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1 rvalbumin-expressing cells mostly in stratum pyramidale.
2 the organization of the hippocampal stratum pyramidale.
3 ks and sources were localized to the stratum pyramidale.
4 d elongate rapidly within strata lucidum and pyramidale.
5 des were carried out in stratum radiatum and pyramidale.
6 1, ripples have maximum amplitude in stratum pyramidale.
7 pendent changes in neuron density in stratum pyramidale.
8 eep compared to superficial layer of stratum pyramidale.
12 This group was found in or near the stratum pyramidale and had axonal projections almost exclusively
13 d hippocampal CA1 field potentials in strata pyramidale and radiatum and assessed neuroplasticity by
17 GLAST staining was highest along the stratum pyramidale and was especially prominent in astrocytes at
18 otential oscillation recorded in the stratum pyramidale, and concomitantly recorded action potentials
19 strocytes in CA1 s. radiatum, CA2 and CA3 s. pyramidale, and molecular layer of the DG, was increased
20 ls), which terminate in the strata radiatum, pyramidale, and oriens, are present throughout the entir
21 rked loss of SP fibers in the strata oriens, pyramidale, and radiatum of the CA3a and CA2 subfields.
22 l, but not vertical, clusters in the stratum pyramidale, as revealed by both cell-type-specific retro
23 up to 150 neurons in the hippocampal stratum pyramidale at approximately 1-mm depth within an intact
26 ve current sources restricted to the stratum pyramidale during SWRs originate from the synaptic outpu
27 s and nearby interneurons in the CA1 stratum pyramidale has been strongly implicated on the basis of
28 lls and PV bistratified cells in the stratum pyramidale; in stratum oriens, HC PV cells were electrop
29 es of hippocampal stratum oriens and stratum pyramidale inhibitory interneurones, before and followin
30 ic IPSPs, dendritic burst firing and stratum pyramidale interneuron activity were all temporally corr
31 siological recordings were made from stratum pyramidale interneurons in which morphology and Kv3.1b-p
32 gest that spatial selectivity of CA1 stratum pyramidale interneurons is inherited from a small cluste
33 were identified using the GIN mice: stratum pyramidale interneurons with lacunosum-moleculare axon a
34 rom pyramidal cells and fast-spiking stratum pyramidale interneurons, we demonstrate that fast gamma
35 minent sprouting was seen in the CA3 stratum pyramidale layer in all rats having 15 daily seizures, r
36 abeling, Purkinje cells, hippocampal stratum pyramidale, locus coeruleus (alpha3); alpha4- discrete l
37 (1) receptor immunoreactivity in the stratum pyramidale neuropil and dentate gyrus inner molecular la
38 active neurons express GFR alpha-1 in the s. pyramidale of CA1 (72%), CA2 (70%) and CA3 (70%) subfiel
39 nificant reductions in the strata oriens and pyramidale of CA1, the stratum pyramidale of CA3, and th
41 atum of CA1, the strata oriens, radiatum and pyramidale of CA3, the dentate molecular layer, and the
44 u hybridization revealed that within stratum pyramidale of the CA1 area, mRNA expression of the Ca(v)
46 ular layer of the dentate gyrus, the stratum pyramidale of the CA1 subregion and subiculum, while the
47 entials and unit activity in the CA1 stratum pyramidale of the hippocampus in the behaving wild-type
48 urons, primarily in or bordering the stratum pyramidale, produced slow membrane potential (0.04 Hz) o
49 of GABAergic terminals at the stratum oriens-pyramidale (SO-SP) or stratum lacunosum-molecular (S-L-M
52 d axons that ramified throughout the stratum pyramidale, suggesting that they are responsible for the
53 ent, a current was injected into the stratum pyramidale via a tungsten electrode positioned within 15
55 gamma oscillations generated around stratum pyramidale, where basket cells selectively innervate pyr
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