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1 with a temperature-sensitive hydrogel as the middle layer.
2 dium or in explants from the superficial and middle layers.
3 om the deepest and most superficial, but not middle layers.
4 pses onto dendritic spines were found in the middle layers.
5 ayers 3 and 4), it was demonstrated that the middle layers (2 and 3) had the greatest ventilation-ind
6 rounded by concentric monolayers of tapetal, middle layer and endothecial cells.
7 in the VNO: the Gi alpha 2-ir neurons in the middle layer and the G(o alpha)-ir neurons in the deep l
8 nd E79 to eliminate neurons destined for the middle layers; and between E33 and E40 to delete neurons
9 anding the retina is that the neurons in its middle layers are varied in type and relatively inaccess
10 em (subperineurial glia, peripheral glia), a middle layer associated with neuronal somata in the cort
11 s, and crack bridging in the shell's tougher middle layers at higher loads.
12       The efficient charge separation in the middle layer, based on Volta's electrophorus, results fr
13 CSP axons from S2 and M1 partly converged on middle layers, but S2-CSP axons extended further dorsall
14 acks tapetal cells, and abnormally maintains middle layer cells.
15  nor haloperidol-treated monkeys exhibited a middle-layer density of parvalbumin-immunoreactive varic
16 a 46, only 12% of the PV-IR terminals in the middle layers formed type I synapses.
17 comprised of modulators (TSGs and OCGs), the middle layer included TFs, and the bottom layer containe
18  are filled with parallel nanosheets and the middle layer is filled with vertical nanofibers.
19                        The fold of inner and middle layers is conserved between T6SS and phage sheath
20                          In contrast, in the middle layers (layers 3b-4), 52% of the PV-IR axon termi
21 ayers, an outer layer made of VP2 and VP5, a middle layer made of VP7, and inner layer made of VP3 th
22                              However, in the middle layers, mean varicosity density was significantly
23 eurons with their cell bodies located in the middle layer (middle 1/3) of the vomeronasal sensory epi
24  can only confirm this for the origin of the middle layer (ml) and tapetum, while young anther develo
25                                  By contrast middle layer molecules remain entangled with capsule lay
26 tallic catalytic site has been buried in the middle layer of a triple-layer complex.
27 g top layer of approximately 20 angstroms, a middle layer of approximately 30 angstroms, and a more d
28  basal layer of two or more alpha-helices, a middle layer of beta-pleated sheet and a top layer forme
29 r of clean ice less than 350 km thick, and a middle layer of mixed rock and ice.
30 , a subpopulation of receptor neurons in the middle layer of the sensory epithelium was immunostained
31  melanin from the lower layer upwards to the middle layer of the skin, which was more dramatic in the
32             The Gi alpha 2-ir neurons in the middle layer of the VNO project to the anterior part of
33 he CB-immunoreactive receptor neurons in the middle layer of the VNO sensory epithelium and CB-immuno
34 tonotopic maps of best frequency (BF) in the middle layers of AI and the anterior auditory field as w
35 ith multiunit microelectrode recordings from middle layers of cortex.
36 y demonstrated a reversal of polarity in the middle layers of entorhinal cortex, whereas ripple oscil
37 nals) were determined in the superficial and middle layers of prefrontal cortex area 9 from 20 matche
38 udying core thalamic systems that project to middle layers of primary sensory cortices.
39                   Cholinergic markers in the middle layers of rat auditory cortex are transiently upr
40 ons were concentrated in the superficial and middle layers of striate cortex, consistent with the kno
41 ny stellate population is encountered in the middle layers of the auditory cortex.
42 ity of PBMCs were localized to the basal and middle layers of the biofilm.
43 rom which to record and labeled cells in the middle layers of the cat auditory and visual cortices to
44 ject in a topographically ordered fashion to middle layers of the cortex in an area-specific manner.
45 alamic nuclei extends across superficial and middle layers of the human DLPFC.
46 sent a novel variant of AMN that affects the middle layers of the macula above the OPL as diagnosed w
47 n a marker of thalamic axon terminals in the middle layers of the prefrontal cortex, the primary zone
48  characteristic SD-OCT lesions involving the middle layers of the retina at the level of the INL.
49 ve spectral-domain OCT lesions involving the middle layers of the retina at the level of the inner nu
50 on of changes in neuronal populations in the middle layers of the retina can be difficult with conven
51 e axons was unchanged in the superficial and middle layers of the schizophrenic subjects but was redu
52 lication labeled dense fiber terminations in middle layers of these same secondary areas in the prima
53  wavelength and color signals project to the middle layers of V1.
54                             The tegument, or middle layer, of herpesviruses comprises both viral and
55 re fields, tonotopy was degraded outside the middle layers or when LFP signals were substituted for u
56 ieces were aligned with through-holes in the middle layer, resulting in microchannels that cross one
57 ial derivative cells and lacks a tapetum and middle layer, resulting in moderate transcriptional devi
58 TENG and direct electrical connection of the middle layer to the earth.
59 immunoreactive puncta in the superficial and middle layers was extremely low in the newborn animals,
60  cartilage explants from the superficial and middle layers were analyzed immediately or after incubat
61 pha-treated samples from the superficial and middle layers were lower after 3 weeks of culture, but n
62 ponsive to chromatic stimuli; those found in middle layers were more strongly selective for motion di

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