ライフサイエンスコーパス: dendrite

1 ioned exclusively at the base of the primary dendrite.

2 cells (DGCs) have a single, complex, apical dendrite.

3 rectly used, especially its tendency to form dendrite.

4 should be important for the stiffness of the dendrite.

5 ly within their soma, rather than the apical dendrite.

6 ing first and being concentrated in proximal dendrites.

7 processing of synaptic inputs allowed for by dendrites.

8 re excited by light falling far beyond their dendrites.

9 elicit Ca(2+) release from lysosomes in the dendrites.

10 he distribution and motility of lysosomes in dendrites.

11 ed orientation of microtubules in vertebrate dendrites.

12 inputs onto CA2 compared with CA1 PN distal dendrites.

13 ptor-dependent calcium spikes in apical tuft dendrites.

14 rom), and have thick, infrequently branching dendrites.

15 null mutation of the IL1RAPL1 gene had more dendrites.

16 d temporoammonic inputs at the distal apical dendrites.

17 sions, termed spines, studding many neuronal dendrites.

18 vivo during formation of axonal branches and dendrites.

19 III spectrin, dendritic spines collapse onto dendrites.

20 e expression of transduction proteins within dendrites.

21 ic spines within individual layer 2/3 neuron dendrites.

22 anding of their distribution and function in dendrites.

23 e presence or absence of h-channels on their dendrites.

24 ial role in the structural dynamics of these dendrites.

25 e integrative properties of the postsynaptic dendrites.

26 sport, much less is known about transport in dendrites.

27 icating hybrid, analog-digital coding in the dendrites.

28 iny neurons and allow visualization of their dendrites.

29 rms) exhibiting bifurcating, V-shaped apical dendrites.

30 ess also significantly affected granule cell dendrites.

31 y synapses at visualized locations along the dendrites.

32 e, arborization pattern, and location of its dendrites.

33 c connections with spines and small-diameter dendrites.

34 lysosomal fusion with the plasma membrane in dendrites.

35 lize microtubules in newly formed high-order dendrites.

36 ranches, leading to shortening or removal of dendrites.

37 MAP1B-LC forms immobile complexes along dendrites.

38 haw cell synapses on their soma and proximal dendrites.

39 differentiated domains such as the axon and dendrites.

40 lithium metal and suppress the formation of dendrites.

41 ective and that selectivity arises in the T4 dendrites.

42 o the locations that receive most input: the dendrites.

43 xonal motor, moves cargo less efficiently in dendrites.

44 s on GFP-immunoreactive MGE cells bodies and dendrites.

45 with tiny somata and, on average, just four dendrites.

46 ith increased smaller mitochondria in D1-MSN dendrites after repeated cocaine.

47 ite effects on the growth and elaboration of dendrites among major classes of brain neurons by PKC-de

48 al deletion of the gene permits extension of dendrite and axon arbors beyond these borders.

49 enerated by oxidative phosphorylation in the dendrite and glycolytically in the cilia using glucose i

50 duce observed plasticity gradients along the dendrite and show that dendritic spike dependent LTP whi

51 ks, such that some molecules function in the dendrite and some are critical in the spine.

52 er, displayed no detectable abnormalities in dendrite and spine morphology of layer V neurons.

53 w neck transmits the incoming signals to the dendrite and supposedly controls the signal propagation.

54 tions distributed uniformly along the apical dendrite and, on average, proximally with respect to OSN

55 ow that lysosomes traffic bidirectionally in dendrites and are present in dendritic spines.

56 be predicted solely by co-stratification of dendrites and axons within the inner plexiform layer.

57 re considered able to inhibit problematic Li dendrites and build safe solid Li-metal batteries.

58 drites and silica nanoparticles consumes the dendrites and can extend the life of the battery by appr

59 te a significant loss of VGLUT1 terminals on dendrites and cell bodies at both 21 days and 3 months p

60 RIbeta is enriched in dendrites and co-localizes with MAP2, whereas RIIbeta is

61 strate that the formation and maintenance of dendrites and functional spines are independent of synap

62 eased spine width and density at sites along dendrites and induction of mushroom-type spines.

63 teries but suffer from the growth of lithium dendrites and low Coulombic efficiency.

64 bserved that FTO is expressed in the nuclei, dendrites and near dendritic spines of mouse dorsal hipp

65 of CCL4 and concomitantly protects neuronal dendrites and pre-synaptic terminals in cortex and hippo

66 showed healthier neurons with thick, uniform dendrites and reduced numbers of activated astrocytes.

67 The reaction between lithium dendrites and silica nanoparticles consumes the dendrite

68 nd adducin, an actin-capping protein, in the dendrites and soma of cultured hippocampal neurons at di

69 er the subheading 'Ca(2+) activity in single dendrites and somata of L5 neurons', the final sentence

70 0.02 mum(2) ), and these terminals contacted dendrites and somata that were significantly larger (1.9

71 significantly higher than the stiffnesses of dendrites and somata.

72 late in recycling endosomes (REs) located in dendrites and spines before reaching the plasma membrane

73 CH axon terminals compared to SR, and in SR dendrites and spines compared to CH.

74 hat (1) GAD-positive terminals mainly target dendrites and spines in the perisomatic neuropil of CG n

75 tween axon terminals of CH and SR or between dendrites and spines of CH and SR.

76 te forward secretory trafficking in neuronal dendrites and spines through a specialized GA-independen

77 and SR axon terminals and between CH and SR dendrites and spines.

78 1 (0.1%) had delayed epithelial healing with dendrites, and 3 (0.4%) had recurrent epithelial defects

79 etermine the signaling patterns in CA1 soma, dendrites, and axons associated with place field formati

80 to investigate the dense meshwork of axons, dendrites, and synapses that form neuronal circuits.

81 NRG2 accumulates on cell bodies and proximal dendrites, and that NMDAR activity is required for shedd

82 ronal communication occurs through axons and dendrites, and the time required for such communication

83 [Cdh1 conditional knockout (cKO)], disrupts dendrite arborization and causes dendritic spine and syn

84 sk variant showed altered MIR137 expression, dendrite arborization, and synapse maturation.

85 model we demonstrate abnormal development of dendrite arbors and dendritic spines in newly generated

86 and the corresponding length of the sensory dendrites are best correlated to tonotopic frequency rep

87 Understanding how active dendrites are exploited for behaviorally relevant comput

88 attenuation properties in the Mauthner cell dendrites arising at least partly from differences in ca

89 s in cone axon terminals and horizontal cell dendrites as well as glutamate release in the outer plex

90 h auditory efferent neuronal cell bodies and dendrites, as well as unlabeled axon terminals, which, i

91 lum (ER) that elaborate throughout the soma, dendrites, axon and presynaptic terminal.

92 Smaller ER-PM contacts occurred throughout dendrites, axons, and in axon terminals.

93 d inhibitory postsynaptic currents in distal dendrites better than GIRK2a.

94 BAergic and cholinergic synaptic drive shift dendrites between different input domains of one postsyn

95 by thinning and fragmentation at the tips of dendrite branches, leading to shortening or removal of d

96 KO mice we identified an increased number of dendrite branching points in CA1 and CA2 hippocampal neu

97 glutamate receptors induces varicosities in dendrites but not in axons.

98 ture neurites and to differentiate them into dendrites, but the existence and nature of this inhibito

99 Such 1D MPS was also observed in dendrites, but the extent to which it exists and how it

100 ify a subset of mRNAs that are translated in dendrites by neuronal ribosomes.

101 1/GABAA receptor signaling pathway of ON-cBC dendrites by the ambient light level facilitates detecti

102 itic arborization results from retraction of dendrites by thinning and fragmentation at the tips of d

103 ically-driven reaction-diffusion pathways on dendrites can perform sequence discrimination on behavio

104 aradigm for interphase design to address the dendrite challenge, paving the way for the development o

105 eferred growth directions of magnesium alloy dendrite change as the type and amount of solute element

106 Moreover, those MF signals arriving onto the dendrite closest to the axon will generate greater CGC e

107 Thus, researchers frequently employ axon-dendrite colocations as proxies of potential connections

108 electrophysiological differences between the dendrites combine to produce stronger attenuation of vis

109 The sensory dendrite contains a ciliary root with a pronounced cross

110 Whether active dendrites contribute to the generation of the dual tempo

111 spatial arrangement of synaptic inputs onto dendrites could play a significant role in cortical comp

112 synchronized excitatory inputs at the distal dendrites could trigger plateau potentials in SPNs.

113 Our findings indicate apical dendrite degeneration as a novel cellular pathology that

114 er's disease (AD), and found profound apical dendrite degeneration of Betz cells in both fALS and sAL

115 found labeling for all three Nav subtypes on dendrites, dendritic spines, and axon terminals, but the

116 em imaging yielded a strong correlation with dendrite density but none of the other parameters includ

117 We found that the dendrite destabilizer Rho protein kinase 2 (Rock2), whic

118 As neuronal dendrites develop, they acquire cell-type-specific featu

119 These mice enable the study of D1-MSN dendrite development in wildtype mice, and its degenerat

120 ncluding neural progenitor proliferation and dendrite development of newborn neurons in the DG.

121 rosophila neurological function and possibly dendrite development.

122 racellular domain is required for regulating dendrite development.

123 This diminishes the formation of dendrites during cycling, and thus Sn4P3 is a relatively

124 bcellular structures that sprout on neuronal dendrites during neurogenesis.

125 hermore, this Golgi-associated mechanism for dendrite establishment might be impaired in a human gene

126 lular levels, adrenergic signaling increases dendrite excitability, but the underlying mechanisms rem

127 rmore, thalamic boutons in M1 targeted spiny dendrites exclusively, whereas approximately 9% of synap

128 As RBC dendrites expand, they form fewer multi-PSD contacts wit

129 Both the outer and inner stratifying dendrites express postsynaptic density (PSD95) immunorea

130 subset of SGNs with type II-like peripheral dendrites extending beneath OHCs.

131 The only OSN dendrite extends to the surface forming a knob projectin

132 s using our system reveals roles for glia in dendrite extension.

133 rons that form a scaffold on which ooDSGC ON dendrites fasciculate.

134 olyte and, for fundamental reasons, inhibits dendrite formation and growth.

135 SEI not only mechanically suppresses lithium dendrite formation but also promotes homogeneous lithium

136 benefit of magnesium is the apparent lack of dendrite formation during charging which is one of the c

137 ed similar defects in Golgi localization and dendrite formation in adult-born neurons.

138 lopmental stages relevant for axon guidance, dendrite formation, and synaptogenesis.

139 n with carbonate electrolytes and suppresses dendrite formation, enabling dendrite-free and stable cy

140 lectrodes, namely high reversibility without dendrite formation, low reduction potentials, and high s

141 peration (100% Coulombic efficiency) with no dendrite formation.

142 Golgi mislocalization and extensive aberrant dendrite formation.

143 s also necessary for motor axonal branch and dendrite formation.

144 icularly the later stages of axon branch and dendrite formation.

145 ode and lithium metal and eliminates lithium dendrite formation.

146 without undergoing passivation or macroscale dendrite formation.

147 and suppresses dendrite formation, enabling dendrite-free and stable cycling over 300 cycles with cu

148 to co-deposit with lithium ions and produce dendrite-free lithium deposits.

149 ighly optimized methods to trace impregnated dendrites from bright-field microscopy images that enabl

150 w neurons develop a single axon and multiple dendrites from common immature neurites.

151 ons work in combination to protect axons and dendrites from mechanical stress and propose that defect

152 the neuronal cytoskeleton protects axons and dendrites from mechanical stress, exploiting mutations i

153 Analysis of unlabeled putative MC dendrites further revealed gap junctions distributed uni

154 stinction between two compartments, axon and dendrite, generates cellular domains that differ in memb

155 rocally reinforcing maintenance of an intact dendrite geometry and a functional synapse-to-nucleus co

156 y uncovers a reciprocal relationship between dendrite geometry, the ability to generate nuclear calci

157 with intact Drosophila larvae, we found that dendrites grow into HSPG-deficient areas but fail to sta

158 Under bending conditions, the Li-dendrite growth can be further aggravated due to bending

159 different transmitter classes locally direct dendrite growth in a competitive manner.

160 ording a promising route to suppress lithium dendrite growth in lithium metal-based batteries.Lithium

161 ical for endosome maturation, viability, and dendrite growth of neurons in vivo.

162 Mechanical suppression of dendrite growth through solid polymer electrolytes (SPEs

163 f the Li anode, resulting in side reactions, dendrite growth, and poor electrodeposition behavior, wh

164 Therefore, synaptic input locally directs dendrite growth, but intra-neuronal dendrite redistribut

165 adult-born DG granule cells, Sema7A promotes dendrite growth, complexity and spine development throug

166 Nevertheless, excessive dendrite growth, infinite relative dimension change, sev

167 al performance and have a large influence on dendrite growth.

168 nd dendrites, where it accelerated spine and dendrite growth.

169 wing to its high reactivity and uncontrolled dendrite growth.

170 are promising candidates to address both the dendrite-growth and electrolyte-consumption problems inh

171 xpression levels control the pruning of GnRH dendrites, highlighting an unexpected role for a vesicul

172 oulombic efficiency and formation of lithium dendrites hinder its practical application.

173 The ventral CA1 dendrites, however, can generate plateau potentials in r

174 , the Shepherd's crook neuron (SCN), extends dendrites in both input regions.

175 nes within layer II and III pyramidal neuron dendrites in Brodmann area 46 dorsolateral prefrontal co

176 We observe that dendrites in carbonate-based electrolytes grow along the

177 oteins to cargo in real time within axons or dendrites in hippocampal neurons.

178 Ascending interneurons with dendrites in matching layers of the nerve cord send axon

179 rior and posterior Wave neurons extend their dendrites in opposite directions to receive somatosensor

180 for clustering AMPARs at endocytic zones in dendrites in response to NMDAR stimulation and for conse

181 mory extinction requires output neurons with dendrites in the alpha and alpha' lobes of the mushroom

182 er glutamatergic synapses depolarize TH cell dendrites in the inner plexiform layer and these depolar

183 In contrast, dendrites in untreated retinae degenerated slowly after

184 ) in mouse retina acquire their bistratified dendrites, in which responses to light onset and light o

185 dynein efficiently navigates both axons and dendrites; in both compartments, dynamic microtubule plu

186 ptors located on ON-center cone bipolar cell dendrites increases the expression and activity of GABAA

187 LC11 dendrites innervate multiple layers of the lobula, and e

188 assessing microstructural myelin, axonal and dendrite integrity in lesional and normal-appearing tiss

189 in the superficial and central areas extend dendrites into the optic tract, suggesting a predominant

190 d that some melanopsin ganglion cells extend dendrites into the outer retina.

191 Translation in dendrites is believed to support synaptic changes during

192 membrane, although their presence at distal dendrites is controversial.

193 icient transport of cargoes within axons and dendrites is critical for neuronal function.

194 lcium activity in populations of neocortical dendrites is increased and synchronised during oscillati

195 In Satb1 mutant mice, ooDSGC dendrites lack ON arbors, and the cells selectively lose

196 um (ER) supports dendritic translation, most dendrites lack the Golgi apparatus (GA), an essential or

197 pposite where visual PSPs invade the lateral dendrite (LD).

198 orm the normal extent of axonal branches and dendrites leading to decreased motor function.

199 to lower order solid species in the form of dendrite-like structures on the edge sites of TMDs have

200 c pathway that can be targeted to ameliorate dendrite loss in pathological conditions.

201 of the nuclear calcium target gene VEGFD, a dendrite maintenance factor, leads to reduced-complexity

202 Our results suggest that active dendrites may therefore constitute a key cellular mechan

203 In dendrites, mitochondrial structure is closely linked to

204 ccessory protein like 1 (IL1RAPL1) regulates dendrite morphology of mice hippocampal neurons and indu

205 electrophysiological membrane properties and dendrite morphology, studied in vivo, play a role in sel

206 ansporter GLT-1 and to attenuated changes in dendrite morphology, synaptic strength, and NMDAR-depend

207 acterized the role of IL1RAPL1 in regulating dendrite morphology.

208 L1RAPL1 mediates the activity of IL-1beta on dendrite morphology.

209 L1RAPL1 mediates the activity of IL-1beta on dendrite morphology.

210 i deposition/dissolution under the skin in a dendrite/moss-free manner.

211 ce factor, leads to reduced-complexity basal dendrites of CA1 neurons, which severely compromises the

212 naptic interactions between apical and basal dendrites of CA1 pyramidal neurons in mouse hippocampal

213 nduces varicosities in the axons but not the dendrites of central neurons by activating TRPV4, a Ca(2

214 und to be unevenly clustered on the soma and dendrites of dopamine neurons within the substantia nigr

215 found that the Ca(2+) signals recorded from dendrites of dorsal horizontal cells were dominated by M

216 tance for most neurological disorders, where dendrites of each neuronal population are densely interm

217 n axis and the second being a sphere made of dendrites of germanium in silicon.

218 ced dendritic arborization within the apical dendrites of hippocampal cornu ammonis 1 and granule cel

219 sed CaV1.2 distributes in clusters along the dendrites of hippocampal neurons.

220 recorded light-evoked Ca(2+) responses from dendrites of individual GACs infected with GCaMP6s in mo

221 ed cortical networks are arranged within the dendrites of individual neurons remains unclear.

222 ed loss of dendritic spines along the apical dendrites of layer (L) 5 pyramidal neurons (PNs) in the

223 We show that dendrites of medial entorhinal cortex neurons are highly

224 The dendrites of neighboring LC11s encode object motion reti

225 Local protein synthesis occurs in axons and dendrites of neurons, enabling fast and spatially restri

226 pproximately 9% of synapses were formed with dendrites of smooth neurons in S1.

227 G-dependent pathway that specifically allows dendrites of space-filling neurons to innervate all targ

228 We used DiOlistic labeling to visualize the dendrites of SPNs selectively labeled for complexin-3.

229 ssion and activity of GABAA receptors on the dendrites of the cells and that surround light responses

230 dent membrane specialization in neighbouring dendrites of the Mauthner cell, we report cross-modal de

231 In these mice, dendrites of the remaining RBCs expand in graded fashion

232 increases arborization and spines of apical dendrites of these neurons in a D1 receptor-dependent ma

233 n induce currents, and cause degeneration of dendrites on murine hippocampal neurons, effects that en

234 Repeated imaging of the same dendrites over 3 weeks enabled longitudinal experiments

235 e separator that slows the growth of lithium dendrites penetrating into the separator is produced by

236 calized exclusively on the soma and proximal dendrites, placing them in a good location to influence

237 pproximately 7 d after birth, with a primary dendrite pointing to the molecular layer, but at this st

238 new feature of neuronal polarity: axons and dendrites preferentially respond to physical and chemica

239 hich target the very distal pyramidal neuron dendrites, provide an unusually strong excitatory drive

240 tory and visual information via two separate dendrites, providing a privileged scenario for in vivo e

241 t each arm of the LPLC2 cross-shaped primary dendrites ramifies in one of these layers and extends al

242 directs dendrite growth, but intra-neuronal dendrite redistributions limit morphological variability

243 nt to which it exists and how it develops in dendrites remain unclear.

244 a loss of a cytoskeletal mechanism in distal dendrites required for dendrite stabilization and arbor

245 ites of the retinal ganglion cell bodies and dendrites, respectively.

246 t putative excitatory inputs cluster at T4's dendrite shafts, while inhibitory inputs localize to the

247 red protection against mutant LRRK2-elicited dendrite shortening, as did inhibiting MCU-mediated calc

248 feature of principal neurons, where tapering dendrites show an inverse distribution of spine size and

249 Dendrite size and morphology are key determinants of the

250 y which input synapse numbers are matched to dendrite size, and by which synaptic inputs from differe

251 ematic co-variation in synapse number and PN dendrite size, suggesting total synaptic conductance is

252 vate multiple layers of the lobula, and each dendrite spans enough columns to sample 75 degrees of vi

253 l mechanism in distal dendrites required for dendrite stabilization and arbor outgrowth.

254 o brain regions with laminar organization of dendrites such as the hippocampus or cerebellum.

255 slation, has been shown to be enriched in NL dendrites, suggesting its potential role in the structur

256 -dependent membrane specialization in M-cell dendrites suited for processing stimuli of different tim

257 Local translation in dendrites supports memory by providing necessary protein

258 owth to provide uniform surface coverage and dendrite suppression, respectively, thereby enabling the

259 rts beta2 signaling to remove Kv1.1 from the dendrite surface.

260 rolonged in networks of neurons by including dendrites.Synaptic plasticity is the neuronal mechanism

261 cific transcription factor that instructs PN dendrite targeting.

262 We interpret these inputs as dendrite-targeting excitation and soma-targeting inhibit

263 ipulations in behaving animals, we show that dendrite-targeting somatostatin (SOM) interneurons are c

264 slower and forms with a lower propensity in dendrites than in axons.

265 ps substantially more slowly in the soma and dendrites than the development of the 1D MPS in axons.

266 dritic spines are protrusions along neuronal dendrites that harbor the majority of excitatory postsyn

267 c spines are small protrusions from neuronal dendrites that make synapses with axons of other neurons

268 gy, consisting of a single axon and multiple dendrites that persist throughout adulthood.

269 M1 and displaced M1 (M1d) cells have dendrites that ramify within the outermost layer of the

270 ely branching central processes (presumptive dendrites) that together extended up to 2 mm dorsally in

271 l link of spindles in the cortex specific to dendrites, the main site of synaptic plasticity.Differen

272 hrough synaptic connection between axons and dendrites, therefore the neuronal connectivity map not o

273 put from entorhinal cortex onto their distal dendrites, these inputs produce a 5- to 6-fold larger EP

274 han in a free medium whereas inside neuronal dendrites this retardation is 70%.

275 e head is through rapid diffusion out to the dendrite through the spine neck with a half-removal time

276 her secretory cargo is locally trafficked in dendrites through a non-canonical pathway remains a fund

277 xcessive MT growth and collapse occur at the dendrite tip, resulting in the formation of aberrant MT

278 Li consumption and much larger curvature of dendrite tips that leads to an enhanced electric driving

279 neuronal types: different PN classes target dendrites to distinct olfactory glomeruli, while PNs of

280 Rod bipolar cells extend their dendrites to form new synapses with healthy rod photorec

281 -clamp recordings from rat TC and TRN neuron dendrites to measure bAPs directly.

282 and translocation of CRTC1 from the cytosol/dendrites to the nucleus of hippocampal neurons in the m

283 in their receptive fields with evenly spaced dendrites to uniformly sample sensory or synaptic inform

284 ve phases for bSC dendritogenesis: orienting dendrites toward TCAs, adding de novo dendritic segments

285 ne potential (DMP) from putative distal-most dendrites using tetrodes in freely behaving rats over mu

286 ause auditory evoked PSPs invade the ventral dendrite (VD), as well as the opposite where visual PSPs

287 SPs are maintained during propagation in the dendrites, we made dendritic and somatic whole-cell reco

288 onstructions to quantify polyribosomes in LA dendrites when consolidation was blocked by the cap-depe

289 reconstructions to examine polyribosomes in dendrites when memory formation was blocked by an inhibi

290 u) was partially retained in cell bodies and dendrites, where it accelerated spine and dendrite growt

291 nce, it is necessary to record from neuronal dendrites, which can generate dendritic action potential

292 Bar(CRH) neurons have unexpectedly long dendrites, which may receive synaptic input from the cer

293 Its neurons have bipolar extension of dendrites, which receive segregated inputs from two ears

294 ost lateral neuropil corresponding to distal dendrites while gephyrin puncta are enriched on neuronal

295 at the soma before backpropagating into the dendrites while undergoing substantial distance-dependen

296 ous EPSP amplitudes increased sharply in the dendrite with distance from the soma (length constant, 5

297 ps into a DGC, consisting of a single apical dendrite with further branches, remains largely unknown.

298 The proportion of dendrites with synaptic input increased from 50% to 80%

299 are predominantly located in pyramidal cell dendrites within the cortex.

300 c terminals, and postsynaptically, at apical dendrites, without inhibiting the soma.