ライフサイエンスコーパス: hydrostatic pressure

1 effect as a function of both temperature and hydrostatic pressure.

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

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

4 for division and maintaining cell shape and hydrostatic pressure.

5 lar space while also regulating interstitial hydrostatic pressure.

6 spectrum to interlayer distance modulated by hydrostatic pressure.

7 Their effect is reversed by hydrostatic pressure.

8 how enhanced DMSP production under increased hydrostatic pressure.

9 iffraction study of these two features under hydrostatic pressure.

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

11 binding sites induced by externally applied hydrostatic pressure.

12 correspondence between osmotic pressure and hydrostatic pressure.

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

14 mechanical stimuli, specifically osmotic and hydrostatic pressure.

15 ction permeability in response to changes in hydrostatic pressure.

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

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

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

19 .9% of mitochondria at 3 days after elevated hydrostatic pressure.

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

21 ic targets for protecting RGCs from elevated hydrostatic pressure.

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

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

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

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

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

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

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

29 ficantly in a linear fashion with increasing hydrostatic pressure.

30 ndence of amide hydrogen exchange on applied hydrostatic pressure.

31 e kinetic effects of varying temperature and hydrostatic pressure.

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

33 position, the spin Hamiltonian is altered by hydrostatic pressure.

34 pplying either an external magnetic field or hydrostatic pressure.

35 bsent-by varying the interlayer spacing with hydrostatic pressure.

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

37 ure deflection or a temporary application of hydrostatic pressure.

38 res, where it becomes extremely sensitive to hydrostatic pressure.

39 rlayer separation of the entire device using hydrostatic pressure.

40 d activation energies strongly influenced by hydrostatic pressure.

41 ificantly reduced by the application of high hydrostatic pressures.

42 01), with no increase in pulmonary capillary hydrostatic pressures.

43 ness and wetting resistance even at elevated hydrostatic pressures.

44 ion of washed chicken muscle exposed to high hydrostatic pressure (0, 200, 400 and 600 MPa) was exami

45 ants and KIEs were examined as a function of hydrostatic pressure (1-2000 bar) and were found to exhi

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

47 mature acini experience significant internal hydrostatic pressure (37 +/- 10.9 Pa).

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

49 High hydrostatic pressure affects the structure, dynamics, an

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

51 Elevated hydrostatic pressure also resulted in a significant, tim

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

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

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

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

56 cal theory, and physiological measurement of hydrostatic pressure and fluid transport in zebrafish to

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

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

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

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

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

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

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

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

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

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 Expressions for velocity field and the hydrostatic pressure are obtained.

74 Here, moderate changes of hydrostatic pressure are used to drive giant and reversi

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

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

77 Here, we have used high hydrostatic pressure as a tool to increase the populatio

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

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

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

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

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

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

84 Hydrostatic pressures can be transmitted between synovia

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

86 Hydrostatic pressure causes a monophasic decrease in the

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

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

92 driven water influx will generate turgor, a hydrostatic pressure considered critical for growth and

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

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

95 Moreover, hydrostatic pressures developed in our synthetic passive

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

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

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

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

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

101 Changes in hydrostatic pressure distribution as well as transmural

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Hydrostatic pressure has little effect on the low-temper

127 Recently, it was demonstrated that high hydrostatic pressure (HHP) (400 MPa for 5 min) induced t

128 n of heat moisture treatment (HMT) with high hydrostatic pressure (HHP) and evaluated its effects on

129 food processing technologies including high hydrostatic pressure (HHP) and high pressure carbon diox

130 Microwave (MAE), high-hydrostatic pressure (HHP) and ultrasound (UAE) assisted

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

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

133 to specifically aggregate beta-lg under high hydrostatic pressure (HHP) in order to separate alpha-la

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

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

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

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

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

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

140 High hydrostatic pressure (HHP) processing is a non-thermal t

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

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

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

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

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

146 ferent procedures: elaboration process, high hydrostatic pressure (HHP), cooking treatment and bioava

147 ple Dawn (PD), and Red) were treated by high hydrostatic pressure (HHP).

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

149 ted the effect of hydrothermal (HT) and high-hydrostatic-pressure (HHP) on the bile salt (BS)-binding

150 antioxidants, which can be extracted by high hydrostatic pressure (HHPE).

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

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

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

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

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

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

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

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

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

160 We find that fluid accumulation creates hydrostatic pressure in the lumen leading to stress in t

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

167 High hydrostatic pressure increases the equilibrium populatio

168 Application of high hydrostatic pressure increases the population of excited

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

170 rce-based measurements involving osmotic and hydrostatic pressure indicate the expansion occurs by ch

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

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

173 Elevated hydrostatic pressure induced ouabain-sensitive alveolar

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

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

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

177 Elevated hydrostatic pressure induces retinal ganglion cell (RGC)

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

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

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

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

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

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

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

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

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

187 Hydrostatic pressure is an important environmental varia

188 Hydrostatic pressure is an important physical parameter

189 Intracellular hydrostatic pressure is an important physiological param

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

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

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

193 omolecular LLPS at low temperatures and high hydrostatic pressures is discussed.

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

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

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

197 p layers of cartilage after cyclic strain or hydrostatic pressure loading.

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

199 Model solution describes luminal fluid flow, hydrostatic pressure, luminal fluid solute concentration

200 fying potentially important relationships to hydrostatic pressure mechanotransduction.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 We demonstrate that hydrostatic pressures of 450 MPa are sufficient to compl

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

217 Hydrostatic pressure offers an alternative to temperatur

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

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

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

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 ult of the previous accumulation of internal hydrostatic pressure (prestress), which is released afte

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

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

238 ine the influence of static and multi-pulsed hydrostatic pressure processing (HPP) treatments on the

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

240 A slightly increased subepithelial hydrostatic pressure produces such unidirectional outwar

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

242 propose a physiological function for DMSP in hydrostatic pressure protection, and that bacteria are k

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

244 The use of hydrostatic pressure reduction makes surgery unnecessary

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

246 Hydrostatic pressure represents an inexpensive and pract

247 Elevated hydrostatic pressure resulted in decreased cystic fibros

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

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

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

251 Application of hydrostatic pressure shifts protein conformational equil

252 Hydrostatic pressure shifts the spectrum from the 425 nm

253 Increasing hydrostatic pressure shows a stabilizing effect on the A

254 Optical absorption under hydrostatic pressure shows that the bandgap of CsPb(2) B

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

256 Here we show that cyclical hydrostatic pressure, similar to that experienced by imm

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

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

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

260 such as lactate dehydrogenase (LDH), against hydrostatic pressure stress (HPS).

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

262 g calculations and a model that balances the hydrostatic pressure, surface tension, and optical press

263 The application of high hydrostatic pressure technology for enzymatic extraction

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

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

266 structural changes when subjected to applied hydrostatic pressures that are both fundamentally intere

267 After elevated hydrostatic pressure, the cellular adenosine triphosphat

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

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

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

271 Under high hydrostatic pressures, the partial inactivation volume f

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

273 isible monomeric constituents by raising the hydrostatic pressure to a few kbar.

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

275 For hydrostatic pressure to drive localized protrusion in an

276 The use of high hydrostatic pressure to investigate structure-function r

277 Reservoirs interfaced with the chip use hydrostatic pressure to passively drive flow through the

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

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

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

281 Elevated hydrostatic pressure triggered mitochondrial fission, ab

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

283 The effect of hydrostatic pressure up to P = 1.7 GPa on the fluctuatio

284 -160 can be used for acidic pH sensing under hydrostatic pressures up to 510 atm, a range suitable fo

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

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

287 467 Da TAMRA by 15%, and permeability under hydrostatic pressure was increased 50% compared with con

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

289 Increasing hydrostatic pressure was shown to inhibit the presence o

290 Elevated hydrostatic pressure was used to probe conformational ch

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

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

293 Intracellular hydrostatic pressures were measured in lenses from mice,

294 Intracellular hydrostatic pressures were measured with a microelectrod

295 through the BV to obtain spatially resolved hydrostatic pressures, which were then combined with Sta

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

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

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

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

300 HIFD significantly increased hydrostatic pressure within the renal vein.