ライフサイエンスコーパス: one another

1 kinematic errors associated with each oppose one another.

2 s over time that make them incompatible with one another.

3 bon makeup, the polymers are immiscible with one another.

4 competing visual locations actively suppress one another.

5 but the clinical groups did not differ from one another.

6 mining if these features were independent of one another.

7 G-quartet disks, which are stacked on top of one another.

8 ting behavior and disease dynamics influence one another.

9 w studies have investigated how these affect one another.

10 ly from low frequency and track tightly with one another.

11 sults have, at times, been inconsistent with one another.

12 ce on the client and their merit relative to one another.

13 influence biofilm formation independently of one another.

14 ts 2 and 3 were unrelated and divergent from one another.

15 urity profiles that differentiated them from one another.

16 ns that only fluoresce on complementing with one another.

17 on, sticking to one another, or walking past one another.

18 en presented regarding their relationship to one another.

19 y states that are readily discriminated from one another.

20 tic populations were most closely related to one another.

21 d AtxA2 are 79% identical and 91% similar to one another.

22 ckly in full sun until they begin to overtop one another.

23 atalysts that complement rather than inhibit one another.

24 mbly on membranes are thus interdependent on one another.

25 etically manipulate cells that interact with one another.

26 ysis results that are difficult to relate to one another.

27 representations of similar events apart from one another.

28 f pairs of fluorine atoms which are ortho to one another.

29 an be difficult when individuals differ from one another.

30 ent combinations intensities were similar to one another.

31 l behavior, many of these studies contradict one another.

32 ms depend on how nation states interact with one another.

33 arranged to immediately become calibrated to one another.

34 y, low variability, and close agreement with one another.

35 whose members cooperate preferentially with one another.

36 the measurements were highly correlated with one another.

37 pair can be regarded as pseudo-replicates of one another.

38 ve social image or do so in combination with one another.

39 h all four 4-bromophenyl substituents cis to one another.

40 ther the competing events are independent of one another.

41 performed by braiding isolated modes around one another.

42 and by a similar extent, in the presence of one another.

43 cithal eggs but have uncertain affinities to one another.

44 lated forms of the MAPK act in opposition to one another.

45 l response patterns which were distinct from one another.

46 species, gametes have to find and recognize one another.

47 otential energy surface before reacting with one another.

48 UL133/8 locus, but are largely distinct from one another.

49 approaches, and these are rarely compared to one another.

50 iral NP and GPC open reading frames replaced one another.

51 atypical depression seem to be antithesis of one another.

52 ter-than-average DNA-level correspondence to one another.

53 from cues that are temporally displaced from one another.

54 ug nystatin are frequently incompatible with one another.

55 l, since all components eventually influence one another.

56 amic positioning of the two ends relative to one another.

57 3 and is required for their association with one another.

58 processes so far considered independent from one another.

59 anetesimals to gravitationally interact with one another.

60 26a isoforms can functionally compensate for one another.

61 Transition dipole moments are orthogonal to one another.

62 ions and how functional terms are related to one another.

63 13 (D/660), which frequently reassorted with one another.

64 r the curve of 0.95 and subtypes of APS from one another.

65 ated effects that may occur independently of one another.

66 non-native plant species are compatible with one another.

67 transparent BNNSs that partially overlapped one another.

68 hen both partners show mutual preference for one another.

69 BON tuning curves are highly correlated with one another.

70 ce of creatinine-based models was similar to one another.

71 ly comparing different interventions against one another.

72 and thermosalience are quite independent of one another.

73 hen sarcomeres are staggered with respect to one another.

74 schemes are independent and do not preclude one another.

75 evaluated their performance in concert with one another.

76 retromer and ESCRT microdomains to regulate one another.

77 registered and functionally integrated with one another.

78 Proteins share similar segments with one another.

79 s with multiple mediators that may depend on one another.

80 not-yet-developed) principles conflict with one another.

81 , and plasma PINP were mutually adjusted for one another.

82 w neurons in those circuits are connected to one another.

83 behavior are actually powerful regulators of one another.

84 s in reward and threat processing potentiate one another.

85 that share components can be insulated from one another.

86 iptional profiles that distinguish them from one another.

87 oups of neurons interact to communicate with one another.

88 elation (r=-0.17; P=0.003) was found between one another.

89 any transcripts only slightly differing from one another.

90 wnregulating efficacies generally paralleled one another.

91 attern and case presentations within 24 h of one another.

92 rom controls ranged from 0.86-0.97; and from one another, 0.75-0.92.

93 cal features of a stimulus can interact with one another [1,2], as when larger stimuli are perceived

94 l properties rendering their separation from one another a challenge of fundamental chemical and glob

95 whereby analysts and decision-makers educate one another about their respective needs and capabilitie

96 e estimates within these areas interact with one another according to their temporal scaling.

97 ks, where familiar individuals can encounter one another after long periods of separation.

98 -1 and MV4-11 could stimulate them to target one another after the addition of daratumumab.

99 penetrance did not significantly differ from one another; ALS cases exhibited earlier age of onset th

100 ; "figure-like" stimuli are coded similar to one another and "ground-like" stimuli are encoded differ

101 70-physically and functionally interact with one another and a subset of NPC components (nucleoporins

102 which CD33 genetics in AD and AML can inform one another and advance human disease therapy.

103 the SCNPs into close spatial proximity with one another and allowing their dynamic covalent crosslin

104 urons, rarely form synaptic connections with one another and are unlikely to contribute to broad inte

105 ll result when skilled practitioners support one another and ascribe to a service philosophy of care.

106 e continuously recalibrated independently of one another and corrections can occur in opposite direct

107 alysis methods were strongly correlated with one another and displayed similar ability to predict imp

108 trongly suggesting that converging CMGs pass one another and dissociate from double-stranded DNA.

109 der to function, proteins frequently bind to one another and form 3D assemblies.

110 Other transitions were simultaneous with one another and had zero-length lags, such as snowpack d

111 , related pathways are spatially proximal to one another and housekeeping-genes tend to be proximal t

112 ural and genetic evolution can interact with one another and influence both transmission and selectio

113 e layers of organization form, interact with one another and influence genome function.

114 tes because they are structurally similar to one another and lack diversity in terms of functional gr

115 Mitofusin proteins are highly diverged from one another and lack strong sequence similarity.

116 e steps that allow mitochondria to attach to one another and merge their outer membranes are unknown.

117 rming tetraspanin-enriched microdomains with one another and other surface molecules.

118 These alternate DL units are related to one another and presented here.

119 -binding head to the membrane repel or crowd one another and regulate conformational equilibria in fa

120 ious aspects of metabolism, may be linked to one another and require protein farnesylation.

121 These proteins bind one another and shape the tubular endoplasmic reticulum

122 patterns were both highly discriminable from one another and similar among people, suggesting consist

123 loop and supporting loop are packed against one another and stabilized by monomer-monomer interactio

124 other bacteria, in an attempt to outcompete one another and survive.

125 When two devices are patterned next to one another and the first one gated through an electroly

126 stry, (2) characterize their relationship to one another and to other Arctic breeds, and (3) estimate

127 CRMP-1 and EVL bind to one another and together accelerate actin filament barbe

128 rtilize and irrigate their crops, connect to one another and travel around the world.

129 d receptors that interact promiscuously with one another and typically appear in combinations.

130 roposed, how these mechanisms are related to one another and which one is dominant for a given tumor-

131 We show that cortex glia tile with one another and with astrocytes to establish unique cent

132 ke the comparison of ion channel models with one another and with experimental data difficult.

133 and lubrication scores were correlated with one another and with potential confounding factors.

134 ution and of the interactions of humans with one another and with their environment.

135 ly control the position of cells relative to one another and within larger cellular assemblies will e

136 en occur in a mutually exclusive manner with one another and, in aggregate, account for the most freq

137 ng, all nonhydrogen atoms were distinct from one another, and allowed an unprecedented level of under

138 to P. leei and P. lifesoni than they are to one another, and contains unique features, including an

139 easy discrimination of these mismatches from one another, and from a fully complementary duplex that

140 Here, we show that Pols IV and V differ from one another, and Pol II, in nucleotide incorporation rat

141 n of these structural components relative to one another, and the overall structure similarity of the

142 functionals are in reasonable agreement with one another, and usually with experiment.

143 iched contigs representing conserved loci to one another; and prepare and manipulate these alignments

144 distinct C. briggsae lineages separated from one another approximately 200,000 generations ago, inclu

145 tothecoides and P. wickerhamii diverged from one another around six million years ago.

146 tic behavior of various CSPs can differ from one another as much as they differ from the well-studied

147 of TMEM219 or IL-13Ralpha2 also phenocopied one another as regards the ability of Chi3l1 to inhibit

148 Rhodococcus that are as distantly related to one another as they are to representatives of other myco

149 these two factors dynamically interact with one another as well as the PDCD4 transcript to maintain

150 rmances of the electrodes were compared with one another as well as with two spectroscopic techniques

151 arts of the tumor are genomically related to one another, as opposed to the mesenchymal component tha

152 CEACAM8 regulate the biological functions of one another, as well as of additional CEACAMs with which

153 ir genes, metabolites, and interactions with one another, as well as with their host collectively, re

154 disorders were significantly associated with one another at baseline and at 3-year follow-up.

155 es despite being easily distinguishable from one another at the network level.

156 lity (for example, ion-pairing) that bind to one another at the oil-water interface.

157 tically unrelated individuals cooperate with one another based on a single shared trait.

158 eLife editors and reviewers consult with one another before sending out a decision after peer rev

159 -rotation fluxes were indistinguishable from one another but rotation phase mattered.

160 resentatives were structurally distinct from one another, but similar to other DRPs in their respecti

161 tioned in a cofacial orientation relative to one another by attachment of the imide group of each PDI

162 on cell surfaces to cross-enhance or inhibit one another by competitive or noncompetitive (allosteric

163 TRN neurons are also coupled to one another by electrical synapses that depend strongly

164 ion, 2) wrapped particles reversibly attract one another by membrane deformation, and 3) a combinatio

165 The two enzymes were metamorphosed into one another by sequentially replacing the loops and heli

166 AOX isoforms cannot be transformed to mimic one another by substituting the variable cysteine residu

167 dioxide nanoparticles that are infused into one another by successive thermal treatments.

168 each component are effectively screened from one another by water.

169 this architecture, with the 2 legs opposite one another, can explain the specificity of Rev for the

170 nd, pairs who exchanged forces whilst facing one another consistently under-reproduced the partner's

171 epidermis are hydraulically sequestered from one another despite their proximity.

172 revealed that they are remarkably similar to one another, despite their differences in geography, mor

173 y assessment methods are not consistent with one another; different risk categories are assigned for

174 imental physiological or physical effects on one another, due to their interest in maximising their o

175 Sensory systems influence one another during development and deprivation can lead

176 de network strengthen their interaction with one another during episodic retrieval.

177 ction of some effectors overlap and regulate one another during infection.

178 l coat protein, although very different from one another, each adopt C3 symmetric structures.

179 A duplexes can preferentially associate with one another even in the absence of proteins.

180 ating three PMDI units in close proximity to one another, exhibits a single output voltage at 2.33 V,

181 g specificities are unlikely to compete with one another for phosphosites in vivo.

182 the sensory cilium and whether they rely on one another for specific transport remains poorly unders

183 lide actin-tropomyosin filaments relative to one another, functions that may explain the role of this

184 t such rings strongly interpenetrate through one another, generating an extensive network of topologi

185 cal and food samples were closely related to one another genetically.

186 sity elongated and aligned their shapes with one another, gliding at relatively high velocities.

187 s of planar molecules can be multiplied with one another graphically or, in the mind's eye, to yield

188 ow these transcription factors interact with one another has recently been revealed from crystallogra

189 Z protofilaments in bundles from sticking to one another, holding them apart at a distance similar to

190 als, but, surprisingly, seem to compete with one another (ie, exert less-than-additive effects) in hu

191 curves of individual cell lineages relate to one another in a developing tissue.

192 e fact that the two sites involved influence one another in a symmetrical manner-can facilitate such

193 CusA, CusB, and CusC are connected to one another in an oligomerization ratio of 3:6:3 CusA/Cu

194 Patches were densely interconnected to one another in both feedforward and feedback directions,

195 tion of Repeat E in female cells phenocopies one another in causing Xist RNA to delocalize from the X

196 age 0, stage 1, and SNAP did not differ from one another in cognitive performance at baseline or over

197 l strategies to communicate and compete with one another in complex environments.

198 Despite differing widely from one another in filament structure and dynamics, these po

199 networks that do not strongly interact with one another in many task contexts.

200 While sister chromatids are segregated from one another in mitosis and meiosis II, specific adaptati

201 of the same order of magnitude and reinforce one another in mode and intermediate waters over the tim

202 unds to be chromatographically resolved from one another in order to be characterized.

203 pes of bladder cancer that might differ from one another in response to various treatments.

204 sional fold where the residues farthest from one another in sequence meet.

205 h knowledge making and decision making shape one another in social-environmental systems.

206 plete SRK and SCR sequences located close by one another in the derived genomic position of the Leave

207 uclei are densely packed and appear to touch one another in the images.

208 e control group and in the opposite order to one another in the intervention group.

209 timulated genes that are located adjacent to one another in the mouse genome.

210 to warming and cooling do not simply mirror one another in the opposite direction, and low temperatu

211 hexagonal grid based on their similarity to one another in the original genomic space and are render

212 d by the remaining nodes that cooperate with one another in the second sub-network.

213 These factors potentially compete with one another in the short time-window when the nascent ch

214 breast cancer (TNBC) cells that differ from one another in their relative tumorigenic abilities.

215 opment, individuals consistently differ from one another in this trait, with higher consolatory tende

216 that PON1, myeloperoxidase, and HDL bind to one another in vivo forming a functional ternary complex

217 illators that are normally weakly coupled to one another in wild-type cells become strongly synchroni

218 antisense Alu elements fold independently of one another into a secondary structure that is conserved

219 Humans readily sort one another into multiple social categories from mere fa

220 NIFICANCE STATEMENT Individuals readily sort one another into social categories (e.g., sex, race), wh

221 amyloids, but the packing of sheets against one another is distinctive relative to soluble proteins.

222 dense forest environments, visual access to one another is often limited, and recognition of social

223 How these events may influence one another is only partly known.

224 and social variables are not independent of one another, making patterns hard to discern using stand

225 d indirect evidence comparing biologics with one another, methotrexate, or placebo.

226 atial distributions of some taxa relative to one another, notably at the border between the mucosa an

227 wo hominin trackways present are parallel to one another, one of which is a composite formed by at le

228 ix 1 of PrP, brought into close proximity to one another only when the alpha helix is intact.

229 ZDs), pentoxifylline, or obeticholic acid to one another or placebo.

230 ompressive strength, and do not bond well to one another or to other materials.

231 ological phases, which, when interfaced with one another or with a topologically trivial phase, give

232 ch as cells reversing direction, sticking to one another, or walking past one another.

233 edly within single patients and compete with one another, providing a vivid clinical example of clona

234 , the objects serve as unknown references to one another, reducing the phase problem to a solvable se

235 Does it make sense for people to hold one another responsible for what they do, as happens in

236 em and analyzing their movements relative to one another reveals that a process of shared decision-ma

237 attractive and aversive odorants neutralize one another's behavioral effects.

238 inding because FoxO1 and FoxA1/A2 facilitate one another's binding to IGFPB1 promoter DNA.

239 es mate with and deposit copulatory plugs on one another's excretory pores.

240 contains structural elements that frustrate one another's folding, and that the two bridges are crit

241 ental retardation protein (FMRP) and bind to one another's mRNA.

242 but often exhibit catalytic promiscuity for one another's reactions, consistent with catalytic promi

243 critical way by which group members regulate one another's self-interest and build cooperation, moral

244 ciously consider how, as scientists, we view one another's unique approaches and argue for the import

245 ing development, cells must communicate with one another, sending and receiving signals that regulate

246 lows the switches to be modularly coupled to one another so that the output of one switch functions a

247 nding how the different dimensions relate to one another spatially is important for conservation prio

248 we demonstrate that they remain tethered to one another subsequent to internalization, arguing that

249 ady state stress on filament turnover cancel one another, such that flow speed is insensitive to fila

250 rs connecting the globular domains of Gag to one another), suggesting that transient encounter comple

251 heterozygous and rarely occur together with one another, suggesting that cells may tolerate only a p

252 were significantly (P < 0.001) correlated to one another, suggesting that these compounds share simil

253 molecular entities of the cell interact with one another suggests that, nevertheless, integration of

254 specific pathway genes that are proximal to one another tend to occupy higher levels in the regulato

255 d cerebellum were more strongly connected to one another than in healthy control subjects.

256 at form polymers are more closely related to one another than they are to other nonpolymerizing membe

257 ed under OMZ conditions were more similar to one another than those deposited in bioturbated interval

258 exhibited larger phenotypic differences from one another than urban populations.

259 g that platelets are physical substrates for one another that establish mechanical feedback loops of

260 and the Allee effect act independently from one another: the Allee effect does not modify the Wolbac

261 within the tetramer reorient with respect to one another; the "rigid body reorientation model" propos

262 heir fold and reorient semi-independently of one another; the linkers connecting the structural domai

263 adaptors may isolate subsets of targets from one another, there is still a strong potential for phosp

264 that as dorsal epidermal cells migrate past one another they produce F-actin-rich protrusions polari

265 As two species diverge from one another, they become increasingly isolated by reprod

266 pper and telluride atoms placed antipolar to one another throughout the lattice with rubidium atoms a

267 re dynamic, overlapping, and may evolve into one another, thus rendering clear-cut definitions diffic

268 nt pipelines above are largely orthogonal to one another; thus GBS-SNP-CROP may be used to augment th

269 dle compartments in close proximity wait for one another to align all chromosomes before entering ana

270 it is not yet clear how they integrate with one another to control cell fate.

271 How these two factors combine with one another to control the course of electrolysis is ana

272 ese trajectories, the helices separated from one another to create a more accessible and dynamic F-bo

273 ays in which the two topics mutually benefit one another to enhance our understanding of the nanoscal

274 s system, are in constant communication with one another to ensure that cardiac output matches the dy

275 egions dynamically engage and disengage with one another to execute everyday actions from movement to

276 hologies, and behaviors in coordination with one another to form a functional body.

277 r of TGN-derived membrane vesicles fuse with one another to form the partitioning membrane.

278 in space and their components may depend on one another to function.

279 ed DNA at the origin, the two CMGs must pass one another to leave the origin and both must remodel on

280 ts where oil and water can be solubilized in one another to provide a unique platform for many differ

281 ally, they can be activated independently of one another to regulate distinct genes.

282 ithin the same parent protein, interact with one another to regulate function.

283 receptors work together (rather than oppose one another) to reduce short-term facilitation when GABA

284 on, PrP(Sc), which may be distinguished from one another using conformation-specific antibodies.

285 ed quorum sensing, bacteria communicate with one another using extracellular signal molecules called

286 s hearing organs to locate and interact with one another via the frequencies of sounds generated by t

287 research microscopy are often isolated from one another, we argue that their combination and integra

288 ine whether these two proteins interact with one another when coexpressed exogenously in COS7 cells.

289 information describing how TFs interact with one another when they do bind.

290 ATCs) offer a survival benefit compared with one another when treating injured children is controvers

291 ss crystalline layers of Si and LN bonded to one another, where the former is patterned and the latte

292 e asked two partners to exchange forces with one another, where the goal was to accurately replicate

293 th pathogens and non-pathogens interact with one another, whether within or outside of the host.

294 to render neighbouring devices invisible to one another, which allows them to be placed closer toget

295 . megalotis) were positively correlated with one another, while the niche breadth dynamics of the het

296 which could be interconverted directly into one another with light.

297 large amount of BNNSs partially overlapping one another with random orientations.

298 ound that X4-LIV and DNA-PKcs interfere with one another with respect to stimulating Artemis activity

299 ntoses are much more structurally similar to one another, with only the axial or equatorial orientati

300 dherin and Na,K-ATPase become separated from one another within the trans-Golgi network, suggesting t