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1 upper layer and detergent-rich phase at the lower layer).
2 layer interface before penetrating into the lower layer.
3 rs: a bell-shaped upper layer and a straight lower layer.
4 ontain high-altitude clouds that obscure its lower layers.
5 iobacillus-related OTUs were detected in the lower layers.
6 upper-layer neurons drives output neurons in lower layers.
7 preserving fine-grained local details in the lower layers.
8 tissue into molecularly dissimilar upper and lower layers.
9 ey have mirror-imaged waveforms in upper and lower layers.
13 In contrast, m2 reactivity was densest in lower layer 4C and in 4A; the latter exhibited a honeyco
15 ells have either (1) dendrites restricted to lower layer 4Calpha and axons specifically targeting lay
19 erentially photobleach fluorescence from the lower layers and allow straightforward observation of de
20 d fibers is not prematurely triggered in the lower layers and is restricted to the upper layers, wher
21 der the streak) have distinct origins in the lower layer, and goosecoid expression distinguishes betw
22 nocomposite is designed, where the upper and lower layers are filled with parallel nanosheets and the
24 e (17)O depletion fluctuates in magnitude in lower layers but is persistently absent up section, prov
25 used a relative reduction of upper layer vs. lower layer cortical neurons, indicating that persistent
28 ontier orbital distribution on the upper and lower layers, facilitating a robust interlayer carrier t
32 crease of synaptic current sinks in layer IV/lower layer II/III at P3-P5 and in the cortical plate/up
34 e bulk of MGV axon terminals are in layer IV/lower layer III with minor projections to supragranular
35 To reevaluate the role of the hypoblast/ADE (lower layer) in patterning the chick ectoderm, we used r
38 tissue replacement), that the hypoblast/ADE (lower layer) is required and sufficient for patterning a
40 We quantified upper-layer (layers II-IV) and lower-layer (layers V-VI) neuron numbers per unit of cor
43 and this phenomenon and the circuit roles of lower layer neocortical interneurones, we combined two-p
44 ons in a defined temporal sequence, in which lower-layer neurons are formed before upper-layer neuron
45 rdrop-shaped cells that rely on Tmc2a, and a lower layer of gourd-shaped cells that rely on Tmc1/2b.
49 Continued expression of NR1-C1 in upper and lower layers of the adult cortex and in CA1 of the hippo
52 not normally include cells derived from the lower layers of the squamous mucosa, the detection of te
54 ctures: (i) von Karman vortex streets in the lower layers of vegetated canopies, (ii) Kelvin-Helmholt
55 iltration of the digested fragments into the lower layer produces a measurable change in optical refl
57 thin and across cortical areas, whereas many lower-layer pyramidal neurons (i.e., layers V-VI) favor
61 e converted to the geographic hierarchy unit Lower Layer Super Output Area (LSOA) level for analysis.
62 ed for different inhaler drugs in England at Lower Layer Super Output Area or 'neighbourhood' level.
63 ange in the distribution of melanin from the lower layer upwards to the middle layer of the skin, whi
66 upper layers (II/III), but enriched only in lower layers (V/VI) of mouse, were cross-correlated to i
68 gory-general learning effects emerged in the lower layers, whereas category-specific improvements eme
69 to inhibit premature TJ complex formation in lower layers while promoting increased tension and TJ st
70 g such RBIs (or RBIs dissected to remove the lower layer with or without tissue replacement), that th