ライフサイエンスコーパス: nonuniform

1 ively), although criteria for diagnosis were nonuniform.

2 tissue, radiation exposures are often highly nonuniform.

3 le and, hence, the local current density, is nonuniform.

4 ukaryotic cells, the density of chromatin is nonuniform.

5 s, the three-dimensional EMD distribution is nonuniform.

6 he ENCODE regions and show that it is highly nonuniform.

7 and the chain density distribution might be nonuniform.

8 calculated to assess the biologic effects of nonuniform absorbed dose including the effects of the un

9 ulated to assess the biologic effects of the nonuniform absorbed dose, including the cold antibody ef

10 aqueous medium and subjected to a spatially nonuniform ac electric field are examined using a simple

11 ted, but the SES disparity was significantly nonuniform across neurocognitive systems.

12 t the DSB-resection machinery is complex, is nonuniform across the genome, and has built-in fail-safe

13 that acknowledges that the mutation rate is nonuniform across the genome.

14 latory neuron output can be stereotyped, yet nonuniform, across network regions.

15 mong individual cells, because of both their nonuniform activity and geometric environment, is an imp

16 Because nonuniform AD deposition by microspheres cannot be deter

17 a positive zeta-potential apparently due to nonuniform adsorption of NOM molecules leading to attrac

18 We assessed the effect of this 'nonuniform age bias' on observed growth trends and find

19 ial induced by the EEF is shown to be highly nonuniform along the cell perimeter and strongly depende

20 in which the interaction of RyR with CaM is nonuniform along the peptide, and the primary effect of

21 leading to slow formation of a structurally nonuniform amorphous precipitate.

22 onal "bulk" PCR often yields inefficient and nonuniform amplification of complex templates in DNA lib

23 ly distributed across the retina, leading to nonuniform analysis of specific visual features at certa

24 tions came from the chemical shift analysis, nonuniform and bell-shaped peak intensity profiles, and

25 This mapping revealed spatially nonuniform and clustered synaptic connectivity patterns.

26 g that antagonist dissociation proceeds in a nonuniform and cooperativity-driven manner, which disfav

27 he distribution of mast cell chymase appears nonuniform and disparate from ACE.

28 hat neurons in the parietal reach region use nonuniform and idiosyncratic frames of reference.

29 thick layers of salts undergo drying that is nonuniform and incomplete.

30 with rinsing off unbound probe, which can be nonuniform and inefficient in thick tissues, thus leadin

31 tentials along the ribosomal exit tunnel are nonuniform and negative.

32 stribution might be simultaneously spatially nonuniform and temporally unstable.

33 ofilin are mechanically heterogeneous (i.e., nonuniform) and display asymmetric shape deformations an

34 Peripherin labeling of outer segments was nonuniform, and EM showed discs arranged in whorllike st

35 particularly animal genomes, have a complex, nonuniform, and nonrandom internal compositional organiz

36 The observed global-warming rate has been nonuniform, and the cause of each episode of slowing in

37 ch two thirds (17/26) were scored as clearly nonuniform, and the majority (11/17) of these nonuniform

38 ubstrates, metabolite isotopologues revealed nonuniform assimilation throughout the metabolic network

39 harmaceuticals and chemotherapeutic drugs is nonuniform at the microscopic level.

40 background noise in systems with spectrally nonuniform background requires complex optimization of a

41 fluctuations, whereas loops show complex and nonuniform behavior.

42 The distribution of these proteins is nonuniform between the bulk sarcolemmal surface and memb

43 ion region in a sequential format produced a nonuniform binding profile in which the majority of the

44 ometric distortion of the embryo resulted in nonuniform blastoderm migration and realignment of the a

45 onuniform, and the majority (11/17) of these nonuniform BMs responded incompletely.

46 that grain borders, light fluctuations, and nonuniform brightness contribute to produce noisy images

47 ly(dimethoxysilane) sheet, which resulted in nonuniform buckling along the polymer surface.

48 Our results demonstrate highly nonuniform Ca2+ signaling among and within individual my

49 e reaction is highly specific, we found that nonuniform capture is a key issue that will need to be r

50 Similar nonuniform cDCS aftereffects on cortical excitability we

51 asma membrane becomes deeply convoluted, and nonuniform cell behaviors begin to emerge.

52 evation of intraocular pressure (IOP) causes nonuniform changes in RNFL reflectance across wavelength

53 spatially varying mobility is attributed to nonuniform charge arising from covalent attachment of am

54 ernal field, the high polarizability of this nonuniform charge system eventually generates the high-e

55 In AD subjects, slower and spatially nonuniform clearance from cortical regions was observed

56 on of metabolic current sinks, caused by the nonuniform collapse of mitochondrial inner membrane pote

57 ed to the synergistic effects of the spatial nonuniform collective quantum confinement of sp(2) domai

58 yancy effects due to the solution containing nonuniform concentrations of substrate and product.

59 Nonuniform conduction and fractionated electrograms were

60 vation breakthrough locations and regions of nonuniform conduction and fractionated electrograms.

61 ng and manipulating spatially inhomogeneous, nonuniform conductivity patterns across a flake of graph

62 additional broadening could result from the nonuniform conformation of bionanoparticles and from the

63 that the tetramer packing within a dyad was nonuniform containing a mix of checkerboard and side-by-

64 The model predicts highly nonuniform contraction with caps of collapsed sarcomeres

65 on these 2D crystals experience a spatially nonuniform Coulomb environment, whose effect on the char

66 nging, however, because MDA generates highly nonuniform coverage of the genome.

67 ted here that ECHO is capable of coping with nonuniform coverage.

68 dersampling particular alleles aggravated by nonuniform coverage; and consequently, (3) ambiguous ide

69 ted hexagonal phase, the lipid monolayer has nonuniform curvature, and cholesterol almost entirely co

70 mixture may redistribute under conditions of nonuniform curvature, such as in the stalk structure.

71 rmal heat generation and therefore spatially nonuniform deformation profiles that drive out-of-plane

72 mal force to the soft boundary, which causes nonuniform deformation.

73 We study the influence of this nonuniform density, which we derive from microscopic ima

74 efects in 2-D NM frameworks, which stem from nonuniform deposition of 2-D NM flakes during layer buil

75 pattern, suggesting spatially and temporally nonuniform developmental features of neural flexibility.

76 spatial network structure to generate highly nonuniform diffusion behavior even at the scale of citie

77 gainst the hydrogel surface yields spatially nonuniform dilution.

78 r trajectories of bacterial motion guided by nonuniform director, (ii) local melting of the liquid cr

79 d NF remained fixed over several months in a nonuniform distribution and exhibited exceptionally slow

80 Its nonuniform distribution between cells and tissues underl

81 eserts." Next, we examine how consistent the nonuniform distribution is between different transcripti

82 We show that nonuniform distribution of cellulose microfibrils and de

83 into and out of these membrane domains, the nonuniform distribution of ciliary membrane components,

84 Additionally, we observed a nonuniform distribution of de novo SVs across offspring.

85 On the basis of DiSLO200 images, significant nonuniform distribution of DR lesions was evident across

86 ma and in vitro HBV infection models shows a nonuniform distribution of HBV CD8(+) T cell epitopes th

87 ven signaling module that contributes to the nonuniform distribution of Kv4 expression, and hence Ito

88 Additionally, the nonuniform distribution of Li ions results in low utiliz

89 supported by the current PBRs is limited by nonuniform distribution of light as a result of self-sha

90 e MT filaments, that is a consequence of the nonuniform distribution of MAP tau proteins along the bu

91 oor accuracy and precision mainly due to the nonuniform distribution of matrix and analyte across the

92 ometric model of the surface remodeling with nonuniform distribution of molecules and a realistic dis

93 es showed that both the human and dogs had a nonuniform distribution of plutonium throughout the lung

94 ity of the glass may be compromised due to a nonuniform distribution of residual water and trehalose

95 first time in any virus-receptor complex the nonuniform distribution of RNA within the capsid.

96 g a substantial amount of missing data and a nonuniform distribution of sequence reads.

97 at the gray-white interface lead to a highly nonuniform distribution of stress in axons, which was mo

98 quantifies both the binding kinetics and the nonuniform distribution of these receptors with respect

99 Nonuniform distribution of tuning within populations of

100 Furthermore, our data unraveled a nonuniform distribution of VGLUT3 in synaptic vesicles.

101 th linked and unlinked sites and displayed a nonuniform distribution on the genetic map around the do

102 g ultralow concentrations of analytes with a nonuniform distribution on the sensor surface.

103 und residues within Steinkreuz soil HA and a nonuniform distribution within Elliott soil HA.

104 nd compared with the experimentally observed nonuniform distribution.

105 o the gene space, where they showed a highly nonuniform distribution.

106 arctic Circumpolar Current, with a spatially nonuniform distribution.

107 ations are believed to be the consequence of nonuniform distributions of activity among the cells or

108 The implications of nonuniform distributions of radioactivity for dosimetry,

109 rtion rate constant lead to the formation of nonuniform domains, and the composition dependence of th

110 ass microspheres could induce a sufficiently nonuniform dose distribution explaining this paradox.

111 Nonuniform dose distributions among disseminated tumor c

112 Evoked Ca(2+) release from the SR was nonuniform (dyssynchronous).

113 ring a train of spin echoes, especially with nonuniform echo spacing applied to complex molecules lik

114 hematical modeling of ECS diffusion required nonuniform ECS dimensions in deep brain, which we call "

115 ters of the mabs is useful in predicting the nonuniform effect of salt on the viscosity of mab soluti

116 To explore the dynamical effects of nonuniform elastic interactions, we calculate the robust

117 cofilin-decorated segments because of their nonuniform elasticity, thereby accelerating filament sev

118 motion of particles under the influence of a nonuniform electric field.

119 based dielectrophoresis (iDEP), the required nonuniform electric fields are generated with insulating

120 separation method via three-dimensional (3D) nonuniform electric fields generated by employing a peri

121 are two electrokinetic phenomena exploiting nonuniform electric fields to exert a force or torque on

122 lectrophoretic forces, in response to the 3D nonuniform electric fields.

123 ces on the opposite sidewalls to produce the nonuniform electric fields.

124 equire a high electrical field and provide a nonuniform electrical field distribution among randomly

125 tion of bacteria in suspensions with spatial nonuniform electrical fields so as to perform specific R

126 nc with an external electric field, creating nonuniform electroosmotic flow distributions.

127 y driven antibody probing stage, we observed nonuniform electrophoretic probe mobility along the chan

128 es and show how they arise from shifting and nonuniform enhancer definitions, and genome-era biases.

129 of solvation can resolve very differently in nonuniform environments than in bulk.

130 In nonuniform environments with position-dependent associat

131 the spaces between obstacles and corners in nonuniform environments.

132 and an ionic contrast agent, resulting in a nonuniform equilibrium partitioning of the ionic contras

133 ibutions across the cortex were consistently nonuniform, establishing between a 73-fold (slow trot) t

134 along the backbone of the substrate protein nonuniform even when the protein gets unfolded.

135 ical core composed of six rings, albeit in a nonuniform fashion, unlike in phenalenyl.

136 in density is distributed over the core in a nonuniform fashion.

137 e population distributions of the biases are nonuniform, featuring asymmetric peaks in the cardinal d

138 The regulation of the nonlinear spatially nonuniform fibrinolytic process in thrombolysis is not c

139 cuss forces acting on a spinner carried by a nonuniform flow and show how the forces confine spinners

140 mented numerically in a variety of unsteady, nonuniform flow configurations where it is shown to accu

141 imulations helped understanding the slightly nonuniform flow field and explained differences in the r

142 es that are not well-suited to analyzing the nonuniform fluxes that govern the electrochemical respon

143 etabolic output, polyploidy can also promote nonuniform genome, transcriptome, and metabolome alterat

144 e model is used to investigate the impact of nonuniform geometrical and electrical properties of the

145 orifice, the cells experience the strongest nonuniform gradient and are drawn toward it by the posit

146 Our results, which establish that nonuniform growth and friction are fundamental determina

147 The nonuniform growth of certain forms of cancer can present

148 they travel inside of the reactor, causing a nonuniform growth of nanomaterials.

149 e oxidative etching of Au(0), which leads to nonuniform growths along different lateral directions to

150 through the narrow hole and generates highly nonuniform heating, which in turn, results in gradients

151 e charges are parameterized to reproduce the nonuniform histone/DNA interaction free energy profile a

152 Our simulations further reveal that the nonuniform histone/DNA interactions in canonical nucleos

153 to blot EM grids and that these manifest in nonuniform ice after vitrification.

154 ntial diffraction intensity decay due to the nonuniform illumination by the X-ray beam.

155 cessing was performed to normalize color and nonuniform illumination of the fundus images to define a

156 e species is modeled taking into account the nonuniform illumination volume.

157 atoms reside on surfaces that are typically nonuniform in composition and structure.

158 The binding is nonuniform in infarcted, periinfarcted, and remote, noni

159 e genealogy, causes the structure of G to be nonuniform in that the variances associated with the pri

160 is associated with LN enlargement as well as nonuniform increases in bulk tissue elasticity and visco

161 nucleation model, indicate that a chemically nonuniform interface presenting different free energy ba

162 trast, bending or twisting filaments imposes nonuniform interface strain and leads to partial interfa

163 e heterogeneity by mitigating the buildup of nonuniform internal stresses associated with volume chan

164 The sciatic nerve (SN) showed increased nonuniform, internodal segments suggesting demyelination

165 o several hundred RyRs, creating a spatially nonuniform intracellular distribution.

166 We investigate the effect of nonuniform intraspecific competitions on coexistence and

167 concluded that, for the same amount of drug, nonuniform ion enhancement for different types of sample

168 resulted in an intriguing formation of small nonuniform islands loaded with Abeta.

169 This work furthers the understanding of nonuniform Li plating and will inspire future studies to

170 However, nonuniform Li-ion flux during repeated Li plating and st

171 This pattern of nonuniform liquid thickness changes again after the filt

172 ganized, with many macromolecules exhibiting nonuniform localization patterns.

173 1 within Foxp3+ cells resulted in global yet nonuniform loss of DNA methylation, derepression of infl

174 s suspended in a paramagnetic liquid under a nonuniform magnetic field, is a powerful tool for determ

175 the energy barriers between stable states in nonuniform magnetic particles on geological timescales.

176 This microwave actuation induces nonuniform Marangoni stresses on the interface, which re

177 Nonuniform matrix ion suppression/enhancement across dif

178 olutions to control bioanalytical risks from nonuniform matrix ion suppression/enhancement even with

179 Therefore, the risk of nonuniform matrix ion suppression/enhancement is usually

180 back was modeled as spatially and temporally nonuniform membrane currents through mechanosensitive ch

181 defects in the tilt orientation that induce nonuniform membrane curvature.

182 Finally, we show that nonuniform membrane properties, along with transient dyn

183 s pressure equilibration models and dynamic, nonuniform membrane tension to account for the shape of

184 microtubules in the spindle is determined by nonuniform microtubule nucleation and the local sorting

185 d coplanar waveguide transducer generating a nonuniform microwave magnetic field.

186 The nonuniform, minimally varying, strain environment sugges

187 trol, and the resulting materials often have nonuniform morphologies with NPs on the external surface

188 nucleotide variant discovery, the sparse and nonuniform nature of the exome capture reaction has hind

189 misdirected assembly are the large size and nonuniform nature of the final particles.

190 In summary, this work unravels the nonuniform nature of the PDL within the 3D structural co

191 ous nucleation underlies our observations of nonuniform nucleation kinetics.

192 ical nonuniformity in this space, indicating nonuniform occupation of cytomorphological states within

193 Nonuniform opening of the angle was predicted when the s

194 Unlike in primates, nonuniform opsin expression across the retina and coexpr

195 overcoming the diffraction limit, a strongly nonuniform optical absorption path length of the light t

196 Recent evidence argues for nonuniform outcomes after fusion, in which cargo is rele

197 If the cortical network is nonuniform over the cell, the cortical contractile eleme

198 ult of mass loss from ice sheets is strongly nonuniform, owing to gravitational, deformational and Ea

199 izure onset in patients with aMCI and AD was nonuniform (P < .001), clustering near the onset of cogn

200 Due to the nonuniform paths of the light traveling in the Au sample

201 Furthermore, we uncovered a nonuniform pattern of reactivation of fear memory traces

202 omputer simulations having both constant and nonuniform peak densities.

203 uide to achieve depth encoding, resulting in nonuniform performance throughout the detector array due

204 ses, including muscular dystrophy, display a nonuniform phenotype.

205 n shear-dependent enhanced diffusivity and a nonuniform platelet distribution.

206 nd medical imaging, SIFT supplements data at nonuniform points in the time domain with the informatio

207 Recovering MAP estimates using simulated, nonuniform priors that correlated with monkeys' choice p

208 eloping tissue, could in principle adopt any nonuniform profile.

209 duction velocity alternans which resulted in nonuniform propagation discontinuities and wave breaks c

210 R architectures, including RG precomplexes, nonuniform R density, specific R arrangements, and immob

211 We thus show how a nonuniform Rac1 distribution on the membrane generates a

212 Ribosomes elongate at a nonuniform rate during translation.

213 ry means of regulating this trade-off is the nonuniform rate of translation elongation that defines t

214 Anatomic models based on nonuniform rational b-spline modeling techniques were us

215 cokinetic modeling and a pediatric series of nonuniform rational B-spline-based phantoms have been us

216 oms was developed using body models based on nonuniform rational B-spline.

217 second software program and transformed to a nonuniform rational basis-spline surface phantom, allowi

218 ssion in mdx and DeltaSIV cells results in a nonuniform redistribution with Na(v)1.5 being specifical

219 t postnatal cortical expansion is strikingly nonuniform: regions of lateral temporal, parietal, and f

220 alignment of F-actin polymers, or spatially nonuniform regulation of F-actin by upstream biochemical

221 our findings instead assign this function to nonuniform release site kinetics.

222 models, an electric field produces a highly nonuniform response of the myocardial wall, with discret

223 Nonuniform sampling (NUS) approaches have the potential

224 pectral "snapshots." Recently, time-resolved nonuniform sampling (NUS) has been proposed as a straigh

225 Nonuniform sampling (NUS) is incorporated to achieve tim

226 Here, we report that 2D FTICR MS using nonuniform sampling (NUS) obtained by randomly skipping

227 e acceleration of nD NMR, ultrafast (UF) and nonuniform sampling (NUS), in the context of metabolomic

228 H correlations with diagonal suppression and nonuniform sampling (NUS).

229 Spectrum-specific optimized nonuniform sampling (SONUS) schemes based on the Cramer-

230 Random phase detection is complementary to nonuniform sampling methods, and their combination offer

231 It can, however, be obtained with nonuniform sampling of the data grid, but optimal proces

232 riteria for PPSC, including 26 patients with nonuniform sampling of the fallopian tubes (group 1) and

233 artifacts and the systematic optimization of nonuniform sampling schedules has remained elusive.

234 hrough combined use of rapid acquisition and nonuniform sampling techniques, we show that these Fab a

235 ed 5D-NMR(13)C-detected NMR experiments with nonuniform sampling to accomplish full resonance assignm

236 h high resolution and sensitivity, extensive nonuniform sampling was employed.

237 irements of isotopic NMR, while a third one, nonuniform sampling, leads to dramatic precision losses.

238 ament-surface interactions lead to a host of nonuniform shape equilibria, in which filaments progress

239 .03) and evidence of cell injury at sites of nonuniform shear profiles that are critical loci for vas

240 ixture of nonplatelet cellular fragments and nonuniform-sized, preactivated platelets mostly lacking

241 ted for surgical deformation, shrinkage, and nonuniform slicing factors in pathologic specimens.

242 This nonuniform slip history reveals a more complex rupture h

243 h the nanochannel surface charges to yield a nonuniform solute concentration across the channel depth

244 patterns with a fixed number of wrinkles and nonuniform spacing and patterns of uniformly spaced wrin

245 ealed that the global signal (GS) exhibits a nonuniform spatial distribution across the gray matter.

246 uantity can also be expected if drugs have a nonuniform spatial distribution inside the tumor, for ex

247 tein self-assembly process involves a highly nonuniform spatial distribution of aggregates.

248 A nonuniform spatial distribution of reward effects across

249 and II of this investigation to account for nonuniform spatial distributions of hydrophobic residues

250 h section was tailored to generate different nonuniform spatial distributions of the electric field a

251 istribution of ganglion cell density and the nonuniform spatial integration across the visual field.

252 These results provide evidence for a nonuniform spatiotemporal deployment of attention during

253 Such a kernel leads to smart stretching with nonuniform spectral resolution, having direct utility in

254 Warped stretch imaging technology utilizes nonuniform spectrotemporal optical operations to compres

255 en by misestimated velocity signals due to a nonuniform speed prior rather than imperfect integration

256 The nonuniform spin-distribution, which dictates the selecti

257 ts indicate that both patterns emerge from a nonuniform stationary instability, supporting a central

258 a at saturating ATP (500 muM), we proposed a nonuniform stepping mechanism in which a UvrD monomer tr

259 These results suggest a nonuniform stepping mechanism that differs from either a

260 w the local step velocity is affected by the nonuniform strain field arising from the dislocation.

261 The resulting nonuniform strain fields induce complex patterns of supe

262 nal functionality is permitted by the unique nonuniform structure of the tissue.

263 Interestingly, we also observe nonuniform subcellular localization of utrophin CH1-CH2

264 pathogenic bacteria adherent even to complex nonuniform substrates.

265 imperfect centering during endoscopy and the nonuniform surface topology of human tissue.

266 ingle dendritic branches can already exhibit nonuniform synaptic integration, with the computational

267 neral problem by mapping the properties of a nonuniform system with Coulomb interactions onto those o

268 s are known to produce significant errors in nonuniform systems, particularly for electrostatic prope

269 s to visualize the cocrystal distribution in nonuniform tablets.

270 This can cause nonuniform temperature changes and uneven photopolymeriz

271 We show that a nonuniform temperature distribution within the battery c

272 ents, suggesting that peeling is caused by a nonuniform tension distribution around the AMR, and that

273 If left ventricular wall thickness seemed nonuniform, the size and location of relatively thickene

274 As a result, aqueous films of nonuniform thickness are formed while the filter paper i

275 model suggests that the helicase displays a nonuniform translocation mechanism in which it moves app

276 ls, charge, and capacitance, the EEF-induced nonuniform transmembrane potential measured in this stud

277 ng results illustrated both local and global nonuniform transport phenomena and the high-resolution C

278 The large nonuniform trapping produced by the microsphere transpor

279 In addition, the nonuniform trapping supports the fact that the granular

280 used commercial IM-MS instruments utilize a nonuniform traveling wave field to propel the ions throu

281 an create unmeasured confounding and lead to nonuniform treatment effects over the propensity score (

282 d location-dependent power changes evidenced nonuniform trends across the population.

283 also studied the biologic implication of the nonuniform tumor AD distribution using radiobiologic mod

284 -dependent intrinsic curvature also leads to nonuniform twist and necessitates consideration of eight

285 resulted in profound defects in barrier and nonuniform, undulating TJ morphology.

286 A nonuniform uptake of water into the tissue at its maximu

287 Nonuniform usage can result from the rearrangement proce

288 DSB-associated ubiquitin structures must be nonuniform, using different linkages for distinct functi

289 ere are expected to be much more tolerant to nonuniform values of 1JCalphaC' (or 1JCalphaC' + 1DCalph

290 erogeneity test was used to test for overall nonuniform variation and also for individual months.

291 f the low-frequency modes in the presence of nonuniform variations in the ENM force constant.

292 gan or tissue donors for infectious risk are nonuniform, varying with the type of allograft, national

293 esults is the formation of cross-sectionally nonuniform viscoelasticity that may have unique applicat

294 mple by partitioning it into droplets with a nonuniform volume distribution.

295 Because biological membranes are diverse and nonuniform, we explore the consequences of lipid diversi

296 rfamily that encloses a central channel with nonuniform width.

297 ion carried by individual neurons was highly nonuniform, with few neurons carrying large amounts of i

298 rders across the world's languages is highly nonuniform, with the majority of languages being either

299 NRL is also nonuniform within single fibers, but how this diversity

300 rsion of the elastic energy, which penalizes nonuniform wrinkle spacing and amplitude, as well as dev