ライフサイエンスコーパス: brain area

1 postarousal, irrespective of sleep stage or brain area.

2 s known about the role of astrocytes in this brain area.

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

4 of targeting this small, thin, and elongated brain area.

5 s at all stages of signal processing in this brain area.

6 as well as in the connections between these brain areas.

7 y impact decoding requirements on downstream brain areas.

8 and abnormal neurophysiology within distinct brain areas.

9 mong populations of neurons across different brain areas.

10 as modeled as partial correlations among 216 brain areas.

11 rgic, and histaminergic systems in selective brain areas.

12 oned stimulus representation in fear-related brain areas.

13 communicate cerebellar computation to other brain areas.

14 lites with decreasing IQ occurred in several brain areas.

15 relevance of these two proteins in specific brain areas.

16 ers were extracted simultaneously from three brain areas.

17 exhibited UPR and hypothyroidism in distinct brain areas.

18 g benefits from optical access to widespread brain areas.

19 umulation leading to neuronal death in focal brain areas.

20 to self-modulate neural patterns in specific brain areas.

21 top-down projections from cortical and other brain areas.

22 tive response properties of neurons in other brain areas.

23 connected with both cortical and subcortical brain areas.

24 with distinct neuronal changes in different brain areas.

25 nderpinned by genetic variability in certain brain areas.

26 ereas low GSCORR was seen in the association brain areas.

27 he visual and functional properties of these brain areas.

28 motor cortex by other schizophrenia-related brain areas.

29 crucial role in communication between remote brain areas.

30 small adjustments of neural circuitry in key brain areas.

31 tory subthalamic region connecting with many brain areas.

32 dulate shared variability within and between brain areas.

33 ps of visuomotor transformations to specific brain areas.

34 trained by behavior and interactions between brain areas.

35 al modulation of alpha activity in posterior brain areas.

36 a product of the concerted activity of many brain areas.

37 neural activity from an extended network of brain areas.

38 l death result, with ensuing thinning of key brain areas.

39 ch activity can be selectively routed across brain areas.

40 functional connection profiles of individual brain areas.

41 ases change this modular architecture within brain areas.

42 ral basis for function specialisation within brain areas.

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

44 o coordinate memory processes across distant brain areas.

45 synaptic transmission and plasticity in many brain areas.

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

47 heterogeneity in this encoding seen between brain areas.

48 ms underlie persistent activity in different brain areas.

49 y move along migratory streams toward target brain areas.

50 technique and evaluating a larger number of brain areas.

51 nce of multisensory evidence in higher-order brain areas.

52 lood flow, and brain temperature in specific brain areas.

53 thickness increases in visual/somatosensory brain areas.

54 caques, three decision-making tasks, and two brain areas.

55 about off-target effects in other organs and brain areas.

56 y directing relevant information to distinct brain areas.

57 of these regions with a number of different brain areas.

58 in the locust central complex and associated brain areas.

59 species homologies, particularly in terms of brain areas.

60 data across modalities, spatial scales, and brain areas.

61 bit altered synaptic function across various brain areas.

62 primary sensory, decision-making, and motor brain areas.

63 erconnectivity between striatal and cortical brain areas.

64 as well as parvalbumin (Pvalb), in cortical brain areas.

65 o such changes in adjacent auditory or other brain areas.

66 rmation processed outside of strictly visual brain areas?

67 (TUS) protocol impacts activity even in deep brain areas: a subcortical brain structure, the amygdala

68 ransformed into standard space to define the brain areas affected by signal loss.

69 d that sensorimotor, parietal, and cingulate brain areas all contributed to the reduced P300 amplitud

70 s specifically activates neurons in distinct brain areas, among which the IPAC is regulated by dopami

71 normal electrical activity begins in a local brain area and propagates before terminating.

72 ess regions are found within a wide range of brain areas and across conventional networks.

73 ce; (c) that viral exchanges occurred within brain areas and across the blood-brain barrier; and (d)

74 flect covariation in morphology of different brain areas and are thought to reflect common trajectori

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

76 Our findings highlight key brain areas and cell types implicated in insomnia, and p

77 ve solutions that require uncovering the key brain areas and cell types mediating the cause of overdo

78 s long-lasting persistent neural activity in brain areas and cells overlapping with the pC1d/e neural

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

80 d reduced serotonin concentration in rostral brain areas and displayed increased anxiety-like behavio

81 ain responses in visual and social cognitive brain areas and in brain areas associated with theory-of

82 rences were seen between groups in the other brain areas and in the analysis of tyrosine hydroxylase

83 ebrain region, receives inputs from numerous brain areas and is a major source of descending sensory

84 euronal and synaptic density across multiple brain areas and modified cognitive performance.

85 neurological impacts across a wide range of brain areas and pathways, our protocol measured 21 large

86 al principle that applies to a wide range of brain areas and sensory, cognitive, and motor processes.

87 edded in population activity across multiple brain areas and sheds further light on how internal stat

88 uch sequence replay is limited to only a few brain areas and sleep states mainly in rodents.

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

90 Categories are encoded in multiple brain areas and tasks, yet it remains unclear how neural

91 pothalamus that project to extrahypothalamic brain areas and the lumbar spinal cord play an important

92 y been observed in different animal species, brain areas, and behavioral states.

93 elation to biological processes, cell types, brain areas, and developmental stages.

94 se population of cells and that they display brain area- and disease-specific properties and function

95 Both temporal and frontoparietal brain areas are associated with the representation of kn

96 This can potentially reveal not only which brain areas are engaged by a task, but also how.

97 Specifically, modules within brain areas are spatially localised.

98 -Fos expression in social motivation-related brain areas, are modified by competition with non-social

99 Prosocial learning recruited similar brain areas as self-relevant learning, but additionally

100 mputations that occur in and across discrete brain areas, as well as how they are progressively alter

101 citability of neurons in clinically relevant brain areas associated with channelopathies.

102 d right posterior cingulate (p(adj) = 0.04), brain areas associated with emotion-regulation and threa

103 visual predictability effect were visible in brain areas associated with semantic processing, and wer

104 sual and social cognitive brain areas and in brain areas associated with theory-of-mind related and e

105 ction, engaging appropriate visual and motor brain areas at the same time.

106 fusion coefficient (ADC) values of different brain areas between two groups of intrauterine growth re

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

108 vealing fast activation of a wide network of brain areas, both including and extending beyond the cor

109 , the posterior slope, and other surrounding brain areas, but not directly from the mushroom bodies.

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

111 orders and neural circuit changes in several brain areas, but the cellular mechanisms that underlie t

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

113 -Sino attenuated inflammation in the injured brain areas by suppressing inflammatory cytokines expres

114 Cerebral hemodynamics of large brain areas can be measured at high spatiotemporal resol

115 We show that expansion and relocation of brain areas can predict terminations of several white ma

116 how populations of neurons in interconnected brain areas communicate is in its infancy.

117 se a computational solution whereby multiple brain areas communicate to suppress the motion attribute

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

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

120 ntly (p < 0.05) higher atrophy rates in many brain areas compared with the control group.

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

122 ased effort-related activity in a network of brain areas consisting of dorsal anterior cingulate cort

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

124 neurons expressing TH are located in several brain areas containing GH-responsive cells.

125 emia, and GH-responsive neurons are found in brain areas containing glucose-sensing neurons that regu

126 s between these higher-order and lower-order brain areas contribute to atypical sensory and cognitive

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

128 C]DASB non-displaceable binding potential in brain areas corresponding to Braak stages 1-3, whereas [

129 C]DASB non-displaceable binding potential in brain areas corresponding to Braak stages 1-6.

130 The amygdala is a brain area critical for the formation of fear memories.

131 Among these brain areas, D1 knockdown in the mPFC decreased social d

132 found that the dominant peak frequency in a brain area decreases significantly along the posterior-a

133 The brain areas demonstrating elevated tau PET binding overl

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

135 thought that cortical projections to distant brain areas derive by and large from glutamatergic neuro

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

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

138 hierarchical representations of higher-order brain areas during complex tasks, such as the production

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

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

141 pose that disease may be transmitted between brain areas either via local diffusion or long-distance

142 Deactivation extended into brain areas encoding low-level sensory representations,

143 inhibitory neurons to LFPI in the different brain areas examined after injury.

144 indicated by Fluoro-Jade C in the different brain areas examined after injury.

145 ent (PHF) tracer [(18)F]Flortaucipir, in all brain areas examined.

146 Synchronized oscillations within and between brain areas facilitate normal processing, but are often

147 nterodorsal thalamic nucleus (ADN) and other brain areas fire already before their preferred directio

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

149 The hippocampus is an essential brain area for learning and memory.

150 mediates defensive responses(6-9), and a key brain area for processing and storing threat memories.

151 The clinical trials should be on the same brain area for the same psychiatric indication." The aut

152 ortical areas are thought to entrain distant brain areas for efficient information transfer and proce

153 or treatment response and to target specific brain areas for innovative neuromodulation therapies.

154 n are highly conserved, its role in specific brain areas for mammalian social behaviors remains large

155 Although NSC might not apply to all brain areas (for example, motor or executive function ar

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

157 a process essential to protecting uninjured brain areas from secondary damage.

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

159 els are processed by first- and higher order brain areas has not been well characterized in any speci

160 er modulations in auditory and motor-related brain areas have been associated with automatic temporal

161 e and functional organization of CFC between brain areas have remained largely unknown.

162 Overlapping all tested brain areas identified unique and shared mutations, with

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

164 Understanding how stimulation of different brain areas impacts such activity is important for gaini

165 c connectivity days later in the amygdala, a brain area implicated in the affective symptoms of stres

166 utamate afferents arising from corticolimbic brain areas implicated in drug addiction and psychiatric

167 xious phenotype via neurochemical changes in brain areas implicated in interoceptive and emotional pr

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

169 and altered functional connectivity between brain areas important for socioemotional behavior, cogni

170 The habenula, an ancient small brain area in the epithalamus, densely expresses nicotin

171 n the precuneus and is connected to multiple brain areas in a body-part-specific manner.

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

173 the evolutionary transformation of specific brain areas in Crustacea.

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

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

176 t only the involvement of a large network of brain areas in supramodal language processing but also t

177 onceptualizes structural connections between brain areas in terms of the relative architectonic diffe

178 nectivity between perceptual and subcortical brain areas in the enjoyment of music.

179 on neuroimaging are similar to the affected brain areas in the myorg PFBC null mouse.

180 The brain areas in which higher volume was correlated with l

181 ns in the brain with observable behavior and brain areas in which they act, in vivo measurement of mu

182 rescence microscopy enable monitoring larger brain areas in-vivo with finer time resolution.

183 teristics of network properties in posterior brain areas, in particular decreased local (segregated)

184 influences the volume change over the whole brain areas including the cortical and subcortical regio

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

186 er with widespread reduced FA values in five brain areas, including left and right corpus callosum, s

187 ry, motor, and spatial signals from multiple brain areas, including the hippocampal system.

188 Several brain areas, including the orbitofrontal cortex (OFC), h

189 ncrease dopamine (DA) concentration in these brain areas, including the striatum, which shapes an abn

190 Although the brain areas indispensable for speech and song learning a

191 An important brain area involved in all these diseases is the striatu

192 1) agonist in the nucleus accumbens (NAc), a brain area involved in mediating social interactions, ch

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

194 Brain areas involved in circadian timing and sleep-wake

195 ical data indicate PPARgamma localization in brain areas involved in drug addiction.

196 ever, the polysynaptic circuitry linking the brain areas involved in feeding behavior to the olfactor

197 nin (5-HT) type 3AB (5-HT(3AB)) receptors in brain areas involved in mood regulation is successful in

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

199 We review the effects of ARHL on brain areas involved in speech perception, from the audi

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

201 the perception of tactile pleasure, but the brain areas involved in their processing remain debated.

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

203 cells (ipRGCs), but the relevant downstream brain areas involved remain elusive.

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

205 of working memory (WM) to mutually exclusive brain areas is at odds with the distributed processing m

206 ction selection interact in decision-related brain areas is still not well understood.

207 B2/nesfatin-1 is expressed in reward-related brain areas, its role in regulating motivation and prefe

208 posterior superior temporal gyrus (pSTG), a brain area known to be important for speech perception.

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

210 ted with atrophy of cortical and subcortical brain areas known for high sensitivity to oxygen supply.

211 cortex of mammals, a hierarchical system of brain areas leads eventually to the selective encoding o

212 cial channels exhibit enhanced activation of brain areas linked to emotional processing during the tr

213 ed profound disruption of neural activity in brain areas linked to social behaviour, social cue proce

214 are often challenging because neurons in one brain area may encode multiple variables, and because ne

215 In parallel, affect-related brain areas may simultaneously exert a disruptive influe

216 erconnectivity with cortical and subcortical brain areas, mediates cognitive and emotional processes

217 iments have provided hints about how various brain areas might contribute to such learning, their pre

218 T), we identified the dorsal striatum as the brain area most altered in DIO-susceptible rats and mole

219 While the cerebellum is one of the brain areas most underestimated in the context of AD, re

220 eural mechanisms are unknown, but neurons in brain areas MT and MST may contribute given their sensit

221 the structural architecture of four distinct brain areas, none of which pertain to the song control s

222 the adult brain, but also identifies several brain areas not usually regarded as cholinergic, includi

223 -18 and IL-37, is also increased in the same brain areas of children with ASD.

224 cell dendrites, has been reported in several brain areas of subjects with major depressive disorder (

225 hese aspects of WM do not map exclusively to brain areas or processing streams; however, the mappings

226 onitor thousands of neurons across connected brain areas or, alternatively, small local networks with

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

228 Here, we show that another brain area, posterior inferotemporal cortex (PITd), also

229 gic neurons receive monosynaptic inputs from brain areas processing important environmental informati

230 ealed hitherto unknown TAAR1 localization in brain areas projecting to the substantia nigra/ventral t

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

232 tionship is often compared across neurons or brain areas, recorded in different sessions, animals, or

233 43 immunohistochemistry on tissue from three brain areas, reflecting a hierarchical pattern of brain

234 Normally activity in brain areas reflects activity in interconnected regions

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

236 onstrated a robust self-other distinction in brain areas related to somatosensory, social cognitive,

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

238 The brain area responsible for seizures is subsequently surg

239 halamus (MBH) was recently implicated as the brain area responsible for this effect.

240 To identify the brain areas responsible for this effect, we first used i

241 In many brain areas, sensory responses are heavily modulated by

242 S, crucial questions remain, including which brain areas should be targeted and in which patients.

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

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

245 ospinal fluid and subsequent action on other brain areas, since icv injection of the same total dose

246 eceptors (CB(1)Rs) in adulthood in a sex and brain area specific manner.

247 the studies, including postmortem interval, brain area studied, age at diagnosis, undergoing treatme

248 telencephalons communicate with higher order brain areas such as prefrontal cortex.

249 In contrast, CO(2) dilates vessels in other brain areas such as the amygdala.

250 g by conveying reward-related information to brain areas such as the ventral tegmental area (VTA).

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

252 In many brain areas, such as the neocortex, limbic structures, a

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

254 an increase in shared representations across brain areas, suggesting that the enhancement was mediate

255 ted signals, and emotional inputs from other brain areas, suggests that, at any given time, its outpu

256 n the human SC into a distributed network of brain areas supporting WM and elucidate the neural mecha

257 ization onto this via the evolution of a new brain area that came to be situated near the jaw region

258 pts autophagy selectively in the striatum, a brain area that controls motor behavior, both in vitro a

259 the nucleus of the solitary tract (NTS), the brain area that receives and integrates sensory informat

260 This receptor is also expressed focally in brain areas that affect reward circuits and addiction.

261 The neural implementation of ARDM includes brain areas that are important for valuation (ventromedi

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

263 Brain areas that control gaze are also recruited for cov

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

265 a growing number of cortical and subcortical brain areas that form distributed networks supporting WM

266 This makes it possible to locate the brain areas that generate predictions about upcoming wor

267 on fluorescence imaging of neurons in deeper brain areas that lie beyond the reach of conventional tw

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

269 associated with activity in fronto-parietal brain areas that play a pivotal role in oculomotor contr

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

271 sociation between lateral and ventral/medial brain areas that respond selectively to different visual

272 In the present study we first identified brain areas that showed an association between cortical

273 derstand the directed information flow among brain areas that underlies complex psychological process

274 Brain areas that were normally correlated could be rapid

275 Therefore, a canonically cognitive brain area, the hippocampus, is sensitive to cerebellar

276 We show that activity in two brain areas-the anterior cingulate cortex and basal fore

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

278 Neuropathologists assess vast brain areas to identify diverse and subtly-differentiate

279 es with wide-ranging effects across multiple brain areas to improve cognitive function.

280 e electrical spikes, and innervate dozens of brain areas to influence physiology, behavior, perceptio

281 addressing the differential vulnerability of brain areas to tau pathology, its cell-to-cell transmiss

282 ingulate and orbito-frontal as well as other brain areas was associated with OCD illness duration, su

283 to regulate synaptic transmission in several brain areas, we investigated whether this form of neuron

284 The brain areas which provide the neuronal substrate for the

285 imaging studies as a set of highly connected brain areas, which are active during wakeful rest and in

286 ural operation across sensory and nonsensory brain areas, which describes neuronal responses as the r

287 matter (WM) degeneration starting from deep brain areas, which is consistent with neuropathological

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

289 ions do not just disable but also disconnect brain areas, which once deprived of their input or outpu

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

291 ular space) when comparing the FUS-sonicated brain area with the contralateral non-sonicated area.

292 n the precuneus and is connected to multiple brain areas with different connectivity for different bo

293 stingly, rodents and macaques shared certain brain areas with high gamma-secretase expression, sugges

294 ion, suggesting greater involvement of these brain areas with illness chronicity.

295 3.52, p = 0.007) was observed in the primary brain areas with in vivo SV2A binding.

296 We examined brain areas with low FA values including caudate nucleus

297 periences, it engages several reward-related brain areas, with activity in the nucleus accumbens (NAc

298 ed nucleus of the stria terminalis (BNST), a brain area within the extended amygdala critically invol

299 ori analyses examined activity in functional brain areas within the right IFG, supplemented by a whol

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