ライフサイエンスコーパス: subdivision

1 art of the dorsal pallium (its ventrolateral subdivision).

2 neurons were detected in the pars lateralis subdivision.

3 nd are distributed largely in the medial CeA subdivision.

4 demonstrate no evidence for host-population subdivision.

5 des 2 and 3, as supports the Gleason score 7 subdivision.

6 izure onset and relates to insula functional subdivision.

7 l entorhinal cortex and of its posteromedial subdivision.

8 the first of three primary vertebrate brain subdivisions.

9 Layers I and II developed early in most subdivisions.

10 of the SEZ to the newly established neuropil subdivisions.

11 in their soma size and distribution among IC subdivisions.

12 nsists of the lateral (CeL) and medial (CeM) subdivisions.

13 onspicuous clusters formed by afferent tract subdivisions.

14 ns with intermediate SSA responses across IC subdivisions.

15 aps characterized the MGB reflecting two MGB subdivisions.

16 ctions of varying densities between the four subdivisions.

17 mportance of task relevance in both thalamic subdivisions.

18 ed into distinct functional and connectional subdivisions.

19 movements, comprises nine or more functional subdivisions.

20 with opposite sign in its ventral and dorsal subdivisions.

21 receptor expression highlighted distinct HF subdivisions.

22 (t28=0.64, p=0.53) or any of its functional subdivisions.

23 ntially correlated relative to the other two subdivisions.

24 other and from adjacent inferior collicular subdivisions.

25 llaterals to both the lateral and medial NTS subdivisions.

26 ional connectivity patterns from the insular subdivisions.

27 mata, dendrites, and axons in all layers and subdivisions.

28 I signals in the cortex relative to amygdala subdivisions.

29 ains multiple developmental compartments and subdivisions.

30 s had lower volumes in striatal and thalamic subdivisions.

31 additional partition into regional or areal subdivisions.

32 ting the dorsolateral versus the dorsomedial subdivisions.

33 ional data, did not coincide with functional subdivisions.

34 pression, which rendered distinctive ventral subdivisions; 2) high alpha2 receptor expression, which

35 on, which rendered distinctive a dorsomedial subdivision; 3) distinct kainate, alpha2 , and muscarini

36 Organization of the data follows a subdivision according to mechanism and substrate classes

37 Organization of the data follows a subdivision according to substrate classes: catalytic di

38 ed fear and brain Fos activation of the mPFC subdivisions, amygdala and periaqueductal gray (PAG).

39 4 the values of PPV3 equalled 26.22% without subdivision and 3.6%, 27.9%, and 88.7% for subcategories

40 Other factors, for example, population subdivision and assortative mating, generate similar sig

41 is of mouse P0-P140 prethalamic histogenetic subdivisions and corresponding nuclear derivatives, in t

42 A neurons were confined to the non-lemniscal subdivisions and exhibited broad receptive fields, while

43 s the inferior pulvinar (PI), which has four subdivisions and numerous connections with other subcort

44 the stereotactic locations both of amygdala subdivisions and of cortical functional brain networks.

45 32) to parcellate rat insula into functional subdivisions and to identify a potential rat SN based on

46 hibit neuroanatomical parcellation within MB subdivisions and topographic projections to the thalamus

47 ious mutations linked to the MHC, geographic subdivision, and adaptive introgression.

48 ocus on the deep history of population size, subdivision, and admixture.

49 he presence of genetic nurturing, population subdivision, and assortative mating.

50 onstructed for genetic nurturing, population subdivision, and assortative mating.

51 triatum likely represents the 4th functional subdivision, and the dorsomedial striatum integrates hig

52 eadily observed, contained the same internal subdivisions, and maintained the topological relationshi

53 The hippocampus has important anatomical subdivisions, and pyramidal neurons of the vulnerable CA

54 at rendered distinctive the two dorsolateral subdivisions; and 4) a dorsomedial region characterized

55 ifferences in staining pattern of particular subdivisions apparently do not affect the general patter

56 Instead, both subdivisions are connected in parallel with the PB and d

57 All three subdivisions are positively correlated with ventral atte

58 were analysed by classical frontal/posterior subdivisions as well as a finer-grained frontal localiza

59 s tetrapartite rostrocaudal and dorsoventral subdivisions, as well as a tripartite radial stratificat

60 eview, we discuss Treg subpopulations, their subdivision based on nonmutually exclusive criteria of o

61 This confirmed that the subdivisions belonged to distinct networks.

62 is supported by tests of admixture, reduced subdivision between North African date palm and P. theop

63 e and volume of distinct layers in different subdivisions, but no changes in neuron number.

64 malian deep cortical layers and/or amygdalar subdivisions, but one-to-one correspondences are controv

65 endrogram was compared with that of its main subdivisions by applying the Fowlkes-Mallows index for d

66 ions were segregated into posterior-anterior subdivisions by emotion.

67 We demonstrate that subdivision can substantially accelerate the crossing of

68 cells, originates from each of the major IC subdivisions (central nucleus, dorsal cortex, and latera

69 y anteroposterior (AP) and dorsoventral (DV) subdivisions, characterized by largely conserved differe

70 ts from the posterior insula cortex (pIC), a subdivision considered as a primary interoceptive cortex

71 In mice and rats, three subdivisions contain visible representations of the myst

72 first ictal change within insula functional subdivision correlated with aura and reflex component.

73 In auditory cortex, cortical subdivision-dependent changes in the terminal distributi

74 Ventrolateral thalamus contains subdivisions devoted to action control as part of a circ

75 study, we demonstrate that multiple thalamic subdivisions display network properties that are capable

76 an participants, we found that most thalamic subdivisions display network properties that are capable

77 tion and fronto-parietal networks; and third subdivision does not have any networks to which it is pr

78 periphery, the main function of many of its subdivisions does appear to be that of a relay station,

79 The LPFC has two subdivisions, dorsal (dLPFC) and ventral (vLPFC), which

80 size: .85; t36 = 2.54, p = .015) and limbic subdivisions (effect size: .74; t36 = 2.23, p = .032) co

81 Neurons in other subdivisions encoded task dimensions such as movement pe

82 ould affect the dentate gyrus, a hippocampal subdivision essential to neurogenesis and cognition, and

83 he brain also tracks experience as segmented subdivisions (events), but the neural basis for encoding

84 marcations and whether additional functional subdivisions exist remain unclear.

85 bcortical connections associated with the PI subdivisions has led to differing results from various g

86 For the whole striatum and its subdivisions (i.e. limbic, associative, and sensorimotor

87 d three molecularly distinct anteroposterior subdivisions, identified as precommissural (PcP), juxtac

88 ey or plateau crossing that can be gained by subdivision, if the process is driven by the deme that c

89 nd were focally directed to a distinctive DR subdivision immunohistochemically characterized as poor

90 In contrast to other BST subdivisions implicated in anxiety-like responses, these

91 Current subdivision in clades and species is based on morphologi

92 variation at population-level, confirm major subdivision in clades and species, and show that the kno

93 medial portion, further implicating this STN subdivision in impulse control disorders.

94 ur results also reveal a stronger population subdivision in K. ocellatus compared to K. hermaphroditu

95 ies both CHOP and R-CHOP were used without a subdivision in separate groups.

96 Thus, we define a fundamental homeostatic subdivision in T reg cell populations based on their loc

97 r functional organization into striped-based subdivisions in human V2 and V3.

98 we provide in vivo evidence for stripe-based subdivisions in humans.

99 al network model to investigate when and how subdivisions in social networks influence disease dynami

100 nuclei and allowed us to propose additional subdivisions in the adult thalamus, whose main afferent

101 he existence of two previously unappreciated subdivisions in the female VMHvl that are involved in di

102 insular projections do not target any of the subdivisions in the hippocampal formation (the dentate g

103 Our findings provide new insights into subdivisions in the mdFP, and will impact current strate

104 nduced patterns of activity to morphological subdivisions in the nTS is challenging.

105 We revealed stripe-based subdivisions in V2 ending at the V1/V2 border.

106 we examined how mating system and population subdivision influence the fitness of the mss + genotype.

107 minimal model that includes only population subdivision into equivalent demes connected by global mi

108 terations x subsets) plays a role, the exact subdivision into iterations and subsets affected all cha

109 tors that regulate PPR specification and its subdivision into placodal domains with distinct identiti

110 ents of 10 human insulinomas permitted their subdivision into three functional groups with similar in

111 more heterogeneous disease than the present subdivision into types 1 and 2 assumes; type 1 and type

112 plate and that delineate the several further subdivisions into which the oral ectoderm per se is part

113 We discovered that one subdivision is preferentially correlated with the defaul

114 ence for the deep layers of its most lateral subdivisions, known also to receive hippocampal inputs.

115 equires a map (or parcellation) of its major subdivisions, known as cortical areas.

116 present study demonstrates that a cerebellar subdivision (mainly lobules VIIb/VIIIa), which exhibits

117 from MGv, and an equal share from the dorsal subdivision (MGd).

118 divisions, as well as from several of their subdivisions (MGv: pars lateralis [LV], pars ovoidea [OV

119 In most PBN subdivisions, more than 50% of CGRP cells dually project

120 pproach, frontal pole volume was compared by subdivision-naive multivariate searchlight analysis base

121 We study the effect of varying the degree of subdivision of a population, and investigate the trade-o

122 dentified a novel role for the anteroventral subdivision of BST in the coordinated inhibition of both

123 s and species, and show that the known major subdivision of C. annuum separates large and bulky fruit

124 we apply Hybrid-Lambda to infer the time of subdivision of certain marine invertebrates under differ

125 solates) and Clade B but did not support the subdivision of Clade A into Clade A1 and A2.

126 ividual highlights the complex migration and subdivision of early human populations in Eurasia.

127 The central concept is that the subdivision of host populations which occurs with habita

128 These findings provide evidence that subdivision of light signaling networks is a component o

129 ay a key role in the formation, shaping, and subdivision of planar plant organs, such as leaves.

130 rom corticospinal tract (CST) neurons in the subdivision of primary motor cortex within the central s

131 Recent evidence supports the subdivision of sensorimotor learning into explicit and i

132 nsification by, for example, prohibiting the subdivision of single lot housing and the conversion of

133 anged into two clusters, SK1 and SK2, with a subdivision of SK2 into SK2a and SK2b.

134 g into account the anatomical and functional subdivision of substantia nigra into dorsal and ventral

135 al abnormalities specifically in the rostral subdivision of the ACC (rACC) in OCD patients.

136 e since the formal proposal of a four-series subdivision of the Cambrian System in 2005.

137 nd that area 8C corresponds to a specialized subdivision of the caudal premotor complex where visual

138 nifestations of polarity in epithelia is the subdivision of the cell surface by cell junctions into a

139 We show that astrocytes in the medial subdivision of the central amygdala (CeM) determine the

140 ression by gating the activity of the medial subdivision of the central amygdala (CeM), the canonical

141 nhanced inhibitory synapses from the lateral subdivision of the central amygdala via A2A receptor act

142 xpression does change with age in a specific subdivision of the CN, but PV does not.

143 ar distinction between the two systems and a subdivision of the core system into ventral, dorsal and

144 traced 16 subtypes of neuron that connect a subdivision of the CX with other regions in the bee's ce

145 3c(+) neurons highlight a previously unknown subdivision of the deep mesencephalic nucleus.

146 Instead we suggest that the subdivision of the deformed microstructure ahead of the

147 l types of DSGCs, converges in a specialized subdivision of the dLGN, and delivers direction-tuned an

148 dings further support the anatomo-functional subdivision of the dorsal attention network in subsystem

149 or organizing the developing nervous system: subdivision of the early neuroepithelium into precursors

150 leus of the stria terminalis (BNST), a major subdivision of the extended amygdala that has been propo

151 t GPR151 is highly conserved, specific for a subdivision of the habenular neurocircuitry, and constit

152 rs were used to assess the functional ON/OFF subdivision of the inner plexiform layer.

153 in the lemniscal division, i.e., the ventral subdivision of the medial geniculate body (MGv).

154 reported that inhibition of the infralimbic subdivision of the medial prefrontal cortex (ilPFC) incr

155 ave reduced activity in the infralimbic (IL) subdivision of the medial prefrontal cortex (mPFC), asso

156 As a subdivision of the medial prefrontal cortex (mPFC), M2 c

157 Cortical areas, such as the dorsal subdivision of the medial superior temporal area (MSTd)

158 0% of their thalamic inputs from the ventral subdivision of the MGN (MGv; the primary/lemniscal audit

159 tion of anatomically distinct outputs from a subdivision of the mouse PFC, the anterior cingulate cor

160 The ventrolateral subdivision of the murine ventromedial hypothalamus (VMH

161 )-expressing neurons in the external lateral subdivision of the PBN (PBel) as being sufficient to sup

162 e two alleles and an illustration of how the subdivision of the population can lead to non-trivial be

163 ns and whisker map organization revealed the subdivision of the posterior group of the thalamus into

164 enlarged hypoglossal nucleus, an additional subdivision of the serotonergic raphe obscurus nucleus,

165 In addition, we provide evidence for a subdivision of the slow/implicit process into distinct m

166 The dorsal subdivision of the SPZ (dSPZ) plays an important role in

167 erely in the caudal sensorimotor striatum, a subdivision of the striatum implicated in habitual contr

168 pha)-expressing neurons in the ventrolateral subdivision of the ventromedial hypothalamic nucleus (vl

169 ptor-expressing neurons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl(Esr1

170 ssing (Esr1(+)) neurons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl) con

171 The ventrolateral subdivision of the ventromedial hypothalamus (VMHvl) con

172 chemogenetic activation of the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl).

173 ssing (Esr1(+)) neurons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl).

174 m, the arcuate nucleus and the ventrolateral subdivision of the ventromedial nucleus of the hypothala

175 nal and temporal specificity in two distinct subdivisions of ACC with different AMPA/N-methyl-D-aspar

176 d in more caudal tracer injections (i.e., in subdivisions of area 24).

177 an in Nissl stain, especially for area 2 and subdivisions of area 5.

178 de level in distinguishing between taxonomic subdivisions of bacteria, and can be more effectively im

179 There are three main subdivisions of calcium channel, defined by the pore-for

180 Here we analyze the connectivity of the subdivisions of dorsal pallium (DD) of an electric gymno

181 ssification schemes, and lacking superfluous subdivisions of genuine types.

182 ing cognitive functions; however, functional subdivisions of human frontal cortex are only coarsely m

183 comparison of the microstructurally informed subdivisions of human frontal pole between depressed pat

184 Here, we demonstrate distinct subdivisions of MPC that are selectively recruited durin

185 f all mt lineages in our dataset belonged to subdivisions of mt haplogroup U5.

186 he broadest sense, the nuclear complexes and subdivisions of nuclear complexes, the topographical arr

187 All four subdivisions of OFC give rise to projections to the dors

188 The different subdivisions of OVLT received glial processes of differe

189 el areas PEipe, PEipi (external and internal subdivisions of PEip), and MIPd.

190 cilitate detailed studies on the role of the subdivisions of PPC in the rat as diverse, higher order

191 erlap of limbic and motor connections within subdivisions of the ACC is not well understood.

192 Social behaviours are not localized to subdivisions of the amygdala even though the inputs and

193 elements consistent with the main anatomical subdivisions of the amygdala that embody distinct functi

194 on of CRF and N/OFQ-related genes in various subdivisions of the amygdala, a critical brain structure

195 d biotinylated dextran amine, were placed in subdivisions of the anterior cingulate area 24b/c and in

196 Extracellular recordings in three different subdivisions of the auditory thalamus in anesthetized mi

197 rities in receptor binding densities between subdivisions of the avian and mammalian HF.

198 fferent connections of two cytoarchitectural subdivisions of the caudolateral frontal cortex, areas 6

199 of the stria terminalis (BST), the two major subdivisions of the central extended amygdala.

200 with four subdivisions of the pulvinar, two subdivisions of the claustrum, and the interlaminar port

201 PHd and PV reactive neurons within the three subdivisions of the CN in middle-aged and aged rhesus ma

202 subtypes that mainly interconnect different subdivisions of the CX.

203 es, and readily distinguished major regional subdivisions of the developing hypothalamus.

204 HF), sequentially contribute to longitudinal subdivisions of the heart tube (HT), with the FHF contri

205 Although individual subdivisions of the hippocampus are difficult to homolog

206 Anatomical subdivisions of the human brain can be associated with d

207 ce imaging at 7 Tesla to identify functional subdivisions of the human EC.

208 erizes the pattern of neurodegeneration in 3 subdivisions of the human GP, and its relation to clinic

209 Subdivisions of the IC were identified based on cytochro

210 led cortical fibers terminating in all three subdivisions of the inferior colliculus.

211 In contrast, in each of three subdivisions of the lateral septum, females had greater

212 n hierarchical clustering approach to derive subdivisions of the LFC based on intrinsic functional co

213 iscal and nonlemniscal (but not polysensory) subdivisions of the medial geniculate body.

214 ctions regarding their nuclear origin in the subdivisions of the MGB and their termination patterns i

215 The different subdivisions of the midbrain periaqueductal gray (PAG) a

216 size, and volume of the different layers and subdivisions of the monkey entorhinal cortex (Eo, Er, El

217 armacologically disinhibited each of the two subdivisions of the mPFC and assessed freezing and downs

218 it activity in the prelimbic and infralimbic subdivisions of the mPFC in behaving rats.

219 od, with similar turnover rates in the major subdivisions of the myocardium.

220 CNS-PNS boundary and connect these two major subdivisions of the nervous system.

221 ius (RI) in the brainstem, innervating three subdivisions of the nucleus mesencephalicus lateralis pa

222 e restricted to either the lateral or medial subdivisions of the OFC in rhesus macaques.

223 eurons (OPNs) of the PCX that project to two subdivisions of the OFC, the agranular insula and the la

224 ence that these accumulations are functional subdivisions of the parasite ER, presumably generated in

225 pattern has been in accurately targeting the subdivisions of the PI with neural tracers.

226 inject bidirectional tracers in the separate subdivisions of the PI, the superior layers of the super

227 We recognize three subdivisions of the posterior parietal cortex (PPC), whi

228 included bidirectional connections with four subdivisions of the pulvinar, two subdivisions of the cl

229 y, physiologically and functionally distinct subdivisions of the SPB tract that underlie affective as

230 We found that, while all four subdivisions of the SPZ share a similar backbone of majo

231 e disparate functions described for anatomic subdivisions of the STN.

232 Structural subdivisions of the striatum and thalamus were identifie

233 xamined as a function of CRP using seeds for subdivisions of the ventral and dorsal striatum associat

234 Neurons in the dorsomedial and central subdivisions of the ventromedial hypothalamus (VMHdm/c)

235 the OFC, yielding altered connectivity-based subdivisions of this region.

236 ent sensory-motor loops run through separate subdivisions of this structure.

237 ected locations, and exhibiting the standard subdivisions of this system.

238 f the inferior colliculus (IC) and its major subdivisions offer a juxtaposition of segregated process

239 different markers did not reveal ganglionic subdivisions or physical compartmentalization in any of

240 ade or anterograde tracers into different IP subdivisions or the MnR and additionally examined the tr

241 boundary setting, specialization of myotome subdivisions or the specific RAR subtype that is require

242 We did find conspicuous network subdivisions organized on the basis of dendritic rather

243 and associative (P = 0.002) and sensorimotor subdivisions (P = 0.007).

244 s with sCJD in 26 cortical and 5 subcortical subdivisions per hemisphere using a semiquantitative sco

245 The right and left insula, as well as insula subdivisions (posterior, ventroanterior, and dorsoanteri

246 Stripe subdivisions preferentially responding to fast temporal

247 These anatomical subdivisions, presented in the form of an atlas includin

248 receptor densities mapped well onto seven HF subdivisions previously described.

249 organization in the adult BG consistent with subdivisions previously identified in anatomical tracing

250 ial layers with a preference for its ventral subdivision, referred to as area 35.

251 tory and trigeminal systems, the arcopallial subdivision related to the tectofugal visual system and

252 We found that several VTA subdivisions share similar cellular compositions in nonh

253 The Mo5 jaw-closing subdivision shows the highest VGluT1+ innervation.

254 sthetized mice revealed a stimulus-specific, subdivision-specific deficit in thalamic sensitivity to

255 pendent differences in striatal and thalamic subdivision structure and functional connectivity.

256 ces in intrinsic network architecture across subdivisions suggest that intrinsic connections shape re

257 Another subdivision that also had left- and right-biased ICs was

258 lack of inbreeding depression and the strong subdivision that characterize natural Caenorhabditis pop

259 One subdivision that presented as distinct left- and right-b

260 orebrain organoids establish major forebrain subdivisions that are positioned with in vivo-like topog

261 utput connectivity playing a greater role in subdivisions that are sparser and less centralized.

262 ained the topological relationships of these subdivisions that could be considered typically mammalia

263 microstructure differs significantly across subdivisions that serve distinct cognitive and affective

264 vl contains two anatomically distinguishable subdivisions that showed differential gene expression, p

265 We identified four subdivisions that were bilaterally symmetrical and one t

266 While there is evidence of arcopallial subdivisions, the internal organization or the arcopalli

267 lear morphological and molecularly delimited subdivisions, the rostral part does not.

268 y conceptualized as including two functional subdivisions: the dorsal component of area V3 (V3d) late

269 diverse isolates and characterize the major subdivisions, their relative diversity, and the level of

270 Within BI-RADS 4 subdivisions there were 359 cases in 4a (45.3%), 215 in

271 While cingulate areas projected to all subdivisions, they preferentially targeted the medial pa

272 the ventromedial hypothalamus, ventrolateral subdivision (VMHvl) revealed distinct patterns of neuron

273 oup, sex, and age on striatum, thalamus, and subdivision volumes were examined.

274 body temperature rhythms, while the ventral subdivision (vSPZ) is critical for rhythms of sleep and

275 One bilateral subdivision was connected to sensorimotor regions and an

276 -state functional connectivity with striatal subdivisions was examined for 926 participants (8-22 yea

277 The connectivity of the main subdivisions was investigated by in vitro tracing techni

278 midbrain, striatal, and prefrontal cortical subdivisions) was measured with kinetic analysis using t

279 independent components (ICs) reflected true subdivisions, we performed functional connectivity analy

280 yards, red wines from the different Bordeaux subdivisions were analysed from different vintages.

281 ubjects and networks, individualized network subdivisions were more valid-more internally homogeneous

282 However, all intra-specific subdivisions were shaped during the Quaternary glaciatio

283 The LM is separated into lateral and medial subdivisions, which project to the oculomotor cerebellum

284 the human EC can be divided into functional subdivisions whose functional connectivity closely paral

285 epressed patients and comparison subjects by subdivision-wise classical morphometric analysis.

286 Subdivision-wise morphometric analysis found a significa

287 Our results demonstrate that subdivision with migration alone can significantly accel

288 We also investigate the case of population subdivision with migration and find that the common clai

289 lt from tracer injections into different NTS subdivisions, with dual retrograde tracing revealing tha

290 st that area 6DR includes rostral and caudal subdivisions, with the former also involved in oculomoto

291 amygdala-CEA-DA path follows macrostructural subdivisions, with the majority of input/outputs converg

292 93-H64 (where "H64" refers to a phylogenetic subdivision within ST1193 that is characterized by the f

293 tivates T cells, thus redefining pDCs; a new subdivision within the CD1C(+) subset of DCs; the relati

294 Our study therefore reveals a fundamental subdivision within the cutaneous somatosensory system, a

295 We characterized three functional subdivisions within the amygdala of each individual.

296 These findings delineate robust natural subdivisions within the ASC population that may allow fo

297 Therefore, we identify previously unknown subdivisions within the EP and reveal the existence of c

298 position of the amygdala and its functional subdivisions within the network organization of the brai

299 gnalling network in the PLLP and link tissue subdivision (Wnt receptor and FGF receptor activity doma

300 he hippocampus and its CA1 and dentate gyrus subdivisions worsened with mild cognitive impairment tha