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1 alamic nucleus and the postsubiculum (dorsal presubiculum).
2 arietal cortex projects only sparsely to the presubiculum.
3 y parahippocampal cortex, parasubiculum, and presubiculum.
4 l trigeminal nucleus, islands of Calleja and presubiculum.
5 axons (at least 10 of 14) branch beyond the presubiculum.
6 om the inferior parietal lobule (IPL) to the presubiculum.
7 as particularly prominent in layer II of the presubiculum.
8 radiatum, stratum lacunosum moleculare, and presubiculum.
9 ied to dMEC, but never by stimuli applied to presubiculum.
10 sters of the retrohippocampus, subiculum and presubiculum.
11 from the retrosplenial cortex combine in the presubiculum.
12 midal neurons in the dorsal portion of mouse presubiculum.
15 e, we summarize the evidence that the dorsal presubiculum (also known as the postsubiculum) is critic
16 e recorded and labeled single neurons in the presubiculum, an area providing one of the major inputs
17 ar termination gradient starting in proximal presubiculum and extending gradually until it covers the
18 ith increases in 1CGU in the pontine nuclei, presubiculum and hippocampus and reductions in somatosen
19 ay be different: bursting cells projected to presubiculum and non-bursting cells projected to entorhi
21 We conclude that the deep layer cells of the presubiculum and parasubiculum are richly interconnected
22 rom deep layer neurons of entorhinal cortex, presubiculum and parasubiculum consisted of one action p
31 A3 stratum radiatum, hilus dentate gyrus and presubiculum, and in the cerebral cortex including agran
32 ts, the interactions with postrhinal cortex, presubiculum, and MEC are mediated predominantly through
34 m the macaque monkey hippocampus, subiculum, presubiculum, and parasubiculum to the entorhinal cortex
35 pal formation (DG, CA1, CA2, CA3, subiculum, presubiculum, and parasubiculum) as well as in the entor
36 ola cinereum, induseum griseum, tenia tecta, presubiculum, and parasubiculum), and in the septum (sep
43 0), right CA4-DG (beta=-0.35, p=0.011), left presubiculum (beta=-0.29, p=0.030), and left fimbria (be
44 applied to the superficial or deep layers of presubiculum, but never by stimuli applied to deep layer
46 FS) interneurons and pyramidal cells in the presubiculum can be distinguished based on physiological
47 oss non-overlapping views, whereas the right presubiculum coded facing direction even across nonconti
48 extensions were found on axons that entered presubiculum, entorhinal cortex or CA1, supporting the n
49 nal subfield volume deficits in the CA1, and presubiculum in FEP at baseline, that further expanded t
50 juxtacellularly recorded single cells in the presubiculum in freely moving rats, finding two classes
51 1, CA2/3, CA4, dentate gyrus, subiculum) and presubiculum layers (PSB1, PSB3) was determined using re
53 (left, p = .035; right, p = .031) and right presubiculum (p = .002) volumes than patients with bipol
54 otentials (IPSPs) were studied in neurons of presubiculum, parasubiculum and medial entorhinal cortex
55 entate gyrus, hippocampus proper, subiculum, presubiculum, parasubiculum and the entorhinal cortex, i
56 orm nucleus, piriform cortex, dentate gyrus, presubiculum, parasubiculum, CA1-CA4 fields, amygdaloid
57 sities of labeled cells were observed in the presubiculum, parasubiculum, entorhinal cortex, and subi
58 mmonis 1-3, dentate gyrus), parahippocampus (presubiculum, parasubiculum, prosubiculum, subiculum, an
59 of the hippocampus as well as the subiculum, presubiculum, parasubiculum, the medial and lateral ento
60 ng the prosubiculum (ProS), subiculum (Sub), presubiculum, postsubiculum (PoS), and parasubiculum (Pa
66 xel pattern analyses indicated that the left presubiculum, retrosplenial complex, and parietal-occipi
68 ese results suggest that OXTR binding in the presubiculum supports pair bonding and parenting behavio
69 larger left hippocampal subfields, including presubiculum that also explains the variability in antis
70 etrosplenial cortex; path distances from the presubiculum to the same targets differ significantly be
71 an interaction model revealed a significant presubiculum volume x group association with antisocial,
72 s than healthy control subjects, but smaller presubiculum volumes were found only in patients with sc
73 r of the dentate gyrus, subiculum proper and presubiculum was indistinguishable from mild and moderat
74 eep MEC was stimulated, but were bursts when presubiculum was stimulated, even in the presence of glu
75 ques, including those in caudate nucleus and presubiculum, were less prominently labelled, amorphous
76 tion-specific translaminar processing in the presubiculum, where neuromodulation facilitates landmark