ライフサイエンスコーパス: dendritic tree

1 y of GluN2A-NMDARs remains similar along the dendritic tree.

2 ies of the soma and different regions of the dendritic tree.

3 as patterns distributed randomly across the dendritic tree.

4 pses, broadening the effective extent of the dendritic tree.

5 Aergic interneuron with a radially symmetric dendritic tree.

6 nputs arriving at different locations on the dendritic tree.

7 high and rather evenly distributed over the dendritic tree.

8 aptic inputs distributed across an extensive dendritic tree.

9 luence signaling in the proximal part of the dendritic tree.

10 nd branching in the elaboration of a complex dendritic tree.

11 ing for both Kv3.3 and Kv3.4 subunits in the dendritic tree.

12 nique report on how an AP invades the entire dendritic tree.

13 were present at high density throughout the dendritic tree.

14 ional integrity of the geometrically complex dendritic tree.

15 nced distribution of synaptic weights on the dendritic tree.

16 egments and gradually encompassed the entire dendritic tree.

17 f somatic cytoplasm extended into the distal dendritic tree.

18 tuft membrane was the least excitable in the dendritic tree.

19 or when they are distributed throughout the dendritic tree.

20 ed high Ca(2+) was established in the distal dendritic tree.

21 pines across approximately 2/3 of the apical dendritic tree.

22 control the activation of a highly excitable dendritic tree.

23 puts placed at different locations along the dendritic tree.

24 different parts of the postsynaptic neuron's dendritic tree.

25 a tonic release of the modulator from their dendritic tree.

26 to the shrinkage of branches throughout the dendritic tree.

27 rons to diversify synaptic tuning across the dendritic tree.

28 the inaccessibility of gap junctions on the dendritic tree.

29 load imposed at the soma by the large basal dendritic tree.

30 apses interconnecting distant regions of the dendritic tree.

31 lthy controls and are distributed across the dendritic tree.

32 e due to their different positions along the dendritic tree.

33 te and efficient cargo delivery throughout a dendritic tree.

34 independent of the site of origin within the dendritic tree.

35 tudes and occur synchronously throughout the dendritic tree.

36 e synapses are spatially segregated on their dendritic tree.

37 among thousands of synapses impinging on the dendritic tree.

38 occurred mainly in the middle portion of the dendritic tree.

39 p the locations of synapses across an entire dendritic tree.

40 voltage attenuation as they spread into the dendritic tree.

41 hannels, and neuromodulatory synapses on the dendritic tree.

42 of synapse morphology and the size of the PC dendritic tree.

43 frequency ranges across wide regions of the dendritic tree.

44 tribution of synaptic inputs from across the dendritic tree.

45 dules containing neurons with a hypertrophic dendritic tree.

46 icted the attenuation of the EPSP across the dendritic tree.

47 rom one primary dendrite to multiple complex dendritic trees.

48 sands of inputs distributed throughout their dendritic trees.

49 ation can also operate in neurons with large dendritic trees.

50 iate laminar distribution of their branching dendritic trees.

51 relatively larger somata and more extensive dendritic trees.

52 d had relatively small somata and restricted dendritic trees.

53 uired for the normal development of neuronal dendritic trees.

54 ut only in select portions of pyramidal cell dendritic trees.

55 in both their sizes and the extent of their dendritic trees.

56 95gfp, often at the extremities of the short dendritic trees.

57 arborization, with longer and more branching dendritic trees.

58 ation and genetic manipulation of individual dendritic trees.

59 ple arithmetic is used by apparently complex dendritic trees.

60 H, NF-M, and NF-L, and are abundant in large dendritic trees.

61 distribution of TH terminals on their spiny dendritic trees.

62 on cells running through the middle of their dendritic trees.

63 ar and nonlinear transformations in extended dendritic trees.

64 icothalamic neurons distributed across their dendritic trees.

65 verall complexity values of apical and basal dendritic trees.

66 ed dendritic spikes in subregions of coupled dendritic trees.

67 lps define the computational compartments in dendritic trees.

68 ng in dendrites maps onto the anatomy of the dendritic tree across behavior, oscillatory network, and

69 ck-propagation of action potentials into the dendritic tree and calcium influx that depends nonlinear

70 Thus, PDE10A is transported throughout the dendritic tree and down the axons to the terminals of th

71 ynaptic inhibition compartmentalized the GAC dendritic tree and endowed all dendritic varicosities wi

72 nerated APs actively backpropagated into the dendritic tree and evoked instantaneous calcium accumula

73 essential functions in forming the neuronal dendritic tree and in maintaining inhibitory connections

74 nt enhanced the length and complexity of the dendritic tree and increased dendritic spine density and

75 ed by the approaching object onto the LGMD's dendritic tree and its membrane potential at the spike i

76 n diameters but approximately 2 times larger dendritic tree and receptive field diameters that formed

77 cone stimulation in the midget ganglion cell dendritic tree and show that L versus M cone opponency a

78 ependent of the position of the spine in the dendritic tree and size of the spine head.

79 arrhythmias in heart and decreased neuronal dendritic tree and spine formation in brain.

80 Geometry of the dendritic tree and synaptic organization of afferent inp

81 ystematically position inputs throughout the dendritic tree and tested the summation of two inputs by

82 functionally profound cross talk between the dendritic tree and the axon initial segment, providing n

83 , the interactions between a ganglion cell's dendritic tree and the local mosaic of bipolar cell axon

84 on the basis of the shape and size of their dendritic tree and the pattern of dendritic ramification

85 terized by a different architecture of their dendritic trees and by a more pronounced separation of C

86 h characterized by broad, sparsely branching dendritic trees and cell bodies intermediate in size bet

87 rom Cx36-KO mice also tended to have simpler dendritic trees and fewer divergent inputs from the TRN

88 es as a result of reduced growth of Purkinje dendritic trees and impaired juvenile social play behavi

89 urthermore, due to high synaptic gain, small dendritic trees and sparse connectivity, neighboring you

90 However, the complex dendritic trees and spines of ICx neurons raises the que

91 Dendritic trees and spines were repeatedly visualized ov

92 l data about the laminar distribution of the dendritic trees and synaptic boutons and the number of s

93 The shape of dendritic trees and the density of dendritic spines can

94 ance that separates adjacent planar Purkinje dendritic trees and the synapse density), we determined

95 While these neurons had smaller dendritic trees and/or formed fewer contacts in specific

96 ffic in vesicles exiting the soma toward the dendritic tree, and also exhibit bidirectional motions,

97 a reduction of CF translocation along the PC dendritic tree, and decreased pruning of CF terminals fr

98 ion of synapses on particular regions of the dendritic tree, and the differentiation of pre- and post

99 orescence transients over the entire primary dendritic tree, and the relative fluorescence increment

100 erally, deafferentation reduced more complex dendritic trees, and caused a moderate decline in dendri

101 receive their synaptic inputs through their dendritic trees, and dendritic spines are the sites of m

102 topically distributed and displayed abnormal dendritic trees, and granule cells were markedly deplete

103 Single NGFCs displayed small dendritic trees, and their characteristically dense axon

104 Silent neurones had the most extensive dendritic trees, and these branched in all directions.

105 Thus, unbiased dendritic trees appear to provide an anatomical substrat

106 ith carbocyanine dyes to quantify changes in dendritic tree architecture as a function of age.

107 mine the size and complexity of the neuronal dendritic tree are unclear.

108 Complex dendritic trees are a distinctive feature of neurons.

109 a comprehensive understanding of how complex dendritic trees are built.

110 Dendritic trees are increased by 250% in length in the l

111 r amacrine cells, including cells with small dendritic trees, as well as for inhibitory interneurons

112 stic growth and retraction achieve efficient dendritic trees both in terms of wire and function.

113 re assembled regularly throughout the entire dendritic tree by the regulated sequential recruitment o

114 synapses placed in the right location on the dendritic tree can exert a powerful impact on backpropag

115 xcitation and inhibition (E/I) within active dendritic trees can significantly impact neuronal functi

116 pikes to propagate more efficiently into the dendritic tree compared with spikes occurring at burst o

117 ting a larger cell body and a more elaborate dendritic tree, compared with OB granule cells.

118 of oligophrenin-1 resulted in reductions in dendritic tree complexity and mature dendritic spine den

119 phila flight motoneuron (MN5) with a complex dendritic tree, comprising more than 4,000 dendritic bra

120 uniform: clusters distributed throughout the dendritic tree contained alpha3, beta3, and, less freque

121 In contrast, dendritic trees demonstrated more limited but isotropic

122 only approximately 0.3 mm (approximately one dendritic tree diameter), the parasubiculum is both one

123 They had the smallest dendritic tree diameter, and their tree size seemed to b

124 types (HA-1, HA-2, and HB) were identified; dendritic tree diameters averaged 25-40 microm.

125 in morphology was the vertical extent of the dendritic tree (distance from soma to fissure), which wa

126 The dendritic trees during lactation elongated ( approximate

127 aptic inhibition in a restricted area of the dendritic tree, endocannabinoids selectively "primed" ne

128 GN synaptic contacts across the complex cell dendritic tree, established by a Hebbian developmental p

129 ctural context of the neural tissue in which dendritic trees exist to drive their generation in silic

130 is elegans polymodal neuron named PVD, whose dendritic tree follows a stereotypical structure charact

131 Photostained dendritic trees formed characteristic spatial mosaics an

132 ntration on intracellular calcium across the dendritic tree from noisy observations at a discrete set

133 We traced dendritic trees from confocal images of the same GAD67-G

134 in three dimensions (3D) by "growing" their dendritic trees from stem branches that were oriented as

135 atiotemporal smoothing of calcium signals in dendritic trees, given single-trial, spatially localized

136 s in the deep cerebellar nuclei, whereas the dendritic trees grew to normal height and branched exten

137 and large multipolar cells with "polarized" dendritic trees; group 3 is composed of less extensive p

138 retinas, ganglion cell receptive fields and dendritic trees grow faster than normal.

139 However, by 6 weeks the dendritic tree had partially recovered and displayed a s

140 The spread of somatic spikes into dendritic trees has become central to models of dendriti

141 The role of spines in Cl(-) diffusion along dendritic trees has not been addressed so far.

142 Other amacrine cells, with small dendritic trees, have been assumed to operate as single

143 onstrate an example of how a single neuron's dendritic tree implements a mathematical step in a neura

144 nerates a predictable, unnaturally patterned dendritic tree in a DMA-1-dependent manner.

145 alters the shape and complexity of the adult dendritic tree in a time-dependent manner.

146 lar plexus and two neurons that have a split dendritic tree in both halves.

147 ibited robust internalization throughout the dendritic tree in response to AMPA application.

148 al fields comparable to the size of a single dendritic tree in the MSO.

149 the branching pattern and orientation of the dendritic tree in the VCN.

150 o NF-L is critical for the growth of complex dendritic trees in motor neurons.

151 urkinje cells have one of the most elaborate dendritic trees in the mammalian CNS, receiving excitato

152 The extent of dendritic trees in the subiculum and fusiform gyrus was

153 n cat primary visual cortex and imaged their dendritic trees in vivo by two-photon microscopy.

154 (the distance between two embranchments in a dendritic tree) in the cerebellum, agreeing with age-mat

155 tory, one inhibitory) that converge onto its dendritic tree; in the other model, inhibition is presyn

156 altered distribution of mitochondria in the dendritic tree, indicating that abnormal mitochondrial d

157 elivered in a restricted part of the basilar dendritic tree invariably produced sustained plateau dep

158 The development of neuronal dendritic trees involves positive and negative control o

159 ts interacting partners in the Purkinje cell dendritic tree is a key mechanism by which mutant forms

160 ion of synaptic currents across an extensive dendritic tree is a prerequisite for computation in the

161 iotemporal pattern of synaptic inputs to the dendritic tree is crucial for synaptic integration and p

162 Integration of synaptic input in dendritic trees is a nonlinear process in which excitato

163 found that the circularity and uniformity of dendritic trees is independent of somatic position on th

164 The wide diversity of dendritic trees is one of the most striking features of

165 he computational function of their elaborate dendritic trees is still mysterious.

166 The structures of dendritic spines and the dendritic tree, key determinants of neuronal function, a

167 complex network of projections that form the dendritic tree, largely at tiny protrusions called dendr

168 ared with the rat (6,009 mum vs. 2,473 mum); dendritic tree length in the central nucleus is increase

169 ory neurons, which possess myelinated distal dendritic tree-like arbors with excitable nodes of Ranvi

170 algorithm is also linear in the size of the dendritic tree, making the approach applicable to arbitr

171 outputs in close proximity throughout their dendritic trees, making them notable exceptions to proto

172 of these channels in a specific part of the dendritic tree might locally alter these signaling proce

173 pyramidal neurons have larger, more branched dendritic trees, more synapses, and perform more complex

174 ectivity subtypes were determined, and their dendritic tree morphologies and axonal stratification pa

175 re reduced in numbers, BP dendritic spreads, dendritic tree morphologies, and cone-bipolar connectivi

176 d spine densities and a broad range of basal dendritic tree morphologies.

177 lassifications rely mainly on differences in dendritic tree morphology and firing patterns.

178 ectivity whereas bipolar cells with the same dendritic tree morphology usually had the same photorece

179 tion in amacrine cells with widely differing dendritic tree morphology, however, is largely unexplore

180 ical dendritic spine density or in the basal dendritic tree morphology.

181 lasses were related to the complexity of the dendritic tree (number of branch points and maximal term

182 In contrast, global integration across the dendritic tree occurs over longer time periods and is ma

183 imately 180,000 excitatory synapses onto the dendritic tree of a Purkinje cell.

184 sity in a region-restricted manner along the dendritic tree of adult-born granule cells (GCs).

185 Amacrine input occurred throughout the dendritic tree of both A8 and A13 types, and numerically

186 hat is heterogeneously distributed along the dendritic tree of C1 neurons.

187 nt of dendritic arbor across the span of the dendritic tree of CA1 pyramidal neurons and reduced long

188 -regions, cell-types and locations along the dendritic tree of CA1 pyramidal neurons, showed diversit

189 ntegration of different inputs targeting the dendritic tree of CA3 pyramidal cells (CA3PCs) is critic

190 s are located throughout the often-elaborate dendritic tree of central neurons.

191 spectrin is present throughout the elaborate dendritic tree of cerebellar Purkinje cells and is requi

192 etal protein present throughout the soma and dendritic tree of cerebellar Purkinje cells, to be requi

193 atial organization of synaptic inputs on the dendritic tree of cortical neurons plays a major role fo

194 cipation is computed autonomously within the dendritic tree of each ganglion cell and relies on feedf

195 n of electrical activity in a portion of the dendritic tree of each neuron in the subpopulation indiv

196 (iii) the spatial electrical pattern in the dendritic tree of each neuron interacts non-linearly wit

197 he horizontal plane, both the somata and the dendritic tree of gastric-projecting neurons were smalle

198 um channels distributed throughout the whole dendritic tree of GP neurons indicates that these channe

199 throughout the proximal-distal extent of the dendritic tree of GP neurons, the density of plasma memb

200 ry drives are widely distributed on the soma-dendritic tree of hypoglossal motoneurons during AS-carb

201 tatory circuit inputs are altered across the dendritic tree of individual neurons under neuroinflamma

202 ed with their anatomical position within the dendritic tree of individual neurons.

203 accompanied by significant increases in the dendritic tree of its principal neurons, but whether thi

204 Quantitative analysis of the basilar dendritic tree of layer V pyramidal cells in frontoparie

205 In both modes, the entire dendritic tree of LTS interneurones behaved as a 'global

206 nd I synaptic organization across the entire dendritic tree of mammalian neurons.

207 d, in part, by stabilizing or remodeling the dendritic tree of motor neurons below the injury site.

208 Our findings suggest that the dendritic tree of motor neurons deprived of descending i

209 e apical tuft is the most remote area of the dendritic tree of neocortical pyramidal neurons.

210 voltage clamp poorly controls voltage in the dendritic tree of neurons, where the majority of synapti

211 0 cortical axons innervate the volume of the dendritic tree of one spiny cell.

212 ibution of excitatory synaptic inputs on the dendritic tree of PV neurons.

213 channels are expressed throughout the entire dendritic tree of rat thalamocortical neurons and that t

214 he results thus support a new picture of the dendritic tree of relay cells which may have implication

215 s were few in number and the staining of the dendritic tree of small cells was not optimal.

216 poral activation patterns of inputs onto the dendritic tree of the LGMD, across three locust species.

217 integration of excitatory inputs within the dendritic tree of the LGMD.

218 Morphologically, the dendritic tree of the physiologically characterized axot

219 l distribution of the afferent inputs on the dendritic tree of the target neurons.

220 Localized delivery of geranylgeraniol to the dendritic trees of CA1 hippocampal neurons via the recor

221 destly influenced by its projection pattern; dendritic trees of cells making transient projections we

222 by forming synapses at optimal locations on dendritic trees of cortical neurons.

223 The dendritic trees of DAPI-3 cells, which range from about

224 ocation, the soma sizes or the extent of the dendritic trees of excitatory and inhibitory interneuron

225 ent modes of signaling, we reconstructed the dendritic trees of five HCs as well as cone axon termina

226 We report that apical, but not basal, dendritic trees of Golgi-impregnated CA3 principal neuro

227 idual dendrites in both the apical and basal dendritic trees of hippocampal neurons to operate as fac

228 The dendritic trees of hippocampal pyramidal cells play impo

229 als, were distributed on all portions of the dendritic trees of injected RTN cells.

230 Dendritic trees of layer 3 neurons largely avoided the c

231 ost of these afferents are integrated in the dendritic trees of Mo7 neurons.

232 Here we show that the dendritic trees of motoneurons innervating a dorsal neck

233 indicate that the length and geometry of the dendritic trees of OT and VP neurons are altered in oppo

234 The dendritic trees of OT neurons shrunk during lactation (

235 The dendritic trees of outer stratifying cells cover the ret

236 napses are widely distributed throughout the dendritic trees of RCA motoneurons, albeit with a strong

237 are performed on synaptic inputs within the dendritic trees of single neurons?

238 ee-dimensional (3D) morphology of individual dendritic trees of six cat alpha motoneurons.

239 In the large dendritic trees of some amacrine cells, such arrangement

240 ely represented in the medial lobe where the dendritic trees of some efferent neurons receive inputs

241 Comparing branching complexity of dendritic trees of supragranular pyramidal neurons and o

242 active thalamic and intracortical inputs on dendritic trees of thalamorecipient cortical neurons in

243 diversity of conscious experience; (ii) the dendritic trees of the neurons in the subpopulation all

244 by NA and 5-HT boutons on the reconstructed dendritic trees of these motoneurons.

245 stigated the morphometry and topology of the dendritic trees of these neurons and the changes induced

246 Reconstructions of the dendritic trees of these OS ganglion cells and measureme

247 ed their localization on the cell bodies and dendritic trees of two amacrine cell populations in the

248 D spatial complexity in the apical and basal dendritic trees of two functionally distinct types of ma

249 pruning is unreliable and ACs elaborate two dendritic trees: one in the IPL and a second projecting

250 Simplification of the apical dendritic tree preceded simplification of basal dendrite

251 nputs can be segregated on the Purkinje cell dendritic tree provides further evidence that these exci

252 discrete synaptic inputs across a non-linear dendritic tree, Purkinje cells integrate parallel fiber

253 Dendritic trees ranged from 10 to 70 microM.

254 ominated by active currents intrinsic to the dendritic tree rather than by the synaptic current enter

255 Their elaborate dendritic tree receives, propagates, and transforms syna

256 and the active electrical properties of the dendritic tree regulates synaptic plasticity.

257 lic and multinucleated neurons with abnormal dendritic trees resembling giant cells.

258 Analysis of the dendritic trees revealed that the tetanus toxin group sh

259 matter trees using the same measures as for dendritic trees shows heteromodal association areas to h

260 The reduction in dendritic tree size was localized to distal dendritic se

261 d within all RGC types exhibit an undersized dendritic tree, spanning about half of the normal area.

262 (ipRGC) types can be distinguished by their dendritic tree stratification and intensity of melanopsi

263 , effectively "throwing their voices" in the dendritic tree, such that distributed inhibitory synapse

264 ts that are often distributed over expansive dendritic trees, suggesting the need for compensatory me

265 striking phosphorylation of Ras-GRF1 in the dendritic tree, supporting a role for Ras activation and

266 ic sites may be distributed along a tortuous dendritic tree that cannot be readily clamped spatially

267 red widespread Ca(2+) signals throughout the dendritic tree that were detectable even in individual s

268 Nerve cells form elaborate, highly branched dendritic trees that are optimized for the receipt of sy

269 y reflecting the growth of randomly oriented dendritic trees that reduce tissue coorientation.

270 led neurons had large and spatially extended dendritic trees that spanned several of these dl-pons su

271 persisted over time and elaborated extensive dendritic trees that stably incorporated themselves thro

272 OFF populations with narrowly monostratified dendritic trees that surprisingly appeared to perfectly

273 ghts a new and powerful direct impact of the dendritic tree (the input region of neurons) on the enco

274 t the surprising result that despite a small dendritic tree, the AII amacrine cell simultaneously per

275 n identifying functional compartments in the dendritic tree, the number and size of which depend on t

276 rong coupling regime, relevant to myelinated dendritic trees, the spike train statistics can be predi

277 ostsynaptic potentials sum across the entire dendritic tree to generate substantial firing rates, pre

278 The ability of synapses throughout the dendritic tree to influence neuronal output is crucial f

279 ls are placed strategically along the entire dendritic tree to modulate most, if not all, of the exci

280 the axosomatic region and propagate into the dendritic tree to provide a retrograde signal that conve

281 roborate the ability of neurons with complex dendritic trees to implement diverse linear and nonlinea

282 show that E/I synapses are regulated across dendritic trees to maintain a constant ratio of inputs i

283 In spines located on the proximal dendritic tree, VSCCs normally open with high probabilit

284 The shift in spine distribution across the dendritic tree was further confirmed with the examinatio

285 segment, axon hillock, soma, and simplified dendritic tree was used to study excitation with an extr

286 Finally, RNA stress granules and smaller dendritic trees were also observed when ribosomal protei

287 Their putative dendritic trees were found to be in close proximity to t

288 Intracallosal NK1IP -n and their dendritic trees were intensely labeled, allowing classif

289 PC dendritic trees were larger and more complex in Nogo-A K

290 rites were smooth or sparsely spiny, and the dendritic trees were mainly restricted to layer I, cover

291 te neurons were evenly distributed and their dendritic trees were symmetric.

292 Tonic neurons, which had long and extensive dendritic trees, were Remak's Type I, II and IV neurons.

293 ping of functional nAChRs along the soma and dendritic tree, whereas the fast uncaging minimized the

294 n coronal section, some neurons had a radial dendritic tree while others had dorso-ventrally elongate

295 e well characterized: amorphs have overgrown dendritic trees with larger synaptic boutons, developmen

296 Here, we labeled the BC dendritic trees with retrograde tracing techniques to an

297 n targeted to distinct regions of a neuron's dendritic tree, with synapses on more distal dendrites n

298 size and NMDAR-driven calcium signals along dendritic trees, with important implications for synapti

299 ns were extensively labeled throughout their dendritic trees, with no evidence of PRV trans-synaptic

300 ll type in the hippocampus, by growing their dendritic trees within their characteristic dendritic fi