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1 arietal cortex projects only sparsely to the presubiculum.
2 y parahippocampal cortex, parasubiculum, and presubiculum.
3 l trigeminal nucleus, islands of Calleja and presubiculum.
4 axons (at least 10 of 14) branch beyond the presubiculum.
5 om the inferior parietal lobule (IPL) to the presubiculum.
6 as particularly prominent in layer II of the presubiculum.
7 radiatum, stratum lacunosum moleculare, and presubiculum.
8 ied to dMEC, but never by stimuli applied to presubiculum.
10 e, we summarize the evidence that the dorsal presubiculum (also known as the postsubiculum) is critic
11 e recorded and labeled single neurons in the presubiculum, an area providing one of the major inputs
12 ar termination gradient starting in proximal presubiculum and extending gradually until it covers the
13 ith increases in 1CGU in the pontine nuclei, presubiculum and hippocampus and reductions in somatosen
14 ay be different: bursting cells projected to presubiculum and non-bursting cells projected to entorhi
16 We conclude that the deep layer cells of the presubiculum and parasubiculum are richly interconnected
17 rom deep layer neurons of entorhinal cortex, presubiculum and parasubiculum consisted of one action p
25 A3 stratum radiatum, hilus dentate gyrus and presubiculum, and in the cerebral cortex including agran
26 ts, the interactions with postrhinal cortex, presubiculum, and MEC are mediated predominantly through
28 ola cinereum, induseum griseum, tenia tecta, presubiculum, and parasubiculum), and in the septum (sep
33 0), right CA4-DG (beta=-0.35, p=0.011), left presubiculum (beta=-0.29, p=0.030), and left fimbria (be
34 applied to the superficial or deep layers of presubiculum, but never by stimuli applied to deep layer
35 FS) interneurons and pyramidal cells in the presubiculum can be distinguished based on physiological
36 oss non-overlapping views, whereas the right presubiculum coded facing direction even across nonconti
37 extensions were found on axons that entered presubiculum, entorhinal cortex or CA1, supporting the n
38 juxtacellularly recorded single cells in the presubiculum in freely moving rats, finding two classes
40 (left, p = .035; right, p = .031) and right presubiculum (p = .002) volumes than patients with bipol
41 otentials (IPSPs) were studied in neurons of presubiculum, parasubiculum and medial entorhinal cortex
42 orm nucleus, piriform cortex, dentate gyrus, presubiculum, parasubiculum, CA1-CA4 fields, amygdaloid
43 sities of labeled cells were observed in the presubiculum, parasubiculum, entorhinal cortex, and subi
44 mmonis 1-3, dentate gyrus), parahippocampus (presubiculum, parasubiculum, prosubiculum, subiculum, an
45 of the hippocampus as well as the subiculum, presubiculum, parasubiculum, the medial and lateral ento
46 ng the prosubiculum (ProS), subiculum (Sub), presubiculum, postsubiculum (PoS), and parasubiculum (Pa
52 xel pattern analyses indicated that the left presubiculum, retrosplenial complex, and parietal-occipi
53 s than healthy control subjects, but smaller presubiculum volumes were found only in patients with sc
54 r of the dentate gyrus, subiculum proper and presubiculum was indistinguishable from mild and moderat
55 eep MEC was stimulated, but were bursts when presubiculum was stimulated, even in the presence of glu
56 ques, including those in caudate nucleus and presubiculum, were less prominently labelled, amorphous
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