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2 at the stratum oriens-pyramidale (SO-SP) or stratum lacunosum-molecular (S-L-M) border, respectively
3 munofluorescence was observed at CA1 and CA3 stratum lacunosum/molecular (SLM) declining to 60% and 6
4 dritic arborization of CA2/3 basket cells in stratum lacunosum moleculare (33% of length, 29% surface
5 the dentate gyrus (P < 0.005) and within the stratum lacunosum moleculare (P < 0.01), the stratum rad
6 quitin and mitochondria accumulations in the stratum lacunosum moleculare (SLM) layer, without loss o
7 ation of GABA(A) receptor-mediated events in stratum lacunosum moleculare interneurons of the rat hip
9 ving rise to the primary theta dipole in CA1 stratum lacunosum moleculare, are conveyed by the tempor
12 rtex (ERC) and then CA1 stratum radiatum and stratum lacunosum-moleculare (CA1-SRLM)--two monosynapti
14 aining cells) and interneurons projecting to stratum lacunosum-moleculare (representing somatostatin/
18 act that a single electrical stimulus of the stratum lacunosum-moleculare (SLM, which contains the PP
19 125)I]alpha-bungarotoxin-positive neurons in stratum lacunosum-moleculare and decreased numbers in st
21 Cajal-Retzius cells target specifically the stratum lacunosum-moleculare and the dentate gyrus, but
23 on-principal neurons at the stratum radiatum-stratum lacunosum-moleculare border (R-LM interneurons)
24 SDF-1 alpha-mediated neuromodulation of the stratum lacunosum-moleculare by directly comparing the p
25 spontaneous action currents from hippocampal stratum lacunosum-moleculare Cajal-Retzius cells of the
26 adiatum receive both signals, while those in stratum lacunosum-moleculare exclusively receive a gluta
27 , activation of beta-adrenergic receptors in stratum lacunosum-moleculare GABAergic networks reduces
28 ion-based coupling in paired recordings from stratum lacunosum-moleculare interneurons by approximate
29 lthough electrical coupling was abolished in stratum lacunosum-moleculare interneurons from knockout
30 litude, kinetically slow synaptic input from stratum lacunosum-moleculare interneurons, anatomically
32 ttern consisted of intense activation of the stratum lacunosum-moleculare of CA1 and the subiculum, c
33 us coeruleus, lateral septum, diagonal band, stratum lacunosum-moleculare of CA1, and various nuclei
34 putamen, the hilus of the dentate gyrus, and stratum lacunosum-moleculare of field CA1 of Ammon's hor
35 r calretinin from its normal position in the stratum lacunosum-moleculare of field CA2 to an alvear p
36 ating the perforant path termination zone in stratum lacunosum-moleculare of the CA1 area as well as
38 ew KT-labeled processes were also present in stratum lacunosum-moleculare of the CA1 region and all l
41 gether with their potential implications for stratum lacunosum-moleculare processing of information i
43 re integrated in the synaptic network of the stratum lacunosum-moleculare via excitatory GABAergic in
44 ns-alveus and their axons which projected to stratum lacunosum-moleculare where they ramified extensi
45 l coupling among hippocampal interneurons of stratum lacunosum-moleculare with different excitability
47 e the apical dendrites project deep into the stratum lacunosum-moleculare, a distance several hundred
48 ate from stratum radiatum to its border with stratum lacunosum-moleculare, both fate maps of pioneer
49 The termination area of this pathway, the stratum lacunosum-moleculare, has the highest concentrat
50 ptic plasticity and dendritic development in stratum lacunosum-moleculare, thus impacting the integra
51 ifically targeted to dendritic spines in the stratum lacunosum-moleculare, which form synapses with p
63 rites in layers 2 to 3 of the neocortex, the stratum lacunosum, the dentate gyrus, and cornu ammonis
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