ライフサイエンスコーパス: dendritic

1 from neuronal dendrites, which can generate dendritic action potentials (DAPs) in vitro, which can p

2 We show that conjugating dendritic alkyl chains to DNA creates amphiphiles that e

3 cal agent of spotted fever, able to activate dendritic and macrophage cells.

4 By operating through dendritic and not just somatic inhibition, SOM-mediated

5 Dendritic and synaptic organization of the ipsilaterally

6 resolving how innate lymphoid, myeloid, and dendritic, and B-cell fate alternatives are excluded by

7 observed in restricted areas in the forming dendritic arbor.

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

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

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

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

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

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

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

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

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

17 patial map of synaptic calcium signals along dendritic arbors of hippocampal neurons and relate this

18 e hippocampi, male neurons have more complex dendritic arbors than female neurons.

19 is expressed in neurons that extend complex dendritic arbors, such as Purkinje cells, targeted in SC

20 e mutants displayed stunted, poorly branched dendritic arbors.

21 firing and, as a result, distance-dependent dendritic attenuation remains consistent across differen

22 ths to late burst spikes and undergo similar dendritic attenuation.

23 The high molecular precision of the dendritic block enabled us to systematically tune the hy

24 -rich membrane ruffles of COS-7 cells and of dendritic branches of neurons.

25 Consistently, dendritic branching and spine density are reduced in cor

26 rons elicits motor abnormalities and affects dendritic branching of Purkinje cells, with no obvious s

27 was shown to be vital for axonal growth and dendritic branching.

28 Mechanistically, this requires local dendritic Ca(2+) influx through Dalpha7nAChRs or through

29 o understanding the stochastic properties of dendritic Ca(2+) spikes in neocortical layer 5 pyramidal

30 ng and maintaining newly formed synapses via dendritic calcium spike-dependent mechanisms.

31 Here, the authors show that dendritic calcium synchronisation correlates with spindl

32 itatory inputs, which can then trigger large dendritic calcium transients due to strong expression of

33 n of dynein to the motility of an endogenous dendritic cargo and found that dynein inhibition elimina

34 r 2 (Th2)-like cells; (iii) interfering with dendritic cell (DC) effector function; and (iv) inhibiti

35 Here, we report that C-type lectin dendritic cell (DC) immunoreceptor (DCIR), a key compone

36 ught to be prototypic representatives of the dendritic cell (DC) lineage, they are now considered to

37 34.5 protein, a virulence factor, stimulates dendritic cell (DC) maturation which is dependent on TAN

38 mune-modulatory functions that could enhance dendritic cell (DC) maturation.

39 Human dendritic cell (DC) response to alpha-(1,3)-glucan polys

40 ted and memory CD4 T cells, macrophages, and dendritic cell (DC) showed chemoattractantDeltadriven ve

41 Dendritic cell (DC) subsets with biased capacity for CD4

42 RNA sequencing was used to characterize dendritic cell (DC) transcripts.

43 y T (Act-A-iTreg) cells on the regulation of dendritic cell (DC)-driven allergic inflammation remain

44 ast, early signatures of innate immunity and dendritic cell activation were highly associated with pr

45 associated cytokine synthesis, and pulmonary dendritic cell activity was assessed.

46 The dendritic cell clade was distinct from a macrophage/mono

47 membrane protein (LAMP) family includes the dendritic cell endocytic receptors DC-LAMP and CD68, as

48 lonic inflammation as a result of defects in dendritic cell function that were associated with abnorm

49 tion and abrogated monocyte, macrophage, and dendritic cell increase in the affected kidneys, whereas

50 , TSLPR(+) mono express higher levels of the dendritic cell marker CD1c.

51 type I interferon responses, suppression of dendritic cell maturation and promotion of inflammatory

52 protease, inflammatory cell recruitment, and dendritic cell maturation.

53 Clec9a (C-type lectin receptor) or DNGR-1 (dendritic cell NK lectin group receptor-1) is preferenti

54 ene expression revealed a novel plasmacytoid dendritic cell precursor preferentially mobilized by ple

55 yte-monocyte progenitors (GMPs) and monocyte-dendritic cell progenitors (MDPs) produce monocytes duri

56 Targeting of myeloid-dendritic cell receptor DC-SIGN by numerous chronic infe

57 reciprocal increase in the CD103(-)CD11b(+) dendritic cell subset.

58 DC-SIGN is a dendritic cell surface structure which participates in b

59 Furthermore, dendritic cell- and IL-2/7-dependent T cell survival was

60 by higher mRNA expression levels of several dendritic cell-associated genes, including CD1, FLT3, CX

61 B cell morphology, having in general a more dendritic cell-like appearance.

62 ion and lymphocyte attraction, together with dendritic cell-mediated cross-priming, are the key eleme

63 Dendritic cell-specific transmembrane protein (DC-STAMP)

64 (CD206+) and MDSCs (Gr1+ CD11b+), increased dendritic cells (CD86+) and cytotoxic T cells (CD8+) in

65 ially expressed by the CD8alpha(+) subset of dendritic cells (CD8alpha(+) DCs) and is involved in sen

66 )-12 by tissue-resident XCR1(+) conventional dendritic cells (cDC1) promoted ILC1 production of IFN-g

67 Dendritic cells (DC) accumulate in the CNS during neuroi

68 , such as HLA-DR4 positivity, indicates that dendritic cells (DC) are of crucial importance to pathog

69 Thymic dendritic cells (DC) delete self-antigen-specific thymoc

70 etermine the mechanism of MSC recruitment by Dendritic Cells (DC), hypothesising that it would be med

71 dhesion molecule-1 for T-cell conjugation to dendritic cells (DC).

72 Dendritic cells (DCs) are activated by pathogens to init

73 Dendritic cells (DCs) are crucial initiators of immune r

74 Mast cells (MCs) and dendritic cells (DCs) are essential innate sentinels pop

75 Although dendritic cells (DCs) are vital for the induction of T-c

76 RPalpha with CD47 preferentially occurred in dendritic cells (DCs) but not in macrophages.

77 cells normally depend on signals from CD8(+) dendritic cells (DCs) for their activation, we used the

78 y susceptibility to TB, we infected with MTB dendritic cells (DCs) from putatively resistant individu

79 Tolerogenic dendritic cells (DCs) have emerged as relevant clinical

80 0, which we found to be produced by CD103(+) dendritic cells (DCs) in T cell-inflamed tumors.

81 Dendritic cells (DCs) initiate immune responses to commo

82 Dendritic cells (DCs) play critical roles in developing

83 Dendritic cells (DCs) promote either tolerogenic or immu

84 The mechanism of dendritic cells (DCs) recruitment across the blood brain

85 Cross-presentation is a critical function of dendritic cells (DCs) required for induction of antitumo

86 that control the presentation of antigens by dendritic cells (DCs) to naive T lymphocytes.

87 emonstrated for the haptotactic migration of dendritic cells (DCs) toward higher concentrations of im

88 Trafficking of tissue dendritic cells (DCs) via lymph is critical for the gene

89 infiltrated MAC387(+) macrophages, T cells, dendritic cells (DCs), and residential macrophages near

90 HIV-1 infection of noncycling cells, such as dendritic cells (DCs), is impaired due to limited availa

91 e of immune reactions with a high density of dendritic cells (DCs), macrophages and T cells.

92 The skin hosts a variety of dendritic cells (DCs), which act as professional APC to

93 Targeting newborn dendritic cells (DCs), which integrate vaccine signals i

94 taining IgG immune complexes (Ig-ICs) by gut dendritic cells (DCs).

95 during pregnancy boosted OVA uptake by fetal dendritic cells (DCs).

96 cific interactions between T lymphocytes and dendritic cells (DCs).

97 ts for the early steps of TLR9 activation in dendritic cells (DCs).

98 from both fungal species with MUTZ-3-derived dendritic cells (DCs).

99 co-cultured with GM-CSF derived bone marrow dendritic cells (G-BMDCs).

100 D25(+)) lymphocytes, tissue macrophages, and dendritic cells (Iba-1(+) and CD83(+)), with a small num

101 une system and specifically monocyte-derived dendritic cells (MDDCs) understudied.

102 litating HIV-1 infection of monocyte-derived dendritic cells (MDDCs), one of the first cell types to

103 of Ly6C(high) monocytes and monocyte-derived dendritic cells (moDC) and lower moDC costimulatory matu

104 7b) on the surface of human monocyte-derived dendritic cells (MoDC) and show only LAMP-2 is internali

105 ells and in CD23-expressing monocyte-derived dendritic cells (moDCs) that represent classical antigen

106 Plasmacytoid dendritic cells (pDCs) are important in antiviral immuni

107 Plasmacytoid dendritic cells (pDCs) were isolated from whole blood, s

108 tumor-infiltrating murine and human myeloid dendritic cells (TIDC) in ovarian cancer.

109 es of different cell types (monocyte-derived dendritic cells [moDCs], PBMCs [peripheral blood mononuc

110 atumorally, including infusion of autologous dendritic cells and even tumor-reactive T lymphocytes.

111 stantiate a critical role for skin migratory dendritic cells and in particular Langerhans cells at go

112 nimals revealed increased numbers of CD1d(+) dendritic cells and increased numbers of iNKT cells.

113 eptor for infection of both monocyte-derived dendritic cells and interstitial dermal dendritic cells,

114 In myeloid-derived dendritic cells and macrophages as well as resting T-cel

115 D40L stimulation derived from human immature dendritic cells and naive B cells to assess the expressi

116 aled that CD40L-responsive genes in immature dendritic cells and naive B cells were significantly enr

117 This process has been defined in dendritic cells and plays a fundamental role in the indu

118 at chemokines produced by intratumoral Batf3 dendritic cells are critical for effector T cell recruit

119 terium tuberculosis-infected macrophages and dendritic cells are limited in their ability to present

120 (IFN-gamma), TNF-alpha, and IL-12 in myeloid dendritic cells are of importance in generating T helper

121 We show that follicular dendritic cells are stiff cells that promote strong B ce

122 s, using bone marrow-derived macrophages and dendritic cells as responders.

123 , leaving macrophages and, to a less extent, dendritic cells as the major infiltrating leukocytes.

124 terferons (IFN-alpha/beta) from plasmacytoid dendritic cells as well as the production of TLR8-depend

125 innate receptor engagement on epithelial or dendritic cells by HDMs that ultimately mediates said in

126 ich prevent prions from infecting follicular dendritic cells can block their spread to the brain.

127 40, CD80, CD83, and CD86 on monocyte-derived dendritic cells from allergic patients was analyzed by u

128 Further, the severe loss of dendritic cells in the draining lymph node had no impact

129 hat Dll4 was expressed on CD11b(+) pulmonary dendritic cells in the lung and draining lymph nodes in

130 turation and cytokine release of bone marrow dendritic cells in vitro.

131 IVM had no major impact on the functions of dendritic cells in vivo and in vitro, IVM impaired T-cel

132 nized mice immunized with long-lived induced-dendritic cells loaded with the pp65 viral antigen (iDCp

133 Our results indicate that macrophages and dendritic cells produce the endocannabinoid, 2-arachidon

134 fect GC B cell responses, the loss of Mer in dendritic cells promotes enhanced T cell activation and

135 Dendritic cells rapidly underwent apoptosis in response

136 UF1 to its cognate receptor, SIGNR1, on dendritic cells resulted in the regulation of intestinal

137 lay a higher frequency of CD11b(+) pulmonary dendritic cells than their WT controls at the baseline a

138 creased numbers of circulating monocytes and dendritic cells that produce more inflammatory cytokines

139 oth fusion proteins matured monocyte-derived dendritic cells through TLR5.

140 ate their initial delivery toward follicular dendritic cells to establish host infection.

141 is suggests that prions exploit conventional dendritic cells to facilitate their initial delivery tow

142 h activated type 2 innate lymphoid cells and dendritic cells to promote differentiation of T-helper 2

143 mmatory cytokines, and recruit monocytes and dendritic cells to the site of damage through a breached

144 Dendritic cells transduced with the adjuvant, an adenovi

145 Decreased CXCL1 production by Nlrp12(-/-) dendritic cells was not due to a difference in CXCL1 pro

146 Indeed, in cultured dendritic cells we found that high salt media potentiate

147 Additionally, both CD8(+) T cells and CD8(+) dendritic cells were identified in the tumor microenviro

148 ssue macrophages, prion trafficking by B and dendritic cells within the lymphoreticular system, intra

149 ols to generate bone marrow-derived cultured dendritic cells yield a heterogeneous mixture, including

150 tic stem cells or bone marrow-derived MSC or dendritic cells) for optimization of appropriate conditi

151 transcript 3 (ILT3), a marker of tolerogenic dendritic cells, also known as LILRB4/LIR5/CD85k, and it

152 as choroid plexus and meningeal macrophages, dendritic cells, and granulocytes.

153 on how cross-talk between epithelial cells, dendritic cells, and innate lymphoid cells translates to

154 T cells, B cells, eosinophils, neutrophils, dendritic cells, and NK cells.

155 anodal prion replication by B and follicular dendritic cells, and potential prion strain selection by

156 th an increase in the number of conventional dendritic cells, CD11b(+) and CD103(+) dendritic cells,

157 ell sorting method to isolate keratinocytes, dendritic cells, CD4+ T effector cells, and CD8+ T effec

158 ed I-A expression on the surface of B cells, dendritic cells, cortical thymic epithelial cells, and m

159 ional dendritic cells, CD11b(+) and CD103(+) dendritic cells, in the lung-draining lymph node, as wel

160 e types of dendritic cells: monocyte-derived dendritic cells, Langerhans cells, and interstitial derm

161 luding Langerhans cells, macrophages, dermal dendritic cells, mast cells, fibroblasts, and lymphatic

162 Dendritic cells, monocytes, and B cells in HCC tumors ex

163 e, often coinciding with loss of circulating dendritic cells, monocytes, B cells, and natural killer

164 e the age-dependent function of conventional dendritic cells, their role in determining immunodominan

165 infection system that utilizes primary human dendritic cells, which display a robust decrease in vira

166 ived dendritic cells and interstitial dermal dendritic cells, yet the virus fully replicates only in

167 s, Langerhans cells, and interstitial dermal dendritic cells.

168 gely due to the recruitment of monocytes and dendritic cells.

169 libraries loaded or not on monocytes-derived dendritic cells.

170 in antigen cross-presentation by Igfbp7(-/-) dendritic cells.

171 ubsets were markedly distinct from PBMos and dendritic cells.

172 exosomes, which are taken up by and activate dendritic cells.

173 ar STING has been studied in macrophages and dendritic cells.

174 important role of SWAP-70 in Cer dynamics in dendritic cells.

175 esses CD11C, a marker typically expressed on dendritic cells.

176 mediated interactions between Treg cells and dendritic cells.

177 t of monocytes that yielded monocyte-derived dendritic cells.

178 en exposure or in vitro by using tolerogenic dendritic cells.

179 of Th17 differentiation cytokines in splenic dendritic cells.

180 g by depleting cross-presenting conventional dendritic cells.

181 ted in its membrane-bound form by follicular dendritic cells.

182 n the interaction between Chlamydia and host dendritic cells.

183 from WAS patients and in WAS-knockout mouse dendritic cells.

184 40 interaction for the function of T, B, and dendritic cells.

185 ses Kaposi's sarcoma, infects three types of dendritic cells: monocyte-derived dendritic cells, Lange

186 eptive field properties exhibited non-random dendritic clustering.

187 Furthermore, mGluR2-mediated dendritic compartmentalization in SACs is important for

188 ep learning can be achieved using segregated dendritic compartments, which may help to explain the mo

189 ndent control over neuronal excitability and dendritic complexity in the development and plasticity o

190 ritic spine density significantly, increased dendritic damage (characterized by swellings/varicositie

191 age-dependent cortical atrophy, neuron loss, dendritic degeneration, and memory deficits.

192 ficits in synaptic proteins and decreases in dendritic density and the frequency of miniature excitat

193 a bortezomib-conjugating intermediate, and a dendritic doxorubicin-affinitive interior.

194 Cilia on dendritic endings of sensory neurons organize distinct t

195 al surface that connect with each other in a dendritic fashion.

196 The dendritic field diameter of melanopsin-expressing cells

197 lytes with metal anodes in fact promote fast dendritic formation, as a result of less Li consumption

198 te interphase, low Coulombic efficiency, and dendritic growth of Li.

199 nown Drosophila HSPG receptor, for promoting dendritic growth of space-filling neurons.

200 engaged by converging GC-inputs and provide dendritic inhibition to the DG circuitry.

201 ivileged scenario for in vivo examination of dendritic integration.

202 , but, surprisingly, decreased depression of dendritic IPSCs isolated after blocking GABAa receptor o

203 SPs, thus indicating a conserved function of dendritic L-type channels from Drosophila to vertebrates

204 otoneurons different functions of axonal and dendritic L-type like calcium channels likely operate sy

205 g de novo dendritic segments, and elongating dendritic length, while maintaining dendritic patterns.

206 cess such differential sensory inputs at the dendritic level?

207 iation more sensitive to synapse timing than dendritic location.

208 mitochondrial dysfunction-mediated selective dendritic loss in Drosophila neurons.

209 expression of Kv1.1 was sufficient to enable dendritic maturation in the absence of sensory input.

210 measured neocortical sub- and suprathreshold dendritic membrane potential (DMP) from putative distal-

211 These complexes restrict AMPAR dendritic mobility, leading to the intracellular trappin

212 Evidence that sex influences dendritic morphogenesis in two models of neurodevelopmen

213 fy NAc neuronal-subtype molecular control of dendritic morphology and related functional adaptations,

214 To address this gap, we quantified dendritic morphology in CA1 pyramidal hippocampal and ad

215 Conversely, dendritic morphology of female cortical neurons is more

216 had no significant effects on soma size and dendritic morphology of VTA neurons but significantly de

217 , which is consistent with the intrinsic non-dendritic nature of Mg deposition in Mg ion batteries.

218 Because rivers are dendritic networks, there is only one dispersal route fr

219 accumulation and bundling of perikaryal and dendritic neurofilaments.

220 Fine-scale dendritic organization was supported by the fact that fu

221 K618A in primary neurons rescues the loss of dendritic outgrowth and number of synapses after treatme

222 l glutamatergic neurons results in excessive dendritic outgrowth within 24 h, resembling the changes

223 lso abolished glutamate transmission-induced dendritic overgrowth.

224 ortem studies have demonstrated considerable dendritic pathologies among persons with schizophrenia a

225 This is associated with reduced dendritic pathology and improved axonal and synaptic pla

226 different spatiotemporal dimensions of J-RGC dendritic patterning to generate the substrate for speci

227 ongating dendritic length, while maintaining dendritic patterns.

228 n the initial post-ONC period, rtACS induced dendritic pruning in surviving neurons.

229 e 1D MPS exists in a substantial fraction of dendritic regions in relatively mature neurons, but this

230 Their composition was dictated by three dendritic regions, i.e., (i) the symmetrical trithiol of

231 enting dendrites toward TCAs, adding de novo dendritic segments, and elongating dendritic length, whi

232 g studies reveal Abeta activates NgRs on the dendritic shaft of neurons, triggering an inhibition of

233 cular trafficking and trap AMPARs inside the dendritic shaft.

234 STDP and for synaptic strengthening by local dendritic spikes.

235 tes excessive protein synthesis and corrects dendritic spine abnormality in Fmr1 knockout mice.

236 Dendritic spine and synapse impairments are features of

237 mpanied by increased local p-tau, changes in dendritic spine density and morphology, and upregulation

238 s microglia-mediated neuronal remodeling and dendritic spine density in the medial PFC.

239 experience with high-fat consumption reduced dendritic spine density in the PFC at both time points.

240 Lower dendritic spine density on layer 3 pyramidal cells in th

241 In D2 MSNs, exposure to HIV-1 Tat reduced dendritic spine density significantly, increased dendrit

242 We observed significant loss of dendritic spine density, abnormal spine morphology, redu

243 uces the motivation for cocaine and reverses dendritic spine density, suggesting a potential target f

244 Tomo-1 overexpression increased dendritic spine density, whereas Tomo-1 knockdown (KD) d

245 dditionally, LTP and LTD are correlated with dendritic spine enlargement and shrinkage that are accom

246 n, is critical for the effects of cocaine on dendritic spine formation and for cocaine-mediated behav

247 h alterations influence cocaine's effects on dendritic spine formation remain unclear.

248 CNS nerve tracts remodels circuitry through dendritic spine loss and hyper-excitability, thus influe

249 Dendritic spine loss is recognized as an early feature o

250 zes the scaffolding protein PSD95, promoting dendritic spine maturation.

251 on of actin filaments, leading to changes in dendritic spine morphology of NAc medium spiny neurons (

252 s of t-SP were assayed during reinstatement: dendritic spine morphology, alpha-amino-3-hydroxy-5-meth

253 iverse effects on NADPH oxidase activity and dendritic spine morphology.

254 uch as nesting and marble burying as well as dendritic spine morphology.

255 ion alters their mobility and also decreases dendritic spine number.

256 euronal populations at single-cell or single dendritic spine resolution in awake monkeys, the techniq

257 Furthermore, we found that average dendritic spine sizes were decreased and increased follo

258 articularly enriched in the neck and base of dendritic spines and largely absent from spine heads.

259 f PERK using GSK2656157 prevents the loss of dendritic spines and rescues memory deficits after TBI.

260 mature features, including the formation of dendritic spines and spontaneously active neuronal netwo

261 Abnormalities in dendritic spines are manifestations of several neurodeve

262 Dendritic spines are protrusions along neuronal dendrite

263 small neuronal compartments, such as single dendritic spines in brain slices.

264 Furthermore, there were fewer dendritic spines in GluN2B S1413L-expressing neurons.

265 transgenic mice produced a 17 +/- 1% loss of dendritic spines in layer 1 of retrosplenial cortex.

266 abnormal development of dendrite arbors and dendritic spines in newly generated dentate gyrus granul

267 as associated with structural alterations of dendritic spines in the CeA and, moreover, whole-cell pa

268 ted BCCAO-induced loss of total and mushroom dendritic spines in the hippocampal CA1 region.

269 in vivo, Lphn2 was specifically targeted to dendritic spines in the stratum lacunosum-moleculare, wh

270 (PD28-42) increased the density of long/thin dendritic spines of layer 5 pyramidal neurons in the adu

271 expressed in the nuclei, dendrites and near dendritic spines of mouse dorsal hippocampal CA1 neurons

272 binds the glutamate receptor, GluRdelta2, in dendritic spines of Purkinje cells.

273 ously found that polyribosomes accumulate in dendritic spines of the adult rat lateral amygdala (LA)

274 There were also fewer and less mature dendritic spines on OGT knockout neurons.

275 he indirect pathway accompanied by decreased dendritic spines on the indirect pathway medium spiny pr

276 al enrichment of actin monomers (G-actin) in dendritic spines regulates spine development and plastic

277 to form synapses and an increased number of dendritic spines that are not in contact with a presynap

278 Dendritic spines usually have a mushroom-like shape, whi

279 sis of presynaptic glutamatergic boutons and dendritic spines was performed on SPNs 1 hour and 1 week

280 We compared dendritic spines within layer II and III pyramidal neuro

281 ins, as well as the detailed architecture of dendritic spines, in mouse brain circuitry.

282 Although PIP2 is also concentrated at the dendritic spines, little is known about the direct physi

283 regulates the actin cytoskeleton supporting dendritic spines, produced spine loss in cortical pyrami

284 e morphogenesis of presynaptic terminals and dendritic spines, suggesting that glutamatergic neurotra

285 d by cAMP-PKA-potassium channel signaling in dendritic spines.

286 regenerated BPs were reduced in numbers, BP dendritic spreads, dendritic tree morphologies, and cone

287 lion cells were distinguished based on their dendritic stratification near either the outer or the in

288 receptors and impairing their access to the dendritic surface and spines.

289 ere formed by a spatially segregated, linear-dendritic telodendrimer containing three segments: a hyd

290 on the development of a proper complement of dendritic tips and transduction proteins in rod bipolar

291 from this study support an association with dendritic trafficking complexes of Ptchd1.

292 Here we define the dendritic trafficking itinerary for key synaptic molecul

293 hile the endoplasmic reticulum (ER) supports dendritic translation, most dendrites lack the Golgi app

294 ynaptic inhibition compartmentalized the GAC dendritic tree and endowed all dendritic varicosities wi

295 re reduced in numbers, BP dendritic spreads, dendritic tree morphologies, and cone-bipolar connectivi

296 the axosomatic region and propagate into the dendritic tree to provide a retrograde signal that conve

297 voltage attenuation as they spread into the dendritic tree.

298 and function of spine synapses in the apical dendritic tuft of layer V pyramidal neurons in the mPFC.

299 educed dendritic arborization, and extensive dendritic varicosities in the cortical neurons of CM-inf

300 lized the GAC dendritic tree and endowed all dendritic varicosities with a small-center, strong-surro