ライフサイエンスコーパス: creep

1 d range expansion has been termed 'Caribbean Creep'.

2 ediated deformation (for example, Coble-type creep).

3 bility to vancomycin are emerging (i.e., MIC creep).

4 xtended slowly in vitro under constant load (creep).

5 iffness), yet did not induce wall loosening (creep).

6 study under more extreme conditions, such as creep.

7 eing an indirect effect mediated by aseismic creep.

8 continuous displacement, due to viscoelastic creep.

9 r than grain boundary sliding or diffusional creep.

10 in the films and occurs through viscoelastic creep.

11 rce, but not so closely coupled to cell wall creep.

12 and is inconsistent with the concept of MIC creep.

13 , while splay and nanoparticles inhibit flux creep.

14 to a factor of 1000 during uniaxial tensile creep.

15 en strain rate and segmental mobility during creep.

16 e sliding behaviour is consistent with fault creep.

17 t consequence of ongoing, localised aseismic creep.

18 er many thermal actuation cycles without any creep.

19 stress concentrations induced by deep fault creep.

20 tions for the observed anisotropic diffusion creep.

21 serves as a stimulus to surface diffusional creep.

22 tching field to pinning-potential-determined creep above it.

23 e of large oocytes, suggesting gravitational creep ages oocytes, with fatal consequences on long time

24 ide the tubules via mainly diffusional Coble creep along the MIEC/metal phase boundary.

25 r regional Garlock fault, triggering shallow creep and a substantial earthquake swarm.

26 nanocrystal stability by surface diffusional creep and dislocation plasticity, respectively, which ex

27 rtz and feldspar relieves stress by aseismic creep and earthquakes are infrequent.

28 s exceptional resistance to high-temperature creep and excellent tolerance to extremely high-dose rad

29 tringite formation, reinforcement corrosion, creep and fatigue, etc.

30 ombining insight from laboratory solid-state creep and friction experiments can successfully explain

31 a diffusion creep, dissolution-precipitation creep and grain boundary sliding.

32 eomorphologic features indicative of viscous creep and hence ground ice have been observed.

33 causes phenomena such as stress relaxation, creep and hysteresis.

34 Total-IVOC emissions from creep and idle operations are substantially higher than

35 he effective activation energy for diffusion creep and lead to a viscosity minimum in the mid-lower m

36 The observed nonlinear relationship of creep and precipitation rates suggests that increased po

37 esulting mechanical properties from both the creep and recovery phases were compared.

38 To do so, confined compression creep and recovery tests were conducted on cartilage exp

39 liance, and behaved more elastic with faster creep and recovery time constants.

40 The magnitudes of creep and relaxation of both HOIPs and IPs are similar,

41 role for xyloglucan) but less extensible in creep and stress relaxation processes mediated by alpha-

42 echanical systems platform, in vitro coupled creep and stress relaxation tests were performed on coll

43 ing cooling, which mechanistically comprises creep and stress relaxation.

44 single crystal by measuring nanoindentation creep and stress relaxation.

45 etworks of cellulose microfibrils influenced creep and tensile stiffness whereas homogalacturonan inf

46 ew clues about designing materials with slow creep and the interplay between material parameters and

47 nite is commonly invoked as the cause of the creep and the low strength of this section of the San An

48 Inconsistent evidence on vancomycin MIC creep and the relevance of the MIC to clinical outcome m

49 equilibrium and non-linear conditions during creep and the transient regime prior to steady flow.

50 s to model the strain behaviour by including creep and this diffusion-controlled phase change.

51 microseismicity related to the accelerating creep and to creep events in the model should be detecta

52 network's plastic deformation also manifests creep and yield regimes depending on the strain rate.

53 model the time scales of stress relaxation, creep, and hysteresis were assessed, and found to be in

54 ese samples exhibit a pronounced increase in creep, and stress relaxation as a function of indentatio

55 ns and pectins elicited greater extension in creep assays of xxt1/xxt2 cell walls compared with wild-

56 tress and high temperature and deformational creep at high stress.

57 rupture at early times followed by aseismic creep at late times.

58 ating the predominant regimes of diffusional creep at low stress and high temperature and deformation

59 the creep rate and reversed the direction of creep at positive pipette potentials.

60 and San Juan Bautista in central California creeps at a rate as high as 28 mm yr(-1), and it is also

61 The results of this study indicate that creeping attachment (i.e., soft tissue recovery) might o

62 o additional root coverage was gained due to creeping attachment between 2 and 6 months for either gr

63 age between 6 months and 2 years, exhibiting creeping attachment of 0.7 +/- 0.6 mm.

64 vements were sustained, suboptimal practices crept back.

65 er from the more traditional viscoelastic or creep-based models in that they incorporate both cell ge

66 rovides innovative measurements of cartilage creep behavior (which has been well-documented in vitro

67 Precise, repeatable measurements of corneal creep behavior can be conveniently obtained using MII at

68 e results showed that heat treatment reduced creep behavior compared to that of untreated wood.

69 Hertzian model that was then used to predict creep behavior for another imposed force.

70 lity resulted, but a significant increase in creep behaviour was observed in the presence of active t

71 ed load' is a dense granular flow bounded by creep below and suspension above.

72 Two variants of creeping bentgrass (Agrostis stolonifera cv palustris),

73 e-specific expression of both genes in rice, creeping bentgrass (Agrostis stolonifera L.) and Arabido

74 ocuments gene flow on a landscape level from creeping bentgrass (Agrostis stolonifera L.), one of the

75 za sativa) miR528 (Osa-miR528) in transgenic creeping bentgrass (Agrostis stolonifera) alters plant d

76 wn patch (Rhizoctonia solani) and stem rust; creeping bentgrass (Agrostis stolonifera) for resistance

77 response to abiotic stress using transgenic creeping bentgrass (Agrostis stolonifera) overexpressing

78 from heterozygous populations of the species creeping bentgrass (Agrostis stolonifera).

79 Most individual creeping bentgrass plants examined are lacking Crs-1.

80 The Crs-1 locus in creeping bentgrass provides a rare example of the evolut

81 the three parental lines used to develop the creeping bentgrass variants.

82 ntified as two putative targets of miR528 in creeping bentgrass.

83 ent land plant lineage and have a flattened, creeping body (the thallus), which grows from apical cel

84 ch fault gouge via dissolution-precipitation creep can explain the reduction in tremor recurrence tim

85 Grain-size reduction and creep cavitation along localized shear zones enhanced fl

86 Creep cavitation in an ex-service nuclear steam header T

87 athelicidin LL-37 killing and daptomycin MIC creep compared to non-USA600 MRSA.

88 nitude and directionality of the cytoplasmic creep compliance (Gamma) in confluent cultures of bovine

89 f-magnitude shift in intracellular effective creep compliance and apparent elastic modulus.

90 Creep compliance as a function of time and temperature w

91 ional (3D) matrices, intracellular effective creep compliance of prostate cancer cells is shown to in

92 ndent viscoelastic moduli and time-dependent creep compliance of the cytoplasm.

93 multiple rheological measurements of cells: creep compliance versus time, complex modulus versus fre

94 grain coarsening, under extremely long-term creep conditions.

95 he recent advances in this field, pure climb creep controlled by diffusion is identified as the key m

96 stification of the power law for subcritical creep crack growth, hitherto considered empirical.

97 cipients with deteriorating renal function ("creeping creatinine") secondary to chronic allograft nep

98 With regard to upward creep, defects were of larger extent with the double- th

99 ing' mechanism that resists high-temperature creep deformation in nickel-based superalloys, where spe

100 ffect raises fundamental questions regarding creep deformation mechanisms.

101 ichment to crystalline defects formed during creep deformation, using combined transmission electron

102 It creeps (deforms plastically with time) at high temperatu

103 Gravitational forces also cause creep displacement of nuclear bodies, resulting in their

104 ocalized shear zones deforming via diffusion creep, dissolution-precipitation creep and grain boundar

105 Our major finding is that postseismic creep dominates the interaction, with earthquake trigger

106 the accumulated polymerases slowly move or 'creep' downstream.

107 resumably due to the activation of power-law creep during the post-earthquake period.

108 chromatin compaction by step-like and slow "creeping" dynamics consistent with a loop-extrusion mech

109 m Aspergillus niger) did not cause cell wall creep, either by itself or in combination with XEG.

110 nase, confirmed the conclusion that to cause creep, endoglucanases must cut both xyloglucan and cellu

111 collectively, such as when confronted with "creeping" environmental problems.

112 ity related to the accelerating creep and to creep events in the model should be detectable.

113 flux: (1) steady-state slip; (2) spontaneous creep events of small displacement with negligible weake

114 gamut of slip styles from stable sliding and creep events to earthquakes.

115 Creep experiments revealed two opposite rheological beha

116 The result: creep exponents obtained from two kinds of tests agree w

117 es to criticality for volcanic eruptions and creep failure.

118 D) is the extra-intestinal manifestation of "creeping fat" (CrF), defined as expansion of mesenteric

119 ically adapted to the MAT contribute to the "creeping fat" of Crohn's disease.

120 In areas of creeping fat, which characterizes inflammation-affected

121 sites of intestinal inflammation is known as creeping fat.

122 enteries is associated with the formation of creeping fat.

123 ts due to their outstanding high temperature creep, fatigue and oxidation resistance.

124 ion-triggering) and intrinsic (secular fault creep) fault processes can lead to SSEs.

125 d ultramafic rocks have been associated with creeping faults in central and northern California, and

126 adderwort traps avoid the adverse effects of creeping flow by generating strong, fast-onset suction p

127 Whitehead paradox need be encountered in the creeping flow regime and (ii) the flux of the factor wil

128 ated streamers in a microfluidic device in a creeping flow regime using both experimental observation

129 on, a mechanism that is not effective in the creeping-flow regime where viscous forces prevent the ge

130 anding the evolution of biofilm streamers in creeping flows.

131 This creeping fluid flow has been shown to affect the morphol

132 ytometry, membrane thermal fluctuations, and creep followed by cell recovery.

133 sses are relaxed over time and which exhibit creep, for three-dimensional (3D) culture of chondrocyte

134 that coda Q-1 may represent the activity of creep fracture in the ductile part of the lithosphere oc

135 ure that specifically decouples irreversible creep from stress relaxation and modulus.

136 Creeping grains beneath the bed-load layer give rise to

137 is boundary has higher rates of interseismic creep, has not generated an earthquake with MJ > 7 (loca

138 g particles in the nucleation mode; and (F3) creep-idle conditions, representing traffic congestion a

139 ge of driving cycles (transient, high-speed, creep/idle) on different ultralow sulfur diesel fuels wi

140 Here, we report very slow creep in BaFe 2(As0.67P0.33)2 films, and propose the exi

141 Molecular processes of creep in metallic glass thin films are simulated at expe

142 mply by flow models which assume dislocation creep in postperovskite.

143 olving the onset of highly localized viscous creep in pre-existing, fine-grained shear zones.

144 The debate on creep in primary consolidation is analysed with a power

145 deformation and flow processes of amorphous creep in response to stress and thermal activations.

146 pproximately logarithmic in time, similar to creep in solids.

147 fective viscosity resulting from dislocation creep in the asthenosphere explains the peculiar retrogr

148 vide the connection between serpentinite and creep in the San Andreas fault, if shear at depth can be

149 s thaliana) hypocotyls, where Cel12A induced creep in wild-type but not in xyloglucan-deficient (xxt1

150 This study investigated "creep" in vancomycin and daptomycin MICs among methicill

151 ements of thermally activated vortex motion (creep) in iron-based superconductors unveiled fast rates

152 iminished unpredictability can allow bias to creep into a trial.

153 Creep is characteristic of disordered solids and reminis

154 SiO(3) bridgmanite resulting from pure climb creep is consequently evaluated and compared with the vi

155 wer law model following an approach in which creep is considered as rate of loading.

156 Voltage-independent creep is expected from the capillary attraction of E(a)

157 "Creep" is an example from everyday life.

158 culations, we attribute the 600% increase in creep life in a prototypical Mg-rare earth (RE)-Zn alloy

159 nexpected, order of magnitude improvement in creep life of alloys upon adding small amounts of elemen

160 ess, primarily enhances the high-temperature creep life.

161 i-based superalloys which almost doubled the creep lifetime.

162 echanical studies of individual nanowires in creep-like conditions to demonstrate that superplastic-l

163 l velocity can be described with a nonlinear creep-like region and a depinning-like region.

164 e to irradiation damage and high-temperature creep, little is known about the mechanical roles of the

165 (Cucumis sativus) hypocotyl walls to undergo creep (long-term, irreversible extension) in response to

166 he equilibrium phase diagram), so this Coble creep mechanism can effectively relieve stress, maintain

167 t cell walls in vitro can extend slowly by a creep mechanism without passive reorientation of innermo

168 emperature and high strain rate by a viscous creep mechanism.

169 ment that induces wall stress relaxation and creep, mimicking wall behaviours during cell growth.

170 lity in this linear regime is described by a creep model of zero-dimensional charges moving within a

171 her dynamic modulus of elasticity and higher creep modulus, meaning that the attachment is stronger a

172 deal, linearly polarizable sphere undergoing creeping motion in viscous medium, we have shown that bo

173 Creeping motion of a Jeffrey fluid in a small width poro

174 ngs suggest that the viscoelastic stretching/creep of axons caused by tension exerted by the growth c

175 reveal glassy behavior involving collective creep of bundles of 2D pancake vortices as well as tempe

176 lts from increases in contact area caused by creep of contacting asperities.

177 ad of external-stress relaxation through the creep of non-liquid-crystal transient networks with exch

178 of temperature conditions and the transient creep of olivine, we explain the transient deformation i

179 as the result of water- and stress-activated creep of olivine.

180 ust have been completely closed by secondary creep of shale in less than a million years.

181 r, the effect of small size on ductility and creep of silicon remains elusive.

182 ligible creep of the sclera and very gradual creep of the cornea.

183 chanical extensions differ from those during creep of the enzymatically loosened wall.

184 Low IOP elicited negligible creep of the sclera and very gradual creep of the cornea

185 mine the type of damage evolution, i.e., the creep or fatigue, during the operation.

186 dditionally, we found no correlation between creeping or locked faults and tremor, contrary to predic

187 econd, and that the first of two shocks in a creep- or intrusion-driven swarm triggers the second, wh

188 Creep penetration experiments with a constant indentatio

189 of bond stiffness via microalloying enhances creep performance of alloys.

190 l effects such as embrittlement, accelerated creep, phase instability, and radiation-altered corrosio

191 sms of the complex processes involved in the creeping porous air and water flow in the presence of ca

192 that deformation of the mechanically unusual creeping portions of the San Andreas fault system is con

193 es during cooling show a good agreement when creep predominates.

194 e link between slab geometry and solid-state creep processes in the mantle.

195 twins, leading to significant improvement in creep properties.

196 the creep strain rate and thereby improving creep properties.

197 new grains that degrade the high-temperature creep properties.

198 y development was the only factor related to creeping proteinuria (hazard ratio, 2.946; 95% confidenc

199 Creeping proteinuria during the first year was associate

200 ths, variation <50%, and increase >/=50% or "creeping proteinuria") (n = 283).

201 Creeping proteinuria, which was present in 35 patients (

202 the seal membrane with low pH decreased the creep rate and reversed the direction of creep at positi

203 luronan, may participate in these changes in creep rate and, in turn, participate in controlling the

204 th applied stress; above that threshold, the creep rate becomes independent of applied stress.

205 at least as early as axial, refractive, and creep rate changes.

206 es; during recovery from induced myopia, the creep rate decreases below normal levels.

207 ce scleral remodeling and changes in scleral creep rate during the development of form deprivation my

208 ress: below a critical stress threshold, the creep rate increases linearly with applied stress; above

209 d levels of the other GAGs, which occur when creep rate is at its peak elevation, and their rapid ret

210 We find a steady-state creep rate of less than 10(-6) per second-six to eight o

211 le deformation under creep, with a secondary creep rate of only ~ 10(-6) s(-1).

212 tly, we observe a biphasic dependence of the creep rate on applied stress: below a critical stress th

213 aracteristics (inversely proportional to the creep rate S) allows the depinning mechanism to be deter

214 c explanation of the well-known variation of creep rate with stress.

215 A change in scleral extensibility (creep rate) is closely associated with the change in axi

216 le in regulating the biomechanical property (creep rate) of the sclera.

217 A biomechanical property of the sclera, creep rate, increases; during recovery from induced myop

218 resistance at 973 K in terms of the minimal creep rate, which is four orders of magnitude lower than

219 el12A from Hypocrea jecorina) induced a high creep rate.

220 tate, and the previously measured changes in creep rate.

221 rameters, we observe a constant deformation (creep) rate that is linearly proportional to the rate of

222 s (TiBw), and a decrease of the steady-state creep rates by augmenting the local volume fractions of

223 limits their practical utility; for example, creep rates in nanocrystalline copper are about four ord

224 ged glaucoma eyes had slower circumferential creep rates in the peripapillary sclera than normal eyes

225 r tan delta and less compliance during shear creep recovery rheology.

226 cue grass Festuca rubra subsp. rubra (strong creeping red fescue) infected with E. festucae.

227 resistance seen in endophyte-infected strong creeping red fescue.

228 ubilization, beta-expansin treatment induced creep, reduced the breaking force and increased the plas

229 and field-driven domain wall velocity in the creep regime are modified in Pt/Co(0.85-1.0 nm)/Pt thin

230 cities have only been observed so far in the creep regime where domain wall velocities are low due to

231 nced mobility, which remain localized in the creep regime, but grow for applied stresses leading to s

232 roperties of the lower-Tc Nd1111 in the flux-creep regime.

233 mantle sluggishly deforms in the dislocation creep regime.

234 y, plasticity, and time-dependent extension (creep) relate to one another, to plant cell wall structu

235 Our results suggest that the enhanced creep resistance achieved by control over chain topology

236 High creep resistance and high electrical conductivity are ob

237 cal structure material exhibits the superior creep resistance at 973 K in terms of the minimal creep

238 at 150 degrees C while also exhibiting good creep resistance at temperatures below its melting trans

239 ent architecture that exhibits a significant creep resistance compared to monolithic Ti6Al4V alloys.

240 a significant improvement of the composites creep resistance due to the network architecture made by

241 rt a novel ferritic alloy with the excellent creep resistance enhanced by coherent hierarchical preci

242 ble structural alloys with high strength and creep resistance for various high-temperature applicatio

243 The degradation of creep resistance in nanocrystalline materials is in part

244 Although the significant improvement of the creep resistance is achieved in the hierarchical-precipi

245 isms lead to a remarkable improvement of the creep resistance of these networked TiBw/Ti6Al4V composi

246 eived great attentions due to their superior creep resistance, as compared to conventional ferritic s

247 sses in other mechanical properties, such as creep resistance, which limits their practical utility;

248 gth combined with extremely high-temperature creep resistance, while maintaining mechanical and therm

249 that of Ti6Al4V alloys, indicating a higher creep resistance.

250 ure and made it possible to obtain excellent creep resistance.

251 The extraordinary creep-resistance of Mg-Nd-based alloys can be correlated

252 operties, and advance the development of the creep resistant materials.

253 s and the fundamental science for developing creep-resistant ferritic alloys.

254 There have been numerous efforts to develop creep-resistant materials strengthened by incoherent par

255 a quantitative link between the macroscopic creep response and the microscopic single-particle dynam

256 le inflation method of measuring the biaxial creep response of ultrathin polymer films.

257 y of EXPB action, we assessed the extension (creep) response of cell walls from diverse monocot famil

258 Creep results in progressive work hardening with disloca

259 Based on the creep results, we show that the second magnetization pea

260 ionless number accounting for diffusive soil creep, runoff erosion, and tectonic uplift, is reminisce

261 Creep-rupture lifetime exceeding 2000 hours at 750 degre

262 rates of thermally activated vortex motion (creep) S(T, H) = |dlnM(T, H)/dlnt|, we reveal glassy beh

263 rancisco' and 'Los Angeles' repeaters on the creeping section of the San Andreas Fault.

264 Voltage-dependent creep seems to arise from electroosmosis in the seal.

265 equences to constrain friction properties of creeping segments.

266 er and lead to processes such as diffusional creep, sliding and rotation.

267 ers concerned with the phenomenon of "myopic creep." Soft contact lens wear by children does not caus

268 imit the range expansion of other 'Caribbean Creep' species.

269 identification of a gene, designated Crs-1 (creeping specific-1), that appears to be in the process

270 t on dislocation movement, thus reducing the creep strain rate and thereby improving creep properties

271 A family of inexpensive, Al2O3-forming, high-creep strength austenitic stainless steels has been deve

272 ls from xxt1/xxt2 and wild-type plants using creep, stress relaxation, and stress/strain assays, in c

273 via integrin-bound microbubbles, enabling a creep test for measuring cellular mechanical property or

274 For each specimen, creep testing was performed using two different forces f

275 Creep tests performed at temperatures between 773 K and

276 controlled load-unload tests to 30 mm Hg and creep tests to 15 and 30 mm Hg.

277 Micro-indentation creep tests were performed on porcine TMJ condylar carti

278 diffusivity results in anisotropic diffusion creep, texture generation, and a strain-weakening rheolo

279 y using Hertzian viscoelastic formulation of creep, the deformation resulting from sustained-force ap

280 by constraining diffusion and implementing a creep theoretical model.

281 a' phases during stress relaxation, while in creep there is no clear monotonic trend in lattice strai

282 Anisotropic diffusion creep therefore provides an attractive alternative expla

283 The transition from creep to strain recovery fits a tensile-compressive line

284 n of domain wall velocities ranging from the creep to the flow regime in Ta/Co40Fe40B20/MgO/TiO2 stru

285 tabilizes them by slowing down gravitational creep to ~2 months.

286 nset is instead a continuous transition from creeping to granular flow.

287 ces an instantaneous deformation followed by creeping to the asymptotic response.

288 nstantaneous deformation followed by gradual creeping to the long-term response.

289 It can be used to identify the creep towards complete antibiotics resistance in bacteri

290 interseismic fault unlocking, slow slip and creep transients, swarm seismicity, and rapid pressure/s

291 K is not a direct (two-state) process, but a creeping transition that takes place through at least on

292 Patches creep up the pipette over time with voltage independent

293 Acidic buffer induced rapid cell wall creep via endogenous alpha-expansins, with negligible ef

294 sappearance of one species of the 'Caribbean Creep' we exposed the non-native crab Petrolisthes armat

295 gillus aculeatus) failed to induce cell wall creep, whereas an endoglucanase that hydrolyzes both xyl

296 urse of hair bundle displacement (mechanical creep), which affects the hair cell's macroscopic MET cu

297 ifunctional xyloglucanase/cellulase, induced creep with only subtle changes in wall appearance.

298 BC nanopaper showed little deformation under creep, with a secondary creep rate of only ~ 10(-6) s(-1

299 ld, California, near the southern end of the creeping zone.

300 historical times, separated by a 150-km-long creeping zone.

301 the region of coseismic slip and the up-dip creeping zone.