ライフサイエンスコーパス: stratum pyramidale

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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 in the deep compared to superficial layer of stratum pyramidale.

6 pias and the organization of the hippocampal stratum pyramidale.

7 ens (35.8%) and CA1 stratum oriens (78.87%), stratum pyramidale (40%), and stratum radiatum (56.6%).

8 e neuroprotection or increased damage in the stratum pyramidale 7 days after reperfusion.

9 This group was found in or near the stratum pyramidale and had axonal projections almost exc

10 similar increases could be detected in both stratum pyramidale and stratum radiatum in area CA1.

11 on spike and the slope of EPSP recorded from stratum pyramidale and stratum radiatum respectively.

12 GLAST staining was highest along the stratum pyramidale and was especially prominent in astro

13 field potential oscillation recorded in the stratum pyramidale, and concomitantly recorded action po

14 orizontal, but not vertical, clusters in the stratum pyramidale, as revealed by both cell-type-specif

15 ty from up to 150 neurons in the hippocampal stratum pyramidale at approximately 1-mm depth within an

16 The zeta-potentials of the CA1 stratum pyramidale, CA3 stratum pyramidal, and dentate g

17 the active current sources restricted to the stratum pyramidale during SWRs originate from the synapt

18 l neurons and nearby interneurons in the CA1 stratum pyramidale has been strongly implicated on the b

19 asket cells and PV bistratified cells in the stratum pyramidale; in stratum oriens, HC PV cells were

20 properties of hippocampal stratum oriens and stratum pyramidale inhibitory interneurones, before and

21 Somatic IPSPs, dendritic burst firing and stratum pyramidale interneuron activity were all tempora

22 ectrophysiological recordings were made from stratum pyramidale interneurons in which morphology and

23 ngly suggest that spatial selectivity of CA1 stratum pyramidale interneurons is inherited from a smal

24 rneurons were identified using the GIN mice: stratum pyramidale interneurons with lacunosum-molecular

25 rdings from pyramidal cells and fast-spiking stratum pyramidale interneurons, we demonstrate that fas

26 Prominent sprouting was seen in the CA3 stratum pyramidale layer in all rats having 15 daily sei

27 glial labeling, Purkinje cells, hippocampal stratum pyramidale, locus coeruleus (alpha3); alpha4- di

28 es in CB(1) receptor immunoreactivity in the stratum pyramidale neuropil and dentate gyrus inner mole

29 the strata oriens and pyramidale of CA1, the stratum pyramidale of CA3, and the dentate hilus.

30 with K+o-sensitive microelectrodes placed in stratum pyramidale of hippocampal subfield CA1.

31 , in situ hybridization revealed that within stratum pyramidale of the CA1 area, mRNA expression of t

32 -coupled to the oscillations recorded in the stratum pyramidale of the CA1 region.

33 he molecular layer of the dentate gyrus, the stratum pyramidale of the CA1 subregion and subiculum, w

34 ield potentials and unit activity in the CA1 stratum pyramidale of the hippocampus in the behaving wi

35 interneurons, primarily in or bordering the stratum pyramidale, produced slow membrane potential (0.

36 ls, with most of their axonal arbours in the stratum pyramidale (SP).

37 ents (EPSCs) on non-pyramidal neurons in the stratum pyramidale (SP).

38 cells had axons that ramified throughout the stratum pyramidale, suggesting that they are responsible

39 of an event, a current was injected into the stratum pyramidale via a tungsten electrode positioned w

40 itude of gamma oscillations generated around stratum pyramidale, where basket cells selectively inner

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