ライフサイエンスコーパス: lower layer

1 upper layer and detergent-rich phase at the lower layer).

2 layer interface before penetrating into the lower layer.

3 iobacillus-related OTUs were detected in the lower layers.

4 upper-layer neurons drives output neurons in lower layers.

5 ontain high-altitude clouds that obscure its lower layers.

6 Furthermore, in a novel pattern, lower layer 2/3 preferentially excited interneurons in o

7 ue-ON' afferents were found in 4A as well as lower layer 2/3.

8 d 5; and bitufted/multipolar CB+ neurones in lower layer 3.

9 In contrast, m2 reactivity was densest in lower layer 4C and in 4A; the latter exhibited a honeyco

10 s were encountered only in deeper cortex, in lower layer 4C.

11 ells have either (1) dendrites restricted to lower layer 4Calpha and axons specifically targeting lay

12 Other neurons in lower layer 4Calpha provide M input to interblobs.

13 d had a peak distribution located in mid- to lower layer 5 in each area.

14 a transparent hydrogel consisting of a stiff lower layer and a compliant upper layer.

15 erentially photobleach fluorescence from the lower layers and allow straightforward observation of de

16 d fibers is not prematurely triggered in the lower layers and is restricted to the upper layers, wher

17 der the streak) have distinct origins in the lower layer, and goosecoid expression distinguishes betw

18 nocomposite is designed, where the upper and lower layers are filled with parallel nanosheets and the

19 e (17)O depletion fluctuates in magnitude in lower layers but is persistently absent up section, prov

20 used a relative reduction of upper layer vs. lower layer cortical neurons, indicating that persistent

21 Hypoblast and endoblast (a second lower layer formed under the streak) have distinct origi

22 crease of synaptic current sinks in layer IV/lower layer II/III at P3-P5 and in the cortical plate/up

23 iding thalamocortical inputs to layer IV and lower layer III of auditory cortex.

24 e bulk of MGV axon terminals are in layer IV/lower layer III with minor projections to supragranular

25 To reevaluate the role of the hypoblast/ADE (lower layer) in patterning the chick ectoderm, we used r

26 id removes one graphene layer and leaves the lower layers intact.

27 tissue replacement), that the hypoblast/ADE (lower layer) is required and sufficient for patterning a

28 We quantified upper-layer (layers II-IV) and lower-layer (layers V-VI) neuron numbers per unit of cor

29 If upper layers are cooler than lower layers, molecular gases will produce absorption fe

30 We previously found that lower layer neocortical interneurones can reach action p

31 and this phenomenon and the circuit roles of lower layer neocortical interneurones, we combined two-p

32 ons in a defined temporal sequence, in which lower-layer neurons are formed before upper-layer neuron

33 rons and in interneurons and was stronger in lower layers of auditory cortex.

34 exi, while Alphaproteobacteria dominated the lower layers of pustular mats.

35 Continued expression of NR1-C1 in upper and lower layers of the adult cortex and in CA1 of the hippo

36 e inhibitor in epidermal adhesion within the lower layers of the human epidermis.

37 not normally include cells derived from the lower layers of the squamous mucosa, the detection of te

38 ediate filaments to form macrofibrils in the lower layers of the stratum corneum.

39 iltration of the digested fragments into the lower layer produces a measurable change in optical refl

40 t and control burst generation of individual lower layer pyramidal neurones.

41 thin and across cortical areas, whereas many lower-layer pyramidal neurons (i.e., layers V-VI) favor

42 Heterotopic lower layer replacement operations strongly suggest that

43 , is independently specified by anteriormost lower layer signals at an early stage.

44 ange in the distribution of melanin from the lower layer upwards to the middle layer of the skin, whi

45 s were highest in layers III/IV or IV and in lower layer V.

46 (18-19 microm) and most commonly located in lower layer V.

47 upper layers (II/III), but enriched only in lower layers (V/VI) of mouse, were cross-correlated to i

48 Stromal cells were suspended in the lower layer, whereas cancer cells were suspended in the

49 to inhibit premature TJ complex formation in lower layers while promoting increased tension and TJ st

50 g such RBIs (or RBIs dissected to remove the lower layer with or without tissue replacement), that th

51 The lower layer, with smaller pore sizes ( approximately 6 n