ライフサイエンスコーパス: distortion

1 nal dynamics could lead to substrate channel distortion.

2 lt leads to an accumulation of heat and thus distortion.

3 self-trapped excitons (STEs) from structural distortion.

4 gh-dimensional data while trying to minimize distortion.

5 complex association that involves gross DNA distortion.

6 The area was corrected for projection distortion.

7 near magnetostriction, leading to a trigonal distortion.

8 to these outlines to quantify and map image distortion.

9 t vulnerability of various alloys to thermal distortion.

10 ntaining vacuoles with endoplasmic reticulum distortion.

11 is only possible at the expense of reactant distortion.

12 nformation effect's purported role in memory distortion.

13 ctra along with Pareto scaling overcomes the distortion.

14 , which involves a strong pseudo-Jahn-Teller distortion.

15 ction and other dimensions of suprathreshold distortion.

16 llary approach in order to reduce anatomical distortion.

17 rporating known degrees and distributions of distortion.

18 ndite phases distinguishable by orthorhombic distortion.

19 or focal asymmetry, mass, and architectural distortion.

20 Am = GUA and FA, that arises from structural distortions.

21 lastic interactions) drive concerted lattice distortions.

22 imal compensation of deterministic nonlinear distortions.

23 d that every use of FIB causes large lattice distortions.

24 e present paper discusses 3 common cognitive distortions: 1) dichotomania, the compulsion to perceive

25 as designed to produce a measure of DW image distortion across the prostate.

26 The paradigm used to induce such distortions (adaptation) can provide powerful insights i

27 e energy gain associated with the tetragonal distortion, allowing the cubic phase to be stable at low

28 nd to the Br end, indicating that the larger distortion also prolongs the lifetime (more STE states).

29 Distinct structural distortions among the axial sites, arising from the nons

30 al complexity or electronic instabilities so distortion analysis methods are useful.

31 Strain/distortion analysis of the (3+1) transition structure hi

32 3.5 in the anticodon loop likely causes tRNA distortion and affects anticodon-codon interaction, whic

33 ergistic or counteracting roles of wavefront distortion and birefringent walk-off, respectively.

34 Lattice distortion and high densities of crystal defects were ob

35 The enabling mechanism is BPLC's lattice distortion and index modulation caused by the action of

36 upled flow &reorientation leading to lattice distortion and index modulation.

37 c radius of potassium-ions causes structural distortion and instabilities even in layered electrodes.

38 the anterior urethra also showed significant distortion and irregular, beaded narrowing.

39 oes not induce structural or microstructural distortion and it can be combined with immunostaining to

40 ated incompatibility can lead to severe peak distortion and loss of resolution and sensitivity in the

41 reased recall examinations for architectural distortion and mass (P < .001) and decreased recall exam

42 unclear how the 5'nuclease mechanisms of DNA distortion and protein ordering robustly mediate efficie

43 We show that information distortion and the overweighting of other people's error

44 on area or features, which were sensitive to distortion and uncertainty in vascular structure, we pro

45 nly overlooked effects: axial electric field distortion and voltage ramping.

46 ) a quantification of the effects of optical distortions and (iv) a comparison with other standard te

47 R186, F187 and K190 stabilise the target DNA distortions and are required for efficient transposon in

48 The competing energetics of polymer chain distortions and chemical mismatch with the substrate gra

49 chtop microscope that is corrected for color distortions and chromatic aberrations, also matching the

50 filler particles resulted in electric field distortions and dissimilar particle behaviors caused by

51 Because these distortions and dissociations of TFS/ENV disrupt tonotop

52 ombination of geometric frustration, lattice distortions and epitaxial engineering.

53 Adsorption leads to measurement distortions and incorrect estimation of the fluid parame

54 All indices improved after surgery, but only distortions and macular volume normalized.

55 e find that thermal gradients cause the most distortions and turbidity causes the most loss.

56 mismatch that can be accommodated by lattice distortions and/or octahedral rotations, ferroelectric-f

57 nces in the subjective propensity to produce distortions, and variations in the degree of trust that

58 Body image distortions are common in healthy individuals and a cent

59 otential perceptual consequences of measured distortions are discussed.

60 In the MOF framework, however, node distortions are found to occur at substantially lower te

61 imulation results confirm that inter-core XT distortions are more relentless for cores fabricated aro

62 concave environments (TON) because framework distortions are required to avoid steric repulsion.

63 nstrained due to a power dependent nonlinear distortion arising from a phenomenon known as the Kerr e

64 t category being particularly susceptible to distortions arising from weight loss.

65 2Re2O7 and induces a parity-breaking lattice distortion as a secondary order.

66 The degree of distortion as well as the overall symmetry of the molecu

67 tic state and form four well-controlled bend distortions as orientational order changes.

68 to a breaking of the trimerous symmetry and distortion at a receptor-binding interface.

69 a structural instability towards tetragonal distortion at low temperatures.

70 ted tomography, there was MV and SB scaffold distortion at the bifurcation with single strut fracture

71 f strain can be useful for measuring lattice distortions at heterojunction boundaries and interfaces.

72 rong link between intermixing and structural distortions at such interfaces is highlighted: intermixi

73 scovery of a general switching of polyhedral distortions at symmetry-disallowed transitions in perovs

74 es the presence of a large amount of defects/distortions at the interfaces.

75 They showed that distortion away from the low-energy solution conformatio

76 esolution; (iii) preprocess data to minimize distortions, blurring and temporal artifacts; (iv) repre

77 on a self-report measure of body perception distortion; but not by pain intensity, time since diagno

78 Preventing octamer distortion by site-specific disulfide linkages inhibits

79 P values can be reframed to lessen distortions by presenting them without reference to a cu

80 mammographic features (masses, architectural distortions, calcifications, focal asymmetries) of lesio

81 We have shown previously that sex ratio distortion can be generated synthetically in the main hu

82 hanism at work here that facilitates lattice distortion can be used to frustrate free relaxation of t

83 ular M6(O)8 nodes studied here, the observed distortions can be mapped to polymorphic forms known for

84 nsitivity measurements and quantification of distortions can objectively assess visual dysfunction in

85 The lattice distortion caused by oxygen concentration gradient withi

86 Here we study the effects of distortions caused by chiral springs and helices on the

87 cterize the nature and magnitude of binaural distortions caused by modern digital behind-the-ear HAs

88 Furthermore, we show how image distortions caused by optically dense structures can be

89 cal approaches to describe and reproduce the distortions caused by reabsorption on emission spectra a

90 Quantifying image distortions caused by strong gravitational lensing-the f

91 orbital, and is then stabilized by a lattice distortion characterized by a hardening of the A1g coher

92 ted hallucinations do not evoke the temporal distortion commonly associated with altered states.

93 d more reliable signal acquisition with less distortion compared with objective based position detect

94 A distortion-corrected Brewster angle microscope (DC-BAM)

95 patterned on its surface that is free of any distortion, coupling, and does not converge to a single

96 Because these distortions degrade and diminish the tonotopic represent

97 analyzed in details using induced molecular distortions, delocatization properties of participating

98 precise moment of the song when a predicted distortion did not occur, consistent with a better-than-

99 The model avoids distortions due to parallax, which occur in simple model

100 electron tomograms including noise and image distortions due to the missing-wedge effects.

101 istortion' or the potential for 'significant distortion' due to susceptibility effects from hip prost

102 ion due to phase transformations and lattice distortions during cycling becomes severe.

103 ervation, to our knowledge, of dynamical DNA distortions during search/interrogation beyond base pair

104 dependency of rate constants of cross-bridge distortion dynamics (c) and force redevelopment (ktr) wa

105 henyldiazomethane is mostly dependent on the distortion effect during the cycloaddition process.

106 This distortion effect is however higher in the alkyl azide c

107 ed, become inextricably interwoven, allowing distortion, elaboration, and even total fabrication.

108 ivation barriers correlate closely with both distortion energies and interaction energies over an act

109 es originate from increased transition state distortion energies and unfavorable interaction energies

110 Dipole distortion energies are responsible for approximately 80

111 states, respectively, the difference in the distortion energies controls the enantioselectivity.

112 ing ligand-substrate steric interactions and distortion energies in the computed transition states.

113 The tuning of distortion energies with substituents in a diazo compoun

114 azido group, which can accommodate decreased distortion energies without predistortion.

115 This is because a large distortion energy ( approximately 43 kcal/mol) is requir

116 The distortion energy of the Diels-Alder reaction transition

117 of the metallacycloadducts are controlled by distortion energy, analogous to their organic counterpar

118 molecules is called the activation strain or distortion energy.

119 reactivity of DDA reactions is controlled by distortion energy.

120 bital interaction, but also to a decrease in distortion energy.

121 es mostly arises from the diene out-of-plane distortion energy.

122 of hands as highly salient body parts, with distortions engaging neural resources that are especiall

123 fficulties), ulceration, and severe anatomic distortion, especially on the face.

124 potential implications of body image and its distortions for the insurance hypothesis.

125 toms possess sp(2) hybrid orbitals with some distortion, forming an extensive conjugated pi-bonding p

126 esented in this paper are aimed at achieving distortion free, compositionally sound and well bonded m

127 organs, which automatically acquires serial distortion-free and registration-free images with endoge

128 sent in conventional raster scans, it is not distortion-free.

129 Separating electronic distortions from intrinsic deformations within the low t

130 flexibility, which allows for a multitude of distortions from the ideal highly symmetric structure.

131 he V2O5 framework couple to local structural distortions, giving rise to small polarons that serves a

132 r, continuous and fine manipulation of these distortions has never been possible.

133 the lattice symmetry by modifying the local distortions, i.e., octahedral bonding angle and length.

134 tion led to excessive microtubule waving and distortion, implying that NEK6 suppresses the aberrant c

135 O2 were not detected because the structural distortions imposed on the tetraoxacyclohexane subunit i

136 stinguished between the three groups of mean distortion in 'non-distorted' image volumes, 1.942 +/- 0

137 ted a means of quantifying and mapping image distortion in clinical prostate MRI cases.

138 m the three equivalent directions of Peierls distortion in the parental 1T phase.

139 pic symmetry breaking leading to robust Bain distortion in the premartensite phase of 10% Pt-substitu

140 nd an experimental reconstruction of lattice distortions in a component of a nanoelectronic prototype

141 bstantially lower temperature than analogous distortions in bulk ZrO2 owing to the nanoscale nature o

142 nses to Gaussian noise to uncover pronounced distortions in coding of rapidly varying acoustic tempor

143 oduce idiosyncratic signatures of perceptual distortions in each observer and suggest that even the m

144 on from phase transformations and structural distortions in Ni-rich LiNi0.8Co0.1Mn0.1O2 using multisc

145 onses and intrinsic spectral backgrounds and distortions in order to extract reliable spectral data.

146 head was positively correlated with gambling distortions in pathological gamblers.

147 Distortions in peer review are driven by economic forces

148 The manipulation of distortions in perovskite structures is critical to tail

149 phragmoplast MT arrays and leads to serious distortions in spindle MT remodeling during mitosis.

150 This suggests that the union of ATP produces distortions in the chains that eliminate the restriction

151 and can therefore be exploited as probes of distortions in the electronic structure at the nanoscale

152 Rietveld analysis shows less distortions in the honeycomb structure of Cu2IrO3 with b

153 Random Projections technique in terms of the distortions in the projections.

154 We analysed lattice distortions in these model crystals by using X-ray diffr

155 onses to Gaussian noise to reveal pronounced distortions in tonotopic coding of TFS and ENV following

156 WM maintenance cause distinct but systematic distortions in WM.

157 e consider how a particular type of temporal distortion, in which the apparent future influences "ear

158 A visual distortions index (%DI) was calculated using 3-dimension

159 We find that duplex distortion induced by a crosslink plays a crucial role i

160 th, which is modulated by the electric field distortion induced by space charge.

161 y, are both attributed to the electric field distortion induced by space charges located in the vicin

162 Distortion-interaction analyses of the transition struct

163 Distortion-interaction analysis indicates that for both

164 Distortion-interaction analysis revealed that attractive

165 The application of distortion/interaction analysis allows us to quantify th

166 Distortion/interaction analysis indicated that the diffe

167 stortion of the substrate, demonstrated by a distortion/interaction analysis.

168 e consistent with predictions made using the distortion/interaction model and were also found to be g

169 The activation strain or distortion/interaction model is a tool to analyze activa

170 The distortion/interaction model shows that interaction domi

171 The distortion/interaction model shows that the increased ac

172 es, while further expanding the scope of the distortion/interaction model.

173 tional theory (M06-2X) and analyzed with the distortion/interaction model.

174 uoromethyl)tetrazine were analyzed using the distortion/interaction-activation strain model.

175 Crystal plastic distortion is highest in the intact segments of broken c

176 stal axes, unless a substantial orthorhombic distortion is imposed.

177 The distortion is predicted to be small and is not discernib

178 factor beta, while the propensity to produce distortions is controlled by a conservation factor K.

179 This pattern, along with extreme body margin distortion, is consistent with onychophoran decay, and i

180 nt protein changes include asymmetric barrel distortion, its interaction with the membrane, and signi

181 ion of linkage groups in case of segregation distortion; (iv) data imputation on VCF files using a ne

182 llic parts produced by AM are susceptible to distortion, lack of fusion defects and compositional cha

183 t the standard error (SE) are susceptible to distortion, leading to overestimation of the existence a

184 rger size of EA, these materials show a high distortion level in their inorganic structures, with EA4

185 gnetic structure and multidomain Jahn-Teller distortions, likely related to its anisotropic thermal p

186 These distortions make overweight and obesity appear less harm

187 Access to novel distortion mechanisms and the ability to switch these di

188 ctural similarity index (SSIM), a perceptual distortion metric based on the human visual system, and

189 work suggests an unusual situation in which distortions might contribute to the preservation rather

190 e a novel one-stranded intercalation and DNA distortion mode.

191 This DNA distortion mutually 'locks' protein and DNA conformation

192 lix by 30 degrees , providing the structural distortion needed for R-loop formation.

193 d that continuum models cannot reproduce the distortions observed in fully atomistic molecular dynami

194 The distortions occurred both for stimuli presented sequenti

195 lus C44 that triggers a rhombohedral lattice distortion occurring between 34 and 39 GPa.

196 to the absence of valvular calcification and distortion of aortic root anatomy in many patients.

197 This distortion of electron density off an interatomic axis i

198 ed stimuli, all programs caused time-varying distortion of ILDs.

199 etrated frameworks, while 2 undergoes simple distortion of linkers.

200 tionally, we observed ablation, blunting, or distortion of microvilli in infected epithelial cells.

201 ation, HbS fiber interaction, and subsequent distortion of RBCs is challenging as they occur at multi

202 It reveals severe distortion of target DNA and flipping of the target aden

203 (PL) studies show a correlation between the distortion of the "PbBr6" octahedron in the 2D layer and

204 This complex revealed unambiguous distortion of the -1 subsite mannoside to an (O)S2 confo

205 Remarkably, EF-4 induces a distortion of the A-site tRNA, allowing it to interact s

206 culations highlight the role of differential distortion of the anhydride-methanol complex in the tran

207 nic charge density accompanied by a periodic distortion of the atomic lattice in quasi-1D or layered

208 Distortion of the catalyst structure, caused by steric c

209 rNTP with normal active site geometry and no distortion of the DNA substrate or nucleotide.

210 e that functionalization leads only to local distortion of the double helix while the overall structu

211 om a tetragonal Jahn-Teller active polaronic distortion of the Fe(2+)O6 octahedra.

212 three different temperatures demonstrate the distortion of the hydrophobic core to be a crucial step.

213 fcc-based structure undergoes a rhombohedral distortion of the La sublattice.

214 In addition, the orthorhombic distortion of the lattice is present at any temperature.

215 is complex shows a remarkable enzyme-induced distortion of the nitro-substituent out of the plane of

216 The distortion of the pi-system from planarity leads to unus

217 patch of a Cu-azurin causes minor structural distortion of the protein blue Cu site and a dramatic ch

218 l that the strain curves associated with the distortion of the reactants in the Diels-Alder reactions

219 The distortion of the shape of the surface wave fronts due t

220 sociated with the seriously trigonal lattice distortion of the SnO6 octehedra, under which the Sn-O1-

221 The major enantiomer is favored by a smaller distortion of the substrate, demonstrated by a distortio

222 This correlation was related to the distortion of TiO6 octahedra observed during neutron dif

223 al resonators, thus resulting in unavoidable distortion of waveforms.

224 For 29% of transducers, some distortions of anechoic structures were observed.

225 re lysis, division and growth defects due to distortions of cell wall biosynthesis.

226 selection bias, measurement error) to cover distortions of conclusions produced by statistical metho

227 : (a) Nonlinear frequency compression caused distortions of high-frequency envelope ITDs and signific

228 phase transition was induced by the enhanced distortions of MgO6 octahedra and VO6 octahedra under hi

229 Moreover, the patterns of idiosyncratic distortions of network synchrony relative to the group c

230 , both associated with local MnO6 octahedral distortions of the (001) LSMO within the first few uc, a

231 and 413 K and totaling 6 mus show transient distortions of the bilayer/water interface (consistent w

232 density wave order is manifested by periodic distortions of the one-dimensional zigzag Ge chains.

233 Here we show that the structural distortions of the perovskite lattice can determine the

234 oupling to hydration-driven Jahn-Teller-like distortions of the Sr coordination environment.

235 We observed voltage-dependent asymmetric distortions of the VDAC-1 barrel and the displacement of

236 l surface to be repelled due to cell elastic distortion, offset by tip-cell adhesion, and indeed such

237 to the martensite phase with additional Bain distortion on further cooling.

238 ng measurement and the influence of waveform distortion on hydrophone corrections.

239 n mechanisms and the ability to switch these distortions on and off through chemical modification fun

240 he atmosphere in lowest order produces phase distortion only.

241 arge density wave with an associated Peierls distortion or a 'Pomeranchuk wave'.

242 NA binding requires a significant structural distortion or partial unfolding.

243 ogically assessed to have, respectively, 'no distortion' or 'significant distortion' or the potential

244 espectively, 'no distortion' or 'significant distortion' or the potential for 'significant distortion

245 xidized Eu(3+)Ti(4+)O2N with the GdFeO3-type distortion (Pnma) as a metastable phase, instead of pyro

246 istic functions can be used to correct image distortions present in more complicated constant linear

247 udden changes in the beam location (fly-back distortion) present in conventional raster scans, it is

248 ed on the mineral surface and that epitaxial distortion previously observed for Pu(IV) sorption occur

249 Error response magnitude depended on distortion probability.

250 calculations not only reproduce the membrane distortions produced by the channel but also accurately

251 nts of auditory brainstem response (ABR) and distortion product otoacoustic emissions (DPOAE) to asse

252 onth, by 4 months, mutants show only minimal distortion product otoacoustic emissions and 70-80 dB th

253 ve I/Wave V ratios in the presence of normal distortion product otoacoustic emissions and normal audi

254 es: (a) electrophysiological tests including distortion product otoacoustic emissions, auditory brain

255 r hair cell (OHC) properties, as measured by distortion product otoacoustic emissions, neither before

256 r-current-driving-voltage, low-mid-frequency distortion-product-otoacoustic-emissions (DPOAEs), and p

257 However, distortion products were found in live but not dead chic

258 nd final measurements, taking into account a distortion rate for each radiograph compared with origin

259 d the substrate induced (pseudo-) tetragonal distortion (ratio of out-of-plane to in-plane lattice pa

260 These distortions, reported here as changes in O-atom location

261 eracts with promoter DNA to initiate the DNA distortions required for transcription bubble formation,

262 coincides with temperature dependent static distortions resulting in pseudocubic local symmetry.

263 The spinal cord showed architectural distortion, severe neuronal loss, and microcalcification

264 hat complex stimulus-responsive out-of-plane distortions such as twist of different chirality, emerge

265 The nature of these distortions supports theories positing that parietal cor

266 Here we describe a CRISPR-Cas9 sex distortion system that targets ribosomal sequences restr

267 l scan images are shown to exhibit less scan distortion than conventional raster scan images.

268 ctures, with EA4Pb3Cl10 having a much larger distortion than that of EA4Pb3Br10, which results in bro

269 6-) reduction is accompanied by a structural distortion that is experimentally manifested by electroc

270 re carried out to reveal the local structure distortion that is responsible for the unusual negative

271 nd our experiments show that SANJAY produces distortions that are 1.44 to 4.15 times smaller than tho

272 ry reveals previously unrecognized framework distortions that balance the C-O bond lengths required f

273 of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interaction

274 However, even in the absence of nonlinear distortion, the practical limit on the transmission thro

275 to frustrate free relaxation of the lattice distortion, thereby prolonging the lifetime of the writt

276 eloped methods to identify and correct these distortions through image-based signal analysis without

277 a situation best avoided by an out-of-plane distortion to a bird-like geometry.

278 , whereas the 4- ion undergoes a Jahn-Teller distortion to an S = 1/2 D3d structure with a small 0.1

279 least one chlorophyll a presenting a slight distortion to its macrocycle.

280 nsitivity, and minimal image interference or distortion to the original field distribution.

281 ualitatively accurate images with negligible distortion to the original field distribution.

282 guided by a theoretical analysis of possible distortions to the pyrochlore lattice, we construct an e

283 ioxocane)-alpha-CD derivative shows a severe distortion toward a narrower elliptical shape for the pr

284 uce cytoplasmic incompatibility or sex-ratio distortion, two parasitic reproductive phenotypes that f

285 y do not cause the large tissue shrinkage or distortions typically associated with other, more compli

286 non-monotonicity arises from the tetragonal distortion under large biaxial strain.

287 ctive sweeps based on linkage disequilibrium distortions under different conditions, including a huma

288 e proposed method correctly reproduced known distortion values and distributions in virtual phantoms.

289 reification, but they can also introduce new distortions via misleading specifications for bias param

290 ooking back to the locus classicus of memory distortion (viz. Bartlett 1932), which in fact provides

291 Segregation distortion was detected for many markers, sometimes as h

292 Distortion was more severe when the primary studies had

293 To reduce these deviations, i.e. image distortions, we use spiral scanning paths, allowing prec

294 . controls = 3.71+/-1.47 %W (P < 0.001); and distortions were 7.61+/-12.6 %DI vs. controls = 0.13+/-0

295 erently substituted 1,3-dipoles is driven by distortion, whereas the difference between azomethine yl

296 factor for SMM behavior is not the degree of distortion which, a priori, would be expected to be the

297 extrusion of consecutive bases and backbone distortions, with a sharp bending of the duplex accompan

298 ragg diffraction intensities enables lattice distortions within a crystal to be imaged at nanometre-s

299 The intermixing and structural distortions within the crystal lattice have been quantit

300 edron provides a general method for studying distortion, yielding parameters that are sensitive to va