ライフサイエンスコーパス: repulsion

1 liver bud formation and laterality via cell repulsion.

2 further inward and receiving stronger water repulsion.

3 ectrons minimize their strong mutual Coulomb repulsion.

4 tether between cells, thereby enabling cell repulsion.

5 way is required for EphB2-stimulated contact repulsion.

6 eractions between neurons through homophilic repulsion.

7 attraction, although some ORN types produced repulsion.

8 1 reverse signaling and causes neuronal axon repulsion.

9 g is essential for cell segregation and cell repulsion.

10 particles, to their effective electrostatic repulsion.

11 s essential for netrin-1/UNC5C-promoted axon repulsion.

12 nt stress fiber, which orchestrates cellular repulsion.

13 WPI by electrostatic repulsion; GA by steric repulsion.

14 ary phase through conspecific attraction and repulsion.

15 d in the behavioral shift from attraction to repulsion.

16 th silica surface because of a strong charge repulsion.

17 ty are equally excluded due to electrostatic repulsion.

18 e deformation and hydration or electrostatic repulsion.

19 a strategy that helped reduce electrostatic repulsion.

20 rocesses by modulating cellular adhesion and repulsion.

21 d by EphB2 signaling that contribute to cell repulsion.

22 n1 and become sensitive to midline Slit-Robo repulsion.

23 d switched netrin tropism from attraction to repulsion.

24 , controls cell morphology, and thereby cell repulsion.

25 y for the solvent and increase interparticle repulsion.

26 on of filopodial protrusion involved in axon repulsion.

27 te to switch the response from attraction to repulsion.

28 nce cue that can mediate both attraction and repulsion.

29 ron density on O-3 increased 1,3-syn-diaxial repulsion.

30 tive cellular effects as F-actin disassembly/repulsion.

31 helix of one protomer breaks to relieve the repulsion.

32 NC5C is involved in netrin-1-mediated axonal repulsion.

33 ork distortions are required to avoid steric repulsion.

34 respectively drive pheromone attraction and repulsion.

35 sfer in competition with destabilizing Pauli repulsions.

36 one entropy and salt-dependent electrostatic repulsions.

37 folding of the glycoligand minimizing steric repulsions.

38 he screened Coulomb and the electron overlap repulsions.

39 riginate from both, hydration and undulation repulsions.

40 pitope, highlighting roles for charge-charge repulsions.

41 n and for those held apart due to long-range repulsions.

42 rotein regions, application of attraction or repulsion, accounting for pairwise distance restraints,

43 ed counterions from solution to avoid charge-repulsion along its backbone and with other PAH molecule

44 mechanistic insights: (i) increased pi...pi repulsions along [100] lead to expansion along the a axi

45 neurotransmitters underlying attraction and repulsion among locusts remains unknown.

46 Despite the repulsion among the anions, the lowest energy states hav

47 gered ABAB stacking that reduces the Coulomb repulsion among the stripes.

48 test the idea that event overlap triggers a "repulsion" among hippocampal representations that develo

49 st LPS contents studied due to electrostatic repulsion and abolishes membrane damage to S. oneidensis

50 ing unspecified social forces of attraction, repulsion and alignment with parameters drawn from obser

51 fluctuation spectrum, and oscillates between repulsion and attraction as a function of wall separatio

52 ut mice in hair growth, wound healing, water repulsion and body temperature regulation.

53 rons can be used to exactly balance both the repulsion and diffraction-broadening.

54 well as for the transition between hydration repulsion and dry adhesion, which favorably compare with

55 ic pair interactions consisting of hard-core repulsion and extra short-range soft-core repulsion beyo

56 ield and a competition between vortex-vortex repulsion and Lorentz force.

57 ge density (r(2) = 0.94) while electrostatic repulsion and loss of positive charge due to destruction

58 disruption of RCP or EphA2 opposes cell:cell repulsion and metastasis in an autochthonous mouse model

59 d endocytic pathway which controls cell:cell repulsion and metastasis in vivo.

60 t repulsion into one that both silences Slit repulsion and potentiates Netrin attraction.

61 ically or genetically disrupts Slit-mediated repulsion and produces severe axon guidance defects in v

62 :Dsg and Dsc:Dsc interactions by same-charge repulsion and promote heterophilic Dsg:Dsc interactions

63 scribe a distinct mechanism to inhibit Robo1 repulsion and promote midline crossing, in which Roundab

64 phorin 3d (Sema3d) mediates endothelial cell repulsion and pulmonary vein patterning during embryogen

65 es outgrowth of the common cardinal vein via repulsion and signals through PlexinD1.

66 Strong Coulomb repulsion and spin-orbit coupling are known to give rise

67 We also characterize the repulsion and steering effect with various excitation vo

68 We demonstrate that cholesterol limits this repulsion and tendency to curve.

69 lecular systems are defined by electrostatic repulsion and the ability of the dominant attractive for

70 sebaceous lipids resulted in impaired water repulsion and thermoregulation, increased rates of UVB-i

71 pulsion to the Thomas-Fermi screened Coulomb repulsion and to the Born-Mayer valence electron overlap

72 ns dominate nearly canceling nuclear-nuclear repulsion and two-electron interactions.

73 lding overcomes intramolecular electrostatic repulsions and forces local dipoles in each layer of the

74 usly mediates NELL2 repulsion, inhibits Slit repulsion, and facilitates Netrin attraction to achieve

75 al than the proximal region of the GC during repulsion, and knockdown of either UNC5C or TUBB3 abolis

76 electron binding energy, the nuclear-nuclear repulsion, and multielectron interactions.

77 t lead to long-range attraction, short-range repulsion, and mutual alignment between adjacent swimmer

78 uch more by electrostatic attraction than by repulsion, and that the filtering capability of the gel

79 egativity, DeltaVNN is the change in nuclear repulsions, and Deltaomega is the change in multielectro

80 itively charged ions to reduce electrostatic repulsions, and induce attractions that can facilitate D

81 y, we demonstrate that electrostatic dye-dye repulsions are negligible for the interdye distance regi

82 NaCl electrolyte concentrations, interfacial repulsions are soft and longer in range, this transition

83 to the next, at odds with any simple Coulomb repulsion argument.

84 the axon guidance field is the importance of repulsion as a guidance mechanism for steering axons to

85 the axon guidance field is the importance of repulsion as a major guidance mechanism.

86 ompensating for intermolecular electrostatic repulsion, as a mechanism to control the length of a sup

87 th I and pH and find that despite the weaker repulsion at higher I and pH, the cluster size remains c

88 uenced surface charge for ALA where enhanced repulsion at pH 7.00 was observed resulting in reduced a

89 The resulting confounding electrostatic repulsion/attraction is strongly influenced by eluent sa

90 at we find is required for subsequent axonal repulsion away from Slit.

91 salt, mainly because of strong electrostatic repulsion between alginate and caseinate.

92 are proposed to be due to the electrostatic repulsion between amino-functionalities and DA.

93 glomeruli, likely owing to contact-mediated repulsion between axons expressing identical combination

94 lectrostatically mimics DNA and can overcome repulsion between basic DNA binding regions of three bZI

95 A contribution of steric repulsion between citrate layers to particle stability i

96 are due to a decrease in closed-shell Pauli repulsion between cycloaddition partners.

97 lated substrate interaction and a long-range repulsion between dots.

98 n fail spectacularly, when the electrostatic repulsion between electrons causes strong correlations.

99 manipulate multi-electron beams, because the repulsion between electrons rapidly alters the beam shap

100 polyanionic cofactors, namely, electrostatic repulsion between four closely spaced cationic lysines w

101 Electrostatic repulsion between helices dominates at low salt concentr

102 Further, the repulsion between like-charged ions is weaker than that

103 ns along the c-axis, driven by electrostatic repulsion between localized electron clouds on Tl and Te

104 r partially desorbed M1 because of increased repulsion between M1 monomers still stuck to the membran

105 an be assigned to shielding of electrostatic repulsion between monomers on the fibril surface or betw

106 caused by the large change in electrostatic repulsion between NPs when the dimers move from intersti

107 s to regulate contact-mediated attraction or repulsion between opposing cells, thereby influencing ti

108 oretical model reveals that in-plane dipolar repulsion between petals in the cluster favors the achir

109 expression; this relieves a native synaptic repulsion between PV cells and pyramidal neurons, thereb

110 proposes a new hypothesis that electrostatic repulsion between sialic residues creates structural con

111 mers in the equilibrium revealed the highest repulsion between the 3-allyloxy group and the isopropox

112 ges (zeta-potential) and hence electrostatic repulsion between the AgNPs.

113 activity is attributed to the smaller steric repulsion between the alkyl group and the lithium surfac

114 primarily from intramolecular electrostatic repulsion between the allosteric and orthosteric ligands

115 and liquid phase environment, results from a repulsion between the electrons of the liquid water and

116 he gas phase because of strong electrostatic repulsion between the extra electrons.

117 nation of capillary action and electrostatic repulsion between the graphene and its container to ensu

118 st-guest complex formation leading to charge repulsion between the host units, as well as an osmotic

119 mobile H2 layers is to decrease the Coulomb repulsion between the negatively charged hydrogen atoms

120 annel is greatly disfavored by electrostatic repulsion between the NTP and the highly negatively char

121 he assembly process is self-limited when the repulsion between the particles is renormalized to balan

122 Upon oxidation, Coulombic repulsion between the positively charged and mechanicall

123 fully expands the cages due to electrostatic repulsion between the positively charged sites.

124 With terminally substituted allenes, steric repulsion between the terminal substituents significantl

125 organic semiconductor devices due to Coulomb repulsion between the two charges.

126 the collector surfaces through electrosteric repulsion between the two interpenetrating charged polym

127 rin skeleton, which alleviates electrostatic repulsion between the two NH protons, and two polarizati

128 attractive forces to overcome the long-range repulsion between the vesicle and membrane.

129 ng, alpha-helix formation, and electrostatic repulsions between acidic side chains, which collectivel

130 ic charge around the anion arise because the repulsions between weakly positively charged H atoms are

131 lipids and cholesterol, a significant push (repulsion) between the low-melting and high-melting lipi

132 teractions at longer range--interparticulate repulsion--between particles that are complexing Eu(III)

133 re repulsion and extra short-range soft-core repulsion beyond the hard core, whose length scale is ro

134 phenomenon is not specific to EphB2/ephrinB1 repulsion but is also present during the formation of bo

135 ptor) is safely large to avoid electrostatic repulsion but, at the same time, amenable to a closer ap

136 igh n-PCM concentration due to electrostatic repulsion, but unstable at intermediate n-PCM concentrat

137 ng pH and salt concentration, due to Coulomb repulsion by charged residues.

138 FVIIa caused potentiation of cell repulsion by the EphB2 ligand ephrin-B1, demonstrating a

139 three intracellular domains, suggesting that repulsion by Unc5, Robo, and Drl, and perhaps repulsion

140 sphere system (alphaBc) and screened Coulomb repulsion combined with short-range attraction (HEWL).

141 sically challenging because inter-electronic repulsion, crystal field, and spin-orbit coupling effect

142 oth surfaces are very hydrophilic, hydration repulsion dominates at small separations and direct attr

143 ocess that is required for subsequent axonal repulsion downstream of the Robo receptor.

144 support parallel ionpair-pi interactions and repulsion-driven ion pairing with self-assembled fluorop

145 Early on, we have argued that repulsion-driven ion-pairing interactions with anionic l

146 in response to self-assembly, i.e., generate repulsion-driven ion-pairing interactions.

147 el membrane were strongly affected by charge repulsion, due to the negative charge of the hydroxyl fu

148 ms: elastic energy of the linker DNA, steric repulsion, electrostatics, and a phenomenological (H4 ta

149 The fitted repulsion energies fall within the theoretical range of

150 The repulsion ensures a minimal distance between the particl

151 ion, and visualized dynamic contact-mediated repulsion events in primary mouse hippocampal neurons ov

152 afficking of EphA2 which generates cell:cell repulsion events that drive tumour cells apart.

153 We find that the repulsion exponent p approximately 6.5 provides an excel

154 We propose the inference of the repulsion exponent through Hierarchical Bayesian uncerta

155 high salinity marine waters by electrosteric repulsion for long time periods.

156 n core creates a very strong but short-range repulsion for oxygen that is consistent with experimenta

157 d to the Born-Mayer valence electron overlap repulsion for various alloys.

158 the balance of the long-range attraction and repulsion forces which stabilizes the cluster patterns a

159 se in the PVDF-BSA and BSA-BSA electrostatic repulsion forces, resulting in a higher deposition rate

160 is was mainly due to the increased hydration repulsion forces, which caused a decrease in the PVDF-BS

161 the interior of the NPC, setting up entropic repulsion forces.

162 al studies identify the cause as interligand repulsion forcing a wider C-Pd-C angle and tilting of th

163 l changes, likely triggered by electrostatic repulsion from a distinct negatively charged environment

164 ord midline by antagonizing Robo1/2-mediated repulsion from midline-expressed Slits and potentiating

165 mpared with acetylene, because of the steric repulsion from the additional substituents.

166 face carboxyl content, despite electrostatic repulsion from the growing negative charge.

167 pair-pi interactions are preferred, despite repulsion from the push-pull dipole.

168 Incipient repulsion from the too short halogen bond increases the

169 atial scales, from long-range attraction and repulsion from the troop's sleeping site, to relatively

170 host chromosome and are therefore "linked in repulsion." Functional complementation of the loci is ac

171 abilization mechanisms: WPI by electrostatic repulsion; GA by steric repulsion.

172 on of the AgNPs as a result of electrostatic repulsion, giving rise to a detectable color change.

173 achment inhibition is based on electrostatic repulsion, high hydrophilicity and the steric hindrance

174 e potential and limitations of electrostatic repulsion-hydrophilic interaction chromatography (ERLIC)

175 le phosphoproteomics, based on electrostatic repulsion-hydrophilic interaction chromatography (ERLIC)

176 illary column operating in the electrostatic repulsion-hydrophilic interaction mode (ERLIC) and coupl

177 dge actin networks forms the basis of mutual repulsion in Drosophila hemocytes.

178 onent 5a and IL-8 induce chemoattraction and repulsion in equal proportions, resulting in the dispers

179 and RhoA signaling necessary for growth cone repulsion in GABAergic interneurons in vitro, which may

180 epulsion by Unc5, Robo, and Drl, and perhaps repulsion in general, involves Trio activity.

181 Hydrogen-hydrogen steric repulsion in naphthalimide-naphthalene (NIN) dyad destab

182 ped interfaces, and long-range electrostatic repulsion in organic media also contribute to the colloi

183 ndependent mechanisms to overcome Slit-Robo1 repulsion in pre-crossing commissural axons have evolved

184 a more important role than A36-driven super-repulsion in promoting the cell-to-cell spread of vaccin

185 nsive approach is taken to study the role of repulsion in the assembly behavior of DNA-NPs, enabling

186 ons is also due to the trend in closed-shell repulsion in the cycloadducts.

187 ing commissural axons to mediate floor plate repulsion in the mouse spinal cord.

188 UBB3 or UNC5C blocked netrin-1-promoted axon repulsion in vitro and caused defects in axon projection

189 d can mediate precrossing semaphorin-induced repulsion in vitro.

190 related to differences in electron-electron repulsions in the conjugated and nonconjugated systems,

191 ntly, with the latter dominating the overall repulsions in the Ld phase.

192 yn isomer fraction increases, intermolecular repulsion increases, resulting in a decrease in the unit

193 model incorporating line tension and dipole repulsion indicated that even small changes in line tens

194 thfinding that simultaneously mediates NELL2 repulsion, inhibits Slit repulsion, and facilitates Netr

195 quence of energetically unfavorable exchange-repulsion interactions among the phenyl side groups.

196 Under extreme pH conditions, charge repulsion interactions within the protein chain can over

197 lian brain by converting a receptor for Slit repulsion into one that both silences Slit repulsion and

198 averted due to a screened long-range Coulomb repulsion intrinsic to disordered q1D materials.

199 Hemocyte collision and subsequent repulsion involves a stereotyped sequence of kinematic s

200 foldamer for strand mimicry in which dipolar repulsion is a central determinant of conformation.

201 most unconventional superconductors, Coulomb repulsion is minimized through the formation of higher a

202 This suggests that neural and perceptual repulsion is not a mechanism to enhance perceptual perfo

203 rast, the complementary parallel ion pair-pi repulsion is spectroscopically irrelevant, in part becau

204 that cannot be cleaved revealed that midline repulsion is still present but longitudinal axon guidanc

205 raction between diamondoids overcomes steric repulsion leading to a cis configuration at the active g

206 ecrease in the range of the steric hydration repulsion, leading to an increase in adhesion at a much-

207 Electrostatic repulsion leads either to autodetachment of electrons or

208 nformation at low force, where electrostatic repulsion leads to a strong excluded volume effect, and

209 n of heterosis generated by a combination of repulsion linkage and dominance.

210 With two loci having repulsion linkage between two inbreds, heterosis in the

211 Computer simulations show that repulsion linkage could influence QTL detection and esti

212 at this previously insurmountable electronic repulsion may be overcome through the use of sufficientl

213 Herein, cation-cation repulsion may play a significant role for the high valen

214 engers cAMP and cGMP modulate attraction and repulsion mediated by neuronal guidance cues.

215 cient in Plxnd1 are resistant to endothelial repulsion mediated by Sema3e but not Sema3d.

216 for relatively thin substrates a short-range repulsion occurs, which prevents the two drops from comi

217 ting both negative DEP (nDEP) attraction and repulsion of B-cells from each a BPE cathode and anode.

218 l molecules and helps overcome the Coulombic repulsion of bringing two cationic species into contact.

219 er and solute channel is responsible for the repulsion of cations.

220 fine balance between surface charges, steric repulsion of coating molecules, and hydration forces aga

221 that polycations can turn electrostatic self-repulsion of DNA into attraction, yet the physical mecha

222 dings indicate that event overlap triggers a repulsion of hippocampal representations-a finding that

223 range of studies from different disciplines, repulsion of particles has been observed over distances

224 lation, and allowing for semaphorin-mediated repulsion of post-crossing axons.

225 How premature semaphorin-induced repulsion of precrossing axons is suppressed in vivo is

226 sequester semaphorins, preventing premature repulsion of precrossing axons prior to subsequent down-

227 idization between them interact via a strong repulsion of range and strength larger than the repulsio

228 PL localization and induce attraction and/or repulsion of retinal neurites in culture, placing them i

229 usion of key DNA-binding residues and charge repulsion of the DNA backbone.

230 Electrostatic repulsion of the highly negatively charged MS2, fr, and

231 of oxidized C147 would lead to electrostatic repulsion of the opposite negatively charged surface.

232 ydrophobic burial of the myristoyl chain and repulsion of the peptidic moiety from the phospholipid h

233 he lipids, possibly due to the higher steric repulsion of the protein coated nanoparticles.

234 Due to the repulsion of the two aryl substituents within the same b

235 ional destabilization of 3-Pheq conformer by repulsion of unidirectional dipoles of the endocyclic ox

236 abled us to consider the entropic undulation repulsions on a fundamental level, without having to tak

237 nt with those seen in systems with competing repulsions on disparate length scales, and remarkably si

238 pacts of skyrmion-skyrmion and skyrmion-edge repulsions on the feasibility of skyrmion-based racetrac

239 of MBONs can, depending on cell type, induce repulsion or attraction in flies.

240 Bacterial motility, and in particular repulsion or attraction toward specific chemicals, has b

241 ard-sphere-like to long-ranged electrostatic repulsion or mixed charge attraction.

242 nt can be achieved through either increasing repulsion or reducing attraction by modifying the fluid

243 cules inside the pore network, as opposed to repulsion or steric hindrance to the diffusion of molecu

244 lation have much less linkage information in repulsion phase than in coupling phase.

245 nation fractions between dominant markers in repulsion phases.

246 emoving the steric hindrance and same-charge repulsion phenomena via multilayer adsorption.

247 ical origins (e.g., electrostatics, exchange-repulsion, polarization, and charge transfer) is a relat

248 ifugal force and interparticle electrostatic repulsion, polycrystalline, single-crystalline and quasi

249 ulsion of range and strength larger than the repulsion predicted by models that neglect ionic correla

250 redistribution according to simple Coulombic repulsion prior to backbone cleavage into C: and Y: ions

251 Inter-droplet repulsion provides electrostatic stabilization of the em

252 ment increased via reduced colloid-collector repulsion (reduced radius of curvature) and increased at

253 Cell repulsion requires bidirectional trans-endocytosis of cl

254 LRT1-3), thereby promoting cell adhesion and repulsion, respectively.

255 hrin-A-EphA2 signaling, which induces a cell repulsion response in RasV12 cells.

256 respectively correlated with attraction- and repulsion-response to gregarious volatiles.

257 , tyramine receptor (TAR) signaling mediated repulsion-response.

258 t dislocations can change from attraction to repulsion, revealing the complex interplay between chemi

259 roles for CHL1 in both axonal extension and repulsion, selectively of DA neurons, suggestive of a ro

260 sential role in netrin-1/UNC5C-mediated axon repulsion.SIGNIFICANCE STATEMENT Proper regulation of mi

261 qualitative differences in receptor-mediated repulsion, suggesting that, despite their highly diverge

262 low HOMOs experience a higher level of Pauli repulsion than those with higher HOMOs.

263 rmation of finite-sized rafts and mediates a repulsion that distributes them evenly throughout the me

264 explicitly show how CIL yields an effective repulsion that promotes cell dispersal, thereby hinderin

265 s of anionic lipids experience electrostatic repulsion that, being exerted asymmetrically, is predict

266 n the aggregation pathway have electrostatic repulsions that are shielded in the high ionic strength

267 Due to electronic repulsion, the antiferromagnetic correlations of the imp

268 rgistic effects of size exclusion and charge repulsion, the novel UF hollow fibers can effectively re

269 Despite the unfavorable Coulombic repulsion, the singlet diradical dianion dimer of NDI sh

270 ascular deformity was related to endothelial repulsion through binding to the UNC5B receptor.

271 m), an antagonist of Slit-Roundabout midline repulsion, through an unknown mechanism.

272 ary locusts caused the behavioral shift from repulsion to attraction.

273 hiking) and are necessary for switching from repulsion to CO2 (a carrier animal cue) in nondauers to

274 able to link the steepness of the interionic repulsion to the Thomas-Fermi screened Coulomb repulsion

275 s with a suitable surfactant provides steric repulsions to prevent particles agglomeration.

276 s usually show uni-directional attraction or repulsion toward their specific cue molecules.

277 the insulating gap is driven by the Coulomb repulsion U on the transition-metal cation, and charge-t

278 under these conditions, due to electrostatic repulsion, unless hydrophilic interaction is superimpose

279 sequences, each intracellular domain elicits repulsion via a common pathway.

280 the very general Valence Shell Electron Pair Repulsion (VSEPR) model to the most esoteric reaction me

281 is stabilized by valence shell electron pair repulsion (VSEPR).

282 The strength of 1,3-syn-diaxial repulsion was evaluated for main types of protecting gro

283 The repulsion was mediated by two mechanisms-activation of a

284 cavitation-induced attraction and hydration repulsion we find a narrow range of contact angle combin

285 lizing force and then varying this colloidal repulsion, we can trigger self-assembly of these nanopar

286 Focusing on Semaphorin/Plexin repulsion, we identified an interaction between the F-ac

287 een phosphorylated Ser-108 and domain 4, but repulsion when Ser-108 is dephosphorylated.

288 to clarify the conditions of attraction and repulsion, which are determined by balance between activ

289 s) must overcome electrostatic strand-strand repulsion, which is moderated by the surrounding atmosph

290 nth depends on coordinated inter-endothelial repulsion, which prevents uncontrolled layering of the e

291 ration measurements show a clear short-range repulsion, which we confirm by considering the spatial s

292 remarkably strong long-range attractions or repulsions, which can be split into three regimes depend

293 , dominated by long-range screened Coulombic repulsion (Wigner glass) and a second one, stabilized by

294 LJ potential models atomistic attraction and repulsion with century old prescribed parameters (q = 6,

295 ng about stabilization due to greater steric repulsion with the box frame.

296 ructures is broken by the presence of vortex repulsions with two different lengthscales, originating

297 sions was mainly attributed to electrostatic repulsion, with droplet aggregation occurring at low pH

298 likely excluded by steric and electrostatic repulsion within the active site supporting the hypothes

299 ional analysis, we reveal that electron pair repulsion within the deprotonated anion is not the reaso

300 e electric field that decays within the core repulsion zone of the surface and hence vanishes in regi