ライフサイエンスコーパス: arborization

1 t signaling pathway that restricts dendritic arborization.

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

3 wth including extensive dendritic and axonal arborization.

4 with animal studies of changes in dendritic arborization.

5 C456S channels promoted dendritic growth and arborization.

6 nule localization, causes similar defects in arborization.

7 and to increase local signaling to regulate arborization.

8 ak function of NHE6 is required for neuronal arborization.

9 evelopment by promoting dendritic growth and arborization.

10 sis, neuronal differentiation, and dendritic arborization.

11 , exogenous BDNF rescues defects in neuronal arborization.

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

13 velo mutant axons also display defects in arborization.

14 nces including differences in axonal density/arborization.

15 tion specificity and BDNF-dependent dendrite arborization.

16 onal migration, axon guidance, and dendritic arborization.

17 spine formation without effect on dendritic arborization.

18 l neurons exhibit severely reduced dendritic arborization.

19 limbic cortex and prelimbic cortex dendritic arborization.

20 kinase substrate, a PKC target that promotes arborization.

21 xtended dendritic length with a more complex arborization.

22 al neurons and promote their lamina-specific arborization.

23 erminal domains leads to simplified neuronal arborization.

24 ivity via RyR-dependent effects on dendritic arborization.

25 lly in the environment for normal motor axon arborization.

26 nce input structure throughout the dendritic arborization.

27 enance, cell death in brain, and optic nerve arborization.

28 ptogenesis, neuronal polarity, and dendritic arborization.

29 romote filopodia during presynaptic terminal arborization.

30 d with the density of an identified neuron's arborization.

31 ocampal neurons, including reduced dendritic arborization.

32 E6AP leads to significant loss of dendritic arborization.

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

34 creases mTOR signaling and promotes dendrite arborization.

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

36 gical defects, including excessive dendritic arborization.

37 pecific circuit motif by modulating neuronal arborization.

38 elongation, but was associated with enhanced arborization.

39 mTOR signaling and increases their dendrite arborization.

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

41 ron for both synapse formation and dendritic arborization.

42 cal neurons significantly increases dendrite arborization.

43 nd aorta consist of sinusoids without normal arborization.

44 euroinflammation and enhanced host dendritic arborization.

45 activity of FAK and of PKC disrupts dendrite arborization.

46 ely to explain the unique patterns of axonal arborizations.

47 nputs paralleled by differences in dendritic arborizations.

48 ct molecular identities and patterning their arborizations.

49 ses of navigation, regeneration and terminal arborizations.

50 arge neuron populations by their wide axonal arborizations.

51 hat molecules shape it throughout the axonal arborization?

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

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

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

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

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

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

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

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

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

61 Although dendritic arborization and densities of excitatory presynaptic ter

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

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

64 atal maturation including abnormal dendritic arborization and impaired neuronal excitability.

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

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

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

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

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

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

71 s, axonal conduction block in the motor unit arborization and of variable axonal conduction.

72 modulating retinal ganglion cell (RGC) axon arborization and presynaptic differentiation.

73 horizontal cells exhibit aberrant dendritic arborization and reduced dendritic self-avoidance within

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

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

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

77 cing defects, indicating that DSCAM mediates arborization and spacing by acting within given cell typ

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

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

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

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

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

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

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

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

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

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

88 in neurons is required for normal dendritic arborization and surface expression of AMPA receptors.

89 Dendrite arborization and synapse formation are essential for wir

90 mined the contribution of netrin to RGC axon arborization and synapse formation at the target.

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

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

93 for the maintenance of established dendritic arborization and synapse number.

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

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

96 Arborizations and boutons within the ventrobasal complex

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

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

99 doublecortin, NeuN), the extent of dendritic arborization, and acquisition of mature cell body morpho

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

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

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

103 DA neurons survived at high numbers, showed arborization, and mediated functional effects in an anim

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

105 te-restricted VCX proteins, promoted neurite arborization, and shRNA-directed knockdown of the VCX ge

106 used a dramatic decrease in dendrite length, arborization, and spine density.

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

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

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

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

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

112 anced neuronal activity, increased dendritic arborizations, and reduced astroglial and microglial act

113 creased excitability and decreased dendritic arborization are associated with downregulation of inwar

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

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

116 adult hippocampal neurogenesis and neuronal arborization, are believed to play an important role in

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

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

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

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

121 ith DSCAM-dependent cell spacing and neurite arborization being mediated through homophilic binding c

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

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

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

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

126 PIKE(-/-) neurons, as the impaired dendritic arborization can be rescued when PI3K/Akt cascade is aug

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

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

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

130 s, and their characteristically dense axonal arborizations covered significant portions of the outer

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

132 s, the axons of certain Drosophila dendritic arborization (da) neurons are capable of substantial reg

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

134 ite pruning of Drosophila class IV dendritic arborization (da) neurons is induced by local caspase ac

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

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

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

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

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

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

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

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

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

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

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

146 These arborization defects occur particularly in late larval d

147 duces cell spacing, cell number and dendrite arborization defects.

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

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

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

151 l-type specific effects in shaping dendritic arborization during postnatal development.

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

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

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

155 or (BDNF), an important mediator of dendrite arborization, for 72 h but not for 24 h or less increase

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

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

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

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

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

161 Consistent segregation of intramuscular CN6 arborization in humans and monkeys suggests functionally

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

163 RF(1) occupancy negatively affects dendritic arborization in mouse organotypic slice cultures, simila

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

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

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

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

168 f a single "principal" glomerulus and sparse arborization in the core of other glomeruli.

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

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

171 eg motoneurons reach their sites of terminal arborization in the leg at the time when their dendrites

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

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

174 egulated PTEN is a key regulator of terminal arborization in vivo.

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

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

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

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

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

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

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

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

183 Their dendritic arborizations indicate selective connectivity with low-f

184 er and observing a segregation of subsequent arborization into superior zones that exhibited minimal

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

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

187 Neuronal arborization is regulated by cell-autonomous and nonauto

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

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

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

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

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

193 CA3) proteins in Drosophila larval dendritic arborization neurons caused neuronal type-specific dendr

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

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

196 ctedly, we found that the class IV dendritic arborization neurons of Drosophila melanogaster larvae r

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

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

199 isingly, after axons of Drosophila dendritic arborization neurons were severed, dendrites were more r

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

201 These class IV dendritic arborization neurons, which are present in every body se

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

203 ions of Drosophila larval class IV dendritic arborization neurons.

204 ic illumination activates class IV dendritic arborization neurons.

205 ption of the normally well ordered dendritic arborization occurs in Purkinje cells from beta-III(-)/(

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

207 rtance of a membrane fusogen in the dendrite arborization of a pair of highly-branched worm sensory n

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

209 tic approach to reduce anxiety and dendritic arborization of amygdaloid neurons of adult male Wistar

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 ARID1B knockdown suppressed dendritic arborization of cortical and hippocampal pyramidal neuro

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

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

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

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

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

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

221 This expression pattern approximates the arborization of ganglion cells (GC) with different tempo

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 Dendritic arborization of neurons is regulated by brain-derived ne

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

229 elopmental changes in the differentiation or arborization of nociceptive sensory neurons.

230 caine administration increases the dendritic arborization of nucleus accumbens neurons, but the under

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

232 showed a marked difference in the dendritic arborization of on-centre retinal ganglion cells in the

233 s and its ability to promote lamina-specific arborization of presynaptic and postsynaptic processes i

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

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

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

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

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

239 We first modeled the selective arborization of RGC axons, mediated by EphA/ephrin-A sig

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

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

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

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

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

245 ulations, nerve terminal sprouting, and poor arborization of the motor nerve terminals, whereas posts

246 Individual fills of HA-ir LNs revealed heavy arborization of the outer ring of a single "principal" g

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

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

249 fects in stereotypic lamina-specific neurite arborization of tyrosine hydroxylase (TH)-expressing dop

250 e by differential sculpting of the dendritic arborizations of an initial pyramidal morphology and tha

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

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

253 Dendritic arborizations of many neurons are patterned by a process

254 al) channels in the cell bodies and terminal arborizations of neurons that innervate the dental pulp

255 the sparse and extended axonal and dendritic arborizations of NPY-PLTS interneurons.

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

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

258 ltrastructural distribution of CHT in axonal arborizations of the mesopontine tegmental cholinergic n

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

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

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

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

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

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

265 Dendritic arborization patterns are consistent anatomical correlat

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

267 stablishment of cell type-specific dendritic arborization patterns is a key phase in the assembly of

268 how how visual function is determined by the arborization patterns of neuronal processes.

269 bipolar cells establish stereotypic neurite arborization patterns to form functional neural circuits

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

271 ed neurons, two-thirds of neurons' dendritic arborizations reached into at least one adjacent barrel

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

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

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

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

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

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

278 hila the dendrites of the class IV dendritic arborization sensory neuron ddaC undergo large-scale pru

279 t dendritic branches of Drosophila dendritic arborization sensory neurons can be positioned either at

280 Subsequent arborization showed a systematic topography, entering a

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

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

283 ent segregation of intramuscular motor nerve arborization suggests functionally distinct superior and

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

285 resulted in dose-dependent loss of dendritic arborization that was blocked with IFNalpha NAb treatmen

286 d highly branched dendritic and local axonal arborizations that contrasted sharply with the sparse an

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

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

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

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

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

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

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

294 pact of Notch signaling specifically on IHBD arborization, we studied the influence of both chronic g

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 enerated developmental deficits in dendritic arborization with concomitant sensory deficits.

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

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

300 deep orbit to the anterior extents of their arborizations within all four rectus EOMs in each orbit.