ライフサイエンスコーパス: proximal dendrite

1 and grouping affected synapses onto the next proximal dendrite.

2 ce between the ablated branches and the next proximal dendrite.

3 mbrane compartments such as the soma vs. the proximal dendrite.

4 d charge density are similar at the soma and proximal dendrite.

5 ed pvBC axons innervating their own soma and proximal dendrites.

6 tive Renshaw cell synapses on their soma and proximal dendrites.

7 that control the spike outputs to axons and proximal dendrites.

8 limited to diffuse staining in the soma and proximal dendrites.

9 single APs and AP trains were restricted to proximal dendrites.

10 tter forming first and being concentrated in proximal dendrites.

11 d VIP boutons associated with TH-IR soma and proximal dendrites.

12 ession was restricted to the cell bodies and proximal dendrites.

13 inhibitory synapses located on the soma and proximal dendrites.

14 d a robust UCP2 input on their perikarya and proximal dendrites.

15 a specific subdomain including the soma and proximal dendrites.

16 re distributed mainly over the cell soma and proximal dendrites.

17 naptic interactions with neuronal somata and proximal dendrites.

18 articipate in triads, and are presynaptic to proximal dendrites.

19 lex clusters concentrated in their somas and proximal dendrites.

20 ys, and outlining the membrane of somata and proximal dendrites.

21 utons outlining a target neuron soma and its proximal dendrites.

22 synaptic plasticity at afferent synapses on proximal dendrites.

23 tions for computations and learning rules in proximal dendrites.

24 CN currents were preferentially expressed in proximal dendrites.

25 ted by LC-NA afferents on their cell soma or proximal dendrites.

26 components mediate transport of nos mRNA in proximal dendrites.

27 c synapses located on the perikarya and most proximal dendrites.

28 thus maintains minus-end-out polarity within proximal dendrites.

29 ervate hundreds of pyramidal cell somata and proximal dendrites.

30 cal roles in the severing and degradation of proximal dendrites.

31 ction of synapses on motor neuron somata and proximal dendrites.

32 tal calcium response independent of the soma/proximal dendrites.

33 ge surface clusters on the neuronal soma and proximal dendrites.

34 cellular output compared to synapses on more proximal dendrites.

35 r inhibitory inputs was found in OT-PVN-RVLM proximal dendrites.

36 sters in the plasma membrane of the soma and proximal dendrites.

37 ng) membrane of multivesicular bodies within proximal dendrites.

38 es primarily of principal cell perikarya and proximal dendrites.

39 from the MOC collaterals on their somata and proximal dendrites.

40 aMK+ pyramidal cell somata or large-caliber (proximal) dendrites.

41 The reverse was true for the contacts with proximal dendrites (33% in the lateral nucleus vs. 46% i

42 o differential input selection at distal and proximal dendrites according to the temporal characteris

43 Within perikarya and large proximal dendrites, almost all of the DAT immunogold par

44 in brain are localized in the cell body and proximal dendrites, alpha 1C subunits in the hippocampus

45 in neuronal perikarya, with some labeling of proximal dendrites; analysis by confocal microscopy reve

46 quilibrium potential is more positive in the proximal dendrite and more negative in the distal dendri

47 urrounding cortical neuronal cell bodies and proximal dendrites and are involved in the control of br

48 n of the Golgi complex, but was dense in the proximal dendrites and axon initial segments emanating f

49 be evoked by both focal stimulation near GC proximal dendrites and by activating sensory inputs in t

50 In CA4 region, the proximal dendrites and cell bodies of mossy cells were i

51 nhibitory inputs enriched on cell bodies and proximal dendrites and excitatory inputs on distal dendr

52 eactivity (alpha 2AAR-ir) was present within proximal dendrites and fine processes.

53 aV1.2 and CaV1.3 channels in cell bodies and proximal dendrites and is closely co-localized with CaV1

54 he differential distribution of NKCC2 on the proximal dendrites and KCC2 on the distal dendrites of s

55 hat exhibit distinct localizations: Kv2.1 in proximal dendrites and Kv4.2 in distal dendrites.

56 ike terminals that made synaptic contacts on proximal dendrites and on somata.

57 injury, most synaptic loses occurred in the proximal dendrites and remaining synapses were decluster

58 ebellum, NRG-2 colocalizes with calbindin in proximal dendrites and soma of Purkinje cells.

59 R1alpha immunoreactivity was mainly found in proximal dendrites and somata and not usually associated

60 n cytoplasmic compartments of the somata and proximal dendrites and was associated with the cytoskele

61 ins, which predominate in the perikaryon and proximal dendrites, and acidic microdomains, which predo

62 micron-sized clusters localized to the soma, proximal dendrites, and axon initial segment of hippocam

63 y by virtue of ParV cell synapses onto soma, proximal dendrites, and axon initial segments.

64 ein was expressed selectively in the somata, proximal dendrites, and axons of cells lying within or n

65 e synaptic contact were found on the somata, proximal dendrites, and distal dendrites.

66 lowly inactivating current expressed only on proximal dendrites, and fast inactivating current predom

67 allowed to direct the beta-galactosidase to proximal dendrites, and in particular to axons.

68 ctive boutons along the motoneurone soma and proximal dendrites, and of immunoreactive cell bodies in

69 more elaborate thorny excrescences on their proximal dendrites, and project more axon collaterals in

70 anied by VC-dependent filopodia sprouting on proximal dendrites, and PSD-95 and VC-dependent quadrupl

71 ssed pro-NRG2 accumulates on cell bodies and proximal dendrites, and that NMDAR activity is required

72 Dendritic APs activated IC only in the proximal dendrites, and this activation decayed within t

73 fewer synaptic contacts on their somata and proximal dendrites, and those contacts were smaller in s

74 n the surface membrane of the soma and large proximal dendrites, and was present also in smaller diam

75 the soma, with the membranes of vesicles in proximal dendrites, and with the plasma membrane on dist

76 On proximal dendrites, approximately 50% of the synapses we

77 In addition, pvLNTB cell bodies and proximal dendrites are contacted by large synaptic termi

78 unding and isolating large segments of their proximal dendrites, as revealed by three-dimensional hig

79 omoted increases in cypin protein levels and proximal dendrite branches.

80 SNAT1 protein was detected in somata and proximal dendrites but not nerve terminals of glutamater

81 In primary neurons, mRNAs are translated in proximal dendrites but repressed in distal dendrites and

82 t only within the CF input territory (smooth proximal dendrites) but also within the PF input territo

83 and is clustered primarily on the somata and proximal dendrites, but not axons, of both principal neu

84 e the plasticity-resistant synapses onto CA2 proximal dendrites, but the mechanisms underlying these

85 nd to 3-5% of all synapses on the somata and proximal dendrites, but, because of their subcellular lo

86 rites, although Na+ channels in the soma and proximal dendrites differ in their inactivation properti

87 dendrite is more hyperpolarized than at the proximal dendrite due to KCC2 activity.

88 ses, the PN axons ran along PV somata and/or proximal dendrites, forming multiple contacts.

89 drites, it is likely that SK channels in the proximal dendrites govern the efficacy of dendrosomatic

90 terminals surround principal cell somata and proximal dendrites, have a privileged and influential po

91 hippocampal CA2 distal dendrites compared to proximal dendrites, however, the functional significance

92 els of L-type calcium channels are in somata/proximal dendrites (i.e., 0-26 mum) and distal dendrites

93 entials always appeared first in the soma or proximal dendrite in response to somatic current injecti

94 the CNS, surrounding neuron cell bodies and proximal dendrites in a mesh-like structure with open "h

95 to labeling of cell bodies along with their proximal dendrites in CA3.

96 Subicular axons, in contrast, excite proximal dendrites in deeper layers.

97 the shape and orientation of the somata and proximal dendrites in horizontal sections, three distinc

98 l for the transport of cargo along axons and proximal dendrites in neurons.

99 These receptors colocalize to proximal dendrites in primary hippocampal neurons.

100 iver powerful inhibition to OFF GC somas and proximal dendrites in the ON layer, rendering the inhibi

101 Morphologically, the numbers of branches of proximal dendrites increased significantly in a subset o

102 of 50 synchronized "gating" synapses on the proximal dendrites increased the relative gain by 17-38%

103 Inhibition directed toward the soma and proximal dendrites is crucial in regulating the output o

104 The decay of IC in the proximal dendrites occurred despite AP amplitude, plus p

105 tion of simulated barrages of EPSCs into the proximal dendrite of layer 5 pyramidal neurons is greate

106 bing fiber at multiple synaptic sites on the proximal dendrite of the Purkinje cell.

107 tal of 5055 terminals on the cell bodies and proximal dendrites of 114 motoneurons from 14 animals we

108 s of the values of these three parameters in proximal dendrites of 15 mouse alpha retinal ganglion ce

109 d terminal boutons surrounded the somata and proximal dendrites of a small subset of neurons, presume

110 erminal fields occupy primarily the soma and proximal dendrites of abducens motor neurons.

111 SK channels are expressed in the somata and proximal dendrites of adult rat CA1 pyramidal cells.

112 form halos of 60-100 inhibitory synapses on proximal dendrites of AI gammaACs.

113 However, in proximal dendrites of all classes of neuron, approximate

114 its were clustered and located on somata and proximal dendrites of all pyramidal cells.

115 d with cholinergic C-boutons on the soma and proximal dendrites of alpha-MNs.

116 ccumulated as large punctate in the soma and proximal dendrites of both corticospinal motor neurons (

117 mber of GABAergic synapses on the somata and proximal dendrites of CA1 pyramidal cells of the hippoca

118 merized actin, was detected in perikarya and proximal dendrites of CA1 pyramidal cells that received

119 s free) within intracellular compartments of proximal dendrites of CA3 hippocampal neurons at times a

120 lly regulated excitatory synapses within the proximal dendrites of CA3 neurons.

121 , form powerful excitatory synapses onto the proximal dendrites of CA3 pyramidal cells.

122 granule cells in the dentate gyrus (DG) and proximal dendrites of CA3 pyramidal neurons.

123 dLGN) and pulvinar nucleus and in somata and proximal dendrites of cells in the thalamic reticular nu

124 llaterals appeared to contact the somata and proximal dendrites of cells within the SPN.

125 presumptive ER-PM junctions on the soma and proximal dendrites of cortical neurons.

126 v2.2(long) are colocalized in the somata and proximal dendrites of cortical pyramidal neurons and are

127 Z form synaptic contacts with the somata and proximal dendrites of CR cells as early as embryonic day

128 terized symmetric contacts on the somata and proximal dendrites of cSLR/AAA cholinergic neurons were

129 mr1 could be detected in the cell bodies and proximal dendrites of DA neurons and that Fmr1 loss-of-f

130 the inhibitory synapses present on soma and proximal dendrites of dentate granule cells.

131 euronal nets (PNs) which surround somata and proximal dendrites of distinct neuron types.

132 ntia nigra pars reticulata (SNr) neurons and proximal dendrites of dopaminergic substantia nigra pars

133 in-positive terminals on the cell bodies and proximal dendrites of efferent cells.

134 ranule cells (GCs) and project back onto the proximal dendrites of GCs.

135 Together, these findings suggest that the proximal dendrites of GnRH neurons are highly excitable

136 evented excitatory axons from synapsing with proximal dendrites of granule cells and raise questions

137 vely asymmetric synapses with the somata and proximal dendrites of hilar ectopic granule cells.

138 hannels are localized mainly in the soma and proximal dendrites of hippocampal pyramidal neurons, but

139 their co-localization in the cell bodies and proximal dendrites of hippocampal pyramidal neurons.

140 n (+) terminals contacting the perikarya and proximal dendrites of host alpha motor neurons.

141 c labeling was observed in the perikarya and proximal dendrites of human spinal motor neurons but not

142 At the ultrastructural level, proximal dendrites of large trigeminal motoneurons, but

143 rves a major structural role in the soma and proximal dendrites of mammalian brain neurons, tethering

144 ly present in large clusters on the soma and proximal dendrites of mammalian brain neurons.

145 sed in high-density clusters on the soma and proximal dendrites of mammalian central neurons; thus, d

146 noreactivity was preserved on the somata and proximal dendrites of motor neurons.

147 that MPO inputs may terminate on the soma or proximal dendrites of neurons exhibiting elevated Fos.

148 tivity in the BNC was observed in somata and proximal dendrites of nonpyramidal neurons, as well as i

149 ies of T currents expressed in cell soma and proximal dendrites of nRT neurones indicate that various

150 rms synapses mostly onto the cell bodies and proximal dendrites of postsynaptic neurons for maximal i

151 e ipsilateral hippocampus are onto spines of proximal dendrites of presumed granule cells.

152 e varicosities were aligned along somata and proximal dendrites of projection neurons providing dense

153 GRIP staining was prominent in perikarya and proximal dendrites of Purkinje cells, whereas Golgi cell

154 s results in numerous spines on the soma and proximal dendrites of Purkinje cells.

155 PV+ targets of PN axons were the somata and proximal dendrites of PV neurons, although there were al

156 ERbeta-ir was primarily in the perikarya and proximal dendrites of pyramidal and granule cells.

157 king GABAergic synapses onto cell bodies and proximal dendrites of pyramidal cells, control pyramidal

158 vate the axon initial segment (AIS) and soma/proximal dendrites of pyramidal cells, respectively.

159 orms was observed within the cell bodies and proximal dendrites of pyramidal neurons, but only the al

160 PFC) that provide inputs onto the somata and proximal dendrites of pyramidal neurons.

161 can form tubular clusters that surround the proximal dendrites of relay cells.

162 rmed symmetric synapses on the perikarya and proximal dendrites of reticulospinal neurons.

163 and mitochondria accumulate in the soma and proximal dendrites of sacsin knockdown neurons.

164 In the motor layer, cell bodies and proximal dendrites of small, multipolar neurons, and lar

165 the extracellular surface of cell bodies and proximal dendrites of specific subsets of neurons in man

166 course of calcium transients in the soma and proximal dendrites of STN neurons during spontaneous fir

167 eling from superficial layers confirmed that proximal dendrites of superficially projecting cells are

168 VLPO selectively targets the cell bodies and proximal dendrites of the histaminergic TMN.

169 d galaninergic inputs to the cell bodies and proximal dendrites of the TMN and other components of th

170 onstructions revealed clusters of PSDs along proximal dendrites of transfected pyramidal neurons in a

171 f projection neurons, 14% formed synapses on proximal dendrites of undefined order, and only 7% estab

172 Although the cell bodies and proximal dendrites of virtually every pyramidal cell app

173 metrical synaptic contacts, primarily on the proximal dendrites of WGA-HRP-labeled motoneurons.

174 lpha1D was found mainly in the cell soma and proximal dendrites ofvasoactive intestinal polypeptide-i

175 tment specific, occurring selectively in the proximal dendrites onto L5 Pyr and not at inputs onto th

176 the majority of ATD synaptic endings contact proximal dendrites or somata.

177 CN but are selectively localized on somata, proximal dendrites, or distal dendrites depending on the

178 s were localized exclusively on the soma and proximal dendrites, placing them in a good location to i

179 In the proximal dendrite, potassium channels were activated by

180 cence was recorded from somatic, nuclear and proximal dendrite regions with high temporal resolution.

181 t a speed of millimeters per minute into the proximal dendrites, resulting in a reversal of the initi

182 NMDA receptors first formed nonsynaptic proximal dendrite shaft clusters within 2-5 d.

183 zones contacting either distal dendrites or proximal dendrites/somata do not change significantly 30

184 Excitatory inputs to the proximal dendrite sum linearly and require precise tempo

185 PCs received stronger inhibition along their proximal dendrites than deep PCs from SST+ interneurons.

186 ve less inhibitory input on their somata and proximal dendrites than granule cells in the GCL.

187 re commonly found within bulging segments of proximal dendrites that were notable for an absence of m

188 In particular, in the proximal dendrite, the spine density was 5 times higher

189 oss of EAAT4 and GLAST, with degeneration of proximal dendrites, the site of climbing fibre innervati

190 as localized to pyramidal cell bodies, thick proximal dendrites, thin distal dendrites, most dendriti

191 microm2 on the soma and initial 25 microm of proximal dendrites to 4-5 per 100 microm2 on the surface

192 limited to neuronal cell bodies and the most proximal dendrites, unlike GLUT3 expression that is obse

193 Kv3.1 protein is distributed along the soma, proximal dendrites, unmyelinated axons, and axon termina

194 s sought at CA1 stratum radiatum synapses in proximal dendrites using postembedding immunogold labeli

195 Inputs to proximal dendrites usually produce large somatic EPSPs t

196 yer (EPL); (2) axodendritic synapses onto GC proximal dendrites via their axon collaterals or termina

197 restricting channelrhodopsin to the soma and proximal dendrites, we are able to reliably evoke action

198 Occasional synapses on GABAergic somata and proximal dendrites were also observed in the dLGN.

199 We found that signals measured from proximal dendrites were relatively sustained compared to

200 pposition to TH-immunoreactive (IR) soma and proximal dendrites were revealed.

201 Mitral cell somata and proximal dendrites were strongly labeled by the mGluR7 a

202 e receptor was restricted to cell bodies and proximal dendrites when a polyclonal antibody raised aga

203 In controls, VGLUT1 synapses were focused to proximal dendrites where they were grouped in tight clus

204 dendrite severing by breaking microtubule in proximal dendrites, where the dendrites subsequently sep

205 a synaptic target preference for somata and proximal dendrites, whereas the remainder of R-LM intern

206 on of Golgi ribbons into the shaft of somato-proximal dendrites, which is consistent with the tetheri

207 from the entorhinal cortex, relative to the proximal dendrites, which receive an intrinsic excitator

208 und in high-density clusters on the soma and proximal dendrites, while Kv2.2 was uniformly distribute

209 ium release that spread through the soma and proximal dendrites without a decline in amplitude or rat