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1 ect brain regions (e.g., the CA1 but not the CA3 region).
2 junction, and hippocampal formation (CA1 and CA3 regions).
3 .g., piriform cortex and hippocampal CA1 and CA3 regions).
4 en the entorhinal cortex and the hippocampal CA3 region.
5 rupted lamination that is most severe in the CA3 region.
6 , and project more axon collaterals into the CA3 region.
7 ) activity in ERC and the dentate gyrus (DG)/CA3 region.
8 ignificantly decreased kainate damage to the CA3 region.
9  staining revealed substantial damage to the CA3 region.
10              Fewer cells were stained in the CA3 region.
11 derlie the hyperexcitability reported in the CA3 region.
12 DG) facilitates synaptic transmission to the CA3 region.
13 se ratios during information encoding in the CA3 region.
14 ghout the molecular layer, as well as in the CA3 region.
15 o a new pattern of output to the hippocampal CA3 region.
16 opment, with VEGFR2 locally expressed in the CA3 region.
17 l gamma generator has been identified in the CA3 region.
18 Cs to identify ectopeptidase activity in the CA3 region.
19 nificant reduction of GAD-67 synapses in the CA3 region.
20 its epileptiform activity in the hippocampal CA3 region.
21  in shaping kainate neurotransmission in the CA3 region.
22 ons of norepinephrine in the rat hippocampal CA3 region.
23 treatments stopped, IBO was infused into the CA3 region.
24 cattered nuclei in the ventral subiculum and CA3 region.
25 ptosis in the KO hippocampus, especially the CA3 region.
26 xcitatory hippocampal neurons of the CA1- or CA3-region.
27 campal mossy fiber synapses of the hilar and CA3 regions.
28  prevented the neuronal loss in both CA2 and CA3 regions.
29 r, non-significant reductions in the CA1 and CA3 regions.
30 all en passant boutons in both the hilar and CA3 regions.
31 ntate gyrus, and pyramidal cell layer of the CA3 regions.
32 somatostatin interneurons in both DG and CA2/CA3 regions.
33 oughout the hippocampus, particularly in the CA3 regions.
34 ed an increase in TLR4 protein levels in the CA3 region 3h after hyperglycemic ischemia.
35 age) appeared in ventral hippocampal CA1 and CA3 regions after 20-min status epilepticus (SE).
36 rgan (SFO) or hippocampus (dentate gyrus and CA3 region) also significantly reduced the fever induced
37  Alzheimer's disease-related proteins in the CA3 region and a switch in amyloid precursor protein pro
38 campal formation is largely localized to the CA3 region and dentate gyrus of aged rats.
39 synapses in the somatosensory cortex and the CA3 region and dentate gyrus of the hippocampus at P30.
40 ed serotonin transporters in the hippocampal CA3 region and in the substantia nigra-reticulata but in
41 -mAbs bound most strongly in the hippocampal CA3 region and induced a significant reduction in Kv1.1
42 DR or FLK1) is expressed specifically in the CA3 region and it is required for dendritic arborization
43 imulating electrodes were placed in the left CA3 region and right angular bundle and a recording elec
44                 The complex circuitry of the CA3 region and the abundance of collateral connections h
45 g development, with strongest effects on the CA3 region and the dentate gyrus (CA3-DG) of the hippoca
46               ATOs were also observed in the CA3 region and the dentate gyrus.
47 n was not seen in the stratum lucidum of the CA3 region and the dentate hilar region, where most alph
48 z) oscillatory patterns are generated in the CA3 region and transferred to the CA1 field.
49 c pump: tPA activity increases along the CA2-CA3 regions and dentate gyrus of the hippocampal formati
50 extranuclear profiles throughout the CA1 and CA3 regions and dentate gyrus, and, in contrast to light
51 including pyramidal cells of the CA1 through CA3 regions and granule cells of the dentate gyrus.
52  lacunosum-moleculare of hippocampal CA1 and CA3 regions and in the molecular layer of the dentate gy
53 tiform bursts both in the hippocampal slice (CA3 region) and in vivo.
54 ed stress causes atrophy of dendrites in the CA3 region, and both acute and chronic stress suppresses
55 myloid deposition in cortex, the hippocampal CA3 region, and dentate gyrus was significantly reduced
56 tion within the mossy fiber terminals of the CA3 region, and in the newly formed mossy fiber aberrant
57 e neuroprotective effects in the dentate and CA3 regions, and that delayed JunB expression in the CA1
58 reshly isolated from rat hippocampus CA1 and CA3 regions are heterogeneous in ion channel expression
59 itory cells in the dentate gyrus, hilus, and CA3 regions as they integrate into hippocampal circuits.
60 mixed hippocampal, CA3 or CA1 cells into the CA3 region at 45 d after lesion, in comparison with "les
61 est a hierarchical internal operation of the CA3 region based on sequential oscillatory activation of
62 for 8 or 16 weeks, volume loss spread to the CA3 region, but not CA1.
63              Injections of beta-FNA into the CA3 region, but not into the ventricles, caused a signif
64  abundantly expressed in hippocampal CA2 and CA3 regions, but there are little known about their phys
65 t epileptiform burst firing generated in the CA3 region by activity-dependent enhancement of recurren
66 nt neuronal death in the hippocampal CA2 and CA3 regions (by 50 and 59%, respectively), by 7 days aft
67  arcuate and dorsomedial nuclei, hippocampal CA3 region, centromedial amygdaloid nucleus and thalamic
68                                  Because the CA3 region contains micro-opioid receptors and receives
69      Furthermore, the enhanced damage to the CA3 region correlated with a worse cognitive outcome aft
70 etic suppression of inputs from the upstream CA3 region during learning impaired coactivity-based con
71 ation of granule neurons that innervated the CA3 region expressed leptin receptors and these cells we
72 m 6 hr to 7 d and in the hippocampal CA1 and CA3 regions from 24 hr to 7 d after HI.
73                                       In the CA3 region, GAD interneuron density was significantly gr
74 sed of the entorhinal cortex and the dentate/CA3 regions hold promise for predicting progression on t
75             Additional studies revealed that CA3 region hypersensitivity, Alzheimer's disease-related
76 he effect of corticosteroids on the human DG/CA3 region implicates the NMDA receptor in human hippoca
77 cellular field potential recordings from the CA3 region in guinea pig hippocampal slices were used to
78 degeneration observed in neighboring CA1 and CA3 regions in both humans and rodent models of TLE.
79 tic remodeling is most prominent, namely the CA3 region, increases that were also inhibited by tianep
80   We found that both the septal and temporal CA3 regions intrinsically generate weakly synchronized d
81                              The hippocampal CA3 region is classically viewed as a homogeneous autoas
82                              The hippocampal CA3 region is essential for pattern completion and gener
83                       A major feature of the CA3 region is its recurrent collateral circuitry, by whi
84                          The hippocampal CA2/CA3 region is thought to be able to rapidly store incomi
85 ative attractor circuitry in the hippocampal CA3 region is thought to be the final arbiter between th
86                              The hippocampal CA3 region is thought to play crucial roles in episodic
87                                          The CA3 region is very striking in this regard: due to the d
88 f excitatory synapses in CA1 and DG, but not CA3 regions is reduced.
89 understand cholinergic modulation within the CA3 region, it is necessary to take into account seconda
90   In mossy fiber synapses of the hippocampal CA3 region, LTP is induced by cAMP and requires the syna
91     We provide evidence that, within the CA2/CA3 region, neurons with higher proportion of distal den
92 locations whereas, in more ventrally located CA3 regions, neurons gradually accumulate information ac
93  cortex and dentate gyrus (DG), the proximal CA3 region of aged rats may switch from its normal funct
94 T-1 mRNA expression in the dentate gyrus and CA3 region of Ammon's horn, increases that were inhibite
95 xtracellularly applied DA in the hippocampal CA3 region of anesthetized rats.
96 x and their targets in the dentate gyrus and CA3 region of hippocampus comprise a system that rapidly
97 learance of locally applied serotonin in the CA3 region of hippocampus in drug- or vehicle-treated ra
98 ect of D-22 to inhibit 5-HT clearance in the CA3 region of hippocampus persisted.
99 , clearance of locally applied 5-HT into the CA3 region of hippocampus was achieved using in vivo ele
100 s of the cortex, by pyramidal neurons of the CA3 region of hippocampus, and by cerebellar Purkinje ne
101 n KO mice in areas including the cortex, the CA3 region of hippocampus, and the lateral dorsal thalam
102                                       In the CA3 region of hippocampus, KT-LI was present in small un
103  Alzheimer's disease-relevant insult, as the CA3 region of long-term ovariectomized rats was profound
104 eu-enkephalin, a neuropeptide present in the CA3 region of OHSCs.
105 ynaptic loss and impaired LTP at hippocampal CA3 region of P301S mice were attenuated by blocking p25
106 form discharges were induced in vitro in the CA3 region of rat hippocampal slices by superfusion with
107 roM) on paired pulse inhibition (PPI) in the CA3 region of rat hippocampal slices.
108      Neural ensembles were recorded from the CA3 region of rats running on T-based decision tasks.
109  CA1 cell grafting into the kainate-lesioned CA3 region of the adult rat hippocampus at early post-ka
110 p-Erk and p-tau accumulated in the hilus and CA3 region of the dentate gyrus, where high levels of zi
111 0, severe = 10.9 +/- 1.3 million neurons) or CA3 region of the hippocampus (sham = 251 +/- 38, mild =
112  5-HT receptor subtypes are expressed in the CA3 region of the hippocampus and high doses of 5-HT red
113 rons, particularly in pyramidal cells in the CA3 region of the hippocampus and in the dorsal cortex.
114 hile relatively few neurons responded in the CA3 region of the hippocampus and the auditory cortex.
115 a higher increase of c-Fos expression in the CA3 region of the hippocampus compared to Trace-trained
116 tivity can be generated intrinsically in the CA3 region of the hippocampus from where it can propagat
117                                          The CA3 region of the hippocampus has been postulated to be
118                                          The CA3 region of the hippocampus is essential for associati
119                                 Although the CA3 region of the hippocampus is often conceptualized as
120                                          The CA3 region of the hippocampus is the major site of sharp
121                                   The dorsal CA3 region of the hippocampus is unique in its connectiv
122                          SERT density in the CA3 region of the hippocampus of the same rats, assessed
123 zed electrophysiological recordings from the CA3 region of the hippocampus performed by Alme et al.,
124                 A recording electrode in the CA3 region of the hippocampus recorded P20-N40 waveforms
125 ntaneous inhibitory neurotransmission in the CA3 region of the hippocampus revealed that loss of SV2A
126 nnections, an architectural component of the CA3 region of the hippocampus that is crucial for AM.
127                Temporary inactivation of the CA3 region of the hippocampus with bilateral infusions o
128         Third, temporary inactivation of the CA3 region of the hippocampus with lidocaine selectively
129 coupled receptor expressed in neurons of the CA3 region of the hippocampus, as transducing OCN's regu
130  BDNF mRNA labeling in the dentate gyrus and CA3 region of the hippocampus, as well as in the basolat
131 d encoding of contextual memory requires the CA3 region of the hippocampus, but the necessary genetic
132 ared to normotensive WKY in caudate putamen, CA3 region of the hippocampus, cingulate cortex, substan
133                                       In the CA3 region of the hippocampus, extensive recurrent assoc
134                                   Within the CA3 region of the hippocampus, glutamatergic mossy fiber
135                        In comparison, in the CA3 region of the hippocampus, LE may have a more limite
136               In mossy fiber synapses of the CA3 region of the hippocampus, long-term potentiation (L
137 ted into each of four different brain areas: CA3 region of the hippocampus, medial septal nucleus, br
138                                       In the CA3 region of the hippocampus, only a few LE-labeled mos
139 , in which astrogliosis is restricted to the CA3 region of the hippocampus, we demonstrate that upreg
140 regulation of c-src mRNA was observed in the CA3 region of the hippocampus, which was accompanied by
141  correlated with neural hyperactivity in the CA3 region of the hippocampus.
142  using a biologically plausible model of the CA3 region of the hippocampus.
143  synchronized epileptiform discharges in the CA3 region of the hippocampus.
144 /-), bgal(+/-) mice, most prominently in the CA3 region of the hippocampus.
145 late excitatory synaptic transmission in the CA3 region of the hippocampus.
146 rehensive description of their action in the CA3 region of the hippocampus.
147 l apical dendrites of pyramidal cells in the CA3 region of the hippocampus.
148 to associational/commissural synapses in the CA3 region of the hippocampus.
149 lare of the CA1 region and all layers of the CA3 region of the hippocampus.
150 e Purkinje neurons of the cerebellum and the CA3 region of the hippocampus.
151 ervical ganglion, into the dentate gyrus and CA3 region of the hippocampus.
152 ssed on distinct neuronal populations in the CA3 region of the hippocampus.
153 ocytosis of synapses and synapse loss in the CA3 region of the hippocampus.
154 ndrites that are particularly evident in the CA3 region of the hippocampus.
155 leptiform bursting activity in the TSC2(+/-) CA3 region of the hippocampus.
156 sy-fiber long-term potentiation (LTP) in the CA3 region of the hippocampus.
157 Mg2+/ high-K+ perfusate were measured in the CA3 region of the intact mouse hippocampus.
158 nization across multiple active zones in the CA3 region of the rat hippocampus.
159               The hippocampal neurons in the CA3 region of these mutant mice are much less sensitive
160 -2.1), cingulate cortex (1.8), CA1, CA2, and CA3 regions of Ammon's horn (1.6-2.0), dentate gyrus (1.
161 ate gyrus and pyramidal cells in the CA1 and CA3 regions of Ammon's horn.
162 ly the anterior piriform cortex, the CA1 and CA3 regions of anterior dorsal hippocampus, anterior and
163                     In the dentate gyrus and CA3 regions of LPS-infused rats, Arc and OX-6 (specific
164 l cFos-ir in the dentate gyrus (DG), CA1 and CA3 regions of the Hipc in response to unilateral NMA in
165 ium ions into stratum radiatum of the CA1 or CA3 regions of the hippocampal slice evoked a fast netwo
166 measured in prefrontal cortex (PFC), CA1 and CA3 regions of the hippocampus (areas important for memo
167 f the function of the dentate gyrus (DG) and CA3 regions of the hippocampus are beginning to be under
168 ta oscillations in the dentate-hilar and CA1-CA3 regions of the hippocampus during exploratory behavi
169 n significant neuronal damage in the CA1 and CA3 regions of the hippocampus for the bicuculline and k
170   We compared the neural activity in CA1 and CA3 regions of the hippocampus in rats running for water
171  receptors were evident in the CA1, CA2, and CA3 regions of the hippocampus of epileptic animals.
172 populations in the cornu ammonis 1 (CA1) and CA3 regions of the hippocampus of freely moving rats.
173             Extracellular fluid from the CA1-CA3 regions of the hippocampus was collected with a 2-mm
174 III of the prefrontal cortex and the CA1 and CA3 regions of the hippocampus were determined.
175 ion volume and neuron density in the CA1 and CA3 regions of the hippocampus were measured 2 wks after
176                               In the CA1 and CA3 regions of the hippocampus, monoamine levels and tur
177 ing upper layer cortical neurons and the CA1-CA3 regions of the hippocampus, were acutely dependent o
178 in in synaptosomes isolated from the CA1 and CA3 regions of the hippocampus.
179  synaptic contact sites, most densely within CA3 regions of the hippocampus.
180  including barrel cortex and CA1 ventral and CA3 regions of the ventral hippocampus: D19 animals had
181 l prefrontal cortex and the CA1, but not the CA3, region of the hippocampus in OVX compared to intact
182 -related firing patterns in the CA1, but not CA3, region of the rat hippocampus were reorganized to r
183 o the CA1 region bilaterally and the CA2 and CA3 region on the right (left P = 0.0024, right P = 0.00
184 om recurrent systems such as the hippocampal CA3 region or the entorhinal cortex.
185                 In neocortex and hippocampal CA3 regions, parvalbumin (PV)-expressing basket cells, a
186 n of mossy fiber synapses in the hippocampal CA3 region, phosphorylated RIM1 acts through an unknown
187                              The hippocampal CA3 region plays an important role in learning and memor
188                  Computational models of the CA3 region predict that blocking mossy-fiber and/or perf
189 ic signaling specifically in the hippocampal CA3 region predominantly in male mice.
190             Potentiation of responses in the CA3 region reflected NMDA receptor-dependent LTP of upst
191          Potentiation of transmission to the CA3 region required LTP in both granule cell-->mossy cel
192 l localization in axons and terminals of the CA3 region results in increased excitability in the CA3
193                      RT-PCR of either CA1 or CA3 regions revealed the presence of KCNQ2, KCNQ3, KCNQ4
194 ons, and pyramidal neurons of the vulnerable CA3 region show significant remodeling after chronic str
195  in a subset of pyramidal neurons in the CA2/CA3 region, suggesting a basis for the epileptic phenoty
196 clude those of the hippocampal CA1, CA2, and CA3 regions, the dentate gyrus, supraoptic nucleus, hypo
197 tivity of the normally resistant hippocampal CA3 region to ischaemic stress, an effect that was gende
198 ially target interneurons in the hippocampal CA3 region to predominantly provide feedforward inhibiti
199 e molecular layer, but left responses in the CA3 region unchanged.
200  gamma oscillations in the mouse hippocampal CA3 region was increased by the activation of NMDA recep
201 ontrolling for baseline volumes, the left DG/CA3 region was significantly larger following memantine
202 aptic responses in preparations in which the CA3 region was surgically isolated from the rest of the
203        To examine synaptic plasticity in the CA3 region, we used aged rats behaviorally characterized
204 d transported along neuronal pathways to the CA3 region where it caused glial cell activation and neu
205 t synapses between individual neurons in the CA3 region, where both sides of the synapses are accessi
206                The bursts originate from the CA3 region, where there is a high degree of recurrent ex
207                                    Since the CA3 region, which is the target of the mossy fibers, rec
208 t inactivating micro-opioid receptors in the CA3 region would cause spatial learning and memory impai

 
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