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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 ning, but how hippocampus activity along its septotemporal axis contributes to flexible adaptation is
4 iological organization of activity along the septotemporal axis is poorly understood.
5 NAP-25 in infected neonates varied along the septotemporal axis of hippocampus and in various anatomi
6 atterns in rats during sleep from the entire septotemporal axis of the CA1 pyramidal layer.
7   This circuit organization exists along the septotemporal axis of the HF, but the circuit connectivi
8  oscillations along the entire extent of the septotemporal axis of the hippocampal CA1 pyramidal laye
9 f granule cell axon reorganization along the septotemporal axis of the hippocampus in control rats an
10 ons are differentially distributed along the septotemporal axis of the hippocampus, and show that the
11  possible functional dissociations along the septotemporal axis of the hippocampus.
12 nd hilar neuron loss occurred throughout the septotemporal axis of the hippocampus.
13 regate neocortical representations along the septotemporal axis of the hippocampus.
14 lling waves that propagate roughly along the septotemporal axis of the hippocampus.
15 esting differentiation of function along the septotemporal axis of this structure.
16 the lamellar axis, while synchrony along the septotemporal axis remained relatively low.
17 rom the labeled mossy cell (1-2 mm along the septotemporal axis), the axon collaterals ramified predo
18 monstrate functional heterogeneity along the septotemporal axis, although precise underlying circuitr
19 tude, and intrahippocampal topography in the septotemporal axis, are correlated with slower excitabil
20        The hippocampus integrates, along its septotemporal axis, substrates of rapid place learning,
21  of the mossy fiber terminal field along the septotemporal axis.
22 granular region for 600-700 microm along the septotemporal axis.
23  layer of the dentate gyrus along the entire septotemporal axis.
24  were more synchronized than those along the septotemporal axis.
25 s correlated along the lamellar, but not the septotemporal, axis during evoked seizures.
26  the direction of information flow along the septotemporal CA3 axis.
27 g functional differentiation across the full septotemporal extent of the hippocampus.
28 erlapping distribution throughout the entire septotemporal extent of the hippocampus.
29 ugh symmetry in their maximal transverse and septotemporal extents (311 +/- 84 microns and 269 +/- 10
30 highly ordered projections into the long, or septotemporal, hippocampal axis.
31 l DG axis, suggesting increased capacity for septotemporal integration.
32 ended through an average of 57% of the total septotemporal length of the hippocampus (summated two-di
33 pyramidal cell place field scale within each septotemporal level attributable to task variations are
34 d of pyramidal cell, a characteristic of the septotemporal level of the hippocampus from which the ce
35            Our results show that, at a given septotemporal level, nearby CA1 neurons receive synaptic
36                          Injections into mid-septotemporal levels of the dentate gyrus (50-75% of the
37 entorhinal neurons that project to different septotemporal levels of the dentate gyrus are linked by
38 e and Diamidino yellow, were injected at all septotemporal levels of the dentate gyrus, and the distr
39 ocampal gene expression data revealed robust septotemporal molecular heterogeneity, leading to the id
40 he dentate granule layer with respect to the septotemporal position of origin of the slice culture, t
41 nce volume, we report significant effects of septotemporal position on the number of granule layer ce
42                                     Although septotemporal relationships of the normal CA3 outflow tr
43 opographical relationship exists between the septotemporal segments of the hippocampus and their ento
44 al hippocampal length, which far exceeds the septotemporal span of axons of granule cells whose compl
45                                          The septotemporal span of the axon arbor extended over 48-82