ライフサイエンスコーパス: BOLD signal

1 ps were found between panic symptoms and the BOLD signal.

2 nsights in the neuronal underpinnings of the BOLD signal.

3 ributed to the observed group differences in BOLD signal.

4 100 Hz) LFP bands were informative about the BOLD signal.

5 1.5-2.0 minutes of RS functional MR imaging BOLD signal.

6 explain different components of the observed BOLD signal.

7 flow (CBF) and volume (CBV) that affect the BOLD signal.

8 ding the spatial specificity of the positive BOLD signal.

9 the population-based neuronal source of the BOLD signal.

10 ning cell-type-specific contributions to the BOLD signal.

11 subsystems using an MDS in the space of the BOLD signal.

12 emodynamic responses that drive the negative BOLD signal.

13 fluctuations (ISFs) in scalp potentials and BOLD signals.

14 local field potential (LFP) activity, and of BOLD signals.

15 Graded hypoxia decreased BOLD signals.

16 phy (fbEEG) are related to the resting-state BOLD signals.

17 as measured by blood oxygen level-dependent (BOLD) signal.

18 es in the blood oxygenation level-dependent (BOLD) signal.

19 ced changes in blood oxygen level-dependent (BOLD) signal.

20 e on the brain blood oxygen level-dependent (BOLD) signal.

21 y measured via blood oxygen level dependent (BOLD) signals.

22 as measured by blood-oxygen-level-dependent (BOLD) signals.

23 pon brain fMRI blood oxygen level-dependent (BOLD) signals.

24 wer (task-off) blood oxygen level-dependent (BOLD) signals.

25 negative blood oxygenation level-dependent (BOLD) signaling.

26 ced response amplitude (percentage change in BOLD signal, 0.65 +/- 0.28 vs 0.89 +/- 0.14; p < 0.01),

27 BOLD signal (7.5 minutes worth) was obtained from 30 sub

28 ency) were computed for each subject at each BOLD signal acquisition duration.

29 bal efficiency stabilized after 2 minutes of BOLD signal acquisition, whereas correlation coefficient

30 ted threshold) stabilized after 5 minutes of BOLD signal acquisition.

31 WM tracts and patterns of condition-related BOLD signal across all GM regions.

32 vestigated the spatial pattern of correlated BOLD signal across eight visual areas on data collected

33 ty, measured by the spatial coherence of the BOLD signal across regions of the brain; and metastabili

34 tinguishable solely from the pattern of fMRI BOLD signals across voxels in the human hippocampus.

35 al patterns of blood oxygen-level-dependent (BOLD) signal across voxels.

36 ing changes in blood-oxygen-level-dependent (BOLD) signal after visual stimulation.

37 ility (measured as the standard deviation of BOLD signal amplitude) in resting state networks (RSNs)

38 Both BOLD signal and CBV decreased from superficial to deep l

39 functional magnetic resonance imaging (fMRI) BOLD signal and electrocorticographic (ECoG) field poten

40 sly and with high spatiotemporal resolution, BOLD signal and LFP during spontaneous activity in early

41 ates positively with the superficial layers' BOLD signal and that beta-power is negatively correlated

42 ain networks readily revealed by spontaneous BOLD signals and their underlying neurophysiology.

43 s well as blood oxygenation level-dependent (BOLD) signal and cerebral blood volume (CBV) and blood f

44 regional blood oxygenation level-dependent (BOLD) signal and correlated symptoms was compared with i

45 tivity are the blood-oxygen-level dependent (BOLD) signal and surface field potential.

46 alient in blood oxygenation level-dependent (BOLD) signals and correlated within specific brain syste

47 mpirical foundation for the widely-used fMRI BOLD signal, and the features of of MRI define a potent

48 ptom severity, blood-oxygen-level-dependent (BOLD) signal, and dorsolateral prefrontal cortex (DLPFC)

49 different brain regions in the resting-state BOLD signal are thought to reflect intrinsic functional

50 n-based optical imaging studies, the highest BOLD signals are localized to the sites of increased neu

51 Changes in BOLD signals are sensitive to the regional blood content

52 (LFOs) of the blood oxygen level-dependent (BOLD) signal are gaining interest as potential biomarker

53 ions (LFOs) of blood-oxygen-level-dependent (BOLD) signals are used to map brain functional connectiv

54 then test the purity of the ventral striatal BOLD signal as a model-free report.

55 e glucose and oxygen consumption, and of the BOLD signal as reported in human studies.

56 nduced deactivations in medial temporal lobe BOLD signal (as compared to periods of rest) demonstrate

57 annot be explained by differences in overall BOLD signal, as average BOLD activity was either equival

58 In this way, we indexed BOLD signals associated with an anticipated need to exer

59 orrelated with blood oxygen level-dependent (BOLD) signal associated with each working memory compone

60 erence in blood oxygenation level-dependent (BOLD) signal associated with the selected and rejected s

61 Here, we demonstrate that the positive BOLD signal at 9.4T can reveal the fine topography of in

62 We calculated the time delay between the BOLD signal at each voxel and the whole-brain signal usi

63 0.2 Hz) inversely correlated fluctuations in BOLD signal at rest.

64 ignal such that TMS to the left LO decreases BOLD signal at the stimulation site (LO) while viewing o

65 the neocortex or thalamus, elicits positive BOLD signals at the stimulus location with classical kin

66 The blood oxygen level-dependent (BOLD) signal at primary olfactory cortex (POC) was weake

67 ations of blood oxygenation level-dependent (BOLD) signals between remote brain areas [so-called BOLD

68 minar-resolved blood-oxygen level-dependent (BOLD) signal by combining data from simultaneously recor

69 (2.35 versus 2.37 mL/min per gram; P=0.91), BOLD signal change (17.3% versus 17.09%; P=0.91), and co

70 a priori defined striatal region of interest BOLD signal change during reward anticipation compared w

71 is was mirrored by a monotonically decreased BOLD signal change in dorsolateral prefrontal cortex on

72 A BOLD signal change in right superior parietal cortex was

73 and S2, as measured by the magnitude of the BOLD signal change to tactile stimuli, was reduced marke

74 gatively (r(2) = 0.09, p < 10(-16)) with the BOLD signal change.

75 ne on striatal blood oxygen level-dependent (BOLD) signal change during anticipation of monetary rewa

76 Mean percent blood oxygen level-dependent (BOLD) signal change was extracted from a priori regions

77 rther assessed blood-oxygen-level-dependent (BOLD) signal change while subjects performed a face-reco

78 motrigine pretreatment prevented many of the BOLD signal changes and the symptoms.

79 ontrast, men exhibited significantly greater BOLD signal changes compared to LF/MC women on bilateral

80 urrent functional magnetic resonance imaging BOLD signal changes in healthy young individuals while t

81 In healthy women, robust task-evoked BOLD signal changes observed under low E(2) conditions w

82 e task-related blood-oxygen level-dependent (BOLD) signal changes during sematic processing and resti

83 rences in blood oxygenation level-dependent (BOLD) signal changes in men compared to EF women, except

84 ng (fMRI) blood oxygenation level-dependent (BOLD) signal changes in response to a mild cold challeng

85 osely parallel blood oxygen level dependent (BOLD) signal changes observed in human functional magnet

86 We also assessed correlations between BOLD signal contrasts and clinical measures in SZs.

87 tional circuits at rest, the extent to which BOLD signals correlate spatially with underlying neurona

88 vestigated the Blood Oxygen Level Dependent (BOLD) signal correlates of interictal epileptic discharg

89 w frequent the blood-oxygen-level-dependent (BOLD) signal correlation between two nodes is negative.

90 by inter-areal blood-oxygen-level-dependent (BOLD) signal correlation, as a proxy for communication i

91 ients, areas exhibiting significant delay in BOLD signal corresponded to areas of hypoperfusion ident

92 ex in terms of blood oxygen level dependent (BOLD) signal cross-correlation in 8 male participants wi

93 halamus after placebo compared with HCs, and BOLD signal decreases in the left hypothalamus after dru

94 uations in the blood-oxygen-level-dependent (BOLD) signals demonstrate consistent temporal correlatio

95 dataset of individuals, using resting state BOLD signals, demonstrated that a functional entropy ass

96 The blood-oxygen-level-dependent (BOLD) signal, detected in fMRI, reflects changes in deox

97 meaningful and meaningless actions elicited BOLD signal differences at bilateral sites in the supram

98 Blood Oxygenation Level Dependent (BOLD) signal differences between tasks were identified b

99 Blood oxygen level dependent (BOLD) signal differences in response to SS and neutral s

100 (opto-fMRI) in mice to test the linearity of BOLD signals driven by locally induced excitatory activi

101 differences in blood oxygen level dependent (BOLD) signal due to risk factors in 74 middle-aged cogni

102 Successful older participants had higher BOLD signal during encoding than average participants, n

103 easing colonic propionate production reduced BOLD signal during food picture evaluation in the caudat

104 ioning left DLPFC with rTMS led to decreased BOLD signal during performance of this reorienting task

105 ontaneous low-frequency fluctuations in fMRI BOLD signal during rest from two separate regions key to

106 Whereas these areas also produced changes in BOLD signal during the dynamic warming stimulus on the c

107 functional magnetic resonance imaging (fMRI) BOLD signal during the performance of the Simon task.

108 RI and a blocked design were used to acquire BOLD signals during implicit (task-unrelated) presentati

109 es in the blood oxygenation level-dependent (BOLD) signal during a cued choice reaction time task.

110 sonance imaging bold oxygen level-dependent (BOLD) signal during decision making at sites within the

111 F) in the blood oxygenation level-dependent (BOLD) signal during resting-state fMRI reflects the magn

112 asures of blood oxygenation-level-dependent (BOLD) signals during the performance of dopamine-depende

113 found that the global phase synchrony of the BOLD signals evolves on a characteristic ultra-slow (<0.

114 Our findings provide evidence that the BOLD signal fluctuates with spatial heterogeneity in mal

115 ic brain activity as measured by spontaneous BOLD signal fluctuations and help to understand propofol

116 the neuronal correlates of these reciprocal BOLD signal fluctuations are unknown.

117 rous studies have measured how low-frequency BOLD signal fluctuations from the brain are correlated b

118 interregional correlations of low-frequency BOLD signal fluctuations in 10 high-functioning particip

119 Analyses of intrinsic fMRI BOLD signal fluctuations reliably reveal correlated and

120 0.015 Hz, commensurate with the frequency of BOLD signal fluctuations seen by fMRI, suggesting that q

121 relevance for the neuronal basis of coherent BOLD signal fluctuations, our procedure may translate in

122 low-frequency blood-oxygen-level-dependent (BOLD) signal fluctuations between major divisions of the

123 scular compartments and other factors to the BOLD signal for different magnet strengths and pulse seq

124 a typical rodent fMRI voxel and predict the BOLD signal from first principles using those measuremen

125 group difference in the skewness of the fMRI BOLD signal from the vPMC, suggesting that the relative

126 phase interactions among resting-state fMRI BOLD signals from human subjects.

127 , we investigated the content-specificity of BOLD signals from various brain regions during a VSTM ta

128 dies using the Blood Oxygen-Level Dependent (BOLD) signal from functional Magnetic Resonance Imaging

129 rs of the blood oxygenation level-dependent (BOLD) signal from its apparent inception on postnatal da

130 n between blood-oxygenation-level-dependent (BOLD) signals from different brain areas.

131 We examined blood oxygen dependent (BOLD) signal functional connectivity using conventional

132 Although the blood oxygen level-dependent (BOLD) signal has been found to correlate preferentially

133 onance imaging blood oxygen level-dependent (BOLD) signal have been shown to exhibit phase coherence

134 ns, where blood oxygenation level-dependent (BOLD) signals have been suggested as correlating with qu

135 frequently accompanied by reductions in the BOLD signal in adjacent regions of cortex.

136 A main effect of reduced BOLD signal in bilateral occipital areas was noted acros

137 nd directionality (positive/negative) of the BOLD signal in both contralateral and ipsilateral sensor

138 ent work with fMRI has demonstrated that the BOLD signal in dopaminergic target areas meets both nece

139 Additional analysis revealed that BOLD signal in heteromodal association cortex typically

140 e the accuracy of word report and reduce the BOLD signal in lateral temporal lobe regions.

141 In Experiment 2, spatial patterns of BOLD signal in medial temporal and posterior midline reg

142 emoglobin oxygen saturation (sO2) levels and BOLD signal in response to carbogen.

143 Significantly greater percent increases in BOLD signal in response to TMT were observed in the ante

144 Oxytocin administration reduces the BOLD signal in reward-related food motivation brain regi

145 rease in response times and increases in the BOLD signal in right frontal and parietal regions when c

146 right DLPFC conditioning revealed decreased BOLD signal in right VLPFC.

147 negative variation (CNV) signal and the fMRI BOLD signal in SMA and VS, (2) the underlying causal con

148 nd a subject-by-subject correlation with the BOLD signal in the amygdala.

149 atility information correlates with the fMRI BOLD signal in the anterior cingulate cortex.

150 BOLD) signal in BAs 9 and 10, and diminished BOLD signal in the anterior cingulate, thalamus, midbrai

151 nts who changed their minds more showed less BOLD signal in the insula and the amygdala when evaluati

152 ger, delayed reward correlates directly with BOLD signal in the lateral orbitofrontal cortex.

153 he risky Stag choice, AVP down-regulates the BOLD signal in the left dorsolateral prefrontal cortex (

154 n performance was positively correlated with BOLD signal in the left posterior hippocampus, parahippo

155 ite (LO) while viewing objects and increases BOLD signal in the left PPA when viewing scenes.

156 l use measures, were associated with greater BOLD signal in the region that differentiated the FHP an

157 iol, a TD by ACE interaction was observed on BOLD signal in the right DLPFC such that TD increased ac

158 During retrieval of the event, the BOLD signal in the same region was modulated by the pers

159 Among GG-homozygotes, BOLD signal in the subgenual cingulate was greater in MD

160 e-brain analysis, methylphenidate attenuated BOLD signal in the ventral striatum during response swit

161 first provide unbiased evidence that the raw BOLD signal in these regions corresponds closely to a re

162 by the decision process, our data show that BOLD signal in this same region reflects the choices we

163 D) signals, it remains controversial whether BOLD signals in a particular region can be caused by act

164 d BOLD activations and local correlations of BOLD signals in a resting state, and whether these spati

165 ng state functional connectivity measures of BOLD signals in different brain regions.

166 he living and intact mammalian brain reveals BOLD signals in downstream targets distant from the stim

167 aspartate (NMDA) receptor antagonist-induced BOLD signals in healthy humans and animals to differing

168 By measuring BOLD signals in human primary visual cortex while varyin

169 e found that the spontaneous fluctuations of BOLD signals in key nodes of RSNs are associated with ch

170 We recorded BOLD signals in occipitotemporal visual cortex of human

171 ective (face minus building, and vice versa) BOLD signals in precuneus and posterior parahippocampal

172 Load-dependent BOLD signals in primary visual cortex (V1) and superior

173 ectively correlated with subsets of cortical BOLD signals in specific task-positive and task-negative

174 Both choices and value-related BOLD signals in striatum, although most often associated

175 neural model that best explains the observed BOLD signals in terms of effective connectivity.

176 based value computation were correlated with BOLD signals in the medial temporal lobe and frontal cor

177 However, the BOLD signals in the right frontal and medial cerebellar

178 e dose of THC exposure were related to lower BOLD signals in the right prefrontal region and medial c

179 BOLD signals in the rostral medial prefrontal cortex (rm

180 model-free reinforcement learning, with fMRI BOLD signals in ventral striatum notably covarying with

181 iride, on blood oxygenation level-dependent (BOLD) signal in a group of 20 healthy participants durin

182 elevated blood oxygenation-level dependent (BOLD) signal in BAs 9 and 10, and diminished BOLD signal

183 with decreased blood oxygen level-dependent (BOLD) signal in Broca's area.

184 etation of the blood oxygen level-dependent (BOLD) signal in fMRI.

185 e) or negative blood oxygen level-dependent (BOLD) signal in functional magnetic resonance imaging (f

186 cortical blood oxygenation level-dependent (BOLD) signal in response to emotionally salient and neut

187 n-related blood oxygenation level-dependent (BOLD) signal in task-positive GM regions.

188 Blood-oxygen-level-dependent (BOLD) signal in the amygdala was examined in children wi

189 and changes in blood oxygen level-dependent (BOLD) signal in the amygdala with a 3T MRI scanner in 16

190 with the blood oxygenation level-dependent (BOLD) signal in the nucleus accumbens and a subject-by-s

191 Moreover, blood-oxygenation-level-dependent (BOLD) signal in the temporo-parietal junction is modulat

192 ncement of the blood oxygen level-dependent (BOLD) signal in V1.

193 found that the blood oxygen level dependent (BOLD) signal in ventromedial prefrontal cortex (vmPFC) w

194 RI) to measure blood oxygen level-dependent (BOLD) signals in 66 infants, 47 of whom were at high ris

195 ations between blood oxygen level-dependent (BOLD) signals in different brain areas.

196 slow intrinsic blood oxygen level dependent (BOLD) signals in normal adults during wake and SWS.

197 a context, and blood oxygen level dependent (BOLD) signals in the ventromedial prefrontal cortex (PFC

198 negative blood oxygenation level-dependent (BOLD) signals in these regions.

199 eater deactivation (task-induced decrease in BOLD signal) in medial parietal regions during successfu

200 omponents was also observed in value-related BOLD signaling, in the form of lateralized biases in str

201 in neural synchrony goes hand-in-hand with a BOLD signal increase in the left dorsolateral prefrontal

202 During cataplexy, suprapontine BOLD signal increase was present in the amygdala, fronta

203 cipants experienced illusory reversals, fMRI BOLD signals increased in anterior cingulate cortex/medi

204 Brain areas showing changes in BOLD signal increases (activations) and decreases (deact

205 h aversive and erotic images produced robust BOLD signal increases in bilateral primary and secondary

206 s with more intact WM further showed greater BOLD signal increases in typical "task-negative" regions

207 refrontal cortex, and the nucleus accumbens; BOLD signal increases were also observed at locus cerule

208 illustrated by quantifying variations in the BOLD signal induced by the morphological folding of the

209 tions in regards to fMRI technology: how the BOLD signal inferences the underlying microscopic neuron

210 een photoacoustically derived sO2 levels and BOLD signal intensity (r = 0.937, P = .005) and partial

211 The BOLD signal intensity and activation volume within the P

212 isplayed a correlation between participants' BOLD signal intensity and reaction time that was selecti

213 Changes in PAI and BOLD signal intensity before and after VDA treatment wer

214 irty-six patients were analyzed for relative BOLD signal intensity increase according to the 16-segme

215 Relative BOLD signal intensity increase was significantly lower i

216 kg/min) and assessed quantitatively (using a BOLD signal intensity index [stress/resting signal inten

217 A BOLD signal intensity index threshold to identify ischem

218 Because the BOLD signal is an indirect measure of neuronal activity

219 s similarly to classic language regions: (i) BOLD signal is higher during sentence comprehension than

220 rol conditions that are more difficult; (ii) BOLD signal is modulated by phonological information, le

221 These results imply that the BOLD signal is more closely coupled to synaptic activity

222 croscopic vascular behavior into macroscopic BOLD signals is at the foundation of physiologically inf

223 r activity and blood oxygen level-dependent (BOLD) signal is of critical importance to the interpreta

224 R) imaging T2* blood oxygen level-dependent (BOLD) signal is sensitive to blood oxygen concentration;

225 RI) using blood oxygenation level-dependent (BOLD) signals, it remains controversial whether BOLD sig

226 irectly applicable, regions with the highest BOLD signals may indicate neurally inactive domains rath

227 delay in blood oxygenation level-dependent (BOLD) signals may be sensitive to perfusion deficits in

228 nt cautionary data concerning the quality of BOLD signals measured from the LC using standard functio

229 Whereas some studies have reported that BOLD signals measured in visual cortex are tightly linke

230 However, blood oxygen level-dependent (BOLD) signals measured via fMRI are very slow [9], so it

231 y, a proxy for blood oxygen level-dependent (BOLD) signal measurement in human functional magnetic re

232 itated by the fact that time resolution of a BOLD signal much lower than that of cognitive processes

233 t anxiety was positively correlated with the BOLD signal of the right parahippocampal gyrus during th

234 first create nodal signals by averaging the BOLD signals of all the voxels in each region, and to th

235 iterature, the blood oxygen level-dependent (BOLD) signal of functional magnetic resonance imaging st

236 The BOLD signal originated primarily from venules, and the C

237 increase in tumor sO2 levels (P = .003) and BOLD signal (P = .001).

238 tudy revealed for the first time contrasting BOLD signal patterns of biased agonists in comparison to

239 a specific cognitive paradigm, modelling the BOLD signal provided new insight into the dynamic causal

240 ion, which correspond to specific changes in BOLD signal reactivity.

241 addition, we assess MD responsiveness using BOLD signal recruitment and multi-task activation indice

242 ed significant blood oxygen level-dependent (BOLD) signal reductions in the amygdala, hippocampus, in

243 dACC BOLD signals reflected two decision biases-to defer comm

244 However, the BOLD signal reflects changes in blood volume and oxygena

245 The BOLD signal related to cue-only trials, regardless of cu

246 1) higher blood oxygenation level-dependent (BOLD) signal related to the eye closure over the visual

247 of the LFP, it is still unclear whether the BOLD signal relates to the activity expressed by each LF

248 Both increases and decreases in BOLD signal reliably followed increases and decreases in

249 esia, as well as rTMS-induced attenuation of BOLD signal response to painful stimuli throughout pain

250 zed but not control mothers showed a greater BOLD signal response to predator odor than a control put

251 lthough applying global signal regression to BOLD signals results in some BOLD anticorrelations that

252 Voxelwise analysis of task-related BOLD signal revealed a significant group-by-abstinence i

253 ns in the blood oxygenation level-dependent (BOLD) signal serve as the basis of functional magnetic r

254 The blood oxygenation level-dependent (BOLD) signal serves as the basis for human functional MR

255 gether, these findings suggest that the vPMC BOLD signal skewness and the temporal relationship of vP

256 s effect is also reflected by changes in the BOLD signal such that TMS to the left LO decreases BOLD

257 Knowledge of the properties of the BOLD signal, such as how linear its response is to senso

258 allodynia produced significant decreases in BOLD signal, suggesting pain-induced activation of endog

259 ous fingers of the two hands elicited higher BOLD signal than stimulation of homologous fingers.

260 The results identified a component of the BOLD signal that can be attributed to significant change

261 us, showed a monotonic variation of the fMRI BOLD signal that scaled with perceived memory strength (

262 een areas, between subjects, or even between BOLD signals that have been preprocessed in different wa

263 100 Hz) neural activity contributes to local BOLD signals, the neural basis of interareal BOLD correl

264 rectly test this assumption by comparing the BOLD signal time courses in each network across differen

265 e-tracking data to a low-temporal resolution BOLD signal to extract responses to single words during

266 eagues use resting-state fluctuations of the BOLD signal to highlight the relevance of networks to hu

267 tionship between cerebral blood flow and the BOLD signal to improve dynamic estimates of blood flow f

268 that psychosis patients showed an increased BOLD signal to LRZ challenge, rather than the decreased

269 at such cross-frequency coupling links local BOLD signals to BOLD correlations across distributed net

270 educe the blood oxygenation level-dependent (BOLD) signal to high-calorie food vs non-food visual sti

271 e behavior and blood oxygen level-dependent (BOLD) signals to decision variables extracted from simul

272 fMRI blood oxygen level-dependent (BOLD) signals to the sight and/or taste of the stimuli w

273 The authors investigated how well BOLD signal tracked prediction error in the striatum and

274 can extract word-level information from the BOLD signal using high-temporal resolution eye tracking.

275 Recording blood oxygenation level-dependent (BOLD) signal using functional magnetic resonance imaging

276 ole-brain blood oxygenation level-dependent (BOLD) signals using functional MRI during an affective S

277 Because previous work investigating BOLD signal variability has been conducted within task-b

278 wn regarding regional changes in spontaneous BOLD signal variability in the human brain across the li

279 onal-MRI-based blood oxygen level-dependent (BOLD) signal variability (SD(BOLD)) in younger and older

280 asy-to-implement analysis approach to assess BOLD-signal variability in event-related fMRI task parad

281 However, higher levels of BOLD-signal variability in the left inferior frontal jun

282 r, our data suggest that neuronally mediated BOLD signal variance generally increases in light sleep.

283 cy fluctuations (fALFF; 0.01-0.08 Hz) of the BOLD signal was compared among the three groups.

284 In the caudate, the reduction in BOLD signal was driven specifically by a lowering of the

285 on, rCBF was measured with [15O]H2O PET, and BOLD signal was measured with fMRI, both during an n-bac

286 a (PPA), significant attenuation in the fMRI BOLD signal was observed for the attended repeated scene

287 BOLD signal was recorded during rest periods before and

288 Conversely, among A-carriers, BOLD signal was smaller in MDD (n = 7) compared with con

289 Resting-state BOLD signal was transformed into frequency space (Welch'

290 occur during early conditioning and amygdala BOLD signaling was unaffected in these patients.

291 The blood oxygen level-dependent (BOLD) signal was measured in a priori brain regions invo

292 The blood-oxygen-level dependent (BOLD) signal was measured to identify regions where the

293 eral, the blood oxygenation level-dependent (BOLD) signal was reduced for the amblyopic eye.

294 phic maps can be achieved using the positive BOLD signal, weakening previous notions regarding the sp

295 y, only decreases in cerebral blood flow and BOLD signal were seen, and these were maximal in hub reg

296 nal MRI (fMRI) blood-oxygen-level-dependent (BOLD) signal were analyzed using a computational model o

297 rences in blood oxygenation level-dependent (BOLD) signal were found in healthy controls (A allele ca

298 power was reflected in the amplitude of the BOLD signal, while the relationship between beta and gam

299 At the lowest odorant concentration, the BOLD signals within POC, hippocampus, and insula were si

300 inhibitory population evoked robust positive BOLD signals within striatum, while downstream regions e