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1 iculum and CA1 eliminated afterdischarges in subicular and CA1 events, but did not de-synchronize the
2 rve to maintain a level of depolarization in subicular and CA1 pyramidal neurons well beyond the dura
3                        Activity from ventral subicular and hippocampal CA1 neurons was recorded in ra
4            Spine density and arborization of subicular apical dendrites were significantly related to
5 od disorders and structural abnormalities of subicular apical dendrites.
6     Primary motor, primary somatosensory and subicular areas barely send projections to either ipsi-
7 coordination of activity between the CA1 and subicular areas during network oscillations.
8  of the projections from the hippocampus and subicular areas matches that of the reciprocal projectio
9 entorhinal cortex to the hippocampus and the subicular areas.
10                                              Subicular axons, in contrast, excite proximal dendrites
11 to implicate Cav3.1-containing T-channels in subicular burst firing, in contrast to several previous
12                Intracellular recordings from subicular bursting and non-bursting cell types and field
13 anus-induced long-term potentiation (LTP) in subicular bursting neurons, but not in subicular regular
14 entata (FD) and hilar region from the CA and subicular cell fields of the rat and conducted in vitro
15                                              Subicular cell patterns during exposure to the large squ
16 number of NMDA receptors in the CA1, CA3 and subicular cell regions of the hippocampus, but not in th
17 aptic potentials (EPSPs) were evoked in both subicular cell types in response to single entorhinal, p
18 n of 5-HT induced in 76% of the investigated subicular cells a hyperpolarization and a reduction of m
19                                    In vitro, subicular cells can be distinguished by their ability to
20                                        Thus, subicular cells can change the size of their spatial pat
21 vantage of multimodal techniques to classify subicular cells in distinct subclasses and have investig
22 ogenetic stimulation or inhibition of bursty subicular cells induced or reduced responses in superfic
23                  These findings suggest that subicular cells may receive converging input from severa
24 vironment-specific spatial patterns, whereas subicular cells show the same pattern in each environmen
25 We found a substantial transformation in the subicular code for space from sparse to dense firing rat
26 while the representational properties of the subicular complex (SC) are relatively underexplored, alt
27 by other networks.SIGNIFICANCE STATEMENT The subicular complex (SC) receives major inputs from the en
28 ing was examined in the hippocampus (HC) and subicular complex (SC).
29                                          The subicular complex and entorhinal cortex also exhibited d
30 extended noncanonical pathways involving the subicular complex and hippocampal subregions CA1 and CA3
31 CA3, the hilus of the dentate gyrus, and the subicular complex of the hippocampal formation; in the p
32 campal region (CA fields, dentate gyrus, and subicular complex) and the adjacent perirhinal, entorhin
33 l formation (dentate gyrus, hippocampus, and subicular complex).
34 pal formation (cornu Ammonis, dentate gyrus, subicular complex, and entorhinal cortex) were readily o
35 lenial, and anterior cingulate cortices, the subicular complex, and the dorsal, medial thalamus.
36 ells receive input from the hippocampus, the subicular complex, and the retrosplenial cortex, suggest
37 he role of the hippocampus, particularly the subicular complex, in the process of learning and rememb
38                                          The subicular complex, including the prosubiculum (ProS), su
39 CA1 (vCA1), perirhinal cortex (Prh), and the subicular complex.
40 discuss equivalencies and extent of the five subicular components in human, monkey, and rodent based
41  improve our understanding of reciprocal CA1-subicular connections and guide future studies on how th
42                Major connections of the five subicular cortices are also summarized based on unified
43               In rodent, most of the typical subicular cortices are located in the dorsal and caudal
44                                     All five subicular cortices exist in human, monkey, and rodent.
45 n prefrontal, somatosensory, entorhinal, and subicular cortices into synchronous transitions between
46 eas such as the cingulate, midcingulate, and subicular cortices.
47 o compare the morphologic characteristics of subicular dendrites in subjects with schizophrenia (n =
48 gnostic group on Sholl analysis of nonapical subicular dendrites nor on Sholl analysis of dendrites o
49 s well with a previous suggestion that local subicular events, purely mediated by excitatory connecti
50 mine the long-term effects of amphetamine on subicular excitability.
51              Our results indicate that local subicular excitatory circuits are connected in a cell ty
52                 Thus, we conclude that local subicular excitatory circuits, connected according to ce
53 exity regulates the organizing principles of subicular GABAergic inhibition, with the interaction of
54                                 Amygdala and subicular (hippocampal) projections overlapped most comp
55             These data strongly suggest that subicular inhibitory neurons receive excitatory input fr
56 tudies demonstrate that: (a) hippocampal and subicular inputs to the entorhinal cortex in the monkey
57 arly C99 production occurs mainly in the CA1/subicular interchange area of the hippocampus correspond
58  support previous work demonstrating altered subicular MAP2 expression in schizophrenia and indicate
59 of diversity regulating GABAergic input onto subicular microcircuits.
60 s hypothesis with a computational model of a subicular network with realistic connectivity.
61 or high-voltage-activated Ca(2+) channels in subicular neuron bursting.
62 counting T-channels as major contributors to subicular neuron physiology.
63 rrents received by regular- vs. burst-firing subicular neurons and their dynamic modulation by the ac
64                     A separate population of subicular neurons encode convex corners of both larger e
65 rent idiosyncrasies by which hippocampal and subicular neurons encoded information and became errors
66                Since in approximately 25% of subicular neurons EPSPs and slow IPSPs were reduced with
67 c diseases, we have also characterized Ih in subicular neurons from rats that have been housed in ind
68 ons exhibited place fields, although ventral subicular neurons had larger fields than hippocampal cel
69  excitatory drive to the hippocampal CA1 and subicular neurons in chronic epilepsy.
70  identify a critical role for CA1-projecting subicular neurons in object-location learning and memory
71 mbrane properties and EPSP/IPSP responses of subicular neurons in rat combined hippocampal-entorhinal
72                                  Encoding by subicular neurons in the task was normally accurate and
73 l cortex and CA1 converge onto single dorsal subicular neurons in vivo.
74 istinction between bursting and non-bursting subicular neurons is a dichotomy and cells do not change
75 hat the afferent circuitry of CA1-projecting subicular neurons is biased by inputs from CA1 inhibitor
76 ramidal and multipolar cells and that single subicular neurons receive convergent inputs from CA1 and
77 that excitability and synaptic plasticity of subicular neurons relies heavily on T-channels.
78 tal portion of the parasubiculum, and distal subicular neurons target the proximal most portion of pa
79 s are non-overlapping with the population of subicular neurons that encode environmental boundaries.
80   The dendritic and axonal morphology of rat subicular neurons was studied in single cells labeled wi
81                            Some non-bursting subicular neurons were antidromically activated by stimu
82 pite the disparate firing rate properties of subicular neurons, we found that neurons at all proximal
83 st prominently in a subtype of microglia and subicular neurons.
84 vior predicts functional differences between subicular neurons.
85 n, so we examined the firing patterns of rat subicular neurons.
86 at this connection may involve only bursting subicular neurons.
87 GABAergic inhibition is essential to prevent subicular-originated epileptiform discharges.
88                                          The subicular-parahippocampal projection has been proposed a
89  signal was found in a network of entorhinal/subicular, posterior and medial parietal, lateral tempor
90                                       At CA1-subicular presynaptic terminals, 5-HT(1B) and GABA(B) re
91   We conclude that both IB and RS classes of subicular principal cells make synaptic contacts in and
92 ats, we studied the bursting behavior of 102 subicular principal neurons and distinguished two popula
93  there was both a rich local axon in CA1 and subicular-projecting branches.
94                                              Subicular projection neurons are themselves classifiable
95                                  The CA1 and subicular projections terminate most densely in Layers V
96 al evidence for the presence of noncanonical subicular projections to CA1.
97 citation-inhibition sequences can be seen in subicular pyramidal and multipolar cells and that single
98            While these findings suggest that subicular pyramidal cell dendrites may be structurally a
99 nd ventral levels, NADPH-diaphorase-positive subicular pyramidal cells and CA1 nonpyramidal cells als
100 utes to the observed functional diversity of subicular pyramidal cells during sharp-wave associated r
101                                              Subicular pyramidal cells have been classified as bursti
102                                              Subicular pyramidal cells may be easily distinguished in
103         Spine density on apical dendrites of subicular pyramidal cells was determined at a fixed dist
104                                              Subicular pyramidal cells were also found to contain NOS
105 both regular- and burst-firing (RFs and BFs) subicular pyramidal cells.
106 riable I(Na) density in cortical layer 6 and subicular pyramidal neurons affects spike patterning and
107                       We tested this idea in subicular pyramidal neurons by using patch-clamp recordi
108                                A majority of subicular pyramidal neurons communicate via bursts of ac
109                                              Subicular pyramidal neurons exhibit low-threshold burst
110                 Axons of neurobiotin-labeled subicular pyramidal neurons were visualized in the apica
111 les and decreased dendritic spine density on subicular pyramidal neurons.
112 hat a Ca(2+) tail current drives bursting in subicular pyramidal neurons.
113 his geocentric information in the entorhinal/subicular region and egocentric direction information in
114 ese data and found that the human entorhinal/subicular region contains a neural representation of int
115 igation, these data implicate the entorhinal/subicular region in assimilating relatively coded knowle
116  to faces and objects, recruits the anterior subicular region of the hippocampus, regardless of wheth
117  discovered prominent BLA innervation in the subicular region of the vHC (vSub).
118 te binding were observed in the CA1 field or subicular region.
119 not label cells in the CA3, dentate gyrus or subicular regions of the hippocampus or in layer 4 of th
120 way linking the dentate gyrus to the CA1 and subicular regions through the hippocampal fissure.
121 jections across the fissure into the CA1 and subicular regions.
122 P) in subicular bursting neurons, but not in subicular regular firing cells.
123                                              Subicular responses to CA1 stimulation consisted of exci
124                       We observed entorhinal/subicular responses to the absolute distance between the
125                          Notably, entorhinal/subicular signals were sensitive to which familiar indiv
126 ry afferents, pharmacologically disinhibited subicular slices generated hyper-synchronous discharges.
127 ctly addressed these two key points in mouse subicular slices.
128 ei lesions in male rats cause a cessation of subicular spatial signaling, reduce spatial memory perfo
129 hat burst firing is functionally relevant to subicular spatially tuned neurons, possibly by serving a
130 here was also evidence of genetic overlap of subicular subfield volumes with schizophrenia.
131 o acid injections into CA1, prosubicular, or subicular subfields produced anterograde label over part
132 rips of neurons in adjacent prosubicular and subicular subfields.
133 ffects of neurotoxic or electrolytic ventral subicular (vSUB) lesions on the acquisition and expressi

 
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