ライフサイエンスコーパス: third-order

1 ries (FA) and first- (1A), second- (2A), and third-order (3A) arterioles using intravital microscopy.

2 First- (1A), second- (2A) and third-order (3A) MAs of pentobarbital-anaesthetized Youn

3 alpha2ARs predominate in distal arterioles (third-order, 3A).

4 iameter, and change in total RMS (P = .019), third-order aberrations (P = .007), and fourth-order abe

5 ocular and corneal total HOAs, particularly third-order aberrations, significantly increased over th

6 ring autoregressive nonlinearities up to the third-order according to the Wiener-Volterra representat

7 Both receptors also localized to third-order amacrine and ganglion cells and their proces

8 alysis is described and demonstrated through third-order analysis of a deisotoped high-resolution mas

9 The formation process was third-order and relatively insensitive to temperature at

10 ence on Co(2+) and inverse orders on proton (third order) and proton acceptor, methylphosphonate (fir

11 for 65s) were evaluated in first, second and third order arterioles and in feed arteries.

12 the square of the number of loci and that of third order as the cube and so on.

13 tivity at least by E14 and are able to drive third-order auditory brainstem neurons by E17.

14 he tonotopic organization of the second- and third-order auditory neurons in nucleus magnocellularis

15 NA), and nucleus laminaris (NL), second- and third-order auditory neurons in the avian brainstem, rec

16 ndependently scored all first-, second-, and third-order biliary branches with a four-point scale fro

17 ked increase in spine density on second- and third-order branches in young adult rats, lesions failed

18 r than the tonic branches in the second- and third-order branches.

19 ) of second-order branching, and 10 (50%) of third-order branching; 17 (85%) in superior mesenteric v

20 Third-order bronchi from autografted or allografted lung

21 Across a third-order catchment in Salt Lake City, Utah, we asked

22 We examined a third-order catchment that transitions from an undisturb

23 ted, and signaling from rod bipolar cells to third order cells was altered.

24 ons offered by the original researchers) and third-order constructs (development of new interpretatio

25 Such analyses allowed exploration of third-order constructs.

26 er distribution, we evaluate the second- and third-order correlation functions, and characterize a mu

27 4A inhibitor, attenuated the constriction of third-order cremasteric arterioles in response to elevat

28 oments which is equivalent to taking a novel third-order cumulant approximation.

29 and proximal and distal, but not second- and third-order, dendrites.

30 etics are observed for [decene] as well as a third order dependence on [water].

31 to a Young's modulus of E = 1.0 terapascals, third-order elastic stiffness of D = -2.0 terapascals, a

32 ress-strain response, and yields second- and third-order elastic stiffnesses of 340 newtons per meter

33 transsynaptic tracer, in anesthetized rats, third-order esophageal neurons (neurons projecting to pr

34 synaptic and retrograde fluorescent tracing, third-order esophageal neurons projecting to pharyngeal

35 Third-order esophageal neurons were identified in the in

36 ith respect to cis-trans isomerization and a third-order folding reaction from competent monomer to t

37 Count-versus-time curves were fit to third-order Fourier series for each LV subvolume to comp

38 xes, NADH supply and glycolysis, and strong (third-order) glycolytic inhibition by protons was requir

39 higher selectivity among habitat types (i.e. third-order habitat selection).

40 entire four dimensional (4D) data sets from third-order instrumentation data.

41 group behavior, but that models that include third-order interactions give a very accurate descriptio

42 We search for third-order interactions, discovering an interaction tha

43 Amacrine cells (ACs) are third-order interneurons in the retina that mediate anta

44 longest interval; the length of the shortest third-order interval; and a composite test.

45 centrations, the folding can be described by third-order kinetics, suggesting nucleation is rate-limi

46 a point of rotation at the jaw joint using a third-order lever mechanism.

47 inary data showed that 90% of bronchi (up to third order) measureable on multiplanar CT reformations

48 at low accumulated hole density to a faster, third order mechanism once the surface hole density is s

49 The perception of motion standstill when the third-order mechanism is nullified indicates that there

50 tants in acetone/water are consistent with a third-order mechanism, and rates and products in ethanol

51 can be explained quantitatively by competing third-order mechanisms in which one molecule of solvent

52 and aortae, and flow-mediated dilatations in third-order mesenteric resistance arteries were improved

53 -myocardial infarction, the myogenic tone of third-order mesenteric resistance vessels is increased,

54 l categories (shape and first-, second-, and third-order metrics).

55 obtained through simulation of a second and third order model, and suggest, for instance, that if th

56 agreement with the true distributions up to third-order moments, but with systematically heavier tai

57 computed entirely in the dorsal stream, and third-order motion may involve two computational process

58 rder motion process and the other by using a third-order motion process.

59 Observers who used third-order motion processing experienced interference w

60 mechanisms within a color pathway but by the third-order motion system at a brain level where binocul

61 The third-order motion system fails when the green/red satur

62 mbination exceeds that of the salience-based third-order motion system in a spatiotemporal frequency

63 minant color motion is perceived only by the third-order motion system, and they have profound implic

64 ate that chromatic motion is detected by the third-order motion system.

65 ition and a more severe interference in dual third-order motion tasks.

66 eir modulatory actions on L-glutamate-evoked third order neuronal firing.

67 tribute to the receptive field properties of third order neurones.

68 ilar time course were observed in second and third order neurones.

69 and synaptic activity of second and perhaps third order neurons.

70 uronal transport of the lectin to second and third order neurons.

71 ssion, and the connections from glomeruli to third-order neurons (neurons in the olfactory cortex of

72 We also examine third-order neurons and local neurons that likely modula

73 redicted connectivity rate from glomeruli to third-order neurons can be tested experimentally.

74 PN signals and enhance their transmission to third-order neurons in a mechanism akin to stochastic re

75 re AMPA receptors on the first-, second- and third-order neurons in the chick ascending auditory path

76 signals from rod and cone photoreceptors to third-order neurons in the inner retina and the brain.

77 peptide receptor antagonists at the level of third-order neurons in the migraine pathway, showing tha

78 second-order dorsal horn neurons project to third-order neurons in the ventrobasal complex of the th

79 d NTS is due to activation of second- and/or third-order neurons of a renal sympathetic afferent path

80 Selective masculinization of third-order neurons transforms their morphology and pher

81 and cones interconnect--retinal second- and third-order neurons underwent dramatic modification, inc

82 ots on days 4 and 5 p.i., and to second- and third-order neurons within sensory regions of the spinal

83 l signals from photoreceptors to second- and third-order neurons, but VGLUT1 is not necessary for int

84 Second- and third-order neurons, including bipolar, horizontal, amac

85 ribution of NMDA and KA/AMPA receptors among third-order neurons.

86 to repulsive odors comprised exclusively of third-order neurons.

87 , and can delineate output connectivity with third-order neurons.

88 neurons activated and eventually sensitized third-order neurons; this sensitization can mediate the

89 les in dilute solutions for potential use in third-order NLO applications.

90 ention thanks to their ability to show large third-order nonlinear effects at moderate power levels a

91 However, the lack of a suitable third-order nonlinear material greatly hinders the devel

92 t-day methods for probing the performance of third-order nonlinear optical (NLO) materials fail to me

93 ltimate speeds can be obtained by exploiting third-order nonlinear optical light-matter interactions

94 rs a strategy for designing high-performance third-order nonlinear optical media.

95 e system suggested here also possess a giant third-order nonlinear susceptibility and may be used to

96 The third-order nonlinear susceptibility of BP has been simp

97 harmonic generation (THG) with an estimated third-order nonlinear susceptibility of chi((3)) = ~3 x

98 ng applications require materials with large third-order nonlinearities and low nonlinear optical los

99 Here, Saouma et al. study the enhancement of third-order nonlinearities in two-dimensional lead iodid

100 arotene, which itself has one of the largest third-order nonlinearities known.

101 Here we report the observation of ultrahigh third-order nonlinearity about 0.45 cm(2)/GW in graphene

102 Z-scan measurements revealed a high third-order nonlinearity with n2 exceeding 10(-9) at a w

103 numerous molecules that function within the third order olfactory neurons for normal olfactory learn

104 he odorant receptive fields of second and/or third order olfactory neurons, and by increases in the c

105 physiology, we now show that two clusters of third-order olfactory neurons have dimorphic pheromone r

106 These are particularly enriched in third-order olfactory neurons of the lateral horn, where

107 e of the metamaterial in terms of a standard third order optical nonlinearity: this shows a clear inv

108 iffraction is due to the ultrafast and large third-order optical nonlinearity of BP.

109 Here, we show that the third-order optical nonlinearity, n 2, of hybrid lead io

110 originates from the interaction between the third-order optical susceptibility of the semiconductor

111 Linux for applying zeroth, first, second and third order partial correlation analysis can be download

112 ed by proton transfer to 1, either directly (third-order pathway) or via anion-assisted proton transf

113 How are second-order (texture-defined) and third-order (pattern-tracking) motions processed in our

114 that involves enhancing the real part of the third-order polarizability (gamma) of cyanine-like molec

115 can then be realized (imaginary part of the third-order polarizability approximately 2.6 x 10(5) x 1

116 th negative real components Re(gamma) of the third-order polarizability, which leads to nonlinear ref

117 We applied a sigmoid function or third order polynomial to the curves and determined the

118 models each ion chromatogram baseline with a third-order polynomial.

119 Coordinate data (x,y) of shapes were fit to third-order polynomials for two sessions, sides, and met

120 Third-order polynomials provided excellent fits (signifi

121 tation of this approach is based on building third-order polynomials which are used to interpolate re

122 At 4.5 d, labeled third-order premotor neurons were found in the pons, mid

123 Labeled third-order premotor neurons were immunoreactive for glu

124 oposed, which is generally applicable to any third-order process in plasmonic nanostructures.

125 An AlN/3C-SiC composite layer enables the third-order quasi-symmetric (QS(3)) Lamb wave mode with

126 This Tafel slope together with an inverse third order rate dependence on H(+) activity establishes

127 lved: (I) dinuclear OAT following an overall third order rate law (N2O); (II) formation of stable oxi

128 ce on catalyst concentration with an overall third-order rate constant (k) of 184 +/- 2 M(-2) s(-1).

129 nion group is expressed as a decrease in the third-order rate constant for activation by phosphite di

130 (I172A) and 25-fold increase (L232A) in the third-order rate constant for phosphite dianion (HPO(3)(

131 ing conformational change that depresses the third-order rate constant for the phosphite-activated re

132 3)C]-GA) in D(2)O, a 25-fold increase in the third-order rate constant for the reaction of the substr

133 The temperature dependence of the third-order rate constant indicates a negative activatio

134 r in cobalt and first order in hydrogen; the third-order rate constant is 106(3) M(-2).s(-1).

135 lO2 decay is a base-assisted reaction with a third-order rate constant of 1.5 x 10(6) M(-2) s(-1) in

136 e TIM-catalyzed isomerization of GAP and the third-order rate constant of 150 M(-2) s(-1) for activat

137 Kinetic analysis indicates a third-order rate law (second order in [1H(H)] and first

138 the corresponding phosphine oxide follows a third-order rate law, first-order in [phosphine] and sec

139 curring under both conditions, with the same third-order rate law, similar selectivity, and the deriv

140 hile the refolding represents a single-stage third-order reaction.

141 le helix is best described by an all-or-none third-order reaction.

142 scatter plots of the data were created, and third-order regression lines were calculated.

143 The thalamus contains third-order relay neurons of the trigeminal system, and

144 Furthermore, the third-order response includes a remarkably low two-photo

145 ession of neuronal remodeling of second- and third-order retinal cells and their synaptic terminals i

146 e rules not only uncover mechanisms by which third-order retinal cells integrate and compute bipolar

147 ikely to be generated by graded responses of third-order retinal cells, most likely amacrine cells.

148 at labeled glial cells, first-, second-, and third-order retinal neurons and processed for confocal m

149 lash electroretinogram (ERG) via activity of third-order retinal neurons, i.e. amacrine and ganglion

150 otoreceptor cell death but spare second- and third-order retinal neurons.

151 activity of hyperpolarizing second- and all third-order retinal neurons; and TTX (tetrodotoxin, 6 mu

152 e 4 m deep HR-MLWs in the riparian zone of a third-order river and analyzed for hydrochemical paramet

153 corneal aberration coefficients, second- and third-order root mean squares of coefficients were the b

154 Among the PZA coefficients, second- and third-order root mean squares of PZA coefficients were t

155 Thus, we propose the use of higher (third order) sample moments to resolve this identifiabil

156 Current analysis methods for third-order separation data use only user-defined subset

157 procedure applied to entire 4D data sets of third-order separation data, which, in this case, is com

158 es followed both second-order (variance) and third-order (skewness) stochastic dominance.

159 They were second or third order, small tributaries of the superior or inferi

160 st-firing neurones tested, first, second and third order spikes in a burst could be made to collide w

161 rporates the indirect effect of non-Gaussian third-order statistics for the unperturbed system in a s

162 We find that the product of the third-order susceptibility and the interfacial potential

163 um tin oxide nanoparticle, with an effective third-order susceptibility up to 3.5 x 10(3) nm V(-2) an

164 ns in arterial diameter) were simulated by a third-order system of nonlinear differential equations.

165 of diagnoses and prescriptions in EHRs as a third-order tensor, and decomposed it using the CP algor

166 and times, they are naturally expressed as a third-order tensor.

167 gher-order Zernike terms, especially for the third-order terms (> 0.21 mum).

168 The ICCs for third-order terms also were high (ICCs, > 0.87); however

169 Third-order terms and Z(4)(0) are repeatable, but not as

170 nd-order spinal cord dorsal horn neurons and third-order thalamic neurons along the pain pathway afte

171 ivity of second order trigemontothalamic and third order thalamocortical neurons in rats.

172 ed the spontaneous and evoked firing rate of third order thalamocortical projection neurons, but not

173 e-specific pathway for courtship hearing via third-order ventrolateral protocerebrum Projection Neuro

174 h-order tetrafoil in myopic-PRK corneas, and third-order vertical coma and fourth-order astigmatism i

175 d sixth-order astigmatism in normal corneas, third-order vertical coma and fourth-order tetrafoil in

176 branching patterns of parental, second-, and third-order vessels leading to circumscribed terminal va

177 iously been found to vary between second and third order with respect to scaffolding protein concentr