ライフサイエンスコーパス: pyramidal neuron

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

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

3 transients in the apical dendritic spines of pyramidal neurons.

4 emistry and electron microscopy in mouse CA1 pyramidal neurons.

5 ir potential to activate or inhibit piriform pyramidal neurons.

6 t and indirect feedforward inhibition to CA3 pyramidal neurons.

7 morphologic changes in perilesional layer 3 pyramidal neurons.

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

9 spatiotemporal spinule dynamics in cortical pyramidal neurons.

10 lationship between cortical interneurons and pyramidal neurons.

11 ons and apical tufts dendrites of excitatory pyramidal neurons.

12 the subiculum and all identified cells were pyramidal neurons.

13 y striatal medium spiny neurons and cortical pyramidal neurons.

14 ivity between each other than with nonmember pyramidal neurons.

15 d astrocyte-mediated tonic inhibition of CA1 pyramidal neurons.

16 on balance and increases excitability of CA3 pyramidal neurons.

17 of apical and basal dendritic arbors of CA1 pyramidal neurons.

18 (PSD), and reduced synaptic transmission of pyramidal neurons.

19 regulated Schaffer collateral pathway LTP in pyramidal neurons.

20 expressed in the brain regions with abundant pyramidal neurons.

21 orated-patch recordings from CA1 hippocampal pyramidal neurons.

22 rmal input-output signal transmission of CA3 pyramidal neurons.

23 neurons, ChAT-VIP neurons did not disinhibit pyramidal neurons.

24 mined using whole-cell recordings in layer V pyramidal neurons.

25 elp to explain the morphology of neocortical pyramidal neurons.

26 ger optogenetic silencing of a subset of CA1 pyramidal neurons.

27 excitability of neocortical layer 2/3 (L2/3) pyramidal neurons.

28 ed the slow AHP component (sAHP) in cortical pyramidal neurons.

29 ndritic Ca(2+) spikes in neocortical layer 5 pyramidal neurons.

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

31 hibitory inputs onto mouse auditory cortical pyramidal neurons.

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

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

34 calization of mGluR2 in mouse frontal cortex pyramidal neurons.

35 hippocampus have focused on disturbances in pyramidal neurons.

36 shape the influence of converging inputs to pyramidal neurons.

37 membrane properties relative to neighboring pyramidal neurons.

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

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

40 examine FMRP mRNA targets in hippocampal CA1 pyramidal neurons, a critical cell type for learning and

41 ility of prelimbic (PL) and infralimbic (IL) pyramidal neurons; a cocaine-induced increase in PL exci

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

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

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

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

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

47 of fear conditioning and extinction on PVIN-pyramidal neuron and SSTIN-pyramidal neuron synapses in

48 olves the coordinated activity of excitatory pyramidal neurons and a specific population of inhibitor

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

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

51 iform discharges were recorded in layer V-VI pyramidal neurons and fast-spiking interneurons in slice

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

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

54 ogy of leading process in radially-migrating pyramidal neurons and its impact on radial migration.

55 KO mice revealed higher E/I ratio in layer 5 pyramidal neurons and lower general protein synthesis.

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

57 Cytoarchitecture and morphology of pyramidal neurons and parvalbumin-positive inhibitory in

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

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

60 ation preserved excitatory synaptic drive to pyramidal neurons and their excitability in the periinfa

61 cipal site of communication between cortical pyramidal neurons and their targets, a key locus of acti

62 We studied pyramidal neurons and two classes of GABAergic interneur

63 D and BD on synaptic connectivity of layer 5 pyramidal neurons and underscore the persistent impact o

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

65 n of task-related coding properties of dmPFC pyramidal neurons and, to a lesser extent, medium spiny

66 lity and action potential properties of L2/3 pyramidal neurons, and identifies Nav1.6 as a new potent

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

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

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

70 find that the effects of D2Rs on prefrontal pyramidal neurons are actually mediated by pathways asso

71 Hippocampal pyramidal neurons are characterized by a unique arboriza

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

73 ng global cerebral ischemia, hippocampal CA1 pyramidal neurons are more vulnerable to injury than the

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

75 r RNAs, which migrate to distal dendrites of pyramidal neurons, are selectively reduced, and their ex

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

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

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

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

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

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

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

83 ere they target not only distal dendrites of pyramidal neurons but also a sparse population of inhibi

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

85 y not essential for synapse formation in CA1 pyramidal neurons but shape synaptic properties and that

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

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

88 inals in vitro reduced firing of hippocampal pyramidal neurons by increasing inhibitory inputs.

89 Inhibiting pyramidal neurons by optogenetically activating somatost

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

91 regulating synaptic receptor trafficking in pyramidal neurons by SorCS2.

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

93 849 3D reconstructions of the basal arbor of pyramidal neurons collected across early postnatal devel

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

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

96 found that Nrp2 is enriched in adult layer V pyramidal neurons, corticostriatal terminals, and in dev

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

98 -expression is limited to a specific type of pyramidal neuron: CT.

99 ls regulates the excitability in hippocampal pyramidal neuron dendrites and are key determinants of d

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

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

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

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

104 DISC1 knock-down to prefrontal layer II/III pyramidal neurons during perinatal development and expos

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

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

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

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

109 ug technology to specifically manipulate CA1 pyramidal neuron excitatory activity, electrophysiology,

110 al pathways by which a subtype of prefrontal pyramidal neurons exerts a powerful top-down influence o

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

112 In rat motor cortex, SMI32-postive pyramidal neurons expressing Kv3.1b were very rare and w

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

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

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

116 Pyramidal neurons from layers II-III of the medial prefr

117 NCI and synaptic dysfunction in pyramidal neurons from layers II-III of the mPFC indepen

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

119 Pyramidal neurons from the hippocampus of Celsr3 knockou

120 round potassium current observed in cortical pyramidal neurons from wild type mice was conspicuously

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

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

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

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

125 CA2 pyramidal neurons have a distinct molecular makeup resul

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

127 Pyramidal neurons in a cluster showed higher than chance

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

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

130 postsynaptic current frequency, measured on pyramidal neurons in acute hippocampal slices at 270 DAT

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

132 excitability and synaptic function in mature pyramidal neurons in addition to regulating early develo

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

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

135 ing whole-cell patch-clamp recordings of CA1 pyramidal neurons in anesthetized rats, we have examined

136 y synaptic currents (mIPSCs) decreased in AI pyramidal neurons in animals with NIHL.

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

138 ritic morphology and intrinsic properties of pyramidal neurons in both deep and superficial layers.

139 everal hours after recovery from SD, layer 5 pyramidal neurons in brain slices from mice of either se

140 Using dynamic clamp in hippocampal CA1 pyramidal neurons in brain slices, we showed that the ef

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

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

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

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

145 oth interneurons in layers (L)1-3 as well as pyramidal neurons in L2/3 and L6 receive direct inputs f

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

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

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

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

150 n of the early development and maturation of pyramidal neurons in mouse mPFC not only demonstrates a

151 oton dendritic micro-dissection on layer-2/3 pyramidal neurons in mouse primary visual cortex.

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

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

154 current clamp recording, we found that L2/3 pyramidal neurons in prefrontal cortex of fmr1(-/y) mous

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

156 Their long-range axons inhibit L5 pyramidal neurons in RSCg via potent synapses onto apica

157 s and axon "en passant" boutons of layer 2/3 pyramidal neurons in S1 of male and female WT and Fmr1 K

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

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

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

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

162 ctivation also inhibited MThal inputs to the pyramidal neurons in the ACC.

163 ity of long/thin dendritic spines of layer 5 pyramidal neurons in the adult PrL-C.

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

165 , trunk and distal tuft dendrites of layer 5 pyramidal neurons in the awake mouse primary visual cort

166 Here, we show that pyramidal neurons in the barrel cortex of BC1 knock out

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

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

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

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

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

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

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

174 tion increases somatic activities of layer 5 pyramidal neurons in the motor cortex respectively.

175 dritic spines on apical dendrites of layer 5 pyramidal neurons in the motor cortex.

176 we also found that D1-expressing deep-layer pyramidal neurons in the mPFC send direct projections to

177 cell lineage determines the connectivity of pyramidal neurons in the neocortex, but the functional r

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

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

180 onnections and somatic activities of layer 5 pyramidal neurons in the primary motor cortex, a cortica

181 Layer (L) 2/3 pyramidal neurons in the primary somatosensory cortex (S

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

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

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

185 It is not known if the other major types of pyramidal neurons in this layer also express this enzyme

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

187 ained whole-cell current-clamp recordings of pyramidal neurons in visual cortex of turtles with unkno

188 excitability in male and female rat cortical pyramidal neurons in vitro and in vivo Using local appli

189 blocker ZD7288 mimicked these effects in BLA pyramidal neurons in wild-type mice but not in Tmem74(-/

190 Pyramidal neurons integrate synaptic inputs from basal a

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

192 ncy adaptation - split layer 5 barrel cortex pyramidal neurons into two clusters: one of adapting cel

193 We now demonstrate that in hippocampal CA1 pyramidal neurons IP(3)- and Ry-receptors are associated

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

195 , daily cocaine injections, t-LTP in layer V pyramidal neurons is induced at +30 ms, a normally ineff

196 a result of KCNQ2 dysfunction in neocortical pyramidal neurons is still unknown.

197 pmental processes of prefrontal layer II/III pyramidal neurons is sufficient to diminish prefrontal-h

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

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

200 For example, layer 3 pyramidal neurons (L3PNs) differ significantly between p

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

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

203 mice revealed that post-mitotic hippocampal pyramidal neurons maintain cyclin A2 expression and that

204 ation of layer- and time-specific changes in pyramidal neurons may be relevant for studies in mouse m

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

206 5-regulated signaling effectors that control pyramidal neuron migration and dendritogenesis.

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

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

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

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

211 Here, in hippocampal pyramidal neurons of both primary cultures and slices, w

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

213 zed all observed excitability defects in CA3 pyramidal neurons of Fmr1 KO mice.

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

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

216 nts (mEPSCs) and NMDA-evoked currents in CA1 pyramidal neurons of rat hippocampal slices, and (iv) re

217 spine density in apical dendrites of layer 5 pyramidal neurons of several neocortical regions that is

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

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

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

221 sitive presynaptic inhibitory boutons around pyramidal neurons of the hippocampal CA3 area.

222 cial role for excitatory synapses connecting pyramidal neurons of the hippocampus and cortex with fas

223 CA1 pyramidal neurons of the hippocampus from these mice exh

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

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

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

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

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

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

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

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

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

233 alized connectivity patterns onto excitatory pyramidal neurons (PNs) and other inhibitory cells.

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

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

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

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

238 er collateral (SC) inputs to hippocampal CA1 pyramidal neurons (PNs) produces a long-term enhancement

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

240 We found that layer 2 and/or 3 pyramidal neurons (PNs) showed sequential activation in

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

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

243 inhibitory (I) synapses received by cortical pyramidal neurons (PNs).

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

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

246 e only population that selectively innervate pyramidal neurons (PyNs) at their axon initial segment (

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

248 Neocortical pyramidal neurons regulate firing around a stable mean f

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

250 previously described thin- and thick-tufted pyramidal neurons, respectively.

251 oid receptor (DOR) agonists disinhibited ACC pyramidal neuron responses to MThal inputs by suppressin

252 em74 or selective knockdown of Tmem74 in BLA pyramidal neurons resulted in anxiety-like behaviors in

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

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

255 Whole-cell recordings in BLA pyramidal neurons revealed lower hyperpolarization-activ

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

257 cell cycle regulatory role to maintain adult pyramidal neuron ribostasis.

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

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

260 Activity in layer 5 pyramidal neuron somata and distal apical trunk dendrite

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

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

263 conditional Lis1 inactivation in excitatory pyramidal neurons, starting in juvenile mouse brain, wer

264 synaptic currents (mEPSCs) onto EC layer III pyramidal neurons, suggesting that these channels decrea

265 xtinction on PVIN-pyramidal neuron and SSTIN-pyramidal neuron synapses in male preadolescent, adolesc

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

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

268 -cAMP/protein kinase A dopamine signaling in pyramidal neurons that in turn pathologically recruits l

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

270 e stimulated M2 cortex harbors glutamatergic pyramidal neurons that project to subcortical structures

271 V1 are shaped by small-world subnetworks of pyramidal neurons that share functional properties and w

272 ation artifacts, we show, in hippocampal CA1 pyramidal neurons, that neuroligin-1 performs two key fu

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

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

275 cells regulate surround suppression to allow pyramidal neurons to optimally encode visual information

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

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

278 ACh exerts two opposing actions in cortical pyramidal neurons: transient inhibition and longer-lasti

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

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

281 ure and transcriptional profile of layer III pyramidal neurons-using cell type- and layer-specific hi

282 enomena while also establishing subthreshold pyramidal neuron V (m) fluctuations as an informative ga

283 Increased excitability of layer II/III pyramidal neurons was accompanied by consistent reductio

284 edforward and feedback inhibitory input onto pyramidal neurons was decreased in GluA1-3 KO.

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

286 In drinking monkeys, evoked firing of OFC pyramidal neurons was reduced, whereas the amplitude and

287 In pyramidal neurons, we found an increase in monocarboxyla

288 Within pyramidal neurons, we identified four major clusters, in

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

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

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

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

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

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

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

296 put of the mPFC is mediated by glutamatergic pyramidal neurons whose activity is coordinated by an in

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

298 mouse cerebral cortex, tracing of individual pyramidal neurons within densely Brainbow-labeled tissue

299 ions (ADPs) in subcortically projecting (SC) pyramidal neurons within L5 of the PFC.

300 es excitability specifically in layer 2/3 of pyramidal neurons within the prelimbic subarea of the pr