ライフサイエンスコーパス: coalescence

1 eater potential surface energy released upon coalescence.

2 hin, inhomogeneous film that has not reached coalescence.

3 lear bodies from immediate sedimentation and coalescence.

4 ate TMT10 reporter ion pairs become prone to coalescence.

5 rise to significant growth of bubbles due to coalescence.

6 e essential to preventing particle growth or coalescence.

7 layed BCR capping and accelerated lipid raft coalescence.

8 cy is reversed if collisions lead to droplet coalescence.

9 in one community dominating after community coalescence.

10 tionally examined population structure using coalescence.

11 ce of higher-affinity B cells even before GC coalescence.

12 eared less able to induce lipid raft and TEM coalescence.

13 te the natural tendency of the liquid toward coalescence.

14 evidence of non-demographic factors driving coalescence.

15 rowding enhances the lateral void growth and coalescence.

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

17 ce and ability to stabilize droplets against coalescence.

18 actin cytoskeleton, preventing their further coalescence.

19 hich emit gravitational waves prior to their coalescence.

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

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

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

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

24 tion in ancestral species can result in deep coalescence, also known as incomplete lineage sorting, w

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

26 Multilocus coalescence analyses suggested that F. albicilla experie

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

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

29 critical composition and the domains undergo coalescence and a circle-to-stripe transition along with

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

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

32 4 suppression causes impaired apical vesicle coalescence and central lumen formation, a phenotype tha

33 akly oscillating hydration force arises from coalescence and depletion of hydration shells as two fil

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

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

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

37 and loss in a population setting, such that coalescence and ILS can be directly addressed.

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

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

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

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

42 Coalescence and solidification of nanoscale droplets res

43 Regions of coalescence and stretching separation of colliding dropl

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

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

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

47 tive coalescence, structural reshaping after coalescence, and surface faceting.

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

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

50 The coalescence artifact was completely removed by lowering

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

52 odels, it is shown how to derive the rate of coalescence, as well as the likelihood of a gene genealo

53 Particle coalescence, assisted by oxygen-induced surface migratio

54 Coalescence-based analyses suggest that the population s

55 Coalescence-based genealogy samplers also indicated that

56 Coalescence-based multi-locus and population genetic ana

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

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

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

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

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

62 of continental crust during supercontinental coalescence-breakup cycles.

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

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

65 The noncoalescence can be switched to coalescence by neutralizing the microgels, and the emuls

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

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

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

69 We prove that the deep coalescence consensus tree problem satisfies the highly

70 We determined that coalescence contributed to the distribution of MVs withi

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

72 This coalescence delayed the overall lipid digestion kinetics

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

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

75 ence, a critical drop size, above which this coalescence does not occur.

76 chanisms hinder nanocluster growth and favor coalescence driven growth.

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

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

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

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

81 The coalescence effects are assigned to racemization of the

82 The coalescence effects are assigned to two different confor

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

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

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

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

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

88 mic, mobile bodies that enlarged by multiple coalescence events, which could be prevented by disrupti

89 he species tree that implies the fewest deep coalescence events.

90 uplications, duplication and losses, or deep coalescence events.

91 detected by the sampling droplet as discrete coalescence events.

92 barriers too high to be measured by (1)H NMR coalescence experiments.

93 tine phases, which was attributed to droplet coalescence, flocculation, and digestion.

94 , one that describes the initial dynamics of coalescence for all drop viscosities, has been missed.

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

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

97 genetics inference methods are based on the coalescence framework.

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

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

100 Whereas coalescence has been thoroughly studied when drops coale

101 oplasmic side occurs abruptly without domain coalescence; hence, the cytoplasmic monolayer is not nea

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

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

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

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

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

107 One approach to account for deep coalescence in phylogenetic analyses is the deep coalesc

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

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

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

111 plications, duplications and losses, or deep coalescence (incomplete lineage sorting) events needed t

112 Coalescence-induced jumping of condensate droplets from

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

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

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

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

117 The mechanisms that govern receptor coalescence into functional clusters--often a critical s

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

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

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

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

122 VSN axonal projections and a delay in axonal coalescence into well defined glomeruli in the AOB.

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

124 Coalescence is an essential phenomenon that governs the

125 Drop coalescence is central to diverse processes involving di

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

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

128 namics of microcrack nucleation, growth, and coalescence is inaccessible experimentally and fast crac

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

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

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

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

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

134 A small extent of coalescence leads to ultraporous dendritic structures, l

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

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

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

138 that microtubule-disrupting drugs abrogated coalescence-mediated MV embedment.

139 Coalescence modeling reveals the speciation of S. manson

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

141 3 to 4 h postinfection and resulted from the coalescence of 0.5- to 2-mum vesicles, possibly bearing

142 for the translocation mechanism propose the coalescence of a substrate-binding TatABC complex with a

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

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

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

146 te an important role for microtubules in the coalescence of ATIs into larger structures, transport of

147 Coalescence of ATIs was confirmed in cells infected with

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

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

150 onstrated that these clusters form after the coalescence of CD90+ cells to form CPs and before the in

151 and scanning electron microscopy showed that coalescence of clustered lipid rafts and TEMs occurs pre

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

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

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

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

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

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

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

159 s compensating for a lack of Sph and second, coalescence of existing nanodomains ending in large-scal

160 Coalescence of flows from these two regions resulted in

161 We observed coalescence of focal adhesion components together with N

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

163 glutinated head-to-head show contact-induced coalescence of GM1 gangliosides (but not zona-binding mo

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

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

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

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

168 e MBCT and MMCT bands is found to persist as coalescence of infrared (IR) vibrational spectra suggest

169 Gag membrane binding is necessary to induce coalescence of lipid rafts and TEMs, either acylation of

170 both assays, suggesting that Gag induces the coalescence of lipid rafts and TEMs.

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

172 mation of a contractile actomyosin ring, and coalescence of lipid rafts between reticulocyte and pyre

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

174 teral correlations were acquired through the coalescence of local microcircuits.

175 The coalescence of major advances in engineering, molecular

176 r complex to regulate the integration and/or coalescence of membrane microdomains, thereby establishi

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

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

179 fit ancestors, in which almost simultaneous coalescence of more than two lineages frequently occurs.

180 y may result from antibody interference with coalescence of MSP1(19)-containing vesicles with the foo

181 owed that nephrogenic aggregates form by the coalescence of multiple cells and then differentiate int

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

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

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

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

186 id particle agglomeration and to control the coalescence of nanoparticles during thermal annealing up

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 ch implies that larger defects are formed by coalescence of noninteracting smaller defects.

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

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

192 ent openings within rhombomeres and eventual coalescence of openings into the hindbrain ventricle lum

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

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

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

196 ind that the signal enhancement is caused by coalescence of polymer-peptide conjugates into "hotspots

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

198 l dendritic refinement occurs just after the coalescence of presynaptic axons.

199 Acoustically mediated coalescence of primary droplets generates single-droplet

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

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

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

203 ammals that is constructed by the glomerular coalescence of sensory neuron axons in the olfactory bul

204 erculosis was progressively enlarged through coalescence of several factors that transformed the prac

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

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

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

208 atropisomers but still slow enough to cause coalescence of some (1)H and (13)C NMR signals at room t

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

210 Non-response to therapy was associated with coalescence of symptoms, chronic opiate use and more sev

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

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

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

214 Coalescence of the embryonic gonad in Drosophila melanog

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

216 This process correlates with coalescence of the hub, but development of CySCs from so

217 e for Fgf signalling in which it enables the coalescence of the lateral line primordium from an initi

218 ase in volume of the vacuolar compartment by coalescence of the organelles into a single large compar

219 lishment of a scaffold for the extension and coalescence of the OSN axons.

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

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

222 rthermore that this interaction results in a coalescence of the two domains leading to collapse of th

223 The coalescence of these clusters creates a rich scenario of

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

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

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

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

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

229 ally the formation, movement, and subsequent coalescence of vacuoles at the junction of the nucleus a

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

231 he general need for caution in ascribing the coalescence of variable-temperature NMR signals of diast

232 Enucleation is caused by the coalescence of vesicles at the nuclear-cytoplasmic junct

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

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

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

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

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

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

239 7+/-45) ripens through cluster diffusion and coalescence only (Smoluchowski ripening).

240 othness and absence of defects (i.e. partial coalescence or irregular shape).

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

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

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

244 rce balance allows the construction of a new coalescence phase diagram.

245 Coalescence, pressure effect on adjacent structures and

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

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

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

249 a new divide and conquer method for the deep coalescence problem based on the Pareto property.

250 nquer method extends the utility of the deep coalescence problem to data sets with enormous numbers o

251 escence in phylogenetic analyses is the deep coalescence problem, which takes a collection of gene tr

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

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

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

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

256 ning and differentiate Ostwald ripening from coalescence processes.

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

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

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

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

261 lfactory sensory neuron (OSN) axon targeting/coalescence, recent work showed that G protein activatio

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

263 Using coalescence simulations of diverging populations, we exp

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

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

266 eps in the process, including site-selective coalescence, structural reshaping after coalescence, and

267 ation alone is sufficient to induce OSN axon coalescence, suggesting an activity-dependent mechanism

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

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

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

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

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

273 hypothesise that in combination with contact coalescence, these mechanisms concentrate important mole

274 30 thousand years, the comparatively recent coalescence time of the extant variation of haplogroup U

275 zygosity generate quite distinct patterns in coalescence-time distributions and gene identity measure

276 The emphasis is on expected coalescence times (proportional to the expected amount o

277 ese distributions to obtain expectations for coalescence times and for homozygosity and heterozygosit

278 ial founder model, deriving distributions of coalescence times for pairs of lineages sampled either f

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

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

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

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

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

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

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

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

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

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

289 During coalescence, two drops first touch and then merge as the

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

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

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

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

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

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

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

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

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