ライフサイエンスコーパス: brain area

1 it as related to the dysfunction of a single brain area.

2 serotonin receptor (dys)function in a limbic brain area.

3 in levels specifically within the stimulated brain area.

4 quires reciprocal excitation across multiple brain areas.

5 ral basis for function specialisation within brain areas.

6 f the excitation were conserved in different brain areas.

7 ency map, which may then be relayed to other brain areas.

8 alpha oscillations in task-relevant sensory brain areas.

9 l processing more than of decoupling between brain areas.

10 ulation structure support hypotheses in many brain areas.

11 es is regulated dynamically across different brain areas.

12 that includes multiple neurotransmitters and brain areas.

13 -20 Hz) beta band power increases in frontal brain areas.

14 was distributed in input neurons in multiple brain areas.

15 timuli are selectively processed in distinct brain areas.

16 tween excitatory neurons located in distinct brain areas.

17 lations of activity synchronized across many brain areas.

18 and dopamine, increase neural gain in target brain areas.

19 ns in total gray matter and (mainly) frontal brain areas.

20 selection requires the interplay of multiple brain areas.

21 ubstrate for learning and memory, in various brain areas.

22 ofiles of stress regulatory genes in various brain areas.

23 entails a very rapid reactivation of sensory brain areas.

24 g neurotoxicity into surrounding, undamaged, brain areas.

25 nputs to a range of cortical and subcortical brain areas.

26 arker of cerebrovascular disease, in several brain areas.

27 of many types recruit common frontoparietal brain areas.

28 glia, provide tonic inhibition of downstream brain areas.

29 ary nucleus, from where they project to many brain areas.

30 , or reward and directly projects to several brain areas.

31 ith dopamine either in the striatum or other brain areas.

32 attempted with varying success in different brain areas.

33 o coordinate memory processes across distant brain areas.

34 synaptic transmission and plasticity in many brain areas.

35 the parahippocampal cortex, but not in other brain areas.

36 heterogeneity in this encoding seen between brain areas.

37 ms underlie persistent activity in different brain areas.

38 ases change this modular architecture within brain areas.

39 etworks are defined as graphs of interacting brain areas.

40 mmetric changes in directed influences among brain areas.

41 namic interactions of reciprocally connected brain areas.

42 can share the same neural circuits in local brain areas.

43 orks are largely conserved between different brain areas.

44 e metabolism in the cingulate and prefrontal brain areas.

45 tracts connecting the hippocampus with other brain areas.

46 onses of less-selective cells in lower-level brain areas.

47 n of such noncanonical organization of these brain areas.

48 ecific neuropathological changes in selected brain areas.

49 d loci: (1) are highly expressed in cortical brain areas; (2) are enriched for ion channel pathways (

50 Clustering of brain areas according to similarity of spectral profiles

51 ructures; (v) accurately align corresponding brain areas across subjects and studies; (vi) analyze da

52 systematically relates to the recruitment of brain areas across two functionally distinct tasks (visu

53 CM patients was best explained by damage in brain areas activated during handgrip.

54 How neurons in this brain area adapt to the changing metabolic environment t

55 ls, cerebral amyloidosis, and the volumes of brain areas affected by Alzheimer disease.

56 s that these DNA glycosylases are present in brain areas affected by neurodegeneration.

57 al excitability have been observed in limbic brain areas after associative learning, but little is kn

58 e represented faithfully by the early visual brain areas; all the information from a certain region o

59 ensembles is regulated differentially across brain areas and adapts dynamically to changes in associa

60 e frequency bands has been described in many brain areas and attributed to numerous brain functions.

61 in early postnatal ZIKV injected mice, some brain areas and cell types display particularly large in

62 discuss neuropharmacological mechanisms, and brain areas and circuits controlling stress-induced rein

63 widespread and variable involvement of other brain areas and circuits.

64 xpression featured in deep categorization of brain areas and developmental stages and brain-specific

65 n those of other amyloid-beta species across brain areas and disease stages.

66 We also provide 3D reconstructions for all brain areas and many of the fiber bundles in the brain o

67 s a promising tool to selectively inactivate brain areas and neural circuits in rat studies of motiva

68 namic prioritization in contralateral visual brain areas and show that this substrate predicts workin

69 d dynamic patterns among molecules, neurons, brain areas and social systems; and the theoretical fram

70 Our model generalizes across brain areas and STDP rules, allowing broad application t

71 ctrophysiological signals synchronize across brain areas and that the topography of this activity is

72 In contrast, PGE2 production in other brain areas and the overall PGE2 level in the brain do n

73 sole brain, profusely innervating different brain areas and the pituitary gland, which could represe

74 -beta, depending on disease stage as well as brain area, and determined how these amyloid-beta specie

75 y measuring the information transfer between brain areas, and by taking reduced information transfer

76 spatial and temporal scales and in different brain areas, and has been hypothesized to affect the neu

77 ony among neurons occurs in many species and brain areas, and has been proposed to help neural circui

78 The receptor is also expressed in other brain areas, and here we examined whether GPR88 function

79 nnectivity, both locally and between distant brain areas, and these long-range changes correlate with

80 ntial dynamics during similar tasks in other brains areas, and clarify the contribution of the striat

81 wever it is currently unknown whether visual brain areas are affected.

82 have established firmly that face-selective brain areas are central to face processing.

83 It is unknown, however, what brain areas are involved in converting vestibular-motion

84 Although a number of brain areas are known to encode such predictions, a deta

85 Specifically, modules within brain areas are spatially localised.

86 al energy supply may underlie the decline in brain areas assigned to food intake regulation and there

87 arises from the lateral hypothalamus [2], a brain area associated with arousal [3-5].

88 a neural level, evaluation of harms engaged brain areas associated with affective and somatosensory

89 ated with enhanced smoking cue-reactivity in brain areas associated with attention and motor preparat

90 ts showed similar increases in activation in brain areas associated with cognitive control.

91 kines in addition to specific alterations in brain areas associated with mood regulation.

92 otinic receptor subtype that is expressed in brain areas associated with motor control.

93 n concentration changes and the fMRI BOLD in brain areas associated with speech comprehension.

94 show that neural variability in a prefrontal brain area at the inferior frontal junction is different

95 ng, which was limited without extra-temporal brain areas available.

96 ne release in the nucleus accumbens shell, a brain area believed to underlie nicotine reward.

97 correcting code-a principle that may hold in brain areas beyond retina.

98 tion because of their projections to several brain areas both in and outside of the hypothalamus, suc

99 re concurrently localized within the same IL brain area but selectively reactive to different environ

100 ,000 genes are present in one or more of the brain areas but only 210 genes, approximately 1.3%, are

101 ns such as RPE are not localized in specific brain areas but, rather, distributed across multiple nod

102 cited activation not only from the sonicated brain area, but also from the network of regions involve

103 (>10 s) duration has been described in many brain areas, but little is known about the role of this

104 idely distributed manner throughout multiple brain areas, but that the striatum may have a privileged

105 PDE10A expression was assessed in different brain areas by rabbit anti-PDE10A antibody immunohistoch

106 To clarify if structural alteration in these brain areas can be verified in a large cohort of adult p

107 s that direct stimulation of memory-relevant brain areas can enhance memory performance, but only whe

108 ught to extract synchronous activity in many brain areas can therefore be combined in a single operat

109 e predictive coding propose that lower-order brain areas compare their inputs to predictions derived

110 ral blood flow and metabolic activity in key brain areas compared with control subjects.

111 ce in trans persons suggests changes in some brain areas concerned with olfaction and voice perceptio

112 e axonal projections, we identified numerous brain areas connected to the BF.

113 Almost all major brain areas contain high and low levels of FMRP cell gro

114 t with prevailing oxidative stress, the same brain areas contained increased DNA 8-oxodG levels and e

115 Acute ischaemic stroke in brain areas contributing to male sexual function may imp

116 The hippocampus is a brain area crucial for episodic memory in humans.

117 ere associated with volumetric reductions in brain areas crucial for attention, (working) memory, and

118 l framework in which neural activity in each brain area depends on a combination of feedforward drive

119 phase of local oscillatory activity within a brain area determines the long-range functional connecti

120 idence of a saliency map in various cortical brain areas, determining the contribution of phylogeneti

121 a neural compensation from auditory sensory brain areas due to visual deprivation.

122 ifferentiated degenerations across different brain areas during brain development.

123 correlates of these computations in multiple brain areas during movement preparation and execution.

124 th auditory sensory and other frontoparietal brain areas during selective listening.

125 twork connectivity impact the recruitment of brain areas during task execution.

126 tigating the functional connectivity (FC) of brain areas during the resting state in human children w

127 ural activity have been observed in numerous brain areas during timekeeping and motor sequence tasks.

128 tory-related signals have been found in many brain areas during various decision-making tasks, but th

129 that link pitch-responsive regions to other brain areas (e.g., frontal cortex) might be altered, and

130 nforcement signals, we found that mesolimbic brain areas encoded both anticipation and prediction err

131 Our results suggest that each brain area engages in different spectral modes that are

132 e more likely to accumulate more in specific brain areas, especially some limbic areas, while full-le

133 for proper functioning of the hippocampus, a brain area essential for learning and memory.

134 The brain areas exhibiting predictability-dependent effects

135 ent of gray matter volumes of the identified brain areas (F = 1.84, P = .18).

136 signal for unexpected orientation in visual brain areas followed by a PE signal for unexpected illum

137 e dorsal raphe nucleus (DRN) is an important brain area for body-weight regulation.

138 the pathological basis for the selection of brain areas for monitoring regional injury and atrophy d

139 ractions between key frontal and subcortical brain areas for response inhibition, by comparing 20 dyn

140 op-down mechanisms of attention that prepare brain areas for target enhancement.

141 mportant to first understand its outputs for brain areas for which the relationship between the stimu

142 disruption of structural connections between brain areas forming a network contributes to determine a

143 ood flow) and in bilateral supra-ventricular brain areas (global cerebral blood flow) and was matched

144 The disruption of coupling between brain areas has been suggested as the mechanism underlyi

145 tterns of coherent activity across different brain areas have been identified during the resting-stat

146 Although several brain areas have been implicated in the generation of at

147 However, these two brain areas have different contributions to the neonatal

148 udy examined whether cortical changes in key brain areas hypothesized to support metacognition contri

149 the course of metreleptin treatment in three brain areas (i.e., hypothalamus, insula/superior tempora

150 y homeostasis and expands the current map of brain areas impacted by GLP-1R activation.

151 n candidate genes in dorsal striatum (DS), a brain area implicated in cue- and context-induced drug r

152 ue, the T1R3 receptor is highly expressed in brain areas implicated in cognition, including the hippo

153 c neurons project to the lateral habenula, a brain area important for generating behavioral avoidance

154 Recent work suggests that the amygdala, a brain area important for processing emotion, may be part

155 unknown if this occurs in cortex, or in any brain area in dTBI.

156 ution we are able to analyse networks within brain areas in a single subject.

157 st glutamatergic deficits in fronto-striatal brain areas in both disorders, this is the first study t

158 functional deficits than higher-order visual brain areas in glaucoma.

159 ions, requires the coordinated engagement of brain areas in local and large-scale networks.

160 Our results emphasize the key role of motor brain areas in providing contextual temporal information

161 We studied these two brain areas in rodents performing interval-timing tasks

162 We locally and reversibly cooled brain areas in songbirds during singing.

163 ated changes in both motor and somatosensory brain areas in which a strengthening of connectivity was

164 In brain areas in which grey matter volumes related to lang

165 dedicated projection interneurons to higher brain areas including the lateral horn and mushroom body

166 es to negative emotional stimuli in multiple brain areas, including amygdala and fronto-limbic region

167 actory) cortex, as well as in limbic-related brain areas, including amygdala and hippocampus.

168 epends on the activity of a large network of brain areas, including frontal, parietal, and visual are

169 and this segregation is maintained in higher brain areas, including regions implicated in learning an

170 ed with increased Fos expression in multiple brain areas, including the BNST, where it was significan

171 the IPS also showed connectivity with other brain areas, including the frontoparietal control networ

172 to working memory has been reported in many brain areas, including the inferior temporal and prefron

173 d motor skills (songs) subserved by distinct brain areas, including the premotor cortical analog HVC,

174 f neural activity dynamically in a number of brain areas-including the striatum and cortex-has been s

175 e stria terminalis (aBNST), but not to other brain areas innervated by VMN(SF1) neurons.

176 Auditory and sensorimotor brain areas interact during the action-perception cycle

177 enhanced neural efficiency in this important brain area involved in both speech production and domain

178 ain, less is known about the amygdala, a key brain area involved in the neural circuitry of fear and

179 BA for expected illumination was observed in brain areas involved in attention to internal representa

180 , there is a striking similarity between the brain areas involved in behavioural activation and effor

181 These observations show that brain areas involved in circadian and metabolic function

182 t of obesity on taste receptor expression in brain areas involved in energy homeostasis, namely the h

183 ion influences the functionality of specific brain areas involved in executive functions.

184 olved goal in face perception is to identify brain areas involved in face processing and simultaneous

185 ll as between the inferior frontal gyrus and brain areas involved in language control, including the

186 d neuroimaging studies have shown that three brain areas involved in learning and memory--the hippoca

187 oscillatory local field activity in several brain areas involved in motor control, but the mechanism

188 tion encoded in piriform is routed to target brain areas involved in multimodal sensory integration,

189 ating odor-driven innate behaviors can, like brain areas involved in odor learning, represent odor ob

190 we report important metabolic variations in brain areas involved in pain processing in a rat model o

191 PPARgamma is densely expressed in brain areas involved in regulation of motivational and e

192 may originate in recurrent input from other brain areas involved in the interpretation of sensory si

193 and neurochemical/neuroreceptor profiles on brain areas involved in these social behaviors.

194 many model of visual recognition posits that brain areas involved in word and face recognition are fu

195 ear which mechanisms are at play in the many brain areas involved in working memory.

196 specific predictions the brain makes and the brain areas involved.

197 he spreading of pathology within and between brain areas is a hallmark of neurodegenerative disorders

198 ition and to the DG, but not the neighboring brain areas, is presented through control experiments.

199 n firing in dorsal lateral striatum (DLS), a brain area known to be involved in habit formation and a

200 romedial prefrontal cortex and the striatum, brain areas known to encode the subjective value of the

201 lations, global mutations of clock genes, or brain area lesions.

202 ingle fiber orientation, relevant to limited brain areas like the corpus callosum, or multiple orient

203 d that also the macroscale wiring profile of brain areas may have an important contribution in shapin

204 n regions, but it is currently unknown which brain areas mediate this effect.

205 vior are due to its local effects in various brain areas, most notably distinct regions of the amygda

206 ered the understanding of inhibition in many brain areas, most notably in the cerebral cortex.

207 The functional activity of brain areas (network nodes) were characterized according

208 e macroscopic scale of around 1,000 or fewer brain areas (network nodes).

209 th neuron-level specificity as a function of brain area, neuronal subtype, and preceding history.

210 top-down communication between the affected brain area, neurovascular unit, and peripheral immune ce

211 nce, loss of vision or audition leads to the brain areas normally associated with these senses being

212 s, the insula is re-emerging as an important brain area not only in the physiological understanding o

213 Analysis of Fos expression in different brain areas of adolescent and adult rats on withdrawal d

214 man society, critically depends on posterior brain areas of the left hemisphere in proficient adult r

215 s communication between neurons in different brain areas on behaviorally relevant timescales.

216 d to global neuroadaptations in a particular brain area or cell type, rendering it impossible to iden

217 ported by homologous, functionally conserved brain areas or by different neurobiological substrates.

218 e under way to target circuit dysfunction in brain areas outside of the traditionally implicated basa

219 Recent studies have identified brain areas outside the hypothalamus that are activated

220 ization of directed influence patterns among brain areas, perhaps reflecting compensatory processes.S

221 uggest that KOR/dynorphin mechanisms in this brain area play a key role in stress-induced alcohol see

222 activity and metabolic correlates in related brain areas, possibly serving different memory functions

223 lead to enhanced ERK1/2 signaling in several brain areas, possibly underlying induction of CP/CPPS-re

224 es linked with such deficits, including some brain areas previously associated with inhibition, persp

225 observed a late interaction effect in visual brain areas, probably corresponding to a high-level PE s

226 rols of appetite by cortical and subcortical brain areas processing external sensory information, rew

227 ovide evidence that connectional topology of brain areas quantified at rest relates to the functional

228 he widespread expression of Dmxl2 in several brain areas raises the intriguing hypothesis that rabcon

229 e and precision significantly depends on the brain area recorded and ongoing task demands.

230 Here, we show that the hypothalamus, a brain area regulating physiological states, provides lon

231 t hearing song activates mTOR signaling in a brain area required for tutor song memorization in males

232 An open question is whether fear-related brain areas respond differently to experienced CS-US con

233 arietal, premotor, and body-selective visual brain areas respond preferentially to a virtual arm seen

234 To provide insight into brain areas responsible for sensorimotor computation, we

235 umed to involve dynamic interactions between brain areas responsible for vision and cognition, but ne

236 repeat behavioral testing to identify which brain areas show cellular adaptations that signal the in

237 can be applied predictively to other paired brain areas showing two-stage learning.

238 tic tool with Neurosynth, we found that this brain area shows strong coactivation patterns with nearl

239 Further, many input neurons across brain areas signaled combinations of these variables.

240 Furthermore, this brain area strongly coactivates with other reward-associ

241 ded the search for abnormalities in specific brain areas such as the hippocampal-amygdala complex and

242 effect was more pronounced in very specific brain areas such as the thalamus, globus pallidus and or

243 xetimide binding was much higher in M1R-rich brain areas, such as the cortex and striatum, than in ce

244 l prostaglandin E2 (PGE2) production in deep brain areas, such as the hypothalamus, which is the site

245 nd how attention modulates LFPs in executive brain areas, such as the lateral prefrontal cortex (LPFC

246 y neuronal and biological adaptations in key brain areas, such as the nucleus accumbens (NAc).

247 ues evoke increased activation in mesolimbic brain areas, such as the nucleus accumbens and the amygd

248 ognitive state, we must learn more about the brain areas supporting attentional selection.

249 xchanged between face-processing centers and brain areas supporting social cognition remains largely

250 ability between pairs of neurons in the same brain area (termed spike count or noise correlation, rSC

251 sdAb accessing a four- to seven-fold greater brain area than IgG.

252 n the lateral parabrachial nucleus (LPBN), a brain area that is also implicated in the response to hy

253 ary storage of information recruits the same brain areas that also process the information.

254 However, whether this model is applicable to brain areas that also use less conventional neurotransmi

255 stently shown that empathy for pain recruits brain areas that are also activated during the first-han

256 eive convergent input from widespread higher brain areas that are capable of carrying diverse pro- an

257 s and related medial temporal lobe circuitry-brain areas that are important for learning and memory.

258 of cellular and synaptic changes in auditory brain areas that are thought to give rise to auditory pe

259 Is there a common, domain-general system of brain areas that evaluates all costs and benefits?

260 Human laughter engages brain areas that facilitate social reciprocity and emoti

261 The brain areas that mediate such incubation are also unknow

262 However, identifying brain areas that play a causal role in decision making h

263 that echolocation in blind people activates brain areas that process light in sighted people.

264 ize network relationships between constitute brain areas that reflect a subject's choice for a face v

265 ng evidence that aSI has profound effects on brain areas that regulate affective states.

266 K/LK-R circuit connects pacemaker neurons to brain areas that regulate locomotor activity and sleep.

267 e circadian rhythm-related gene mPer2 within brain areas that regulate motivation and emotion.

268 Brain areas that responded during cold allodynia were al

269 daptations may alter dmPFC connectivity with brain areas that target its deep vs superficial layers a

270 t the protocerebral bridge with two adjacent brain areas, the posterior optic tubercles.

271 t dependence varies among neurons and across brain areas, there are strong shared qualitative charact

272 Like primates, the rat brain areas thought to be involved in visual object reco

273 These brain areas thus likely integrate visual and propriocept

274 bations reflecting the capability of a given brain area to propagate neuronal activity to other regio

275 in brain networks link functionally related brain areas to accomplish thought and action, but this m

276 map that displays the frequency of different brain areas to be affected by these processes.

277 stigated the causal contribution of specific brain areas to implicit attitudes toward violence.

278 nality reduction has been applied in various brain areas to study the activity of populations of neur

279 variations in the connectivity pattern of a brain area (topology) relates to its activity during tas

280 Distinct brain areas tracked the likelihood of new observations g

281 coarse and equivocal information about which brain areas underlie amusia.

282 exploited multistable perception to identify brain areas uniquely activated in association with these

283 of recently activated, GFP+ neurons in these brain areas using whole-cell electrophysiology in brain

284 se in phosphorylated tau was seen, including brain areas vulnerable in AD, as well as relatively spar

285 cortex Brodmann area 47/12 with these three brain areas was lower in the medicated than the unmedica

286 Using a metaanalysis across the two brain areas, we identified a core set of 235 genes (q <

287 of 1-s long data segments for atlas-defined brain areas were clustered into spectral profiles ("fing

288 y convey motion signals accessible in higher brain areas, whenever abrupt shifts in visual objects or

289 ain expression sites in rodents, such as the brain areas where in mammals the median preoptic nucleus

290 though all sensory circuits ascend to higher brain areas where stimuli are represented in sparse, sti

291 n receives afferent projections from several brain areas which provide multiple neurochemical inputs

292 e information flow between language-relevant brain areas, which is required for linguistic processing

293 ng can enhance top-down modulation by higher brain areas while reducing bottom-up sensory drives.

294 ibuted differently across disease stages and brain areas, while N-terminally truncated amyloid-beta40

295 lations of tdTomato-positive neurons in most brain areas with patterns that matched P2X4 mRNA distrib

296 ed functional connectivity between different brain areas with resting state functional magnetic reson

297 ignals and coordinating commands from higher brain areas with the step cycle.

298 l amyloid increase in functionally connected brain areas, with a particular focus on intrinsic functi

299 Brain areas within the lateral parietal cortex (LPC) and

300 itate information transfer within and across brain areas, yet their underlying mechanisms remain hotl