ライフサイエンスコーパス: asymmetry

1 all biological membranes is a distinct lipid asymmetry.

2 flip-flop of lipids and thus "scramble" this asymmetry.

3 es stemming from their inherent out-of-plane asymmetry.

4 t role in shaping the energetic cost of gait asymmetry.

5 d KCNQ1 have been implicated in establishing asymmetry.

6 after lipid exchange and after scrambling of asymmetry.

7 onstrated by their better perception of gait asymmetry.

8 lar and anatomical defects in the left-right asymmetry.

9 articularly for drug permeation and membrane asymmetry.

10 ernal structural symmetry that show sequence asymmetry.

11 Pelvic vestiges also showed left-side larger asymmetry.

12 ctors that define cellular and organismal LR asymmetry.

13 nded brain representations, termed the alpha asymmetry.

14 (k (1) = 11 s(-1)) without apparent kinetic asymmetry.

15 t role in shaping the energetic cost of gait asymmetry.

16 used to help establish the origin of chiral asymmetry.

17 conductor nanowire with precisely engineered asymmetry.

18 insulator-metal transition show a pronounced asymmetry.

19 propagation and a stronger inter-hemispheric asymmetry.

20 both significant directional and fluctuating asymmetry.

21 ry valuable tool to study functions of lipid asymmetry.

22 unilamellar liposomes showing a stable lipid asymmetry.

23 otential biological response to diel warming asymmetry.

24 ll cycle delay is sufficient to disrupt Ace2 asymmetry.

25 ed by a divergent response of LAI to warming asymmetry.

26 ficient to drive population-level behavioral asymmetries.

27 language experience shape speech processing asymmetries.

28 t this was not the case for population-level asymmetries.

29 tually exclusive mechanisms may explain this asymmetry: 1) Higher dispersal rate of North American ma

30 n of irregular ring shapes (21%) and disease asymmetry (23%) in comparison to other modes of inherita

31 erstand the establishment of left-right (LR) asymmetry, a limiting factor is that most animals are or

32 les as effectors of membrane and cytoplasmic asymmetry across fungi and animals.

33 lecular knot transmits information regarding asymmetry across length scales, from Euclidean point chi

34 of the NE and suggest ways to generate lipid asymmetry across the NE despite its direct continuity wi

35 We evaluated the vertical asymmetry across the temporal raphe of the deep retinal

36 etaphase delay is sufficient to disrupt Ace2 asymmetry after release, and that Ace2 asymmetry is rest

37 g differential stress, but not compositional asymmetry alone, can increase the bending modulus.

38 Asymmetry also induces distinct inter-subunit interactio

39 We have investigated whether such asymmetry also occurs in reconstitution assays with the

40 However, asymmetry among sub-structures is fundamentally importan

41 left-Handers (LH)) of language task-induced asymmetries and intrinsic connectivity strength of the s

42 owever, the mechanisms regulating centrosome asymmetry and biased centrosome segregation are unclear.

43 (2019) utilize neurofeedback to train alpha asymmetry and causally impact measures of spatial attent

44 re mechanism for the biogenesis of molecular asymmetry and cell polarity.

45 ses distinctive features, including cellular asymmetry and differentiation during the cell cycle.

46 Asymmetry and distorsion of the foveal avascular zone we

47 ream determinant linking SPB age, functional asymmetry and fate.

48 nts, we characterize the degree of inter-eye asymmetry and frequency of irregular hyperAF ring morpho

49 Nevertheless, both asymmetry and irregular ring morphologies are also obser

50 had the highest proportions of both disease asymmetry and irregular ring morphology.

51 This model shows the importance of initial asymmetry and its reinforcement by mechanical feedback w

52 ive decomposition of water and fat with echo asymmetry and least-squares estimation (IDEAL) technique

53 During early divisions, furrow ingression asymmetry and midbody inheritance is consistent, suggest

54 The assay preserved endosomal membrane asymmetry and protein composition, providing a platform

55 for normal development, including left-right asymmetry and renal tissue homeostasis.

56 uter-leaflet lipid, 4) verification of lipid asymmetry and stability, and 5) determination of protein

57 dy we characterized the effects of step time asymmetry and step length asymmetry on energy cost durin

58 m s(-1) while a range of values of step time asymmetry and step length asymmetry were enforced.

59 Hemispheric asymmetry and symptom lateralization in PD is linked to

60 novel decision-making task with both reward asymmetry and temporal uncertainty.

61 Funnel plot asymmetry and trim-and-fill revealed a clear publication

62 The relationship between spatiotemporal gait asymmetry and walking energetics is currently under deba

63 This lipid asymmetry, and in particular the exclusion of phospholip

64 , central keratoconus index, index of height asymmetry, and index of height decentration differed bet

65 l autoregulation and cerebral autoregulation asymmetry, and poor long-term clinical outcomes in acute

66 ns between language lateralization and motor asymmetries are much weaker than previously assumed with

67 These asymmetries are well captured by a simple model for the

68 As such, mechanisms involved in lipid asymmetry are fundamental to our understanding of OM lip

69 Other contributions to the link-usage asymmetry are instead, as we show, self-organized in nat

70 Some of these cases of "link-usage asymmetry" are local in nature and can be mechanisticall

71 SOT are identified, i.e., the lateral Pt-Co asymmetry as well as out-of-plane injected spin currents

72 Notch regulates this asymmetry, as when inhibited, symmetric divisions produc

73 earchers for decades due to their pronounced asymmetries at the population level.

74 anioplasty is the only option to correct the asymmetry at the skull in LC.

75 MRI in 19 patients did not reveal consistent asymmetries between hemispheres or regions.

76 ctions can induce an alignment of behavioral asymmetries between individuals (i.e., population-level

77 Such ideological asymmetries between left- and right-wing activism hold c

78 idget and parasol ganglion cells, consistent asymmetries between their ON and OFF types (that signal

79 ver resolution was observed, consistent with asymmetry between DNA ends in earlier intermediates.

80 fin web, and unexpectedly, the evolution of asymmetry between dorsal and ventral hemitrichia.

81 There was a small but significant asymmetry between left and right iliopsoas muscle volume

82 fic endosperm defects; second, the extent of asymmetry between reciprocal F1 seed size is correlated

83 Asymmetry between right and left eyes was present (media

84 rent pulling velocities and variable tension asymmetry between the inner and outer membrane leaflets.

85 adus, an icy moon of Saturn, exhibits strong asymmetry between the northern and southern hemispheres,

86 ively well, the majority still simulates its asymmetry between warm (El Nino) and cold (La Nina) phas

87 p = 0.05 pineal) and cerebral autoregulation asymmetry (both p < 0.001).

88 al processes, complicating the use of chiral asymmetry by itself as a definitive biosignature.

89 nt detergent removal, 3) generation of lipid asymmetry by partial exchange of outer-leaflet lipid, 4)

90 epigenetic patterns involved in hemispheric asymmetry by profiling DNA methylation in isolated prefr

91 Cells ensure this asymmetry by regulating the biogenesis of lipid A, the c

92 e Mla pathway maintains outer membrane lipid asymmetry by transporting phospholipids between the inne

93 We also show that assessment of joint asymmetry can reveal significant differences between ind

94 Most striking is the asymmetry caused by the absence of the second cyclic nuc

95 lysis of the muscle alone can resolve breast asymmetry, corroborating that muscle is a key contributo

96 er some conditions in vivo the loss of lipid asymmetry could trigger ordered domain formation.

97 e system into polyhedra of increasing volume asymmetry delays the onset of macroscopic phase separati

98 The magnitude of asymmetry depends on network features such as network si

99 We found that a comparable alpha asymmetry developed over the visual cortex.

100 Moreover, the strength of individual-level asymmetries differed between strains, but this was not t

101 This asymmetry directs McrC binding so that it engages a sing

102 We found that MAKR2 is required for the PIN2 asymmetry during gravitropism by acting as a negative re

103 o cooperative interactions with severe power asymmetries (e.g., the cleaner-client fish mutualism [9]

104 We found that structural asymmetry (e.g. 5- or 2-nt overhang) has no impact on ac

105 levels of auditory processing, a hemispheric asymmetry emerged, with delta and beta band (3/15 Hz) re

106 st animals are ordinarily invariant in their asymmetry, except when manipulated or mutated.

107 briefly surveys evidence showing that clear asymmetries exist within the temporal lobe structures su

108 petent conformation, leading to a structural asymmetry explaining the low nucleation efficiency of pu

109 showing the highest functional connectivity asymmetry (FCA).

110 s model has anticipated analogous centrosome asymmetries featured in self-renewing stem cell division

111 JC templates IgA oligomerization and imparts asymmetry for pIgR binding and transcytosis.

112 Our objective was to assess gait asymmetry (GA) and bilateral coordination of gait (BCG),

113 Their intrinsic asymmetry gives rise to a variety of interesting propert

114 n individuals drives alignment of behavioral asymmetries, greater alignment at the population-level s

115 Consequently, asymmetry has been attributed to account for the added e

116 by Abeta small-animal PET and tested if such asymmetries have an association with microglial activati

117 n only the top four predictive features (CI, asymmetry, hyperchromatism, and cytologic atypia) outper

118 How lipid asymmetry impacts ordered lipid domain (raft) formation

119 Therefore, we investigated Abeta asymmetries in Abeta mouse models examined by Abeta smal

120 Hemispheric asymmetries in ADC maturation ages were assessed using t

121 A functional perspective helps explain asymmetries in blame and praise: we propose that while b

122 ituations in which there are adviser-advisee asymmetries in expertise.

123 ntexts we measured individual and population asymmetries in individual behaviors (circling asymmetry,

124 or system that commands left-right locomotor asymmetries in mammals.

125 Intriguingly, our results revealed distinct asymmetries in morphology of the labial and lingual side

126 Asymmetries in motor behavior, such as human hand prefer

127 cross the retinal surface corresponding with asymmetries in the statistics of natural visual space an

128 pact angle and direction can be diagnosed by asymmetries in the subsurface structure of the Chicxulub

129 iations across various language task-induced asymmetries in this group.

130 We show that the stroke-induced asymmetry in a sensorimotor (cylinder) test is reversed

131 ults define the neuronal substrate for motor asymmetry in a vertebrate and support the idea that hapl

132 result supports current models of prefrontal asymmetry in affect, and lays the groundwork for further

133 he T and V liposomes, we observed a striking asymmetry in both lipid and content mixing stimulated by

134 anzee brain, as well as, a general rightward asymmetry in brain regions.

135 ated [CO(2)], meaning insect herbivory drove asymmetry in carbon for nutrient exchange between symbio

136 radigm for the generation and maintenance of asymmetry in cell membranes.

137 ompletely or almost completely suppressed by asymmetry in cholesterol-containing SM+POPC outside/POPC

138 ally, there was no statistically significant asymmetry in correct grading using SS-OCTA and FA.

139 In neurons of PD patients, hemispheric asymmetry in DNA methylation is greater than in controls

140 urons of different modules displayed a clear asymmetry in favor of connections from faster to slower

141 invertebrate traces [8], and even behavioral asymmetry in fossil non-human primates [9, 10].

142 indings support the hypothesis that vertical asymmetry in global processing is a 3-D (not a 2-D) phen

143 e test a novel hypothesis that this vertical asymmetry in global processing is a 3-D phenomenon assoc

144 canner, we found that the extent of vertical asymmetry in global visual processing in human subjects

145 According to this hypothesis, the asymmetry in global visual processing is a 3-D (rather t

146 le neural mechanisms underlying the vertical asymmetry in global visual processing.

147 n reciprocal F1 seed size is correlated with asymmetry in HSI; and third, inferred differences in the

148 propose that the establishment of centriole asymmetry in mitosis primes biased interphase MTOC activ

149 mutations in nucleosomes shows the opposite asymmetry in NER-proficient skin cancers, but not in NER

150 Hemispheric asymmetry in neuronal DNA methylation patterns is largel

151 long disease course have greater hemispheric asymmetry in neuronal epigenomes than those with a short

152 With aging, there is a loss of hemispheric asymmetry in neuronal epigenomes, such that hemispheres

153 Hemispheric asymmetry in neuronal processes is a fundamental feature

154 g from the nontumor hemisphere may attenuate asymmetry in patients with tumors near ipsilateral hand

155 We also observed a dorsoventral asymmetry in photoreceptor density, with greater density

156 In rare instances, paleontologists can infer asymmetry in predatory or foraging behavior, including p

157 This asymmetry in R-loop structure may explain the uniformity

158 he original double-strand break repair model-asymmetry in recombination intermediates and D-loop migr

159 e TF gene and its target genes have inherent asymmetry in regulation, even when their promoters are i

160 y formed by finger-like extensions generates asymmetry in stem cell divisions.

161 cs, but it remains unclear why people reduce asymmetry in step lengths, but prefer asymmetry in step

162 Here, we assessed how preferred asymmetry in step times and step lengths of healthy huma

163 reduce asymmetry in step lengths, but prefer asymmetry in step times.

164 ce of expected substrate- and oxygen-induced asymmetry in the anodic-to-cathodic charge ratio.

165 We discuss the asymmetry in the context of magnetospheric current and v

166 A small north-south asymmetry in the dayside auroral energy flux was identif

167 Based on near-complete asymmetry in the directionality of hybridization and dec

168 gs: First, there is a transcriptional strand asymmetry in the distribution of mononucleotide repeat t

169 ment relies on conserved factors that induce asymmetry in the early embryo.

170 ase, thereby establishing anterior-posterior asymmetry in the handplate.

171 Infinitesimal asymmetry in the ice shell thickness due to random pertu

172 In contrast, an asymmetry in the occupancy is induced by anisotropic sha

173 often occur at particular times of day, any asymmetry in the rate of change between the daytime and

174 studies with yeast vacuolar SNAREs uncovered asymmetry in the results of lipid mixing assays.

175 in interaction networks, and find a striking asymmetry in the roles of activating and deactivating pr

176 ted polarity crescent defined by BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) and BREVIS RADI

177 ssue cell polarity protein BASL (BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE) in the simplifying co

178 this work, we show that there is significant asymmetry in the summer-time temperature response of ele

179 s reveal that [Formula: see text] induces an asymmetry in the transport cycle based on the following

180 g establishment and regulation of epigenetic asymmetry in the zygote remains obscure.

181 nergy of the photoelectrons and introduce an asymmetry in their emission direction, at variance with

182 We found that preferred step time asymmetry increased with greater speed differences while

183 Both the optimal and preferred step time asymmetry increased with greater speed differences, whil

184 tient cells, accompanied by replication fork asymmetry, increased interorigin distances, replication

185 The asymmetry index (AI) was calculated between tracer uptak

186 We used an asymmetry index (AI) where positive AI indicates a great

187 , such as a newly introduced length-weighted asymmetry index and the global segment-length distributi

188 xpected effects on individual and population asymmetries: individual-level asymmetries were strong an

189 ation times due to the electron spin spatial asymmetry induced by chemical bond polarization involvin

190 When we incorporate this asymmetry into integral projection models, the predicted

191 Regulation of membrane asymmetry is a fundamental characteristic of membrane bi

192 dmill walking and tested the hypothesis that asymmetry is adapted to optimize metabolic energy cost.

193 cs (MD) simulations, we discovered that this asymmetry is already present in the wild-type (WT) RIIbe

194 at the fin tip analogous to a fleshy "palm." Asymmetry is also observed in cross-sectional areas of d

195 This asymmetry is also present during syllables presentation,

196 e the main current carrier, this north-south asymmetry is consistent with the previous finding that l

197 n modes of the x = 0.34 compound reveals the asymmetry is enhanced in the antiferromagnetic state.

198 ides strong support for models in which this asymmetry is established early in the embryo.

199 nduction of conformational and thermodynamic asymmetry is expected to affect the pathways leading to

200 How allelic asymmetry is generated remains a major unsolved problem

201 ate models, we here show that simulated ENSO asymmetry is largely proportional to subsurface nonlinea

202 h an artefact may inadvertently arise if NCP asymmetry is lost during image processing.

203 A detailed description of this functional asymmetry is missing, and the underlying models are wide

204 However, the emergence of asymmetry is not inevitable.

205 tterns, frequency-specific inter-hemispheric asymmetry is one major feature of meditation, and that m

206 Ace2 asymmetry after release, and that Ace2 asymmetry is restored after cytokinesis.

207 index of surface variance, index of vertical asymmetry, keratoconus index, central keratoconus index,

208 cifically, we explore the link between power asymmetry, lay theories of peace, and preference for con

209 ative to the excitatory input, and that this asymmetry leads to the timing difference.

210 and lateral (D1 versus D2 branch) excitation asymmetry, making Chl(D1) the chromophore with the lowes

211 ce-evolution model, we demonstrate that this asymmetry may form spontaneously, without any noticeable

212 This asymmetry may link to the intrinsic allosteric regulatio

213 One such mechanism, the Maintenance of lipid asymmetry (Mla) pathway has been proposed to extract mis

214 Magnetic transfer ratio asymmetry (MTR(asym)) at 3.0 ppm was used as the pH-sens

215 e then detail how bacteria regulate OM lipid asymmetry, negative membrane curvature, and the phosphol

216 e of nucleosomes, consistent with the repair asymmetry observed in yeast nucleosomes.

217 Results: Relevant asymmetries of Abeta deposition were identified in at le

218 Asymmetries of amyloid-beta (Abeta) burden are well know

219 TEMENT The principles underlying hemispheric asymmetries of auditory speech processing remain debated

220 be understood, the mechanisms that shape the asymmetries of individual organs remain less clear.

221 In regions that showed warming asymmetry of >0.5 degrees C (equivalent to mean surface

222 d 95.8% of participants showed resting pupil asymmetry of <=0.5 mm and <= 1.0 mm, respectively.

223 irst, we introduce a measure to quantify the asymmetry of a community's feasibility domain using the

224 scrambling of liposomes mimicking the charge asymmetry of bacterial membranes with 20 mol % of 1-palm

225 hosphatidylglycerol (PG), mimicking this key asymmetry of bacterial membranes.

226 The functional roles of the lipid asymmetry of biomembranes are attracting increasing atte

227 oduce molecular multipole moments and charge asymmetry of full-length antibodies instead of only loca

228 nd, there is a strong transcriptional strand asymmetry of indels across 2,575 whole genome sequenced

229 gent-based protocol for scrambling the lipid asymmetry of liposomes and maybe cells without compromis

230 Concomitant asymmetry of microglial activation indicates a neuroinfl

231 Here, we investigated the asymmetry of motor contributions to auditory speech proc

232 n the listener's native language affects the asymmetry of motor influences on auditory speech discrim

233 ne whose deletion generates left-side larger asymmetry of pelvic vestiges in extant, closely related

234 NUS appears to be influenced by the negative asymmetry of precipitation anomalies.

235 The asymmetry of processing of speech sounds is affected by

236 ralized top-down motor influences can affect asymmetry of speech processing in the auditory system.

237 n of a "four-lane" swimming pattern with the asymmetry of the cell distribution of up to 40%.

238 We show that as the asymmetry of the feasibility domain increases the relati

239 Altogether, the asymmetry of the interchange was not due to higher origi

240 which allowed us to characterize hemispheric asymmetry of the other functions and compare their funct

241 ge excitations for the conspicuous lineshape asymmetry of the x = 0.34 compound.

242 rinciple to control over ultra-large optical asymmetry on a wider scope of chiral materials.

243 fects of step time asymmetry and step length asymmetry on energy cost during steady-state walking on

244 However, the influence of membrane asymmetry on proteins is poorly understood, and novel as

245 US for the different products, with negative asymmetries over the Great Plains and positive asymmetri

246 ymmetries over the Great Plains and positive asymmetries over the southwestern CONUS.

247 We propose a new set of generalized asymmetry parameters which are sensitive to interference

248 in a single quantum state via anisotropy and asymmetry parameters.

249 e find that intrinsic differences in the Wnt asymmetry pathway already exist between seam cells at 20

250 symmetrization occurs via changes in the Wnt asymmetry pathway, leading to aberrant Wnt target activa

251 energy reduction and suggest that step time asymmetry plays a dominant role in shaping the energetic

252 energy reduction and suggest that step time asymmetry plays a dominant role in shaping the energetic

253 fore, better simulating the dynamics of ENSO asymmetry potentially reduces uncertainty in future proj

254 iction can help address emergent information asymmetry problems and in doing so improve price efficie

255 In-cell data suggest that asymmetry promotes synaptic complex formation, and modif

256 peed differences while preferred step length asymmetry remained constant and nearly symmetric.

257 Despite this asymmetry, resident immune cells in the liver are consid

258 The general tendency of dominant negative asymmetry response for ecosystem productivity across the

259 This asymmetry resulted from complex 3D spirals and vaginal f

260 subregion showing the highest reward-related asymmetry (RRA) overlapped with the region showing the h

261 thermodynamics-inspired method, "disassembly asymmetry score classification (DASC)", that resolves AC

262 Perturbations to OM lipid asymmetry sensitize the cell to antibiotics.

263 Flat keratometry, inferior-superior dioptric asymmetry, skewed radial axis, logarithm of keratoconus

264 ontaneously, without any noticeable a priori asymmetry (such as a giant impact or a monopole structur

265 This asymmetry suggests that higher-order cognitive and neura

266 osely approximated magnitudes of step length asymmetry that are observed in clinical populations.

267 2D bilayer nanosheets due to the structural asymmetry that arises from heteromeric self-association.

268 ar genome, giving rise to an extreme genomic asymmetry that is ancestral to all extant eukaryotes.

269 Because of this asymmetry, the net-negative charge at the inner leaflet

270 at warmer temperatures show relatively more asymmetry; thus, the idiosyncrasy of responses is higher

271 ge keratoconus/ in variables of the vertical asymmetry to 90 degrees and the central corneal thicknes

272 increased their preferred value of step time asymmetry to coincide with the lowest energy cost.

273 copolymers with insufficient conformational asymmetry to form Frank-Kasper phases in the neat-melt s

274 ectural distortions (15 malignant), and five asymmetries (two malignant).

275 The observed asymmetry, very small in the unperturbed state, expands

276 This vertical asymmetry was absent in 0 g.

277 Asymmetry was also not apparent under hindering or assis

278 Asymmetry was associated with higher variance of tracer

279 The absolute magnitude of this asymmetry was greater in CPs relative to HSs.

280 DaT asymmetry was greater in the PD group than other groups.

281 Asymmetry was introduced by partial, outside-only exchan

282 our results show that preferred step length asymmetry was not optimal even with extensive experience

283 However, no such asymmetry was observed in assays performed in the presen

284 This asymmetry was observed in cones and rods, but it was mor

285 ucer, polydiacetylene (PDA) with high chiral asymmetry was obtained from achiral diacetylene monomers

286 Lipid asymmetry was stable for more than 7 days at 23 degrees

287 on with other individuals affects behavioral asymmetries, we systematically manipulated the social en

288 c and amygdala processes exhibit hemispheric asymmetry, we investigated changes in synaptic plasticit

289 Furthermore, the two types of asymmetries were found to be significantly correlated ac

290 d by the social context but population-level asymmetries were mild or absent.

291 and population asymmetries: individual-level asymmetries were strong and modulated by the social cont

292 and interhemispheric cerebral autoregulation asymmetry were assessed using mixed random effects model

293 alues of step time asymmetry and step length asymmetry were enforced.

294 cluded that reconstitution and generation of asymmetry were successful.

295 ell communities are maintained by population asymmetry, where stochastic behaviors of multiple indivi

296 evergreen forests show a persistent positive asymmetry, whilst (natural) grasslands appear to have tr

297 symmetries in individual behaviors (circling asymmetry, wing use) and dyadic behaviors (relative posi

298 hock adduction, suggesting greater movement asymmetry with an increase in the back slope (n = 30).

299 Results indicate disease asymmetry with slightly worse vision and more advanced d

300 (heterotypic) types of cells, with a marked asymmetry within heterotypic pairs.