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1 s/alveus and innervated stratum radiatum and oriens.
2 ty at all; half of these were in the stratum oriens.
3 n the stratum radiatum and/or in the stratum oriens.
4 X neurons were most prevalent in CA1 stratum oriens.
5 campal subregions, CA1 stratum radiatum, and oriens.
6 y of the recording electrodes in the stratum oriens.
7 rneurons with cell bodies in the CA1 stratum oriens.
8 diatum and pyramidale but not in the stratum oriens.
9 tate supragranular layer and the CA3 stratum oriens.
10 -moleculare and decreased numbers in stratum oriens.
12 um radiatum and, to a lesser extent, stratum oriens; (3) perforant pathway-associated interneurons (n
13 f NAAG-immunoreactive neurons in CA3 stratum oriens (35.8%) and CA1 stratum oriens (78.87%), stratum
14 n CA3 stratum oriens (35.8%) and CA1 stratum oriens (78.87%), stratum pyramidale (40%), and stratum r
15 ive labeling of SOM-expressing neurons in s. oriens, a Cre recombinase-dependent construct for channe
16 s extending into all CA subfields in stratum oriens, adapting firing patterns and a pronounced "sag"
17 rm potentiation (LTP) in hippocampal stratum oriens-alveus (O/A) interneurons requires co-activation
18 ry synapses onto hippocampal interneurons in oriens-alveus (OA-INs) which is induced by activation of
19 nd dendrites, which were confined to stratum oriens-alveus and their axons which projected to stratum
21 ls in CA1 and interneurones near the stratum oriens-alveus border revealed excitatory connections tha
22 a of CA1 pyramidal neurons and stratum (st.) oriens-alveus inhibitory interneurons in rat hippocampal
23 interneurones were classified as horizontal oriens-alveus interneurones by the pronounced 'sag' in r
24 cemaking activity in rat hippocampal stratum oriens-alveus interneurones was studied using whole-cell
26 on basilar dendrites extend into the stratum oriens-alveus while the apical dendrites project deep in
29 citatory synapses between principal cell and oriens/alveus (O/A) interneurons, a particular form of N
30 on of the alpha5-GABA(A)R in the CA1 stratum oriens/alveus (O/A) using a combination of immunohistoch
31 erneurons within the hippocampal CA1 stratum oriens/alveus (O/A), with preferential innervation of or
32 had horizontal dendrites restricted to str. oriens/alveus and innervated stratum radiatum and oriens
33 of distal dendritic branches within stratum oriens/alveus elicited fast Ca2+ transients, which showe
34 matostatin (SOM) interneurons in CA1 stratum oriens/alveus fire during hippocampal theta and investig
35 neurons were comprised almost exclusively of oriens/alveus interneurons with lacunosum-moleculare axo
36 somatostatin interneurons in the CA1 stratum oriens and dentate hilus (which themselves do not expres
38 in-expressing cells predominantly in stratum oriens and parvalbumin-expressing cells mostly in stratu
39 ese structures were also observed in stratum oriens and piriform cortex, and in cerebellar Purkinje c
40 showed significant reductions in the strata oriens and pyramidale of CA1, the stratum pyramidale of
41 ns and were highly significant in the strata oriens and radiatum of both CA1 and CA3 subfields and in
43 s were decreased significantly in the strata oriens and radiatum of CA3, in the dentate granule cell
44 ymmetric synapses was observed in the strata oriens and radiatum of the CA3a and CA2 regions, and a f
45 y 71.82% and 77.53% reduction in the stratum oriens and radiatum, respectively, when compared with co
46 siological properties of hippocampal stratum oriens and stratum pyramidale inhibitory interneurones,
47 ing subfield preference, innervating stratum oriens and stratum radiatum of CA2 and CA1 but stopping
48 ensin II binding was detected in the stratum oriens and stratum radiatum of the CA1 and CA2 subfields
51 rane polarization of deep (closer to stratum oriens) and superficial (closer to stratum radiatum) rat
52 co-expression was located in CA1/CA3 stratum oriens, and GAD67/alpha5 co-expression was predominantly
53 nses, was localized primarily to the stratum oriens, and had axonal projections to the stratum lacuno
54 in calbindin-positive neurons in the stratum oriens, and in a small number of interneurons that did n
56 nate in the strata radiatum, pyramidale, and oriens, are present throughout the entire transverse ext
57 C), axo-axonic (AAC), bistratified (BiC) and oriens-bistratified (O-BiC) cells, were distinguished by
58 corded from the hippocampal fissure and str. oriens but not the coherence between signals derived fro
59 ngs, Nkx2.1-Cre+ interneurons in the stratum oriens, but not Chrna2-Cre+ or Htr3a-GFP+ cells, receive
61 us, delivered extracellularly in the stratum oriens, caused a reduction in spike frequency adaptation
63 roglia in the denervated hippocampal stratum oriens did not migrate extensively, whereas human immuno
65 ssion to hippocampal interneurons in stratum oriens does not require NMDA receptors and the induction
66 king interneurons in the hippocampal stratum oriens exhibit a form of long-term potentiation of excit
67 cells in the stratum pyramidale; in stratum oriens, HC PV cells were electrophysiologically distinct
68 iological properties differentiating stratum oriens horizontal interneurons from pyramidal neurons of
72 igh-frequency priming stimulation in stratum oriens inhibits subsequent LTP in the stratum radiatum o
74 he resting membrane potential of CA1 stratum oriens interneurones persistently increased following ex
75 rinic receptor (mAChR) activation on stratum oriens interneurones using whole-cell patch clamp record
76 s of gamma activity, two distinct classes of oriens interneurones, oriens lacunosum-moleculare (O-LM)
77 h and Girk in the same population of stratum oriens interneurons and that the modulation of these ion
78 ency spiking activity in a subset of stratum oriens interneurons controlling electrogenesis in pyrami
79 emporally correlated with spiking in stratum oriens interneurons demonstrating intrinsic theta-freque
82 caine) was detected in 30-50% of CA1 stratum oriens interneurons of various morphological classes.
83 red recordings between pyramidal neurons and oriens interneurons were obtained to determine whether L
87 alpha7, beta2 and beta3 subunits in stratum oriens interneurons; and beta2-4 in pyramidal neurons.
92 wo distinct classes of oriens interneurones, oriens lacunosum-moleculare (O-LM) and trilaminar cells,
94 l-Retzius cells receive GABAergic input from oriens lacunosum-moleculare cells and that this input ha
95 x2-1 intersection identified a population of oriens lacunosum-moleculare INs that predominantly targe
99 both synaptic and intrinsic potentiation in oriens-lacunosum moleculare (O-LM) interneurons followin
101 pses, we recorded mGluR1-mediated EPSCs from oriens-lacunosum moleculare (O-LM) interneurons in acute
102 CP) AMPA receptors has been characterized in oriens-lacunosum moleculare (O-LM) interneurons, which e
103 rt a surprising divergence among hippocampal oriens-lacunosum moleculare (O-LM) projecting interneuro
104 ypes of visualised presynaptic interneurone, oriens-lacunosum moleculare (O-LMC), basket (BC), axo-ax
106 icompartment neurons [pyramidal, basket, and oriens-lacunosum moleculare (OLM) cells] generated theta
107 al pyramids and facilitating inputs onto 7/7 oriens-lacunosum moleculare and 5/5 burst firing, sparse
108 veus (O/A), with preferential innervation of oriens-lacunosum moleculare cells (OLMs) through dendrit
109 essing basket, axo-axonic, bistratified, and oriens-lacunosum moleculare cells, innervating different
110 n intrinsic excitability of basket cells and oriens-lacunosum moleculare interneurons in epileptic an
111 urs in NDNF-positive neurogliaform cells and oriens-lacunosum moleculare interneurons in the mouse hi
112 h low probability to somatostatin expressing oriens-lacunosum-moleculare (O-LM) interneurons (INs), a
113 tro to study activity of pyramidal cells and oriens-lacunosum-moleculare (O-LM) interneurons during r
115 ct interneuron types--basket, axo-axonic and oriens-lacunosum-moleculare cells--visualized and define
117 r of the oscillatory activity in the stratum oriens lamina of CA3, but for the kainate-induced oscill
118 l cortex layers V and VI, the subiculum, the oriens layer of CA1, the medial septum, the diagonal ban
119 We also found massive cell death in the oriens layer of the hippocampus on P1 and in regions sur
121 c plasticity in stratum radiatum and stratum oriens layers of both ventral and dorsal hippocampal CA1
122 eurons in the stratum pyramidale and stratum oriens layers of KO hippocampus may contribute to reduce
123 agonist G1: G1 increased PSD95-IR in strata oriens, lucidum, and radiatum of CA3 in ovariectomized m
126 tively) on GABAergic interneurons in stratum oriens of area CA1 of the hippocampus were examined by u
127 labeled neurons were also detected in the s. oriens of CA1 (52%), CA2 (27%) and CA3 (36%) subfields.
128 ron microscopy (cortex, CPN, and the stratum oriens of CA1), PROT labeling was observed primarily wit
130 though significant, increases in the stratum oriens of CA3 (30%), the subiculum (20-30%) and the pres
131 eposits were found in the subiculum, stratum oriens of hippocampal field CA1, and the hilus of the de
132 ons possessing somata located within stratum oriens of hippocampal slices were classified according t
134 ive neurons could be observed in the stratum oriens of the Ammon's horn and subiculum, fewer were see
136 m the hippocampal fissure and stratum (str.) oriens of the CA1 region and (2) between CA1 stratum rad
137 7-immunopositive interneurons in the stratum oriens of the CA1 region of the hippocampus, accompanied
139 of the CA1 and CA2 subfields, in the stratum oriens of the CA3 subfield, and in the molecular layer o
143 c profiles were most concentrated in stratum oriens of the hippocampal CA1 region and dentate inner m
144 (1A)-AR EGFP-expressing cells in the stratum oriens of the hippocampal CA1 region confirmed that thes
145 n in the mossy fiber pathway and CA3 stratum oriens of the hippocampus during limbic epileptogenesis.
146 tin (SOM)-expressing neurons in stratum (s.) oriens of the hippocampus exhibit axonal sprouting beyon
148 re, such as the stratum radiatum and stratum oriens of the hippocampus, the molecular and granular la
150 tterns, are primarily located in the stratum oriens or pyramidale, have sparsely spiny dendrites, and
153 Surprisingly, paired radiatum and unpaired oriens pathway potentiated, unless the pre-post delay wa
154 sely, the exact same 5 ms pairing in stratum oriens potentiated both pathways, as did AP-bursts alone
155 sine receptors counteracted unpaired stratum oriens potentiation following pairing in stratum radiatu
156 in a marked loss of SP fibers in the strata oriens, pyramidale, and radiatum of the CA3a and CA2 sub
157 lation of GABAergic terminals at the stratum oriens-pyramidale (SO-SP) or stratum lacunosum-molecular
159 d in the stratum radiatum of CA1, the strata oriens, radiatum and pyramidale of CA3, the dentate mole
160 e distribution of alpha2A-AR-I in the strata oriens, radiatum, and lacunosum-moleculare of hippocampa
162 Horizontal interneurones in the stratum oriens showed firing preference to inputs at theta frequ
163 egulate synaptic transmission in the stratum oriens (SO) and lacunosum-moleculare (SLM) of the dCA1 a
167 we investigated I(M) in hippocampal stratum oriens (SO) interneurons, both from wild-type and transg
168 a down-regulation of GAD(67) in the stratum oriens (SO) of CA2/3 in both groups; CA1 only showed cha
171 ticularly between strata radiatum and strata oriens, suggesting a functional heterogeneity among hipp
172 racted DNA from laser-microdissected stratum oriens tissue of cornu ammonis 2/3 (CA2/3) and CA1 postm
174 tanic stimulation of the stratum radiatum or oriens were analysed using intracellular and multichanne
175 ified interneurones (n = 43) located in str. oriens were recorded in order to compare their functiona
176 on fluorescence intensity in the CA1 stratum oriens, where CA2 axons preferentially project, and that
177 volved in mediating synaptic potentiation in oriens, whereas NMDA and adenosine receptors counteracte