ライフサイエンスコーパス: sublayer

1 ory weights onto pyramidal cells in the deep sublayer.

2 ly with the thickness of the aqueous viscous sublayer.

3 om passing ON bipolar cells axons in the OFF sublayer.

4 Raman microscopy was unable to visualize the sublayer.

5 uling propensity that occurs in the membrane sublayer.

6 nanoparticles fabricated on a thin metallic sublayer.

7 e between the nanoparticles and the metallic sublayer.

8 in the inner third of the IPL, within the ON sublayer.

9 ) monostratify at the outer limit of the OFF sublayer.

10 noble metal A and strongly correlated BO(2) sublayers.

11 drite growth and drives arbors into adjacent sublayers.

12 ect swarms consisting of several overlapping sublayers.

13 es that have strayed from the DS circuit IPL sublayers.

14 visual encoding within inner plexiform layer sublayers.

15 rbit coupling alternating between the cerium sublayers.

16 l retina and [Formula: see text] for retinal sublayers.

17 es, where it additionally forms two distinct sublayers.

18 ntified six physiological layers and further sublayers.

19 l cell types in the deep and superficial CA1 sublayers.

20 by non-DS neurons projecting to adjacent IPL sublayers.

21 sublayers and OFF-dominant responses in OFF sublayers.

22 elopment into eye-specific layers and ON/OFF sublayers.

23 al arbors that are highly specific for these sublayers.

24 a grinding tool recovered at Grotta Paglicci sublayer 23A [32,614 +/- 429 calibrated (cal) B.P.], Sou

25 g is observed between the surface (77)Se and sublayer (77)Se sites due to spin diffusion in the Cd(77

26 he feasibility of regenerating the tethering sublayer after binding was investigated.

27 eal that the UO(x) film is composed of three sublayers: an approximately 38 A thick layer of U(3)O(8)

28 lid electrolyte interphase, a porous Li(3)Bi sublayer and a solid binder (welding porous Li(3)Bi onto

29 the compaction of dense-selective layer and sublayer and helps to retain membrane performance during

30 The superior sublayer and medial division also stain strongly for GAB

31 ion each project to the SC/NOT; the superior sublayer and medial division of the PrGC are connected r

32 This increase was both sublayer and projection-class specific, restricted to co

33 presents a convenient platform for studying sublayer and temperature-dependent phenomena over indivi

34 ed Dm-DRA1 and Dm-DRA2) stratify in separate sublayers and exclusively contact polarization-sensitive

35 cking, orthogonal microcracking in laminated sublayers and geometrically corrugated junctions between

36 sponses, showing ON-dominant responses in ON sublayers and OFF-dominant responses in OFF sublayers.

37 weakens the Cu-Cu bonds between the top- and sublayer, and further stabilized at 1/3 ML when H adsorb

38 ally exact near-wall behavior in the viscous sublayer, and is consistent with the near balance of tur

39 as the epithelium, mucosa, cartilage and its sublayers, and glands at a resolution higher than any cl

40 chronological order from deep to superficial sublayers; and (3) whereas the average GCP proliferation

41 Carbons from these two alternating sublayers are exposed to different chemical environments

42 s intercalated between aliphatic hydrocarbon sublayers at or near room temperature.

43 Layer V has three sublayers based on the types of neuron and their sublami

44 nderneath the separation chamber-fluorescent sublayer-based visualization (FSV).

45 of the boundary layer (including the viscous sublayer, buffer layer, and logarithmic layer), recovers

46 terize the thicknesses of individual retinal sublayers by macular optical coherence tomography (OCT)

47 mpling techniques show how an adsorbed water sublayer can enhance NO(2) adsorption on calcite compare

48 Thus, CA1 pyramidal cells in adjacent sublayers can address their targets jointly or different

49 the UO(x)/substrate interface; the adjacent sublayer consists of an approximately 900 A thick single

50 chically structured composites in which each sublayer contributes a distinct function to yield a mech

51 ctions were selective for neurons in certain sublayers: corticospinal neurons in upper layer 5B and c

52 e was produced, consisting of a rough nickel sublayer covered by an outer, compact, smooth PTFE layer

53 in texture spatially confined within each Se-sublayer due to strong sublayer-localised electric dipol

54 The amorphization of the crystalline silicon sublayer during irradiation and/or heating can provide a

55 campus and assessed the relationship between sublayer dynamics and learning.

56 laminar distribution, but cortical layers or sublayers enriched for one isoform do not correlate with

57 ium-Bruch's membrane, with thinning in other sublayers, especially the outer nuclear layer (ONL) (p <

58 al symmetry of the quasicrystal is broken in sublayers, forming a random tiling of rectangles, large

59 ariably be controlled by the laminar viscous sublayer, grain roughness, form drag from bedforms, or t

60 ease in the density of very large neurons in sublayer Illc.

61 in local dielectric properties of the VO(2) sublayer in the course of the temperature-tuned insulato

62 ology-aware loss function to segment retinal sublayers in OCT images from patients with STGD1.

63 ons residing in the deep and superficial CA1 sublayers in rats.

64 inals in separate inner (ON) and outer (OFF) sublayers in response to light intensity increments and

65 lear layer and send their processes into two sublayers in sublaminae a and b of the inner plexiform l

66 nement of retinogeniculate axons into ON/OFF sublayers in the ferret lateral geniculate nucleus (LGN)

67 rsely, UNC5C misexpression within DS circuit sublayers inhibits dendrite growth and drives arbors int

68 phases that result exhibit biomacromolecular sublayers intercalated between aliphatic hydrocarbon sub

69 the overall spin-orbital texture for each Se sublayer is in strict adherence to time-reversal symmetr

70 se force that is confined within the viscous sublayer; it has its maximum at the wall and decays expo

71 xamined geniculocortical inputs to these two sublayers labeled by tracer or virus injections or an an

72 nfined within each Se-sublayer due to strong sublayer-localised electric dipoles orientated along the

73 The ON sublayer occupied 75% of the IPL thickness, including bo

74 layer characterized by a middle hydrophobic sublayer of 7-8 A with lower scattering length density a

75 to the deep, rather than to the superficial, sublayer of CA1.

76 st that the predilection of a extremely thin sublayer of inner Bruch's membrane for accumulating lipi

77 re Brn3a-immunoreactive neurons in the inner sublayer of layer 10.

78 al density in layer Cm, the minor in the top sublayer of layer A).

79 terial-specific temperatures within a turbid sublayer of poly(tetrafluoroethylene) (PTFE) through a h

80 Recently active neurons in the superficial sublayer of stratum pyramidale displayed larger post-syn

81 ed the problem by p-doping of the underlying sublayer of the bilayer HTLs.

82 radually coupling neurons in the superficial sublayer of the CA1 stratum pyramidale to whole-populati

83 on solid medium revealed a fragile sac-like sublayer of the exosporium basal layer, to which caps we

84 n line with the extended thickness of the ON sublayer of the inner plexiform layer in the microbat re

85 bottlebrush endings in the most superficial sublayer of the SGS.

86 rkably similar to those found in the viscous sublayer of turbulent wall-bounded flows.

87 and two almost symmetrical hydrophilic outer sublayers of 6-8 A with higher scattering length density

88 The superlattice consists of alternating sublayers of crystalline thiolate lamellae and chain-end

89 coding dynamics between deep and superficial sublayers of hippocampal CA1, suggesting how the hippoca

90 H2-Mv(-) VSNs reside in the lower and upper sublayers of the basal layer, respectively.

91 with axonal projections limited to specific sublayers of the cerebellar cortex.

92 Addressing individual sublayers of the deep entorhinal cortex in future experi

93 igment epithelium (INL-RPE) and the specific sublayers of the photoreceptor: inner nuclear layer-exte

94 ottlebrush endings arrayed within the middle sublayers of the SGS.

95 r lies in the lower part of sublamina a (OFF sublayer) of the inner plexiform layer where it costrati

96 s ramify broadly throughout sublamina a (OFF sublayer) of the inner plexiform layer.

97 ndary between sublaminae a and b (OFF and ON sublayers) of the inner plexiform layer, occupying the n

98 tial connectivity is established by neuronal sublayer positioning and actual connectivity in this fra

99 long-range axonal targets or their layer or sublayer positions, but by both, in specific combination

100 evolution reaction (POER), while the Mo-rich sublayer promotes charge transfer and enhances the oxida

101 onment, while their counterparts in the deep sublayer provide a more flexible representation that is

102 pe-specific chemogenetic silencing of either sublayer revealed independent geometric codes.

103 na includes the retinorecipient and superior sublayers, rostrally, and the medial division, caudally.

104 skinned FO membrane comprises a fully porous sublayer sandwiched between (i) a truly dense skin for s

105 od targets relatively unaffected regions for sublayer segmentation, ensuring accurate boundary deline

106 (-ir) was seen in all layers except area and sublayer specific bands in layer 4.

107 We find sublayer-specific arbor specializations within the inner

108 Despite shared topology, sublayer-specific manifolds displayed distinct geometric

109 ese observations indicate that at least some sublayer-specific projections emerge by elimination of e

110 However, the development of sublayer-specific projections was not always precise fro

111 quasi-two-dimensional systems with inherent sublayer stacking orders.

112 The retinorecipient sublayer stains most intensely for GABA and SP.

113 The sublayer streaks seem to be passive and are often simply

114 segmentation, and termination on the viscous sublayer streaks, and they coincide with local concentra

115 ach target, tSbC RGC axons occupy a specific sublayer, suggesting that they restrict their input to s

116 ateral LSO axonal bands that occupy adjacent sublayers supports the idea that the initial establishme

117 ks (MOFs) crystal growth via the assembly of sublayer surfaces and has important implications in unde

118 projections, and uncovers the structures of sublayer surfaces and their evolution to stable surfaces

119 The structural characterization of sublayer surfaces of MIL-101 is reported by low-dose sph

120 ay simulations is a growing saline diffusive sublayer that drives a time-dependent melt rate.

121 anoscale outer layer and a slower microscale sublayer that relax by different mechanisms.

122 tree shrew striate cortex, we identified two sublayers that differ in their intracortical and thalami

123 and allows objective measurements of corneal sublayer thickness and backscattering.

124 As the LaCoO3 sublayer thickness approaches its fundamental limit (i.e

125 When comparing the rate of retinal sublayer thickness change over time (mean follow-up 3.9

126 oreceptor outer segments). OCT-based retinal sublayer thickness measurements are feasible in STGD1 pa

127 e enables to form noninvasive images of thin sublayers through highly turbid overlayers.

128 layer, followed by a lateral motion of GeTe sublayer to the final, low energy structure.

129 In contrast, films without DIO exhibit three-sublayer vertical phase morphology with phase separation

130 Automated segmentation of retinal sublayers was performed with manual correction as needed

131 ctional partition of the IPL into ON and OFF sublayers was shown by using antibodies against vesicula

132 t CA1 place cells located in the superficial sublayer were more active in cue-poor environments and p

133 In contrast, place cells located in the deep sublayer were more active in cue-rich environments and u

134 alyses of the retina, choroid, and choroidal sublayers were performed, and associations with clinical

135 r occupies the upper part of sublamina b (ON sublayer), where it costratifies with ON alpha dendrites

136 ode surface and grow into the porous Li(3)Bi sublayer, which ameliorates pressure (stress) changes.

137 Se atoms sink to form a new Cu(2)Se sublayer, while the original subsurface Cu atoms are lif

138 ea catalysis, or bridged to form a networked sublayer with complimentary properties.

139 The Li(3)Bi sublayer with its high ionic/electronic conductivity rat

140 A combination of the neutral gold sublayer with the antimicrobial properties of silver nan

141 We find that the magnetopause has sublayers with thickness comparable to the ion scale.

142 rs and subsequently On-center and Off-center sublayers within the dorsal lateral geniculate nucleus (

143 eams in transverse slices were restricted to sublayers within the molecular layer, conducting slowly

144 argets and restrict their arbors to specific sublayers within these targets.