ライフサイエンスコーパス: dendritic

1 ectual disability, that are characterized by dendritic aberrations.

2 experiments we show that vinculin can bundle dendritic actin networks through rapid binding and filam

3 a metal anode has been primarily hindered by dendritic and "dead" Na formation that leads to low Coul

4 perisynaptic GluD1 labeling at putative axo-dendritic and axo-spinous glutamatergic synapses, and in

5 in the adult retina, with significantly less dendritic and axon terminal labeling in TRPM1 knockout c

6 We propose that delta-catenin regulates the dendritic arbor by coordinating the dynamics of individu

7 The dendritic arbor of neurons constrains the pool of availa

8 aptation of glutamatergic synapses-along the dendritic arbor.

9 and other effectors to sculpt the developing dendritic arbor.

10 autophagy mechanism to sculpt the developing dendritic arbor.

11 comes to stress by preventing loss of D1-MSN dendritic arbor.

12 Class I ventral posterior dendritic arborisation (c1vpda) proprioceptive sensory n

13 well as adult stages for maintaining normal dendritic arborization and sensory function to regulate

14 ure at birth encodes regionally differential dendritic arborization and synaptic formation.

15 f the ASD risk gene Taok2, as a regulator of dendritic arborization in sensory neurons.

16 How neuronal growth control programs tune dendritic arborization to ensure function is still not f

17 endrite self-avoidance, synapse development, dendritic arborization, spine maturation, and prevention

18 , is less synaptically targeted and promotes dendritic arborization.

19 numerous short dendrites that formed a dense dendritic arborization; they also exhibited a very dense

20 However, the mechanisms of how dendritic arbors develop to promote functional and prope

21 f retinal amacrine cells that do not develop dendritic arbors in relation to the spatial positioning

22 is known about the postnatal development of dendritic arbors of cortical pyramidal neurons and the i

23 results in DG granule cells with simplified dendritic arbors, reduced dendritic spine density, and d

24 romotes the stabilization of DG granule cell dendritic arbors, spines, and synapses, whereas it restr

25 gration of synaptic inputs across a neuron's dendritic arbour.

26 We propose that the dendritic architecture of pyramidal neurons might determ

27 GFD delivered intraventricularly to preserve dendritic architecture, reduce stroke-induced brain dama

28 cinergic cells were smaller in soma size and dendritic area, but over ten-fold more numerous than D-s

29 mination of neuronal morphology demonstrated dendritic atrophy and dendritic spine loss in dorsal str

30 d of mitochondria to induce inflammation and dendritic atrophy.

31 r and thalamic vacuolation and Purkinje cell dendritic atrophy.

32 rs: (1) the location of the input within the dendritic branch (proximal vs distal), (2) the strength

33 Their dendritic branches run along the direction of contractio

34 sis posits that synapse formation stabilizes dendritic branches, but this hypothesis has not been cau

35 weeks, adult-born neurons gained additional dendritic branches, formed a second primary dendrite, ac

36 treatment was associated with greater apical dendritic branching complexity, spine density, and inhib

37 to identify signaling pathways that regulate dendritic branching downstream of TDP-43.

38 , this cell type modulates the extent of its dendritic branching when faced with a variable number of

39 by which TDP-43 dysfunction interferes with dendritic branching, and may define pathways for therape

40 pyramidal neurons in the ACC did not exhibit dendritic Ca(2+) spikes as prominently found in the apic

41 pute and validate transfer functions between dendritic calcium signals of specific neurons and vascul

42 Development and function of conventional dendritic cell (cDC) subsets, cDC1 and cDC2, depend on t

43 e most strongly enriched in AD, and we found dendritic cell (CLEC7A, amphiregulin/AREG, EREG) and mac

44 lopment, only one contributed to intrathymic dendritic cell (DC) differentiation, predominantly of pl

45 The most upregulated gene was the dendritic cell (DC) marker CD209a only in PVPV-Akt1KO th

46 Dendritic cell (DC) maturation is a prerequisite for the

47 ns and marks Langerhans cells (LC), the only dendritic cell (DC) population of the epidermis.

48 Generation of pDCs from bone marrow dendritic cell (DC) progenitors and their maintenance is

49 Although GM-CSF has been widely used in dendritic cell (DC) research, the mechanisms, factors, a

50 isease, which is attributed to a loss of the dendritic cell (DC) subset conventional DC2.

51 Recently, another dendritic cell (DC) subset, termed merocytic DCs (mcDCs)

52 Dendritic cell (DC) subsets are abundantly present in ge

53 microenvironment diminishes the efficacy of dendritic cell (DC)-based cancer immunotherapy.

54 s can recognize and eliminate the follicular dendritic cell (FDC) reservoir of HIV-bound immune compl

55 is currently much interest in how different dendritic cell and macrophage populations contribute to

56 CD38 as a critical regulator of plasmacytoid dendritic cell function in response to influenza virus.

57 show in this study that conventional type 1 dendritic cell IL-27 production in the draining lymph no

58 otch signaling in CD8(+) T cell responses to dendritic cell immunization, Listeria infection, and vir

59 vorinostat (VOR) and AGS-004, an autologous dendritic cell immunotherapeutic, on the HIV reservoir.

60 the miRNAs to regulate Th2 polarization and dendritic cell maturation.

61 Here, we quantify dendritic cell migration under well-defined 2-dimensiona

62 lymphoid cells (ILC2s) and monocyte-derived dendritic cell numbers in the mediastinal lymph nodes, a

63 The dendritic cell receptor Clec9A facilitates processing of

64 Although conventional dendritic cell subsets have received much attention for

65 (-/-) mice lacking the CD103(+) conventional dendritic cell type 1 (cDC1) subpopulation important for

66 G9Calpha(-/-)CD8(+) T-cell cytotoxicity and dendritic cell-induced proliferation, they failed to suf

67 d was able to 1) inhibit bone marrow-derived dendritic cell-mediated T cell functions and reduce seru

68 systemic increase of cf-mt-DNA that promotes dendritic cell-mediated, age-specific inflammatory respo

69 ynergies between TNF and IFNbeta controlling dendritic cell-T cell crosstalk.

70 t the extent of activation in a plasmacytoid dendritic cell-type I IFN-T/B lymphocyte network.

71 ive changes in vasculature and maturation of dendritic-cell subsets with chronicity, with FOXK1 actin

72 Dendritic cells "patrol" the human body to detect pathog

73 firmed increased frequencies of conventional dendritic cells (3.1% versus 2.1%; P = 0.023) and CD4 TN

74 aride (LPS)-primed mouse bone marrow-derived dendritic cells (BMDC).

75 F8(+) type 1 and IRF4(+) type 2 conventional dendritic cells (cDC1s and cDC2s, respectively) is well

76 Type 1 conventional dendritic cells (cDC1s) are typically thought to be dysr

77 ndicates Batf3-dependent conventional type 1 dendritic cells (cDC1s) rarely found within the tumor my

78 ther myeloid subsets, including conventional dendritic cells (cDCs) and monocyte (MO) subsets, expres

79 ty by acting as danger signals recognized by dendritic cells (DC) facilitating the establishment of a

80 After ischemic injury to the myocardium, dendritic cells (DC) respond to cardiomyocyte necrosis,

81 epidermal Langerhans cells (LC), and dermal dendritic cells (DC).

82 re-associated DNA damages that are sensed by dendritic cells (DCs) and activates the host cytosolic D

83 receptor (TLR) recruitment to phagosomes in dendritic cells (DCs) and downstream TLR signaling are e

84 Dendritic cells (DCs) and other innate immune cells patr

85 We show that NVP was readily taken up by dendritic cells (DCs) and promoted DC maturation and ant

86 Dendritic cells (DCs) are antigen-presenting cells contr

87 Dendritic cells (DCs) are antigen-presenting cells subdi

88 Dendritic cells (DCs) are highly susceptible to extrinsi

89 Dendritic cells (DCs) are professional APCs, which sampl

90 Airway dendritic cells (DCs) are recognized as important factor

91 aive CD4 T cells were primed via antigen and dendritic cells (DCs) at fever temperatures, the Th2 swi

92 Dendritic cells (DCs) develop in the bone marrow from ha

93 hat accessible DNA elements in skin-resident dendritic cells (DCs) exhibit the highest enrichment of

94 ined.Objectives: To examine the role of lung dendritic cells (DCs) in T follicular helper (Tfh)-cell

95 tion of a population of tolerogenic CD103(+) dendritic cells (DCs) in the spleen.

96 Migratory dendritic cells (DCs) in tumors transport antigens and s

97 The formation of mammalian dendritic cells (DCs) is controlled by multiple hematopo

98 Dendritic cells (DCs) participate in the pathogenesis of

99 Dendritic cells (DCs) play a central role in the early i

100 Dendritic cells (DCs) play a critical role in shaping ad

101 monocytes, resident tissue macrophages, and dendritic cells (DCs) present in every tissue in the bod

102 mast cells (MCs) were studied; in addition, dendritic cells (DCs) purified from the draining lymph n

103 -cell lung cancers, we identify a cluster of dendritic cells (DCs) that we name 'mature DCs enriched

104 ntima is thought to be populated by vascular dendritic cells (DCs) that, during hypercholesterolemia,

105 ent upon NFkappaB-p65 and IL-6 expression in dendritic cells (DCs), as well as aryl hydrocarbon recep

106 mphocytes (CTLs) and CD103+ cross-presenting dendritic cells (DCs), as well as up-regulation of MHC c

107 absence of SIGN-R1(+) macrophages, DCIR2(+) dendritic cells (DCs), which play a key role in priming

108 ptive immune responses via interactions with dendritic cells (DCs).

109 (IFN) responses in mouse bone marrow-derived dendritic cells (DCs).

110 herapy (PDT) and promoting the maturation of dendritic cells (DCs).

111 Furthermore, immature dendritic cells (iDC) responded to mCD40L with enhanced

112 and B. licheniformis Monocytes and immature dendritic cells (iDCs) responded differentially to the P

113 mmune responses in mouse bone marrow-derived dendritic cells (mBMDCs) and a synergistic response in b

114 CD11c(+) macrophages/dendritic cells (MDCs) are increased and display the cla

115 , CD8 T, B, and NK cells, monocytes, myeloid dendritic cells (mDCs), and plasmacytoid dendritic cells

116 up by a population of IRF4+ dermal migratory dendritic cells (migDC2) that similarly upregulate surfa

117 allergy model and on human monocyte-derived dendritic cells (moDCs) and PBMCs.

118 alters TLR7-MyD88 signaling in plasmacytoid dendritic cells (pDCs) and blunts systemic production of

119 Plasmacytoid dendritic cells (pDCs) are robust producers of IFNalpha

120 oid dendritic cells (mDCs), and plasmacytoid dendritic cells (pDCs) from three individuals with ZIKV

121 Plasmacytoid dendritic cells (pDCs) produce abundant type I IFNs (IFN

122 Plasmacytoid dendritic cells (pDCs) produce type I interferon (IFN-I)

123 Plasmacytoid dendritic cells (pDCs) require a particularly tight regu

124 que lungs include the influx of plasmacytoid dendritic cells (pDCs), an Interferon (IFN)-responsive m

125 esponse in both mouse and human plasmacytoid dendritic cells (pDCs).

126 s, CD8(+) T cells, B cells, macrophages, and dendritic cells after systemic delivery in mice.

127 y and detect couplings between monocytes and dendritic cells and between erythrocytes and basophils t

128 subpopulations of ductal cells, macrophages, dendritic cells and cancer cells have spatially restrict

129 HDM + DEP exposed bone marrow derived dendritic cells and IL33 pulsed BMDC promote a mixed Th2

130 APCs, resulting in an 11.5-fold increase of dendritic cells and infiltration of lymphocytes througho

131 The interaction of dendritic cells and macrophages with a variety of rigid

132 ss both mMHCII antigen presentation in mouse dendritic cells and MHCII-dependent CD4(+) T cell activa

133 Antigen-presenting cells (APCs) including dendritic cells and monocytes instruct naive T cells to

134 d the frequencies and activation profiles of dendritic cells and monocytes present in the blood and l

135 bers of the microbiota regulate plasmacytoid dendritic cells and monocytes via TLR7 and MyD88 signali

136 ions by recruiting FOXP3(+)T cells, CD11c(+) dendritic cells and natural killer cells.

137 umor cell-derived lactate activates GPR81 in dendritic cells and prevents presentation of tumor-speci

138 esponses in the lungs that is independent of dendritic cells and T-cell priming in the draining lymph

139 ection in mice, with increased maturation of dendritic cells and the induction of protective CD8(+) T

140 ls have sustained contacts with intratumoral dendritic cells and tumor targets compared with low-avid

141 Dendritic cells are efficient at capturing microbes when

142 d systemic lupus erythematosus, plasmacytoid dendritic cells are not effector cells, have lost capaci

143 mulator of maturation of bone marrow-derived dendritic cells compared to E. coli LPS.

144 ed activation of primary bone marrow-derived dendritic cells ex vivo.

145 The role of dendritic cells in bone homeostasis, however, is not und

146 e factors associated with TNBC, whereas CD83 dendritic cells in the ALNs(-) were associated with the

147 d monocytes rapidly replaced macrophages and dendritic cells in tumors following administration of an

148 diated immune complex delivery to follicular dendritic cells in vivo.

149 kin fibroblasts or mouse bone marrow-derived dendritic cells infected with the protozoan parasite Tox

150 re observed in most CD11c(+)CD103(+) myeloid dendritic cells migrating to mediastinal draining lymph

151 ponses to cancer and virally-infected cells, dendritic cells must capture antigens present in tissues

152 In their search, dendritic cells perform a random walk by amoeboid migrat

153 remodeling of light and dark zone follicular dendritic cells required CXCL12-dependent crosstalk with

154 d for the development of conventional type 1 dendritic cells that are essential for cross-presentatio

155 1 (LYVE-1) mediates the docking and entry of dendritic cells to lymphatic vessels through selective a

156 preceded by poor activation of conventional dendritic cells type 2 (cDC2) due to reduced type 1 inte

157 ization efficacy by targeting and activating dendritic cells via C-type lectin receptors and reduce s

158 opria macrophages, and mesenteric lymph node dendritic cells were examined.

159 D56(dim) natural killer cells, monocytes and dendritic cells were not reduced in number and hence rel

160 Neutrophils and dendritic cells when migrating in confined environments

161 ifying a potential role for PD-L1 expressing dendritic cells within the lymph node in regulation of a

162 fessional' phagocytes (such as monocytes and dendritic cells) and 'non-professional' phagocytes, such

163 itors, monocytes, macrophages, and classical dendritic cells) are controlled by signals from the M-CS

164 und that histologic grade, intratumoral S100 dendritic cells, and CD8 T lymphocytes and CD57 natural

165 mmunity and comprise monocytes, macrophages, dendritic cells, and granulocytes.

166 late both iNKT-mediated activation of thymic dendritic cells, and iNKT availability in extrathymic si

167 including basal keratinocytes, fibroblasts, dendritic cells, and lymphocytes.

168 l responses of human monocytes, macrophages, dendritic cells, and neutrophils in response to stimulat

169 c cellular sources, rather than plasmacytoid dendritic cells, are responsible for interferon producti

170 nts and in their dependence on B7-expressing dendritic cells, B cells, and thymic epithelial cells.

171 by a dynamic mixture of macrophage subtypes, dendritic cells, granulocytes, and lymphocytes.

172 Bone marrow-derived macrophages and dendritic cells, lamina propria macrophages, and mesente

173 We also find that monocytes, neutrophils, dendritic cells, natural killer cells, innate lymphoid c

174 of six CBMPs containing regulatory T cells, dendritic cells, or macrophages; patient selection and i

175 D8 T cells, as they have natural tropism for dendritic cells, preeminent inducers of CD8 T cell immun

176 hritis), mainly inflammatory macrophages and dendritic cells, were characterized by co-expression of

177 ing that IL-36 acts directly on plasmacytoid dendritic cells, where it potentiates toll-like receptor

178 edullary thymic epithelial cells (mTECs) and dendritic cells, whereas TRP1 expression was restricted

179 ily, is the prototypic endocytic receptor of dendritic cells, whose ligands include phosphorothioated

180 s autoreactivity by stimulating plasmacytoid dendritic cells-(pDCs)-Type I interferon (IFN-I) and act

181 olated cf-mt-DNA capable of activating human dendritic cells.

182 as T follicular helper cells and follicular dendritic cells.

183 ion or functions of T cells, macrophages and dendritic cells.

184 -presented by professional APC, specifically dendritic cells.

185 duced expression of IFN-I in macrophages and dendritic cells.

186 fferentiation, predominantly of plasmacytoid dendritic cells.

187 anslational profile of renal macrophages and dendritic cells.

188 7 macrophages and murine bone marrow-derived dendritic cells; we now show that SLP-8321 and SLP-5818

189 epression-like behaviors by restoring D1-MSN dendritic complexity.

190 However, if electrical synapses were in axo-dendritic connections, where chemical synapses occur, th

191 dritic fields to approximate a uniformity in dendritic density across the retina.

192 idence for a conserved role of Tao kinase in dendritic development and function of sensory neurons, s

193 ured organization of E and I synapses across dendritic domains as well as within individual dendritic

194 unique arborization subdivided in segregated dendritic domains receiving distinct excitatory synaptic

195 e contacted by multiple BC4s through ongoing dendritic elaboration between 1 and 6 months of age-well

196 Langerhans cells and inflammatory dendritic epidermal cells (IDEC) are located in the epid

197 in a displacement of the normally occurring dendritic epidermal T cells (DETC) concomitant with an a

198 ss, enhanced corneocyte fragility, decreased dendritic epidermal T cells, and an exaggerated percutan

199 e that mismatches in the opposing actions on dendritic excitability may relate to these compounds' ce

200 Small changes in the kinetics of dendritic excitatory currents amplify when reaching the

201 NPY treatment reduces the complexity of the dendritic extent of anxiogenic BLA principal neurons, ma

202 achieve a constant coverage by varying their dendritic field area inversely with the local density of

203 ense axonal arborization that overlapped the dendritic field.

204 faced with a variable number of overlapping dendritic fields to approximate a uniformity in dendriti

205 d larger nuclei, thicker dendrites, and more dendritic filopodia than all other groups.

206 findings as to the nature of the changes in dendritic function in CA1 and PFC neurons based on the p

207 lar milieu.SIGNIFICANCE STATEMENT Changes in dendritic function, and voltage-gated ion channels in pa

208 Dendritic galactose moieties have a high affinity for ga

209 rent suite of techniques utilised to analyse dendritic growth in all-solid-state cells.

210 BDNF-dependent gene expression and neuronal dendritic growth mediated by the CREB transcription fact

211 e distinct mechanisms by which they regulate dendritic growth to generate their characteristic covera

212 otites, but inconsistent with an origin from dendritic growth.

213 show that the interplay between somatic and dendritic inhibition balances the increased excitatory w

214 interneurons mediating both perisomatic and dendritic inhibition in the somatosensory cortex.

215 ic calcium dysregulation is due to a loss of dendritic inhibition via decreased NMDAR currents and re

216 In so doing, amantadine enhances dendritic integration of excitatory synaptic potentials

217 overcomes a soma-retention signal to achieve dendritic localization.

218 iently impregnated for accurate quantitative dendritic measurements, descriptions of neuronal morphol

219 cking; however, the mechanism that regulates dendritic microtubule organization is still unclear.

220 Concurring with these dendritic mitochondrial changes, oligomycin A-insulted n

221 eficits, cognitive dysfunction, and abnormal dendritic morphogenesis.

222 Dendritic morphologies were also unaffected.

223 Interestingly, altered neuronal dendritic morphology is a common theme among several neu

224 We demonstrate that the dendritic nature of the hepatic artery, portal vein and

225 Perfusable dendritic networks in cell-laden hydrogels may help sust

226 e synthesis of DNA brick nanostructures with dendritic oligonucleotides attached to the outer surface

227 f their extensive arborisation and nonlinear dendritic operations.

228 ionally distinct prior to their segregation, dendritic outgrowth, and synapse formation.

229 Although the molecular machinery of dendritic patterning in c1vpda has been extensively stud

230 sity, and inhibition, indicative of enhanced dendritic plasticity and filtering of signals integrated

231 X (FX) suggests that increased constitutive dendritic protein synthesis yields exaggerated mGluR5-de

232 mulated neuronal growth cone development and dendritic protrusion formation, and we noted that ZBP1 a

233 actin mRNA localization resulted in abnormal dendritic protrusions and growth cone dynamics.

234 e in mediating depression-like behaviors via dendritic remodeling of NAc D1-MSNs and may prove a usef

235 ronal output were mediated by changes in the dendritic reversal potential for GABA.

236 coring the importance of connectivity within dendritic river systems.

237 n experience-dependent negative regulator of dendritic segment number during the visual critical peri

238 ction selectivity independently within small dendritic segments (<10um) with remarkable accuracy.

239 of GluN2B-NMDARs between proximal and distal dendritic segments, whereas the topography of GluN2A-NMD

240 ndritic domains as well as within individual dendritic segments.

241 ic cytoskeletal protein enriched in neuronal dendritic shafts.

242 The membrane properties, soma-dendritic shape, and intrastriatal and extrastriatal syn

243 the technology to calcium imaging of entire dendritic spans of neurons as well as neural ensembles w

244 pattern (subthreshold or suprathreshold for dendritic spikes), and (3) the stimulation of neighborin

245 Taken together, our results suggest that the dendritic spine abnormalities are primary developmental

246 ck of OTR expression correlates with reduced dendritic spine densities in selected cortical regions o

247 on and synaptic plasticity but had increased dendritic spine density compared with young WT.

248 ls with simplified dendritic arbors, reduced dendritic spine density, and diminished excitatory synap

249 greater vGlut1/PSD95 colocalization, higher dendritic spine density, and enhanced evoked AMPAR and N

250 a recruits Ror2 and Ryk receptors to enhance dendritic spine density, leading to nociceptive sensitiz

251 ved cognitive function, synaptic plasticity, dendritic spine density, microglial morphology, and brai

252 tal cortex neurons leads to perturbations in dendritic spine development and hypoconnectivity, which

253 ity (PSD), which is critical for synapse and dendritic spine development.

254 t time, the ongoing, steady-state changes in dendritic spine dynamics in the dorsal horn associated w

255 ed the role of sleep in experience-dependent dendritic spine elimination of layer 5 pyramidal neurons

256 oenergetics, enhances synaptic viability and dendritic spine formation, and increases turnover of neu

257 n corticospinal neurons, where they regulate dendritic spine formation, axon elongation, and pontine

258 PS2APP;Trem2(ko) mice also exhibited more dendritic spine loss around plaque and more neurofilamen

259 orphology demonstrated dendritic atrophy and dendritic spine loss in dorsal striatum D1-MSNs from mic

260 In addition, Tet3 cKO mice exhibit increased dendritic spine maturation in the ventral CA1 hippocampa

261 functional synaptic plasticity and abnormal dendritic spine morphology, but little is known about ho

262 ost-synaptic currents accompanied changes in dendritic spine nano-architecture, and single-synapse cu

263 Together, our data indicate dendritic spine plasticity is MSN subtype specific, impr

264 However, it remains unclear if the dendritic spine plasticity is MSN subtype specific.

265 Assess occurrence of the dendritic spine scaffolding protein Drebrin as a pathoph

266 ion flow, in driving synaptic weakening and dendritic spine shrinkage during synaptic plasticity.

267 ergic transmission, synaptic plasticity, and dendritic spine structure.

268 the NMDAR is required to maintain NMDARs at dendritic spine synapses and mediates the direct extrace

269 both enhanced mEPSC frequency and increased dendritic spine-density.

270 + transients were also generated on discrete dendritic spine-like structures on the melanocytes.

271 kinases are contained in axon terminals and dendritic spines adjacent to the synaptic membrane, whic

272 ion, we identified changes in pyramidal cell dendritic spines and axon initial segments consistent wi

273 that most of them were excitatory, targeting dendritic spines and displaying a macular shape, regardl

274 tau species and related signaling to protect dendritic spines and processes from Abeta-induced injury

275 knock-in mice enabled thorough evaluation of dendritic spines and synapses on pathway-identified SPNs

276 tion alone can induce tau mislocalization to dendritic spines and synaptic deficits in cultured rat h

277 studies have reported downsizing and loss of dendritic spines following sleep deprivation.

278 We present a concise review of the role of dendritic spines in neuropathic pain and outline the pot

279 Structural plasticity of dendritic spines is a key component of the refinement of

280 otein that suppresses synaptic plasticity in dendritic spines of hippocampal neurons.

281 MIA increases plastic dendritic spines of the intrinsically bursting neurons a

282 terminals, presynaptic mitochondria, and in dendritic spines of xCT(-/-) mice.

283 Formation of dendritic spines on newborn neurons was also impaired fo

284 Here, we profiled the in vivo dynamics of dendritic spines over time on the same superficial dorsa

285 triatal medium spiny neurons, the density of dendritic spines, or the density or ultrastructure of co

286 her small compartments like primary cilia or dendritic spines.

287 n and long-term maintenance of dendrites and dendritic spines.

288 12 noon and processed for quantification of dendritic spines.

289 in synthesis-dependent structural changes of dendritic spines.

290 m the dendrite tips, thereby smoothening the dendritic surface.

291 ues than Control cases in seven of the eight dendritic system measures.

292 Dendritic systems of 20 neurons per region in each brain

293 rewire, two contact new cones within stable dendritic territories, whereas one expands its dendrite

294 lanocytes, melanosomes mature and traffic to dendritic tips, where they are transferred to adjacent e

295 ls had a normal complement of TRPM1 at their dendritic tips, while GPR179 accumulation was partially

296 genes establish phrenic MN organization and dendritic topography through the regulation of phrenic-s

297 y of GluN2A-NMDARs remains similar along the dendritic tree.

298 targeting distal apical dendrites and apical dendritic tufts of pyramidal neurons in layer I, and rar

299 nergic modulation were mediated, in part, by dendritic voltage-gated calcium channels (VGCCs): pharma

300 ic factor (BDNF) enhances co-localization of dendritic ZBP1 and PAT1 within granules that also contai