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1 s and parvalbumin-expressing cells mostly in stratum pyramidale.
2 rent sinks and sources were localized to the stratum pyramidale.
3 In CA1, ripples have maximum amplitude in stratum pyramidale.
4 n age-dependent changes in neuron density in stratum pyramidale.
5 al based on their radial position within the stratum pyramidale.
6 the perisomatic perineuronal net in the CA2 stratum pyramidale.
7 in the deep compared to superficial layer of stratum pyramidale.
8 pias and the organization of the hippocampal stratum pyramidale.
9 ens (35.8%) and CA1 stratum oriens (78.87%), stratum pyramidale (40%), and stratum radiatum (56.6%).
12 ositive synaptic sites on CA1 neurons in the stratum pyramidale and stratum oriens layers of KO hippo
14 on spike and the slope of EPSP recorded from stratum pyramidale and stratum radiatum respectively.
16 field potential oscillation recorded in the stratum pyramidale, and concomitantly recorded action po
17 with ZIP1 predominantly expressed in the CA3 stratum pyramidale, and ZIP3 primarily localized to the
18 orizontal, but not vertical, clusters in the stratum pyramidale, as revealed by both cell-type-specif
19 ty from up to 150 neurons in the hippocampal stratum pyramidale at approximately 1-mm depth within an
20 spikes of putative excitatory neurons in CA1 stratum pyramidale based on waveform sorting and validat
22 ctive neurons in the superficial sublayer of stratum pyramidale displayed larger post-synaptic respon
23 the active current sources restricted to the stratum pyramidale during SWRs originate from the synapt
25 l neurons and nearby interneurons in the CA1 stratum pyramidale has been strongly implicated on the b
26 asket cells and PV bistratified cells in the stratum pyramidale; in stratum oriens, HC PV cells were
27 properties of hippocampal stratum oriens and stratum pyramidale inhibitory interneurones, before and
28 Somatic IPSPs, dendritic burst firing and stratum pyramidale interneuron activity were all tempora
29 ectrophysiological recordings were made from stratum pyramidale interneurons in which morphology and
30 ngly suggest that spatial selectivity of CA1 stratum pyramidale interneurons is inherited from a smal
31 rneurons were identified using the GIN mice: stratum pyramidale interneurons with lacunosum-molecular
32 rdings from pyramidal cells and fast-spiking stratum pyramidale interneurons, we demonstrate that fas
34 glial labeling, Purkinje cells, hippocampal stratum pyramidale, locus coeruleus (alpha3); alpha4- di
35 es in CB(1) receptor immunoreactivity in the stratum pyramidale neuropil and dentate gyrus inner mole
38 , in situ hybridization revealed that within stratum pyramidale of the CA1 area, mRNA expression of t
40 he molecular layer of the dentate gyrus, the stratum pyramidale of the CA1 subregion and subiculum, w
41 ield potentials and unit activity in the CA1 stratum pyramidale of the hippocampus in the behaving wi
42 interneurons, primarily in or bordering the stratum pyramidale, produced slow membrane potential (0.
43 ssion (index of neuronal activation) in dCA3 stratum pyramidale (SP) glutamatergic and GABAergic neur
44 imaging of dorsal CA1 (dCA1) neurons in the stratum pyramidale (SP) in head-fixed mice performing a
47 the local-field potential recorded from the stratum pyramidale, stratum radiatum, and stratum lacuno
48 cells had axons that ramified throughout the stratum pyramidale, suggesting that they are responsible
49 during sleep/rest, we identified ripples in stratum pyramidale that feature current sinks in stratum
51 of an event, a current was injected into the stratum pyramidale via a tungsten electrode positioned w
52 itude of gamma oscillations generated around stratum pyramidale, where basket cells selectively inner