ライフサイエンスコーパス: hydrostatic pressure

1 Their effect is reversed by hydrostatic pressure.

2 iffraction study of these two features under hydrostatic pressure.

3 e caused by muscle contraction or changes in hydrostatic pressure.

4 binding sites induced by externally applied hydrostatic pressure.

5 by a modest (approximately 40%) increase in hydrostatic pressure.

6 correspondence between osmotic pressure and hydrostatic pressure.

7 equired for fragmenting a magma at such high hydrostatic pressure.

8 mechanical stimuli, specifically osmotic and hydrostatic pressure.

9 ction permeability in response to changes in hydrostatic pressure.

10 ppa B (NFkappaB) translocation with elevated hydrostatic pressure.

11 s its pseudo wild-type (WT*) counterpart, to hydrostatic pressure.

12 ernary stability when exposed to 2-3 kbar of hydrostatic pressure.

13 .9% of mitochondria at 3 days after elevated hydrostatic pressure.

14 y as much as 60% after exposure to 3 kbar of hydrostatic pressure.

15 ic targets for protecting RGCs from elevated hydrostatic pressure.

16 ressure-induced changes after the release of hydrostatic pressure.

17 /or whose growth is altered as a function of hydrostatic pressure.

18 ng the conformation of the X-ray window with hydrostatic pressure.

19 eases in apical surface area when exposed to hydrostatic pressure.

20 and fungi, protrusion is driven primarily by hydrostatic pressure.

21 ap osmotic pressure to the axial drop in sap hydrostatic pressure.

22 e and the ratio of the shear stress with the hydrostatic pressure.

23 ficantly in a linear fashion with increasing hydrostatic pressure.

24 ndence of amide hydrogen exchange on applied hydrostatic pressure.

25 e kinetic effects of varying temperature and hydrostatic pressure.

26 nes were also characterized as a function of hydrostatic pressure.

27 an adaptive manner in response to changes in hydrostatic pressure.

28 typified by simulated ischemia and elevated hydrostatic pressure.

29 screened for the ability to grow at 280-atm hydrostatic pressure.

30 an be dissociated by the application of high hydrostatic pressure.

31 ure deflection or a temporary application of hydrostatic pressure.

32 cess could be completely reversed under high hydrostatic pressure.

33 l potential changes caused by alterations in hydrostatic pressure.

34 ross-sectional area increased with increased hydrostatic pressure.

35 rlayer separation of the entire device using hydrostatic pressure.

36 d activation energies strongly influenced by hydrostatic pressure.

37 e Cav1.3 channels when varying intracellular hydrostatic pressure.

38 F-actin network and changes in intracellular hydrostatic pressure.

39 for division and maintaining cell shape and hydrostatic pressure.

40 lar space while also regulating interstitial hydrostatic pressure.

41 spectrum to interlayer distance modulated by hydrostatic pressure.

42 ificantly reduced by the application of high hydrostatic pressures.

43 ness and wetting resistance even at elevated hydrostatic pressures.

44 High hydrostatic pressures (1-2 kbar), combined with low, non

45 ture media were subjected to three different hydrostatic pressures (2 atm, 1 atm, and 0.03 atm) for 2

46 Elevated hydrostatic pressure (24 hours) increased microglial IL-

47 neously during the application of changes in hydrostatic pressure (-500 to +500 mm Hg) to exposed den

48 val of isolated RGCs at ambient and elevated hydrostatic pressure (+70 mm Hg).

49 essive age-related increase in intracellular hydrostatic pressure, along with, increased intracellula

50 Elevated hydrostatic pressure also resulted in a significant, tim

51 This apparent absence has been attributed to hydrostatic pressure, although direct evidence is wantin

52 ndard hyphal form requires a balance between hydrostatic pressure and a resistive cell wall.

53 he fundamental band gap with the increase in hydrostatic pressure and a semiconductor to metal transi

54 atments (sterilisation, pasteurisation, high hydrostatic pressure and baking) was proven.

55 smotic water inflow, which raises vestibular hydrostatic pressure and forces water, salt, and glucose

56 lion cell (RGC) cultures exposed to elevated hydrostatic pressure and in a mouse model of glaucoma.

57 mic changes in the dissected aorta depend on hydrostatic pressure and on the percentage of aortic wal

58 rnal shell of peptidoglycan opposes internal hydrostatic pressure and prevents membrane rupture and d

59 le is known about the relative importance of hydrostatic pressure and shell mechanics, however.

60 monstrated during the response to increasing hydrostatic pressure and subsequent regulatory volume de

61 We measured internal hydrostatic pressure and the force exerted during claw a

62 heated to the supercooled liquid state under hydrostatic pressure and then quenched to room temperatu

63 In this study, the effect of high hydrostatic pressure and thermal treatments on antimicro

64 e allergenicity of walnuts subjected to high hydrostatic pressure and thermal/pressure treatments was

65 dissection flap were measured at increasing hydrostatic pressures and at increasing fractions of dis

66 assively by manipulating surface tension and hydrostatic pressure, and actively using external pumps.

67 ing their response to hot, cold, osmotic and hydrostatic pressure, and mechanical stimulation of expo

68 orten in response to fluid flow and elevated hydrostatic pressure, and promote increased transcriptio

69 s of anesthesia, the response of proteins to hydrostatic pressure, and protein engineering.

70 ncluding mechanical deformation, fluid flow, hydrostatic pressure, and streaming potentials; however,

71 control of permeability, under diffusive and hydrostatic pressures, and its contribution to the contr

72 However, moderate hydrostatic pressure applied to the isolated DHO subunit

73 In this model, membrane tension and hydrostatic pressure are the basic factors responsible f

74 RGC apoptosis induced by elevated hydrostatic pressure arises substantially through TRPV1,

75 We used high hydrostatic pressure as a tool for exploring the conform

76 phloem is permitted by maintaining sieve sap hydrostatic pressure at a value that is spatially nearly

77 n are now ordinarily successfully reduced by hydrostatic pressure (barium enema).

78 sed to various intensities of ultrasound and hydrostatic pressures before measuring their size distri

79 rtmentalizes the cytoplasm and increases the hydrostatic pressure between the nucleus and the leading

80 tally, it has been observed that increase in hydrostatic pressure can both increase and decrease prot

81 The present work demonstrates that high hydrostatic pressure can increase protein folding by red

82 tron diffraction experiments reveal that the hydrostatic pressure can push the Tmstr to a lower tempe

83 Hydrostatic pressures can be transmitted between synovia

84 It is well known that high hydrostatic pressures can induce the unfolding of protei

85 Hydrostatic pressure causes a monophasic decrease in the

86 The responses of rabbit urinary bladder to hydrostatic pressure changes and to electrical stimulati

87 lood pressure, did not show correlation with hydrostatic pressure changes in the joints.

88 Over a wide range of temperatures, hydrostatic pressure changes of 2.5 kbar yield large and

89 ressure probe, small and highly reproducible hydrostatic pressure clamp (PC) and pressure relaxation

90 A40) displayed growth impairment at elevated hydrostatic pressure concomitant with diminished cis-vac

91 duction is expected to directly modulate the hydrostatic pressure conditions for the low-resistance p

92 ofold lower in occludin-depleted cells under hydrostatic pressure conditions.

93 erved a strong correlation between force and hydrostatic pressure, consistent with hydrostatic skelet

94 y distress syndrome (ARDS) excludes only the hydrostatic pressure contribution.

95 Application of hydrostatic pressure controllably tunes A15 Cs(3)C(60) f

96 need for optical imaging, and viscosity and hydrostatic pressure corrections, as required by other m

97 Moreover, hydrostatic pressures developed in our synthetic passive

98 plificability of hazelnut DNA, however, high-hydrostatic pressure did not affect.

99 counter force on the complementary system, a hydrostatic pressure difference across the membrane can

100 o induce in molecular dynamics simulations a hydrostatic pressure difference across the membrane, fro

101 ly isolated from each other by using a small hydrostatic pressure difference; this feature can be use

102 Oncotic and hydrostatic pressure differences control the movement of

103 Small hydrostatic pressure differences produced by removal of

104 o a mismatch in electroosmotic flow rates or hydrostatic pressure differentials along the microetched

105 Changes in hydrostatic pressure distribution as well as transmural

106 hat observed earlier with CYP3A4, increasing hydrostatic pressure does not cause either a complete di

107 ics of the outer shell, rather than internal hydrostatic pressure, dominates stiffness.

108 es among the groups were less pronounced for hydrostatic pressure-driven flux and J(osm).

109 BSA)), osmotic filtration flux (J(osm)), and hydrostatic pressure-driven flux.

110 The temporal variations of the hydrostatic pressure, electric impedance and potential a

111 The extent of denaturation of WPI in a high hydrostatic pressure environment (600MPa for 600s) was a

112 to be higher than its denaturation in a high hydrostatic pressure environment at ambient temperature

113 tic continuum or viscous liquid require that hydrostatic pressure equilibrates essentially instantane

114 they can be dissociated to monomers by high hydrostatic pressure even after 1 h of incubation.

115 e coupling differs as a result of the higher hydrostatic pressure experienced by venules relative to

116 d WSe2, crystals has been studied at various hydrostatic pressures experimentally by photoreflectance

117 Attendant lowering of the reservoir's hydrostatic pressure facilitates the subsequent transfer

118 Our results show that the existence of the hydrostatic pressure field makes the transformation both

119 We show that under a hydrostatic pressure field, the unit cell dimension of a

120 o FMVD is the reduction in fetal-side inflow hydrostatic pressure (FIHP) following increased flow rat

121 Hydrostatic pressures, fixed charges and/or osmoles in t

122 ls were subjected to 0, 30, 60, or 100 mm Hg hydrostatic pressure for 2 hours, and the cells were har

123 Electron microscopy showed that elevated hydrostatic pressure for 3 days induced abnormal cristae

124 enaturant concentrations and the use of high hydrostatic pressure for simultaneous solubilization and

125 We also show that DC101 induces a hydrostatic pressure gradient across the vascular wall,

126 enses from various species, an intracellular hydrostatic pressure gradient goes from approximately 34

127 trinsic (active) forces move lymph against a hydrostatic pressure gradient in most regions of the bod

128 and an increase in the glomerular capillary hydrostatic pressure gradient.

129 r any substantial bulk flow at physiological hydrostatic pressure gradients.

130 different root zones under both osmotic and hydrostatic pressure gradients.

131 mall intestine in the absence of osmotic and hydrostatic pressure gradients.

132 lecules that stabilize proteins against high hydrostatic pressure has been classified as piezolytes,

133 Hydrostatic pressure has little effect on the low-temper

134 High hydrostatic pressure (HHP) did not produce any effect on

135 High hydrostatic pressure (HHP) has been used to pre-conditio

136 The application of high hydrostatic pressure (HHP) in winemaking for substitutio

137 High hydrostatic pressure (HHP) is a non-thermal technique fo

138 Although the effect of high hydrostatic pressure (HHP) on aqueous soluble and integr

139 The effect of high hydrostatic pressure (HHP) on flaxseed protein structure

140 The effects of high hydrostatic pressure (HHP) on wine stability were studie

141 The influence of high hydrostatic pressure (HHP) processing in parallel with o

142 ncounter mechanical stresses, including high hydrostatic pressure (HHP) stress.

143 er, we explored the potential for using high hydrostatic pressure (HHP) to promote disintegration of

144 n this study, the effects of thermal or high hydrostatic pressure (HHP) treatment of a milk base in t

145 The impact of high hydrostatic pressure (HHP) treatments on volatile compos

146 tructure and allergenicity responses to high hydrostatic pressure (HHP) was modelled.

147 , sonication (UAE), microwave (MAE) and high hydrostatic pressures (HHP).

148 nerve head astrocytes subjected to elevated hydrostatic pressure (HP) for 1 to 5 days.

149 objective was to explore the effect of high hydrostatic pressure (HP) on proteolysis by different pr

150 A sub-lethal hydrostatic pressure (HP) shock of approximately 100 MPa

151 ession of these genes is altered by elevated hydrostatic pressure (HP).

152 re subjected to independent manipulations of hydrostatic pressure, hypoxia, and glucose deprivation i

153 vitro, moderate (2.5 MPa, 1 Hz) intermittent hydrostatic pressure (IHP) treatment suppresses basal MM

154 Glycerol addition or the application of high hydrostatic pressure improved the final refolding yields

155 The model also predicts that peak levels of hydrostatic pressure in articular cartilage increase bet

156 how an external perturbation such as applied hydrostatic pressure in CdGeP(2):Mn induces a two serial

157 re we report the suppression of magnetism by hydrostatic pressure in elemental chromium, a simple cub

158 any marine invertebrates and fish respond to hydrostatic pressure in order to regulate their depth an

159 tensity did not change by the application of hydrostatic pressure in the presence or absence of chlor

160 We investigated the effects of high hydrostatic pressure in the range of 1--3 kilobars on te

161 f single-ring heptameric GroEL (SR1) by high hydrostatic pressure in the range of 1-2.5 kbar.

162 dissociation of tetradecameric GroEL by high hydrostatic pressure in the range of 1-2.5 kbar.

163 ined them at ambient or elevated (+70 mm Hg) hydrostatic pressure in vitro and used ELISA and immunoc

164 types were dissolved and refolded using high hydrostatic pressures in combination with either elevate

165 We measured intracellular hydrostatic pressures in mouse lenses using a microelect

166 ays affected by increased renal interstitial hydrostatic pressure include spinal neurons located at l

167 In contrast, elevated hydrostatic pressure increased copper toxicity, but did

168 High hydrostatic pressure increases the equilibrium populatio

169 Application of high hydrostatic pressure increases the population of excited

170 cytosis and its sensitivity to intracellular hydrostatic pressure, independently of its action on the

171 Changes in hydrostatic pressure induce changes in both the abundanc

172 Exposure to elevated hydrostatic pressure induced a fourfold increase in RGC

173 We also measured the hydrostatic pressure induced by the confinement, which w

174 Elevated hydrostatic pressure induced ouabain-sensitive alveolar

175 To model hydrostatic pressure-induced edema in vitro, we develope

176 this study was to determine whether elevated hydrostatic pressure induces mitochondrial fission and d

177 d Nanodiscs was very low, demonstrating that hydrostatic pressure induces neither substrate dissociat

178 Elevated hydrostatic pressure induces retinal ganglion cell (RGC)

179 enables a straightforward estimation of the hydrostatic pressure inside a walled cell.

180 solvent exchange after rapidly dropping the hydrostatic pressure inside the NMR sample cell from den

181 lebs, in which the edge is driven forward by hydrostatic pressure instead of actin.

182 Our data reveal a link between hydrostatic pressure, interstitial convection, and invas

183 s that oxidative stress is an early event in hydrostatic pressure/IOP-induced neuronal damage.

184 demand for novel technologies, such as high hydrostatic pressure, irradiation, ultrasound, filtratio

185 phinone reductase by NADH} and suggests that hydrostatic pressure is a sensitive probe of nuclear qua

186 Hydrostatic pressure is a useful tool in the study of va

187 lustering of the dynamic response to applied hydrostatic pressure is also seen, indicating localized

188 Hydrostatic pressure is an important environmental varia

189 Hydrostatic pressure is an important physical parameter

190 Intracellular hydrostatic pressure is an important physiological param

191 of protection factors and their response to hydrostatic pressure is consistent with a structural reo

192 characteristic of the open conformation, as hydrostatic pressure is increased from 1 to 2000 bar.

193 loading pathways and the mechanisms by which hydrostatic pressure is maintained in the minor vein phl

194 Hydrostatic pressure is used to perturb the manifold of

195 NLC behaviour yet reported: under increasing hydrostatic pressure its crystal structure expands in on

196 sing other perturbations (e.g. [P(i)] jumps, hydrostatic pressure jumps and temperature jumps and sin

197 delicate balance between an inner drive-the hydrostatic pressure known as turgor-and an outer restra

198 Third, we find that elevated hydrostatic pressure, long known to reverse anesthesia,

199 fying potentially important relationships to hydrostatic pressure mechanotransduction.

200 Neon is used as a chemically inert, near-hydrostatic pressure medium that prevents collapse of th

201 thylcholanthrene (3-MC; 25 muM) at levels of hydrostatic pressure mimicking shallow (0.1 megapascal o

202 roduce a fabrication method that relies on a hydrostatic pressure mismatch between the buffer and pol

203 lyte such as fluorescein that the additional hydrostatic pressure mode enables to stabilize the conce

204 ity (NAC), an extremely rare property, as at hydrostatic pressure most materials shrink in all direct

205 Increase in hydrostatic pressure, much like increase in temperature,

206 In response to increasing hydrostatic pressure, NH(4)NbWO(6) and RbNbWO(6) both in

207 ated ion channel conductances in response to hydrostatic pressure of 1 cmH2O (P<0.05).

208 Under a hydrostatic pressure of 1.52 GPa, Zn(CN)2 undergoes a fi

209 Furthermore, a cell hydrostatic pressure of 16.8 +/- 1.7 Pa and an interstit

210 present study shows that application of high hydrostatic pressure of 600MPa for 15min at ambient temp

211 native, yet pressure stable, conformation by hydrostatic pressure of about 300 MPa.

212 ate transition is completed by applying high hydrostatic pressure of up to 40 GPa.

213 pressing single-crystal coesite SiO(2) under hydrostatic pressures of 26-53 GPa at room temperature,

214 measurements at high temperatures and quasi-hydrostatic pressures of about three gigapascals on prev

215 Hydrostatic pressure offers an alternative to temperatur

216 s we assessed the effects of temperature and hydrostatic pressure on lethal and sublethal (respiratio

217 s in AXCP from the effect of temperature and hydrostatic pressure on rate constants.

218 sis was used to test the effects of elevated hydrostatic pressure on the binding of BamHI to its cogn

219 In this study, the effects of hydrostatic pressure on the folding reactions of AKe wer

220 al framework for interpreting the effects of hydrostatic pressure on the physical events leading to p

221 The effects of pH and hydrostatic pressure on the reaction of H463F tryptophan

222 The effects of hydrostatic pressure on the static magnetism in Eu(Fe0.9

223 -temperature studies, whereas the effects of hydrostatic pressure on the structure and properties of

224 The differential impact of elevated hydrostatic pressure on the temperature dependencies of

225 The effect of hydrostatic pressure on the tryptophan (Trp) synthase al

226 Here we investigate the effect of hydrostatic pressure on the vestibular hair cells locate

227 Biomechanical stimuli, such as hydrostatic pressure or compression, have been used to e

228 This suggests that either changes in hydrostatic pressure or transmural pressure distribution

229 = 300 K-40 mK, magnetic field B = 0-25T and hydrostatic pressure P = 0-17 kbar.

230 ance, thus increasing intrasplenic capillary hydrostatic pressure (P(c)) and fluid efflux into the ly

231 Rapid changes in hydrostatic pressure (P-jump) and temperature (T-jump) w

232 Hydrostatic pressure perturbs the spectra of the H463F l

233 ce, efferent resistance (RE), and glomerular hydrostatic pressure (PGLO).

234 demonstrate limited tolerance of increasing hydrostatic pressure (pressure exerted by the overlying

235 is unclear how the low temperature and high hydrostatic pressure prevalent in the deep sea affect to

236 The effect of high hydrostatic pressure processing (650MPa/9min) on molecul

237 Neutrophils exposed to elevated gas but not hydrostatic pressure produce MPs according to the potenc

238 haviour at higher pressures, indicating that hydrostatic pressure promotes the appearance of nodes in

239 h is generated by actomyosin contraction and hydrostatic pressure, pushes the cell out of confinement

240 over the temperature range 298-318 K and the hydrostatic pressure range 0.1-250 MPa [porphyrin ligand

241 The use of hydrostatic pressure reduction makes surgery unnecessary

242 sulting from mechanically induced changes in hydrostatic pressure regulate the metabolic activity of

243 the characterization of a gene necessary for hydrostatic pressure regulation of gene expression in th

244 In a natural environment, different hydrostatic pressures represent distinct ecosystems with

245 Elevated hydrostatic pressure resulted in decreased cystic fibros

246 of the CYP119 T213A mutant under increasing hydrostatic pressure resulted in variation of the N-aryl

247 terial pressure (RAP) and renal interstitial hydrostatic pressure (RIHP) has been shown under conditi

248 Renal interstitial hydrostatic pressure (RIHP) is a link between increased

249 Application of hydrostatic pressure shifts protein conformational equil

250 Hydrostatic pressure shifts the spectrum from the 425 nm

251 Increasing hydrostatic pressure shows a stabilizing effect on the A

252 study investigated the effects of sustained hydrostatic pressure (SHP; up to 4 cm H2O) on human umbi

253 as not affected by low temperature, but high hydrostatic pressure significantly enhanced the synergis

254 this oligomer is destabilized by increasing hydrostatic pressure, similar to the behavior of globula

255 The application of high hydrostatic pressure slows folding by orders of magnitud

256 or greater) and more evidence that elevated hydrostatic pressure stabilizes cells and enzymes at hig

257 These results indicate that increased hydrostatic pressure stimulates release of ATP from the

258 nerve fibres were selected that responded to hydrostatic pressure stimuli and their responses to the

259 -ferromagnetically below 3.8 K, and moderate hydrostatic pressure suppresses the anti-ferromagnetic o

260 The application of high hydrostatic pressure technology for enzymatic extraction

261 form of CcO even more sensitive to elevated hydrostatic pressure than monomeric CcO containing all 1

262 'Anomalous' pressures--large departures from hydrostatic pressure that are not explicable in terms of

263 owed that mouse lenses have an intracellular hydrostatic pressure that varied from 335 mm Hg in centr

264 After elevated hydrostatic pressure, the cellular adenosine triphosphat

265 ear to be responsive to modest positional or hydrostatic pressure, the choriocapillaris capacity is,

266 On elevation of hydrostatic pressure, the fission-linked protein, Drp-1

267 With the increase of the hydrostatic pressure, the magnetic state of Eu evolves f

268 Under high hydrostatic pressures, the partial inactivation volume f

269 At a given hydrostatic pressure, this area increased with increased

270 at piezolytes counteract the effects of high hydrostatic pressure through effects on the volumetric p

271 Here we use small changes in hydrostatic pressure to drive giant inverse barocaloric

272 For hydrostatic pressure to drive localized protrusion in an

273 ing cell was achieved by applying a positive hydrostatic pressure to its interior through a patch-cla

274 involved in protein-DNA recognition, we used hydrostatic pressure to perturb the binding of the BamHI

275 une the density of bosons and gigapascals of hydrostatic pressure to regulate the underlying interact

276 r transitions have been observed by applying hydrostatic pressure to, for example, Langmuir films of

277 emonstrates the potential for application of hydrostatic pressures to interpenetrated framework syste

278 Elevated hydrostatic pressure triggered mitochondrial fission, ab

279 t to the stability of dimeric CcO, 3 kbar of hydrostatic pressure triggers multiple structural and fu

280 Escherichia coli has been subjected to high hydrostatic pressure under a variety of conditions, and

281 -160 can be used for acidic pH sensing under hydrostatic pressures up to 510 atm, a range suitable fo

282 teins with predefined response to changes in hydrostatic pressure using computational approaches.

283 by use of bilateral catheters, and increased hydrostatic pressure was achieved by raising 1 catheter

284 ull micropipette system (SNMS)-for measuring hydrostatic pressure was adapted for the mouse eye.

285 467 Da TAMRA by 15%, and permeability under hydrostatic pressure was increased 50% compared with con

286 ase of ZnO during phase transition under non-hydrostatic pressure was observed and could be attribute

287 Increasing hydrostatic pressure was shown to inhibit the presence o

288 Elevated hydrostatic pressure was used to probe conformational ch

289 ity, determined from flow through gels under hydrostatic pressure, was compared with predictions obta

290 n cytochrome P450eryF applicable at elevated hydrostatic pressures, we introduce a laser dye Fluorol-

291 Intracellular hydrostatic pressures were measured in lenses from mice,

292 Intracellular hydrostatic pressures were measured with a microelectrod

293 c axis of its trigonal cell under increasing hydrostatic pressure, while contracting along the a axis

294 rome c oxidase is very resistant to elevated hydrostatic pressure with almost no perturbation of its

295 oplet formation is achieved by applying weak hydrostatic pressures, with liquid-filled pipette tips a

296 We used changes in hydrostatic pressure within a microscope optical chamber

297 produces regional fluctuating, intermittent hydrostatic pressure within the articular cartilage of l

298 2), With BE stretching, hydrostatic pressure within the BE cytoplasm is reduced

299 HIFD significantly increased hydrostatic pressure within the renal vein.

300 External hydrostatic pressure would generate an influx of water i