ライフサイエンスコーパス: arborization

1 E6AP leads to significant loss of dendritic arborization.

2 y of dendritic spines via regulating F-actin arborization.

3 creases mTOR signaling and promotes dendrite arborization.

4 longation and, to a lesser extent, dendritic arborization.

5 gical defects, including excessive dendritic arborization.

6 pecific circuit motif by modulating neuronal arborization.

7 elongation, but was associated with enhanced arborization.

8 mTOR signaling and increases their dendrite arborization.

9 acellular Ca(2+) concentration and dendritic arborization.

10 ron for both synapse formation and dendritic arborization.

11 cal neurons significantly increases dendrite arborization.

12 nd aorta consist of sinusoids without normal arborization.

13 euroinflammation and enhanced host dendritic arborization.

14 activity of FAK and of PKC disrupts dendrite arborization.

15 t signaling pathway that restricts dendritic arborization.

16 ise control of axon outgrowth, guidance, and arborization.

17 wth including extensive dendritic and axonal arborization.

18 with animal studies of changes in dendritic arborization.

19 C456S channels promoted dendritic growth and arborization.

20 nule localization, causes similar defects in arborization.

21 and to increase local signaling to regulate arborization.

22 ak function of NHE6 is required for neuronal arborization.

23 evelopment by promoting dendritic growth and arborization.

24 sis, neuronal differentiation, and dendritic arborization.

25 , exogenous BDNF rescues defects in neuronal arborization.

26 s NDL PCB-enhanced RyR activity to dendritic arborization.

27 velo mutant axons also display defects in arborization.

28 nces including differences in axonal density/arborization.

29 tion specificity and BDNF-dependent dendrite arborization.

30 spine formation without effect on dendritic arborization.

31 l neurons exhibit severely reduced dendritic arborization.

32 limbic cortex and prelimbic cortex dendritic arborization.

33 kinase substrate, a PKC target that promotes arborization.

34 xtended dendritic length with a more complex arborization.

35 al neurons and promote their lamina-specific arborization.

36 ivity via RyR-dependent effects on dendritic arborization.

37 ase Tao as a negative regulator of dendritic arborization.

38 lly in the environment for normal motor axon arborization.

39 nce input structure throughout the dendritic arborization.

40 ther with its Rac1-GAP activity to terminate arborization.

41 ubstantial reduction in axonal outgrowth and arborization.

42 BAI1 as an important regulator of dendritic arborization.

43 y outgrowth, selective routing, and terminal arborization.

44 onal migration, axon guidance, and dendritic arborization.

45 synaptically targeted and promotes dendritic arborization.

46 erminal domains leads to simplified neuronal arborization.

47 arge neuron populations by their wide axonal arborizations.

48 sized cortical columns, or limited dendritic arborizations.

49 ely to explain the unique patterns of axonal arborizations.

50 nputs paralleled by differences in dendritic arborizations.

51 ct molecular identities and patterning their arborizations.

52 hat molecules shape it throughout the axonal arborization?

53 These processes facilitate dendritic arborization(2,3), prevent formation of autapses(4) and

54 ic phenotypes and regulation of cytoskeletal arborization(3,4).

55 stic reduction in the complexity of neuronal arborization, affecting both axonal and dendritic outgro

56 ewborn neurons had longer dendrites and more arborization after MR imaging-guided focused ultrasound,

57 s protected neurons and maintained dendritic arborization after oxygen-glucose deprivation.

58 and physiological properties such as axonal arborization and action potential amplitude of individua

59 demonstrate a dramatic reduction in synaptic arborization and active zone number at NMJs following C9

60 IL2 bipolar sensory neurons undergo dendrite arborization and axon remodeling during dauer developmen

61 nditional knockout (cKO)], disrupts dendrite arborization and causes dendritic spine and synapse loss

62 og KPC-1 is required for dauer IL2 dendritic arborization and dauer-specific nictation behavior.

63 ion of CaMKIIalpha-E183V increases dendritic arborization and decreases both dendritic spine density

64 ckdown in cortical neurons impairs dendritic arborization and dendrite self-avoidance.

65 d known normal expansions in basal dendritic arborization and dendritic spine pruning during the tran

66 Although dendritic arborization and densities of excitatory presynaptic ter

67 t THBS4 and SPARCL1 both increased dendritic arborization and doubled synapse numbers in cultured neu

68 ) in astrocytes mimicked LPS-induced process arborization and elongation, while application of a NF-k

69 er injury, transient hypoxemia disrupted SPN arborization and functional maturation during a critical

70 were accompanied by a decrease in dendritic arborization and increased proportions of immature filop

71 nk between release site development and axon arborization and introduce a novel mechanism that govern

72 remains arduous when the neuron has complex arborization and long projection.

73 of G(PFC)E mice relate to sparser dendritic arborization and lower spine density.

74 rim9 similarly exhibited excessive dendritic arborization and mislocalization of cell bodies in vivo

75 are largely driven by their different axonal arborization and myelination profiles.

76 architectural processes, including dendritic arborization and neuronal density decreases, were inferr

77 We show that postembryonic arborization and neurosecretory terminal targeting of th

78 neurons to regulate dauer-specific dendritic arborization and nictation.

79 sential role for the development of neuronal arborization and of dendritic spines independent of syna

80 By virtue of their extensive axonal arborization and perisomatic synaptic targeting, cortica

81 ne cortex, and increases both pyramidal cell arborization and PSD-95 expression in the cortex of WT b

82 rol, such as: less synapses, lower dendritic arborization and reduced spine density.

83 dult stages for maintaining normal dendritic arborization and sensory function to regulate escape and

84 al organization to maintain proper dendritic arborization and sensory function, providing a strong li

85 ncentration-dependent increases of dendritic arborization and soma size in both mouse and human cultu

86 M) for 72 hours in vitro increased dendritic arborization and soma size in primary cultures.

87 gi-Cox stained tissue, we compared dendritic arborization and spine density of prelimbic layer III ne

88 uced a cell-autonomous decrease in dendritic arborization and spine development in pyramidal neurons,

89 neuron morphogenesis by regulating dendrite arborization and spine formation during cortical circuit

90 Cdc42 to promote neuronal growth, dendritic arborization and spine formation.

91 es during a time of robust cortical dendrite arborization and spine formation.

92 s displayed a marked impairment in dendritic arborization and spine growth.

93 CA3 region and it is required for dendritic arborization and spine morphogenesis in hippocampal neur

94 imensional imaging and analysis of dendritic arborization and spine morphometry.

95 imensional imaging and analysis of dendritic arborization and spine morphometry.

96 eurogenesis and the development of dendritic arborization and spines in the dentate gyrus, in which n

97 er II/III pyramidal neurons, S-SDS increases arborization and spines of apical dendrites of these neu

98 Dendrite arborization and synapse formation are essential for wir

99 elated developmental alteration in dendritic arborization and synapse formation, our findings provide

100 n the developing brain, such as in dendritic arborization and synapse formation.

101 lacking protocadherin-alpha showed defective arborization and synaptic density of prefrontal cortex c

102 th encodes regionally differential dendritic arborization and synaptic formation.

103 rodevelopmental processes, including neurite arborization and the regulation of neurogenesis.

104 tory cascade is temporally required for 5-HT arborization and upregulation of the 5-HT axon arborizat

105 SERT were delivered to the extensive axonal arborizations and accumulated in bouton-like structures.

106 SP4 leads to cell-autonomous feminization of arborizations and loss of courtship in the dark.

107 ulator differed, with 5-HT exhibiting denser arborizations and TH-ir processes being sparser.

108 abnormal spine morphology, reduced dendritic arborization, and extensive dendritic varicosities in th

109 ts, including muscle targeting and dendritic arborization, and in a highly specific walking defect in

110 SALM1 on the cell surface affects dendritic arborization, and intracellular motifs regulate its dend

111 the analysis of synaptic density, dendritic arborization, and neurogenesis.

112 processes including axon guidance, dendrite arborization, and synapse formation.

113 which can influence the sprouting response, arborization, and synapse formation.

114 t showed altered MIR137 expression, dendrite arborization, and synapse maturation.

115 stimulation of neurite outgrowth, dendritic arborization, and synaptogenesis all exhibited bidirecti

116 beginning with specification, outgrowth, and arborization, and terminating with formation and maturat

117 CNTN4/APP in promoting target-specific axon arborization, and they highlight the importance of this

118 Axonal branching and terminal arborization are fundamental events during the establish

119 re mutant, errors in both dendritic and axon arborizations are observed.

120 yramidal neuron spine turnover and dendritic arborization as a function of age in transgenic mice exp

121 pression reduces the complexity of dendritic arborization, associated with altered electrophysiologic

122 e apical dendrites show a complex transverse arborization at the level of layer 7.

123 born neurons resulted in truncated dendritic arborization at the time of synaptic integration.

124 nic stem cells, directly increased dendritic arborization, augmented synapse numbers, doubled dendrit

125 hway promotes cortical neuron basal dendrite arborization but also repels axons.

126 fects chromatin ultrastructure and dendritic arborization, but alters cognitive skills rather than mo

127 ate that both Pcdh18b and Nap1 regulate axon arborization by affecting the density of filopodia along

128 RNAi screen in Drosophila class IV dendritic arborization (C4da) neurons and identified the conserved

129 pruning using Drosophila class IV dendritic arborization (c4da) neurons as a model.

130 e, dendrites of Drosophila class IV dendrite arborization (C4da) neurons grow synchronously with thei

131 n blunts mossy fiber sprouting and dendritic arborization caused by ECS.

132 The mutation causes a proximal shift in arborization coincident with decreased beta-spectrin loc

133 ic restraint stress also increased dendritic arborization, complexity and spine density of pyramidal

134 ichrochaetes, neurons with shorter dendritic arborization (DA) and reduced complexity, diminished lar

135 dendritic surface of the polymodal dendritic arborization (da) neuron of the Drosophila peripheral ne

136 Using Drosophila dendritic arborization (da) neurons as a model, we identified the

137 n sense harsh or gentle touch with dendritic arborization (da) neurons in the body wall and can detec

138 Drosophila dendritic arborization (da) neurons lack centrosomes and therefore

139 r to regulate the morphogenesis of dendritic arborization (da) neurons of the Drosophila larval perip

140 Using Drosophila class IV dendritic arborization (da) neurons we test in vivo the effects of

141 hing of Drosophila larval class IV dendritic arborization (da) neurons, but their specific regulatory

142 By studying the Drosophila dendritic arborization (da) neurons, we discovered a role of the d

143 e we show that Drosophila class IV dendritic arborization (da) neurons, which tile the larval body wa

144 ized in Drosophila larval class IV dendritic arborization (da) neurons.

145 s that the dendrites of Drosophila dendritic arborization (da) sensory neurons are properly restricte

146 (tricluster deletion) led to a severe axonal arborization defect and loss of self-avoidance.

147 ame S922A construct can also rescue dendrite arborization defects in gamma-Pcdh null neurons cell aut

148 ermore, kat80 depletion results in dendritic arborization defects in sensory and motor neurons, affec

149 by ALA/ALC was accompanied by a reversal of arborization deficits in SCZ cINs.

150 thways that regulate Purkinje cell dendritic arborization downstream of mutant TRPC3, we employed tra

151 increased dosage of Ube3A/E6AP in dendritic arborization during brain development.

152 riched RhoGAP, plays a key role in dendritic arborization during early neuronal development in the ne

153 x puzzle in neurons with extensive dendritic arborization, encompassing a combinatorial diversity of

154 with somata in the pars intercerebralis and arborizations extending throughout the brain and ventral

155 ns as they establish laminar and retinotopic arborization fields within the same region of neuropil.

156 borization and upregulation of the 5-HT axon arborization gene, Protocadherin-alphac2, during postnat

157 Dendritic arborization (Golgi Sholl analyses), spine morphology, a

158 nated axons: (1) branches of a single axonal arborization have variable AP waveforms independent of m

159 itive gene expression and promotes dendritic arborization in a nuclear Ca(2+)-dependent manner.

160 rtners, many have a high percentage of their arborization in adjacent segments, and many have branche

161 nal morphology, dendritic spine density, and arborization in brain cortex subjected to Plasmodium ber

162 nts) leads to a further increase of terminal arborization in certain NGF-rich peripheral tissues.

163 nflux through L-VGCCs and inhibits dendritic arborization in cultured rat cortical neurons and in the

164 c spines and allostatic atrophy of dendritic arborization in early adulthood.

165 analysis of MSNs revealed increased neuronal arborization in GPRIN3 KO and modified passive and activ

166 We found increased dendritic arborization in isolated cortical pyramidal neurons from

167 afish pcdh18b is involved in regulating axon arborization in primary motoneurons.

168 ng cascades, and enhancement of axodendritic arborization in rat immortalized hippocampal neurons, mo

169 risk gene Taok2, as a regulator of dendritic arborization in sensory neurons.

170 ases are required for axon specification and arborization in subsets of mouse neurons.

171 Here we explore: (a) if dendritic arborization in the amygdala follows the pattern of prot

172 ype 4 bipolar cells, had defects in dendrite arborization in the Dscam mutant retina, whereas other c

173 buted throughout the cell body and dendritic arborization in the GL, but, at P20, when the glomerular

174 Because of their arborization in the lobula complex, we called these cell

175 as relatively delayed maturation of neuronal arborization in the prefrontal cortex compared with sens

176 mediate a later stage of axon development - arborization in the target field.

177 amics of RNA and LPS in retinal axons during arborization in vivo.

178 atment with a PKC activator reduces dendrite arborization in wild-type cortical neurons.

179 lusters of labeled neurons and terminal axon arborizations in area 1.

180 V/VI, and are characterized by dense axonal arborizations in layer I.

181 wever, the size and complexity of the axonal arborizations in non-SCN regions are less elaborate than

182 ensive filigree of TH-immunoreactive (TH-ir) arborizations in the appendage neuromeres, as well as th

183 er, ESNP-derived neurons formed dense axonal arborizations in the inner molecular layer and throughou

184 ear the esophageal foramen that gave rise to arborizations in the protocerebral bridge.

185 cluster (mcPNs) predominantly have dendritic arborizations in the sexually dimorphic macroglomerular

186 in sets of genetically defined neurons with arborizations in the targeted layers.

187 appeared to exhibit "basket-like" dendritic arborizations in two MGC compartments and made connectio

188 ity exists in AP waveforms across the axonal arborization independent of axon morphology.

189 Their dendritic arborizations indicate selective connectivity with low-f

190 Impaired terminal arborization is accompanied by a reduction in the streng

191 presynaptic puncta, suggesting that reduced arborization is accompanied by increased synaptogenesis

192 Dendritic arborization is highly regulated and requires tight cont

193 a complete analysis of itch-sensing terminal arborization is missing.

194 Neuronal arborization is regulated by cell-autonomous and nonauto

195 f a signaling pathway important for dendrite arborization is regulated.

196 atures including characteristic size, shape, arborization, location and synaptic patterns.

197 own to regulate the development of dendritic arborization, much less is known about the mechanisms th

198 unction of the UPS during class IV dendritic arborization neuron dendrite pruning and link the UPS to

199 ies, here we report that class III dendritic arborization neurons are touch sensitive and contribute

200 val Drosophila peripheral class IV dendritic arborization neurons degenerate during metamorphosis in

201 r for dendritic growth in class IV dendritic arborization neurons in the larva.

202 ckdown of RhoBTB in the Drosophila dendritic arborization neurons resulted in a decreased number of d

203 revious live imaging in Drosophila dendritic arborization neurons showed that while microtubules are

204 ry neurons, class III and class IV dendritic arborization neurons, tile the body wall.

205 organ and the peripheral class IV dendritic arborization neurons--to regulate light avoidance.

206 ions of Drosophila larval class IV dendritic arborization neurons.

207 Reduced pyramidal cell arborization occurs with stress and MDD, and may diminis

208 Furthermore, vmPFC DBS reversed CSDS-induced arborization of 5-HT dendrites in the DRN and increased

209 ar zone (SGZ) neuroblasts, and the dendritic arborization of adult-generated dentate gyrus neurons.

210 tical astroglia and found that developmental arborization of astroglial processes and expression of f

211 ate and quantitatively analyze developmental arborization of astroglial processes.

212 We observed unexpectedly large dendritic arborization of CA2/3 basket cells in stratum lacunosum

213 xpressing macrophages causing stellation and arborization of cell shape.

214 Sprouting and arborization of CGRP+TrkA+ sensory nerve fibers within t

215 ARID1B knockdown suppressed dendritic arborization of cortical and hippocampal pyramidal neuro

216 nt AP propagation failures across the axonal arborization of cultured rat hippocampal neurons (mixed

217 cerebellar slice cultures inhibits dendritic arborization of developing GCs, a critical step in circu

218 in the mouse results in decreased dendritic arborization of developing neurons.

219 icate the ability of ECS to induce dendritic arborization of differentiating granule cells as a relev

220 sed a significant reduction in the dendritic arborization of E11 motoneurons.

221 A2 expression had no effect on the dendritic arborization of E6 motoneurons.

222 ransmission; and (iv) the size and dendritic arborization of gastric-projecting DMV neurones was incr

223 Genetic deletion of Trim9 elevated dendritic arborization of hippocampal neurons in vitro and in vivo

224 1 is required by Sema3A to promote dendritic arborization of hippocampal neurons, and Sema3A regulate

225 The molecular mechanisms underlying the axon arborization of mammalian neurons are poorly understood

226 lts in reduction of motoneurons and aberrant arborization of motor axons.

227 ated only in the past 5 years that extensive arborization of nerve fibres has a dominant role in regu

228 Dendritic arborization of neurons is regulated by brain-derived ne

229 reduced the number, migration and dendritic arborization of newborn neurons.

230 re critical for achieving radially symmetric arborization of On starburst amacrine cell (SAC) dendrit

231 ibitory structure largely precedes dendritic arborization of primary motor neurons, suggesting that t

232 Cobl deficiency impaired proper dendritic arborization of Purkinje cells and led to low-complexity

233 tion, likely through dendritic outgrowth and arborization of Purkinje cells in the mouse cerebellum.

234 is processes, particularly for the postnatal arborization of Purkinje cells representing the source f

235 KPC-1 is also necessary for dendritic arborization of PVD and FLP sensory neurons.

236 the first description of the morphology and arborization of single corneal axons and identify three

237 ity of AMPA receptors regulate the dendritic arborization of spinal cord motoneurons during a critica

238 l period of development alters the dendritic arborization of spinal motoneurons in ovo.

239 ed in specific deficits in the extension and arborization of sympathetic fibers in their final target

240 ing to a temporal delay in the extension and arborization of the gland tree in mammary fat pads.

241 tion of Rumi in VSMCs results in progressive arborization of the IHBD tree, whereas deletion of Rumi

242 a marked loss of Purkinje cells and reduced arborization of the remaining ones.

243 Defects in arborization of these bipolar cells could not be attribu

244 ainst AstA, AT, and TK in the brain revealed arborizations of AstA- and TK-positive neurons in primar

245 mately 35,000), different from the dendritic arborizations of CA1 basket cells.

246 Dendritic arborizations of many neurons are patterned by a process

247 europil possesses four layers defined by the arborizations of such columnar inputs.

248 rotocerebrum that overlapped with the axonal arborizations of TH1-AC1.

249 The arborizations of the astrocytes can extend across neuron

250 d, but new clock cells differentiate and the arborizations of their axons increase in complexity, as

251 aspects (cell bodies, axon tracts, terminal arborization) of a lineage, we were able to describe pro

252 om sensory neurons can perturb either axonal arborization or nerve terminal maturation, depending on

253 y play a role in synaptic plasticity, axonal arborization, or functional diversity of the circuit.

254 led an altered colony growth, morphology and arborization pattern in LASP-1 knockdown cells.

255 We provide the first description of the arborization pattern of single corneal axons.

256 of the cell body, ascending axon, dendritic arborization pattern, and dye coupling, is highly simila

257 , are greatly influenced by the size, shape, arborization pattern, and location of its dendrites.

258 Dendritic arborization patterns are consistent anatomical correlat

259 glion (TG) display characteristic growth and arborization patterns during development.

260 fered in cell body shape and size, dendritic arborization patterns, and medial-lateral position withi

261 lize the morphology and properties of axonal arborization profiles obtained from publicly available a

262 sal (BA), amygdala possess complex dendritic arborizations, receive potent excitatory drive, and medi

263 sed axonal rewiring, and augmented dendritic arborization, resulting in long-term functional ameliora

264 The E6AP-dependent remodeling of dendritic arborization results from retraction of dendrites by thi

265 vity rhythms, including PDF accumulation and arborization rhythms in the small ventrolateral neuron (

266 eurones, increasing their size and dendritic arborization; RYGB did not reverse these morphological a

267 By minimizing gaps and overlaps within the arborization, self-avoidance facilitates complete covera

268 crb2b is required for podocyte foot process arborization, slit diaphragm formation, and proper nephr

269 lf-avoidance, synapse development, dendritic arborization, spine maturation, and prevention of apopto

270 R2 and ephrinB2 in vivo to control dendritic arborization, spine morphogenesis and hippocampal circui

271 amidal neurons are characterized by a unique arborization subdivided in segregated dendritic domains

272 morphologies with a variety of axon terminal arborizations subserving their functions.

273 Previous models of neuronal dendrite arborization suggested that contact-dependent self-avoid

274 alyses, and impaired mitochondrial function, arborization, synapse formation and synaptic GABA releas

275 ynaptic connectivity by increasing dendritic arborization, synapse formation, and synaptic transmissi

276 arly-life adversity on hippocampal dendritic arborization, synapse number and memory-function.

277 Variation in location of arborization territory for identified astrocytes was gre

278 hat are in part due to impoverished neuronal arborization that may be treatable by enhanced TrkB sign

279 ion; they also exhibited a very dense axonal arborization that overlapped the dendritic field.

280 larly showed defects in synaptic density and arborization that were reversed by inhibitors of protein

281 terations in both basal and apical dendritic arborization that were significantly associated with the

282 NPN axons, when stained, formed dense local arborizations that overlapped their dendritic fields to

283 yramidal neurons possess elaborate dendritic arborizations that receive functionally distinct inputs,

284 ely innervate hairy skin with large terminal arborizations that resemble the receptive fields of C-ta

285 striosomes form highly unusual bouquet-like arborizations that target bundles of ventrally extending

286 hort dendrites that formed a dense dendritic arborization; they also exhibited a very dense axonal ar

287 generate time-lapse movies of complex neural arborization through automated image registration.

288 ing pathway whereby Rem2 regulates dendritic arborization through interactions with Ca(2+)/calmodulin

289 hat target tissues exert control of terminal arborization through secretion of trophic factors.

290 ronal growth control programs tune dendritic arborization to ensure function is still not fully under

291 n impact of BDNF on plasticity and dendritic arborization, we complimented direct rCBF comparisons wi

292 Deficits in mitochondrial function and arborization were reversed by alpha lipoic acid and acet

293 and hippocampal neuronal cells and dendritic arborization, when evaluated at the above post-exercise

294 e an inhibitory component, and form terminal arborizations which are cell-type dependent, extensive,

295 ealed deficits in axonal growth and terminal arborization, which can be prevented by reintroduction o

296 downstream of TDP-43 that mediate dendritic arborization, which may provide potential new avenues fo

297 ity of acetylcholinesterase-positive process arborization, which was significantly increased when ana

298 enerated developmental deficits in dendritic arborization with concomitant sensory deficits.

299 ntinued to increase in density, showing axon arborizations with projections into the deeper muscle le

300 rexpression in adult mice enhanced dendritic arborization within the apical dendrites of hippocampal