ライフサイエンスコーパス: one another

1 w studies have investigated how these affect one another.

2 ly comparing different interventions against one another.

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

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

5 performed by braiding isolated modes around one another.

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

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

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

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

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

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

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

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

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

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

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

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

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

19 26a isoforms can functionally compensate for one another.

20 hen both partners show mutual preference for one another.

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

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

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

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

25 representations of similar events apart from one another.

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

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

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

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

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

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

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

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

34 an be difficult when individuals differ from one another.

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

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

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

38 any transcripts only slightly differing from one another.

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

40 y states that are readily discriminated from one another.

41 from cues that are temporally displaced from one another.

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

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

44 l response patterns which were distinct from one another.

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

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

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

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

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

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

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

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

53 processes so far considered independent from one another.

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

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

56 that share components can be insulated from one another.

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

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

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

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

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

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

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

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

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

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

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

68 urity profiles that differentiated them from one another.

69 iptional profiles that distinguish them from one another.

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

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

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

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

74 ting behavior and disease dynamics influence one another.

75 l, since all components eventually influence one another.

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

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

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

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

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

81 atalysts that complement rather than inhibit one another.

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

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

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

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

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

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

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

89 atypical depression seem to be antithesis of one another.

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

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

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

93 mining if these features were independent of one another.

94 ther the competing events are independent of one another.

95 and thermosalience are quite independent of one another.

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

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

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

99 influence biofilm formation independently of one another.

100 ated effects that may occur independently of one another.

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

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

103 behavior are actually powerful regulators of one another.

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

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

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

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

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

109 mbly on membranes are thus interdependent on one another.

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

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

112 kinematic errors associated with each oppose one another.

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

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

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

116 transparent BNNSs that partially overlapped one another.

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

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

119 wnregulating efficacies generally paralleled one another.

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

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

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

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

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

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

126 s in reward and threat processing potentiate one another.

127 schemes are independent and do not preclude one another.

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

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

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

131 retromer and ESCRT microdomains to regulate one another.

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

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

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

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

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

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

138 competing visual locations actively suppress one another.

139 -1 and MV4-11 could stimulate them to target one another after the addition of daratumumab.

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

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

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

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

144 cithal eggs but have uncertain affinities to one another.

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

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

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

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

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

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

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

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

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

154 arranged to immediately become calibrated to one another.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

175 Transition dipole moments are orthogonal to one another.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 tic populations were most closely related to one another.

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

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

195 en presented regarding their relationship to one another.

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

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

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

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

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

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

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

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

204 hen sarcomeres are staggered with respect to one another.

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

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

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

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

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

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

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

212 ent combinations intensities were similar to one another.

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

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

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

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

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

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

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

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

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

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

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

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

225 3 and is required for their association with one another.

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

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

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

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

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

231 oups of neurons interact to communicate with one another.

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

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

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

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

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

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

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

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

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

241 ns that only fluoresce on complementing with one another.

242 evaluated their performance in concert with one another.

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

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

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

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

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

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

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

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

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

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

253 the measurements were highly correlated with one another.

254 BON tuning curves are highly correlated with one another.

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

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

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

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

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

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

261 ug nystatin are frequently incompatible with one another.

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

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

264 registered and functionally integrated with one another.

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

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

267 70-physically and functionally interact with one another and a subset of NPC components (nucleoporins

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

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

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

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

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

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

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

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

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

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

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

279 etically manipulate cells that interact with one another.

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

281 anetesimals to gravitationally interact with one another.

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

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

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

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

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

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

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

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

290 whose members cooperate preferentially with one another.

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

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

293 otential energy surface before reacting with one another.

294 13 (D/660), which frequently reassorted with one another.

295 Proteins share similar segments with one another.

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

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

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

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

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