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 The polynomial order P = 2 (third order accurate) was found to closely match the Dir

8 ales, and multiple teams also work together (third-order alliances).

9 is dependent upon being well connected with third-order allies, independently of the effect of their

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

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

12 ived control-oriented linearized model is of third order and relates small deviations of the stator v

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

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

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

16 ameter of feed arteries, first-, second- and third-order arterioles supplying the GM using intravital

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

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

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

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

21 improves upon the nonsparse case, where the third-order autocorrelation is required for uniformly or

22 d second-order) and between-group alliances (third-order), based on cooperation between two or more s

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

24 Both methods give very similar third-order Birch-Murnaghan equations of state with bulk

25 imentally demonstrated solving a small-scale third-order Boolean satisfiability problem based on inte

26 ighlight the nuanced behaviors of second and third-order branch points by winding around embedded EPs

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

28 to clearly visualize the vasculature beyond third-order branches of the hepatic and portal veins.

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

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

31 Third-order bronchi from autografted or allografted lung

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

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

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

35 iors, marsh edges, first-order channels, and third-order channels, can result in spatial variation in

36 Our OPO device, based on the third-order (chi((3))) nonlinearity in a silicon nitride

37 The second- (chi(H(2)O)((2))) and third-order (chi(H(2)O)((3))) optical susceptibilities o

38 ng Mott transition dynamics-form a nanoscale third-order circuit element.

39 almologic subfields, questions of second and third order cognitive complexity, and on image-based que

40 element theoretically requires a minimum of third-order complexity (for example, three dynamical ele

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

42 Such analyses allowed exploration of third-order constructs.

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

44 se models may be good in terms of predicting third-order correlations and the probability of multiple

45 extent to which the pairwise model predicts third-order correlations, and (3) its ability to predict

46 ot observed for pairwise nor for higher than third-order correlations.

47 4A inhibitor, attenuated the constriction of third-order cremasteric arterioles in response to elevat

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

49 cific role for proper elaboration of higher, third-order dendrites both in male and in female mice.

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

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

52 The results show that applying positive third order dispersion values to short pulses is favoura

53 acoustoelasticity formulation to obtain the third order elastic coefficient, referred to as nonlinea

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

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

56 nd no previous demonstration of any isolated third-order element(6-8).

57 emonstrate simple transistorless networks of third-order elements that perform Boolean operations and

58 cal properties of a parametrically encircled third-order EP (EP3), emerging from two connected second

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

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

61 Third-order esophageal neurons were identified in the in

62 ral substrates for first-order (Fourier) and third-order (feature-tracking) motion perception.

63 orionic arteries from FGR pregnancies and in third-order femoral arteries from hypoxic chicken embryo

64 expression and H(2)S production and enhanced third-order femoral artery dilator responses to the H(2)

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

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

67 We focused on a subset of third-order glutamatergic lateral horn neurons (LHNs) an

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

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

70 The dynamics induced by second- and third-order harmonics resemble smooth stretchings and tr

71 able to access a reaction mechanism that is third order in surface-hole density, which is assigned t

72 ion loss of 3.2 dB to 5.1 dB and out-of-band third order input intercept point greater than 41 dBm ar

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

74 Second and third order interactions of these features pose a substa

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

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

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

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

79 10) or dispersion-engineered resonators with third-order Kerr nonlinearity(11).

80 monstrate an analogous mechanism and overall third-order kinetics, due to similar complexation from a

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

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

83 ted division schedule of 3D (relative to the third-order macromeres of the A, B and C quadrants).

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

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

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

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

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

89 aphy was used to assess vascular function in third-order mesenteric arteries.

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

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

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

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

94 A linear third-order model performs better, but only non-linear m

95 accounting for data heterogeneity, show that third-order modulational instabilities do not significan

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 argely segregated by taste modality, whereas third-order neurons have more projections outside the SE

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

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

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

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

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

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

121 ygrosensory systems and an initial survey of third-order neurons that could directly modulate behavio

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

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

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

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

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

127 grate into the 25 um deep wells, leaving the third-order neurons, such as amacrine and ganglion cells

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

129 ll first, second and lateral horn-associated third-order neurons.

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

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

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

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

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

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

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

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

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

139 order harmonic generation and extremely high third-order nonlinear optical properties in MTPs suggest

140 Third-order nonlinear optical susceptibility chi((3)) of

141 BP exhibits a high third-order nonlinear susceptibility ([Formula: see text

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

143 response is further analyzed to retrieve the third-order nonlinear susceptibility for franckeite crys

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

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

146 Furthermore, the third-order nonlinear susceptibility of gerstleyite crys

147 Additionally, the third-order nonlinear susceptibility of gillulyite cryst

148 Furthermore, the third-order nonlinear susceptibility of teallite crystal

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

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

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

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

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

154 e-locking inside microresonators with either third-order nonlinearity(10) or with semiconductor gain(

155 ed extensive activation in regions up to the third order of axonal projections following optogenetic

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

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

158 nd these v-PNs synapse upon separate sets of third order olfactory neurons.

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

160 We studied this problem in Kenyon cells, the third-order olfactory neurons in the fruit fly Drosophil

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

162 tory inputs and memory-related feedback onto third-order olfactory neurons.

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

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

165 silicon-based photonic circuits utilize the third-order optical nonlinearity, but an analogous integ

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

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

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

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

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

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

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

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

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

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

176 Third-order polynomials provided excellent fits (signifi

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

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

179 Labeled third-order premotor neurons were immunoreactive for glu

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

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

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

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

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

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

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

187 The third-order rate constant for the demetalation of chloro

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

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

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

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

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

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

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

195 ylpiperazine showed the reaction to follow a third-order rate law with a second-order dependence upon

196 ylpiperazine showed the reaction to follow a third-order rate law with a second-order dependence upon

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

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

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

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

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

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

203 modulational instabilities are ineffective, third-order resonances negligible and the largest waves

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

205 t agreement with numerical evaluation of the third-order response of the XXZ spin chain.

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

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

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

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

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

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

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

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

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

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

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

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

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

219 Deformation Theory (FSDT), and Reddy (R) or Third-order Shear Deformation Theory (TSDT).

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

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

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

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

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

225 coherent regime, despite the large nonlinear third-order susceptibility of graphene, has so far prove

226 One of such complexes exhibits a very large third-order susceptibility over 10(-10) esu with low non

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

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

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

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

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

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

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

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

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

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

237 Five third-order themes emerged for survivors: 1) increased d

238 We first prove that third-order (triple) correlation describes network activ

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

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

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

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

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