ライフサイエンスコーパス: coalescence

1 g or Smoluchowski ripening (NC diffusion and coalescence).

2 while divalent cations resulted in extensive coalescence.

3 in one community dominating after community coalescence.

4 tionally examined population structure using coalescence.

5 mproving both centrosome clustering and pole coalescence.

6 evidence of non-demographic factors driving coalescence.

7 ce and ability to stabilize droplets against coalescence.

8 role of host resources in driving community coalescence.

9 actin cytoskeleton, preventing their further coalescence.

10 hich emit gravitational waves prior to their coalescence.

11 at more than [Formula: see text] to prevent coalescence.

12 eater potential surface energy released upon coalescence.

13 hin, inhomogeneous film that has not reached coalescence.

14 s sinter slowly by crystallite migration and coalescence.

15 lear bodies from immediate sedimentation and coalescence.

16 ate TMT10 reporter ion pairs become prone to coalescence.

17 rise to significant growth of bubbles due to coalescence.

18 e essential to preventing particle growth or coalescence.

19 ing emulsions that were resistant to droplet coalescence.

20 layed BCR capping and accelerated lipid raft coalescence.

21 cy is reversed if collisions lead to droplet coalescence.

22 interactions, while chitosan also prevented coalescence.

23 various models, such as Ostwald ripening and coalescence.

24 rowding enhances the lateral void growth and coalescence.

25 on for silicic acid, followed by the micelle coalescence.

26 mixing and periodic takeovers by neighbors (coalescence), after which neutral evolution reestablishe

27 of lineage B2, allowing us to refine younger coalescence age estimates for these two clades.

28 romotes increasing marine richness, but that coalescence alone has only a small negative or stabilizi

29 sweeps in the presence of such within-sweep coalescence, although the effects of multiple recombinat

30 Moreover, coalescence analyses suggest that a Patagonian sub-popul

31 Multilocus coalescence analyses suggested that F. albicilla experie

32 a long time before the last glacial maximum; coalescence analysis (as implemented in the program IMa2

33 Genome-based coalescence analysis estimated that the population of th

34 To stabilize a colloidal system against coalescence and aggregation, the surface of each solute

35 nts or colloids stabilize structures against coalescence and alter the mechanical properties of the i

36 cs: an unexpected correlated motion prior to coalescence and an independent motion otherwise.

37 The ring-coalescence and annealing model for the formation of C(6

38 as a physical barrier blocking spindle pole coalescence and bipolarity.

39 Bayesian coalescence and birth-death analyses were performed with

40 4 suppression causes impaired apical vesicle coalescence and central lumen formation, a phenotype tha

41 inus are sufficient for robust viral protein coalescence and filamentous VLP formation and suggest th

42 s F, or P plus F, induced both viral protein coalescence and formation of filamentous VLPs that resem

43 essfully stabilizing enzymatic cargo against coalescence and fusion in discrete protocellular populat

44 The second step, however, involves droplet coalescence and is proportional to temperature.

45 s (microL droplets) through a combination of coalescence and Laplace pressure-driven flow.

46 ion experiments, such as contactless droplet coalescence and mixing, solid-liquid encapsulation, abso

47 asingly popular because they can accommodate coalescence and multilocus data sets.

48 hysical mechanism triggering droplet-droplet coalescence and observe a cutoff distance from the cente

49 Diffusion of the lipid domains, coalescence and reduction in domain size were observed u

50 Coalescence and solidification of nanoscale droplets res

51 Regions of coalescence and stretching separation of colliding dropl

52 um-diameter epithelial tubules form by cell coalescence and structural maturation.

53 ous layer, contribute to the delayed droplet coalescence and subsequent phase separation.

54 to the study of electron beam induced defect coalescence and to long range rippling in graphene.

55 ic microbubble behaviors: stable cavitation, coalescence and translation, and inertial cavitation.

56 coarsening dynamics are mediated by Brownian coalescence and, to a lesser degree, Ostwald ripening.

57 scale required to stabilize droplets against coalescence, and we show that the interface should be co

58 sion of the intervening solvent and particle coalescence are enabled by near-perfect co-alignment via

59 The coalescence artifact was completely removed by lowering

60 ttention to community-community encounters ('coalescence') as likely an important factor shaping natu

61 Particle coalescence, assisted by oxygen-induced surface migratio

62 the split parasitic intra-cavity modes into coalescence at an exceptional point of the resulting thr

63 Coalescence-based analyses suggest that the population s

64 Coalescence-based genealogy samplers also indicated that

65 Coalescence-based multi-locus and population genetic ana

66 Beyond the computational demands, coalescence-based simulation strategies have to be recon

67 ometrical organization that we term "angular coalescence." Based on this phenomenon, we propose a cla

68 lates multiple processes, such as lipid raft coalescence, BCR diffusion, microclustering, and endosom

69 Glucose esters delayed, but did not prevent coalescence, because the oil droplets diameter doubled d

70 multiple individuals, focusing on the first coalescence between any two individuals.

71 on-spherical droplets and the sudden halt of coalescence between individual droplets.

72 e merging process is caused by dipole-dipole coalescence between the daughter droplets.

73 of continental crust during supercontinental coalescence-breakup cycles.

74 eous interface, stabilizing droplets against coalescence but not preventing their eventual sedimentat

75 ibition of c-kit by imatinib reduced cluster coalescence, but allowed cluster phosphorylation and F-a

76 s model stabilizers, we show that multi-body coalescence can occur in both water-in-oil and oil-in-wa

77 rsening of Ptnano from crystal migration and coalescence can occur in low temperature fuel cells.

78 ontrolled, and droplet digestion, as well as coalescence, can be visualized.

79 torque that completes alignment and enables coalescence.Crystal growth is a fundamental process, imp

80 fitting of dimer coagulation, isolation, and coalescence (DCIC) measurements.

81 This coalescence delayed the overall lipid digestion kinetics

82 ene flow, this method allows calculating the coalescence densities efficiently.

83 cleation, nanocluster surface diffusion, and coalescence depends on the material and the overpotentia

84 anocoating that facilitates feedback between coalescence-driven growth and capillary-driven motion on

85 d SUMO interaction motif (SIM), and that APB coalescence drives telomere clustering.

86 tabilized nanoemulsions were destabilized by coalescence due to insufficient interfacial charge.

87 Sucrose esters prevented coalescence during 7days since the droplets diameter did

88 regular oblong shapes formed due to arrested coalescence during polymerization, occurring as a result

89 The coalescence effects are assigned to two different confor

90 this paper, we show that in the presence of coalescence effects, the set of displayed trees is not s

91 In the subsequent Phase II, coalescence elevates the molecular complexity further by

92 liquid coating can stabilize bubbles against coalescence even when the particles alone cannot.

93 n that the ability of a species to survive a coalescence event is best predicted by a community-level

94 Second, we demonstrate how coalescence events could negatively affect the ability t

95 , because of the small sample size, only few coalescence events occur in that period.

96 detected by the sampling droplet as discrete coalescence events.

97 Furthermore, using a community coalescence experiment, we found that the bacterial comm

98 the mixing of entire communities (community coalescence), for example, flooding events, host excreti

99 is purely attractive and leads to drop-drop coalescence, for relatively thin substrates a short-rang

100 genetics inference methods are based on the coalescence framework.

101 The latter limit allows us to characterize coalescence, genetic diversity, and the speed of adaptat

102 ropriate mechanism for droplet transport and coalescence has always been a challenge.

103 Whereas coalescence has been thoroughly studied when drops coale

104 The full coalescence, however, constrains the lower limit of volu

105 e that Birnaviridae reassortment requires VF coalescence.IMPORTANCE Reassortment is common in viruses

106 um or air, many important situations involve coalescence in a dense surrounding fluid, such as oil co

107 m the ER to newly formed LDs, and induces LD coalescence in a tubulin-dependent manner.

108 ce in a dense surrounding fluid, such as oil coalescence in brine.

109 By contrast, lack of coalescence in conspecific accessions of abundant and of

110 erve significant differences in chromosome X coalescence in disease-implicated lymphocytes isolated f

111 Despite suboptimal coalescence in the absence of P, the M and F proteins, w

112 Citrem-stabilized emulsion showed extensive coalescence in the gastric environment, which reduced li

113 The emulsion produced with Tween 20 resisted coalescence in the gastric phase and showed the highest

114 lized emulsions showed aggregation with some coalescence in the gastric phase, and casein provided be

115 nanocrystalline grain size regime, but loop coalescence in the ultra-fine grain size regime.

116 lpha/beta activity was associated with VAMP3 coalescence in WT and Fyn-deficient cells.

117 Coalescence-induced jumping of condensate droplets from

118 re-engineering of carbon bonds evolves via a coalescence-induced reconfiguration of sp(2) hybridizati

119 hylene glycol (PEG)-rich aqueous phase, with coalescence inhibited by adsorbed ~130-nm diameter lipos

120 ntractile pulses, disrupting both actomyosin coalescence into apical foci and cycles of Myo-II assemb

121 o fluorescently activated subpopulations for coalescence into colour-indexed output.

122 emperatures in transition areas, even before coalescence into full thickets.

123 go rapid proliferation at this site prior to coalescence into germinal centers (GCs).

124 the inward diffusion of vacancies and their coalescence into larger voids.

125 High light induces Vipp1 coalescence into localised puncta within minutes, with n

126 r, spinodal decomposition or nucleation, and coalescence into multiple layers.

127 Invadopodia dynamics and their coalescence into rosettes were also dependent on Rac1, f

128 looping, yet neither crumpling nor HSP gene coalescence is affected.

129 Coalescence is an essential phenomenon that governs the

130 iting growth, cluster surface diffusion, and coalescence is essential and opens new, exciting possibi

131 The revelation of multi-body coalescence is expected to help better understand Picker

132 The coalescence is extremely slow, decelerating process, res

133 fluid and, for oil fractions exceeding 0.6, coalescence is observed.

134 n of small graphene domains is observed, yet coalescence is prevented by the limited residence time i

135 Furthermore, coalescence is promoted by repulsive latex and silica pa

136 We hypothesize that VF coalescence is required for the reassortment of the Birn

137 s with a larger N have higher probability of coalescence is responsible for the emergence of the scal

138 We established that the main reason for coalescence is the commonly accepted maximum ion target

139 hod, Minimal-Assumption Genomic Inference of Coalescence (MAGIC), that reconstructs key features of t

140 mmary methods': BUCKy, MP-EST, minimize deep coalescence, matrix representation with parsimony and th

141 where we pinpoint high-level spread using a coalescence measurement, is efficient when sequence data

142 A combination of techniques including coalescence measurements, line shape analysis, and selec

143 ormance of the different C++ highly reusable coalescence mergers (binary, multiple, hybrids) are give

144 hip in the more complicated duplication-loss-coalescence model.

145 Coalescence modeling reveals the speciation of S. manson

146 of population genetics theory, specifically, coalescence modeling, to intrainfection populations of B

147 standing reconciliations in duplication-loss-coalescence models with multiple samples per species.

148 We implement a self-coalescence module (SCM) for the controlled reconstituti

149 3 to 4 h postinfection and resulted from the coalescence of 0.5- to 2-mum vesicles, possibly bearing

150 The coalescence of a member of this population offers a poss

151 ic liquid with nitric acid (HNO(3)), and the coalescence of a solid particle (CuSO(4).5H(2)O) and a w

152 features such as lymph node calcification or coalescence of adjacent lymph nodes were also compared.

153 Pt-Fe3O4, followed by surface diffusion and coalescence of Ag onto the Pt surface to form the Ag-Pt-

154 Pt-Fe3O4 seeds, which is consistent with the coalescence of Ag through a surface-mediated process and

155 n orientational migration, the intraparticle coalescence of Au satellites at QD surfaces transforms i

156 We show that this coalescence of BCR microclusters depends on the actin-re

157 actant-stabilized brine-in-oil emulsions via coalescence of brine droplets on our dye-sensitized TiO2

158 Kilonovae produced by the coalescence of compact binaries with at least one neutro

159 llotropes and carbon-rich materials from the coalescence of cyclocarbon molecules.

160 of the past, fresh insights have come from a coalescence of different experimental and theoretical ap

161 sition and a spectral collapse, that is, the coalescence of discrete energy levels into a continuous

162 b models cannot account for the fast, direct coalescence of dislocation loops seen experimentally.

163 om thermal degradation of the buffer or from coalescence of dissolved gas.

164 w that it is possible to realize the natural coalescence of droplets through Marangoni effect without

165 tion in bulk proceeds through the continuous coalescence of droplets until the system undergoes compl

166 ttachment and spindle tension to promote the coalescence of early spindle pole foci that produces a b

167 oliferation, differentiation, migration, and coalescence of endothelial cells.

168 We observed coalescence of focal adhesion components together with N

169 biology to enable symbiosis, and an exciting coalescence of genome mining, lipid profiling, and trace

170 mitrella patens caulonemal cells through the coalescence of growing MT plus ends.

171 This effect was achieved through the dynamic coalescence of ILT3, BCRs, and phosphatidylinositol-3,4,

172 ranscription-PCR analysis suggested that the coalescence of inclusion bodies is a strategy to efficie

173 seconds, as well as monitor the movement and coalescence of individual aggregates into larger structu

174 Here, we review the emerging coalescence of infectious disease epidemiology around a

175 prouting lymphangiogenesis, and the other by coalescence of isolated lymphatic cells.

176 rmation of a contractile actomyosin ring and coalescence of lipid rafts between reticulocyte and pyre

177 ns grow via two mechanisms 1), collision and coalescence of liquid domains, and 2), Ostwald ripening.

178 usion of cell aggregates by analogy with the coalescence of liquid droplets and ignore the complex st

179 Cavities grow through coalescence of micro-cavities to form micro-cracks first

180 sed to elucidate the initiation, growth, and coalescence of microfractures leading to macroscopic fai

181 by incorporating the nucleation, growth, and coalescence of microscopic gas bubbles in a molding proc

182 Roles of Ran and importin beta in the coalescence of microtubule organizing centers (MTOCs) an

183 iour of Pickering emulsions-the simultaneous coalescence of multiple droplets in a single event.

184 the condensate droplet jumping is induced by coalescence of multiple droplets of different sizes, and

185 ation was consistent with an actin-dependent coalescence of multiple early replicative sites.

186 termed insulator bodies that result from the coalescence of multiple protein-bound insulators.

187 From Raman spectroscopy, we observe coalescence of nanotubes during breakdown, which stabili

188 le structures and was required for effective coalescence of NMY-2 filaments into large contractile fo

189 have developed a methodology to quantify the coalescence of oil-in-water emulsion droplets during lip

190 nt receptors (OR) are strongly implicated in coalescence of olfactory sensory neuron (OSN) axons and

191 main olfactory epithelium (MOE), and on the coalescence of OSN axons into approximately 3,600 glomer

192 ochastic, inelastic collisions of ejecta and coalescence of partially-sintered agglomerates.

193 ssure processing to drive the attachment and coalescence of PbS nanocubes along directed crystallogra

194 e perversion-perversion interaction, and the coalescence of perversions that finally leads to a linea

195 mall soluble oligomers, or through the rapid coalescence of pre-existing monomeric IgG1 nuclei into a

196 This ensures that the coalescence of precursors into a single deposit is restr

197 Acoustically mediated coalescence of primary droplets generates single-droplet

198 TCR territories to contract, leading to the coalescence of protein islands and formation of stable T

199 Here, we show that the coalescence of protein-induced DNA bubbles can mediate a

200 initiates the process, followed by on-target coalescence of remaining IDP segments.

201 n eukaryotic cells, diverse stresses trigger coalescence of RNA-binding proteins into stress granules

202 h bubble in the trail results from the early coalescence of several microscopic bubbles, themselves d

203 that the age-dependent deposit forms through coalescence of smaller aggregates, two deposits rapidly

204 roceeds by Ostwald's step rule through which coalescence of soluble monomers leads to the formation o

205 sapiens appears to have originated from the coalescence of South and, possibly, East-African source

206 chromosome configurations, whereby the final coalescence of supernumerary poles into a bipolar array

207 manipulate protein distributions by inducing coalescence of supposedly cholesterol-enriched domains.

208 Numerical simulations demonstrate that the coalescence of TFAM-induced bubbles can explain experime

209 binding requires conditions consistent with coalescence of the 5 and 3 sites in a complex (I, initia

210 e supercooled liquid state, promote the fast coalescence of the amorphous nanoparticles at relatively

211 powered by the surface energy released upon coalescence of the condensed water phase around the cont

212 Coalescence of the embryonic gonad in Drosophila melanog

213 otal volume of the glomeruli (TGV) formed by coalescence of the fluorescent axons.

214 properties of the olive cells, improving the coalescence of the oil droplets due to substantial cellu

215 ion and extraction of samples via orthogonal coalescence of the plug with a static array of sample dr

216 It is believed that the coalescence of the primary M7C3 carbides is ascribed to

217 The coalescence of these clusters creates a rich scenario of

218 Unzipping is then followed by coalescence of these densely clustered multiple uncurled

219 A new study demonstrates that coalescence of these nuclei is driven by the expression

220 outer shell (cortical bone), which forms by coalescence of thin trabeculae at the metaphysis (cortic

221 .The strength of long bones is determined by coalescence of trabeculae during corticalization.

222 ment may be a consequence of a defect in the coalescence of trabeculae into the developing ventricula

223 chniques are compared, specifically from the coalescence of two droplets in holographic optical tweez

224 nal magnetohydrodynamical simulations of the coalescence of two massive stars and follow the evolutio

225 re-existing amorphous nanocluster (Au) or by coalescence of two separate amorphous sub-nanometre clus

226 Addition of LPS provoked coalescence of VAMP3 and its interaction with synaptosom

227 model in which myosin II-mediated forces and coalescence of vIFs at mature FAs are required for endop

228 a nanoscale Kirkendall process-for example, coalescence of voids as they grow and reversal of mass d

229 el and provides a mechanism for severing and coalescence of vortex lines, so that the questions relat

230 res are formed through compressive mesoscale coalescences of spherical gold nanoparticles, which is f

231 This coalescence on a small set of model species comes with s

232 growth, surface diffusion, aggregation, and coalescence on the growth mechanism and morphology of th

233 7+/-45) ripens through cluster diffusion and coalescence only (Smoluchowski ripening).

234 th scales without using an explicit model of coalescence or recombination, allowing it to analyze arb

235 In this report, we study coalescence pathways of circularly shaped two-dimensiona

236 the constituent rods leads to three atypical coalescence pathways that are not found in other simple

237 Coalescence, pressure effect on adjacent structures and

238 stabilization of the emulsion, with droplet coalescence prevented even for submonolayer interfacial

239 ly crosslinking DNA, BAF promotes chromosome coalescence, preventing nuclear membranes from enwrappin

240 During embryonic gonad coalescence, primordial germ cells (PGCs) follow a caref

241 For these methods the calculation of the coalescence probability density of a genealogy requires

242 This evolution was the result of a two-stage coalescence process of microscopic junctions made betwee

243 Furthermore, we induce the coalescence process with optical forces, leading to a ro

244 ence times of the phylogenetic tree follow a coalescence process.

245 otion revealed the droplets growth and their coalescence processes and clearly demonstrated the diffe

246 We identify magnon localisation and coalescence processes, whereby localised magnetic textur

247 gh surface tension analysis, foam formation, coalescence rate and foam characteristics (using coffee

248 lready provided concrete measurements on the coalescence rates and has allowed us to test the theory

249 antitative measurements of cluster velocity, coalescence rates, and proliferation rates.

250 iform grain growth due to grain rotation and coalescence rather than the thermally and the stress-ass

251 plication and gene loss or only multispecies coalescence, recent work has combined these phenomena th

252 ese problems by introducing sparse trees and coalescence records as the key units of genealogical ana

253 Moreover, during chromosome X coalescence significant changes in Xist, H3K27me3, and X

254 Using coalescence simulations of diverging populations, we exp

255 ral lineages; and to model hybridization and coalescence simultaneously.

256 two juxtaposed branches are transported to a coalescence station, where they merge after the accumula

257 We hypothesize that the coalescence temperature (Tc) corresponds to the barrier

258 ng to the two diastereoisomers at a range of coalescence temperatures in the VT NMR spectra and occur

259 ns arise in other free-surface flows such as coalescence that also exhibit singularities.

260 tural enemies; (f) habitat fragmentation and coalescence that promote homogeneous, species-depleted l

261 Through nanoparticle re-orientation and coalescence, the nanowires collapse into ordered UO(2) n

262 tals such as monomer attachment and particle coalescence, the synthesis of zinc chalcogenide quantum

263 opulations and the Iraqis was inferred using coalescence theory in the Migrate-n program.

264 30 thousand years, the comparatively recent coalescence time of the extant variation of haplogroup U

265 ndrial data were less accurate when a longer coalescence time was assumed.

266 liquid-film case, leading often to a shorter coalescence time, as observed in recent experiments.

267 harsh environments, which result in shorter coalescence times and keep populations in regions of the

268 selection can be calculated in terms of the coalescence times of random walks.

269 election, on any weighted graph, in terms of coalescence times of random walks.

270 Our method relies on calculating the coalescence times of random walks.

271 Moreover, coalescence times of the phylogenetic tree follow a coal

272 ationship between Wright's F(ST) and average coalescence times to develop an analytic theory describi

273 onary history, including the distribution of coalescence times, by integrating information across gen

274 andom phylogenies with the same sampling and coalescence times, to reduce the false positive rate.

275 s, nanowires and nanosheets, with nanosecond coalescence times.

276 ondensation to enrich DNA repair factors and coalescence to cluster telomeres.

277 lexes at heminodes and promotes their timely coalescence to form the mature node of Ranvier.

278 time coalescent simulation while restricting coalescence to node pairs with overlapping or near-overl

279 xchange of matter are prepared by inhibiting coalescence to produce acoustically trapped lattices of

280 tes of genetic domain wall annihilations and coalescences to simulations modeling the population as a

281 ew method, transition probability-structured coalescence (TPSC), replaces the discrete migration even

282 An [PbI(6) ](4-) octagon coalescence transformation mechanism coupled with metal

283 f homologous chromosome X colocalization (or coalescence), typically associated with initiation of X-

284 pi compared to 0.22 mum/s at 22 hpi), and VF coalescence was dependent on an intact microtubule netwo

285 coalescence, while in the SN100C solder this coalescence was not significant.

286 during tangential tether extraction, and no coalescence was observed during multiple tether extracti

287 d cellular spaces with liquid-like KGs whose coalescence was restricted by keratin filament bundles.

288 sappeared from view in 58.3% of eyes, drusen coalescence was seen in 70.8% of eyes, and new RPE pigme

289 By studying picoliter droplet coalescence, we demonstrate that surfactants can signifi

290 charge state, and study of the onset of peak coalescence when the resolution at the fundamental frequ

291 med via two mechanistic pathways: (1) nuclei coalescence, where the Ag nanoparticles absorbed onto th

292 amorphous nanoparticles takes place by fast coalescence which is dominated by facet-free surface dif

293 ch the chromosome establishes sites of polyP coalescence, which recruit Ppk1 to promote the in situ s

294 nt cations resulted in aggregation and minor coalescence, while divalent cations resulted in extensiv

295 sion in SnAgCu solder causes void growth and coalescence, while in the SN100C solder this coalescence

296 nodomain formation, destruction, and dynamic coalescence with a domain lifetime of 220+/-60 ms.

297 d protein production, likely through reduced coalescence with cytoplasmic ribonucleoprotein granule c

298 ions, while the onset of peak broadening and coalescence with shorter separations suggests the limita

299 rk (TGN) is believed to be mediated by their coalescence with specific lipids, but how these membrane

300 ic storage vesicles likely occurs upon their coalescence with the Rab27a-hMunc13-4 compartment and re