ライフサイエンスコーパス: subdivision

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

2 e striatum (r=-0.23, p=0.41) or any striatal subdivision.

3 the NADPH-d distribution pattern in a brain subdivision.

4 or types, often without obvious criteria for subdivision.

5 rine cells, primarily located in the rostral subdivision.

6 off collaterals to, or were located in, this subdivision.

7 nd follow the brain's established functional subdivision.

8 that innervated the rostrocentral, gustatory subdivision.

9 neurons were detected in the pars lateralis subdivision.

10 ns with intermediate SSA responses across IC subdivisions.

11 aps characterized the MGB reflecting two MGB subdivisions.

12 ctions of varying densities between the four subdivisions.

13 mportance of task relevance in both thalamic subdivisions.

14 ed into distinct functional and connectional subdivisions.

15 movements, comprises nine or more functional subdivisions.

16 receptor expression highlighted distinct HF subdivisions.

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

18 similar to each other than to rat and mouse subdivisions.

19 the relative contributions of key anatomical subdivisions.

20 cal signatures for most of the brain's major subdivisions.

21 ts of B(max) and K(D) in functional striatal subdivisions.

22 titioned into medial (MFP) and lateral (LFP) subdivisions.

23 ) and the limbic (effect size=1.04) striatal subdivisions.

24 of the SEZ to the newly established neuropil subdivisions.

25 in their soma size and distribution among IC subdivisions.

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

27 onspicuous clusters formed by afferent tract subdivisions.

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

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

30 Subdivision 4 acidobacterial sequences tended to follow

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

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

33 he tuberal (rostral) and mammillary (caudal) subdivisions, according to the prosomeric model.

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

35 cide with and contribute to the proportional subdivision and expansion of these primordia.

36 ese motoneurons reside in the caudal central subdivision and have 10 or more poorly branched dendrite

37 eetles is correlated with greater population subdivision and higher speciation rate.

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

39 Integrating LID into residential subdivisions and increasing population density by buildi

40 pallium itself (dorsomedial and dorsocentral subdivisions and nucleus taenia); (2) other diencephalic

41 macaque area 32 has subgenual and pregenual subdivisions and the extent to which they are comparable

42 chniques were used for the identification of subdivisions and their boundaries.

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

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

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

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

47 urhood relationships between fine anatomical subdivisions are associated with discrete neuronal subty

48 These subdivisions are linked by circuitry intrinsic to DD its

49 ortical afferent projections of one of these subdivisions, area PE.

50 hypothesis that they may form as continuous subdivisions around the lateral ventricle.

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

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

53 n pallium, expression in the ventral pallial subdivisions became distinct during prehatch development

54 Most gene expression-defined pallial subdivisions began as one ventral or dorsal domain that

55 This confirmed that the subdivisions belonged to distinct networks.

56 e CT axons that innervated NTS rostrolateral subdivision both in the adult and in P15 rats were morph

57 The central subdivision (BSTLcn) and the juxtacapsular subdivision (

58 l subdivision (BSTLcn) and the juxtacapsular subdivision (BSTLJ) are two BSTL regions that lie above

59 nces in cDNA content between these two brain subdivisions but, more importantly, between the LIS1 com

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

61 We demonstrate that subdivision can substantially accelerate the crossing of

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

63 In the rostrocentral subdivision, compared with the CT terminal field, GSP ap

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

65 TeO, respectively, indicating that each Imc subdivision contains one of the two cell types hodologic

66 In both subdivisions, CT terminals reached morphological maturit

67 dence that the Arabian horse breed has clear subdivisions depending on the traditional maternal based

68 port the continuum hypothesis of avian brain subdivision development around the ventricle and influen

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

70 nal connectivity, and that activity in these subdivisions differentially encodes values for expected

71 Whereas IX and LV filled the rostrolateral subdivision diffusely, CT projected only to the dorsal a

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

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

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

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

76 Assessing the extent to which population subdivision during cladogenesis is necessary for long-te

77 These subdivisions each included two parts of the mesopallium,

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

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

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

81 eactive for CB or CR varied depending on the subdivisions examined, with the highest percentage of co

82 marcations and whether additional functional subdivisions exist remain unclear.

83 Each subdivision expression profile had a different temporal

84 demonstrate unique roles for each of the two subdivisions for monetary reward and thermal pain percep

85 trast, deletions that involved the medial PB subdivision had minimal effects on arousal during hyperc

86 r, a parcellation of the monkey OFC into two subdivisions has been suggested based on its intrinsic a

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

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

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

94 ) and medial-caudal (putative shell, pshell) subdivisions in humans.

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

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

97 The genes included those that define brain subdivisions in the adult and some that are also involve

98 olecular profiling to discover that distinct subdivisions in the avian pallium above and below the ve

99 development these domains fold into distinct subdivisions in the dorsal and ventral avian pallium, fo

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

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

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

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

104 he identification of the main boundaries and subdivisions in the optic, paraventricular, tuberal, and

105 fore could unequivocally be used to identify subdivisions in the urodele brain similar to other verte

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

107 lei with sensorimotor, cognitive, and limbic subdivisions, indicative of functional organization.

108 ccompanying paper show that these structures/subdivisions initially form continuous gene expression d

109 In arthropods, body subdivision into a region with locomotory appendages ("t

110 s well with anatomical evidence suggesting a subdivision into an anterior (45A) and posterior part (4

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

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

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

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

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

116 Such a functional subdivision is similar to mammalian cortico-basal gangli

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

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

119 The caudal nidopallium (NCM) and subdivision L3 of field L were more selective than other

120 e, we identified three PI chemoarchitectonic subdivisions, lateral central (PIcl), medial central (PI

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

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

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

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

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

126 olution of this primordium may be related to subdivision of an early pansensory domain.

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

128 The lateral subdivision of CEA (CEl) contains a subpopulation of GAB

129 CeL output, thereby disinhibiting the medial subdivision of CeA and releasing fear expression.

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

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

132 the supplementary motor area, and the caudal subdivision of dorsal premotor cortex, as well as affere

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

134 Recent evidence highlights a subdivision of GABAergic neurons within anterior bed nuc

135 l phenotype of GABAergic neurons across each subdivision of LS and in cingulate cortex (Cg) and media

136 The precise and remarkable subdivision of myelinated axons into molecularly and fun

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

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

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

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

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

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

143 is the specification of the germ layers, the subdivision of the blastula embryo into endoderm, mesode

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

145 apses onto inhibitory neurons in the lateral subdivision of the CeA (CeL).

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

147 The centromedial amygdala (CeM), a subdivision of the central amygdala (CeA), is believed t

148 Recent studies indicate that the lateral subdivision of the central amygdala (CeL) is essential f

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

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

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

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

153 Injections were made into the dorsal subdivision of the cochlear nucleus in order to restrict

154 ly in the core and typically within a single subdivision of the cochlear nucleus.

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

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

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

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

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

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

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

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

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

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

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

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

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

168 0% of their thalamic inputs from the ventral subdivision of the MGN (MGv; the primary/lemniscal audit

169 The ventrolateral subdivision of the murine ventromedial hypothalamus (VMH

170 essing neurons in the outer external lateral subdivision of the parabrachial nucleus that project to

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

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

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

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

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

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

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

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

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

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

181 Monkey and human subdivisions of area 32 are more similar to each other t

182 Receptor fingerprints of both subdivisions of area 32 differed between species in size

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

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

185 ssion on Ang II and TGF-beta activity in all subdivisions of cardiac tissues except for the central z

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

187 The L2b and L1 subdivisions of field L had the least selectivity and to

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

189 to the dorsolateral and dorsomedial pallial subdivisions of gymnotiform fish arise from the preglome

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

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

192 calize trait diffusivity changes to specific subdivisions of limbic fiber pathways, including the for

193 stress syndrome (PaO2/FIO2 < 300 mm Hg), and subdivisions of mild, moderate, and severe acute respira

194 Previous work has suggested that anatomical subdivisions of mPFC make distinct contributions to fear

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

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

197 vulgaris-leucoagglutinin (PHA-L), into four subdivisions of OFC.

198 ed by chandelier cells across major cortical subdivisions of piriform cortex is lacking.

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

200 projections from the dorsocaudal and medial subdivisions of premotor cortex (areas 6DC and 6M), from

201 l, and connectional data no consensus on the subdivisions of the adult telencephalon of ray-finned fi

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

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

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

205 olecular specification, and connectivity the subdivisions of the anuran alar hypothalamus possess man

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

207 We describe the divisions and subdivisions of the auditory thalamus including the medi

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

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

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

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

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

213 sivity between patient and control groups in subdivisions of the corpus callosum, cingulum, and forni

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

215 r also functionally associate with different subdivisions of the hippocampus along its longitudinal a

216 Although individual subdivisions of the hippocampus are difficult to homolog

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

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

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

220 Subdivisions of the IC were identified based on cytochro

221 Large cells, which are found in all subdivisions of the IC, may form an exception.

222 ed the external lateral and lateral crescent subdivisions of the lateral PB more than doubled the lat

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

224 aris leucoagglutinin were aimed at different subdivisions of the LHb.

225 ize gene expression patterns in the regional subdivisions of the mammalian brain, we integrated spati

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

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

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

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

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

231 d octopaminergic/tyraminergic neurons in all subdivisions of the mushroom body.

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

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

234 humans, little is known about any functional subdivisions of the OFC except for a rather coarse media

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

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

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

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

239 elements such as bones and cartilages), and subdivisions of the skeletal system.

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

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

242 In the larval zebrafish, subdivisions of the subpallium have been proposed using

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

244 zation that encompasses both the STN and two subdivisions of the ZI, and that the group of cortical a

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

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

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

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

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

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

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

252 Thus, the teleost PAG may have functional subdivisions playing different roles in vocal-auditory i

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

254 Stripe subdivisions preferentially responding to fast temporal

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

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

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

258 that neurons from the external and internal subdivisions project to the Ipc and the TeO, respectivel

259 In the caudal NTS, the ventrolateral subdivision received notable innervation from CT, GSP, a

260 elopment of compartmentalization of distinct subdivisions recently identified in the brain of adult a

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

262 Layers I-III of primate and rodent area 32 subdivisions share more similarities in their receptor d

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

264 idence that the NADPH-d system in main brain subdivisions should be cautiously approached for compara

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

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

267 perception, action, and cognition (including subdivisions such as attention, expectation, and imagina

268 tioning them into dorsal and ventral pallial subdivisions surrounding the mesopallium lamina.

269 chick neural tube, we uncover a form of cell subdivision that abscises apical cell membrane and media

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

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

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

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

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

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

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

277 to be in the sequential fixation regime for subdivision to significantly accelerate crossing.

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

279 One bilateral subdivision was connected to sensorimotor regions and an

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

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

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

283 the overall striatum and functional striatal subdivisions were determined by a Patlak analysis using

284 ffect of ATP was higher in the ventrolateral subdivision, which is densely innervated from outside th

285 X innervate and overlap in the rostrolateral subdivision, which is primarily targeted by the lingual

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

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

288 Subdivision-wise morphometric analysis found a significa

289 d tonotopic arrangement of AN fibers in each subdivision with a clear indication of isofrequency lami

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

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

292 ween striatal heritability in the functional subdivisions, with the greatest heritability estimates o

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

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

295 studies suggest that the lateral and medial subdivisions within aPFC may support metacognitive judgm

296 monstrated a conservation of intraprosomeric subdivisions within prosomeres 1, 2, and 3 (p1, p2, and

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

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

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