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1 d in hippocampus, at mossy fiber synapses of stratum lucidum.
2 F pathway, including the MF terminal zone of stratum lucidum.
3 nd crossed the pyramidal layer to run in the stratum lucidum.
4 amidale, and ZIP3 primarily localized to the stratum lucidum.
5               In most laminae, except in CA3 stratum lucidum, about 15% of PR-immunoreactive profiles
6 f Kv3.4 immunoreactivity was detected in the stratum lucidum and hilus of dentate gyrus in areas corr
7                         Many interneurons in stratum lucidum and stratum radiatum receive both signal
8 voked by MF stimulation in interneurons from stratum lucidum and stratum radiatum, but not in interne
9 of CA3 neurons and lower GluR1 levels in the stratum lucidum area where MF-CA3 synapses reside but no
10 nputs to fast-spiking basket cells and spiny stratum lucidum cells were found to be numerous, but the
11 g ivy cells, and the septum-projecting spiny stratum lucidum cells.
12 rease of the immunostaining for GluK2 in the stratum lucidum in CA3, and of the amplitude and decay t
13 3 expression in mossy fiber at hilus and CA3 stratum lucidum in contrast with an enhanced expression
14 ABA(A) receptor-mediated synaptic input onto stratum lucidum inhibitory interneurons was shunting in
15  This finding suggested that the survival of stratum lucidum inhibitory neurons might be the primary
16              Interestingly, MF inputs to CA3 stratum lucidum interneurons (SLINs) undergo long-term d
17 figuration, we recorded from CA3 hippocampal stratum lucidum interneurons and pyramidal cells to moni
18         Thus, mossy fiber innervation of CA3 stratum lucidum interneurons occurs via two parallel sys
19 of stratum radiatum interneurons, whereas in stratum lucidum interneurons only GABAergic responses we
20 , the simultaneous MF GABAergic responses of stratum lucidum interneurons, but not of stratum radiatu
21 lutamatergic LTD, which is known to exist on stratum lucidum interneurons, coexists in the same pathw
22 tate gyrus granule cells and hippocampal CA3 stratum lucidum interneurons.
23 tive excitatory presynaptic terminals in the stratum lucidum of area CA3a/b.
24  significant increases in binding density in stratum lucidum of CA3 (hippocampal mossy fiber zone) in
25 eled peptide and observed highest binding in stratum lucidum of CA3 subfield, known to contain inhibi
26 port of biocytin following its ejection into stratum lucidum of CA3 was used to label granule cells f
27 ated Kv1.1 and Kv1.4 immunoreactivity in the stratum lucidum of CA3, indicating that these subunits a
28 nd aligned along dendritic shafts within the stratum lucidum of CA3.
29 as found in all lamina but was most dense in stratum lucidum of CA3.
30 opic granule cells following injections into stratum lucidum of CA3b of hippocampal slices obtained f
31 udes both the hilus of the dentate gyrus and stratum lucidum of the CA3 area was the lightest immunol
32 taining in the mossy fibers at the hilus and stratum lucidum of the CA3 area.
33 ostsynaptic distribution was not seen in the stratum lucidum of the CA3 region and the dentate hilar
34 approximately 100-200 nm in diameter) in the stratum lucidum of the CA3b field of the rat ventral hip
35 shown that the interneurons of the hilus and stratum lucidum receive this dual monosynaptic input on
36 ) glutamatergic and GABAergic neurons and in stratum lucidum (SL) GABAergic neurons during reconsolid
37 apse with dentate granule cells, and (2) the stratum lucidum (SL) of CA3, where the mossy fibers trav
38 nnervation pattern that is restricted to the stratum lucidum (SL).
39 s (CA3: SMI-32) and in the MF terminal zone (stratum lucidum: SMI-31) were nearly parallel to the pro
40                                           In stratum lucidum, where the mossy fiber axons course, mor