipantIDs | plos_journals_1312288676 doaj_primary_oai_doaj_org_article_f469ae0f4317446ebe7a4609eb98bd7b pubmedcentral_primary_oai_pubmedcentral_nih_gov_2263138 proquest_miscellaneous_70420071 proquest_journals_1312288676 gale_infotracacademiconefile_A472656116 gale_incontextgauss_ISR_A472656116 gale_incontextgauss_IOV_A472656116 gale_healthsolutions_A472656116 pubmed_primary_18350136 crossref_citationtrail_10_1371_journal_pone_0001794 crossref_primary_10_1371_journal_pone_0001794 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2008-03-19 |
PublicationDateYYYYMMDD | 2008-03-19 |
PublicationDate_xml | – month: 03 year: 2008 text: 2008-03-19 day: 19 |
PublicationDecade | 2000 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: San Francisco – name: San Francisco, USA |
PublicationTitle | PloS one |
PublicationTitleAlternate | PLoS One |
PublicationYear | 2008 |
Publisher | Public Library of Science Public Library of Science (PLoS) |
Publisher_xml | – name: Public Library of Science – name: Public Library of Science (PLoS) |
References | RM Birn (ref49) 2006; 31 VD Calhoun (ref65) 2001; 14 MJ Lowe (ref11) 1998; 7 S Achard (ref7) 2006; 26 HD Critchley (ref29) 2005; 493 KA Celone (ref68) 2006; 26 SC Baker (ref59) 1997; 27 VD Calhoun (ref61) 2006; 25 JL Vincent (ref5) 2007; 447 JS Damoiseaux (ref22) 2007 MJ McKeown (ref62) 1998; 6 MD Greicius (ref52) 2007 ZV Segal (ref58) 2006; 63 HD Critchley (ref30) 2004; 7 M De Luca (ref20) 2006; 29 D Mantini (ref34) 2007; 104 MD Greicius (ref51) 2004; 101 JS Damoiseaux (ref19) 2006; 103 AT Newton (ref24) 2007; 28 KJ Friston (ref63) 1993; 13 YO Li (ref69) 2007 MD Fox (ref15) 2006; 103 M Liotti (ref31) 2000; 48 J Xiong (ref12) 1999; 8 M Hampson (ref13) 2002; 15 VJ Kiviniemi (ref72) 2005; 23 AJ Bell (ref70) 1995; 7 D Cordes (ref9) 2001; 22 VD Calhoun (ref66) 2004; 22 CF Beckmann (ref71) 2004; 23 AB Waites (ref26) 2005; 24 KL Phan (ref28) 2002; 16 MJ Lowe (ref35) 2000; 12 D Cordes (ref10) 2000; 21 L Ma (ref47) 2007; 25 ME Raichle (ref41) 2001; 98 JC Rajapakse (ref64) 2006; 25 AG Garrity (ref50) 2007; 164 M Martin (ref57) 1990; 10 BJ Harrison (ref42) 2007; 91 E Svoboda (ref45) 2006; 44 B Biswal (ref8) 1995; 34 M Fukunaga (ref48) 2006; 24 VD Calhoun (ref67) 2004; 29 F Esposito (ref33) 2006; 70 MD Greicius (ref17) 2003; 100 M Hampson (ref14) 2006; 31 WW Seeley (ref6) 2007; 27 S Ogawa (ref1) 1990; 87 CF Beckmann (ref18) 2005; 360 P Fransson (ref25) 2006; 44 ME Raichle (ref4) 2005; 493 V Kiviniemi (ref36) 2004; 22 J Pujol (ref43) PA Lewis (ref60) 2005; 25 M Hampson (ref23) 2004; 15 ME Raichle (ref2) 2006; 29 P Fransson (ref21) 2007; 104 DA Gusnard (ref39) 2001; 98 M Yucel (ref44) 2007; 64 MD Fox (ref16) 2005; 102 D Wechsler (ref55) 1999 AD Craig (ref37) 2002; 3 DP Kennedy (ref53) 2006; 103 D Sabatinelli (ref46) 2006; 156 E Zarahn (ref73) 1997; 5 DD Price (ref38) 2000; 288 AR Damasio (ref27) 2000; 3 KA McKiernan (ref40) 2003; 15 EM Reiman (ref32) 1997; 58 DM Clark (ref56) 1985; 48 MD Fox (ref3) 2007; 8 YF Zang (ref54) 2007; 29 15167557 - Neuroreport. 2004 Jun 7;15(8):1315-9 12030820 - Neuroimage. 2002 Jun;16(2):331-48 17027761 - Brain Res Bull. 2006 Oct 16;70(4-6):263-9 17636560 - Hum Brain Mapp. 2008 Aug;29(8):910-21 17329432 - J Neurosci. 2007 Feb 28;27(9):2349-56 17679639 - Arch Gen Psychiatry. 2007 Aug;64(8):946-55 16818864 - Arch Gen Psychiatry. 2006 Jul;63(7):749-55 16087444 - Philos Trans R Soc Lond B Biol Sci. 2005 May 29;360(1457):1001-13 10846154 - Science. 2000 Jun 9;288(5472):1769-72 16254998 - J Comp Neurol. 2005 Dec 5;493(1):167-76 11034865 - Neuroimage. 2000 Nov;12(5):582-7 9153677 - Psychol Med. 1997 May;27(3):565-78 17274023 - Hum Brain Mapp. 2007 Nov;28(11):1251-66 17670949 - Proc Natl Acad Sci U S A. 2007 Aug 7;104(32):13170-5 8417010 - J Cereb Blood Flow Metab. 1993 Jan;13(1):5-14 7584893 - Neural Comput. 1995 Nov;7(6):1129-59 16254997 - J Comp Neurol. 2005 Dec 5;493(1):154-66 2124706 - Proc Natl Acad Sci U S A. 1990 Dec;87(24):9868-72 9673671 - Hum Brain Mapp. 1998;6(3):160-88 8524021 - Magn Reson Med. 1995 Oct;34(4):537-41 11835612 - Hum Brain Mapp. 2002 Apr;15(4):247-62 16945915 - Proc Natl Acad Sci U S A. 2006 Sep 12;103(37):13848-53 15070770 - Proc Natl Acad Sci U S A. 2004 Mar 30;101(13):4637-42 11259662 - Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4259-64 11039342 - AJNR Am J Neuroradiol. 2000 Oct;21(9):1636-44 15976020 - Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9673-8 14964560 - IEEE Trans Med Imaging. 2004 Feb;23(2):137-52 16399673 - J Neurosci. 2006 Jan 4;26(1):63-72 17210143 - Biol Psychiatry. 2007 Sep 1;62(5):429-37 12154366 - Nat Rev Neurosci. 2002 Aug;3(8):655-66 16702548 - Proc Natl Acad Sci U S A. 2006 May 23;103(21):8275-80 17080441 - Hum Brain Mapp. 2007 Jul;28(7):663-72 11498421 - AJNR Am J Neuroradiol. 2001 Aug;22(7):1326-33 15850739 - Neuroimage. 2005 May 1;25(4):1214-23 14730305 - Nat Neurosci. 2004 Feb;7(2):189-95 16919409 - Brain Dev. 2007 Mar;29(2):83-91 15316570 - Neuropsychopharmacology. 2004 Nov;29(11):2097-17 16788060 - Proc Natl Acad Sci U S A. 2006 Jun 27;103(26):10046-51 11559959 - Hum Brain Mapp. 2001 Nov;14(3):140-51 17021177 - J Neurosci. 2006 Oct 4;26(40):10222-31 15607089 - Magn Reson Imaging. 2004 Nov;22(9):1181-91 9558644 - Neuroimage. 1998 Feb;7(2):119-32 16632379 - Neuroimage. 2006 Jul 15;31(4):1536-48 12506194 - Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):253-8 17329470 - Am J Psychiatry. 2007 Mar;164(3):450-7 18063564 - Cereb Cortex. 2008 Aug;18(8):1856-64 16568940 - IEEE Eng Med Biol Mag. 2006 Mar-Apr;25(2):79-90 11209064 - Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):676-82 16997067 - Magn Reson Imaging. 2006 Oct;24(8):979-92 17476267 - Nature. 2007 May 3;447(7140):83-6 16806314 - Neuropsychologia. 2006;44(12):2189-208 17878310 - Proc Natl Acad Sci U S A. 2007 Sep 25;104(39):15531-6 10913505 - Biol Psychiatry. 2000 Jul 1;48(1):30-42 16568942 - IEEE Eng Med Biol Mag. 2006 Mar-Apr;25(2):102-11 15010111 - Magn Reson Imaging. 2004 Feb;22(2):197-203 17015076 - Prog Brain Res. 2006;156:93-103 17704812 - Nat Rev Neurosci. 2007 Sep;8(9):700-11 9430503 - J Clin Psychiatry. 1997;58 Suppl 16:4-12 15382248 - Hum Brain Mapp. 2005 Jan;24(1):59-68 16260155 - Neuroimage. 2006 Feb 15;29(4):1359-67 17222714 - Magn Reson Imaging. 2007 Jan;25(1):47-56 9345548 - Neuroimage. 1997 Apr;5(3):179-97 12729491 - J Cogn Neurosci. 2003 Apr 1;15(3):394-408 16497520 - Neuroimage. 2006 Jun;31(2):513-9 10524607 - Hum Brain Mapp. 1999;8(2-3):151-6 15919598 - Magn Reson Imaging. 2005 May;23(4):531-7 16776593 - Annu Rev Neurosci. 2006;29:449-76 17307337 - Schizophr Res. 2007 Mar;91(1-3):82-6 11017179 - Nat Neurosci. 2000 Oct;3(10):1049-56 16879844 - Neuropsychologia. 2006;44(14):2836-45 |
References_xml | – volume: 103 start-page: 13848 year: 2006 ident: ref19 article-title: Consistent resting-state networks across healthy subjects. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0601417103 – volume: 104 start-page: 15531 year: 2007 ident: ref21 article-title: Resting-state networks in the infant brain. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0704380104 – volume: 23 start-page: 137 year: 2004 ident: ref71 article-title: Probabilistic independent component analysis for functional magnetic resonance imaging. publication-title: IEEE Trans Med Imaging doi: 10.1109/TMI.2003.822821 – volume: 64 start-page: 946 year: 2007 ident: ref44 article-title: Functional and biochemical alterations of the medial frontal cortex in obsessive-compulsive disorder. publication-title: Arch Gen Psychiatry doi: 10.1001/archpsyc.64.8.946 – volume: 8 start-page: 151 year: 1999 ident: ref12 article-title: Interregional connectivity to primary motor cortex revealed using MRI resting state images. publication-title: Hum Brain Mapp doi: 10.1002/(SICI)1097-0193(1999)8:2/3<151::AID-HBM13>3.0.CO;2-5 – year: 1999 ident: ref55 article-title: Wechsler Abbreviated Scale of Intelligence Manual. – volume: 10 start-page: 669 year: 1990 ident: ref57 article-title: On the induction of mood. publication-title: Clin Psychol Rev doi: 10.1016/0272-7358(90)90075-L – volume: 44 start-page: 2836 year: 2006 ident: ref25 article-title: How default is the default mode of brain function? Further evidence from intrinsic BOLD signal fluctuations. publication-title: Neuropsychologia doi: 10.1016/j.neuropsychologia.2006.06.017 – volume: 27 start-page: 2349 year: 2007 ident: ref6 article-title: Dissociable intrinsic connectivity networks for salience processing and executive control. publication-title: J Neurosci doi: 10.1523/JNEUROSCI.5587-06.2007 – volume: 7 start-page: 119 year: 1998 ident: ref11 article-title: Functional connectivity in single and multislice echoplanar imaging using resting-state fluctuations. publication-title: Neuroimage doi: 10.1006/nimg.1997.0315 – volume: 91 year: 2007 ident: ref42 article-title: Task-induced deactivation of midline cortical regions in schizophrenia assessed with fMRI. publication-title: Schizophr Res doi: 10.1016/j.schres.2006.12.027 – volume: 21 start-page: 1636 year: 2000 ident: ref10 article-title: Mapping functionally related regions of brain with functional connectivity MR imaging. publication-title: AJNR Am J Neuroradiol – volume: 16 start-page: 331 year: 2002 ident: ref28 article-title: Functional neuroanatomy of emotion: a meta-analysis of emotion activation studies in PET and fMRI. publication-title: Neuroimage doi: 10.1006/nimg.2002.1087 – volume: 29 start-page: 1359 year: 2006 ident: ref20 article-title: fMRI resting state networks define distinct modes of long-distance interactions in the human brain. publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.08.035 – volume: 25 start-page: 79 year: 2006 ident: ref61 article-title: Unmixing fMRI with independent component analysis. publication-title: IEEE Eng Med Biol Mag doi: 10.1109/MEMB.2006.1607672 – volume: 27 start-page: 565 year: 1997 ident: ref59 article-title: The interaction between mood and cognitive function studied with PET. publication-title: Psychol Med doi: 10.1017/S0033291797004856 – volume: 156 start-page: 93 year: 2006 ident: ref46 article-title: The neural basis of narrative imagery: emotion and action. publication-title: Prog Brain Res doi: 10.1016/S0079-6123(06)56005-4 – volume: 22 start-page: 1181 year: 2004 ident: ref66 article-title: A method for comparing group fMRI data using independent component analysis: application to visual, motor and visuomotor tasks. publication-title: Magn Reson Imaging doi: 10.1016/j.mri.2004.09.004 – volume: 44 start-page: 2189 year: 2006 ident: ref45 article-title: The functional neuroanatomy of autobiographical memory: a meta-analysis. publication-title: Neuropsychologia doi: 10.1016/j.neuropsychologia.2006.05.023 – volume: 29 start-page: 83 year: 2007 ident: ref54 article-title: Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. publication-title: Brain Dev doi: 10.1016/j.braindev.2006.07.002 – volume: 102 start-page: 9673 year: 2005 ident: ref16 article-title: The human brain is intrinsically organized into dynamic, anticorrelated functional networks. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0504136102 – volume: 15 start-page: 247 year: 2002 ident: ref13 article-title: Detection of functional connectivity using temporal correlations in MR images. publication-title: Hum Brain Mapp doi: 10.1002/hbm.10022 – year: 2007 ident: ref69 article-title: Estimating the number of independent components for functional magnetic resonance imaging data. publication-title: Hum Brain Mapp – ident: ref43 article-title: Posterior cingulate activation during moral dilemma in adolescents. publication-title: Human Brain Mapping – volume: 58 start-page: 4 year: 1997 ident: ref32 article-title: The application of positron emission tomography to the study of normal and pathologic emotions. publication-title: J Clin Psychiatry – volume: 26 start-page: 10222 year: 2006 ident: ref68 article-title: Alterations in memory networks in mild cognitive impairment and Alzheimer's disease: an independent component analysis. publication-title: J Neurosci doi: 10.1523/JNEUROSCI.2250-06.2006 – year: 2007 ident: ref52 article-title: Resting-State Functional Connectivity in Major Depression: Abnormally Increased Contributions from Subgenual Cingulate Cortex and Thalamus. publication-title: Biol Psychiatry – volume: 31 start-page: 1536 year: 2006 ident: ref49 article-title: Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI. publication-title: Neuroimage doi: 10.1016/j.neuroimage.2006.02.048 – volume: 493 start-page: 167 year: 2005 ident: ref4 article-title: Intrinsic brain activity sets the stage for expression of motivated behavior. publication-title: J Comp Neurol doi: 10.1002/cne.20752 – volume: 28 start-page: 663 year: 2007 ident: ref24 article-title: Task demand modulation of steady-state functional connectivity to primary motor cortex. publication-title: Hum Brain Mapp doi: 10.1002/hbm.20294 – volume: 25 start-page: 1214 year: 2005 ident: ref60 article-title: Brain mechanisms for mood congruent memory facilitation. publication-title: Neuroimage doi: 10.1016/j.neuroimage.2004.11.053 – volume: 100 start-page: 253 year: 2003 ident: ref17 article-title: Functional connectivity in the resting brain: a network analysis of the default mode hypothesis. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0135058100 – volume: 360 start-page: 1001 year: 2005 ident: ref18 article-title: Investigations into resting-state connectivity using independent component analysis. publication-title: Philos Trans R Soc Lond B Biol Sci doi: 10.1098/rstb.2005.1634 – volume: 493 start-page: 154 year: 2005 ident: ref29 article-title: Neural mechanisms of autonomic, affective, and cognitive integration. publication-title: J Comp Neurol doi: 10.1002/cne.20749 – volume: 25 start-page: 47 year: 2007 ident: ref47 article-title: Detecting functional connectivity in the resting brain: a comparison between ICA and CCA. publication-title: Magn Reson Imaging doi: 10.1016/j.mri.2006.09.032 – year: 2007 ident: ref22 article-title: Reduced resting-state brain activity in the “default network” in normal aging. publication-title: Cereb Cortex – volume: 101 start-page: 4637 year: 2004 ident: ref51 article-title: Default-mode network activity distinguishes Alzheimer's disease from healthy aging: evidence from functional MRI. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0308627101 – volume: 288 start-page: 1769 year: 2000 ident: ref38 article-title: Psychological and neural mechanisms of the affective dimension of pain. publication-title: Science doi: 10.1126/science.288.5472.1769 – volume: 103 start-page: 10046 year: 2006 ident: ref15 article-title: Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0604187103 – volume: 48 start-page: 1595 year: 1985 ident: ref56 article-title: Constraints of the effects of mood on memory. publication-title: J Pers Soc Psychol doi: 10.1037/0022-3514.48.6.1595 – volume: 23 start-page: 531 year: 2005 ident: ref72 article-title: Midazolam sedation increases fluctuation and synchrony of the resting brain BOLD signal. publication-title: Magn Reson Imaging doi: 10.1016/j.mri.2005.02.009 – volume: 22 start-page: 197 year: 2004 ident: ref36 article-title: Comparison of methods for detecting nondeterministic BOLD fluctuation in fMRI. publication-title: Magn Reson Imaging doi: 10.1016/j.mri.2003.09.007 – volume: 6 start-page: 160 year: 1998 ident: ref62 article-title: Analysis of fMRI data by blind separation into independent spatial components. publication-title: Hum Brain Mapp doi: 10.1002/(SICI)1097-0193(1998)6:3<160::AID-HBM5>3.0.CO;2-1 – volume: 3 start-page: 1049 year: 2000 ident: ref27 article-title: Subcortical and cortical brain activity during the feeling of self-generated emotions. publication-title: Nat Neurosci doi: 10.1038/79871 – volume: 12 start-page: 582 year: 2000 ident: ref35 article-title: Correlations in low-frequency BOLD fluctuations reflect cortico-cortical connections. publication-title: Neuroimage doi: 10.1006/nimg.2000.0654 – volume: 14 start-page: 140 year: 2001 ident: ref65 article-title: A method for making group inferences from functional MRI data using independent component analysis. publication-title: Hum Brain Mapp doi: 10.1002/hbm.1048 – volume: 103 start-page: 8275 year: 2006 ident: ref53 article-title: Failing to deactivate: resting functional abnormalities in autism. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0600674103 – volume: 26 start-page: 63 year: 2006 ident: ref7 article-title: A resilient, low-frequency, small-world human brain functional network with highly connected association cortical hubs. publication-title: J Neurosci doi: 10.1523/JNEUROSCI.3874-05.2006 – volume: 34 start-page: 537 year: 1995 ident: ref8 article-title: Functional connectivity in the motor cortex of resting human brain using echo-planar MRI. publication-title: Magn Reson Med doi: 10.1002/mrm.1910340409 – volume: 24 start-page: 59 year: 2005 ident: ref26 article-title: Effect of prior cognitive state on resting state networks measured with functional connectivity. publication-title: Hum Brain Mapp doi: 10.1002/hbm.20069 – volume: 48 start-page: 30 year: 2000 ident: ref31 article-title: Differential limbic–cortical correlates of sadness and anxiety in healthy subjects: implications for affective disorders. publication-title: Biol Psychiatry doi: 10.1016/S0006-3223(00)00874-X – volume: 29 start-page: 2097 year: 2004 ident: ref67 article-title: Alcohol intoxication effects on simulated driving: exploring alcohol-dose effects on brain activation using functional MRI. publication-title: Neuropsychopharmacology doi: 10.1038/sj.npp.1300543 – volume: 15 start-page: 1315 year: 2004 ident: ref23 article-title: Changes in functional connectivity of human MT/V5 with visual motion input. publication-title: Neuroreport doi: 10.1097/01.wnr.0000129997.95055.15 – volume: 3 start-page: 655 year: 2002 ident: ref37 article-title: How do you feel? Interoception: the sense of the physiological condition of the body. publication-title: Nat Rev Neurosci doi: 10.1038/nrn894 – volume: 70 start-page: 263 year: 2006 ident: ref33 article-title: Independent component model of the default-mode brain function: Assessing the impact of active thinking. publication-title: Brain Res Bull doi: 10.1016/j.brainresbull.2006.06.012 – volume: 98 start-page: 4259 year: 2001 ident: ref39 article-title: Medial prefrontal cortex and self-referential mental activity: relation to a default mode of brain function. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.071043098 – volume: 5 start-page: 179 year: 1997 ident: ref73 article-title: Empirical analyses of BOLD fMRI statistics. I. Spatially unsmoothed data collected under null-hypothesis conditions. publication-title: Neuroimage – volume: 164 start-page: 450 year: 2007 ident: ref50 article-title: Aberrant “default mode” functional connectivity in schizophrenia. publication-title: Am J Psychiatry doi: 10.1176/ajp.2007.164.3.450 – volume: 13 start-page: 5 year: 1993 ident: ref63 article-title: Functional connectivity: the principal-component analysis of large (PET) data sets. publication-title: J Cereb Blood Flow Metab doi: 10.1038/jcbfm.1993.4 – volume: 104 start-page: 13170 year: 2007 ident: ref34 article-title: Electrophysiological signatures of resting state networks in the human brain. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0700668104 – volume: 7 start-page: 1129 year: 1995 ident: ref70 article-title: An information-maximization approach to blind separation and blind deconvolution. publication-title: Neural Comput doi: 10.1162/neco.1995.7.6.1129 – volume: 29 start-page: 449 year: 2006 ident: ref2 article-title: Brain work and brain imaging. publication-title: Annu Rev Neurosci doi: 10.1146/annurev.neuro.29.051605.112819 – volume: 447 start-page: 83 year: 2007 ident: ref5 article-title: Intrinsic functional architecture in the anesthetized monkey brain. publication-title: Nature doi: 10.1038/nature05758 – volume: 31 start-page: 513 year: 2006 ident: ref14 article-title: Connectivity-behavior analysis reveals that functional connectivity between left BA39 and Broca's area varies with reading ability. publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.12.040 – volume: 25 start-page: 102 year: 2006 ident: ref64 article-title: Exploratory analysis of brain connectivity with ICA. publication-title: IEEE Eng Med Biol Mag doi: 10.1109/MEMB.2006.1607674 – volume: 8 start-page: 700 year: 2007 ident: ref3 article-title: Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. publication-title: Nat Rev Neurosci doi: 10.1038/nrn2201 – volume: 87 start-page: 9868 year: 1990 ident: ref1 article-title: Brain magnetic resonance imaging with contrast dependent on blood oxygenation. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.87.24.9868 – volume: 98 start-page: 676 year: 2001 ident: ref41 article-title: A default mode of brain function. publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.98.2.676 – volume: 22 start-page: 1326 year: 2001 ident: ref9 article-title: Frequencies contributing to functional connectivity in the cerebral cortex in “resting-state” data. publication-title: AJNR Am J Neuroradiol – volume: 15 start-page: 394 year: 2003 ident: ref40 article-title: A parametric manipulation of factors affecting task-induced deactivation in functional neuroimaging. publication-title: J Cogn Neurosci doi: 10.1162/089892903321593117 – volume: 24 start-page: 979 year: 2006 ident: ref48 article-title: Large-amplitude, spatially correlated fluctuations in BOLD fMRI signals during extended rest and early sleep stages. publication-title: Magn Reson Imaging doi: 10.1016/j.mri.2006.04.018 – volume: 63 start-page: 749 year: 2006 ident: ref58 article-title: Cognitive reactivity to sad mood provocation and the prediction of depressive relapse. publication-title: Arch Gen Psychiatry doi: 10.1001/archpsyc.63.7.749 – volume: 7 start-page: 189 year: 2004 ident: ref30 article-title: Neural systems supporting interoceptive awareness. publication-title: Nat Neurosci doi: 10.1038/nn1176 – reference: 16818864 - Arch Gen Psychiatry. 2006 Jul;63(7):749-55 – reference: 14964560 - IEEE Trans Med Imaging. 2004 Feb;23(2):137-52 – reference: 12030820 - Neuroimage. 2002 Jun;16(2):331-48 – reference: 17476267 - Nature. 2007 May 3;447(7140):83-6 – reference: 15316570 - Neuropsychopharmacology. 2004 Nov;29(11):2097-17 – reference: 17015076 - Prog Brain Res. 2006;156:93-103 – reference: 17670949 - Proc Natl Acad Sci U S A. 2007 Aug 7;104(32):13170-5 – reference: 11034865 - Neuroimage. 2000 Nov;12(5):582-7 – reference: 11259662 - Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4259-64 – reference: 15382248 - Hum Brain Mapp. 2005 Jan;24(1):59-68 – reference: 15976020 - Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9673-8 – reference: 17080441 - Hum Brain Mapp. 2007 Jul;28(7):663-72 – reference: 16945915 - Proc Natl Acad Sci U S A. 2006 Sep 12;103(37):13848-53 – reference: 16399673 - J Neurosci. 2006 Jan 4;26(1):63-72 – reference: 16632379 - Neuroimage. 2006 Jul 15;31(4):1536-48 – reference: 16919409 - Brain Dev. 2007 Mar;29(2):83-91 – reference: 17307337 - Schizophr Res. 2007 Mar;91(1-3):82-6 – reference: 10524607 - Hum Brain Mapp. 1999;8(2-3):151-6 – reference: 14730305 - Nat Neurosci. 2004 Feb;7(2):189-95 – reference: 8417010 - J Cereb Blood Flow Metab. 1993 Jan;13(1):5-14 – reference: 17636560 - Hum Brain Mapp. 2008 Aug;29(8):910-21 – reference: 11039342 - AJNR Am J Neuroradiol. 2000 Oct;21(9):1636-44 – reference: 16568942 - IEEE Eng Med Biol Mag. 2006 Mar-Apr;25(2):102-11 – reference: 16997067 - Magn Reson Imaging. 2006 Oct;24(8):979-92 – reference: 15919598 - Magn Reson Imaging. 2005 May;23(4):531-7 – reference: 11017179 - Nat Neurosci. 2000 Oct;3(10):1049-56 – reference: 11559959 - Hum Brain Mapp. 2001 Nov;14(3):140-51 – reference: 11835612 - Hum Brain Mapp. 2002 Apr;15(4):247-62 – reference: 15167557 - Neuroreport. 2004 Jun 7;15(8):1315-9 – reference: 12729491 - J Cogn Neurosci. 2003 Apr 1;15(3):394-408 – reference: 9153677 - Psychol Med. 1997 May;27(3):565-78 – reference: 9430503 - J Clin Psychiatry. 1997;58 Suppl 16:4-12 – reference: 18063564 - Cereb Cortex. 2008 Aug;18(8):1856-64 – reference: 16776593 - Annu Rev Neurosci. 2006;29:449-76 – reference: 12506194 - Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):253-8 – reference: 15850739 - Neuroimage. 2005 May 1;25(4):1214-23 – reference: 17222714 - Magn Reson Imaging. 2007 Jan;25(1):47-56 – reference: 17329470 - Am J Psychiatry. 2007 Mar;164(3):450-7 – reference: 17329432 - J Neurosci. 2007 Feb 28;27(9):2349-56 – reference: 16497520 - Neuroimage. 2006 Jun;31(2):513-9 – reference: 17027761 - Brain Res Bull. 2006 Oct 16;70(4-6):263-9 – reference: 8524021 - Magn Reson Med. 1995 Oct;34(4):537-41 – reference: 16788060 - Proc Natl Acad Sci U S A. 2006 Jun 27;103(26):10046-51 – reference: 17679639 - Arch Gen Psychiatry. 2007 Aug;64(8):946-55 – reference: 17704812 - Nat Rev Neurosci. 2007 Sep;8(9):700-11 – reference: 16806314 - Neuropsychologia. 2006;44(12):2189-208 – reference: 10846154 - Science. 2000 Jun 9;288(5472):1769-72 – reference: 12154366 - Nat Rev Neurosci. 2002 Aug;3(8):655-66 – reference: 16702548 - Proc Natl Acad Sci U S A. 2006 May 23;103(21):8275-80 – reference: 16568940 - IEEE Eng Med Biol Mag. 2006 Mar-Apr;25(2):79-90 – reference: 9673671 - Hum Brain Mapp. 1998;6(3):160-88 – reference: 17021177 - J Neurosci. 2006 Oct 4;26(40):10222-31 – reference: 17878310 - Proc Natl Acad Sci U S A. 2007 Sep 25;104(39):15531-6 – reference: 2124706 - Proc Natl Acad Sci U S A. 1990 Dec;87(24):9868-72 – reference: 10913505 - Biol Psychiatry. 2000 Jul 1;48(1):30-42 – reference: 16254998 - J Comp Neurol. 2005 Dec 5;493(1):167-76 – reference: 16087444 - Philos Trans R Soc Lond B Biol Sci. 2005 May 29;360(1457):1001-13 – reference: 15070770 - Proc Natl Acad Sci U S A. 2004 Mar 30;101(13):4637-42 – reference: 16879844 - Neuropsychologia. 2006;44(14):2836-45 – reference: 7584893 - Neural Comput. 1995 Nov;7(6):1129-59 – reference: 11498421 - AJNR Am J Neuroradiol. 2001 Aug;22(7):1326-33 – reference: 16260155 - Neuroimage. 2006 Feb 15;29(4):1359-67 – reference: 15607089 - Magn Reson Imaging. 2004 Nov;22(9):1181-91 – reference: 17210143 - Biol Psychiatry. 2007 Sep 1;62(5):429-37 – reference: 9558644 - Neuroimage. 1998 Feb;7(2):119-32 – reference: 11209064 - Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):676-82 – reference: 15010111 - Magn Reson Imaging. 2004 Feb;22(2):197-203 – reference: 9345548 - Neuroimage. 1997 Apr;5(3):179-97 – reference: 17274023 - Hum Brain Mapp. 2007 Nov;28(11):1251-66 – reference: 16254997 - J Comp Neurol. 2005 Dec 5;493(1):154-66 |
SSID | ssj0053866 |
Score | 2.3486202 |
Snippet | There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI resting-state studies.... Background There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI... BACKGROUND: There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI... Background There is growing interest in the nature of slow variations of the blood oxygen level-dependent (BOLD) signal observed in functional MRI... |
SourceID | plos doaj pubmedcentral proquest gale pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | e1794 |
SubjectTerms | Adult Affect Alcohol Alzheimer's disease Alzheimers disease Brain Brain - physiology Brain architecture Brain mapping Cognitive ability Emotions Experiments Female Functional anatomy Functional magnetic resonance imaging Humans Hypotheses Independent component analysis Magnetic Resonance Imaging Male Memory Mood Networks Neural networks Neuroimaging Neuroscience/Behavioral Neuroscience Neuroscience/Cognitive Neuroscience NMR Nuclear magnetic resonance Oxygen Psychiatry Radiology and Medical Imaging/Magnetic Resonance Imaging Recall Reference Values Studies |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Nb9QwELXQnrggSoEGSmshJOCQNo4T27nRIqqCBEhAUW-WHduAVJIV2T3w75mJvWmDKpUD13isJM_j-ZDHbwh5VqjgHLiyXPIy5JUqqtwogYe8wXheQsDhxwLZD-L0rHp3Xp9fafWFNWGRHjgCdxggfzO-COjoIHWBd0pTiaLxtlHWSYvWF3zeJpmKNhh2sRDpohyX7DCty8Gy7_zByBHTVDNHNPL1T1Z5sbzoh-tCzr8rJ6-4opO75E6KIelR_PYtcst398hW2qUDfZGopF9uk1fve5f6c9E-UIv9ICh24wCHlY93iWgX68AHan_TwTj6s-8dhUQ9ssreJ2cnb768Ps1Tz4S8laVa5cyDv1ZVZYSpAaGmCK31RtZly73h3BVly8AANsLVgZlS1JY3gTkjWWvBWTn-gCw6QGmH0MAwfGBeuAYZcCwSiHpluXTCN2AoM8I3AOo2EYpjX4sLPZ6SSUgsIh4aYdcJ9ozk06xlJNS4Qf4Y12aSRTrs8QEoiU5Kom9Skozs48rqeLd02tT6qJIAgWBMZOTpKIGUGB3W3Hwz62HQbz9-_Qehz59mQs-TUOgBjtakew7wT0i1NZPcQUXb_PYAILCyVEpIGNrdKN_1w_vTMJgDPOMxne_Xg5ZghDFszMjDqKmXICs8Q-YwV850eIbsfKT78X0kHIcQnTOuHv2PpXhMbseSG56zZpcsVr_W_gnEdSu7N27hP5UdS0s priority: 102 providerName: Directory of Open Access Journals – databaseName: Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwELZguXBBlFdDC7UQEnBIG8dZ2zlBi6gKUovUUrQ3y4ntLVKVLM3uof-eGcebElQB1_VE2nyelzPjbwh5nSlvLYSyVPLcp4XKitQogUVebxzPIeFwoUH2RBydF19m01n84NbFtsq1TwyO2rY1fiPfY5zluVJCiveLnylOjcLqahyhcZfcQ-oybOmSs-HABbYsRLwuxyXbi7uzu2gbtxuYYspiFI4Ca__gmyeLy7a7LfH8s3_yt4B0-JA8iJkk3e-3foPccc0jshFttaNvI6H0u8fkw3Fr45Qu2np6gFMh6CnSazTzNGSb9KTvBu9odU3PjKXHbWspjvUI1x6ekPPDT98-HqVxckJay1wtU-YgaquiMMJMq1KVma8rZ-Q0r7kznNssrxm4wVLYqWcmF9OKl55ZI1ldQciy_CmZNIDSJqGeYRLBnLAl8uBUSCPqVMWlFa4Ed5kQvgZQ15FWHKdbXOpQK5NwvOjx0Ai7jrAnJB2eWvS0Gv-QP8C9GWSRFDv80F7NdbQx7eGob1zmMSeCUy6opzSFyEoHEFRWVgnZwZ3V_Q3TwbT1fiEBAsGYSMirIIHEGA123szNquv056_f_0Po7HQk9CYK-RbgqE287QDvhIRbI8lNVLT1a3f6RtMTsr1WvtuXd4ZlcApY6TGNa1edluCKMXlMyLNeU29AVlhJ5vCsHOnwCNnxSvPjItCOQ6LOGVfP__6ntsj9vqWGp6zcJpPl1cq9gLxtWb0MxvkLq5dBXg priority: 102 providerName: ProQuest |
Title | Modulation of Brain Resting-State Networks by Sad Mood Induction |
URI | https://www.ncbi.nlm.nih.gov/pubmed/18350136 https://www.proquest.com/docview/1312288676 https://www.proquest.com/docview/70420071 https://pubmed.ncbi.nlm.nih.gov/PMC2263138 https://doaj.org/article/f469ae0f4317446ebe7a4609eb98bd7b http://dx.doi.org/10.1371/journal.pone.0001794 |
Volume | 3 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3Nb9MwFLe27sIFMb5WGF2EkIBDqjhObeeAYJ1aBlIL6ijqLXJip0OqktK0Ervwt_Oe4waKitjFh_q5Un55X86zf4-QF4HMtYZQ5gsW5n4kg8hXkmORN1eGhZBwGHtAdswvp9HHWW92QLY9Wx2A1d6tHfaTmq4W3R_fb96Cwb-xXRsE3S7qLsvCdC0DTBwdkiOITQJNdRQ1dQWwblu9xKzF52HA3GW6f_3LTrCynP6N524tF2W1Ly39-3TlH-FqeI_cdXmmd14rxjE5MMV9cuwsufJeObrp1w_Iu1GpXQ8vr8y9PvaM8CZIvlHMfZuLeuP6rHjlpTfeldLeqCy1h00_7KWIh2Q6HHy5uPRdXwU_E6Fc-9RATJdRpLjqpbGMgzxLjRK9MGNGMaaDMKPgJGOuezlVIe-lLM6pVoJmKQQ0zR6RVgEonRAvp5hiUMN1jCw5KZKMGpkyobmJwZm2CdsCmGSOdBx7XywSW0kTsPmo8UgQ9sTB3iZ-s2pZk278R76P76aRRcps-0O5mifOApM84rEyQY4ZE-yBQXmFingQG4Ag1SJtkzN8s0l9_7Qx_OQ8EgABp5S3yXMrgbQZBZ7LmatNVSUfPn29hdDVZEfopRPKS4AjU-4uBDwT0nHtSJ6gom0fuwIQaBhKyQVMnW6Vb__0WTMNLgPrQKow5aZKBDhqTC3b5HGtqb9BllhnZrBW7OjwDrK7M8W3a0tKDmk8o0w-uQ1GT8md-tgN82l8Slrr1cY8g9xunXbIoZgJGOUFxXH4vkOO-oPx50nHfi3pWHPG8efgFxjuUV0 |
linkProvider | Scholars Portal |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3fb9MwELZGeYAXxPi1wKAWAgEP2eI4tZMHBBswtWwt0n6gvhkndgrSlJSlFdo_xd_IXeJkFE3Ay17rS9V8Pn93rs_fEfIsiHNjIJT5koe5H8VB5OtY4CFvri0PIeGwdYHsRAxPoo_TwXSN_GzvwmBZZcuJNVGbMsP_yLcZZ2EYx0KKN_PvPnaNwtPVtoVG4xb79vwHbNmq16P3ML_Pw3Dvw_G7oe-6CviZDOOFzyxEtDiKtNCDNImTIM9Sq-UgzLjVnJsgzBhQRCLMIGc6FIOUJzkzWrIsBTo3HL73GrkOgTfAFSWn3QYPuEMIdz2PS7btvGFrXhZ2q1amSaKV8Fd3CehiQW9-WlaXJbp_1mv-FgD3bpNbLnOlO42rrZM1W9wh644bKvrSCVi_ukvejkvjuoLRMqe72IWCHqKcRzHz6-yWTprq84qm5_RIGzouS0OxjUh9zeIeObkSTO-TXgEobRCaM0xamBUmQd2dFGVLbZxyaYRNgJ49wlsAVeZkzLGbxqmqz-YkbGcaPBTCrhzsHvG7p-aNjMc_7HdxbjpbFOGuPyjPZsqtaZVHItE2yDEHg101LAepIxEkFiBIjUw90seZVc2N1o5K1E4kAQLBmPDI09oChTgKrPSZ6WVVqdGnz_9hdHS4YvTCGeUlwJFpd7sC3gkFvlYsN9DR2teu1MXK8shm63yXD_e7YSAhPFnShS2XlZJA_ZiseuRB46kXIMd4cs3hWbniwyvIro4U377WMuewMeCMxw___qP65MbweHygDkaT_UfkZlPOw32WbJLe4mxpH0POuEif1AuVki9XzQy_AJyZffE |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3fb9MwELZGkRAviPFrgUEtBAIessZxYicPCDZGtTJW0MZQ34wT2wVpSsrSCu1f46_DlzgZQRPwstf6UjWfz9-d6_N3CD0JEqOUDWU-p6HxoySIfJkwOOQ1UtPQJhy6LpCdsr3j6N0snq2hn-1dGCirbDmxJmpV5vAf-YhQEoZJwjgbGVcW8XF3_Grx3YcOUnDS2rbTaFxkX5_9sNu36uVk18710zAcv_30Zs93HQb8nIfJ0ifaRrckiiSTcZYmaWDyTEsehznVklIVhDmxdJEyFRsiQxZnNDVESU7yzFK7ovZ7r6CrnMYE1hifdZs9yyOMuat6lJOR84ytRVnorVqlJo16obDuGNDFhcHipKwuSnr_rN38LRiOb6IbLovF243braM1XdxC644nKvzciVm_uI1eH5TKdQjDpcE70JECH4K0RzH360wXT5tK9ApnZ_hIKnxQlgpDS5H6ysUddHwpmN5Fg8KitIGwIZDAEM1UCho8GUiY6iSjXDGdWqr2EG0BFLmTNIfOGieiPqfjdmvT4CEAduFg95DfPbVoJD3-Yb8Dc9PZgiB3_UF5OhdufQsTsVTqwEA-ZnfYdmlwGbEg1RaCTPHMQ0OYWdHcbu1oRWxH3ELACGEeelxbgChHAe49l6uqEpMPn__D6OiwZ_TMGZnSwpFLd9PCvhOIffUsN8DR2teuxPkq89Bm63wXDw-7YUtIcMokC12uKsFtGIDE1UP3Gk89BzmBU2xqn-U9H-4h2x8pvn2tJc_tJoESmtz_-48aomuWE8T7yXT_AbreVPZQn6SbaLA8XemHNn1cZo_qdYrRl8smhl-HEIIn |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Modulation+of+Brain+Resting-State+Networks+by+Sad+Mood+Induction&rft.jtitle=PloS+one&rft.au=Harrison%2C+Ben+J&rft.au=Pujol%2C+Jesus&rft.au=Ortiz%2C+Hector&rft.au=Fornito%2C+Alex&rft.date=2008-03-19&rft.pub=Public+Library+of+Science&rft.issn=1932-6203&rft.eissn=1932-6203&rft.volume=3&rft.issue=3&rft.spage=e1794&rft_id=info:doi/10.1371%2Fjournal.pone.0001794&rft.externalDBID=IOV&rft.externalDocID=A472656116 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1932-6203&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1932-6203&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1932-6203&client=summon |