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1                                         Both interlaminar and intralaminar differences in the dynamic
2 ll considered to establish only local (i.e., interlaminar and short-range) connections.
3   Another specialized type of astrocyte, the interlaminar astrocyte, abundantly populates the superfi
4                                              Interlaminar astrocytes (ILA) in the cerebral cortex pos
5                       These primate-specific interlaminar astrocytes are located in the superficial l
6                        Here we modeled human interlaminar astrocytes in humanized glial chimeric mice
7  of humans exhibits a radial distribution of interlaminar astrocytes in the supragranular layers.
8 imates are additional populations of layer 1 interlaminar astrocytes that extend long (millimeter) fi
9 ere consistently found in the subpial area ("interlaminar" astrocytes), the deep isocortical layers,
10 on and further thickening of the retina with interlaminar bridges.
11 stack design, on the basis of the concept of interlaminar carbon-nanotube forests that would provide
12              The extension of this theory to interlaminar circuitry also accounts for a sub-class of
13 nd dendritic fields support the concept that interlaminar communication is mediated in part via conta
14       Specifically, our results suggest that interlaminar communication within human temporal neocort
15 al horn, and that suggest a critical role in interlaminar communication.
16 s of lamina I form intersegmental as well as interlaminar connections and may govern large numbers of
17 emerge requires a precise description of the interlaminar connections and the quality of information
18  are discussed with reference to the role of interlaminar connections in mediating physiological inte
19  and detection studies necessary to decipher interlaminar connections involved in systems-level conso
20 all is unknown but essential for deciphering interlaminar connections involved in systems-level memor
21 ual cortex for investigating and replicating interlaminar connectivity changes using non-invasive EEG
22 iological correlations support the idea that interlaminar connectivity is mediated via translaminar d
23  interblobs, and the innate lineage-specific interlaminar connectivity within cortical columns.
24                Recent research suggests that interlaminar correlated firing between minicolumns durin
25                                  Strength of interlaminar correlations in Arc expression and modulati
26                                              Interlaminar correlations in Arc expression modulated by
27 patterns for distribution of strong and weak interlaminar correlations.
28 a specific reduction in excitatory ascending interlaminar cortical circuits resulting in decreased ac
29                       One hypothesis is that interlaminar cortical processing might be dedicated to a
30 mory recall, we studied multiple profiles of interlaminar coupling.
31 mposite samples with simulated flaws such as interlaminar delamination.
32                        Furthermore, although interlaminar differences were encountered, the pattern o
33  these synaptic connections display the same interlaminar directional preference as those observed in
34 alyzed contrast agent spread during cervical interlaminar epidural steroid injections (CILESIs) by us
35                          Conclusion Cervical interlaminar epidural steroid injections have injectate
36 ransforaminal ESIs are more efficacious than interlaminar ESIs, and that fluoroscopy can improve trea
37               These layers receive intrinsic interlaminar excitatory and inhibitory relays from layer
38 e demonstrate remarkable improvements in the interlaminar fracture toughness, hardness, delamination
39 risons to identify when laminar activity and interlaminar functional interactions showed surround sup
40 g feedback obeys hierarchical interareal and interlaminar gradients opposite to the flow of ascending
41                   An integrated treatment of interlaminar, horizontal, orientational and endstopping
42                             Stimulus-induced interlaminar information flow within V1 dominated upward
43                                       Strong interlaminar inhibitory inputs are found, particularly f
44 uch inhibition in this network; however, the interlaminar instantiation of inhibitory processes remai
45            We suggest that these reciprocal, interlaminar interactions may represent a "Helmholtz mac
46                             These "PGN-like" interlaminar interneurons innervated restricted regions
47                  Pharmacologically, PGN-like interlaminar interneurons were also similar to PGN neuro
48 contralateral neuroforamen in every cervical interlaminar level.
49 edle placement (43%; 36 of 83) than in other interlaminar levels (19.5%; 97 of 498; P < .001).
50 To retrospectively evaluate flow patterns of interlaminar lumbar epidural steroid injections and comp
51                                     However, interlaminar mapping experiments demonstrated a phase re
52                     Thus, neurons within the interlaminar microcircuits participate in various functi
53 he effective elastic chains via shearing the interlaminar molecular chains, which provides an additio
54 dimension lamellar structure with the aid of interlaminar n-n interaction.
55 formed by PGN cells and allowed the PGN-like interlaminar neurons to participate in the generation of
56  LGNd revealed that both PGN and a subset of interlaminar neurons were parvalbumin-positive.
57 lateral geniculate nucleus (LGN), the medial interlaminar nucleus (MIN), the lateral posterior nucleu
58 btype, except for patchy label in the medial interlaminar nucleus and the ventralmost C laminae.
59 geniculate nucleus (the C laminae and medial interlaminar nucleus).
60 geniculate nucleus (the C laminae and medial interlaminar nucleus).
61 ject more heavily to the C layers and medial interlaminar nucleus.
62 gnated the parvocellular, magnocellular, and interlaminar pathways.
63 ed recently that theta to high-gamma PAC and interlaminar phase coherence at theta frequencies can be
64 pressed only by neurons in the S laminae and interlaminar plexuses of the dorsal lateral geniculate n
65 ed by neurons in principal and S laminae and interlaminar plexuses.
66 y all neurons in principal and S laminae and interlaminar plexuses.
67                                 Feed-forward interlaminar population correlations were stronger on hi
68 , two subdivisions of the claustrum, and the interlaminar portions of the lateral geniculate nucleus,
69                           This suggests that interlaminar prefrontal cortical microcircuits are playi
70 e from cortico-cortical interactions between interlaminar prefrontal cortical microcircuits, whereas
71 rtex possess a soma in layer I and extend an interlaminar process that runs perpendicular to the pia
72                               We showed that interlaminar processes contact neurons, pia, and capilla
73    We described two distinct cell types with interlaminar processes that have been referred to as ILA
74 red or stereotypical spatial organization of interlaminar relations in neuronal activity distribution
75                     Detailed organization of interlaminar relations in neuronal activity underlying r
76 ory recall, changes in strength of analogous interlaminar relations occurred largely in parallel but
77 ibits staggered cut distributions, while the interlaminar shear mitigates the cut-induced mechanical
78             A similar trend was observed for interlaminar shear strength (ILSS) testing.
79 d disorganized patches with no corresponding interlaminar spaces in the LGN.
80                                         Both interlaminar spike and field correlations revealed a seq
81 cial SC evoked a pattern of intralaminar and interlaminar spread that was distinct from the spread ev
82 h the nanotube forests providing much-needed interlaminar strength and toughness under various loadin
83 ing co-localization of RCL1 with the layer 1 interlaminar subclass of astrocytes found exclusively in
84 ocortex, hippocampus, striatum, midline, and interlaminar thalamic nuclei, hypothalamus, brainstem, P
85  were instead strongly excited by descending interlaminar (vertical) input from layer 2/3 pyramidal n
86 ratification according to type of injection (interlaminar vs. transforaminal) likewise showed no sign
87                Our results indicate that the interlaminar zone in between laminae A and A1 and A1 and
88 hout the PGN and are concentrated within the interlaminar zones (IZs) of the dLGN, regions distinguis
89 aminae, and denser staining was found in the interlaminar zones and the C laminae.
90                                          The interlaminar zones contained RFd cells, RFb cells, or bo
91 leus (LGNd) contains interneurons within the interlaminar zones situated between the laminae correspo
92 bsent in the PGN and sparsely present in the interlaminar zones, but were numerous in the A and C lam