ライフサイエンスコーパス: dendritic arborization

1 on of neuronal migration, axon guidance, and dendritic arborization.

2 al connectivity via RyR-dependent effects on dendritic arborization.

3 igh-impedance input structure throughout the dendritic arborization.

4 tion, synaptogenesis, neuronal polarity, and dendritic arborization.

5 es in hippocampal neurons, including reduced dendritic arborization.

6 ns in vivo, and APP overexpression increased dendritic arborization.

7 ression of E6AP leads to significant loss of dendritic arborization.

8 a role in neuronal development by regulating dendritic arborization.

9 f nonstimulated kinase activity in enhancing dendritic arborization.

10 of Wnt-2, and expression of Wnt-2 stimulates dendritic arborization.

11 d axonal elongation and, to a lesser extent, dendritic arborization.

12 neurons from mice lacking Dvl1 show reduced dendritic arborization.

13 in the growth and branching of Purkinje cell dendritic arborization.

14 composition resulted in dramatic changes in dendritic arborization.

15 pposing effects of BDNF on RGC axonal versus dendritic arborization.

16 increasing retinal BDNF levels inhibits RGC dendritic arborization.

17 inization), and enhancing synaptogenesis and dendritic arborization.

18 roperties of the most distal branches of the dendritic arborization.

19 axons; however, it did reduce the extent of dendritic arborization.

20 o: large cell body, long axon, and extensive dendritic arborization.

21 l morphological defects, including excessive dendritic arborization.

22 es in intracellular Ca(2+) concentration and dendritic arborization.

23 naptic neuron for both synapse formation and dendritic arborization.

24 reduced neuroinflammation and enhanced host dendritic arborization.

25 y-dependent signaling pathway that restricts dendritic arborization.

26 consistent with animal studies of changes in dendritic arborization.

27 neurogenesis, neuronal differentiation, and dendritic arborization.

28 way couples NDL PCB-enhanced RyR activity to dendritic arborization.

29 opodia and spine formation without effect on dendritic arborization.

30 nt cortical neurons exhibit severely reduced dendritic arborization.

31 rmal infralimbic cortex and prelimbic cortex dendritic arborization.

32 several hundred micrometers of their apical dendritic arborizations.

33 vious reduction in these regions occurred in dendritic arborizations.

34 us, and amygdala and is compartmentalized to dendritic arborizations.

35 synaptic inputs paralleled by differences in dendritic arborizations.

36 ositive immature neurons displayed increased dendritic arborization after chronic fluoxetine treatmen

37 retinal neurotrophin levels at the onset of dendritic arborization and assessed the resulting arbor

38 urin homolog KPC-1 is required for dauer IL2 dendritic arborization and dauer-specific nictation beha

39 al expression of CaMKIIalpha-E183V increases dendritic arborization and decreases both dendritic spin

40 d Cdh8 knockdown in cortical neurons impairs dendritic arborization and dendrite self-avoidance.

41 n the cytoarchitecture of neurons, including dendritic arborization and dendritic spines, and that se

42 Although dendritic arborization and densities of excitatory presy

43 M2 cells displayed a more complex dendritic arborization and higher input resistance, yet

44 s in postnatal maturation including abnormal dendritic arborization and impaired neuronal excitabilit

45 se defects were accompanied by a decrease in dendritic arborization and increased proportions of imma

46 lacking Trim9 similarly exhibited excessive dendritic arborization and mislocalization of cell bodie

47 ly in IL2 neurons to regulate dauer-specific dendritic arborization and nictation.

48 TR4-/- cerebellum, as evidenced by aberrant dendritic arborization and reduced calbindin staining in

49 ese mutant horizontal cells exhibit aberrant dendritic arborization and reduced dendritic self-avoida

50 ed to control, such as: less synapses, lower dendritic arborization and reduced spine density.

51 licited concentration-dependent increases of dendritic arborization and soma size in both mouse and h

52 e (1-10 muM) for 72 hours in vitro increased dendritic arborization and soma size in primary cultures

53 Using Golgi-Cox stained tissue, we compared dendritic arborization and spine density of prelimbic la

54 ule cell proliferation and maintenance of PC dendritic arborization and spine density.

55 ASPR2 produced a cell-autonomous decrease in dendritic arborization and spine development in pyramida

56 Dendritic arborization and spine formation are critical

57 nal FXDY1 expression is sufficient to reduce dendritic arborization and spine formation, hallmarks of

58 all GTPase Cdc42 to promote neuronal growth, dendritic arborization and spine formation.

59 ent neurons displayed a marked impairment in dendritic arborization and spine growth.

60 on three-dimensional imaging and analysis of dendritic arborization and spine morphometry.

61 by three-dimensional imaging and analysis of dendritic arborization and spine morphometry.

62 te adult neurogenesis and the development of dendritic arborization and spines in the dentate gyrus,

63 K and TNIK in neurons is required for normal dendritic arborization and surface expression of AMPA re

64 P in ASD-related developmental alteration in dendritic arborization and synapse formation, our findin

65 ntiation in the developing brain, such as in dendritic arborization and synapse formation.

66 required for the maintenance of established dendritic arborization and synapse number.

67 The dendritic arborization and voltage-activated channel com

68 With ipsilateral dendritic arborizations and contralateral axonal branchi

69 -tubulin, doublecortin, NeuN), the extent of dendritic arborization, and acquisition of mature cell b

70 root and peripheral nerves, ultrastructure, dendritic arborization, and afferent axosomatic synapses

71 density, abnormal spine morphology, reduced dendritic arborization, and extensive dendritic varicosi

72 ical defects, including muscle targeting and dendritic arborization, and in a highly specific walking

73 ichment of SALM1 on the cell surface affects dendritic arborization, and intracellular motifs regulat

74 s included the analysis of synaptic density, dendritic arborization, and neurogenesis.

75 PbTx-2 stimulation of neurite outgrowth, dendritic arborization, and synaptogenesis all exhibited

76 d with enhanced neuronal activity, increased dendritic arborizations, and reduced astroglial and micr

77 Increased excitability and decreased dendritic arborization are associated with downregulatio

78 layer 5 pyramidal neuron spine turnover and dendritic arborization as a function of age in transgeni

79 miR-128 expression reduces the complexity of dendritic arborization, associated with altered electrop

80 ion in newborn neurons resulted in truncated dendritic arborization at the time of synaptic integrati

81 blation affects chromatin ultrastructure and dendritic arborization, but alters cognitive skills rath

82 sults indicate that developing RGCs modulate dendritic arborization by integrating signals from discr

83 n in vivo RNAi screen in Drosophila class IV dendritic arborization (C4da) neurons and identified the

84 ila peripheral sensory neurons, the class IV dendritic arborization (C4da) neurons, that completely d

85 Having shown previously that class IV dendritic arborization (C4da) sensory neurons in Drosoph

86 vities in PIKE(-/-) neurons, as the impaired dendritic arborization can be rescued when PI3K/Akt casc

87 ements: long axon tracts and terminal axonal/dendritic arborizations carrying synapses.

88 of tamalin blunts mossy fiber sprouting and dendritic arborization caused by ECS.

89 onfocal microscopy and analyzed according to dendritic arborization, cell depth, dendritic terminal m

90 Chronic restraint stress also increased dendritic arborization, complexity and spine density of

91 Axons and dendritic arborization could be resolved in primate reti

92 rganized michrochaetes, neurons with shorter dendritic arborization (DA) and reduced complexity, dimi

93 servation, we observed that the structure of dendritic arborization (da) neuron dendritic filopodia c

94 ory neurons, the axons of certain Drosophila dendritic arborization (da) neurons are capable of subst

95 Drosophila dendritic arborization (da) neurons contain subclasses o

96 In each hemisegment, six dorsal cluster dendritic arborization (DA) neurons elaborate stereotypi

97 he roles of Fmr1 in dendritic development of dendritic arborization (DA) neurons in Drosophila larvae

98 larvae can sense harsh or gentle touch with dendritic arborization (da) neurons in the body wall and

99 ntal dendrite pruning of Drosophila class IV dendritic arborization (da) neurons is induced by local

100 Drosophila dendritic arborization (da) neurons lack centrosomes and

101 rk together to regulate the morphogenesis of dendritic arborization (da) neurons of the Drosophila la

102 Insect dendritic arborization (da) neurons provide an opportuni

103 Using Drosophila class IV dendritic arborization (da) neurons we test in vivo the

104 and branching of Drosophila larval class IV dendritic arborization (da) neurons, but their specific

105 lexus of multidendritic sensory neurons, the dendritic arborization (da) neurons, innervates the epid

106 ct dendrite branching complexity in class IV dendritic arborization (da) neurons, suggesting that nos

107 By studying the Drosophila dendritic arborization (da) neurons, we discovered a rol

108 Here we show that Drosophila class IV dendritic arborization (da) neurons, which tile the larv

109 -avoidance of all four classes of Drosophila dendritic arborization (da) neurons.

110 of class III and IV, but not class I and II, dendritic arborization (da) neurons.

111 ally localized in Drosophila larval class IV dendritic arborization (da) neurons.

112 ion ensures that the dendrites of Drosophila dendritic arborization (da) sensory neurons are properly

113 level of Cut immunoreactivity in individual dendritic arborization (da) sensory neurons correlates w

114 Drosophila dendritic arborization (da) sensory neurons display clas

115 Single-cell clones of shrub mutant dendritic arborization (DA) sensory neurons in Drosophil

116 r (Ahr), regulates dendrite diversity in the dendritic arborization (da) sensory neurons.

117 Furthermore, kat80 depletion results in dendritic arborization defects in sensory and motor neur

118 ffector pathways that regulate Purkinje cell dendritic arborization downstream of mutant TRPC3, we em

119 SD-related increased dosage of Ube3A/E6AP in dendritic arborization during brain development.

120 a brain-enriched RhoGAP, plays a key role in dendritic arborization during early neuronal development

121 ct RGC-cell-type specific effects in shaping dendritic arborization during postnatal development.

122 to reduce cytoskeletal stability and permit dendritic arborization early in postnatal development.

123 prevented the otherwise dramatic increase in dendritic arborizations elicited by brain-derived neurot

124 s a complex puzzle in neurons with extensive dendritic arborization, encompassing a combinatorial div

125 gh morphological aspects, such as axonal and dendritic arborization, have been well characterized, le

126 defined by their early birthdate and unique dendritic arborizations, have been observed in the mushr

127 ation, neuronal polarity, axon guidance, and dendritic arborization, highlighting the importance of "

128 tin 11 small hairpin RNAs showed (i) reduced dendritic arborization; (ii) decreased density and incre

129 a(2+)-sensitive gene expression and promotes dendritic arborization in a nuclear Ca(2+)-dependent man

130 on preferentially affects the maintenance of dendritic arborization in adults.

131 Knock-out of APP or Reelin decreased dendritic arborization in cortical neurons in vivo, and

132 calcium influx through L-VGCCs and inhibits dendritic arborization in cultured rat cortical neurons

133 We found increased dendritic arborization in isolated cortical pyramidal ne

134 n-1/PlexA4 signalling cascade controls basal dendritic arborization in layer V cortical neurons, but

135 chronic CRF(1) occupancy negatively affects dendritic arborization in mouse organotypic slice cultur

136 mely N-cadherin and alphaN-catenin, enhances dendritic arborization in rat hippocampal neurons, an ef

137 Here we explore: (a) if dendritic arborization in the amygdala follows the patte

138 decreased microgliosis and prevented loss of dendritic arborization in the brains of HIVE mice.

139 es as well as significantly increased apical dendritic arborization in the cortex compared with APOE4

140 lls as well as proper neuronal migration and dendritic arborization in the developing cerebral cortex

141 is distributed throughout the cell body and dendritic arborization in the GL, but, at P20, when the

142 eurones were relatively large with extensive dendritic arborization in the horizontal dimension and a

143 in the molecular layer, significantly larger dendritic arborization in the molecular layer, and a mor

144 tressed rats, but not in controls, decreased dendritic arborization in the mPFC predicted impaired at

145 Instead, apical dendritic arborization in the OFC was increased by 43%.

146 ance columns as well as in the regulation of dendritic arborization in visual cortex of higher mammal

147 Golgi stains after birth reveal restricted dendritic arborizations in MGv cells and dichotomous bra

148 Corrected for atrophy, the "dendritic arborization index" was significantly reduced

149 Their dendritic arborizations indicate selective connectivity

150 us retina during retinal ganglion cell (RGC) dendritic arborization indicates that BDNF is spatially

151 Dendritic arborization indices negatively correlated wit

152 Thus, RGC dendritic arborization is controlled in a complementary

153 Dendritic arborization is required for proper neuronal c

154 mechanism for the growth and maintenance of dendritic arborization is unclear.

155 cell-autonomous simplification of pyramidal dendritic arborizations leading to reduced inhibitory sy

156 antitative aspects of soma area and proximal dendritic arborization, measures that were consistent ac

157 ins are known to regulate the development of dendritic arborization, much less is known about the mec

158 ependent function of the UPS during class IV dendritic arborization neuron dendrite pruning and link

159 oural studies, here we report that class III dendritic arborization neurons are touch sensitive and c

160 type 3 (SCA3) proteins in Drosophila larval dendritic arborization neurons caused neuronal type-spec

161 of the larval Drosophila peripheral class IV dendritic arborization neurons degenerate during metamor

162 e regulator for dendritic growth in class IV dendritic arborization neurons in the larva.

163 Unexpectedly, we found that the class IV dendritic arborization neurons of Drosophila melanogaste

164 Knockdown of RhoBTB in the Drosophila dendritic arborization neurons resulted in a decreased n

165 Previous live imaging in Drosophila dendritic arborization neurons showed that while microtu

166 Surprisingly, after axons of Drosophila dendritic arborization neurons were severed, dendrites w

167 In Drosophila class IV dendritic arborization neurons, dendritic tiling, which

168 s of sensory neurons, class III and class IV dendritic arborization neurons, tile the body wall.

169 These class IV dendritic arborization neurons, which are present in eve

170 e Bolwig's organ and the peripheral class IV dendritic arborization neurons--to regulate light avoida

171 sive functions of Drosophila larval class IV dendritic arborization neurons.

172 Dendritic illumination activates class IV dendritic arborization neurons.

173 nesis on postnatal day 1 (P1) with a peak in dendritic arborization occurring at P21.

174 Disruption of the normally well ordered dendritic arborization occurs in Purkinje cells from bet

175 subgranular zone (SGZ) neuroblasts, and the dendritic arborization of adult-generated dentate gyrus

176 e therapeutic approach to reduce anxiety and dendritic arborization of amygdaloid neurons of adult ma

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

178 ARID1B knockdown suppressed dendritic arborization of cortical and hippocampal pyram

179 n ex vivo cerebellar slice cultures inhibits dendritic arborization of developing GCs, a critical ste

180 2 deletion in the mouse results in decreased dendritic arborization of developing neurons.

181 T and implicate the ability of ECS to induce dendritic arborization of differentiating granule cells

182 ession caused a significant reduction in the dendritic arborization of E11 motoneurons.

183 ion of GluA2 expression had no effect on the dendritic arborization of E6 motoneurons.

184 synaptic transmission; and (iv) the size and dendritic arborization of gastric-projecting DMV neurone

185 pses that are distributed across much of the dendritic arborization of hippocampal CA1 pyramidal neur

186 Genetic deletion of Trim9 elevated dendritic arborization of hippocampal neurons in vitro a

187 ally, Farp1 is required by Sema3A to promote dendritic arborization of hippocampal neurons, and Sema3

188 Dendritic arborization of neurons is regulated by brain-

189 eptor ALK5 reduced the number, migration and dendritic arborization of newborn neurons.

190 epeated cocaine administration increases the dendritic arborization of nucleus accumbens neurons, but

191 l analysis showed a marked difference in the dendritic arborization of on-centre retinal ganglion cel

192 tatory-inhibitory structure largely precedes dendritic arborization of primary motor neurons, suggest

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

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

195 permeability of AMPA receptors regulate the dendritic arborization of spinal cord motoneurons during

196 a critical period of development alters the dendritic arborization of spinal motoneurons in ovo.

197 on as, but commonly exceeding the extent of, dendritic arborization of the postsynaptic neuron.

198 rons emerge by differential sculpting of the dendritic arborizations of an initial pyramidal morpholo

199 of approximately 35,000), different from the dendritic arborizations of CA1 basket cells.

200 the axon terminals of bipolar cells and the dendritic arborizations of ganglion cells suggests the p

201 Within the dendritic arborizations of L3 cells, individual inputs i

202 Dendritic arborizations of many neurons are patterned by

203 In the central nervous system, dendritic arborizations of neurons undergo dynamic struc

204 rply with the sparse and extended axonal and dendritic arborizations of NPY-PLTS interneurons.

205 d by presynaptic ChR2 expression, within the dendritic arborizations of recorded neurons.

206 ean hamsters cause structural changes in the dendritic arborizations of the CA3 pyramidal neurons and

207 lar number of synapses with both on separate dendritic arborizations (ON-OFF RGCs).

208 cate a developmental plasticity in the final dendritic arborization pattern of central olfactory neur

209 Dendritic arborization patterns are consistent anatomica

210 The establishment of cell type-specific dendritic arborization patterns is a key phase in the as

211 We also describe axonal and dendritic arborization patterns of three pyramidal cell

212 s that differed in cell body shape and size, dendritic arborization patterns, and medial-lateral posi

213 Based on dendritic arborization patterns, four major cell types w

214 Integration of inputs by a neuron depends on dendritic arborization patterns.

215 econstructed neurons, two-thirds of neurons' dendritic arborizations reached into at least one adjace

216 not the basal (BA), amygdala possess complex dendritic arborizations, receive potent excitatory drive

217 , their distribution and the extent of their dendritic arborizations relative to functional compartme

218 on, increased axonal rewiring, and augmented dendritic arborization, resulting in long-term functiona

219 The E6AP-dependent remodeling of dendritic arborization results from retraction of dendri

220 s of DMV neurones, increasing their size and dendritic arborization; RYGB did not reverse these morph

221 In Drosophila the dendrites of the class IV dendritic arborization sensory neuron ddaC undergo large

222 found that dendritic branches of Drosophila dendritic arborization sensory neurons can be positioned

223 precursors decreased dendritic branching of dendritic arborization sensory neurons, which was partia

224 m-free dispersed culture developed extensive dendritic arborizations, spontaneous synaptic activity a

225 IFNalpha resulted in dose-dependent loss of dendritic arborization that was blocked with IFNalpha NA

226 Layer 5 pyramidal neurons possess elaborate dendritic arborizations that receive functionally distin

227 The morphology of dendritic arborizations, the biochemical composition of

228 of a behavioral relationship with increased dendritic arborization, these changes may be related to

229 ng pathway that couples neuronal activity to dendritic arborization through enhanced Wnt synthesis an

230 y a signaling pathway whereby Rem2 regulates dendritic arborization through interactions with Ca(2+)/

231 ackpropagation of action potentials into the dendritic arborization was impacted only slightly by den

232 f the known impact of BDNF on plasticity and dendritic arborization, we complimented direct rCBF comp

233 omerular and granular neurons with extensive dendritic arborization were found in the olfactory bulb.

234 n-immunoreactive perikarya and the extent of dendritic arborizations were decreased in Rpe65 knockout

235 d that increasing NF-H and/or NF-M inhibited dendritic arborization, whereas increasing NF-L alleviat

236 se TrkB isoforms had differential effects on dendritic arborization: whereas full-length TrkB increas

237 g pathways downstream of TDP-43 that mediate dendritic arborization, which may provide potential new

238 neurons generated developmental deficits in dendritic arborization with concomitant sensory deficits

239 Type B neurones had the most complex dendritic arborization, with longer and more branching d

240 BDNF can differentially modulate axonal and dendritic arborization within a single neuronal populati

241 Cav-1 overexpression in adult mice enhanced dendritic arborization within the apical dendrites of hi

242 Thus, BDNF reduces RGC dendritic arborization within the retina and increases a

243 express neuronal markers and have extensive dendritic arborizations within the SP, WM, and to the ov