ライフサイエンスコーパス: asymmetry

1 cal expansion, thereby establishing physical asymmetry.

2 ials, can be manifested in sibling cell size asymmetry.

3 t non-Mendelian segregation depended on this asymmetry.

4 id gradients that underlie the generation of asymmetry.

5 lizing on two geometric properties: size and asymmetry.

6 er model to the interface accounting for the asymmetry.

7 holoprosencephaly and defects in left-right asymmetry.

8 nance and initial establishment of cell size asymmetry.

9 he Mla system preserves outer membrane lipid asymmetry.

10 however, new findings reveal their synaptic asymmetry.

11 pulling excited carrier away under built-in asymmetry.

12 the upper atmosphere, causing a north-south asymmetry.

13 w cell cycles regardless of their mother-bud asymmetry.

14 ce demonstrated disrupted callus healing and asymmetry.

15 tant for maintenance of outer membrane lipid asymmetry.

16 the PPV remains low even at high degrees of asymmetry.

17 ated GluN1 subunits further reflect receptor asymmetry.

18 -cell snail embryos, preceding morphological asymmetry.

19 ved wave stress tensor has an apparent index asymmetry.

20 difference corresponded to the degree of MA asymmetry.

21 deficiency leads to loss of plasma membrane asymmetry.

22 anied by a modulation of the cells' fore-aft asymmetry.

23 tes of cost were not sensitive to changes in asymmetry.

24 natomic sites identified 2 types of anatomic asymmetry.

25 ositioning and the establishment of physical asymmetry.

26 tical, regardless of geometrical or material asymmetries.

27 d show development-dependent gene expression asymmetries.

28 al timing of developing regions and regional asymmetries.

29 s, specifically sensitive to lipid and water asymmetries.

30 ehavioral consequences such as visual search asymmetries.

31 This generates membrane phospholipid asymmetry, a property important in many cellular process

32 Vertebrate hearing organs manifest cellular asymmetries across the radial axis that underlie afferen

33 lls naturally retain their bond distribution asymmetry after division by rapidly replenishing Ft-Ds b

34 Mode hybridization and structural asymmetry allow address-ing different input polarization

35 This filter asymmetry, along with differences in intracellular and e

36 Funnel plot asymmetry among SLC6A3 studies was identified and attrib

37 Apart from their in-plane inversion asymmetry, an additional degree of freedom allowing spin

38 cal for development by establishing cellular asymmetries and orientation within the plane of an epith

39 ginates fundamentally from local atomic site asymmetries and therefore centrosymmetric materials may

40 rge nonlinearities with suitable geometrical asymmetries and/or topological features.

41 lators can exhibit both strong electron-hole asymmetry and a strong deviation from a linear dispersio

42 defined glaucoma." Association between vCDR asymmetry and disc plus field defined glaucoma.

43 erms of two biologically relevant variables, asymmetry and ellipticity, allowing us to quantify the o

44 lopment reveals the interplay between tissue asymmetry and growth that helps our hearts take shape.

45 , accompanied in some individuals by cranial asymmetry and incisor malocclusion.

46 ple mechanical devices which combine spatial asymmetry and nonequilibrium to produce counterintuitive

47 The results suggest an inter-hemispheric asymmetry and olfactory cortical functional separation t

48 conversion by plasmonic antennas: Structural asymmetry and plasmon hybridization through strong coupl

49 on prevents the development of mitotic aster asymmetry and spindle pole movement towards the subdomai

50 d microtubule tyrosination to induce spindle asymmetry and that non-Mendelian segregation depended on

51 at these dsRBD homodimers display structural asymmetry and that this unusual self-association mechani

52 ss suppresses AML cell polarity and division asymmetry, and CDC42 constitutes a useful target to alte

53 50th, 97.5th, and 99.5th percentiles of vCDR asymmetry are 0.05, 0.19, and 0.26, respectively.

54 unction with spindle positioning and spindle asymmetry are key determinants for correct cleavage furr

55 the molecular mechanisms underlying spindle asymmetry are unknown.

56 Asymmetry arises by a combination of selective pruning a

57 ived MT (GDMT) distribution, we find that MT asymmetry arises from nonrandom nucleation sites at the

58 The crystal structure of apo-FAcD exhibits asymmetry around the dimer interface and cap domain, pri

59 Measurements revealed increased asymmetry around the ferryl moiety, consistent with incr

60 loped model accounts for direction-dependent asymmetry, as well as for short- and long-term plasticit

61 systems to support molecular and functional asymmetries at electrical synapses.

62 We have identified sequential left-right asymmetries at the poles, which bias the buckling in opp

63 ity at one length scale can be translated to asymmetry at a different scale is largely not well under

64 erturbation of its inherent left-right (L-R) asymmetry at larval stages, that the dorsal habenulo-int

65 novel model of electrical synapse molecular asymmetry at the level of an intracellular scaffold that

66 channels that are correlated with functional asymmetry at the synapse [3, 4].

67 data identify a genetic basis for molecular asymmetry at vertebrate electrical synapses and show the

68 Here I present evidence of marked asymmetries between members of a functional pair of sust

69 The confinement also leads to a notable asymmetry between anions and cations of the same diamete

70 tunneling is most enhanced (a) when the bond asymmetry between C-H bond breaking and O-H bond formati

71 The asymmetry between critical heating and cooling rates dis

72 Importantly, we demonstrate a temporal asymmetry between miR-155 and miR-146a expression during

73 spatial information of the odorant into the asymmetry between the axonal activities.

74 ternative states are driven by a fundamental asymmetry between the inoculum population and the stably

75 with a uniform polarization that leads to an asymmetry between the number of soft modes on opposing s

76 The strong compositional asymmetry between the polar Cu2N and the vacuum gap brea

77 This implies some asymmetry between the two sides of the spindle, but the

78 Despite this asymmetry, both cell types show strong nonlinear integra

79 Modeling suggested that not only search asymmetries but also the asymmetric transfer of VPL depe

80 g questions about the evolutionary origin of asymmetry, but it also provides insight into the mechani

81 be involved in generating physical division asymmetry, but nonetheless is important for specifying d

82 Disruption of this asymmetry by ATP-independent phospholipid scrambling is

83 le anchored damage strengthens selection for asymmetry by creating additional fitness variance, it ha

84 P4-ATPases), which establish plasma membrane asymmetry by flipping specific phospholipids from the ex

85 We highlight the importance of the flow asymmetry by showing that many of the asymmetric growth

86 had vCDR determined in both eyes, with vCDR asymmetry calculated as the absolute value of the differ

87 This asymmetry can be modulated by the kinetic parameters of

88 We show how network asymmetry can now be incorporated in the many allometric

89 in which carrier propagation exhibits parity asymmetry, can remove elastic backscattering and provide

90 This asymmetry caused a rise in the mitochondrial calcium con

91 Model calculations confirmed that this asymmetry caused the rise in [Ca(2+) ]m during diastole

92 We propose that such ESD asymmetries could be used by all nervous systems to supp

93 anterior temporal lobes and the presence of asymmetry could be useful in differential diagnosis.

94 ndent of the nucleosomal DNA sequence or the asymmetry created by the presence of a linker DNA.

95 At a higher vCDR asymmetry cutoff of >/=0.30, the PPV increases to 37.7%.

96 The asymmetry, detected at the distal elongation zone, was b

97 Interestingly, asymmetry develops in a protracted dorsoventral wave, wh

98 to the cell cortex and maintaining cell size asymmetry during asymmetric cell division of Drosophila

99 The emergence of learning-dependent asymmetry during reversal learning was associated with d

100 n provide a simple and reliable mechanism of asymmetry establishment.

101 lucidate the mechanisms involved in physical asymmetry establishment.

102 that is essential to mouse embryo left-right asymmetry establishment.

103 These asymmetries exist across several species, and are depend

104 We propose that this asymmetry exists to compensate for inherent and variable

105 ze the effects of heterogeneity, anisotropy, asymmetry, follicular diffusion, and location of the mai

106 the ParA system can exploit this biochemical asymmetry for directed cargo transport.

107 elected because of the pronounced mother-bud asymmetry for these proteins distributions, Trx2p as ind

108 g it more likely that spinal gene expression asymmetries form the molecular basis of handedness.

109 RNAi morphology mutant have a range of shape asymmetries, from wild-type T. brucei (highly chiral) to

110 tter group included the maintenance of lipid asymmetry genetic pathway as a key determinant in protec

111 revious ocular surgery, or trauma and an IOP asymmetry greater than 5 mm Hg between eyes were exclude

112 The prevalence of vCDR asymmetry >/=0.20 among white, black, and Hispanic adult

113 The odds of vCDR asymmetry >/=0.20 are 1.44 times higher per 10-year incr

114 The sensitivity and specificity of vCDR asymmetry >/=0.20 for disc plus field defined glaucoma a

115 Vertical cup-to-disc ratio asymmetry >/=0.20 occurs in 2.1% of U.S. adults without

116 ypothesis that population-level, directional asymmetry has evolved as an adjunct to social behaviour.

117 ivated by experimental evidence of such flow asymmetry, here we explore the patterns of internal ring

118 s responsible for creating sibling cell size asymmetry; however, how the cortex causes the depolymeri

119 umber of models of mechanical and structural asymmetries in actomyosin contraction have been posited.

120 ver, human fetuses already show considerable asymmetries in arm movements before the motor cortex is

121 n for why swimming cells tend to have strong asymmetries in cell shape or propulsion.

122 ng manifests distinct types of morphological asymmetries in different contexts.

123 ithin the islet, which generates topological asymmetries in glucose responsiveness and proliferation.

124 erstanding of the ontogenesis of hemispheric asymmetries in humans.

125 es of the temporal binding window, revealing asymmetries in its size and plasticity depending on the

126 to quantify seasonal travel and directional asymmetries in Kenya, Namibia, and Pakistan, across a sp

127 Furthermore, any sex-based asymmetries in life history or behaviour (skewed sex rat

128 Transfer asymmetries in model behavior also depended on having di

129 well as tissue-level mechanisms, that drive asymmetries in organ formation.

130 a nonlinear model that incorporates observed asymmetries in PPT-ANPP relationships.

131 amination, however, functional pairs exhibit asymmetries in receptive field size and response kinetic

132 and enzymes that form and stabilize cortical asymmetries in response to diverse inputs.

133 Asymmetries in responses to climate change have the pote

134 d three measures designed to assess possible asymmetries in the distribution of movements across spac

135 show an absence of carbon (C) 1s signal, no asymmetries in the oxygen (O) 1s peak, and a Zn:O intens

136 veal that this material exhibits significant asymmetries in the Pb-I pair distribution functions.

137 metric, nonsinusoidal features, specifically asymmetries in the ratio between the sharpness of the be

138 responses in awake mice, we find surprising asymmetries in the spatial processing of eye-specific vi

139 ertebrates exhibit striking left-right (L-R) asymmetries in the structure and position of the interna

140 epigenetically regulated by miRNA expression asymmetries in the TGF-beta signaling pathway and latera

141 We report brain asymmetries in the tiny, dorsal tubular nervous system o

142 chanism for propagation of membrane polarity asymmetry in axonal degeneration.

143 We find significant asymmetry in both olfactory and orbitofrontal cortical o

144 le in establishing PS and PE plasma membrane asymmetry in budding yeast.

145 Nine patients (36%) had a greater than 20% asymmetry in ERG values between the 2 eyes.

146 creating and maintaining transbilayer lipid asymmetry in eukaryotic cell membranes.

147 uctural changes in cortical bone, as well as asymmetry in fracture healing.

148 s based on visual or analytical detection of asymmetry in funnel plots.

149 l rotation as they swim, arising from chiral asymmetry in hydrodynamic drag or propulsion bending the

150 with negatively charged DMPG, causing strong asymmetry in lipid bilayer.

151 which adhesion complexes maintain front-rear asymmetry in migrating cells.

152 nucleation at the Golgi generates MT network asymmetry in motile vertebrate cells.

153 derstand in greater depth the role of chiral asymmetry in nature inclusive of both earth and space.

154 rization electrical field, which strengthens asymmetry in organic-c-Si heterojunction solar cell thro

155 orphogenetic events that generate anatomical asymmetry in other regions of the digestive tract remain

156 hibits growth at nascent new poles, creating asymmetry in polar growth.

157 variation in visuospatial bias: hemispheric asymmetry in posterior alpha power measured before targe

158 Our findings highlight a possible asymmetry in protein-ligand association by suggesting th

159 change material to achieve a high degree of asymmetry in radiative heat transfer.

160 elt treadmill, which can impose a left-right asymmetry in step lengths.

161 Voltage asymmetry in the binding kinetics indicated that rhodami

162 n U.S. adults and assess the utility of vCDR asymmetry in the diagnosis of glaucoma.

163 Hence, there is an apparent asymmetry in the evolutionary interactions between Inga

164 These findings imply an asymmetry in the geomorphic response of badlands to eros

165 A left-skewed asymmetry in the germination rate with temperature was r

166 hibiting increased carbon uptake due to both asymmetry in the interannual distribution of rainfall (e

167 dy of antimatter, to see if there is a small asymmetry in the laws of physics that govern the two typ

168 Second, asymmetry in the levels of noise variation (expression f

169 try of ring closure but the role of possible asymmetry in the material flow into the growing membrane

170 Notably, there was a hemispheric asymmetry in the MDMR-based MFG findings, with literacy

171 st with recent observations of particle-hole asymmetry in the N=0/N=1 Landau levels of bilayer graphe

172 y N2c target-selection signal; and, finally, asymmetry in the onset time of the subsequent neural evi

173 Asymmetry in the outer membrane has long defined the cel

174 eparatory attention across the visual field; asymmetry in the peak latency of the early N2c target-se

175 cies in timing judgments but reveal a robust asymmetry in the perception and neural coding of synchro

176 The resulting asymmetry in the phonon line shape, conspicuous at low t

177 ole pair excitations can induce a pronounced asymmetry in the phonon line shape, known as the Fano re

178 Whisker-tracking analysis revealed an asymmetry in the position of the whiskers: they oriented

179 ibution of rainfall (extrinsic forcing), and asymmetry in the response of gross primary production (G

180 Such asymmetry in the transport is mainly caused by a Cdc42-

181 The directional asymmetry in the ultrafast laser writing is qualitativel

182 valence of vertical cup-to-disc ratio (vCDR) asymmetry in U.S. adults and assess the utility of vCDR

183 or several breaths and are accompanied by an asymmetry in vibrissa positioning toward the same side o

184 Asymmetry in visual acuity was found in 31% of patients.

185 (right: p=0.512; left: p=0,430) affected the asymmetry in volumes of maxillary sinuses.

186 Associations between the asymmetry index of the 95th percentile and functional, c

187 The asymmetry index of the 95th percentile within individual

188 The asymmetry index of the 95th percentile within the entire

189 The asymmetry index of the 95th percentile within the medio-

190 ral P = 0.02, lenticular P = 0.01) while the asymmetry index of the 95th percentile within the pulvin

191 An asymmetry index was used to compare R2* within the thala

192 asures and gestation corrected age, regional asymmetries, infant sex, as well as newborn growth measu

193 Thus, selfish meiotic drivers exploit the asymmetry inherent in female meiosis to bias their trans

194 t of coupling is controlled by the degree of asymmetry introduced.

195 Left-right (LR) asymmetry is a fundamental feature of internal anatomy,

196 an Dynamics simulations suggest that binding asymmetry is a general feature of reversible gels, arisi

197 Modelling experiments imply that this asymmetry is caused by active conductances expressed in

198 This asymmetry is dynamically averaged through conformational

199 Tip asymmetry is enhanced by curving of ventral elements in

200 Our model predicts that this asymmetry is greatest in the radially-expanding transiti

201 This asymmetry is maintained by the Mla pathway, a six-compon

202 Furthermore, we found that cellular asymmetry is maintained throughout the cell cycle and is

203 Vertical cup-to-disc ratio asymmetry is predictive of prevalent glaucoma, but the P

204 The direction of this asymmetry is the opposite between cancers with mutated p

205 While chemical asymmetry is widely recognized as the cornerstone of cat

206 n result from the physical polarity and size asymmetry itself, as well as the subsequent activation o

207 s are semiconductors with intrinsic in-plane asymmetry, leading to direct electronic bandgaps, distin

208 s are similar, then the proposed microscopic asymmetry leads to effective contraction of random 1D ac

209 uencing' (cap-SMRT-seq) and newly developed 'asymmetry linker-mediated nested PCR walking' (ALN-walki

210 /5 alpha-syn results in progressive forelimb asymmetry, loss of striatal dopaminergic terminal densit

211 ing type: calcifications, asymmetry or focal asymmetry, mass, and architectural distortion.

212 The asymmetry might result from the two MTOCs being in disti

213 Moreover, the direction of strand asymmetry observed in cancers with mutated polymerase de

214 This form of physical asymmetry occurs in several metazoan cells, but the unde

215 al techniques to search for generalities and asymmetries of aboveground NPP (ANPP) and belowground NP

216 Suture interval asymmetry of >2 mm (OR, 3.18; 95% CI, 1.31-7.70; P = 0.0

217 Using the inherent geometrical asymmetry of a conically shaped nanopore, we examine how

218 the kinetics of SPB maturation, control the asymmetry of astral microtubule organization between the

219 voltage rectification of gap junctions on an asymmetry of cell-to-cell signaling.

220 al SemiSWEET, which potentially explains the asymmetry of eukaryotic SWEETs.

221 HXMS reveals a dynamic asymmetry of flexible and ordered regions common to both

222 Skewness (asymmetry of gray-level pixel distribution), kurtosis (p

223 the origin and multiple components of mirror asymmetry of individual NPs and their assemblies.

224 n upper and lower boundaries of Ag layer and asymmetry of LA and TA phonons propagation through inter

225 Neurally, looming bias was reflected in an asymmetry of late event-related potentials associated wi

226 in the analysis of forward-backward angular asymmetry of low energy electron emission.

227 Deletion of the plpA gene abolishes the asymmetry of MglA localization, increases the frequency

228 Given the physical asymmetry of mycobacteria, the models that describe coor

229 fer mechanisms between MI and IM interfaces: asymmetry of plasmon-polariton interactions on upper and

230 perconducting LSCO (x = 0.35) film, the spin asymmetry of reflectivity shows a very small static magn

231 romoters within such pairs revealed emerging asymmetry of regulatory elements.

232 sponsible for initiating and maintaining the asymmetry of ring closure but the role of possible asymm

233 Asymmetry of Scx-mutant callus was not due to muscle unl

234 The interhemispheric asymmetry of sleep depth associated with the FNE was fou

235 Here, we characterize the transmembrane asymmetry of small unilamellar liposomes consisting of z

236 The key element is a pronounced asymmetry of surface hopping energies-that is, a kinetic

237 Specifically, we found that the functional asymmetry of the ACx (tonotopy and isofrequency axes) is

238 y, or curvature-inducing agent, or intrinsic asymmetry of the bilayer; it is solely driven by the lar

239 guiding the establishment of the left-right asymmetry of the body in the vertebrate left-right organ

240 criteria (vertical cup-to-disc ratio >/=0.6, asymmetry of the cup-to-disc ratio >/=0.2 between eyes,

241 Steering can be achieved by varying the asymmetry of the distal part of the ovipositor by protra

242 We assume that the asymmetry of the Ft-Ds bond distribution around the cell

243 ion in non-magnetic solids is induced by the asymmetry of the global crystal space group has limited

244 The asymmetry of the interface approximately doubles the siz

245 , and recaptures the experimentally observed asymmetry of the intermediate aperture shapes during clo

246 ariant and T2D or glycemia and highlight the asymmetry of the LDL-C-T2D relationship and/or the gene/

247 that these cancers demonstrate a substantial asymmetry of the mutations between the leading and the l

248 listic rotation was observed with increasing asymmetry of the nanoparticle morphology.

249 theoretically according to the morphological asymmetry of the nanoparticles.

250 leuronectiformes), which display substantial asymmetry of the olfactory organs and forebrain.

251 m of three Gaussian curves suggests that the asymmetry of the three ATPase-dependent 120 degrees powe

252 The asymmetry of the trion PL peak and resulting peak red-sh

253 lse front tilt gives rise to the directional asymmetry of the ultrafast laser writing.

254 The specification of left-right asymmetry of the visceral organs is precisely regulated.

255 rial membrane, preserving the characteristic asymmetry of these membranes.

256 Second, the asymmetry of venous drainage in the pathological cerebra

257 PS asymmetry on the plasma membrane depends on the activiti

258 d according to finding type: calcifications, asymmetry or focal asymmetry, mass, and architectural di

259 .001) and decreased recall examinations for asymmetries (P </= .001).

260 y reading (p = .04), and the index of height asymmetry (p = .014).

261 Asymmetry parameters, distributions of the sum of the tw

262 In response to this asymmetry, participants gradually adjust their foot plac

263 phery defines the polarization, with greater asymmetry promoting cell proliferation.

264 anatomy, yet the emergence of morphological asymmetry remains one of the least understood phases of

265 er an active mechanism is necessary for this asymmetry remains unsolved.

266 Moreover, dimer asymmetry sets up differential hydrolysis rates for each

267 Vertical cup-to-disc ratio asymmetry should initiate a more comprehensive glaucoma

268 in the symmetry-breaking step of left-right asymmetry specification.

269 We demonstrated that such asymmetry strongly depends on junctional conductance and

270 al Poschl-Teller potential which contains an asymmetry term.

271 Multiple factors contribute to the asymmetry that include 5f electrons being present in mic

272 n the anterior temporal lobe with a leftward asymmetry that was not observed in healthy controls.

273 his contractility must rely on a microscopic asymmetry, the precise mechanism of which is not complet

274 of energetic cost associated with a range of asymmetries to determine whether symmetry is the energet

275 The ability to use asymmetry to operate molecular-level machines or macrosc

276 determinant in organizing microtubule aster asymmetry to power nuclear dynein-dependent separation.

277 gs reveal that H1 imparts a strong degree of asymmetry to the nucleosome, which is likely to influenc

278 This asymmetry, unobserved in other Hsp90 homologs, is due to

279 size and intervention effects on funnel plot asymmetry, using empirical datasets and illustrative sim

280 (3) A description of peak asymmetry via leading/trailing half-widths vs relative h

281 Each 0.10 increase in vCDR asymmetry was associated with a 2.57 times higher adjust

282 ide of space ipsilateral to TN, and (2) this asymmetry was consequent to an increased estimated poten

283 ON stimulation, forelimb asymmetry was exacerbated, indicating alpha-syn overexpr

284 sidues to proline, functional and structural asymmetry was observed.

285 o examine why bacteria evolved deterministic asymmetry, we modeled the effect of damage anchored to t

286 To uncover the origins of asymmetry, we performed molecular dynamics simulations o

287 n six diverse fitness measures (ulna length, asymmetry, weight-at-weaning, testes volume, reproductiv

288 These gene expression asymmetries were epigenetically regulated by miRNA expre

289 , which affects how J-RGCs sample space; (3) asymmetry, which contributes to direction-selectivity; (

290 hanism for transcription-associated mutation asymmetry, which is frequently observed in human cancers

291 lipid flippases that regulate lipid membrane asymmetry, which is important for vesicle formation.

292 We conclude that this asymmetry, which is supported by molecular docking studi

293 ydrolysis, the dimer undergoes a flip in the asymmetry while remaining in a closed state for the seco

294 gs in zebrafish; southpaw directs left-right asymmetries, while squint and cyclops function earlier t

295 Ignoring the trion asymmetry will result in over estimating the trion bindi

296 Then, asymmetry with depth and follicular diffusion are studie

297 in receptive field size and degree of ON-OFF asymmetry with IPL depth.

298 This asymmetry, with lipopolysaccharide (LPS) or lipooligosac

299 e defining characteristic of the OM is lipid asymmetry, with phospholipids comprising the inner leafl

300 consequently, the strength of the rotational asymmetry within the CH2D group.