ライフサイエンスコーパス: connectivity

1 , morphology, distribution, and input-output connectivity.

2 ial-correlation-based measures of functional connectivity.

3 often characterized by alterations in brain connectivity.

4 eading to a weak characterization of habitat connectivity.

5 ygdala (BLA) and their reciprocal inhibitory connectivity.

6 fferent goals, and thereby promote migratory connectivity.

7 ss-function landscape (LFL) along with their connectivity.

8 rmance nor its associations with hippocampal connectivity.

9 estimate verbal memory performance based on connectivity.

10 ision in response to increased mitochondrial connectivity.

11 in the OFC, as well as by increased HPC-OFC connectivity.

12 e their intrinsic properties, as well as the connectivity.

13 Auckland because of its better road network connectivity.

14 and identified gene clusters with functional connectivity.

15 s their ability to modulate functional brain connectivity.

16 tter imbalance and impaired neuronal network connectivity.

17 al step during the establishment of neuronal connectivity.

18 approach for concisely representing network connectivity.

19 typical search time as a function of network connectivity.

20 t involve disruptions in large-scale network connectivity.

21 trength (R = 0.33, P = .03) of resting-state connectivity.

22 r propose a role for abnormal cortico-limbic connectivity.

23 dominantly associated with higher functional connectivity.

24 disordered prefrontal-hippocampal functional connectivity.

25 cies was indirect and related to river-ocean connectivity.

26 t concurrently increased sensory, brain-wide connectivity.

27 s between memory performance and hippocampal connectivity.

28 ereotypy in sensory responses despite random connectivity.

29 TMS elicited (1) an increase in dlPFC global connectivity, (2) induction of negative dlPFC-amygdala c

30 These results suggest that recurrent connectivity, a hallmark of biological visual systems, m

31 on behavior, neural activity, and functional connectivity across multiple nodes of brain stress and r

32 inks to response requires integrating neural connectivity, activity, and behavior.

33 Understanding how structural connectivity affects the interplay between networks will

34 arison across many neurons of morphology and connectivity after imaging or co-registration within a c

35 dendrite strive to shorten while preserving connectivity, aggregate wiring length would remain low.

36 estimating stroke-induced changes in network connectivity aggregated over the duration of several min

37 culations but also to evaluate the energetic connectivities among the minima.

38 ferences in global efficiency and functional connectivity among 12 regions comprising a previously de

39 Lack of focused conservation and connectivity among bear subpopulations could further fra

40 Together with the extensive cross-connectivity among pharyngeal neurons, which is more wid

41 o widen access to all stakeholders, seamless connectivity (an internet of things) and maintenance of

42 ontal cortex (mPFC) combined with seed-based connectivity analysis with the striatum recapitulated th

43 nts on chromosome 18q23 in regulating neural connectivity and alcohol use behavior, potentially via d

44 rate how climate change may increase habitat connectivity and alter the distributions of shrub herbiv

45 dults with distinct influences on functional connectivity and an ability to differentially influence

46 he delayed enhancing effects on BLA synaptic connectivity and anxiety-like behavior.

47 line brain morphology, resting-state network connectivity and clinical response after 24-weeks of ant

48 echnique enables the visualization of glycan connectivity and discrimination between regioisomers.

49 in turn, leads to a change in neural circuit connectivity and disruption of normal behavior.

50 o investigate the relationship between brain connectivity and duration of IA.

51 Taken together, rTMS induced lasting connectivity and excitability changes from the site of s

52 rease of neuronal activity restores synaptic connectivity and function in the sensory-motor circuit t

53 Acknowledging the relation between network connectivity and functionality, we compare the robustnes

54 on of adequate conservation measures is that connectivity and genetic structure of populations are po

55 ss, in association with neonatal hippocampal connectivity and infant memory.

56 Larger decreases in amygdala-frontal connectivity and insula-parietal connectivity were assoc

57 Relationships between functional connectivity and OCD symptoms pre- and post-CBT were exa

58 Our findings imply that low connectivity and plasticity provide protective mechanism

59 ciency alters neuronal function and synaptic connectivity and results in perturbed processing of soun

60 to then explore whether CMR affects OP1/OP4 connectivity and sensorimotor recovery after stroke.

61 redicted clinical outcome, while both global connectivity and TMS/EEG changes tracked clinical outcom

62 Both variants have identical network connectivity and were compared to each other and to expe

63 attention has been devoted to its intrinsic connectivity and whether its local excitatory circuits a

64 elationships between structural white matter connectivity and word production in a cross-sectional st

65 ts indicate that genetic identity determines connectivity (and therefore, function), providing a fram

66 ty, (2) induction of negative dlPFC-amygdala connectivity, and (3) local and distributed changes in T

67 insights into RGC type classification, brain connectivity, and cytoarchitectonic.

68 ivariate pattern analysis (MVPA), functional connectivity, and functional alignment, have become powe

69 ed vmPFC value signals, vmPFC-frontoparietal connectivity, and the impact of impulsivity during decis

70 ly dynamic pattern of whole-brain functional connectivity, and this encoding is enhanced in individua

71 dual-oriented approach to examine functional connectivity, and trained a linear support vector regres

72 Functional connectivity architecture of the rat SN is supported by

73 f work has focused on habitat patch area and connectivity (area-isolation paradigm).

74 , heterogeneous neural activity, and circuit connectivity, as well as to explore optimization in neur

75 le patch clamp has not been used to study LH connectivity, aside from a limited dataset of MCH neuron

76 i, this finding did not extend to functional connectivity at rest in our population.

77 on the basis of excitability and functional connectivity at the time of learning.

78 s on mPFC and ventral hippocampus functional connectivity before and after adolescence.

79 best-known genetic risk for AD, affect brain connectivity before the onset of symptomatic AD.

80 (abDGC) maturation so mapping the functional connectivity between abDGCs and local interneurons is re

81 Complementary increases and decreases of connectivity between both temporal and occipital lobes p

82 cles, smaller volumes and altered functional connectivity between brain areas important for socioemot

83 ausal modelling-that estimates the effective connectivity between brain regions from resting-state fM

84 determine whether patterns of resting-state connectivity between brain regions predict differential

85 This work identifies a new pathway of connectivity between brainstem auditory neurons and indi

86 antly encompassed decreased interhemispheric connectivity between cortical motor networks independent

87 ortantly, effort demand modulated functional connectivity between dACC and face-responsive or house-r

88 ceptual dimensions is linked with functional connectivity between frontal and perceptual regions and

89 ults collectively indicate that preferential connectivity between functionally matched patches is a p

90 with MDD had higher resting-state functional connectivity between hippocampus and sgACC, associated w

91 Connectivity between left PCC and right posterior cerebe

92 ameter and stacking, a decrease in energetic connectivity between photosystem II (PSII) reaction cent

93 ew connectivity motifs, including axo-axonic connectivity between projection neurons, feedback, and l

94 uit mapping revealed functional, di-synaptic connectivity between SCN(VIP) neurons and dorsomedial hy

95 harming others was associated with stronger connectivity between sgACC and dorsolateral prefrontal c

96 ssociated with later reduction of functional connectivity between social brain default mode (DMN) sub

97 Altered connectivity between task-positive and task-negative net

98 and similarly to lorazepam and also reduced connectivity between the amygdala and the anterior cingu

99 Functional connectivity between the anterolateral EC and the anteri

100 ectivity findings highlight reduced positive connectivity between the default mode network and salien

101 within the executive network, but increased connectivity between the executive network and the rest

102 e patients with AN failed to show functional connectivity between the hypothalamus and the reward-rel

103 s by demonstrating functional and structural connectivity between these regions and temporal lobe fac

104 ve to imagined drinking, implying functional connectivity between these two regions is needed before

105 hese findings demonstrate that resting state connectivity can be leveraged to produce generalizable m

106 rrangement of habitat patches (and resulting connectivity) can influence metapopulation dynamics.

107 c action, with only OXT inducing large-scale connectivity changes of potential therapeutic relevance.

108 Global connectivity changes predicted clinical outcome, while b

109 crostructure was only observed in boys, with connectivity changes restricted to girls.

110 address this, we investigated the structural connectivity changes that accompany visual hallucination

111 rogram, but this program lacks the necessary connectivity component.

112 A third connectivity configuration represented an intermediate c

113 Slower, structural changes in random connectivity, consistent with rewiring and pruning proce

114 intrinsic network-level analysis (intrinsic connectivity contrast, ICC) to resting-state fMRI data a

115 Whether connectivity contributes to tissue volume loss in schizo

116 tional (functional variability, global brain connectivity) correlates of depression and negative affe

117 torhinal connectivity increases, and CA1-CA3 connectivity decreases, with the number of changes.

118 versus WT septic mice, although the tempo of connectivity differed.

119 spatiotemporal fluctuations of wetlandscape connectivity driven by stochastic hydroclimatic forcing,

120 rmation of structural and functional network connectivity during early development.

121 dies have investigated changes in structural connectivity during the first 2 years of formal schoolin

122 volumes (nodes) and white matter structural connectivity (edges) within 9 well-characterized network

123 his suggests that in xylem networks with low connectivity, embolism spread between conduits leading t

124 edicted by functional rather than structural connectivity, emphasizing a complex interplay between an

125 lidation dataset used to identify structural connectivity explaining change in depressive symptoms.

126 seline difference between OP1/OP4 functional connectivity (FC) at rest in stroke versus healthy adult

127 We quantified functional connectivity (FC) of reward neurocircuitry using nucleus

128 order (ADHD), but their impact on functional connectivity (FC) remains unclear.

129 d network processes behind the RS-functional connectivity (FC) spatiotemporal patterns, we systematic

130 Functional connectivity (FC) studies have identified at least two l

131 ltered spatiotemporal patterns of functional connectivity (FC), even during interictal resting state

132 However, due to complex and uncertain brain connectivity features in the cognitive domains, it remai

133 Resting-state functional connectivity findings highlight reduced positive connect

134 ed these networks with those in humans using connectivity fingerprinting.

135 This baseline hypo-connectivity for non-remitters also distinguished them f

136 al data on life history timing and migratory connectivity from previous studies, eBird and band recov

137 o investigate APOE epsilon4 effects on brain connectivity from the perspective of multimodal connecto

138 lei) and locally and shedding light onto the connectivity, geometry, topology, and dynamics of bondin

139 l striatum and aberrant intrinsic functional connectivity (iFC) between distinct cortical networks an

140 udy, we calculate the within/between-network connectivity in 528 college students, and Pearson correl

141 ation of atrophy using seed-based functional connectivity in a large (n = 1000) normative connectome.

142 a reduction in prefronto-striatal structural connectivity in accounting for action selection performa

143 re transient configurations of motor network connectivity in acute stroke.

144 etion of LAR-RPTPs had no effect on synaptic connectivity in cultured neurons or in vivo, but impaire

145 Spindle density modulated connectivity in distinct hippocampal-cortical networks d

146 particularly strong theta band event-related connectivity in dystonia.

147 le healthy control children showed increased connectivity in frontal and limbic hubs over time, child

148 ically, this manifests as aberrant effective connectivity in intrinsic connections involving inhibito

149 Our findings show that genetic connectivity in M. alfredi extends for several hundred k

150 ving the understanding of altered functional connectivity in mental disorders.

151 iques, we identified a subnetwork of reduced connectivity in Parkinson's disease hallucinations.

152 bWPLI is most appropriate for characterising connectivity in populations with limited availability of

153 ction fraction was associated with decreased connectivity in select networks.

154 broadly tuned in vivo and show non-specific connectivity in slice.

155 hus directly controlling formation of neural connectivity in the brain.SIGNIFICANCE STATEMENT The for

156 conditioning exhibited increased functional connectivity in the cingulate cortex, retrosplenial cort

157 e influence of PVs on feedforward functional connectivity in the circuit.

158 antennal lobe, the CSDn has more distributed connectivity in the LH, preferentially synapsing with pr

159 ng technique for the study of activation and connectivity in the lightly sedated awake mouse brain an

160 larger number of CTs in daily life had lower connectivity in the posterior temporal language network.

161 ver time, children with PME showed increased connectivity in the superior parietal cortex and striatu

162 Ketamine thus normalized fronto-striatal connectivity in TRD participants but disrupted it in HVs

163 left hemisphere, we find that CA1-entorhinal connectivity increases, and CA1-CA3 connectivity decreas

164 Per river basin, we quantified a connectivity index (CI) for each fish species by combini

165 uage network, providing evidence that innate connectivity instructs the later refinement of cortex.

166 Habitat connectivity is a key factor influencing species range d

167 Functional brain connectivity is a promising metric for identifying treat

168 Ecosystem connectivity is an essential consideration for marine sp

169 Sex-specific synaptic connectivity is beginning to emerge as a remarkable, but

170 isplay highly labile dynamics, when synaptic connectivity is continuously modified due to noise or st

171 to determine the extent to which structural connectivity is correlated with consciousness threshold,

172 Importantly, connectivity is impaired by insults, which mimic the dia

173 Axonal connectivity is largely built during embryonic developme

174 This disruption of synaptic connectivity is linked to working memory impairment and

175 e structural design of robust MOFs with high connectivity is provided.

176 The trimming of long-range network connectivity leads to a more local, clustered network an

177 Deletion similarities identified at the connectivity level could be related to the redundant ass

178 Here, we used functional connectivity magnetic resonance imaging to examine whole

179 to upstream and downstream regulators using connectivity mapping, and predicted biological pathways

180 Moreover, reconstructed functional connectivity maps exhibit good correspondence with the o

181 n microscopy volume to reveal new long-range connectivity maps of complete populations of neurons in

182 Dynamic Connectivity Maps showed a striking difference between d

183 xhibit good correspondence with the original connectivity maps, indicating that the model recovers fu

184 Here we integrate anatomical and functional connectivity measurements with behavioural assays to cre

185 gests that the combination of regional-scale connectivity measures and local-scale environmental cond

186 These findings identify a synaptic connectivity mechanism of cones and illustrate how inter

187 the potential advantages of fMRI functional connectivity methods for improving our understanding of

188 chronization (characterized by the algebraic connectivity metric) caused by abnormal neuronal firing

189 We review how connectivity might be used to identify an optimal TMS ta

190 inhibitory interneurons, with stereotypical connectivity motifs that may follow specific plasticity

191 Here, we find new connectivity motifs, including axo-axonic connectivity b

192 Investigating the brain connectivity networks, we successfully identified a robu

193 The different modes of action and pathway connectivities of EDS1 family members go some way to exp

194 y pattern that is characterised by increased connectivity of (a) broadly distributed delta networks,

195 t study we assessed the effect on functional connectivity of a familiar contextual stimulus presented

196 oliferation of hippocampal NSCs and synaptic connectivity of adult-born neurons are inversely correla

197 gnaling drives the functional maturation and connectivity of basal VSNs.

198 atches and can increase or decrease with the connectivity of crop fields to other habitats.

199 d a unique possibility for investigating the connectivity of dozens of tightly spaced M1 sites, which

200 ion interactions and improves the functional connectivity of grapevine gene co-expression networks.

201 ate evolutionary tree, including distinctive connectivity of human temporal gray matter.

202 ironmental modifications may enhance genetic connectivity of malaria vectors.

203 landscape conversion may reduce the genetic connectivity of marten populations in the northeastern U

204 The connectivity of mitochondria is regulated by a balance b

205 Importantly, proteins that increase the connectivity of multicomponent condensates have higher c

206 Here, we present a method for finding the connectivity of networks for which the dynamics are spec

207 Functional connectivity of neural oscillations (oscillation-based F

208 d picture of the heterogeneous structure and connectivity of pores within a model EPS polymer.

209 fy the behavioral state-dependent functional connectivity of pyramidal neurons and vasoactive intesti

210 Inspired by the sparse and random connectivity of real neuronal circuits, we present a mod

211 neurons likely underlie enhanced reciprocal connectivity of S1BC after unilateral deprivation consis

212 nalysis to describe spatial organization and connectivity of social groups.

213 Structural brain connectivity of the amygdala, fornix, uncinate fasciculu

214 The functional connectivity of the anterior cingulate cortex (ACC) was

215 w examines the morphology, organization, and connectivity of the DCN and their associated nuclei.

216 r sertraline, as did greater between-network connectivity of the default mode and executive control n

217 ng with the brain's structure and functional connectivity of the default mode network (DMN); and (3)

218 MRI structural measures and functional connectivity of the DMN were recorded at baseline.

219 circuit analysis we have mapped the afferent connectivity of the mouse RE using retrograde Fluoro-Gol

220 al-adaptation mechanism where the structural connectivity of the network itself changes such that it

221 tional pathway evaluation procedure sets the connectivity of the objective function in the target sys

222 d multiple concurrent stressors (RMS) on the connectivity of the posterior parietal cortex (PPC) in a

223 The connectivity of the regio- and stereoisomers were determ

224 hat is, sprawl as measured through the local connectivity of the street network.

225 s between changes in activity and functional connectivity of the stress response circuitry and variat

226 ograde neuroanatomical tracing confirmed the connectivity of the SubM and VLO.

227 s having unique properties from the size and connectivity of their sub-nanometer pores, the Si/Al rat

228 To resolve the precise connectivity of these circuits, we first mapped mouse vi

229 accurately described the widths, angles and connectivity of veins.

230 e BNAM hydrodynamic model, we found enhanced connectivity over previously developed 2-D models and un

231 L_INST and EL_LIT showed greatest functional connectivity overlap with structures in the Default Mode

232 ty configuration represented an intermediate connectivity pattern compared to the preceding two, and

233 all meditation conditions displayed a common connectivity pattern that is characterised by increased

234 oment activity cofluctuations to the overall connectivity pattern.

235 ry modifications affecting the temporal lobe connectivity pattern.

236 ing to evaluate changes in global functional connectivity patterns in 15 patients with glioblastoma.

237 en brain regions, may be a useful measure of connectivity patterns in neural networks for studying th

238 We additionally found that connectivity patterns involving task control networks an

239 Specifically, functional connectivity patterns of brain regions between and withi

240 n order to identify resting state functional connectivity patterns that predict individual-difference

241 ve approaches have the advantage of studying connectivity patterns under different conditions directl

242 These distinct connectivity patterns were substantiated by analyses of

243 ayers have distinct intra- and interregional connectivity patterns, and therefore determining which l

244 ualize both activation levels and functional connectivity patterns, in head-restrained awake and beha

245 the basis of robust and distinct functional connectivity patterns, prominently within the frontopari

246 In this respect, the correct disulfide connectivity plays a decisive role.

247 lness was not restored, the functional gamma connectivity remained reduced, but there was a significa

248 n terms of cell types and the rules of their connectivity represents a fundamental challenge to the n

249 Building long distance connectivity requires interfaces that map quantum inform

250 Understanding the principles of neuronal connectivity requires tools for efficient quantification

251 tive measurements of thickness, spacing, and connectivity, reveal that Namapoikia produced approximat

252 imaging (MRI), and resting state functional connectivity (rs-fc) were collected from African America

253 Cross-sectional resting state functional connectivity (rsFC) studies in humans identified a circu

254 identifiable using resting-state functional connectivity (RSFC).

255 This semi-parallel, scalable connectivity schema likely contributes to flexible contr

256 oAs for compounds with unrelated structures, connectivity scores, and binding targets.

257 hip and the principal gradient of functional connectivity strongly predicted the type and frequency o

258 Network analysis techniques explored the connectivity structure of c-sIgE, and differential netwo

259 bridge the gap between high-density cellular connectivity studies in rodents and imaging-based analys

260 Analyses of brain connectivity suggest network organisation is a better wa

261 This connectivity suppressed redundant responses and was nece

262 piking and in gamma-band (40 to 90 Hz) power/connectivity that fed forward up the cortical hierarchy

263 G(N) proteins, they all share similar domain connectivity that resembles glycoproteins from unrelated

264 Crucial decisions involving cell fate and connectivity that shape the distinctive development of t

265 radeoff between confirmation bias and social connectivity through analytic results.

266 ights of recovery sleep restored hippocampal connectivity to baseline levels, but did not fully resto

267 ft V3/V3A as the area with the most specific connectivity to migraine coordinates compared to control

268 scene recognition task, impaired hippocampal connectivity to multiple prefrontal and default mode net

269 exclusively focused on cortical areas, with connectivity to subcortical networks less extensively ex

270 r the anteromedial pallidum exhibited higher connectivity to the positively correlated networks than

271 Here we decompose resting-state functional connectivity using a temporal unwrapping procedure to as

272 pecies have similar degrees of xylem network connectivity (vessel grouping) with largely solitary ves

273 The same connectivity was adversely influenced by polygenic risk

274 oved in all the materials groups, trabecular connectivity was diminished when the biomaterials receiv

275 Functional connectivity was found both between similar (homotypic)

276 Resting-state functional connectivity was largely unaltered in children with in u

277 l magnetic resonance imaging, and functional connectivity was measured using generalized psychophysio

278 , the reduction in the strength of rich-club connectivity was significantly associated with the parti

279 Inspired by the cortical connectivity, we built models of excitatory and inhibito

280 Finding a lack of local connectivity, we used optogenetic circuit mapping to stu

281 ala-frontal connectivity and insula-parietal connectivity were associated with larger PTSD symptom re

282 gdala-ventromedial prefrontal cortex (vmPFC) connectivity when processing threat-related cues.

283 or middle-down level to preserve the key PTM connectivity, which condensed-phase separations failed t

284 ange, and that improving passage and fluvial connectivity will be important climate adaptation tactic

285 State-of-the-art tools used to probe connectivity with cell-type-specific resolution have exp

286 We isolated the patterns of subcortical connectivity with cortical resting-state networks (RSNs)

287 l afferents but some differences in afferent connectivity with other brain regions.

288 mammalian claustrum, owing to its widespread connectivity with other forebrain structures, has been h

289 ortex, and ventral striatum, has substantial connectivity with the hypothalamus.

290 y, the aMCC showed an increase in functional connectivity with the insula during imagined thirst rela

291 of the VWFA is earmarked at birth due to its connectivity with the language network, providing eviden

292 ability is associated with global structural connectivity, with higher fractional anisotropy associat

293 s topographic modulation of cortico-thalamic connectivity within cortico-basal-ganglia-thalamic circu

294 velopment of structural and functional brain connectivity within distributed association networks coi

295 In general, higher connectivity within the default mode network predicted b

296 r the structural cut-off degree based on the connectivity within the hubs.

297 ed quadruple whole-cell recordings to screen connectivity within the LH with standard methodology we

298 were consistent with ultra-sparse intrinsic connectivity within the LH.

299 ucible ketamine CFP, consistent with reduced connectivity within the primary cortices and within the

300 However, we found decreased functional connectivity within the sensory-motor, lateral sensory-m