ライフサイエンスコーパス: deform

1 cells disaggregate, orientate with flow, and deform.

2 ude when droplets are jammed but only weakly deformed.

3 iving in the harbor area were reported to be deformed.

4 that can be squeezed out when the nucleus is deformed.

5 ntly even if its cortical contraction cannot deform a near-rigid ECM, but then the contraction of the

6 he cell can also migrate even if it fails to deform a stiff nucleus, but then it has to be able to su

7 opological transitions that either refine or deform a tissue.

8 ments at high pressures and temperatures, we deformed a mixture of bridgmanite and magnesiowustite un

9 However, they have potential to deform according to their local energy environment.

10 1 mm, the collagen fiber network in the MVAL deforms according to an affine kinematics model.

11 ility and spermatogenesis defects, including deformed acrosomal formation, degenerative elongating sp

12 pha-proteobacteria display the same membrane deforming activity and are able to partially overcome th

13 ther plastically anisotropic/layered solids, deform and accommodate strain.

14 nents: the entry time required for a cell to deform and enter a constriction, which is dominated by t

15 can generate sufficient mechanical stress to deform and even disrupt soft epithelial cell monolayers,

16 currently available needle delivery systems deform and move soft tissue and organs, leading to a non

17 iting efficient locomotion by its ability to deform and negotiate flexures and bends.

18 to form fibers in red cells, causing them to deform and occlude the circulation.

19 ole in transmitting force to the membrane to deform and reorganize lipid bilayer structure.

20 ess and viscosity indices and were easier to deform and to break.

21 ts rheology, which determines its ability to deform and to dynamically evolve(2).

22 uring mitotic exit, however, centrosomes are deformed and fractured by those same forces, which is a

23 ights are displayed and shown to define both deformed and recovered structures.

24 rienced by mechanoreceptors when the skin is deformed and then simulates the spiking response that wo

25 ting channels through the collagen matrix by deforming and tearing apart collagen fibers and that the

26 to distinguish between normal, mechanically deformed, and pathological skin tissues.

27 contrast, overexpression of MoGSK1 produced deformed appressoria in M. oryzae.

28 ferative glomerulonephritis, liver fibrosis, deforming arthropathy and increased anti-DNA antibodies.

29 largely aligned in the uncombed threads and deform as a single composite unit that is 5-10x stronger

30 Cancer cells deform as they move through while blood cells remain int

31 r soft matter, the nanoMIPs were observed to deform at binding to HTR: while no relevant changes were

32 When the electron clouds become more deformed at a longer emitting wavelength due to reduced

33 erlying cytoskeleton are expected to locally deform axisymmetrically when indented by a spherical tip

34 These collective findings point toward a deformed B cell repertoire as a fundamental component of

35 monstrates a continuously accreting, shallow-deforming, bed and invariant basal conditions.

36 When deformed beyond the linear regime, the aggregation flows

37 When deformed beyond their elastic limits, crystalline solids

38 one remodeling, which result in enlarged and deformed bones in one or more regions of the skeleton.

39 ease presenting with 3 severely fibrotic and deformed bowel loops separated by 2 diseased segments wi

40 ents presenting with 3 severely fibrotic and deformed bowel loops separated by 2 diseased segments wi

41 ted to the complex flow field induced by the deformed bubble shape.

42 in matrix components, we found that biofilms deform by buckling, and that adhesion transmits these fo

43 Many areas of the Earth's crust deform by distributed extensional faulting and complex f

44 butions, and continues to hold for fractures deformed by applied stress and by chemical erosion as we

45 ics simulation model of a biopolymeric shell deformed by axial forces exerted at opposing poles.

46 ile the dendrites of ddaD were more strongly deformed by backward locomotion.

47 every texture in contact with the liquid is deformed by capillary stresses.

48 osition Fe50Mn30Co10Cr10 (at.%) was severely deformed by FSP and evaluated for its microstructure-mec

49 iron-molybdenum alloy powder was extensively deformed by high energy milling, so to refine the bcc ir

50 the surface of mDia1-coated latex beads, and deformed by manipulating both ends through attached bead

51 Micro-pillars on B2 phase deformed by plastic barreling while L1(2) micro-pillars

52 ongation, where the membrane is then further deformed by polymerizing actin filaments; and 3) pinch-o

53 whereas for larger grain sizes the material deforms by direct amorphization along shear planes.

54 with deeper serrations, serrated petals and deformed carpels.

55 Although mild osmotic stress deforms caveolae and alters interactions between the cav

56 ngated cell shape in normal gravity and this deformed cell shape got rescued to normal one by applyin

57 resulted in disordered arrangement of cells, deformed cell shapes, altered cell structure, and a shor

58 and the transit time required for the fully deformed cell to travel inside the constriction, which m

59 egulates cellular behaviors: cytoskeleton is deformed, cell tentacles are significantly shortened, an

60 In addition, undeformed cells and fully deformed cells were simultaneously characterized via ele

61 wo-dimensional finite element simulations of deforming cells reveal that as a cell protrudes under th

62 In motile, rapidly deforming cells such as human neutrophils, bulk cytoplas

63 How ESCRTs bind and deform cellular membranes and ultimately produce vesicle

64 Direct observation of deformed cellulose fibrils following partial enzymatic d

65 the 3D network of dislocation boundaries in deformed crystalline materials is unknown and critical f

66 l holds for both elastically and plastically deformed crystals and, unless there is significant or co

67 Mechanically pre-deformed crystals taken over the thermal phase transitio

68 and female Erk5 (fl/fl) mice had a severely deformed curved thoracic spine, with an associated loss

69 gammaS-DNA structure reveals that the partly deformed DNA runs symmetrically across central groove be

70 polyhedra in crystalline compounds are often deformed due to structural complexity or electronic inst

71 We find that they deform during flight and, depending on size, quench prio

72 The membrane deforming dynamin family members MxA and MxB are large G

73 we show that the latter can be electrically deformed either radially or along selectable directions,

74 They deform elastically when weakly confined and swell to the

75 oduced exophytic growth, whereas large ducts deformed endophytically.

76 lar connectivity and geometry information of deforming epithelial tissues, and computational tools to

77 rrent artificial microrobots cannot actively deform, exhibiting at best passive bending under externa

78 Dynamic F-actin deforms exocytosed membrane into microvilli.

79 The same lavas, deformed experimentally at volcanic conduit temperature

80 It contains a membrane-deforming F-BAR domain as well as a Src homology 3 (SH3)

81 e hydromechanical parameters of the actively deforming fault.

82 ons as well as flower and pod abnormalities (deformed flower and pod).

83 l physical model of particle dispersion in a deforming fluid domain to show that transport of organel

84 d mitochondrial degeneration, mitophagy, and deformed foot processes in podocytes.

85 demonstration, we applied AFMOTs to trap and deform freely floating individual cells.

86 cells or cell aggregates can induce bands of deformed gel, extending to surprisingly long distances i

87 Moreover, the deformed graphene could exhibit a band-gap, allowing an

88 omic positions and the strain map within the deformed graphene layer, and demonstrate the tip-induced

89 dicting a rapid transition from spherical to deformed ground states, with (78)Ni as the turning point

90 chemoreceptors in live cells by artificially deforming growing cells of Escherichia coli in curved ag

91 15 biophysical parameters from cells as they deform in a microfluidic stretching flow field via high-

92 feature of biomaterials is their ability to deform in response to certain external bio-stimuli.

93 many molecular crystals are soft and can be deformed in a similar way as rubber or plastic, this per

94 The model indicates that the substrate is deformed in the ground state (GS) of the reaction and pa

95 y, that if a crystal's unit cell elastically deforms in an inhomogeneous manner, the yield stress is

96 cooling to room temperature and subsequently deforms in compression, tension, and torsion.

97 it is today, and that its mantle sluggishly deforms in the dislocation creep regime.

98 ated as percentage of insects that were dead/deformed, infertile, or fertile and subjected to chi-squ

99 The extent to which the polymer chains can deform influences the packing density of the JNPs at the

100 ps of Na3Bi and Cd3As2 Generically, the arcs deform into a Fermi pocket, similar to the surface state

101 cell contractility, model epithelia smoothly deform into invaginated or evaginated shapes similar to

102 We track changes in cell shape as cells deform into microfluidic constrictions, and we calibrate

103 we show that RBCs successively tumble, roll, deform into rolling stomatocytes, and, finally, adopt hi

104 olecules, since all the components twist and deform into the same chiral configuration when compresse

105 as the complex eigenvalues of the system are deformed into a two-dimensional flat band enclosed by an

106 olae formation, the cell membrane is locally deformed into curved morphologies.

107 ee degrees of freedom, which can be actively deformed into numerous specific shapes through embedded

108 Third, from prophase onward, chromosomes are deformed into sequential arrays of half-helical segments

109 quitous in nature and understanding how they deform is crucial in geology, nuclear engineering, micro

110 tes compressive stresses on the nucleus that deform it and cause rupture of nuclear membranes.

111 e substrate and the elastic energy needed to deform it, allowing to use bubbles to study elastic prop

112 ts exerting active forces on the membrane to deform it, and 2) the large-scale membrane deformation i

113 crotubules push onto the nuclear envelope to deform it, which results in fission into two daughter nu

114 her the protein binds to unbent DNA and then deforms it, or if bent DNA conformations are 'captured'

115 ds of microscopy demonstrate that PIEZO1 can deform its shape towards a planar structure.

116 ing changes in the hierarchical structure of deforming joints are constrained by destructive sample t

117 f torons within quasi-hexagonal periodically deformed lattices.

118 rnia, and identify seismicity in an actively deforming localized zone penetrating the lithospheric ma

119 of a sample of cold rolled aluminum, further deformed locally by a hardness indentation.

120 realization of steady-state BPs embedded in deformed magnetic vortex cores in asymmetrically shaped

121 s, are remarkably similar to olivines within deformed mantle peridotites, but inconsistent with an or

122 and elucidate how re-encountering previously deformed material hinders performance.

123 ction of energy delivered to the plastically deformed material is responsible for readjustments of de

124 eorganizations are stable in a homogeneously deformed material.

125 a fundamental understanding of how proteins deform membrane.

126 92A and -92B in cooperation with Cby1 induce deformed membrane-like structures containing the small G

127 density was continuously associated with the deforming membrane.

128 ncovers a new paradigm for how a BAR protein deforms membrane.

129 to nucleation of new perfect crystals within deformed metals during annealing, in particular how and

130 Analysis of deformed Mg and Zr microstructures reveals that local tw

131 hree terms: the elastic energy stored in the deformed micro-cylinder, the interfacial energy within t

132 ividual 1.2 mum ZIF-8 microcrystals, and the deformed microcrystals partially recovered after pressur

133 stead we suggest that the subdivision of the deformed microstructure ahead of the boundary plays the

134 Deforming miniature semiconductor-based sensors with hig

135 ochemically relevant degrees of freedom in a deformed molecule, and spotlight selected applications o

136 Here, we use FETs with a deformed monolayer graphene channel for the detection of

137 ry suggests that nanocrystals can be made to deform more controllably than previously thought.

138 f stress within the film causes the holes to deform more substantially than the pillars.

139 on, we observe nanoscale recovery of heavily deformed nacre that restores its mechanical strength on

140 physical-transformation into 3D structurally deformed nanostructures.

141 repared by other methods, the cast nanowires deform nearly homogeneously with much lower strength but

142 Therefore a deforming network is expected to exhaust all possible be

143 Nuclei deformed nonmonotonically under constant load.

144 uitively, we find that even when the droplet deforms noticeably under the influence of gravity, the r

145 a radioactive nucleus-can contain heavy and deformed nuclei, offering high sensitivity for investiga

146 do divide are either multinucleated, display deformed nuclei, or undergo cell division at a much slow

147 e from mechanical stress on chromatin in the deformed nucleus.

148 origin for interactions between any membrane-deforming objects, from nanometre-sized proteins to micr

149 al impacts, causing the sphere to maintain a deformed, oblong shape.

150 Biological cells deform on a nanometer scale when their transmembrane vol

151 it was understood that phyllosilicates could deform only by dislocation glide along layers and could

152 results in stable trapping will also exert a deforming optical stress on the surface of the particle.

153 e in addition to melting-point depression in deformed or damaged crystals relative to their pristine

154 ynamics of the skeleton when the membrane is deformed or perturbed by parasites, the role lipids play

155 The deforming outer accretionary wedge may decouple the stre

156 imine hydroboration with regeneration of the deformed phosphorous triamide 1.

157 solids in which the microscopic elements can deform plastically in response to stresses on them.

158 s of Pd82Si18 is attributed to an ability to deform plastically in the absence of crack nucleation th

159 ssed sufficiently, solid materials yield and deform plastically via reorganization of microscopic con

160 , we report that silicon at small scales may deform plastically with time at lower temperatures (400

161 It creeps (deforms plastically with time) at high temperatures (~80

162 l3 mutants exhibit dramatically enlarged and deformed plastids in the shoot apical meristem, and deve

163 At the grain boundaries of plastically deforming polycrystals, strain transfer mechanisms can a

164 ing stomatocytes, and, finally, adopt highly deformed polylobed shapes for increasing shear stresses,

165 ibute to the chronic inflammatory and tissue-deforming processes characteristic of CRS.

166 cases, lipid transfer proteins, and membrane-deforming proteins in virus replication.

167 nced(5,7-9) in molecules containing octupole-deformed radium isotopes(10,11).

168 ullerene reduces the interaction between the deformed reactants along the entire reaction coordinate.

169 the stronger interaction energy between the deformed reactants.

170 ilaments portray non-Hookean behavior - they deform reversibly at a few hundred picoNewtons and stiff

171 onic surface mount devices is shown that can deform reversibly into various 3D shapes including hemis

172 Drosophila R1-6 photoreceptors, resulting in deformed rhabdomeric structure.

173 the reduction of friction coefficient of the deformed sample.

174 pressure of 1.1 gigapascals, dehydration of deforming samples containing only 5 vol% of antigorite s

175 gh chi((2)) and chi((3)) nonlinearities in a deformed silica microcavity.

176 MAG-bound vesicles are deformed similarly, regardless of the ganglioside or its

177 deformation, they can safely be considered (deformed) single crystals with a high concentration of d

178 e number of charged defects originating from deformed sp(2) carbons and covalent defects from photo/t

179 riction stir processed, annealed and tensile-deformed specimens.

180 freezing (IF) effect also causes droplets to deform, split, and grow tails.

181 auge volume in the bulk of the sample in the deformed state, then anneal the sample and map the exact

182 aphic orientations from those present in the deformed state.

183 -sensing platform for living organisms under deformed states.

184 e and in situ when cells are in mechanically deformed states.

185 eyond this stronghold, caused by a competing deformed structure.

186 rticles, the yield is poor and includes many deformed structures.

187 tive VPS26-VPS29-VPS35 trimer and a membrane-deforming subunit of sorting nexin (SNX)-Bin, Amphyphysi

188 ion-induced nanoporosity found in the highly deformed surface layer, a phenomenon that has been linke

189 ature undercuts and grooves that accommodate deformed surface microstructures, effectively enhancing

190 cimens, indicating transition from flat to a deformed surface.

191 -organized, mechanochemical processes on the deforming surface.

192 ynamics using the theory of active fluids on deforming surfaces and develop a numerical approach to s

193 The rate of deformed templating does not depend on the concentration

194 attributed to the stochastic nature of rare deformed templating events.

195 hetic prions, a new mechanism referred to as deformed templating was introduced.

196 um, and regulation by the normal forces that deform the cross-section of the flagellum.

197 , but then it has to be able to sufficiently deform the ECM.

198 s generate the requisite force to physically deform the innermost layer of luminal cells, compelling

199 system can work in synergy to significantly deform the linear configuration of CO(2) and reduce the

200 The ability to deform the liquid metal couples geometric changes to Jou

201 o the stiffness or to the energy required to deform the material remains unclear.

202 ve pathways abrogated the ability of CAFs to deform the matrix and suppressed vascularization.

203 Actin dynamics generate forces to deform the membrane and overcome the cell's high turgor

204 receptors at the endosome and simultaneously deform the membrane to generate intraluminal vesicles (I

205 This argues that Bax acts at short range to deform the membrane.

206 Here we used a direct force probe to locally deform the nucleus by applying a transient tensile stres

207 of the cortex has to be able to sufficiently deform the nucleus.

208 sin complex generates the force necessary to deform the plasma membrane into a pit.

209 ntensity of the electron beam not to melt or deform the quartz nanotip without a metal coating.

210 We show that all resulting growths that deform the skin tissue architecture regress, irrespectiv

211 high temperatures induced during lasing can deform the substrate polymer, altering existing micro- a

212 To change conformation, a protein must deform the surrounding bilayer.

213 Epithelial tissues mechanically deform the surrounding extracellular matrix during embry

214 ves fixation and cryosectioning, which could deform the tissues.

215 that the spine tips indented and plastically deformed the substrate.

216 based microphones that respond to stimuli by deforming the device in thickness directions, this hydro

217 ing some of the energetic cost incurred from deforming the DNA.

218 of the vacuum Rabi frequency is obtained by deforming the EMNZ region without detuning a bound eigen

219 The method utilizes pulsed electric fields deforming the interface between an aqueous and an oil ph

220 PS optimally opened the SB ostium without deforming the main vessel (MV) bioresorbable vascular sc

221 anism by which actin filament polymerization deforms the cell membrane is unknown, largely due to lac

222 stallography that this TPP1 disease mutation deforms the conformation of two critical amino acids of

223 toconus (27%), a corneal disease that slowly deforms the cornea in young people; and sequellae of inf

224 In California, water storage deforms the crust as snow and water accumulates during t

225 horizontal duction, particularly adduction, deforms the disc and peripapillary vasculature.

226 NEC deforms the inner nuclear membrane (INM) around the caps

227 Its shape deforms the membrane locally into a dome.

228 We show that mechanical stretch deforms the nucleus, which cells initially counteract vi

229 ell confinement below a resting nucleus size deforms the nucleus, which expands and stretches its env

230 The pressure from the tumour deforms the surrounding tissue leading to changes in sti

231 The ablation plasma deforms the topology of the external magnetic field, for

232 th the ability of biocrystals to elastically deform, the inherent crystal structure of the principal

233 As the structure absorbs light and deforms, the conditions of illumination change, and this

234 uclear movement, and the ability of cells to deform their nucleus to invade through confined spaces.

235 of controlling equilibration by mechanically deforming their samples.

236 The extent by which forces deform tissues critically depends on the rheological pro

237 ient the cytoskeleton to produce forces that deform tissues.

238 ched vascular network, WBCs have to strongly deform to pass through the narrowest capillaries and bif

239 r defect-free graphene nanosheets, which can deform to remain ultraconformal during the expansion and

240 Red blood cells must deform to squeeze through these narrow vessels, transien

241 tically aligned pairs of EM maps (one map is deformed to fit the other map), and results in visualizi

242 below 42 HU for ZTACSEC For ATAC, the atlas deformed to MR in-phase was segmented to air, inner air,

243 amorphous carbon is surprisingly stable and deforms to a high breaking strength, without crack propa

244 he resistance to ice flow that arises as ice deforms to negotiate bed topography.

245 stability of lawsonite, while the sample was deforming, to test whether the lawsonite dehydration rea

246 Instead mosquitoes rely on damping by deforming two forelimbs and buckling of the proboscis, w

247 ve independent families with a progressively deforming type of OI, in whom we identified four homozyg

248 ative positions so that this structure could deform under force field.

249 evelop ultrasoft mechanosensors that visibly deform under less than 10 Pascals of cell-generated stre

250 MTs deformed under contractile load into sinusoidal buckles,

251 indium tin oxide, is reversibly structurally deformed under the application of an electric field, and

252 ng dielectrics whereby they are mechanically deformed under the application of an electric field.

253 nds of the type observed in metallic glasses deforming under mechanical stress.

254 th between particles can alter how a lattice deforms under applied mechanical force.

255 serve as a model matrix that MSCs can easily deform unless the film is enzymatically cross-linked, wh

256 soft actuators are liquid-filled shells that deform upon the application of electric fields; they exc

257 whole EV population and/or if the EVs become deformed upon binding to the surface.

258 rocks, granular materials, and the earth all deform via intermittent slips or "quakes".

259 Slowly strained solids deform via intermittent slips that exhibit a material-in

260 HfN specimens deformed via four-point bend tests at room temperature a

261 ctile deformation into localized shear zones deforming via diffusion creep, dissolution-precipitation

262 Aluminium typically deforms via full dislocations due to its high stacking f

263 at its absence results in an accumulation of deformed virus particles retaining the scaffold protein

264 and morphological properties of cells while deforming were critical for this classification.

265 Deformed wing virus (DWV) and infestation with the ectop

266 Deformed wing virus (DWV) and its vector, the mite Varro

267 e presence of black queen cell virus (BQCV), deformed wing virus (DWV) and sacbrood virus (SBV) in ma

268 Deformed wing virus (DWV) and the closely related Varroa

269 erentially expressed genes (DEGs) in brains, deformed wing virus (DWV) and the proportion and intensi

270 ic mite Varroa destructor and the associated deformed wing virus (DWV) apparently playing key roles.

271 Deformed wing virus (DWV) from the family Iflaviridae, t

272 Deformed wing virus (DWV) has become the most well-known

273 The picornavirus-like deformed wing virus (DWV) has been directly linked to co

274 been well documented for the replication of deformed wing virus (DWV) induced by Clothianidin in hon

275 s transformed the previously inconsequential Deformed Wing Virus (DWV) into the most important honey

276 Deformed wing virus (DWV) is a persistent pathogen of Eu

277 Transmission of mite-borne virus such as Deformed Wing Virus (DWV) was also enhanced by mites fee

278 seases (Nosema sp. and the Varroa-associated Deformed wing virus (DWV)) affect bees' behavioural perf

279 This specialist honeybee mite vectors deformed wing virus (DWV), an important re-emerging hone

280 ollinator, suffer considerable losses due to Deformed wing virus (DWV), an RNA virus vectored by the

281 e global epidemic of the single stranded RNA Deformed wing virus (DWV), driven by the spread of Varro

282 vestigated whether another key bee pathogen, Deformed Wing Virus (DWV), may also have originated in E

283 Deformed wing virus (DWV), the main viral pathogen of ho

284 is due, in part, to the high viral loads of Deformed wing virus (DWV), transmitted by the ectoparasi

285 Among these is Deformed wing virus (DWV), which has been frequently lin

286 ure of iflavirids [sacbrood bee virus (SBV), deformed wing virus (DWV)] and dicistrovirids [Israeli a

287 Our results demonstrate that deformed wing virus infected drones are competitive to m

288 lation with drones showing comparatively low deformed wing virus infections served as control.

289 d that seven of the 30 queens had high-level deformed wing virus infections, in all tissues, includin

290 Deformed wing virus is an important contributor to honey

291 esent, was removed from the mated queens for deformed wing virus quantification, leading to the detec

292 ical brood signals are induced by Varroa and Deformed Wing Virus, and elicit hygienic response in the

293 ts in Pennsylvania, USA for three pathogens (deformed wing virus, black queen cell virus, and Vairimo

294 mples tested positive for the replication of Deformed wing virus, Black queen cell virus, or Israeli

295 In an environment with high prevalence of deformed wing virus, queens (n = 30) were trapped upon t

296 tic mite Varroa destructor associated to the Deformed Wing Virus.

297 with complex form factors that continuously deform with the robot's movement.

298 mulate textures, suggests that olivines were deformed within melt-rich mush piles accumulating within

299 hat amorphous aluminum oxide can permanently deform without fracture at room temperature and high str

300 corresponds to the transition from coarse to deformed xenoliths.