戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  prefrontal cortex, basolateral amygdala, or hippocampal CA1 region.
2 -801 on LTD and NMDAR signaling in the mouse hippocampal CA1 region.
3 naptic plasticity in slice recordings of the hippocampal CA1 region.
4 the medial entorhinal cortex (MECIII) to the hippocampal CA1 region.
5 nes) profiles in the stratum radiatum in the hippocampal CA1 region.
6 f total and mushroom dendritic spines in the hippocampal CA1 region.
7 es and microglial cells were observed in the hippocampal CA1 region.
8 ces spontaneous epileptiform activity in the hippocampal CA1 region.
9 ning and long-term potentiation (LTP) in the hippocampal CA1 region.
10 ined if nicotine modulates DP and LTD in the hippocampal CA1 region.
11 ction of long-term potentiation (LTP) in the hippocampal CA1 region.
12 pulations and functional capabilities of the hippocampal CA1 region.
13 voked synaptic potential recorded in the rat hippocampal CA1 region.
14 eurite processes of remaining neurons of the hippocampal CA1 region.
15 the brain such as the pyramidal cells of the hippocampal CA1 region.
16 ons facilitate GABAergic transmission in the hippocampal CA1 region.
17 er research into the complex workings of the hippocampal CA1 region.
18 ioral changes and synaptic plasticity in the hippocampal CA1 region.
19 engram cells) in both the dorsal and ventral hippocampal CA1 regions.
20 nd Archaerhodopsin in pyramidal cells in the hippocampal CA1 region, achieving high quality recording
21 a feedforward inhibitory microcircuit in the hippocampal CA1 region, an increased excitability of pyr
22 l impairments and increased apoptosis in the hippocampal CA1 region and cortex.
23 e most concentrated in stratum oriens of the hippocampal CA1 region and dentate inner molecular layer
24 own histone acetyltransferases (HATs) in the hippocampal CA1 region and find that K-acetyltransferase
25 th altered in vivo network activities in the hippocampal CA1 region and impaired synaptic function.
26 nd high-frequency ripple oscillations in the hippocampal CA1 region and is linked to experience, but
27 ynaptic maturation are largely normal in the hippocampal CA1 region and somatosensory cortex at stage
28 ng RTN3 will develop RIDNs, initially in the hippocampal CA1 region, and later in other hippocampal a
29 tum oriens layers of both ventral and dorsal hippocampal CA1 regions, and again in both control and k
30 ssociated virus-based Eva1c knockdown in the hippocampal CA1 region annuls NAD(+)-induced memory impr
31                               Neurons in the hippocampal CA1 region are particularly sensitive to oxi
32 mation and impaired synaptic function in the hippocampal CA1 region as the result of epigenetic-depen
33 fect on GluR1 phosphorylation at T840 in the hippocampal CA1 region, bath application of NMDA induced
34 ts of the study show that ERalpha in the rat hippocampal CA1 region but not the uterus undergoes enha
35 xpressing cells in the stratum oriens of the hippocampal CA1 region confirmed that these cells were i
36                 Catecholamine release in the hippocampal CA1 region consolidates an object location m
37 n analysis, was significantly reduced in the hippocampal CA1 region, cortex, striatum, and thalamus i
38 he anterior cingulate, basolateral amygdala, hippocampal CA1 region, dentate gyrus, nucleus accumbens
39 theless, knockdown of synaptotagmin-1 in the hippocampal CA1 region did not impede acquisition of rec
40 sed with lentiviral shRNA-HCN1 in the dorsal hippocampal CA1 region displayed antidepressant- and anx
41 tions of glutamate were not increased in the hippocampal CA1 region during a 2-h postmortem interval,
42    Spatially firing "place cells" within the hippocampal CA1 region form internal maps of the environ
43 stigation of transcriptome plasticity in the hippocampal CA1 region in aging and AD models and sugges
44 e show that, in the pyramidal neurons of the hippocampal CA1 region in mice, blocking postsynaptic ex
45 s associated with learning and memory in the hippocampal CA1 region in rats.
46 nd the density of axospinous synapses in the hippocampal CA1 region in young rats, yet this is attenu
47                                          The hippocampal CA1 region is crucial for converting new mem
48 ts indicate that the induction of LTD in the hippocampal CA1 region is dependent on ionotropic, rathe
49                                          The hippocampal CA1 region is highly vulnerable to ischaemic
50 ther knockdown of HCN1 protein in the dorsal hippocampal CA1 region is sufficient to produce antidepr
51                                       In the hippocampal CA1 region, low-frequency stimulation (LFS;
52 haffer-collateral synapses, respectively, to hippocampal CA1-region neurons.
53 elicited long-term potentiation (LTP) in the hippocampal CA1 region of 28-day-old control animals.
54               Inhibitory synapses in the rat hippocampal CA1 region of acute slices were studied usin
55                      LAMTOR1 deletion in the hippocampal CA1 region of adult mice results in alterati
56                 The IFNbetaKO results in the hippocampal CA1 region of both male and female HIVgp120t
57 ls were trained on two memory tasks, and the hippocampal CA1 region of each was analyzed on an indivi
58  pyramidal neurons freshly isolated from the hippocampal CA1 region of immature (2- to 10-day-old) an
59 s and perisomatic inhibitory synapses in the hippocampal CA1 region of juvenile and adult male offspr
60 l cells and modified GABAergic inputs in the hippocampal CA1 region of LRRC8A bKO.
61  characterized events accompanying SD in the hippocampal CA1 region of murine brain slices, using who
62  postsynaptic density (PSD) thickness in the hippocampal CA1 region of NCK1-deficient mice.
63 not theta burst stimulation, is perturbed in hippocampal CA1 region of old but not young htau mice.
64 erties of basal synaptic transmission in the hippocampal CA1 region of PSD-93 and PSD-95 mutant mice
65 rays of electrodes in the dorsal and ventral hippocampal CA1 region of rats and recorded the neuronal
66 -phase long-term potentiation (L-LTP) in the hippocampal CA1 region of rodents.
67 of interneurons-theta-driving neurons in the hippocampal CA1 region of the mouse-to characterize the
68 inous synaptic density and plasticity in the hippocampal CA1 region of young female rats but fails to
69 reases the axospinous synapse density in the hippocampal CA1 region of young female rats but fails to
70 1 mice, a subpopulation of astrocytes in the hippocampal CA1 region prominently expressed nAChRbeta4
71 that nicotine reverses stabilized LTP in the hippocampal CA1 region, providing the first evidence tha
72 actic viral expression of Cre-recombinase in hippocampal CA1 region pyramidal neurons at postnatal da
73 nstem, excitatory and inhibitory synapses on hippocampal CA1-region pyramidal neurons, and inhibitory
74 n to principal excitatory cells (PCs) in the hippocampal CA1 region, regulating incoming inputs and m
75       Electrophysiological recordings in the hippocampal CA1 region revealed that short-term and long
76 taGABA(A)R) expression in the dentate gyrus, hippocampal CA1 region, thalamus, and striatum but not i
77 lidate our dual-channel miniscope, we imaged hippocampal CA1 region that co-expressed a dynamic calci
78                         Specifically, in the hippocampal CA1 region, the NL3(R451C) mutation caused a
79 aptic plasticity of pyramidal neurons in the hippocampal CA1 region to maintain an appropriate homeos
80 side-out laminated regions spanning from the hippocampal CA1 region to neocortex undergo a slow 'reve
81  showed abnormal long-term plasticity in the hippocampal CA1 region together with deficits in learnin
82 lation-mediated synaptic potentiation in the hippocampal CA1 region was significantly reduced compare
83  pyramidal cells and field recordings in the hippocampal CA1 region, we investigated the specific con
84 ever, reduction of amyloid deposition in the hippocampal CA1 region, where RIDNs predominantly formed
85 ctor 2) phosphorylation in astrocytes in the hippocampal CA1 region, which promotes protein synthesis
86 d induction of long-term potentiation in the hippocampal CA1 region without affecting basal synaptic