ライフサイエンスコーパス: pyramidal

1 Granular, zymogen-rich pyramidal acinar cells in normal glands predominated ove

2 l feedback inhibition during synchronous CA1 pyramidal activity.

3 us, and stimulus-evoked response profiles of pyramidal and inhibitory neurons belonging to deep and s

4 r primary sensory areas have elucidated that pyramidal and inhibitory neurons belonging to distinct l

5 ale mice to monitor the activity of putative pyramidal and inhibitory neurons located in deep and sup

6 lication and associated firing alteration of pyramidal and interneuron populations led to lasting cha

7 of tiagabine on GABAergic modulation of deep pyramidal and interneuronal cell populations.

8 tial (LFP), and increases calcium signals in pyramidal and neuronal nitric oxide synthase (nNOS)-expr

9 nt pitches on different facets of an inverse pyramidal array, a multiplexing structure-color filter i

10 reaction of a judiciously selected trigonal pyramidal building block, 1,3,5-Tris(4-aminophenyl)adama

11 At hippocampal pyramidal CA3-CA1 synapses, RIM-BP2 loss has a mild effe

12 ng interneurons mediate distinct features of pyramidal cell activity(4-6), the SCG2-dependent reorgan

13 havior in rats by optogenetically inhibiting pyramidal cell and interneuron subpopulations.

14 levels in murine cortex, and increases both pyramidal cell arborization and PSD-95 expression in the

15 Reduced pyramidal cell arborization occurs with stress and MDD,

16 erage the precise targeting of chandelier-to-pyramidal cell connectivity to understand how homeostati

17 is prediction, hippocampal gamma rhythms and pyramidal cell coupling to theta phase are significantly

18 Their inhibition of pyramidal cell dendrites and of fast-spiking, parvalbumi

19 a-aminobutyric acid interneurons that target pyramidal cell dendrites, has been reported in several b

20 In addition, we identified changes in pyramidal cell dendritic spines and axon initial segment

21 gamma power is increased with pyramidal cell disinhibition and with remission from MDD

22 M rapidly activated biophysically unique PFC pyramidal cell ensembles.

23 whether and how burst propensity relates to pyramidal cell heterogeneity.

24 in forebrain GABAergic synapses resulting in pyramidal cell hyperexcitability and disruptions in netw

25 nappreciated role for MRs in controlling CA2 pyramidal cell identity and in facilitating CA2-dependen

26 r identified multiple classes of isocortical pyramidal cell in a pattern matching their known organiz

27 GABA, excess PNN deposition likely increases pyramidal cell inhibition.

28 ults indicate that progenitor cells generate pyramidal cell lineages with a wide range of sizes and l

29 a type of GABAergic interneuron that control pyramidal cell output through axo-axonic synapses that t

30 iggers as well as converging effects on Drd1-pyramidal cell signaling that underlie the antidepressan

31 HT(4)R acutely in the mPFC or targeting mPFC pyramidal cell terminals in the DRN might constitute a s

32 ce that the classical CA3, CA1 and subiculum pyramidal cell types all exhibit prominent and spatially

33 easuring spike transmission probabilities in pyramidal cell-interneuron spike cross-correlations that

34 crossed with mouse lines labeling excitatory pyramidal cells (PCs) and inhibitory PV cells.

35 kes initiated in the distal trunk of layer 5 pyramidal cells (PCs) underlie nonlinear dynamic changes

36 Patch-clamp recordings of ventral CA1 pyramidal cells 24 h after a single systemic administrat

37 all membrane time constants observed in both pyramidal cells and interneuron cell bodies, the low-fre

38 late phase of spike-frequency adaptation in pyramidal cells and is recruited later than both SK and

39 H and EM to reconstruct hundreds of cortical pyramidal cells and show that more superficial cells rec

40 onal assemblies composed of interneurons and pyramidal cells are prominent in the somatosensory corte

41 be connectomic principles for the control of pyramidal cells at their apical dendrites and support di

42 is well described in principal glutamatergic pyramidal cells but poorly understood in GABAergic inhib

43 ion of GABA release and synaptic inputs onto pyramidal cells erode the emergence of functional topogr

44 These pyramidal cells express specialized nicotinic acetylchol

45 innervation of apical dendrites of cortical pyramidal cells in a region between layers (L) 1 and 2 u

46 onal properties of L2, L3 and subtypes of L5 pyramidal cells in cortex.

47 ing electrophysiological recordings from CA1 pyramidal cells in freely moving mice, we report that a

48 was used to examine the role of neocortical pyramidal cells in generating spasms.

49 hat was tested on basolateral amygdala (BLa) pyramidal cells in mouse brain slices.

50 iGluSnFR variants in vitro, transfection of pyramidal cells in organotypic hippocampal cultures, and

51 NKA transport activity in single hippocampal pyramidal cells in situ We have found that neuronal NKA

52 ns and found that activating Drd1 expressing pyramidal cells in the mPFC produces rapid and long-last

53 tic inhibition onto dendrites of hippocampal pyramidal cells is increased.

54 We found that, in pyramidal cells of visual and prefrontal cortices and hi

55 und that increases in the activity of either pyramidal cells or individual ChCs during this temporal

56 Our models explain how the activation of pyramidal cells or PV(+) cells can trigger SWRs, as show

57 FICANCE STATEMENT A minimal model of layer 5 pyramidal cells replicates all known features crucial fo

58 Only L3 pyramidal cells showed homogeneous inhibitory input frac

59 Remarkably, acute chemogenetic inhibition of pyramidal cells successfully corrected memory deficits a

60 Chemogenetic activation of neocortical pyramidal cells supported these observations, as it incr

61 nput was at least about 2-fold larger for L5 pyramidal cells than for all others.

62 ection window of direct excitatory inputs to pyramidal cells whereas increasing [GABA] through GABA u

63 In hippocampal pyramidal cells, a small subset of dendritic spines cont

64 tive/nitrosative stress of prefrontal cortex pyramidal cells, and ultimately improved the behavior of

65 ver, many neuronal classes, such as cortical pyramidal cells, are electrically extended objects.

66 inal cortex layer 2, putative CA1-projecting pyramidal cells, but not putative dentate gyrus/CA3-proj

67 utamatergic input to mouse prefrontal cortex pyramidal cells, leading to antidepressant-relevant acti

68 Here, we show how the interactions between pyramidal cells, parvalbumin-positive (PV(+)) basket cel

69 Among putative pyramidal cells, preferred phase tiles phase space, but

70 distal dendritic regions respectively of CA1 pyramidal cells, PV-iLTD and SST-iLTP coordinate a repri

71 CA3 pyramidal cells, the targets of DGC-derived mossy fibers

72 ivation of interneurons suppressed firing of pyramidal cells, unexpectedly the majority of interneuro

73 tors in hippocampal interneurons but not CA1 pyramidal cells, which is consistent with the expression

74 s pathological hyperactivity of motor cortex pyramidal cells, while concurrently activating somatosta

75 aired mitochondrial function in both PVI and pyramidal cells.

76 pulations and the resulting disinhibition of pyramidal cells.

77 synaptic plasticity between interneurons and pyramidal cells.

78 firing rate changes of interneurons but not pyramidal cells.

79 ptic ratio is thus specific for the types of pyramidal cells.

80 distinctive subcellular localization within pyramidal cells.

81 imate the membrane potential perturbation in pyramidal cells.

82 ven as they flip from exciting to inhibiting pyramidal cells.

83 ld larger for L2 than L3 and L5 thick-tufted pyramidal cells.

84 tic responses and somatic spike rates within pyramidal cells.

85 in interneurons and GluN1/2A/2B receptors in pyramidal cells.

86 eurons, which target the distal dendrites of pyramidal cells.

87 etection window for excitatory inputs to CA1 pyramidal cells.

88 put patterns in perisomatic dendrites of CA1 pyramidal cells.

89 considers electronic delocalization between pyramidal diradical resonance structures and associated

90 etamine activates mTORC1-4E-BP signalling in pyramidal excitatory cells of the cortex(8,14).

91 anel criteria and Lublin criteria, a Kurtzke pyramidal functional subscore of at least 2 (defined as

92 h Expanded Disability Status Scale score and pyramidal functional system score.

93 )(4)], 2-U(PN)NMes, exhibits a unique square pyramidal geometry in contrast to the expected trigonal

94 the Zn center was determined to have square-pyramidal geometry with four Zn-N bonds in the equatoria

95 d by X-ray crystallography, showing a square pyramidal geometry with two coordinated nitrate anions.

96 e composed of micron-scale needles featuring pyramidal heads supported by undercut stem regions with

97 hyperexcitability that appeared only in CA3 pyramidal hippocampal neurons that were derived from pat

98 reatment (lithium responders) and not in CA3 pyramidal hippocampal neurons that were derived from pat

99 neuron populations led to lasting changes in pyramidal-interneuron connection weights as indicated by

100 iative and non-associative reorganization of pyramidal-interneuron connections triggered by the optog

101 trodes in the dentate granule layer and pCA3 pyramidal layer can also record mossy cells, thus introd

102 pposite pattern, with decreases in total and pyramidal layer thickness from motor to frontal associat

103 ower than ideal c/a ratio promotes non-basal pyramidal <c + a> slip and deformation twinning in epsil

104 tal coordination, (2) a thiophilic, trigonal pyramidal metalloid (Pb(II)) that binds to these sulfurs

105 ranslocation through silicon-based truncated pyramidal nanopores.

106 tic tectum of other teleost fish: the tectal pyramidal neuron (PyrN).

107 Modulation of pyramidal neuron activity alone had little effect on bas

108 tational model highlights that a decrease in pyramidal neuron activity induced by DBS or by a stimula

109 on activity, (2) ventral hippocampal (vHipp) pyramidal neuron activity, and (3) the number of parvalb

110 ) imaging up to 20 kHz in the rat layer five pyramidal neuron axon we found that activity-dependent i

111 and (2) ongoing population activity of such pyramidal neuron clique is temporally linked to the acti

112 ts cortical microcircuit features (including pyramidal neuron depth and glial expression) and allowed

113 ession restored HCN1 channel trafficking and pyramidal neuron excitability in the BLA of Tmem74(-/-)

114 nt with the effects of chronic reductions in pyramidal neuron firing, and enhancement of this activit

115 s of maternal choline supplementation on CA1 pyramidal neuron gene expression in the Ts65Dn mouse mod

116 Shank3 in vS1 inhibitory interneurons led to pyramidal neuron hyperactivity and increased stimulus se

117 5-regulated signaling effectors that control pyramidal neuron migration and dendritogenesis.

118 out and Cullin 5 knockdown cause hippocampal pyramidal neuron mislocalization and development of mult

119 n utero electroporation resulted in abnormal pyramidal neuron morphology, polarization, and positioni

120 es was attenuated, likely reflecting reduced pyramidal neuron spiking.

121 microcircuit alterations resulted in reduced pyramidal-neuron firing and increased phase locking to c

122 In a previous study, we showed that pyramidal-neuron specific conditional knockout (cKO) of

123 ed the frequency of spontaneous IPSCs in CA1 pyramidal neurons >twofold (KA: P = 0.04; pilocarpine: P

124 Thus, in L4 pyramidal neurons (considered a single transcriptional c

125 uman and nonhuman primate neocortex, layer 3 pyramidal neurons (L3PNs) differ significantly between d

126 Layer 5 pyramidal neurons (L5PNs) in particular are thought to b

127 was used to compare the soma size of typical pyramidal neurons (n = 2,238) across all three cortical

128 chronized activation of excitatory layer 2/3 pyramidal neurons (PNs) and to a lesser degree layer 4 n

129 arvalbumin-expressing interneurons (PVs) and pyramidal neurons (PNs) by dLGN, LP, and cortical feedba

130 ctions, we recorded extracellularly from CA2 pyramidal neurons (PNs) in male mice during social behav

131 enetically-labeled layer 2/3 (L2/3) cortical pyramidal neurons (PNs) in vivo.

132 rimary visual cortex, various populations of pyramidal neurons (PNs) send axonal projections to disti

133 tostatin-positive Martinotti cells (MCs) and pyramidal neurons (PNs) was strongly enhanced, with no a

134 that contacted the axon initial segments of pyramidal neurons (PNs).

135 number of spontaneously active putative BLA pyramidal neurons 1-2 weeks, but not 5-6 weeks post stre

136 nsity and destabilized spines of hippocampal pyramidal neurons 4 weeks after intracerebroventricular

137 nation of how a class of prefrontal cortical pyramidal neurons achieve efficient integration of subth

138 and show that populations of human cortical pyramidal neurons and cerebellar Purkinje cells show sig

139 Setd1a targets are highly expressed in pyramidal neurons and display a complex pattern of trans

140 , Drd1 and Drd2 dopamine receptor expressing pyramidal neurons and found that activating Drd1 express

141 P) in the Schaffer collateral pathway of CA1 pyramidal neurons and in vitro blocked LTP-induced surfa

142 ronger synapses between coactivated cortical pyramidal neurons and neurons in the dorsal striatum (DS

143 in the physiology and structure of premotor pyramidal neurons and support recovery of function.

144 development of dendritic arbors of cortical pyramidal neurons and the influence of experience.

145 l state-dependent functional connectivity of pyramidal neurons and vasoactive intestinal peptide-expr

146 Hippocampal pyramidal neurons are characterized by a unique arboriza

147 atosensory cortex (S1) of mice, layer 5 (L5) pyramidal neurons are major outputs to downstream areas

148 Layer 5 pyramidal neurons are the main output neurons of the cor

149 ptic strength of vHIP inputs onto layer five pyramidal neurons as contributing factors of aberrant vH

150 identify a projection-defined subtype of PFC pyramidal neurons as key mediators of impulse control.

151 nput from infragranular layers to layers 2/3 pyramidal neurons as the key component of hyperexcitable

152 illations by increasing activity in cortical pyramidal neurons at the frequency of slow waves restore

153 those observed in other felids, with typical pyramidal neurons being the most prominent neuronal type

154 tly differentiated 87.4% of complete typical pyramidal neurons between the African leopard and cheeta

155 ed spontaneous and stimulus-evoked firing in pyramidal neurons but reduced activity in interneurons.

156 inhibition of Fos-activated hippocampal CA1 pyramidal neurons by parvalbumin-expressing interneurons

157 regulating synaptic receptor trafficking in pyramidal neurons by SorCS2.

158 849 3D reconstructions of the basal arbor of pyramidal neurons collected across early postnatal devel

159 at spatial and temporal activity patterns of pyramidal neurons correlated with their topographical po

160 potassium channels in dendrites of cortical pyramidal neurons counter-intuitively promote rather tha

161 Activation of layer 2/3 pyramidal neurons drives fast oscillations throughout de

162 We observed complete activation of CA1 pyramidal neurons during brief seizures, followed by a s

163 ontal cortex (dlPFC), where microcircuits of pyramidal neurons enable persistent firing in the absenc

164 nobutyric acid (GABA)-ergic interneurons and pyramidal neurons evoke cortical gamma oscillations, whi

165 tory synapse between hippocampal CA3 and CA1 pyramidal neurons exhibits long-term potentiation (LTP),

166 y to investigate the development of cortical pyramidal neurons following migration and maturation of

167 different timescales in cultured hippocampal pyramidal neurons from mice of either sex.

168 High-activity L4 pyramidal neurons had greater intrinsic excitability and

169 role in synaptic facilitation in hippocampal pyramidal neurons has been difficult due to size limitat

170 of inhibitory synaptic transmission onto OFC pyramidal neurons in a regionally selective manner.

171 Moreover, pyramidal neurons in A25 had a heightened density of NMD

172 s and reduced kainate-evoked currents in CA1 pyramidal neurons in acute hippocampal slices.

173 d Immunoglobulin-like receptor B (PirB) from pyramidal neurons in adult mouse hippocampus results in

174 A novel population of pyramidal neurons in ALM layer 2 may mediate this proces

175 We found enhanced excitation of CA1 pyramidal neurons in astrocyte-specific ephrin-B1 KO mal

176 nd (2) an increased number of cFos-activated pyramidal neurons in CA3, an outcome that appears to pro

177 We used in vivo 2-photon imaging of pyramidal neurons in cortical layers L4 and L2/3 of awak

178 cterized excitatory inputs contacting single pyramidal neurons in ferret primary visual cortex (V1) b

179 nnel dysfunction in hyperexcitability of CA3 pyramidal neurons in Fmr1 knock-out (KO) mice.

180 ical dendrites and apical dendritic tufts of pyramidal neurons in layer I, and rarely target other in

181 and electrophysiological properties of human pyramidal neurons in long-term brain slice cultures.

182 enetic activation of small ensembles of L2/3 pyramidal neurons in mouse barrel cortex while simultane

183 hological and functional characterisation of pyramidal neurons in mouse mPFC during the first postnat

184 esults also demonstrate that Drd1-expressing pyramidal neurons in mPFC mediate the rapid antidepressa

185 ction was significantly increased in layer V pyramidal neurons in mPFC of D(2)R-GSK-3beta(-/-) mice,

186 atments further suppressed the activities of pyramidal neurons in PrL, suggesting that EA treatments

187 endrites of many neurons, including cortical pyramidal neurons in sensory cortex, is characterized by

188 istributions in perisomatic dendrites of CA1 pyramidal neurons in slices from adult male rats.

189 Furthermore, L5 pyramidal neurons in the ACC did not exhibit dendritic C

190 om the distal apical dendrite to the soma in pyramidal neurons in the ACC, which was significantly be

191 the apical dendrite and soma of layer 5 (L5) pyramidal neurons in the anterior cingulate cortex (ACC)

192 ce and adulthood on the activity of putative pyramidal neurons in the BLA and corticoamygdalar plasti

193 tonic inhibition is significantly reduced in pyramidal neurons in the CA1 region of the hippocampus i

194 atively, somatodendritic measures of typical pyramidal neurons in the cheetah were generally larger t

195 For neural activity, individual layer 2/3 pyramidal neurons in the cingulate and medial secondary

196 production of excitatory synapses in layer 5 pyramidal neurons in the cortex and increases seizure su

197 bitory postsynaptic currents (sIPSCs) on CA1 pyramidal neurons in the hippocampus.

198 cellular compartment-specific innervation of pyramidal neurons in the mammalian cerebral cortex.

199 ysfunction to layer V intrinsically bursting pyramidal neurons in the prefrontal cortex of mice.

200 excitatory synaptic transmission in layer V pyramidal neurons in the prelimbic mPFC.

201 reduced tonic inhibition in hippocampal CA1 pyramidal neurons in the Rett syndrome mice, reveal a po

202 rtal (postnatal day 21-40) EE on DA neurons, pyramidal neurons in the ventral hippocampus, and projec

203 ndent dendritic spine elimination of layer 5 pyramidal neurons in the visual (V1) and frontal associa

204 drites and dendritic spines of supragranular pyramidal neurons in tissue from human frontal and occip

205 The development of the dendritic arbor in pyramidal neurons is critical for neural circuit functio

206 e propose that the dendritic architecture of pyramidal neurons might determine burst-firing by settin

207 to studying the phenotype of CA3 hippocampal pyramidal neurons of 6 patients with BD compared with 4

208 of sorting receptors, is highly expressed in pyramidal neurons of CA2, as well as ventral CA1, a circ

209 citatory and inhibitory inputs to individual pyramidal neurons of layer 2/3 of the mouse visual corte

210 e show that frontal association cortex (FrA) pyramidal neurons of mice integrate auditory cues and ba

211 (DLPFC) gray matter and layer 3 and layer 5 pyramidal neurons of subjects with schizophrenia or bipo

212 ments occur in glutamatergic synapses in the pyramidal neurons of the anterior cingulate cortex (ACC)

213 analyzed the dendritic spine morphologies in pyramidal neurons of the hippocampal and Cortical layer

214 CA1 pyramidal neurons of the hippocampus from these mice exh

215 as postsynaptic recognition molecules in CA1 pyramidal neurons of the hippocampus, where they are loc

216 egulates plastic thin spines on layer II/III pyramidal neurons of the medial prefrontal cortex via CX

217 d rapid Golgi staining on the layer IV and V pyramidal neurons of the parietal cortex and the CA1 bas

218 m that adjusts neuronal excitability in L2/3 pyramidal neurons of the PFC and may thereby modulate th

219 ansiently expressed in a subset of layer 5-6 pyramidal neurons of the prefrontal cortex (PFC).

220 Genes associated with intelligence implicate pyramidal neurons of the somatosensory cortex and CA1 re

221 ntegration of feedback excitation from local pyramidal neurons onto mouse CA1 PV+ cells.

222 s are not affected by removal of Pcdhgs from pyramidal neurons or glial cells.

223 ed contrast, reduced Tiam1 expression in CA1 pyramidal neurons produced no effect on glutamatergic sy

224 verexpression of miR-218 selectively in mPFC pyramidal neurons promotes resilience to CSDS and preven

225 Neocortical pyramidal neurons regulate firing around a stable mean f

226 s specifically disrupted, whereas input onto pyramidal neurons remained intact.

227 ecific gene expression profiling of cortical pyramidal neurons revealed aberrant regulation of genes

228 gical recordings from female layer V PrL-PFC pyramidal neurons revealed CB1R-dependent CORT-induced s

229 Chemogenetic stimulation of IL pyramidal neurons reversed EtOH-driven fear memory overg

230 layers, and layer 2/3 (but not deeper layer) pyramidal neurons show bias for front-to-back motion spe

231 recording from pairs of neighboring cortical pyramidal neurons showed a reduction of synchronous spon

232 larger population of low contrast preferring pyramidal neurons than deeper layers, and layer 2/3 (but

233 We find that ensembles of CA2 pyramidal neurons that are active during social explorat

234 hibition of auditory responses in deep-layer pyramidal neurons that is selective for behaviorally rel

235 n the cortex regulate feedback inhibition of pyramidal neurons through suppression of somatostatin-ex

236 are necessary for the dendritic outgrowth of pyramidal neurons to the superficial strata of the hippo

237 oth feedforward and feedback inhibition onto pyramidal neurons underscoring the importance of glutama

238 This suggests that frontal pyramidal neurons use a different integration scheme com

239 We found that the response of FrA pyramidal neurons was more pronounced to Gaussian noise

240 somatostatin-positive interneurons (SOM) to pyramidal neurons were altered in a layer- and site-spec

241 is revealed that gene sets of layer 5b and 6 pyramidal neurons were enriched in DEGs of the mPFC down

242 In contrast, gene sets of layer 5a pyramidal neurons were enriched in upregulated DEGs of t

243 l small-world cliques preferably incorporate pyramidal neurons with similar visual feature tuning, an

244 ological recordings of mouse CA1 hippocampal pyramidal neurons, AK-42 acutely and reversibly inhibits

245 inhibition and intrinsic excitability in CA1 pyramidal neurons, and rescue the phenotype of increased

246 oral summation of AON inputs within piriform pyramidal neurons, and suggest that the AON could powerf

247 level was very low in hippocampal and cortex pyramidal neurons, but strongly expressed in the corpus

248 coordinating the spike timing of excitatory pyramidal neurons, but the role distinct inhibitory circ

249 to reduce local GABAergic transmission onto pyramidal neurons, disrupt prefrontal excitatory-inhibit

250 ty strongly shapes the spiking pattern of GC pyramidal neurons, eliciting phase-locked spiking across

251 ult knockout mice, there were fewer cortical pyramidal neurons, interneurons, cholinergic basal foreb

252 Given the diversity of CA2/CA3 pyramidal neurons, it is currently unknown whether and h

253 complexity and spine density of upper layer pyramidal neurons, leading to an excitation/inhibition i

254 activation of Channelrhodopsin 2-expressing pyramidal neurons, or 200 ms silencing of Archeorhodopsi

255 ms silencing of Archeorhodopsin T-expressing pyramidal neurons, to generate local cortical UP, or DOW

256 In pyramidal neurons, we found an increase in monocarboxyla

257 g with an increased spine density in layer V pyramidal neurons, were detected in D(2)R-GSK-3beta(-/-)

258 nitial segment and somatodendritic domain of pyramidal neurons, where it interacts directly with the

259 ogical and transcriptional trajectory of PFC pyramidal neurons, which could enhance vulnerability to

260 a subset of dorsomedial PFC (dmPFC) layer 5 pyramidal neurons, which project to the subthalamic nucl

261 calization of mGluR2 in mouse frontal cortex pyramidal neurons.

262 hippocampus have focused on disturbances in pyramidal neurons.

263 shape the influence of converging inputs to pyramidal neurons.

264 membrane properties relative to neighboring pyramidal neurons.

265 ed VENs, but also fork cells and a subset of pyramidal neurons.

266 d for perception of cortical activity is ~14 pyramidal neurons.

267 transients in the apical dendritic spines of pyramidal neurons.

268 emistry and electron microscopy in mouse CA1 pyramidal neurons.

269 ir potential to activate or inhibit piriform pyramidal neurons.

270 t and indirect feedforward inhibition to CA3 pyramidal neurons.

271 morphologic changes in perilesional layer 3 pyramidal neurons.

272 ion but not on the PV+ perisomatic puncta on pyramidal neurons.

273 spatiotemporal spinule dynamics in cortical pyramidal neurons.

274 lationship between cortical interneurons and pyramidal neurons.

275 ons and apical tufts dendrites of excitatory pyramidal neurons.

276 the subiculum and all identified cells were pyramidal neurons.

277 y striatal medium spiny neurons and cortical pyramidal neurons.

278 on balance and increases excitability of CA3 pyramidal neurons.

279 apical dendrite of S1 (somatosensory cortex) pyramidal neurons.

280 hibitory inputs onto mouse auditory cortical pyramidal neurons.

281 d pattern of findings was also identified in pyramidal neurons.

282 aptic localization of SR and d-serine in CA1 pyramidal neurons.

283 tamatergic excitatory synapses onto piriform pyramidal neurons; and while these inputs are not as str

284 the axon initial segment (AIS) of excitatory pyramidal neurons; the subcellular domain where action p

285 ition is exploited to induce either a NiO(5) pyramidal or a NiO(6) octahedral structure at the SCO/LN

286 In vitro patch-clamp recordings from L5B pyramidal output neurons showed age-related nAChR subuni

287 ng, while passive isoforms usually bind to a pyramidal plane at slower rates.

288 irst show that in response to repeated tones pyramidal (Pyr) neurons in male mouse auditory cortex (A

289 This contrasts starkly with the pattern of pyramidal recruitment, which is greatly delayed.

290 s three isomers in solution including square-pyramidal [Ru(PPh(3))(2)(C(6)H(4)PPh(2))(ZnMe)] (5), tha

291 he ReB(3)(-) cluster is shown to have a near-pyramidal structure, while ReB(4)(-) is found to be a pl

292 Confirmation of the 3D, pyramidal structures was verified and supported by a com

293 with focal cord lesions and correlated with pyramidal subscore (r ranging from -0.53 to -0.40; P < .

294 CK+ interneurons make stronger synapses onto pyramidal tract (PT) cells over nearby intratelencephali

295 ells also inhibit the apical dendrites of L5 pyramidal tract (PT) cells to suppress action potential

296 with the structural integrity of either the pyramidal tract (PT) or alternate motor fibers (aMF).

297 Pyramidal tract neurons (PTNs) within macaque rostral ve

298 In addition, the initial state of layer 5 pyramidal tract neurons contained a memory trace of the

299 corticothalamic (CT) neurons in layer 6 and pyramidal tract-type (PT) neurons in layer 5B.

300 Our data further show that pyramidal-tract neurons in the cortex collateralized wit