ライフサイエンスコーパス: oxygen concentration

1 The Cu effect increased with oxygen concentration.

2 f both Steps due to the increasing dissolved oxygen concentration.

3 f 100, 200, and 300 mum to measure the local oxygen concentration.

4 plays a key role in determining atmospheric oxygen concentration.

5 e, with semidiurnal pH fluctuations, or with oxygen concentration.

6 re populations can be reversed by changes in oxygen concentration.

7 21% oxygen, 4% oxygen, or with LPS at either oxygen concentration.

8 sive element (ORE), maximally active at a 4% oxygen concentration.

9 etically costly, that is, under non-limiting oxygen concentration.

10 cenarios such as irradiance or environmental oxygen concentration.

11 led conditions of temperature, pressure, and oxygen concentration.

12 ility was largely independent of the O-MWCNT oxygen concentration.

13 s of the active form of FNR as a function of oxygen concentration.

14 oxygen-nitrogen mixer generates differential oxygen concentration.

15 on between tumor vascular leakage and median oxygen concentration.

16 olic ROS production is directly dependent on oxygen concentration.

17 with aqueous solutions of controlled pH and oxygen concentration.

18 uitment maneuvers, mean airway pressure, and oxygen concentration.

19 to environmental factors such as glucose and oxygen concentration.

20 o fluctuations in Late Paleozoic atmospheric oxygen concentration.

21 a response promoter elements on the basis of oxygen concentration.

22 ced by either CoCl2 or decreased atmospheric oxygen concentration.

23 grate systems for monitoring and controlling oxygen concentration.

24 ssue-specific variations in redox stress and oxygen concentration.

25 including genes for adaptations to elevated oxygen concentrations.

26 benthic fluxes, and in-sediment nutrient and oxygen concentrations.

27 id in solution, under the same conditions of oxygen concentrations.

28 ing the respiratory rate and enhancing local oxygen concentrations.

29 ltured human placental cells under different oxygen concentrations.

30 se (RuBisCO) to CO2 under conditions of high oxygen concentrations.

31 survive in environments subject to changing oxygen concentrations.

32 eriods of low water table and high dissolved oxygen concentrations.

33 nt of XaXa hESCs derived under physiological oxygen concentrations.

34 ans sense and respond to reductions in local oxygen concentrations.

35 macrophages, fewer blood vessels, and lower oxygen concentrations.

36 ogenize the upper water column and cause low oxygen concentrations.

37 when the strain is cultivated under elevated oxygen concentrations.

38 upon interaction with the membrane at normal oxygen concentrations.

39 are often mechanically ventilated with high oxygen concentrations.

40 artificial porous scaffolds under different oxygen concentrations.

41 ux and redox states to changed substrate and oxygen concentrations.

42 g pathway to allow adaptation to fluctuating oxygen concentrations.

43 ocyte cultures were studied at 21, 5, and 2% oxygen concentrations.

44 e in its average speed moving away from high oxygen concentrations.

45 etween the HMP groups subjected to different oxygen concentrations.

46 injury caused by treatment with high inhaled oxygen concentrations.

47 tained limiting extant nitrite and dissolved oxygen concentrations.

48 rihydrite and goethite under variable pH and oxygen concentrations.

49 ured EE during walking under three different oxygen concentrations.

50 econd-order kinetics depending on tannin and oxygen concentrations.

51 and degradation in response to both iron and oxygen concentrations.

52 endence on both organic carbon and dissolved oxygen concentrations.

53 e oxidative peak is proportional to absolute oxygen concentrations.

54 temperatures (25-70 degrees C) and dissolved oxygen concentrations (0-100% O2 in the gas phase).

55 ) = 0.999) over the whole range of dissolved oxygen concentrations (0-43 ppm).

56 f which included a major rise in atmospheric oxygen concentrations [1, 2], extreme climatic fluctuati

57 in the AlS-IACW system under high dissolved oxygen concentrations (3-6 mg L(-1)) without specific co

58 ed photosynthesis at various irradiances and oxygen concentrations; (3) the response of gs to ci is s

59 Second, cultivation at human bloodstream oxygen concentration (5% relative to 21% atmospheric) si

60 e thermal degradation of tires under various oxygen concentrations (7-30%/Bal.

61 In support of this rise in oxygen concentrations, a large database shows a marked c

62 urn allows cancer cells to survive under low oxygen concentrations-a condition that generally kills n

63 The results show that the oxygen concentration affects the selection pressure, cel

64 Our model illustrates how even low oxygen concentrations allow the cell to perform essentia

65 ith taurine, k(1) was shown to depend on the oxygen concentration allowing calculation of a second-or

66 ts that P. aeruginosa responds to changes in oxygen concentration along a continuum rather than havin

67 Moreover, cytokines evaluation and oxygen concentration analysis revealed in this microenvi

68 we have analysed the influence of the tissue oxygen concentration and extra-cellular matrix density o

69 ange bias magnitude by varying the interface oxygen concentration and Fe-O bonding.

70 RT caused significant increases in tumor oxygen concentration and hemoglobin oxygen saturation.

71 uggest that it is the combined effect of the oxygen concentration and matrix density that creates an

72 mental factors, including water temperature, oxygen concentration and metal contamination, may influe

73 strategy to simultaneously visualize tissue oxygen concentration and microvascular permeability by u

74 at different hyperpolarization levels, local oxygen concentration and microvascular permeability of O

75 Constant maternal villous oxygen concentration and perfect fetal capillary membran

76 checking its compatibility with a change of oxygen concentration and pH.

77 ury and inflammation is characterized by low oxygen concentration and poor supply of nutrients.

78 tal methods enable both precise control over oxygen concentration and real-time imaging of cell behav

79 Here, the effects of oxygen concentration and temperature on the kinetic isot

80 was inhibited by endorepellin independent of oxygen concentration and that only a combination of both

81 ism for the observed sensitivity to elevated oxygen concentration and the decreased lifespan of the m

82 he possible values of the membrane-dependent oxygen concentration and the oxygen diffusion gradients.

83 gen peroxide increased with temperature, pH, oxygen concentration and the presence of phosphate buffe

84 on, and suggests that increasing atmospheric oxygen concentrations and a progressive oxygenation of t

85 e drop-tube furnace was used under different oxygen concentrations and CO(2) versus N(2) to study the

86 tal conditions and can survive low dissolved oxygen concentrations and high water temperatures.

87 development, the fetus is exposed to varying oxygen concentrations and must be able to quickly adapt

88 volved a significant increase in atmospheric oxygen concentrations and oxygenation of the surface oce

89 ems in the kilohertz regime at physiological oxygen concentrations and shed important light on the mu

90 n is seen as marking the rise in atmospheric oxygen concentrations and the evolution of non-photosynt

91 it fluctuations in blood flow that influence oxygen concentrations and therapeutic resistance.

92 for increased glycolysis under non-limiting oxygen concentrations and therefore do not fully explain

93 sitive to influent conditions (i.e., nitrate/oxygen concentration) and are 3-14 times higher compared

94 trolled, including assay media, temperature, oxygen concentration, and in the case of permeabilized s

95 and induce shifts in ocean temperature, pH, oxygen concentration, and productivity, which in turn co

96 dose, photosensitizer concentration, tissue oxygen concentration, and singlet oxygen production in r

97 irradiance, water matrix absorbance, singlet oxygen concentration, and the virus-specific apparent se

98 .32 mg/L of dissolved oxygen) at ambient air oxygen concentrations (approximately 200 hPa at 980 mbar

99 by which cells sense and respond to ambient oxygen concentration are fundamental to cell survival an

100 The observed ring-like patterns of oxygen concentration are modeled using thermophoretic fo

101 In normal cells, intracellular oxygen concentrations are directly sensed by prolyl hydr

102 Oxygen concentrations are hypothesized to decrease in ma

103 Because oxygen concentrations are important in normal lung physi

104 tric oxide (NO) and nitrous oxide (N2O) when oxygen concentrations are limiting.

105 a Clark ultramicroelectrode to determine the oxygen concentration as a function of time.

106 Oxygen concentrations as low as 0.5% did not alter the g

107 rends conform well to changes in atmospheric oxygen concentration, as predicted by modeling, and indi

108 ypothesis that ASB4 function is regulated by oxygen concentration, ASB4 interacts with the factor inh

109 high pH to limiting values that depended on oxygen concentration at < or = 0.97 mM oxygen.

110 The local oxygen concentration at each spectrally resolved proton

111 permitted semiquantitative determination of oxygen concentration at the mitochondria using calibrati

112 an phosphate, ocean sulfate, and atmospheric oxygen concentration at this time.

113 may detrimentally impact taxa that avoid low oxygen concentrations (Beroe, doliolids), but favour tax

114 ivity for the coupling reaction for adsorbed oxygen concentrations between 0.01 and 0.1 monolayer, wh

115 ze that tissue recovery is a function of the oxygen concentration, blood pressure, location on the va

116 ntial for biosynthesis of active MBH at high oxygen concentrations but dispensable under microaerobic

117 Independent of atmospheric oxygen concentration calculated EE has the same sign for

118 nce, the sensitivity of zooplankton to ocean oxygen concentrations can have direct implications for a

119 The oxygen diffusion coefficient (DbO2), oxygen concentration (cbO2), and oxygen permeability (Db

120 To monitor fluctuations in oxygen concentration, cells use sensory proteins often c

121 able of recommended mean airway pressure and oxygen concentration combinations, or individually titra

122 The influence of process parameters, such as oxygen concentration, concentration of initial volatile

123 ombined effects of temperature, pressure and oxygen concentration constrain the fundamental ecologica

124 ssion of many phosphorescent compounds, thus oxygen concentration could in many cases be derived dire

125 Oxygen concentrations decreased quickly during the first

126 Hypoxia induced in a time- and oxygen-concentration-dependent manner increased associat

127 Oxygen concentration did not impact the anthocyanin degr

128 een cells were cultured in BMP4 + SCF at low-oxygen concentrations did we recapitulate the expansion

129 We show that the dissolved oxygen concentration does not appear to affect AgNP form

130 Dissolved oxygen concentrations dropped from approximately 50-60 m

131 otection is related to a decrease of singlet oxygen concentration due to OCP action.

132 red with 2D materials reflects the change in oxygen concentration due to thermal desorption, which we

133 rate was almost identical and independent of oxygen concentrations due to simultaneous volatilization

134 ninvasive sensor that can accurately measure oxygen concentration during cell culture while being com

135 severe acute lung damage and decreased blood oxygen concentration during influenza virus infection wi

136 nt in children after cardiac arrest, initial oxygen concentration during resuscitation of newborns, a

137 A shift toward higher atmospheric oxygen concentration during the late Proterozoic has bee

138 nal function and morphology in dependence of oxygen concentrations during HMP in a porcine donation a

139 High oxygen concentrations during the Carboniferous may have

140 ssfully transition the broad fluctuations in oxygen concentrations encountered in the host.

141 dium refreshment, direct/indirect treatment, oxygen concentration, etc.), in primary cultures of norm

142 Here, we show that, at high dissolved oxygen concentrations, FeS accelerates NCU(IV) reoxidati

143 to the effect of a high fraction of inspired oxygen concentration (FiO(2)) during the perioperative p

144 uctuations in temperature, pH, and dissolved oxygen concentration following the variation in the phot

145 nventional methods and tools used to control oxygen concentration for cell studies, and then highligh

146 ntific literature on the appropriate initial oxygen concentration for use during neonatal resuscitati

147 on of positive-pressure ventilation, initial oxygen concentrations for initiation of resuscitation in

148 e acceptors, while likely conserving limited oxygen concentrations for other essential functions such

149 kinetic models have then been used to deduce oxygen concentration from TACs.

150 g correlation between RCT values and surface oxygen concentrations from X-ray photoelectron spectrosc

151 The lattice distortion caused by oxygen concentration gradient within the silver nanopart

152 the order of 10(-14) N, is generated by the oxygen concentration gradient, which in turn produces an

153 ow-affinity components, HemAT can respond to oxygen concentration gradients under both hypoxic (0-10

154 nction, the physiological values of cerebral oxygen concentration have remained elusive because high-

155 and nutrient-rich conditions and avoid high oxygen concentration, high salinity, and high density of

156 rd, CCS mitochondrial import is regulated by oxygen concentration: high (20%) oxygen prevents import,

157 ependent (BOLD) signal is sensitive to blood oxygen concentration; however, this signal is also sensi

158 Accordingly, decreased oxygen concentration (hypoxia) is a major stressor that

159 Regions of low oxygen concentration (hypoxia) occur in both normal huma

160 rs frequently contain large regions with low oxygen concentrations (hypoxia).

161 ygen sensing probe to study the variation in oxygen concentration in a viable multicellular 3D human

162 larger in diameter can be comparable to the oxygen concentration in air-saturated water, suggesting

163 , or four orders of magnitude lower than the oxygen concentration in air-saturated water.

164 ong onshore-offshore transects was driven by oxygen concentration in an area with an oxygen minimum z

165 Considering that the oxygen concentration in cancerous tissue can be less tha

166 rier embedded in collagen gel that increases oxygen concentration in culture 6-fold.

167 sent from global sediments since the rise in oxygen concentration in Earth's early atmosphere.

168 The oxygen concentration in explants was quantified using mi

169 nd enables the determination of the absolute oxygen concentration in individual moving droplets.

170 hem to efficiently migrate toward an optimal oxygen concentration in microaerobic niches.

171 n by molecular oxygen to transduce the local oxygen concentration in the 3D tissue scaffold.

172 ield potentials (LFPs) and changes in tissue oxygen concentration in the absence of spikes.

173 of the peripheral nervous system that senses oxygen concentration in the blood and responds to change

174 ation, digestion, and many pathologies alter oxygen concentration in the blood and tissue.

175 zero-stress state after step changes of the oxygen concentration in the breathing gas.

176 d glycolysis are increased regardless of the oxygen concentration in the cell, a phenomenon known as

177 Oxygen concentration in the cornea at a known depth was

178 Oxygen concentration in the cornea is modulated by UV-A

179 Varying the oxygen concentration in the medium can induce the transi

180 Metaproteogenomics showed that higher oxygen concentration in the midgut drives lignocellulose

181 The operational oxygen concentration in the originating full scale plant

182 The excess oxygen concentration in the photosynthetic membranes of

183 dy establishes the importance of physiologic oxygen concentration in the propagation and function of

184 nylalanine concentration, time, temperature, oxygen concentration in the reaction atmosphere, and the

185 A low oxygen concentration in the tissue gives rise to a tumou

186 th a small apoptotic potential, while a high oxygen concentration in the tissue gives rise to a tumou

187 benzene, for in vivo oximetry and imaging of oxygen concentration in tissues using electron paramagne

188 unique opportunities for measurement of the oxygen concentration in tumors using EPR methods.

189 Additional experiments with altered oxygen concentrations in conditions of feedback-limited

190 It is thought that oxygen concentrations in excess of 4% decreased the deco

191 g method to directly monitor fluctuations in oxygen concentrations in mouse models.

192 l technologies are revealing vanishingly low oxygen concentrations in nitrite-rich OMZs, indicating t

193 Furthermore, dissolved oxygen concentrations in streambed pore water were signi

194 High oxygen concentrations in the 90% treatment resulted in d

195 , which causes dysentery, encounters varying oxygen concentrations in the gastrointestinal tract, whi

196 Tumor hypoxia, characterized by low oxygen concentrations in the microenvironment of most so

197 apply this proxy to estimate past dissolved oxygen concentrations in the near surface waters of the

198 of multiple unit neural activity and tissue oxygen concentrations in the striate cortex of anaesthet

199 e OMZ margin are abundant at lower dissolved oxygen concentrations, including sulphur-cycling Chromat

200 Low blood oxygen concentrations increase fetal plasma catecholamin

201 r and tetragonality increase with decreasing oxygen concentration, indicating the crystal structure i

202 Oxygen concentration influenced the percentage of lysoph

203 omparing modified atmosphere packaging (MAP; oxygen concentration initially below 0.5%) packaging wit

204 of a system to remotely monitor and control oxygen concentration inside a device for 3D cell culture

205 he response of DosP activation to increasing oxygen concentration is a complex function of its ligand

206 ontrolled process and that a rapid change in oxygen concentration is a critical factor in detachment

207 been linked to hyperoxic conditions because oxygen concentration is a key physiological control on b

208 ng negative feedback regime when atmospheric oxygen concentration is of order pO2 approximately 0.1 P

209 e in modified atmosphere packaging where the oxygen concentration is reduced below 2%.

210 Yet adaptations to low-oxygen concentrations leading to anaerobiosis have indep

211 n increasing temperature and/or a decreasing oxygen concentration led to an elevated NOB/AOB ratio an

212 ia-induced activation of ATM correlates with oxygen concentrations low enough to cause a replication

213 emperatures (<6 degrees C) and low dissolved oxygen concentrations (<1-3 ml l(-1)).

214 y 0.02-0.08 mg/L of dissolved oxygen) at low oxygen concentrations (<50 hPa) and 4-8 hPa (approximate

215 tion suggests that Archaean upper-atmosphere oxygen concentrations may have been close to those of th

216 observed at higher EBCT where low dissolved oxygen concentrations may have limited biological activi

217 and the contemporary increase of atmospheric oxygen concentrations may have promoted the appearance o

218 d by use of the Microtox assay and dissolved oxygen concentration measurements.

219 s in pH or temperature but were sensitive to oxygen concentrations (N2-saturated kobs = 9.10 +/- 0.32

220 e critical validation: the measured ratio of oxygen concentrations near the midplanes of liquid disor

221 lls when they were cultured at a physiologic oxygen concentration of 5%.

222 Low dissolved oxygen concentration of subsurface environments is a lim

223 The enterprising solution is to increase the oxygen concentration of the air in the train from 21% to

224 erfusion and heart rate independently of the oxygen concentration of the inhaled gas, and did not eli

225 centration, or CDC) increased as the surface oxygen concentration of the O-MWCNTs or pH increased, fo

226 vative of strain PAO1 each grew at dissolved oxygen concentrations of less than 3 microM.

227 To investigate the influence of oxygen concentration on the degradation process, ohmic h

228 e have investigated the impact of the tissue oxygen concentration on the growth and evolutionary dyna

229 n, Fe(III)-EDDS concentration, pH value, and oxygen concentration on the homogeneous Fenton degradati

230 iogeochemical model that simulates dissolved oxygen concentrations on the shelf in response to varyin

231 wing lengths, that size tracked atmospheric oxygen concentrations only for the first 150 Myr of inse

232 for a number of key parameters, such as pH, oxygen concentration or primary production (PP).

233 Jurassic boundary to the present, we modeled oxygen concentrations over the past 205 million years.

234 re of arterial oxygen to fractional inspired oxygen concentration (PaO(2)/F(I)O(2)) ratio, and age.

235 re of arterial oxygen to fractional inspired oxygen concentration (PaO2/FiO2, P/F) ratio has been the

236 proteomic studies indicated that the ambient oxygen concentration plays a role in V. cholerae virulen

237 ng maximum size to atmospheric environmental oxygen concentration (pO(2)) until the end of the Jurass

238 Moreover, a higher oxygen concentration promotes NO conversion.

239 panied by corresponding changes in dissolved oxygen concentrations, proxy data reflecting oxygenation

240 By lowering the internal oxygen concentration, pulsation alleviates the problem o

241 uronal and behavioural responses to a narrow oxygen concentration range close to atmospheric levels.

242 From the FE models, glucose, lactate, and oxygen concentration ranges for unloaded healthy human T

243 e of arterial oxygen to fraction of inspired oxygen concentration ratio (DeltaPa(O(2))/Fi(O(2))).

244 This wide range of oxygen concentrations recommended for resuscitation high

245 Every 1% increase in oxygen concentration reduces the equivalent altitude by

246 ng water PCBs, lipid fraction, and dissolved oxygen concentration (regulating gill ventilation).

247 ted numerical model can quantify the spatial oxygen concentration related to different scenarios such

248 tely 2.4 billion years ago, when atmospheric oxygen concentrations rose from less than 10(-5) of the

249 ommunity structure also depend on geography, oxygen concentration, salinity, temperature, and other e

250 many of the adaptive responses to decreased oxygen concentration, such as enhanced glucose uptake an

251 rozoic Era (850-542 million years ago), when oxygen concentrations sufficiently rose to permit the ex

252 Dissolved oxygen concentrations suggest that microbial respiration

253 The rate increased in proportion to oxygen concentration, suggesting that the superoxide is

254 est metazoans probably needed relatively low oxygen concentrations, suggesting additional environment

255 at the Vb isozyme produces NO at much higher oxygen concentrations than the Va isozyme.

256 2-dependent growth of a host bacterium at an oxygen concentration that inhibited growth of the host c

257 ct on the form of a TAC; it is only the mean oxygen concentration that matters.

258 l and translational responses to surrounding oxygen concentrations that suggest both are important in

259 nto the bone marrow may be encouraged by low oxygen concentrations that trigger metabolic and molecul

260 lence of oxidized BP that is associated with oxygen concentration, the power density can be precisely

261 forms that persist in settings with variable oxygen concentrations, the capacity to perceive and modu

262 At saturating oxygen concentrations, the D(kcat/Km) was 10.6 +/- 0.6 a

263 The tissue oxygen concentration thus affects the tumour at both the

264 By increasing the oxygen concentration to 25%, the equivalent altitude is

265 ring ammonia oxidation in N. europaea at low oxygen concentrations to detoxify NO produced by reducti

266 se in which E. coli cells migrated away from oxygen concentrations to which they are normally attract

267 Above the 3-8% oxygen concentration typical of most tissues, we find th

268 The equilibrium stromal oxygen concentration under atmospheric oxygen at 3 mW/cm

269 rbon nanotubes (O-MWCNTs) of varying surface oxygen concentrations under a range of aquatic condition

270 sor into the 3D tissue scaffold and regulate oxygen concentration via the control of purging gas flow

271 r symbiotic nitrogen fixation in response to oxygen concentration via the sensor protein FixL.

272 ) value with 1,2-[2H4]-choline at saturating oxygen concentration was independent of pH in the range

273 When the oxygen concentration was lower than 22 muM and under the

274 iated at 3, 9, 18, and 30 mW/cm(2) while the oxygen concentration was measured.

275 the algorithm in a dynamic situation, where oxygen concentration was modulated to induce a change in

276 Oxygen concentration was the predominant environmental f

277 summer) with contrasting abiotic condition (oxygen concentration, water temperature and transparency

278 For low oxygen concentration we observe tumours with a fingered

279 , by monitoring the real-time fluctuation of oxygen concentration, we illustrated the formation of hy

280 ce that allows spatio-temporal variations in oxygen concentrations, we report the discovery that S. r

281 By experimental simulation of varying oxygen concentrations, we show that hypoxia followed by

282 subsets of this dataset, depth, season, and oxygen concentration were significant drivers of viral c

283 The potency of sulfide was enhanced when oxygen concentrations were low.

284 In addition, soil oxygen concentrations were lower in the low and mid-mars

285 ps of, e.g., nitrogen monoxide, benzene, and oxygen concentrations were obtained at a near microscopi

286 s as the bacteria are exposed to atmospheric oxygen concentrations when leaving the reservoir host gu

287 he pH on oxidation was more important at low oxygen concentrations, where deltalog k/deltapH was 0.85

288 4]-choline were pH-independent at saturating oxygen concentrations, whereas they decreased at high pH

289 ned ruthenium complex for sensing changes in oxygen concentration which resulted from oxidation of AT

290 that kidney formation is highly dependent on oxygen concentration, which is largely regulated by von

291 pression was sensitive to changes in ambient oxygen concentrations, while its dimerization partner HI

292 is platform, photonic measurements of pH and oxygen concentration with high precision in the distal a

293 actic behavior enables cells to seek optimal oxygen concentration with maximal efficiency.

294 Plants respond to reductions in internal oxygen concentrations with adaptive mechanisms (for exam

295 invariance of the spin Hall angle for higher oxygen concentrations with the bulk properties of the fi

296 ized conditions, we observed lower dissolved oxygen concentrations with the protocatechuic acid/proto

297 The excess oxygen concentration within the plesiomorphic cyanobacte

298 Excess oxygen concentrations within individual cells of the apo

299 hen microbial respiration depleted dissolved oxygen concentrations within the biomat.

300 is verified by measurement of the change in oxygen concentration, yielding a Faradaic efficiency of