ライフサイエンスコーパス: tension

1 the first trimester occurs under low oxygen tension.

2 storage capacity under both compression and tension.

3 ta between 5.6% biaxial compression and 2.1% tension.

4 lation against opposing forces like membrane tension.

5 odel incorporating an internal electrostatic tension.

6 in complexes that is autoinhibited under low tension.

7 8 cells with time and with increasing oxygen tension.

8 ilization of cortex correlate with increased tension.

9 o-pole axis without a detectable increase in tension.

10 between marginal band rigidity and cortical tension.

11 lium, mediated by cell membrane adhesion and tension.

12 TMAO, however, reduces the surface tension.

13 ause these sites are hot spots of epithelial tension.

14 nically cycled and stressed to failure under tension.

15 eparation and provided a source for membrane tension.

16 ne to form in body sites with increased skin tension.

17 otein composition, interaction, and cellular tension.

18 unding solution and dominated by interfacial tension.

19 s a continuous load-bearing layer, resisting tension.

20 osphorylation, suggesting elevated monolayer tension.

21 face-active molecules that can lower surface tension.

22 TNNT2p.K217del caused increased passive tension.

23 ules behaved like semi-flexible fibres under tension.

24 lled pore in response to changes in membrane tension.

25 te, whereas it is largely disordered without tension.

26 spatial variations in membrane recycling and tension.

27 a targeted consent process can resolve these tensions.

28 KO rendered the cells sensitive to membrane tensions.

29 the subsequent 6 at near-physiologic oxygen tensions.

30 r efficient catalysis under different oxygen tensions.

31 ng for successful budding at higher membrane tensions.

32 s and quantify their viscosities and surface tensions.

33 es robust vesiculation even at high membrane tensions.

34 sions generated during platelet adhesion and tensions above 54 piconewton generated during platelet c

35 Tension across Madin-Darby canine kidney cell monolayers

36 e force experiments and simulations to apply tension across the substrate binding domain (SBD) of hea

37 Changes in tension across VE-cadherin observed using ratio-metric o

38 lular tension, and that the highest recorded tensions across vinculin are associated with adhesion as

39 Undulations and line tension act synergistically: the gain in energy due a mi

40 hat has to survive high environmental oxygen tensions, adapt to oxygen limitation in the intestine an

41 e formation, we show that the application of tension alone, or in combination with matrix remodelling

42 a axons also actively maintain contractility/tension along the circumferential direction.

43 haracterized by physiological extremes of O2 tension and blood flow.

44 havior of the mycelium is non-linear both in tension and compression.

45 nger tubules with dependence on the membrane tension and CTxB concentration.

46 tin/myosin disrupting drugs relaxed the hoop tension and decreased when microtubule disrupting drug r

47 of ZO-1/ZO-2 elevates the apical epithelial tension and effective viscosity.

48 n automated drop tensiometer for interfacial tension and elastic modulus determination with oscillati

49 embly is governed by the anisotropic surface tension and elasticity at the interface of beads with th

50 signaling platform, and provider of passive tension and elasticity in myocytes.

51 y scaling resistance under moderate uniaxial tension and fatigue.

52 onally greater lowering of the vesicle lysis tension and hydration repulsive pressure that combine to

53 tivated, resulting in increased cytoskeletal tension and impaired cell-cell adhesion.

54 This transition is governed by oxygen tension and involves the large-scale production of bacte

55 red, increase in isolated sphincter muscle's tension and largely suppressed the local PLR in vivo.

56 he process reached a steady state where line tension and lateral crowding balanced.

57 x microelasticity, with increases in nuclear tension and nuclear stiffness resulting from increases i

58 reduced (P < 0.001) at constant arterial CO2 tension and pH (P = 0.27 and P = 0.23, respectively); en

59 thway that confers resistance to high oxygen tension and protects cells from undergoing ferroptosis i

60 ced coupling is very robust against membrane tension and substrate interactions.

61 a new approach to the nature of interfacial tension and the impact this has on concepts used to defi

62 t significantly affect the maximal isometric tension and the rates of force activation (kACT) and red

63 on-induced increase in endothelial monolayer tension and thereby moderate inflammation-induced juncti

64 on in lower layers while promoting increased tension and TJ stability in the granular layer 2.

65 a transparent model based on the concurrent tensioning and sliding of the translocating knotted chai

66 us conventional (e.g. shear, compression and tension) and nano-indentation loading geometries, our fi

67 a: see text] stands for vapor-liquid surface tension, and [Formula: see text] stands for the liquid d

68 substitution level, with diminished surface tension, and a longer time was needed for both water and

69 hesion protein stabilization, focal adhesion tension, and cancer cell migration is CSD dependent.

70 f epithelial barrier formation, cytoskeletal tension, and cell adhesion, underscoring the complexity

71 s provide evidence that a balance of torque, tension, and elasticity stabilizes neurons against mecha

72 , area covered by the protein coat, membrane tension, and force from actin polymerization on bud form

73 inotropic insufficiency, increased diastolic tension, and premature contractions; ranolazine treatmen

74 chial index, increased transcutaneous oxygen tension, and reduced rest pain.

75 died while controlling membrane composition, tension, and shape.

76 ivation coincide with areas of high cellular tension, and that the highest recorded tensions across v

77 ivers were perfused at high perfusate oxygen tensions, and the subsequent 6 at near-physiologic oxyge

78 ntation, we show that the resolution to this tension-and the adaptation of social behavior in this ga

79 uction of cell contact length and depends on tension anisotropy between NBs and their neighbors.

80 osin-driven circumferential contraction/hoop tension applies a squeezing force on the microtubule bun

81 ntral furrow, in which actomyosin fibres and tension are directed along the length of the furrow.

82 lations, we conclude that tissue interfacial tensions are sufficient to explain cell sorting in aggre

83 These rotations reduce the bond tension around Na and effectively soften the short Na-O

84 The decrease of the line tension around the thicker ordered domain constitutes an

85 tionally implicate the broad use of membrane tension as a mechanism to drive abscission.

86 hompson emphasised the importance of surface tension as a potential driving force in establishing cel

87 ication behaviour in relation to interfacial tension as modelled using phase-field methodology is sho

88 ial for junctional integrity and contractile tension at epithelial ZA.

89 NMIIa a critical function of enhancing line tension at the cell boundary surrounding the TEMs by pro

90 se that this relocation of H3T3ph depends on tension at the centromere and is required to promote bi-

91 alized active tension (AT (norm)) and active tension at the resting sarcomere length (T (req), reflec

92 To ensure maximal sensitivity, tip links are tensioned at rest, resulting in a continuous influx of C

93 didate parameters included normalized active tension (AT (norm)) and active tension at the resting sa

94 l basis of the stable 2HB state and offers a tension-based rationale for an optimal NL length to ensu

95 Myosin VIIa is responsible for tension bearing and the transduction mechanism in the st

96 -cadherin coordinates tissue polarization of tension-bearing adherens junction (AJ) and F-actin organ

97 an persistently generate this metaphase-like tension before biorientation, likely stabilizing sister

98 We measured the line tension between coexisting Ld and Lo domains close to th

99 The resulting tension between cooperative and competitive interactions

100 opose a model in which the local variance in tension between junctions determines whether actomyosin-

101 We describe an intriguing tension between phenotypic complexity and evolvability t

102 Our review showed the tension between standardising handovers and making them

103 This electrostatic tension between the Cu(+) and Cu(0) surface sites respon

104 ever, and it is uncertain how differences in tension between the inner and outer leaflets of the memb

105 The latter structure indicates how tension between the two motor domains keeps their cycles

106 ore how society might reasonably resolve the tension between these two objectives as well as evaluate

107 We worry that such a framing may exacerbate tensions between "competing" scientific perspectives and

108 interstitial gaps depends on the mechanical tensions between cells and at gap surfaces, and on the d

109 action forces, yet little is known about how tension borne by an individual SF is governed by SF geom

110 ted, buckled, and bundled as well as undergo tension buildup during the structural reorganization.

111 er ductility; and also show strengthening in tension but weakening in compression with decreasing wir

112 stoderm expansion by reducing tissue surface tension, but also drive blastoderm thinning by inducing

113 Reduction of maternal arterial oxygen tension by 50% over 30 min resulted in a subseiuent sign

114 In response to a low oxygen tension, C. jejuni increases the transcription and activ

115 holesterol depletion also increases membrane tension, Ca(2+) spikes frequency and intracellular Ca(2+

116 ected to measure Young's modulus and surface tension can also provide both qualitative and quantitati

117 This tension can be ameliorated by unveiling the constructed

118 n to increase axial tension, suggesting that tension can be coupled in the axial and circumferential

119 crose particles, Young's modulus and surface tension can be quantified as a function of RH.

120 ur findings provide evidence that mechanical tension can regulate cell-cycle dynamics in regenerating

121 issues highlighting the key areas of ethical tension central to evaluating physician-assisted suicide

122 viscosity, mu, and the water/oil interfacial tension coefficient, sigma.

123 vation, and the onset of piconewton integrin tension coincides with calcium flux.

124 For the molecule under tension, contour length, bending rigidity and intrinsic

125 es were truly solvent-free and that membrane tension could be controlled over a physiological range.

126 The mapping of global interfacial tension coupled with free energy dissipation has been us

127 s to the elastic data show that the internal tension decreases with salt, from [Formula: see text]5 p

128 As membrane tension decreases, protrusion resumes and buckling disap

129 ctive cell movements, further highlight that tension-dependent adaptation of AJs regulates cell-cell

130 compact to linear form, and subsequently, a tension-dependent local transition to a state with high

131 that FN-bound alpha5beta1 integrin promotes tension-dependent malignant transformation through engag

132 ubsequently activated to bind GPIbalpha in a tension-dependent manner.

133 their compositions unexpectedly appear to be tensioned differently compared to phosphorus congeners.

134 h nascent adhesions under rigidity-dependent tension downstream of SFK activity.

135 de ribbon and single-atom chain, linked by a tension-driven (negative-pressure) transformation.

136 active distal-exo adduct becomes inert under tension due to poor mechanochemical coupling.

137 ection and to successfully dampen aggressive tension during the imagination of aggressive behavior.

138 s act as cues to orient the cytoskeleton and tension during ventral furrow formation.

139 eral process of minimizing the system's line tension energy, because of the lowering of line interfac

140 response revealed that the droplet monolayer tension equilibrated over time, likely by insertion of l

141 maintaining substantial lowering of surface tension, even for partial surface coverage.

142 duces experimentally measured values of ring tension, explains why nodes move bidirectionally, and sh

143 ly bleb from concave regions, where membrane tension facilitates membrane-cortex detachment.

144 ound that diapedesis is facilitated when the tension fluctuations in the VEC monolayer were increased

145 s has on concepts used to define interfacial tension for a two phase system with material exchange ac

146 ess on tonality cues than controls in rating tension for Western melodies.

147 n generate up to 1.7 mN (3.2 kPa) of passive tension force and 300 muN (0.56 kPa) of active tension f

148 nsion force and 300 muN (0.56 kPa) of active tension force in response to external stimulation.

149 tion protocol differentiated between passive tension (Fpassive) attributable to cardiomyocytes or to

150 different microtubule attachment features or tension from biorientation to SAC satisfaction nor how t

151 The surface tension (gamma) of xylem sap plays a key role in stabili

152 We propose that the tension generated by the E-cadherin/AmotL2/actin filamen

153 on levels: 12-54 piconewton (nominal values) tensions generated during platelet adhesion and tensions

154 degradation was independent of cytoskeletal tension generation and presentation of engineered adhesi

155 remodelling, in the absence of cytoskeletal tension generation, as a previously unknown strategy to

156 To test the hypothesis that normal-tension glaucoma (NTG) is caused by an increased pressur

157 owering intraocular pressure (IOP) in Normal Tension Glaucoma (NTG) patients.

158 n associated with POAG (including the normal tension glaucoma (NTG) subgroup), 8 with PACG and 2 with

159 K1 gene recapitulate the phenotype of normal tension glaucoma in human patients with a TBK1 gene dupl

160 TBK1 gene is associated with 1-2% of normal tension glaucoma, a common cause of vision loss and blin

161 ls lead to optic neuropathies such as normal tension glaucoma.

162 linear elasticity and the response to large tensions governed by an effective spring constant that s

163 xtension regimes, with the response to small tensions governed by linear elasticity and the response

164 These findings suggest that tension gradients can lead to patterning and differentia

165 ge in overall surface properties for surface tensions >10 mN/m, indicative of a bimodal behavior.

166 the placebo group (infusion site pain, n=1; tension headache, n=1); one patient in the placebo group

167 Interfacial tension (IFT) studies have shown a decrease in IFT at th

168 ly, pY14Cav1 enhanced CSD-dependent vinculin tension in focal adhesions, dampening force fluctuation

169 Tension in GUVs also influences the action of AMPs, wher

170 ajectories of single DNA hairpins held under tension in high-resolution optical tweezers.

171 at the tips of the stereocilia, activated by tension in interciliary tip links, and anomalous mechano

172 Our study uncovers a new role of mechanical tension in neural development: the regulation of axon fa

173 stereocilia of hair cells and opened by the tension in specialized molecular springs, the tip links,

174 2, a class-II myosin, is the major source of tension in the contractile ring, but how Myo2 is anchore

175 is based on the mechanical interplay between tension in the plasma membrane and stresses that develop

176 Although tension in the plasma membrane is generally considered t

177 w does not necessarily mean increased oxygen tension in the tissue.

178 dergoes similar conformational changes under tension in the two-head bound (2HB) state, whereas it is

179 s, amusics used timbre cues to judge musical tension in Western and Indian melodies.

180 The ITS also calibrated integrin molecular tensions in platelets and revealed two distinct tension

181 sistent with these experiencing the greatest tensions in the plant xylem network.

182 lar incision, asymmetric suture position and tension, inadequate correction, and lash location.

183 me constants for diameter reduction and rest tension increase of slackened axons.

184 t during cytokinesis progression, mechanical tension increased substantially along the direction of t

185 We show that when cortical tension increases faster than cross-linkers can unbind,

186 the marginal band will coil, whereas if the tension increases more slowly, the marginal band may sho

187 n of the marginal band rigidity and cortical tension increases the ability of the cell to withstand f

188 During protrusion, as membrane tension increases, velocity slows, and the lamellipodium

189 D cell shape information, transduced through tension-independent mechanisms, can regulate phenotype.

190 assembly, we find it is essential to recruit tension indicators, such as BubR1 and 3F3/2, to erroneou

191 ed with changes in effective plasma membrane tension induce significant spatiotemporal alterations in

192 of tension, suggesting that the hypo-osmotic tension induced the dispersion of caveolin-1 from the ca

193 in regulating endocytosis, whether membrane tension inhibits or facilitates endocytosis remains deba

194 Spicules are shown to occur when magnetic tension is amplified and transported upward through inte

195 This hoop tension is balanced by the restoring force of the microt

196 discovered that the termination of integrin tension is coupled with the exposure of phosphatidylseri

197 y nodes move bidirectionally, and shows that tension is generated by myosin pulling on barbed-end-anc

198 The tension is impulsively released to drive flows, heat pla

199 ring marshals actomyosin forces to generate tension is not settled.

200 lly: the gain in energy due a minimized line tension is proportional to domain radius and thus primar

201 This tension is resolved by reversible unfolding of the linke

202 opipette aspiration to show that anisotropic tension is sufficient to rescue the resolution, but not

203 nty-six amusics and 26 matched controls made tension judgments on Western (familiar) and Indian (unfa

204 Anal canal pressure and EAS length-tension (L-T) were measured for 15 weeks after which the

205 sions in platelets and revealed two distinct tension levels: 12-54 piconewton (nominal values) tensio

206 e illustrating that, in ambient air, surface tension lowering can prevail over the reduction in the R

207 Surface tension lowering caused by organic surfactants, which di

208 tablish a quantitative link between cortical tension, material properties and morphogenesis of an ent

209 abilizing cellular focal adhesions in a high-tension mode, paralleling effects of actin stabilization

210 Sensing bilayer tension, MscL channels are sensitive to changes in the b

211 vement cell shapes within an epidermis under tension must involve mechanical wall heterogeneities acr

212 me measures were the Rating for Premenstrual Tension observer and self-ratings completed every 2 week

213 sin network into a bundle and the buildup of tension occurring during the transformation.

214 lia of inner ear hair cells are gated by the tension of 'tip links' interconnecting stereocilia.

215 All diastereomers exhibit a minimum surface tension of about 28 mN/m without a significant differenc

216 n every case the transition occurs at a line tension of approximately 0.3 pN.

217 found that DRG neurons had a plasma membrane tension of approximately 54 pN/mum, and the tension was

218 both CA and MC had no effect on the surface tension of BSA/air interfaces.

219 The surface tension of matrices, and the wettability and diffusion o

220 e relatively high volatility and low surface tension of most organic solvents.

221 rmal and adhesion-reduced ectoderm, cortical tension of the free cell surfaces at gaps does not retur

222 ty caveolin-1 increased after increasing the tension of the plasma membrane through hypo-osmotic trea

223 GPA leads to an increase in the cytoskeletal tension of the red cell and a reduction in the bending m

224 e VECs can separately perturb the junctional tensions of VECs to result in the opening of gaps before

225 Increased tension on the E-cadherin complex promoted the junctiona

226 ixing point of the liquids, with interfacial tensions on the order of 20 mN m(-1).

227 Membrane tension plays various critical roles in the cell.

228 cular force microscopy, leveraging molecular tension probes and fluorescence polarization microscopy

229 microscopes, these easy-to-use membrane DNA tension probes can be broadly used to measure intercellu

230 d a novel strategy to construct membrane DNA tension probes to visualize tensile forces at cell junct

231 tDNA replication by removing DNA topological tensions produced during mtDNA transcription, but it app

232 gest that an asymmetric increase in cortical tension promotes filament reorientation along the cytoki

233 means of a modified version of the iso-flux tension propagation theory, and extensive molecular dyna

234 ctor related to poor concentration and inner tension (r=-0.32; 95% CI=-0.51, -0.08).

235 tension ratings, amusics provided comparable tension ratings for Western and Indian melodies on both

236 While controls assigned significantly lower tension ratings to Western melodies compared to Indian m

237 , thus showing a tonal familiarity effect on tension ratings, amusics provided comparable tension rat

238 othesized to facilitate protein interaction, tension regulation, and trafficking in biological membra

239 plants, with livers perfused at lower oxygen tensions, reperfused uneventfully.

240 and gamma are the viscosity and the surface tension, respectively.

241 ankle brachial index, transcutaneous oxygen tension, rest pain, and walking capacity after cell ther

242 ns of the SSB-ssDNA complex under mechanical tension revealed a multitude of possible pathways for ss

243 to a previous figure upon which the surface-tension scheme in Fig.1 should have included the followi

244 ld have included the following: "The surface-tension scheme in Fig.1b is adapted from Fig.1a in Noh,

245 Finally, the Rating for Premenstrual Tension scores in the second and third estradiol/progest

246 Mechanistically, the tension sensing cell-matrix adhesion molecule, vinculin,

247 e localization and function of a VE-cadherin tension sensor (TS) in vivo.

248 ported lipid bilayer platform as well as DNA tension sensor technologies.

249 logies such as high-resolution live imaging, tension sensors, and force-mapping techniques are provid

250 icient, D, as a function of applied membrane tension, sigma-as an indirect assay for determining func

251 monstrated that choice of a very low surface tension solvent is critical in successfully activating c

252 ed surface areas provided that lower surface tension solvents, such as n-hexane and perfluoropentane,

253 ient onto banana surfaces, and lower surface tension (ST, 25.4mN/m) than the critical ST (35.2mN/m) o

254 oss different ECM stiffness and cytoskeletal tension states.

255 Implantation of tension-stimulated tissues results in neotissues that ar

256 We also show that tension stimulation can be translated to a human cell so

257 e the effects of intermittent and continuous tension stimulation on tissue formation, we show that th

258 ted to manipulations known to increase axial tension, suggesting that tension can be coupled in the a

259 rgent and increased after the application of tension, suggesting that the hypo-osmotic tension induce

260 role of caveolae in counterpoising membrane tensions, syndapin III KO skeletal muscles showed pathol

261 As a consequence of the dependence on tension/tension ratios, the presence of gaps does not de

262 nd fluctuation spectra reveal a high nuclear tension that matches trends from traction force microsco

263 biologically relevant changes in VE-cadherin tension that occur as the dorsal aorta matures and upon

264 Aligned collagen fibers support elevated tensions that promote the folding of interfaces along pa

265 lic vulnerability can protect the xylem from tensions that would induce embolism and disruption of wa

266 ew light on how the interplay among membrane tension, the lamellipodial actin network, and adhesions

267 se the spectrin filaments are under entropic tension, the thermal random motion of the voltage-gated

268 gative pressure as explained by the cohesion-tension theory by coating hydrophobic surfaces and nanob

269 ons of plasma membranes that buffer membrane tension through their deformation.

270 Circumferential tension thus can regulate axonal diameter and volume, as

271 ues cytokinesis failure by reducing cortical tension, thus making it easier for the cell to divide wh

272 ressure rate product, pressure time product, tension time index), and high postextubation phase angle

273 030) and myocardial oxygen demand were seen (tension-time index, P=0.024; rate-pressure product, P=0.

274 ong the anterior intestinal portal generates tension to elongate the foregut and heart tube.

275 lizes and tunes EGFR activity and junctional tension to inhibit premature TJ complex formation in low

276 strong surface activity that reduces surface tension to low values when concentrated as they are in p

277 n factor complex stabilized under low oxygen tension to mediate cellular responses, including cell fa

278 We applied tension to the whole organ in situ by transverse deflect

279 ytoskeletons of adjacent cells, serving as a tension-transducer.

280 icellular junctions, propose a new model for tension transmission at tAJs, and discuss key open quest

281 nstriction by cleaving fibronectin to impair tension transmission in airway smooth muscle (ASM).

282 l produced by an increase in plasma membrane tension triggers the positioning of new rows of adhesion

283 ; tube elongation thus builds local membrane tension until the membrane undergoes scission through ly

284 From these parameters, and from surface-tension values measured previously, we estimated the val

285 a microfluidic viscometer driven by surface tension was developed to reduce the sample volume requir

286 Monolayer tension was measured through vinculin localization at th

287 The distribution of integrin tension was shown to be spatially regulated through two

288 tension of approximately 54 pN/mum, and the tension was significantly decreased to approximately 29

289 es), pKa, and the inverse calculated surface tension was significantly lower although still present,

290 a(2)(+)-sensitivity and passive myofibrillar tension were decreased in heterozygous fiber bundles, bu

291 -rated scores on the Rating for Premenstrual Tension were significantly increased (more symptomatic)

292 Arterial blood CO2 tension when increased by 25 mm Hg can induce MBF to the

293 ent STEMI exhibited increased LV wall active tension when normalized by SBP.

294 LSCs home in bone marrow areas at low oxygen tension, where HSCs are physiologically hosted.

295 on of gravity, centrifugal force and surface tension, which can be accounted for using only the spin

296 tions of buffer, we induced quantifiable DHB tension, which could be related to channel activity.

297 et size or increases with decreasing surface tension, which is sensitive to surfactants.

298 show that this barrier grows with increasing tension, which may slow down or prevent membrane budding

299 Quantitatively, membrane tension will alter gating energetics in proportion to th

300 eeper hybridization conforms to the classic "tension zone" model, where alleles are lost via reduced