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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 se ratios during information encoding in the 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 ghout the molecular layer, as well as in the CA3 region.
12 o a new pattern of output to the hippocampal CA3 region.
13 ) activity in ERC and the dentate gyrus (DG)/CA3 region.
14 l gamma generator has been identified in the CA3 region.
15 Cs to identify ectopeptidase activity in the CA3 region.
16 nificant reduction of GAD-67 synapses in the CA3 region.
17 its epileptiform activity in the hippocampal CA3 region.
18 in shaping kainate neurotransmission in the CA3 region.
19 ons of norepinephrine in the rat hippocampal CA3 region.
20 treatments stopped, IBO was infused into the CA3 region.
21 cattered nuclei in the ventral subiculum and CA3 region.
22 ptosis in the KO hippocampus, especially the CA3 region.
23 derlie the hyperexcitability reported in the CA3 region.
24 xcitatory hippocampal neurons of the CA1- or CA3-region.
25 campal mossy fiber synapses of the hilar and CA3 regions.
26 prevented the neuronal loss in both CA2 and CA3 regions.
27 r, non-significant reductions in the CA1 and CA3 regions.
28 all en passant boutons in both the hilar and CA3 regions.
29 ntate gyrus, and pyramidal cell layer of the CA3 regions.
30 oughout the hippocampus, particularly in the CA3 regions.
33 rgan (SFO) or hippocampus (dentate gyrus and CA3 region) also significantly reduced the fever induced
34 Alzheimer's disease-related proteins in the CA3 region and a switch in amyloid precursor protein pro
36 ed serotonin transporters in the hippocampal CA3 region and in the substantia nigra-reticulata but in
37 imulating electrodes were placed in the left CA3 region and right angular bundle and a recording elec
40 n was not seen in the stratum lucidum of the CA3 region and the dentate hilar region, where most alph
42 c pump: tPA activity increases along the CA2-CA3 regions and dentate gyrus of the hippocampal formati
43 extranuclear profiles throughout the CA1 and CA3 regions and dentate gyrus, and, in contrast to light
45 lacunosum-moleculare of hippocampal CA1 and CA3 regions and in the molecular layer of the dentate gy
47 ed stress causes atrophy of dendrites in the CA3 region, and both acute and chronic stress suppresses
48 myloid deposition in cortex, the hippocampal CA3 region, and dentate gyrus was significantly reduced
49 tion within the mossy fiber terminals of the CA3 region, and in the newly formed mossy fiber aberrant
50 e neuroprotective effects in the dentate and CA3 regions, and that delayed JunB expression in the CA1
51 reshly isolated from rat hippocampus CA1 and CA3 regions are heterogeneous in ion channel expression
52 itory cells in the dentate gyrus, hilus, and CA3 regions as they integrate into hippocampal circuits.
53 mixed hippocampal, CA3 or CA1 cells into the CA3 region at 45 d after lesion, in comparison with "les
54 est a hierarchical internal operation of the CA3 region based on sequential oscillatory activation of
57 abundantly expressed in hippocampal CA2 and CA3 regions, but there are little known about their phys
58 t epileptiform burst firing generated in the CA3 region by activity-dependent enhancement of recurren
59 nt neuronal death in the hippocampal CA2 and CA3 regions (by 50 and 59%, respectively), by 7 days aft
60 arcuate and dorsomedial nuclei, hippocampal CA3 region, centromedial amygdaloid nucleus and thalamic
63 ation of granule neurons that innervated the CA3 region expressed leptin receptors and these cells we
66 sed of the entorhinal cortex and the dentate/CA3 regions hold promise for predicting progression on t
68 cellular field potential recordings from the CA3 region in guinea pig hippocampal slices were used to
69 tic remodeling is most prominent, namely the CA3 region, increases that were also inhibited by tianep
70 We found that both the septal and temporal CA3 regions intrinsically generate weakly synchronized d
74 ative attractor circuitry in the hippocampal CA3 region is thought to be the final arbiter between th
77 understand cholinergic modulation within the CA3 region, it is necessary to take into account seconda
78 In mossy fiber synapses of the hippocampal CA3 region, LTP is induced by cAMP and requires the syna
79 locations whereas, in more ventrally located CA3 regions, neurons gradually accumulate information ac
80 T-1 mRNA expression in the dentate gyrus and CA3 region of Ammon's horn, increases that were inhibite
82 x and their targets in the dentate gyrus and CA3 region of hippocampus comprise a system that rapidly
83 learance of locally applied serotonin in the CA3 region of hippocampus in drug- or vehicle-treated ra
85 , clearance of locally applied 5-HT into the CA3 region of hippocampus was achieved using in vivo ele
86 s of the cortex, by pyramidal neurons of the CA3 region of hippocampus, and by cerebellar Purkinje ne
87 n KO mice in areas including the cortex, the CA3 region of hippocampus, and the lateral dorsal thalam
89 Alzheimer's disease-relevant insult, as the CA3 region of long-term ovariectomized rats was profound
91 ynaptic loss and impaired LTP at hippocampal CA3 region of P301S mice were attenuated by blocking p25
92 form discharges were induced in vitro in the CA3 region of rat hippocampal slices by superfusion with
95 CA1 cell grafting into the kainate-lesioned CA3 region of the adult rat hippocampus at early post-ka
96 p-Erk and p-tau accumulated in the hilus and CA3 region of the dentate gyrus, where high levels of zi
97 0, severe = 10.9 +/- 1.3 million neurons) or CA3 region of the hippocampus (sham = 251 +/- 38, mild =
98 5-HT receptor subtypes are expressed in the CA3 region of the hippocampus and high doses of 5-HT red
99 rons, particularly in pyramidal cells in the CA3 region of the hippocampus and in the dorsal cortex.
100 hile relatively few neurons responded in the CA3 region of the hippocampus and the auditory cortex.
101 a higher increase of c-Fos expression in the CA3 region of the hippocampus compared to Trace-trained
102 tivity can be generated intrinsically in the CA3 region of the hippocampus from where it can propagat
107 ntaneous inhibitory neurotransmission in the CA3 region of the hippocampus revealed that loss of SV2A
110 coupled receptor expressed in neurons of the CA3 region of the hippocampus, as transducing OCN's regu
111 BDNF mRNA labeling in the dentate gyrus and CA3 region of the hippocampus, as well as in the basolat
112 d encoding of contextual memory requires the CA3 region of the hippocampus, but the necessary genetic
113 ared to normotensive WKY in caudate putamen, CA3 region of the hippocampus, cingulate cortex, substan
118 ted into each of four different brain areas: CA3 region of the hippocampus, medial septal nucleus, br
120 , in which astrogliosis is restricted to the CA3 region of the hippocampus, we demonstrate that upreg
121 regulation of c-src mRNA was observed in the CA3 region of the hippocampus, which was accompanied by
138 -2.1), cingulate cortex (1.8), CA1, CA2, and CA3 regions of Ammon's horn (1.6-2.0), dentate gyrus (1.
140 ly the anterior piriform cortex, the CA1 and CA3 regions of anterior dorsal hippocampus, anterior and
142 l cFos-ir in the dentate gyrus (DG), CA1 and CA3 regions of the Hipc in response to unilateral NMA in
143 ium ions into stratum radiatum of the CA1 or CA3 regions of the hippocampal slice evoked a fast netwo
144 measured in prefrontal cortex (PFC), CA1 and CA3 regions of the hippocampus (areas important for memo
145 f the function of the dentate gyrus (DG) and CA3 regions of the hippocampus are beginning to be under
146 ta oscillations in the dentate-hilar and CA1-CA3 regions of the hippocampus during exploratory behavi
147 n significant neuronal damage in the CA1 and CA3 regions of the hippocampus for the bicuculline and k
148 We compared the neural activity in CA1 and CA3 regions of the hippocampus in rats running for water
149 receptors were evident in the CA1, CA2, and CA3 regions of the hippocampus of epileptic animals.
150 populations in the cornu ammonis 1 (CA1) and CA3 regions of the hippocampus of freely moving rats.
153 ion volume and neuron density in the CA1 and CA3 regions of the hippocampus were measured 2 wks after
155 ing upper layer cortical neurons and the CA1-CA3 regions of the hippocampus, were acutely dependent o
157 including barrel cortex and CA1 ventral and CA3 regions of the ventral hippocampus: D19 animals had
158 l prefrontal cortex and the CA1, but not the CA3, region of the hippocampus in OVX compared to intact
159 -related firing patterns in the CA1, but not CA3, region of the rat hippocampus were reorganized to r
160 o the CA1 region bilaterally and the CA2 and CA3 region on the right (left P = 0.0024, right P = 0.00
163 n of mossy fiber synapses in the hippocampal CA3 region, phosphorylated RIM1 acts through an unknown
167 l localization in axons and terminals of the CA3 region results in increased excitability in the CA3
169 ons, and pyramidal neurons of the vulnerable CA3 region show significant remodeling after chronic str
170 in a subset of pyramidal neurons in the CA2/CA3 region, suggesting a basis for the epileptic phenoty
171 clude those of the hippocampal CA1, CA2, and CA3 regions, the dentate gyrus, supraoptic nucleus, hypo
172 tivity of the normally resistant hippocampal CA3 region to ischaemic stress, an effect that was gende
174 gamma oscillations in the mouse hippocampal CA3 region was increased by the activation of NMDA recep
175 aptic responses in preparations in which the CA3 region was surgically isolated from the rest of the
177 d transported along neuronal pathways to the CA3 region where it caused glial cell activation and neu
178 t synapses between individual neurons in the CA3 region, where both sides of the synapses are accessi
181 t inactivating micro-opioid receptors in the CA3 region would cause spatial learning and memory impai
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