ライフサイエンスコーパス: connectivity

1 fiber innervation and bidirectional synaptic connectivity.

2 en intrinsic membrane properties and network connectivity.

3 erves in closer proximity to maintain larval connectivity.

4 easures of greenspace structure to calculate connectivity.

5 e maintenance of interhemispheric functional connectivity.

6 al oscillatory activity may underpin network connectivity.

7 jection neurons (PNs) with apparently random connectivity.

8 events during the establishment of synaptic connectivity.

9 nase-1 has a pivotal role in cocaine-induced connectivity.

10 via the demonstrated differential functional connectivity.

11 infiltration of the neuropil alters synaptic connectivity.

12 e channels, thus providing clear evidence of connectivity.

13 cuit exhibits a distinct pattern of synaptic connectivity.

14 establish a framework for modulatory neuron connectivity.

15 e stimulation site were used as a measure of connectivity.

16 with strong asymmetric patterns of dispersal connectivity.

17 neously determining their effect on synaptic connectivity.

18 mpair synaptic function and functional brain connectivity.

19 produced by neurons with different synaptic connectivity.

20 e for patients with abnormal amygdala-insula connectivity.

21 rse morphology, physiological properties and connectivity.

22 nge, in conjunction with remodeling of local connectivity.

23 ns, and systematically varied their synaptic connectivity.

24 aging is central to the study of human brain connectivity.

25 first applied to capture the aberrant brain connectivity.

26 imotor network strength and interhemispheric connectivity.

27 e amygdala-to-ventromedial prefrontal cortex connectivity.

28 vation as well as measures of inter-regional connectivity.

29 nzene rings to those with cis- or trans-bent connectivities.

30 , cerebellar dentate nuclei (DNs) functional connectivity abnormalities in multiple sclerosis (MS) to

31 ly play a role in variability and functional connectivity abnormalities.

32 o mouse brain slice preparation that retains connectivity across the extended circadian system.

33 madic herding could shape discrete routes of connectivity across the mountains of Asia.

34 s a progressive, selective decline in neural connectivity, affecting hippocampal efferent pathways do

35 somatic and visual effects, and higher gamma connectivity along the dorsal visual pathways when the r

36 ental boundary currents are likely to change connectivity among a network of MPAs spanning over 1000

37 component-level associations with functional connectivity among brain regions, especially between inf

38 w that larger phenotypic variation increases connectivity among predators and their prey as well as t

39 The metabolic connectivity analyses crucially supported the neuroprote

40 Functional and effective connectivity analyses suggest reorganization in long-ran

41 Our results show that differential connectivity analysis can provide new insights into the

42 al magnetic resonance imaging and functional connectivity analysis to estimate network-level connecti

43 fiber bundle reconstruction and graph-based connectivity analysis.

44 vioral assays to determine their patterns of connectivity and ascribe functional roles in reinforceme

45 elationship between the spatial structure of connectivity and correlated variability in neural circui

46 network of good responders has differential connectivity and distinct ontologies (eg, proapoptosis e

47 They differ in their connectivity and firing patterns and, therefore, in thei

48 the effects of climate change on population connectivity and genetic diversity of C. monodonta.

49 Patients with FO had higher within-DMN connectivity and greater anticorrelation between SN and

50 ses revealed sex-specific changes in network connectivity and identified distinct alterations in the

51 e extent of the association between striatum connectivity and individual differences in food craving

52 lia-mediated GPCR signaling in interneuronal connectivity and inhibitory circuit formation.

53 This framework enables connectivity and mapping projects in individual laborato

54 ed by the stroke due to loss of white matter connectivity and network integrity.

55 roducing an avalanche of data on both neural connectivity and neural activity.

56 bid depression in OCD, we examined effective connectivity and neurochemical signatures in the pregenu

57 nt study provides a detailed analysis of the connectivity and neuronal properties of lamprey pretecta

58 This pattern corresponds to shifts of connectivity and overlapping cognitive processes along a

59 te data set to test hypotheses of population connectivity and refugial isolation in the web-toed sala

60 the bond stabilities of a polymer, yielding connectivity and sequence information.

61 ablishing the specificity of thalamocortical connectivity and the receptive fields (RFs) of postsynap

62 results in loss of structural and functional connectivity and, hence, compromise of functional networ

63 MRI-based indications of possible subtending connectivity and, if confirmed, they are going to be a m

64 aggregation of neurons into clusters, local connectivity, and bundling of long-range axons.

65 d networks, networks with distance-dependent connectivity, and those with broad degree distributions.

66 Although changes in resting-state brain connectivity are a transdiagnostic key finding in neurod

67 Even though models with random feedforward connectivity are capable of creating computationally rel

68 ta suggest that developmental plasticity and connectivity are impaired in sensory systems in DS model

69 with high crystallinity and good interdomain connectivity are obtained.

70 e conservation implications of generally low connectivity are that the loss (or protection) of any no

71 Changes in synaptic strength and connectivity are thought to be a major mechanism through

72 ormalities in synaptic plasticity and neural connectivity, are currently suggested to underlie their

73 a dissociation between aberrant internetwork connectivity as a distinctive feature of psychosis and a

74 ature of psychosis and aberrant intranetwork connectivity as a transdiagnostic feature of psychiatric

75 investigate experience-dependent changes in connectivity as they related to later memory.

76 , pore type, sample size and associated pore connectivity, as well as theoretical base and interpreta

77 spill contingency planning, and fish larval connectivity assessment are among the many activities th

78 l, we combined local and international scale connectivity assessments with stage 2 to evaluate possib

79 pressed patients show abnormalities in brain connectivity at rest, including hyperconnectivity within

80 sted whether the therapies altered effective connectivity at the lower (primary) or higher (secondary

81 ia in T1D might affect the brain's intrinsic connectivity at very young ages.

82 Furthermore, connectivity attenuation among reward-processing regions

83 Neural connectivity-based categorization revealed an atypical p

84 We identified a tripartite connectivity-based parcellation of SN with a limbic, cog

85 82 youth ages 8-22 to show that white matter connectivity becomes increasingly optimized for a divers

86 vides prospective validation that functional connectivity between an individual's rTMS cortical targe

87 is diffuse, weak and sustained it can boost connectivity between co-active brain regions.

88 However, the intricacies of connectivity between different pairs of MPAs were notewo

89 s associated with beta/gamma power and gamma connectivity between frontoparietal regions and the visu

90 iction and enhanced resting-state functional connectivity between hubs of the reading/language networ

91 experiments reveal bidirectional functional connectivity between MS1 and FRU neurons.

92 ongenitally blind showed enhanced functional connectivity between parietal and frontal regions in the

93 ene-flow that was inefficient in maintaining connectivity between populations.

94 ynamic effect on interhemispheric functional connectivity between primary sensory cortices.

95 ial neuropathic pain show altered functional connectivity between regions within the brainstem pain-m

96 In the training dataset, connectivity between the DBS electrode and a distributed

97 Long-range functional connectivity between the hippocampus and other forebrain

98 ousal would manifest with reduced functional connectivity between the LC and key brain regions involv

99 with an increase in resting-state functional connectivity between the mid-insula and the ventral stri

100 ed that dot periodicity modulated functional connectivity between the parietal operculum (related to

101 This raises the possibility that anatomical connectivity between the PFC and mediodorsal thalamus ma

102 s revealed that levodopa increased effective connectivity between the posterior putamen and other are

103 More negative pretreatment connectivity between the sgACC and the default mode netw

104 ulated after selective devaluation, and that connectivity between this region and general value codin

105 ontrol group and differentially modulate the connectivity between TPJ and ventral striatum.

106 ing was associated with decreased functional connectivity both between the bilateral OFC and between

107 ropogenic disruption of hydrological habitat connectivity by dams is the major factor reducing climat

108 ic stimulation were used to study structural connectivity, cerebral blood flow (CBF), and corticospin

109 We used slice electrophysiology to measure connectivity changes associated with song learning in th

110 pecialization is driven largely by inherited connectivity constraints that do not require sensorimoto

111 thalamocortical, as well as corticocortical, connectivity contribute to auditory dysfunction in schiz

112 Dorsal striatum connectivity correlated with food craving and predicted

113 dopamine release but also in dopamine neuron connectivity, cotransmission, modulation, and activity.

114 Somatosensory connectivity could be an important target for recovery o

115 The model shows how asymmetric connectivity could enhance the representation of imbalan

116 ld be a generalizable model that takes brain connectivity data as input and generates predictions of

117 cal analysis to task-related fMRI functional connectivity data from 20 human participants and found t

118 SZ offspring were found to show connectivity deficits of the brain's central rich club (

119 suggesting that the resting-state functional connectivity depends on direct structural connections, a

120 rrents as proxies, showed a reduced level of connectivity despite short distances between some of the

121 fferent bird cohorts and temporal changes in connectivity driven by the invasion of an exotic food re

122 ntegrates graph theory and changes in larval connectivity due to potential reductions in planktonic l

123 The authors used amygdala-based connectivity during a threat-attention task and a random

124 that pretreatment frontostriatal functional connectivity during reward processing is predictive of r

125 esponses in anterior insula and insula-vmPFC connectivity during self-esteem updates.

126 ons and analyses of edge weights and network connectivity during subnetwork construction processes, y

127 e principles governing interareal functional connectivity dynamics (FCD) remain elusive.

128 demiological dynamics of fish and bryozoans, connectivity effects, and hydrothermal drivers.

129 However, there are situations where connectivity exists without a nursing mechanism, and the

130 nergy of diversity and decreasing density of connectivity favors cooperation in a biological network.

131 to which initial changes in brain functional connectivity (FC) associated with the first MPH dose in

132 -cortical and cortico-subcortical functional connectivity (FC) networks.

133 elps to prioritize the facets of the brain's connectivity for future genomic studies.

134 parieto-occipital regions, with directional connectivity from parieto-occipital regions to PFC, rega

135 eines that can have three possible disulfide connectivities: globular (Cys(I)-Cys(III) and Cys(II)-Cy

136 insufficient data on intracranial electrical connectivity has precluded a direct test of this hypothe

137 sized that individual differences in network connectivity impact the recruitment of brain areas durin

138 s show that incorporating distance-dependent connectivity improves the extent to which balanced netwo

139 nectivity analysis to estimate network-level connectivity in 50 patients with FEP, 50 patients with m

140 tegorization revealed an atypical pattern of connectivity in a depressed patient subset that would be

141 evealed a significant increase of structural connectivity in a frontolimbic network.

142 -neuron ablation and optogenetics to explore connectivity in acute slice preparations.

143 of an in silico chemical network with random connectivity in an environment that makes strong thermod

144 SHAM) rats had lower/higher structural connectivity in anterior/posterior corpus callosum.

145 or cingulate cortex showed weaker functional connectivity in at-risk than control participants (p < .

146 early adulthood, while increased structural connectivity in centromedial amygdala-anterior vmPFC whi

147 tional magnetic resonance imaging functional connectivity in conjunction with lower neuronal density,

148 agic ratio rules", which capture the role of connectivity in determining the electrical conductance o

149 sed analyses demonstrated reduced functional connectivity in frontal brain regions and increased func

150 and right dorsolateral prefrontal functional connectivity in healthy controls, a region implicated in

151 Ising model couplings to infer the synaptic connectivity in in silico networks of neurons and compar

152 el indicated that the parental caudate-vmPFC connectivity in infancy predicted lower child externaliz

153 Additionally, MVPD outperformed univariate connectivity in its ability to explain independent varia

154 The reduced functional connectivity in left orbitofrontal-both thalamic regions

155 efined by distinct patterns of dysfunctional connectivity in limbic and frontostriatal networks.

156 uld be predicted from baseline resting-state connectivity in locomotor-related networks.

157 euroimaging, alterations of brain functional connectivity in major depressive disorder (MDD) patients

158 dely used to infer the underlying structural connectivity in neuronal networks.

159 is study shows lower levels of anatomical RC connectivity in nonpsychotic young offspring of SZ patie

160 ontal brain regions and increased functional connectivity in posterior brain regions of postweaning s

161 The disruption in anatomical RC connectivity in SZ offspring was associated with increas

162 We find that connectivity in the Bind condition is less integrated wi

163 fect of bilingualism by showing an increased connectivity in the executive control and the default mo

164 antly lower whole-brain intrinsic functional connectivity in the medial prefrontal cortex (mPFC).

165 context (spatial distribution within cells, connectivity in the network, participation in supramolec

166 th models implicating disrupted PFC-thalamic connectivity in the pathophysiology of schizophrenia and

167 children with ASD showed atypical functional connectivity in this circuit.

168 It remains unclear whether and how connectivity in various neurophysiological frequency ran

169 We found that maintaining dispersal connectivity incidentally through representation-only re

170 ies indicate that differences in sterics and connectivity, independent of stacking, significantly aff

171 on spectroscopy (TOCSY) provides unique spin connectivity information for the analysis of a large num

172 There is gathering consensus that altered connectivity is a hallmark of the autistic brain.

173 Qubit connectivity is an important property of a quantum proce

174 types, their distributions, and patterns of connectivity is critical for understanding the propertie

175 plexed mechanism help to explain how complex connectivity is encoded and robustly established during

176 g network depend on how much of the inferred connectivity is eventually retained.

177 Although the importance of network connectivity is increasingly recognized, identifying syn

178 These findings indicate that transplant connectivity is largely dictated by the circuitry of the

179 refrontal cortex (PFC), and decreased MD-PFC connectivity is observed in schizophrenia patients.

180 leads to a mitochondrial structure of higher connectivity is shown to substantially enhance conductiv

181 xcitatory neuronal networks and microcircuit connectivity is warranted to improve the accuracy of pre

182 recent advances in resting-state functional connectivity magnetic resonance imaging (rs-fcMRI) and t

183 The DRN group tends to exhibit decreased connectivity mainly in areas of sensorial and motor cont

184 The Connectivity Map (CMAP) represents an unprecedented reso

185 perturbational profiling studies such as the connectivity map and library of integrated network-based

186 nsequently, a dynamic and cell-type-specific connectivity map has never been constructed from simulta

187 axons and dendrites, therefore the neuronal connectivity map not only depicts the underlying anatomy

188 r, we constructed a three-dimensional global connectivity map of promoters and enhancers, revealing t

189 Using a connectivity map, we identified prostaglandin E1 (PGE1)

190 n this study, we infer high resolution brain connectivity matrices using diffusion imaging data from

191 reductions in amygdala-prefrontal functional connectivity may be associated with severity of suicidal

192 We develop a connectivity measure that successfully classifies networ

193 fferences in traits and behavior using brain connectivity measures derived from neuroimaging data.

194 The association between connectivity measures, structural changes, and the princ

195 Functional connectivity metrics have been widely used to infer the

196 PET imaging with F(18)-AV1451 and functional connectivity MRI (fcMRI) in the context of amyloid-PET i

197 by using 1,3,5 silyl benzene precursors, the connectivity of a silicon atom within the network extend

198 y is linked to alterations in the functional connectivity of dorsal striatal networks relevant to foo

199 resting-state functional MRI, and functional connectivity of executive function-related Crus I/II in

200 The connectivity of individual modulatory neurons can be com

201 However, the connectivity of individual modulatory neurons to their t

202 ifferential effects of MD and BD on synaptic connectivity of layer 5 pyramidal neurons and underscore

203 esonance imaging tractography to examine the connectivity of LIS1-deficient neurons.

204 e generative model, yet better explained the connectivity of most regions.

205 diameters <10 nm, which we attribute to low connectivity of organic matter-hosted and clay-associate

206 The connectivity of rocks' porous structure and the presence

207 ntiated startle and resting-state functional connectivity of the amygdala in traumatized humans.

208 Additionally, interhemispheric functional connectivity of the bilateral precentral gyri positively

209 The resting-state functional connectivity of the following three regions with the SCC

210 observed when going from isomers with linear connectivity of the fused benzene rings to those with ci

211 aggression was found to positively modulate connectivity of the left amygdala to the posterior thala

212 s only accounting for half of the story: the connectivity of the nodes unaffected by the attack.

213 herefore, we aimed to examine the functional connectivity of the striatum in excess-weight versus nor

214 Neonatal functional connectivity of the ventral attention and default mode n

215 Studies on the functional properties and connectivity of these neurons are hindered by the lack o

216 Therefore, a modular strategy based on the connectivity of tpy-Ru(2+) -tpy was employed to construc

217 Here, we characterized the cell-specific connectivity of VTA dopamine neurons, their mRNA transla

218 y systematically bias perceptions of network connectivity or the prevalence of certain traits.

219 blishment and maintenance of proper synaptic connectivity, our understanding of their role in brain f

220 rately recover the direction and presence of connectivity paths in individual participants.

221 Directed functional connectivity paths within a depression-relevant network

222 compared the neural activity and functional connectivity pattern in the cerebellum between PD patien

223 The connectivity pattern of afferented EVC suggests adaptive

224 e the visual processing capacity whereas the connectivity pattern of deafferented EVC may reflect the

225 This connectivity pattern was highly specific for delusional

226 Recent studies have shown diverse connectivity patterns across the thalamus, but whether t

227 xt-specific profiles, revealed in the static connectivity patterns linked to increased reward or cogn

228 led that amisulpride changed the whole-brain connectivity patterns of individual OFC subregions.

229 gram of the ACx with an investigation of the connectivity patterns of inhibitory subclasses.

230 the lineage, neurotransmitter phenotype, and connectivity patterns of phrenic premotor neurons, which

231 endritic tree morphologies, and cone-bipolar connectivity patterns were restored in regenerated retin

232 KEY POINTS: Despite sparse connectivity, population-level interactions between mitr

233 Regression analysis showed that reduction in connectivity predicted therapy-induced improvement in pa

234 In addition to intra-cortical connectivity, prefrontal projection neurons innervate su

235 This same connectivity profile predicted response in an independen

236 In the latter group, connectivity remained elevated 15 min post-AIH (30%; p =

237 gnificance of this extensive thalamocortical connectivity remains largely unknown.

238 echanism, and the biological meaning of such connectivity remains obscure.

239 onsidered when interpreting tractography and connectivity results.

240 Using the summed SCC functional connectivity scores for these three regions, overall cla

241 dication, whereas negative summed functional connectivity scores were associated with remission to me

242 by striatal activations and corticostriatal connectivity similar to other human affiliative bonds; h

243 rating the challenge of identifying critical connectivity sites for conservation in the presence of g

244 Actomyosin bundle size, connectivity, spacing, and orientation are regulated by

245 Aberrant ventral striatum functional connectivity specifically predicts future risk for depre

246 depends in part on characteristics including connectivity, stability and heterogeneity.

247 notype individuals showed greater functional connectivity strength among smokers but not nonsmokers.

248 Functional connectivity strength was negatively associated with sev

249 Intrinsic functional connectivity strength, a whole-brain, data-driven, graph

250 aken together, we propose that intercellular connectivity supported by the fusome uniquely increases

251 nt, and highlight selective changes in brain connectivity supporting increases in task complexity.SIG

252 how large-scale cortico-cortical functional connectivity systematically reconfigures across states.

253 weaker corticothalamic task-based functional connectivity (tbFC) (F1,77 = 5.87; P = .02).

254 We identify zones of high air-borne connectivity that geographically correspond with previou

255 n about possible changes in synaptic circuit connectivity that may underlie these hearing deficits.

256 icating fundamental differences in selective connectivity that seem unexpected for closely related sp

257 orks of marine reserves that maximize larval connectivity, thus allowing exchanges between population

258 The anomalies in functional connectivity tied to clinically significant inattention

259 gdala volume and stronger bilateral amygdala connectivity to brain regions involved in sensory proces

260 We used data-driven parsing of neural connectivity to reveal subgroups present across depresse

261 with clinical response including structural connectivity to supplementary motor area and functional

262 cerebellum regions; and amygdala functional connectivity to the left ventral and right rostral prefr

263 on tractography and resting state functional connectivity) to identify connections reliably associate

264 thy controls) using resting state functional connectivity, tracing studies conducted in non-human pri

265 itope maps of diverse mAbs and the disulfide connectivity underlying E1E2 native conformation.

266 and reliable fingerprints of the structural connectivity underlying the neural processing of olfacto

267 be and compare the structural and functional connectivity using both traditional 2D greenspace models

268 ed with analyses of voxel mirrored homotopic connectivity (VMHC) and probabilistic fibre tracking.

269 Then, the triple network connectivity was analyzed and compared between PTSD and

270 Task-related amygdala-based functional connectivity was assessed.

271 reased centromedial amygdala-rACC functional connectivity was associated with greater anxiety and dep

272 Positive summed functional connectivity was associated with remission with CBT and

273 Functional connectivity was calculated between 47 regions of intere

274 d found that systems-level neural functional connectivity was diminished in fetuses that would subseq

275 Functional connectivity was examined by cross-correlating C-IN disc

276 somatosensory cortex and discovered that the connectivity was not consistent with any of these main t

277 The mPFC-vlPFC connectivity was positively correlated with depressive s

278 Based on DD connectivity, we illustrate the close similarity, and po

279 Given the potential changes in connectivity, we show that our graph-theoretical approac

280 Responses, sensitivity and presumed connectivity were rapidly enhanced by synchronous stimul

281 Areas of high connectivity, where shifting climates converge, are pres

282 TLE are associated with disturbances in ARAS connectivity, which are part of the widespread network d

283 Increased levels of interhemispheric connectivity with age were diminished by atDCS, suggesti

284 , associative and motor frontal hyper-direct connectivity with anterior and posterior subregions of t

285 statistical mechanics model that correlates connectivity with mechanical response.

286 acunarity (+139%), indicating a poor network connectivity with network interruptions.

287 rmine the implications of increased thalamic connectivity with sensory cortex.

288 ypical humans resulted in altered functional connectivity with the inferior parietal lobule, and chil

289 al processor with no preferential functional connectivity with the language system.

290 mediodorsal thalamus (MD) shares reciprocal connectivity with the prefrontal cortex (PFC), and decre

291 underlying the generation of dHb neurons and connectivity with their midbrain target.

292 youths, CD/CU+ youths showed diminished CMA connectivity with ventromedial/orbitofrontal regions.

293 However, no study has used functional connectivity within a distributed reward network, assess

294 c properties of individual neurons or on the connectivity within neural circuits to maintain the pers

295 ing is instantiated by changes to functional connectivity within premotor circuits, but whether the s

296 he beta band [14] and to modulate long-range connectivity within the default mode network [15].

297 ncy were correlated with baseline functional connectivity within the DMN and baseline parasympathetic

298 o the mother's infant and stronger intrinsic connectivity within the medial amygdala network.

299 tworks, whereas during task it was driven by connectivity within these networks.

300 n that lesion's unique pattern of functional connectivity, without the need for pre-existing or hidde