ライフサイエンスコーパス: CA1 stratum radiatum

1 pse and post-synapse, and synapse density in CA1 stratum radiatum.

2 under the control of mTOR, increased in area CA1 stratum radiatum.

3 increase in MMP-3 expression and activity in CA1 stratum radiatum.

4 ughout the HF, but slightly more numerous in CA1 stratum radiatum.

5 teristic pattern, with zeta prominent in the CA1 stratum radiatum.

6 naptophysin immunoreactivity was enhanced in CA1 stratum radiatum.

7 teral-induced excitatory field potentials in CA1 stratum radiatum.

8 the dentate gyrus inner molecular layer and CA1 stratum radiatum and in (ii) postsynaptic densities

9 ency recorded from GABAergic interneurons in CA1 stratum radiatum and induced membrane depolarization

10 r, with the entorhinal cortex (ERC) and then CA1 stratum radiatum and stratum lacunosum-moleculare (C

11 r.) oriens of the CA1 region and (2) between CA1 stratum radiatum and the dentate molecular layer.

12 spinophilin-immunoreactive spine numbers in CA1 stratum radiatum and the inner and outer molecular l

13 organization, especially in the hippocampal CA1 stratum radiatum, and also diminishes GABA-mediated

14 hin two less-defined hippocampal subregions, CA1 stratum radiatum, and oriens.

15 s well as basal synaptic transmission in the CA1 stratum radiatum appeared unaffected, whereas sponta

16 c potentials (fEPSPs) were recorded from the CA1 stratum radiatum following stimulation of the Schaff

17 ted charge transfer onto postnatal day 11-15 CA1 stratum radiatum hippocampal interneurons but is wit

18 alpha7-containing nAChRs in rat hippocampal CA1 stratum radiatum interneurones in slices, we describ

19 Schaffer collateral excitatory synapses onto CA1 stratum radiatum interneurones versus pyramidal cell

20 receptors on the membrane of rat hippocampal CA1 stratum radiatum interneurons and pyramidal cells in

21 ere investigated in outside-out patches from CA1 stratum radiatum interneurons from thin slices of ra

22 nAChR, on GABAergic activity in hippocampal CA1 stratum radiatum interneurons in acute rat brain sli

23 of this PAM on both CA1 pyramidal cells and CA1 stratum radiatum interneurons in immature hippocampu

24 These data suggest that rat hippocampal CA1 stratum radiatum interneurons in the slice possess a

25 uced by exogenous application of agonists to CA1 stratum radiatum interneurons was approximately 65%

26 cortex (ERC) and CA1 apical neuropil layer [CA1-stratum radiatum lacunosum moleculare (SRLM)] thickn

27 layer 5 pyramidal neurons of the RSG to the CA1 stratum radiatum/lacunosum-moleculare of the dorsal

28 rates of FM1-43 destaining from terminals in CA1 stratum radiatum, mostly representing excitatory ter

29 ed the subcellular localization of CaMKII in CA1 stratum radiatum of adult rat hippocampus, by using

30 ARs or NMDARs in serial sections through the CA1 stratum radiatum of adult rats.

31 We tested this hypothesis in the CA1 stratum radiatum of hippocampal slices from juvenile

32 duction in clustered gephyrin is detected in CA1 stratum radiatum of rTMS-treated anaesthetized mice.

33 reservation of GluN1/GluN2A receptors in the CA1 stratum radiatum region during BZ withdrawal.

34 increased synaptogenesis in the hippocampal CA1 stratum radiatum (sr) and enhances memory in young a

35 1, GluN2A, and GluN2B subunits was sought at CA1 stratum radiatum synapses in proximal dendrites usin

36 In the hippocampal CA1 stratum radiatum, the values of the CB1 receptor-imm

37 through coded serial electron micrographs of CA1 stratum radiatum to determine the: (1) frequency of

38 Axospinous synapses from the CA1 stratum radiatum were analyzed using systematic rand

39 Axons in CA1 stratum radiatum were evaluated with 3D reconstructi

40 s of adjacent protoplasmic astrocytes in the CA1 stratum radiatum were injected with fluorescent intr

41 xonal and glial pTrkB-ir and pTrkB-ir in the CA1 stratum radiatum were more abundant in high-estradio