ライフサイエンスコーパス: septotemporal

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1 e domains of cells projecting to septal, mid-septotemporal, and temporal levels of the dentate gyrus

2 molecular layer bilaterally along the entire septotemporal axis and LTP-induced activation of PATE in

3 iological organization of activity along the septotemporal axis is poorly understood.

4 NAP-25 in infected neonates varied along the septotemporal axis of hippocampus and in various anatomi

5 atterns in rats during sleep from the entire septotemporal axis of the CA1 pyramidal layer.

6 oscillations along the entire extent of the septotemporal axis of the hippocampal CA1 pyramidal laye

7 f granule cell axon reorganization along the septotemporal axis of the hippocampus in control rats an

8 ons are differentially distributed along the septotemporal axis of the hippocampus, and show that the

9 possible functional dissociations along the septotemporal axis of the hippocampus.

10 nd hilar neuron loss occurred throughout the septotemporal axis of the hippocampus.

11 regate neocortical representations along the septotemporal axis of the hippocampus.

12 lling waves that propagate roughly along the septotemporal axis of the hippocampus.

13 esting differentiation of function along the septotemporal axis of this structure.

14 rom the labeled mossy cell (1-2 mm along the septotemporal axis), the axon collaterals ramified predo

15 monstrate functional heterogeneity along the septotemporal axis, although precise underlying circuitr

16 The hippocampus integrates, along its septotemporal axis, substrates of rapid place learning,

17 of the mossy fiber terminal field along the septotemporal axis.

18 granular region for 600-700 microm along the septotemporal axis.

19 layer of the dentate gyrus along the entire septotemporal axis.

20 the direction of information flow along the septotemporal CA3 axis.

21 g functional differentiation across the full septotemporal extent of the hippocampus.

22 erlapping distribution throughout the entire septotemporal extent of the hippocampus.

23 ugh symmetry in their maximal transverse and septotemporal extents (311 +/- 84 microns and 269 +/- 10

24 highly ordered projections into the long, or septotemporal, hippocampal axis.

25 l DG axis, suggesting increased capacity for septotemporal integration.

26 ended through an average of 57% of the total septotemporal length of the hippocampus (summated two-di

27 pyramidal cell place field scale within each septotemporal level attributable to task variations are

28 d of pyramidal cell, a characteristic of the septotemporal level of the hippocampus from which the ce

29 Our results show that, at a given septotemporal level, nearby CA1 neurons receive synaptic

30 Injections into mid-septotemporal levels of the dentate gyrus (50-75% of the

31 entorhinal neurons that project to different septotemporal levels of the dentate gyrus are linked by

32 e and Diamidino yellow, were injected at all septotemporal levels of the dentate gyrus, and the distr

33 ocampal gene expression data revealed robust septotemporal molecular heterogeneity, leading to the id

34 he dentate granule layer with respect to the septotemporal position of origin of the slice culture, t

35 nce volume, we report significant effects of septotemporal position on the number of granule layer ce

36 Although septotemporal relationships of the normal CA3 outflow tr

37 opographical relationship exists between the septotemporal segments of the hippocampus and their ento

38 al hippocampal length, which far exceeds the septotemporal span of axons of granule cells whose compl

39 The septotemporal span of the axon arbor extended over 48-82

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