ライフサイエンスコーパス: dendritic tree

1 voltage attenuation as they spread into 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 luence signaling in the proximal part of the dendritic tree.

6 Aergic interneuron with a radially symmetric dendritic tree.

7 nputs arriving at different locations on the dendritic tree.

8 or when they are distributed throughout the dendritic tree.

9 high and rather evenly distributed over the dendritic tree.

10 aptic inputs distributed across an extensive dendritic tree.

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

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

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

14 were present at high density throughout the dendritic tree.

15 ional integrity of the geometrically complex dendritic tree.

16 nced distribution of synaptic weights on the dendritic tree.

17 egments and gradually encompassed the entire dendritic tree.

18 f somatic cytoplasm extended into the distal dendritic tree.

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

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

21 the inaccessibility of gap junctions on the dendritic tree.

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

23 control the activation of a highly excitable dendritic tree.

24 puts placed at different locations along the dendritic tree.

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

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

27 to the shrinkage of branches throughout the dendritic tree.

28 te and efficient cargo delivery throughout a dendritic tree.

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

30 tudes and occur synchronously throughout the dendritic tree.

31 e synapses are spatially segregated on their dendritic tree.

32 among thousands of synapses impinging on the dendritic tree.

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

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

35 hannels, and neuromodulatory synapses on the dendritic tree.

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

37 frequency ranges across wide regions of the dendritic tree.

38 tribution of synaptic inputs from across the dendritic tree.

39 dules containing neurons with a hypertrophic dendritic tree.

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

41 rom one primary dendrite to multiple complex dendritic trees.

42 sands of inputs distributed throughout their dendritic trees.

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

44 iate laminar distribution of their branching dendritic trees.

45 relatively larger somata and more extensive dendritic trees.

46 d had relatively small somata and restricted dendritic trees.

47 uired for the normal development of neuronal dendritic trees.

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

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

50 95gfp, often at the extremities of the short dendritic trees.

51 arborization, with longer and more branching dendritic trees.

52 ation and genetic manipulation of individual dendritic trees.

53 ple arithmetic is used by apparently complex dendritic trees.

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

55 distribution of TH terminals on their spiny dendritic trees.

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

57 icothalamic neurons distributed across their dendritic trees.

58 verall complexity values of apical and basal dendritic trees.

59 ed dendritic spikes in subregions of coupled dendritic trees.

60 lps define the computational compartments in dendritic trees.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 Dendritic trees and spines were repeatedly visualized ov

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 In contrast, dendritic trees demonstrated more limited but isotropic

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

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

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

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

110 The dendritic trees during lactation elongated ( approximate

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

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

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

114 Photostained dendritic trees formed characteristic spatial mosaics an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 0 cortical axons innervate the volume of the dendritic tree of one spiny cell.

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

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

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

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

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

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

191 Morphologically, the dendritic tree of the physiologically characterized axot

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

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

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

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

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

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

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

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

200 The dendritic trees of hippocampal pyramidal cells play impo

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

202 Dendritic trees of layer 3 neurons largely avoided the c

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

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

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

206 The dendritic trees of OT neurons shrunk during lactation (

207 The dendritic trees of outer stratifying cells cover the ret

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 Dendritic trees ranged from 10 to 70 microM.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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