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1  4-6 of training, rats received posttraining intrahippocampal (1 microgram/0.5 microliter) or intraca
2                                              Intrahippocampal (10 micrograms), but not intra-dorsal s
3 ntra-dorsal striatal (2 micrograms), but not intrahippocampal (2, 5, or 10 micrograms) injection of A
4  either physostigmine (systemic=0.075 mg/kg; intrahippocampal=20, 40 ng/muL) or saline.
5 These findings support the development of an intrahippocampal AAV.NPY-Y2R therapy for treating seizur
6                                              Intrahippocampal Abeta(1-40) injection resulted in prono
7 d P33 (Experiment 1), or following bilateral intrahippocampal administration of 2.5 or 5.0 microg per
8 ogies for at least six months after a single intrahippocampal administration of an adeno-associated v
9                                 In addition, intrahippocampal administration of anisomycin (100 mug/m
10                                     Further, intrahippocampal administration of biotin-labeled CAA mu
11                                 In contrast, intrahippocampal administration of BN 50730 had no effec
12 - to long-term memory observed in vivo after intrahippocampal administration of picomolar amounts of
13 abolished hPAC and the amnesia caused by the intrahippocampal administration of reconsolidation block
14                            We show here that intrahippocampal administration of SP triggers self-sust
15                                 Furthermore, intrahippocampal administration of SPK100.NPY-Y2R reduce
16                     Here we show that direct intrahippocampal administration of the adeno-associated
17 er experiments using the plus-maze, in which intrahippocampal administrations of pharmacological agen
18 genesis and the balance of entorhinal versus intrahippocampal afferents.
19    Hippocampal CA1 pyramidal neurons receive intrahippocampal and extrahipppocampal inputs during the
20 ng-term behavioral consequences of systemic, intrahippocampal and intra-medial prefrontal cortex admi
21          Here, we evaluated the influence of intrahippocampal ANI infusions on allocentric spatial na
22                               Sensitivity to intrahippocampal anisomycin was observed only in the pro
23 g to birds, and birds expanded the system of intrahippocampal axon collaterals, relative to turtles a
24 wo-dimensional spatial topology, whereas the intrahippocampal CA3-DG projections concurrently produce
25                            All patients with intrahippocampal calcification and the control cohort de
26                            The prevalence of intrahippocampal calcification appears to increase with
27           Eleven (23.4%) of 47 patients with intrahippocampal calcification had calcification within
28                              The presence of intrahippocampal calcification was assessed by four read
29                                              Intrahippocampal calcification was demonstrated in 47 (1
30                 The anatomic distribution of intrahippocampal calcification was similar to that descr
31 cations and a matched control cohort without intrahippocampal calcification.
32   Differences in proportion of patients with intrahippocampal calcifications across different age gro
33 stories were reviewed in those patients with intrahippocampal calcifications and a matched control co
34 ity was observed in epileptic mice receiving intrahippocampal CGE progenitors.
35  throughout a 14-day monitoring period in an intrahippocampal chemoconvulsant mouse model that develo
36 tion to synaptic plasticity processes via an intrahippocampal circadian transcriptional clock.
37 e discovered a network event generated by an intrahippocampal circuit formed by a subset of CA2 pyram
38 elationships between different components of intrahippocampal circuitry derived from experimental pat
39  results demonstrate that temporally precise intrahippocampal communication is critical for spatial p
40 e histological changes occurred with altered intrahippocampal connectivity and abnormal behavior; inc
41  and pathological core, indicating perturbed intrahippocampal connectivity.
42 ovariance patterns to characterize efficient intrahippocampal connectivity.
43  intrahippocampal flatmap, with accompanying intrahippocampal coordinate system, are presented; they
44  manipulated hippocampal IL1 signaling using intrahippocampal delivery of IL1 receptor antagonist (IL
45 bserved in HDAC3-FLOX mice were abolished by intrahippocampal delivery of Nr4a2 small interfering RNA
46                                              Intrahippocampal delivery of plasminogen to plg(-/-) mic
47 histochemistry showed that focal deletion or intrahippocampal delivery of RGFP136 resulted in increas
48                                  Single-dose intrahippocampal delivery of the interneurons in a mouse
49                     M40 alone, either icv or intrahippocampal, did not affect choice accuracy in eith
50  by hippocampal volumetrics, analysis of the intrahippocampal distribution of T2 signal, and apparent
51 demonstrated that intracerebroventricular or intrahippocampal E(2) infusion immediately after object
52                      Forty minutes following intrahippocampal E2 or vehicle administration, tissues w
53                  Systemic (Experiment 1) and intrahippocampal (Experiment 2) injections of the acetyl
54 an Alzheimer's disease, we initiated chronic intrahippocampal expression of IFNgamma through delivery
55 onstructing a computer graphics quantitative intrahippocampal flatmap, with accompanying intrahippoca
56                                           An intrahippocampal gamma generator has been identified in
57                                              Intrahippocampal gamma oscillation emerges in the CA3 re
58 p is sufficient to explain the generation of intrahippocampal gamma-frequency oscillations.
59 nhancing effects of posttraining systemic or intrahippocampal glucocorticoid administration on memory
60 e memory enhancement induced by intra-BLA or intrahippocampal glucocorticoid receptor agonist adminis
61                                              Intrahippocampal IL1ra prevented synaptic dysfunction, p
62  In vivo studies demonstrated that bilateral intrahippocampal implants continued to secrete GDNF that
63 istered intraperitoneally (0.2 mg/kg) or via intrahippocampal infusion (5.0 microg/side) immediately
64                    We show that pre-training intrahippocampal infusion of a COX-2 specific inhibitor
65                          We demonstrate that intrahippocampal infusion of an EphA antagonist immunoad
66 e behavioral outcomes was examined by either intrahippocampal infusion of cholinergic receptor antago
67 s subsequently received an intra-amygdala or intrahippocampal infusion of either 20% DMSO or the MAPK
68                                              Intrahippocampal infusion of leptin produced a similar a
69 l activity only in male hippocampal neurons, intrahippocampal infusion of oAbeta or genetic suppressi
70                                 In contrast, intrahippocampal infusion of SB203580, a specific inhibi
71                                        Thus, intrahippocampal infusion of the CB1R antagonist SR14171
72                Experiment 1 established that intrahippocampal infusion of the D(1)/D(5) dopaminergic
73 blocked by the postextinction or postnovelty intrahippocampal infusion of the NMDA receptor antagonis
74                    Next, we demonstrate that intrahippocampal infusion of the protein synthesis inhib
75 assessed network activity after a unilateral intrahippocampal infusion of ZIP in anesthetized rats.
76 urrents were not affected by Zn(2+) Finally, intrahippocampal infusion of Zn(2+) elicited rapid epile
77                                              Intrahippocampal infusion studies with the AMPA-specific
78 DHT, or 3alpha-diol via Silastic capsules or intrahippocampal infusions had greater analgesia (tail f
79                        In addition, although intrahippocampal infusions of 40 ng of physostigmine inc
80                  We examined the capacity of intrahippocampal infusions of an alpha5 subunit-selectiv
81 , in addition to blocking protein synthesis, intrahippocampal infusions of ANI cause the suppression
82               Control studies confirmed that intrahippocampal infusions of anisomycin inhibited prote
83                                      We used intrahippocampal infusions of antisense oligodeoxynucleo
84 sent experiments examined whether unilateral intrahippocampal infusions of glucose would enhance spon
85 d the memory retrieval impairment induced by intrahippocampal infusions of RU 28362 given 60 min befo
86 y retrieval impairment induced by concurrent intrahippocampal infusions of RU 28362.
87 to the novelty, animals were given bilateral intrahippocampal infusions of vehicle (VEH), of the prot
88                                     Further, intrahippocampal inhibition of ERK activation or DNA met
89 fter infusion, an effect that was blocked by intrahippocampal inhibition of ERK or PI3K activation.
90 cement in middle-aged females was blocked by intrahippocampal inhibition of ERK or PI3K activation.
91 er memory training and that acute, selective intrahippocampal inhibition of GluT4-mediated glucose tr
92                    Here we report that acute intrahippocampal inhibition of PKMzeta disrupts place ce
93                                       VGF by intrahippocampal injection also had novel activity in an
94 ligonucleotide Fli-1 Gapmer administered via intrahippocampal injection decelerated pericyte loss, de
95                                              Intrahippocampal injection of 2.5 micrograms of the 3 be
96   A molecular biology approach combined with intrahippocampal injection of a gamma-secretase inhibito
97               Finally, we show that a single intrahippocampal injection of a specific oligomeric anti
98                            Here we show that intrahippocampal injection of ASC specks resulted in spr
99 nduction of alphaS aggregation following the intrahippocampal injection of E46K alphaS fibrils in M20
100  task, followed by a unilateral posttraining intrahippocampal injection of either estradiol (1.0 micr
101 a Morris water maze after a single bilateral intrahippocampal injection of either saline or the selec
102 Experiment 2, the memory enhancing effect of intrahippocampal injection of estradiol was blocked by p
103                                  Conversely, intrahippocampal injection of JNKs inhibitors sp600125 (
104 ating limbic areas in rats made epileptic by intrahippocampal injection of kainic acid, and in patien
105 n and reactive gliosis, which was induced by intrahippocampal injection of kainic acid.
106                        We also show that the intrahippocampal injection of naturally secreted Abeta i
107                                          The intrahippocampal injection of p17 in mice reduces their
108  Finally, induction of status epilepticus by intrahippocampal injection of pilocarpine induced biphas
109                                              Intrahippocampal injection of PUFA-CE-lipApoE4 was suffi
110           The model is induced by unilateral intrahippocampal injection of tetanus toxin.
111                                          The intrahippocampal injection of the selective A2A receptor
112                                        After intrahippocampal injection, and by contrast to the LRR-d
113 y to impair long-term potentiation and, upon intrahippocampal injection, caused spatial memory defici
114                               Rats receiving intrahippocampal injections of 192 IgG-saporin (SAP-HPC)
115                                              Intrahippocampal injections of adeno-associated virus ve
116                                   Similarly, intrahippocampal injections of an anti-Abeta antibody re
117                                              Intrahippocampal injections of BN 52021 decreased the la
118                                              Intrahippocampal injections of estradiol delayed 2 hr po
119                                              Intrahippocampal injections of estradiol enhance memory
120 etention test escape latencies of rats given intrahippocampal injections of estradiol were lower than
121                               Rats receiving intrahippocampal injections of glutamate predominantly d
122                   We evaluated the impact of intrahippocampal injections of NMDA on CCR5 expression i
123                             In Experiment 2, intrahippocampal injections of physostigmine significant
124                                 Furthermore, intrahippocampal injections of RhoA antisense oligodeoxy
125 g from systemic, intracerebroventricular and intrahippocampal injections of the protein synthesis inh
126 nalyzed in wild-type and nSTAT3KO mice after intrahippocampal kainate (IHKA) injection as a model of
127 ed in two rat models of SE-induced epilepsy: intrahippocampal kainate and systemic administration of
128 ion in the absence of injury, and unilateral intrahippocampal kainate injections into the transgenic
129                      We utilized the chronic intrahippocampal kainate mouse model of temporal lobe ep
130 trophy (granule cell dispersion) produced by intrahippocampal kainate.
131          We induced SE in adult male mice by intrahippocampal kainic acid (KA) infusion.
132 ivo model of temporal lobe epilepsy based on intrahippocampal kainic acid (KA) injection.
133 l cell death, accompany CAST depletion after intrahippocampal kainic acid administration to mice, and
134        To address this question, we used the intrahippocampal kainic acid mouse model of temporal lob
135 9 in the rapid-kindling rat model and in the intrahippocampal kainic acid mouse model.
136  are consistent with previous studies in the intrahippocampal kainic acid rat model of chronic epilep
137  range of 250-600 Hz [fast ripples (FRs)] in intrahippocampal kainic acid-treated rats with spontaneo
138 within the infrahippocampal cleft as well as intrahippocampal location of graft-derived cells express
139                                              Intrahippocampal microdialysis was performed in freely b
140 ular concentration profile of ethanol during intrahippocampal microdialysis with 1 M ethanol was esti
141          The predominant effect of the first intrahippocampal microdialysis with ethanol was a decrea
142 w that encoding of novel PAs is sensitive to intrahippocampal microinfusion of the NMDA antagonist d-
143                         Here, we report that intrahippocampal microinfusions of anisomycin in urethan
144                                      Whereas intrahippocampal microinjection of a conjugate of native
145                                              Intrahippocampal modulation of the EtOH-maintained respo
146  of adenosine and other extrahippocampal and intrahippocampal modulators in regulating SC synaptic fu
147                             In experiment 3, intrahippocampal muscimol infusions did not disrupt the
148              In the current studies, we used intrahippocampal muscimol microinfusions to transiently
149                            To understand how intrahippocampal networks interact during REM sleep, we
150 ished by LTP-like synaptic plasticity within intrahippocampal networks.
151  excitotoxic brain injury; in neonatal rats, intrahippocampal NMDA injection stimulates expression of
152        Field patterns, recorded from various intrahippocampal or entorhinal cortex sites, were used t
153                                              Intrahippocampal or intracerebroventricular E(2) infusio
154 kt phosphorylation was increased 5 min after intrahippocampal or intracerebroventricular E(2) infusio
155 latency to burying behavior was increased by intrahippocampal or intraseptal injection of 2.5 and 5 m
156                    The anxiolytic effects of intrahippocampal or intraseptal injection of pregnanolon
157                              Most excitatory intrahippocampal pathways are characterized by significa
158 trast, the lack of behavioral improvement by intrahippocampal physostigmine infusion in the PF rats,
159 after 15 min, and this effect was blocked by intrahippocampal PI3K, but not ERK, inhibition.
160 tated the extinction, which was inhibited by intrahippocampal protein synthesis inhibitor anisomysin,
161                This observation (systemic vs intrahippocampal) provides further support for the desig
162 iber projection, and its relationship to the intrahippocampal Purkinje cell protein 4 gene-expression
163                     Electrocorticographic or intrahippocampal recordings of epileptogenesis (from the
164 hese novel results demonstrate that a single intrahippocampal Reelin infusion into the dorsal hippoca
165 t examines the effects of repeated or single intrahippocampal Reelin infusions on measures of depress
166               The present study utilises the intrahippocampal route to further investigate CGS 21680-
167             Parallel studies have found that intrahippocampal scopolamine (Scop) blocks contextual fe
168 electrical stimulation can quickly terminate intrahippocampal seizures and suppress secondary general
169 cover the synaptic mechanisms underlying the intrahippocampal spread of gamma oscillations, we record
170 F levels that is dependent on the pattern of intrahippocampal stimulation.
171 ariate profile of age-related differences in intrahippocampal structures and show that HC maturity as
172 acterized by the differential development of intrahippocampal subfields and associated networks.
173 d reversible morphological reorganization of intrahippocampal subregions involved in information proc
174 hibitory theta signaling also contributes to intrahippocampal synchrony.
175 l effects on synchrony reflect the different intrahippocampal targets of these inputs.
176 trahippocampal structures depend both on the intrahippocampal topographic origin and magnitude of hip
177 res, such as their incidence, magnitude, and intrahippocampal topography in the septotemporal axis, a
178 NSC) grafting in the irradiated brain, where intrahippocampal transplantation of hNSC ameliorated rad
179                                              Intrahippocampal transplantation of human neural stem ce
180 g athymic nude rats followed 2 days later by intrahippocampal transplantation with human neural stem
181          In vivo, C57BL/6 mice that received intrahippocampal WNK463 experienced delayed onset of kai

 
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