ライフサイエンスコーパス: bend

1 ochord markers (col2a1a and col9a2) appeared bent.

2 act IgE is significantly less asymmetrically bent.

3 ending can be controlled from flat to highly bent.

4 roplastics than samples from inner and outer bends.

5 ments for commonly used climbing and sailing bends.

6 pressing crack formation upon stretching and bending.

7 ing strain, 50% compressing strain and fully bending.

8 of its two main resonant modes, rocking and bending.

9 pedicels or sexual organs or slower peduncle bending.

10 Static during upright free bending.

11 lar vesicles, suggesting a role for membrane bending.

12 twisting; and Supera and Viabahn restricted bending.

13 of RNA duplexes bound to the core also shows bending.

14 curred in maize roots, preceding hydrotropic bending.

15 ruled out as an explanation for the downward bending.

16 th the winged-helix domains to stabilize DNA bending.

17 formed by brain capillary endothelial cells (bEnd.3 cells).

18 mouse brain-derived microvessel endothelial, bEnd.3, Madin-Darby canine kidney transfected with multi

19 ssure), while the tube was held straight and bent 90 degrees.

20 heterogeneous, site-specific, and programmed bending actuations.

21 One bent aldehyde stands out as unable to assemble into high

22 at 1513, 1464, and 1139 cm(-1) CH(2), CH(3) bend and C-O-C stretch represented structural changes.

23 , the intracellular halves of the S6 helices bend and rotate by about 100 deg, exposing different res

24 ense strand does not alter the 'clover leaf' bend and sugar puckers that are critical for anchoring t

25 of the filament, which exhibits an intrinsic bend and twist.

26 e combination of Walden-inversion "umbrella" bending and asymmetric stretching of the SC(alpha) and C

27 arged lipids in the bilayer altered membrane bending and binding properties of BIN1 and so did the ma

28 the three-point-bend test in which both the bending and crack-parallel compression are statically de

29 rvations indicate that the cellular membrane bending and curvature sensing activities of endophilin c

30 G608G mouse model may increase the risk for bending and deformation, which could result in the skele

31 We suggest that the bending and looping of DNA by PRC2, independent of PRC2'

32 third of the arms performed relatively less bending and more shortening and elongation as compared w

33 Here, a vector bending and orientation distinguishing curvature sensor,

34 its contour length, due to thermally driven bending and rotation on the membrane, and that height st

35 ents that best discriminate angles (vertical bending and slide distance) also have the greatest influ

36 This approach includes membrane bending and stretching deformations into the model, prod

37 lso confer stability of the OLED to repeated bending and to extensive postprocessing, e.g. via reacti

38 bent); and a hybridized method based on fire bending and toasting followed by a 12 h fill with water

39 also alter the mechanical response of DNA to bending and twisting constraints, both of which are impo

40 high linearity, as well as insensitivity to bending and twisting deformations-features that are impo

41 identified that substantially affected helix bending and twisting motions in the entire TMD.

42 ur findings suggest that the accumulation of bending and twisting stresses as the filament elongates

43 s, and that this is manifested through rapid bending and/or rotation of pedicels or sexual organs or

44 e bending/toasting protocols, including fire bent and fire toasted (fire-bent); water bent and fire t

45 ire bent and fire toasted (fire-bent); water bent and fire toasted (water-bent); and a hybridized met

46 bridged molecule reconstructs into the trans-bent and linear structures prevail over the interatomic

47 bridged molecule reconstructs into the trans-bent and linear structures.

48 7 docks onto ORC-Cdc6, and the origin DNA is bent and positioned adjacent to the open DNA entry gate,

49 d transfer structure, target DNA is severely bent and the TTAA target is unpaired.

50 The bent and tilted arrangement of complex components limits

51 The two IgAs are bent and tilted with respect to each other, forming dist

52 re-bent); water bent and fire toasted (water-bent); and a hybridized method based on fire bending and

53 l, the crystals of 1b and 1c visibly expand, bend, and fracture, mainly along specific crystallograph

54 actuators that can extend, contract, twist, bend, and perform a combination of these motions in 3D s

55 e auxin, leading to asymmetric growth, organ bending, and subsequent reset of auxin distribution back

56 measurement of baseline FPA foreshortening, bending, and twisting associated with each posture.

57 ational change, where the difference between bending angles of neighboring PFs tends to be larger com

58 exible detectors can be operated at multiple bending angles without a deterioration in detection perf

59 Mechanical deformations of DNA such as bending are ubiquitous and have been implicated in diver

60 witching behaviors after repeated mechanical bending as well as organic synapses capable of emulating

61 tion of the signs and magnitudes of the band bending as well as the valence band offsets.

62 Optical refraction causes light to bend at interfaces between optical media.

63 -in electric field that originates from band bending at heterostructure interfaces induces polar symm

64 is folded into three segments and the heads bend back and interact with each other and the tail(3-7)

65 We experimentally analyze the bending behavior of biomimetic beams covered with tunabl

66 pronounced and reversible tunability in the bending behavior of biomimetic scale covered beam, which

67 lement that calculates both the membrane and bending behavior via displacement degrees of freedom for

68 Long actin filaments bend between attachment sites in the coat and the base o

69 n governed by the displacement of the weaker bent bond as determined by the presence of electron-with

70 The bent bond/antiperiplanar hypothesis (BBAH) orbital model

71 These results were analyzed through the bent bond/antiperiplanar hypothesis (BBAH) orbital model

72 es can be uniformly rationalized through the bent bond/antiperiplanar hypothesis (BBAH).

73 ncoming nucleophiles displace one of the two bent bonds of bicyclic oxocarbenium ion intermediates in

74 etween groups at C(2) and the two tau bonds (bent bonds) of oxocarbenium ion intermediates formed und

75 iradical resonance structures and associated bent bonds, as it applies to aromatic, nonaromatic, and

76 ized wrinkle is categorized into three modes-bending, buckling, and sliding.

77 the Y269 residue is required for proper DNA bending by APE1, providing evidence for the importance o

78 resence of 6mA could repress DNA binding and bending by mitochondrial transcription factor (TFAM).

79 These findings show that epithelial bending can be achieved by a morphogenetic mechanism of

80 tering the strings of the bow, the degree of bending can be controlled from flat to highly bent.

81 hronically-infected individual from whom the bent CDRH3 bNAbs were derived.

82 sults demonstrate that both the straight and bent CDRH3 classes of HCV bNAb can be elicited in a sing

83 ficiency and binary coding along large-angle bending channels for bit-error-free acoustic data transm

84 of-of-concept, an X-ray phase contrast under bending conditions was constructed using a 5x5 pixelated

85 filaments (PFs) and less cooperative outward bending conformational change, where the difference betw

86 t elastic constant compared to the splay and bend constants.

87 (cholesteric LCs, cubic blue phases, achiral bent-core LCs, etc.) and lyotropic LCs (DNA LCs, nanocel

88 Melting of the bent crystal starts at the kink and often appears as spl

89 also lower on the convex (outer) side of the bent crystal.

90 In the bending curves, a drastic decrease in the viscosity of t

91 ility with negligible degradation after 1600 bending cycles (up to 60 degrees ) are demonstrated.

92 e performance degradation after one thousand bending cycles and exceptional room-temperature gas sens

93 Multiple bending cycles caused a marked deterioration of the phot

94 h less than 9% variation, followed by 10 000 bending cycles with a radius of 125 mum.

95 nced by 100 taping, 100 scratching, and 1000 bending cycles.

96 om less than 5% to ~50% for the ratio of the bending deflection to the original length of the pillars

97 t the micropillars with different degrees of bending deformation can be configured in any spatial pat

98 Note that bending deformations are reversible, while stretching de

99 Therefore, bending deformations need only be considered in reversib

100 ature with diverse geometrical (cylindrical, bent, disk, etc.) and chemical (neutral, ionic, etc.) na

101 this article, we demonstrate that an intense bend distortion applied to the LC molecular director whi

102 The bend distortion is analog to the magnetic field in metal

103 lowest excited state undergo a Renner-Teller bending distortion upon excitation.

104 To investigate whether a straight versus bent disulfide bond-containing CDRH3 is specific to part

105 microscopy, we show that human XPA binds and bends DNA by ~60 degrees as a monomer.

106 with a working model in which monomeric XPA bends DNA, displays episodic phases of linear diffusion

107 nds to unbent DNA and then deforms it, or if bent DNA conformations are 'captured' by protein binding

108 g to a macroscopic crossover from an initial bending-dominated softening regime to a stretching-domin

109 redicts a detailed stress pattern related to bending down to 450 km, followed by unbending as the sla

110 Allowing the GDD tube to bend during needle perforation increases the risk of ver

111 ost two orders of magnitude smaller than the bend elastic constant (21 pN).

112 formation allowing to determine the membrane bending elasticity, a property related to hydrodynamics

113 of the bilayer, its excess surface area, and bending elasticity.

114 ydrogel can work as a stretching/compressing/bending electrode, maintaining its stable output under c

115 ased on the Helfrich formulation of membrane bending energy as we previously first applied to lipid-p

116 de-off between the need to minimize both the bending energy of the stiff plectonemes and the volume o

117 cybertechnologies, such as social digibots, bend epistemological conventions of life and culture alr

118 dylinositol 3-kinase (PI3K) and the membrane-bending ESCRT factors, are required for reconstitution o

119 characterize this response using three-point bending experiments at various temperature profiles.

120 lves a plasmonic sandwich immunoassay on a U-bent fiber optic probe with gold plasmonic (AuNP) labels

121 D-photodetector pair, 200 mum fused silica U-bent fiber probe and 60 nm (20 x ) AuNP labels gave LoDs

122 e text] state of Abeta42, encoding for the U-bend fibril, should form earlier than the structure with

123 Elastic energy stored in bent filaments, whose presence was confirmed by cryo-ele

124 echniques, inherently sensitive to mesoscale bending fluctuations, show up to a threefold increase in

125 of the pit, increasing actin nucleation and bending for increased force production.

126 ematic domains, periodically intermixed with bend-free smectic-A domains.

127 ether continuously, providing a menagerie of bend-free textures akin to the packing of focal conic do

128 of packing hyperboloid "diabolic" domains in bend-free textures of liquid crystals.

129 Our purpose was to investigate how bending GDD tubes affects the performance of needle perf

130 m existing inorganic nanocoils with flexible bending geometries, the built-in lattice misfit between

131 ss favorable in the order dibridged -> trans-bent -> linear for both C(2)H(2) and Si(2)H(2).

132 ed that microtubules elongate by addition of bent guanosine triphosphate tubulin to the tips of curvi

133 NMR structural determination indicated a bent helix in solution and bound to MDM2.

134 a 12 h fill with water at 80 degrees C (fire-bent + hot water), were trialed in triplicate.

135 mic analysis of the elongation zone prior to bending identified IAA response and lignin synthesis/wal

136 proline-rich linker region cause an overall bend in the PRD structure.

137 ovskite solar cells, the doping-induced band bending in perovskite effectively facilitates hole extra

138 d orbital can be controlled by the degree of bending in the structures and that the energy of the hig

139 s transposition, how RAG can stabilize sharp bends in target DNA, and why replacement of residue 848

140 e, at higher speed and performed larger tail bends, indicating that Somatostatin 1.1 inhibits spontan

141 traight (individuals who clear infection) or bent (individuals with chronic infection) conformation.

142 s a result of significant thermodynamic band bending induced by ligand attachment and Ni(II) binding.

143 omprises a system wherein the extent of band bending induced by metal ion binding is the primary driv

144 shown excellent photocurrent stability under bending induced stress up to 0.32%.

145 By utilizing a bending-induced ferroelastic transition of TIPS-P, flexi

146 On the other hand, bending-induced intracellular stresses are more concentr

147 The localized effect of bending-induced stresses may be important in processes l

148 degrees Mn providing the strong, singular C bend initiating escape and the 2 degrees Mn conferring w

149 brating tube sensor, a piece of glass tubing bent into a tuning-fork shape and filled with any desire

150 Hydrotropic bending involves coordinated adjustment of spatial cell

151 Epithelial bending is a fundamental process that shapes organs duri

152 How membrane bending is accomplished is not yet fully understood but

153 at additional pressure generated by membrane bending is negligible, compared to pressures generated b

154 that protamine loops DNA in multiple steps, bending it into a loop.

155 n in perylene diimides where the molecule is bent, like a bow, along its long axis.

156 Small size, together with bending, localize high stress near the surface of the be

157 res increases in the order dibridged < trans-bent < linear, in contrast to acetylene, C(2)H(2), for w

158 eliminary experiments with a liquid jet at a bending magnet X-ray beamline demonstrate the feasibilit

159 , 2020), a novel concept of applying reverse bending magnets to adjust the energy-dependent path leng

160 ctor that is widely used to characterize DNA bending mechanics.

161 an essential part of the cell's machinery to bend membranes.

162 When excited by using laser light, such bent microcrystals act as active optical microwaveguides

163 Past studies suggested that meander-bend migration, levee-deposition, or migration of (super

164 ally mapping the Ti-O stretching and Ti-O-Ti bending modes, we reveal how structural order parameters

165 e scale is given by membrane properties: its bending modulus and its surface tension, which arises fr

166 Further, the effective bending modulus is highly sensitive to the geometry of t

167 This large bending modulus is in part due to the 45 nm separation b

168 Our calculations show that the effective bending modulus of the nuclear envelope is an order of m

169 can then estimate the active torques and the bending modulus of the tissue.

170 stituents, quantified as a decrease in their bending modulus, area compressibility modulus, and visco

171 fragments cause a reduction in the membrane-bending modulus, as measured by a method based on atomic

172 positional asymmetry alone, can increase the bending modulus.

173 tions of vanishing area strain and vanishing bending moment differ.

174 curvature that balances torques due to both bending moments and differential stress, with sometimes

175 een the two membranes, which supports larger bending moments in the structure.

176 ngth structure is observed, indicating hinge bending motions at the linker region connecting the head

177 th characteristic ring twisting and bridge-H bending motions enables rational design of functional pr

178 without losing crystallinity, undergo prompt bending motions in response to stimuli, and self-heal ef

179 otein internal dynamics, which include hinge-bending motions, are needed to explain the short-ranged

180 Hinge-bending movements in proteins comprising two or more dom

181 at even at these relatively small scales the bending movements of limbs and ctenes conform to the pat

182 pplication of a dynamical methodology to the bending movements of shoots of common beans (Phaseolus v

183 egates are the most mobile, and the two beta-bend mutants have the strongest changes at the F4 site t

184 nding mixing with N-C-N sigma-bonding of the bent N-C-N framework.

185 , and even the long-predicted, elusive splay-bend nematic phase.

186 We show that although the DNA-bending nonhistone proteins make the chromatin irregular

187 ds, we examine how the interplay between DNA-bending nonhistone proteins, histone tails, intrachromat

188 a partnering gold ion only a distinct N-Au-P bending occurs, revealing a potential mechanism for the

189 ocates relative to the pore concomitant with bending of a GGxGG motif in the pore helices.

190 The coordinated bending of cilia requires mechanoregulation by the radia

191 inding led to a 3-fold increase in the local bending of DNA's helical backbone without evidence of DN

192 In particular, bending of epithelia is thought to result from active to

193 (SOCB) approach captures 3D nonlinear Euler bending of filaments with high fidelity at low cost.

194 We highlight mechanical stretching and bending of membranes and the importance of membrane defo

195 large rocking motions of the gating ring and bending of pore-lining helices.

196 by magnetic-field-assisted lithography, the bending of the actuator can be controlled by switching t

197 4L and N512Y substitutions appear to prevent bending of the beta3-beta4 loop that is required to cont

198 STAT3 in complex with monobody MS3-6 reveals bending of the coiled-coil domain, resulting in diminish

199 tub inversion proceed through the successive bending of the linkers and the barrier for isopropyl-sub

200 , we performed computational analysis of the bending of the nuclear envelope under applied force usin

201 erated actomyosin forces generate epithelial bending of the wing disc pouch.

202 Branches and bends of arteries are exposed to complex blood flow patt

203 receptor consisting of a calix[4]arene and a bent oligophenylene loop ("molecular squid"), was obtain

204 tudying the effect of cyclic conjugation and bending on the incorporated pai-systems.

205 In this study, a label-free ultrasensitive U-bent optical fiber-based immunosensor for the determinat

206 2D material and substrate could dominate the bending or stretching processes, leading to inefficiency

207 on while allowing flexural deformation under bending or twisting.

208 ation transforms the linear trans COE into a bent or C-shape form.

209 nd regardless of whether a cell is straight, bent or curved.

210 e locations, magnitudes, and modes (stretch, bend, or press) of mechanical deformation.

211 he organization of the nucleoid by bridging, bending, or wrapping the DNA.

212 some combination of four basic deformations: bending (orally, aborally; inward, outward), torsion (cl

213 Upon ATP binding, a phosphate binding loop bends over the active site to recognize ATP and bring th

214 ucture, and can be reversibly and repeatedly bent over 90 degrees.

215 curvature and SNARE force-generated membrane bending promote fusion pore formation and expansion.

216 binding and remodeling by ORC, and that DNA bending promotes Mcm2-7 loading in vitro.

217 The resistance of the envelope to bending, quantified by the flexural stiffness, helps det

218 erent volumes of sweat (20, 50, and 100 uL), bending radii (10, 15, 20 mm), charging/discharging stab

219 d clotting time, even when flexed to a 35 mm bend radius.

220 amino acid residue is located within a hinge-bending region or within an intradomain region.

221 R results is that in the prediction of hinge-bending regions a long-range correlation is at play betw

222 cysteine has the lowest propensity for hinge-bending regions and proline has the highest, even though

223 lity to recognise sequence features of hinge-bending regions and to be able to predict them from sequ

224 Hinge-bending regions demarcate protein domains and collective

225 As hinge-bending regions have been previously shown to occur freq

226 ach that focused solely on interdomain hinge-bending regions, the method provides a modest and statis

227 acids that either favour or disfavour hinge-bending regions.

228 ence features that favour or disfavour hinge-bending regions.

229 its 3D orientation and 3D shape, as well as bending-related mechanical force.

230 We also found negative bend resistance at 1/q fractions for electrical probes p

231 ative (upward bending) to positive (downward bending), resulting in a "weeping" inflorescence phenoty

232 n of plastic organic single crystals such as bending results in a small yet significant decrease in t

233 eam ESCRT-induced alteration of the Gaussian bending rigidity and their crowding in concert with the

234 uid lipid membranes, its effects on membrane bending rigidity are assumed to be nonuniversal; i.e., c

235 imensional liquid crystalline membranes with bending rigidity of a few kT exhibit unusual properties

236 eport that cholesterol locally increases the bending rigidity of DOPC membranes, similar to saturated

237 depending on the substrate curvature and the bending rigidity of the lipid domains.

238 s cholesterol's role in controlling membrane bending rigidity over mesoscopic length and time scales

239 show up to a threefold increase in effective bending rigidity with increasing cholesterol content app

240 the diseased lipid membrane has a 25% lower bending rigidity, thus destabilizing smooth [Formula: se

241 has no significant influence on the membrane bending rigidity.

242 The bent section of the crystal was found to be mechanically

243 sensitivity of - 1.4 nm/ degrees as a vector bending sensor and - 17.5 nm/m(-1) as a curvature sensor

244 , whereas other primates have flat feet that bend severely in the midfoot(7,10,11).

245 We achieve this stress by bending single-crystal silicon microbeams using an in si

246 onfined to within one to two cell lengths of bending sites.

247 ich favors the nearby presence of the highly bent stalk structure or prestalk dimple.

248 ng, CSC mice were characterized by decreased bending stiffness and bony bridging of the fracture call

249 Additionally, increased footwear bending stiffness did not affect muscle activity (all se

250 Hence, footwear bending stiffness does not appear to alter the volume of

251 Overall, increased footwear bending stiffness lengthened ground contact time (p = 0.

252 Particularly, it is shown that the bending stiffness of the biomimetic scale covered beam c

253 provide a convenient template to tailor the bending stiffness of the underlying slender substrate du

254 footwear conditions that varied in shoe sole bending stiffness, modified by carbon fiber plates.

255 me strongly and exponentially depends on the bending stiffness, which accounts for more than half the

256 be induced when the fibrils are subjected to bending stress exceeding a certain threshold.

257 We find IrB(2) O(-) has a closed-shell bent structure (C(s) , (1) A') with BO(-) coordinated to

258 nal unpaired regions (bubbles) into strongly bent structures, and suggest how XPG complexes may bind

259 d PIN3 re-polarization and shoot gravitropic bending termination.

260 nts a simple modification of the three-point-bend test in which both the bending and crack-parallel c

261 Furthermore, the 3-point bending test revealed increased bone strength in female

262 p were both left-canted with similar angular bends that mirrored one another and correspond with the

263 t just simply halt biodiversity loss, but to bend the curve of biodiversity loss to stable or increas

264 Although the migrating tissue is able to bend the fiber for some time, it eventually recoils befo

265 e sites with time, lowering the stress while bending the beam plastically.

266 f these structures suggest that protamine is bending the DNA to achieve this curvature rather than in

267 Despite some recent progress on bending the emissions curve, RCP8.5, the most aggressive

268 Bending the tube after perforation could close a slit an

269 labeled DNA construct, we show that Pol beta bends the gapped DNA substrate less than indicated by pr

270 in the complex and suggests that the protein bends the RNA upon binding.

271 ion with dextral strike-slip kinematics that bent the layers in the contact area without obliterating

272 ated by a model protein involved in membrane bending, the N-terminal homology domain (ENTH) of Epsin1

273 electrostatic interactions regulate membrane bending: the ratio of negatively charged lipids in the b

274 eguides using AFM is non-invasive, and after bending their emissive spectral output remains unaltered

275 ones were loaded to failure with three-point bending to assess strength.

276 ctuation into life-like motions, from simple bending to walking, for example.

277 crystals of three N-benzylideneanilines were bent to an arbitrary angle, sliced out from a bundle int

278 hoot gravity responses from negative (upward bending) to positive (downward bending), resulting in a

279 tion to control barrels (3 years old), three bending/toasting protocols, including fire bent and fire

280 aged in barrels produced with the different bending/toasting protocols.

281 d by barrel use (new versus neutral) than by bending/toasting protocols.

282 d form earlier than the structure with the S-bend topology, which is in accord with Ostwald's rule ra

283 g and closing pressures of slits made in the bent tube were significantly lower, frequently leaking a

284 d such as bleeding, vitreous tube placement, bent tubes, etc.

285 ng electrochemical cell array can be readily bent, twisted and stretched without affecting its device

286 Remarkably, in the bending/unbending regions, down-dip compression occurs c

287 esults in dramatic DNA distortions including bending, unwinding and base flipping.

288 nfirmed the presence of peaks related to N-H bending vibration, C-N stretching and symmetric, and asy

289 Membrane bending was also reduced in BIN1 mutants where negative

290 Curiously, BIN1 membrane binding and bending was diminished in cells where the membrane's cha

291 Bending was the most common deformation observed, althou

292 , including fire bent and fire toasted (fire-bent); water bent and fire toasted (water-bent); and a h

293 rive extracellular fluid flow by propagating bending waves from their base to tip.

294 e both the strength and direction of whisker bending were informative cues to pole location.

295 hain overcrowding-induced asymmetric lamella bending, which is further confirmed by correlating cryst

296 reas eugenol was 10-fold higher in the water-bent wines.

297 trial at a clinical pharmacology unit (West Bend, Wisconsin) was conducted in 48 healthy participant

298 rsoventral (DV) shear and lateral transverse bending ('wishboning').

299 t dramatic mechanical effects by cracking or bending with the release of N(2).

300 tubes, but this time the tube was allowed to bend within the 3.5-mm open prongs of a needle holder du