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1 te granule cells, dentate hilar neurons, and hippocampal pyramidal cells.
2 in controlling the rate, burst and timing of hippocampal pyramidal cells.
3 age gradient for fast synaptic inhibition in hippocampal pyramidal cells.
4 rents by the muscarinic agonist carbachol in hippocampal pyramidal cells.
5 es at the GABAergic synapses in dendrites of hippocampal pyramidal cells.
6 e slightly fewer dendritic spines in the CA1 hippocampal pyramidal cells.
7 utside-out patches from acutely isolated CA1 hippocampal pyramidal cells.
8 nal signaling endosomes to transport Akt1 in hippocampal pyramidal cells.
9 es dendritic hyperexcitability in entorhinal-hippocampal pyramidal cells.
10 AMPA receptor-mediated synaptic responses in hippocampal pyramidal cells.
11 he biophysical and integrative properties of hippocampal pyramidal cells.
12 l patch clamp techniques on acutely isolated hippocampal pyramidal cells.
13 s back-propagate into the dendritic arbor of hippocampal pyramidal cells.
14 te in small spots along the dendrites of CA1 hippocampal pyramidal cells.
15 imulation of the Schaffer collaterals in CA1 hippocampal pyramidal cells.
16 F) mRNA levels occurred in granule cells and hippocampal pyramidal cells.
17 of dentate granule cells, hilar neurons, and hippocampal pyramidal cells.
18 ows brief membrane depolarization in rat CA1 hippocampal pyramidal cells, a process called depolariza
19                                           In hippocampal pyramidal cells, a prominent elevation of Ca
20                                           In hippocampal pyramidal cells, a rise in Ca(2+) releases e
21                                           In hippocampal pyramidal cells, a small subset of dendritic
22 pecific gamma oscillations, implemented onto hippocampal pyramidal cells along their somato-dendritic
23                                              Hippocampal pyramidal cells also exhibit spatial selecti
24                                           In hippocampal pyramidal cells, AMPA receptors are heterome
25 translation of GluA1-4 mRNAs in dendrites of hippocampal pyramidal cells and CA1 interneurons but not
26  ligands are synthesized by neurons, such as hippocampal pyramidal cells and cerebellar granule cells
27 een described for principal neurons, such as hippocampal pyramidal cells and cerebellar Purkinje cell
28 By using both immunofluorescence of cultured hippocampal pyramidal cells and EM postembedding immunog
29 jections have a unique topography and target hippocampal pyramidal cells and interneurons.
30 uses a rapid exocytosis of AMPA receptors in hippocampal pyramidal cells and is constitutively requir
31                           We found that many hippocampal pyramidal cells and most interneurons discha
32  the spatial signal carried by the firing of hippocampal pyramidal cells and specifically reduces the
33 ound transform the integrative capacities of hippocampal pyramidal cells and their dendrites.
34 l-4-isoxazole propionate (AMPA) receptors in hippocampal pyramidal cells, and on glutamate transporte
35                                              Hippocampal pyramidal cells are called place cells becau
36 ary to widely-held assumptions in the field, hippocampal pyramidal cells are not a major target of NR
37                                         Many hippocampal pyramidal cells are scattered in the plexifo
38 erefore, is the extent to which theories see hippocampal pyramidal cells as representing nonspatial i
39 ecific intracellular immunoreactive sites in hippocampal pyramidal cells, astroglia, and in microglia
40 y TBPB potentiates NMDA receptor currents in hippocampal pyramidal cells but does not alter excitator
41  Rab5 endosomes in primary cultures of mouse hippocampal pyramidal cells by live-cell imaging and sho
42 ptors increases membrane excitability in CA1 hippocampal pyramidal cells by reducing the slow calcium
43  from the soma into dendrites was studied in hippocampal pyramidal cells by simultaneous extracellula
44                                              Hippocampal pyramidal cells can be divided into place ce
45         Here we find that the spike times of hippocampal pyramidal cells can be predicted more accura
46 rominent injury to dentate hilar neurons and hippocampal pyramidal cells, dentate granule cells of an
47 rchitecture and lineage relationships of the hippocampal pyramidal cells, dentate granule cells, and
48 ing KA administration, the large majority of hippocampal pyramidal cells die in the FVB/N (FVB) mouse
49  stargazin lacking the PDZ-binding domain in hippocampal pyramidal cells disrupts synaptic AMPA recep
50                                           In hippocampal pyramidal cells, dopamine acts at D1 recepto
51 semble activity correlations expressed among hippocampal pyramidal cells during behavior persists dur
52               The correlated activity of rat hippocampal pyramidal cells during sleep reflects the ac
53 c deletion of either mGlu(3) or mGlu(5) from hippocampal pyramidal cells eliminated effects of mGlu(3
54                                              Hippocampal pyramidal cells encode an animal's location
55                                              Hippocampal pyramidal cells encode memory engrams, which
56 rate that activation of mGlu(3) receptors in hippocampal pyramidal cells enhances hippocampal-depende
57                              Place fields of hippocampal pyramidal cells expand asymmetrically when a
58 ial segment (AIS) in low-density cultures of hippocampal pyramidal cells following GABAergic and glut
59 ts indicate that the amplitude of the AHP in hippocampal pyramidal cells from aged animals is depende
60                   By contrast, the firing of hippocampal pyramidal cells from slices of the same age
61 tionally considered a homogeneous cell type, hippocampal pyramidal cells have been recently shown to
62                In the actively foraging rat, hippocampal pyramidal cells have strong spatial correlat
63  rescue using whole-cell recordings from CA1 hippocampal pyramidal cells in brain slices.
64 s inhibition of the M-current in rat CA1/CA3 hippocampal pyramidal cells in primary neuron cultures.
65 ysiological NKA transport activity in single hippocampal pyramidal cells in situ We have found that n
66 -evoked (NMDA-evoked) firing rate of rat CA1 hippocampal pyramidal cells, in vivo.
67  conducted in excised patches collected from hippocampal pyramidal cells indicated that thiocyanate d
68       We report the selective recruitment of hippocampal pyramidal cells into patterned network activ
69                  The axon initial segment of hippocampal pyramidal cells is a key subcellular compart
70                            The firing of rat hippocampal pyramidal cells is determined both by the an
71 Aergic synaptic inhibition onto dendrites of hippocampal pyramidal cells is increased.
72 GluR-induced change in the firing pattern of hippocampal pyramidal cells is thus the result of multip
73 hat KChIP2, which is abundantly expressed in hippocampal pyramidal cells, is essential for IA regulat
74 s recorded from both below and above the CA1 hippocampal pyramidal cell layer became highly coherent.
75 ty and mRNA are found at lower levels in the hippocampal pyramidal cell layer, dentate granule cell l
76 lopregnanolone administration on spontaneous hippocampal pyramidal cell neural activity.
77                            The inhibition of hippocampal pyramidal cells occurs via inhibitory intern
78 lta GABA(A) receptors (GABARs) occurs in the hippocampal pyramidal cells of female mice at pubertal o
79 eptors (mGluRs), are shown to coexist in CA1 hippocampal pyramidal cells of juvenile (11-35 day-old)
80 e genes undergo a sustained up-regulation in hippocampal pyramidal cells only of mice and rats that h
81  constitute two key GABAergic controllers of hippocampal pyramidal cell output.
82                                              Hippocampal pyramidal cells (PCs) express many GABAAR su
83      In any given environment, a fraction of hippocampal pyramidal cells (PCs) is active at specific
84                                              Hippocampal pyramidal cells (PCs) release glutamate with
85 he synaptic excitation and inhibition of CA1 hippocampal pyramidal cells (PCs), cells known to partic
86 apid changes in spatial coding properties of hippocampal pyramidal cells (PCs).
87 hermoregulation, brain estrogen content, and hippocampal pyramidal cell physiology.
88                       The dendritic trees of hippocampal pyramidal cells play important roles in the
89 ected learning and related reorganization of hippocampal pyramidal cell population dynamics.
90 otentials back-propagating into dendrites of hippocampal pyramidal cells provide sufficient postsynap
91                                              Hippocampal pyramidal cells (PYRs) of the mammalian brai
92                              The activity of hippocampal pyramidal cells reflects both the current po
93                       The phase of spikes of hippocampal pyramidal cells relative to the local field
94  and GABA-negative dentate hilar neurons and hippocampal pyramidal cells remained immunonegative.
95                                 Tests in CA1 hippocampal pyramidal cells reveal that a slow AHP is re
96                Cerebellar Purkinje cells and hippocampal pyramidal cells revealed substantial immunor
97                  Modeling experiments in CA1 hippocampal pyramidal cells revealed that both mutations
98 atch clamp recordings of acutely dissociated hippocampal pyramidal cells revealed that the D1 dopamin
99                                              Hippocampal pyramidal cells show high expression of alph
100                         However, in isolated hippocampal pyramidal cells, simulated ischaemia evokes
101                        Here we show in mouse hippocampal pyramidal cells that LTP at individual synap
102 f the presynaptic contacts between a pair of hippocampal pyramidal cells that used biologically reali
103                                       In CA1 hippocampal pyramidal cells, the fAHP is carried by the
104                                In individual hippocampal pyramidal cells, the range of GABA(A) revers
105 c transmission in retinal ganglion cells and hippocampal pyramidal cells to determine, at a cellular
106 xtrinsic factors modulate the sensitivity of hippocampal pyramidal cells to kainic acid.
107 f glutamate receptors in distal dendrites of hippocampal pyramidal cells triggers voltage-dependent C
108                                In the brain, hippocampal pyramidal cells use temporal as well as rate
109                              The activity of hippocampal pyramidal cells was recorded while adult (10
110 was insufficient to injure hilar neurons and hippocampal pyramidal cells, was nonetheless sufficient
111 ndritic and axonal arbors of biocytin-filled hippocampal pyramidal cells were reconstructed.
112 e pyramidal layers of cortex, and changes in hippocampal pyramidal cells were smaller.
113 entate granule cells, hilar mossy cells, and hippocampal pyramidal cells, were devoid of detectable S
114  A notable exception is found in a subset of hippocampal pyramidal cells where the axon emerges from
115                          Transfection of CA3 hippocampal pyramidal cells with BoNtE-resistant SNAP-25
116                          The spike timing of hippocampal pyramidal cells with respect to the theta rh

 
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