ライフサイエンスコーパス: energy requirement

1 th BD, especially in brain, which has a high-energy requirement.

2 in a substantial net decrease of the overall energy requirement.

3 d if an increased body size incurs a greater energy requirement.

4 modifications, showed predictable activation energy requirement.

5 en submaximal force and hence decreasing the energy requirement.

6 apacitor hybrid device as a solution to this energy requirement.

7 hout development to accommodate the animals' energy requirements.

8 ter expression is proportional to the cell's energy requirements.

9 The noninferiority margin was <10% of total energy requirements.

10 es, producing high effluent quality with low energy requirements.

11 stem to help rapidly growing pups meet their energy requirements.

12 ing limb collision, thereby reducing overall energy requirements.

13 be used for asymmetric photolysis with lower energy requirements.

14 nificant portion of deviations from expected energy requirements.

15 nd its ability to cope with altered cellular energy requirements.

16 nto how the corneal epithelium regulates its energy requirements.

17 its of agreement for energy intake/estimated energy requirements.

18 rdized to provide 50% of the daily estimated energy requirements.

19 y a suitable device configuration and assess energy requirements.

20 er, IC is strongly recommended for assessing energy requirements.

21 tide levels, couples metabolic pathways with energy requirements.

22 e provided and were isocaloric to individual energy requirements.

23 aptation of the left ventricle to changes in energy requirements.

24 al/d), which matched their individual, daily energy requirements.

25 population turnover rates and extremely low energy requirements.

26 hed food records were within 5% of estimated energy requirements.

27 rogen purification because of inherently low energy requirements.

28 ocean is a byproduct of microbial carbon and energy requirements.

29 rimary energy source for meeting the heart's energy requirements.

30 counting for 61.6% (2.2%) of estimated daily energy requirements.

31 s (n = 56), providing 20% of daily estimated energy requirements.

32 t self-reported dietary records to estimated energy requirements.

33 scale with size as a result of mass-related energy requirements.

34 ate did not alter ventricular defibrillation energy requirements.

35 nd is dependent solely on glycolysis for its energy requirements.

36 for children is discussed in light of their energy requirements.

37 iate source of glucose to support the cell's energy requirements.

38 on-chip systems with very low foot-print and energy requirements.

39 on has become crucial for fulfilling present energy requirements.

40 r are scarce, precluding an understanding of energy requirements.

41 compared to abundant small species with low energy requirements.

42 signals with extremely small footprints and energy requirements.

43 d combustion efficiency, and decreased laser energy requirements.

44 r 4-d food record and adjusted for estimated energy requirements.

45 global markets to satisfy their material and energy requirements.

46 nd fuel catabolism during prolonged elevated energy requirements.

47 [2.3 +/- 0.3 MJ; energy restriction (ER)] of energy requirements.

48 carboxylic acid (TCA) cycle to satisfy their energy requirements.

49 ailor their metabolic pathways to meet their energy requirements.

50 signalling fine-tune glycolytic flux to meet energy requirements.

51 , 2.73%), energy intake adjusted for minimum energy requirements (3.86%; 95% CI: 0.06%, 7.96%), total

52 eit with a significantly higher mean (+/-SD) energy requirement (36.6+/-19.8 J vs. 11.1+/-8.5 J).

53 surveyed, energy intake adjusted for minimum energy requirements (-4.49%; 95% CI: -8.77%, -0.15%) and

54 from baseline to sham phase (defibrillation energy requirements 50% = 12 +/- 1 J vs. 13 +/- 1 J, res

55 ly change during hypothermia (defibrillation energy requirements 50% = 14 +/- 2 J vs. 15 +/- 2 J, res

56 kcal, P =.02) or relative to estimated daily energy requirements (66.5% [3.1%] vs 57.0% [2.9%], P =.0

57 ration index (Z(p)=1) at the lowest specific energy requirements (8.92 kJ/kg).

58 heightened vulnerability are the substantial energy requirements, a strong excitatory drive, and a un

59 Energy requirements alone can explain how population den

60 Knowledge of energy requirements among relatively healthy elderly is

61 The energy requirement and associated carbon footprint of mi

62 mpact on land, water use, nutrients, albedo, energy requirement and cost, so have fewer disadvantages

63 Increased energy requirement and metabolic reprogramming are hallm

64 At baseline, 63% of infants met their energy requirement and most did not receive enough folat

65 sponsiveness of adipose tissue to changes in energy requirements and availability.

66 ent a framework to estimate the economy-wide energy requirements and carbon emissions associated with

67 the effects of hypothermia on defibrillation energy requirements and cardiac electrophysiology.

68 stems to better understand and constrain the energy requirements and costs of these air capture syste

69 he accuracy of calculating variables such as energy requirements and drug and dialysis dosages can be

70 water, the former consistently underestimate energy requirements and have a high degree of variabilit

71 her trophic level prey, (2) they have higher energy requirements and higher prey consumption, (3) the

72 berty is a time of rapid growth and changing energy requirements and is a risk period for obesity.

73 ce that the ability of mitochondria to sense energy requirements and localize properly within axons i

74 Energy requirements and nutrient intakes are commonly es

75 omas because of increased amino acid use for energy requirements and protein synthesis.

76 Traditionally thought to fuel energy requirements and provide building blocks for bios

77 e proximal tubule that by virtue of the high energy requirements and reliance on aerobic metabolism r

78 Thus, climate change may reduce time and energy requirements and the chance of mortality or vagra

79 fer considerably in their food availability, energy requirements and threats, and these differences c

80 t daily energy expenditure (DEE) to estimate energy requirements and to assess subject compliance.

81 GR-LACS may contribute to the provision of energy requirements and to the biosynthesis of steroid p

82 lid foods were provided at 125% of estimated energy requirements and were consumed ad libitum.

83 fects of ambient temperature on total winter energy requirements, and a relatively narrow combination

84 st, sample requirement, reagent consumption, energy requirements, and production of waste products ar

85 Electrical energy requirements are ensured by a photovoltaic cell t

86 Gallium nitride cradle-to-gate energy requirements are estimated to be similar to silic

87 Changes in gene expression, metabolism, and energy requirements are hallmarks of cancer growth and s

88 Basal energy requirements are higher in adolescents with sickl

89 erestimated PAL, new predictive equations of energy requirements are proposed.

90 Because energy requirements are substantially increased during a

91 Currently over 80% of the world's energy requirements are supplied by the combustion of fo

92 in IBB (sIBB) with approximately 70% reduced energy requirement as compared with the classical import

93 high cardioversion efficiency but with lower energy requirements as compared to whole ventricle inter

94 The subjects then consumed 25% of energy requirements as fructose- or glucose-sweetened be

95 n by ETV was accomplished through disfavored energy requirements as well as steric constraints during

96 The energy requirements as well as the temporal and spatial

97 uits must be able to identify and respond to energy requirements, as well as the amount of energy ava

98 requirement for high levels of iron to meet energy requirements associated with their rapid growth.

99 hought to be critical in supporting neuronal energy requirements at the synapse, and bioenergetic fai

100 akfast consisting of 20% of subject-specific energy requirements between 2 successive scans.

101 met more than 100% of their daily metabolic energy requirements by markedly increasing their feeding

102 batrosses during Levy movements exceed daily energy requirements by nearly fourfold, and approached y

103 stomy in ALS patients who fail to meet their energy requirements by oral intake.

104 riction (25% calorie restriction of baseline energy requirements); calorie restriction with exercise

105 Some or all of the energy requirements can be satisfied using renewable ene

106 s microalgal biomass with at least 80% lower energy requirement compared to traditional processes.

107 restimated and underestimated, respectively, energy requirements compared with those obtained by bica

108 ameters and scale-up effects showed that the energy requirement could be substantially reduced to 0.9

109 Investigation of the energy requirements demonstrated that the proton motive

110 ody's resting metabolic rate (RMR) and daily energy requirements (DER) expressed in glucose-gram equi

111 Studies that examined dietary energy requirements (DERs) of patients undergoing mainte

112 tput (ERWBC) was compared with the estimated energy requirements/Dietary Reference Intakes equation (

113 Energy requirements differed by age (P: = 0.001), feedin

114 ceive a formula diet containing 60% of daily energy requirement (DR group) or ad-libitum food during

115 king to eat (or not) can prevail over actual energy requirements due to emotional disturbances result

116 represent saving of 5-65% of the electrical energy requirements due to the vapor separation process.

117 um falciparum depends on glucose to meet its energy requirements during blood-stage development.

118 Accumulated lipids are catabolized to meet energy requirements during dormancy (diapause), which oc

119 In this work, we explore fundamental energy requirements during mammalian cell movement.

120 bstantial change in the temporal and spatial energy requirements during parasite differentiation.

121 Energy requirements during pregnancy remain controversia

122 ption of glucose or fructose as 25% of daily energy requirements (E) differentially affected plasma a

123 trimesters were not increased as compared to energy requirements early in pregnancy (34+/-53 kcal/d,

124 Energy requirement (EE/O) for the treatment of PFOA and

125 Caloric intake exceeded the estimated energy requirement (EER) for ideal body weight in 1995 b

126 in 2%) approximated TER-CF was the estimated energy requirement (EER) formula at the active level (EE

127 002 Dietary Reference Intake (DRI) estimated energy requirements (EER) noted that DLW studies in adul

128 o undergo conformational changes with little energy requirement (eg, point mutations and post-transla

129 Energy requirements equaled the sum of TEE and energy de

130 t zero, low, medium, and high proportions of energy requirements (Ereq) on circulating lipid/lipoprot

131 There is a paucity of data concerning the energy requirements (ERs) of preschool-age children with

132 dies was developed to enable comparison with energy requirements estimated by 17 commonly used predic

133 The energy requirements exponentially decay with the number

134 dulates the proton electrochemical potential energy requirement for activation of the chloroplast ATP

135 irements in children with CF against a total energy requirement for children with CF (TER-CF) derived

136 the energy profiles indicates that the free energy requirement for decarboxylation of 2,6-dimethoxyb

137 rature than wild-type gB, indicating a lower energy requirement for fusion activation.

138 titution, which may in turn indicate a lower energy requirement for fusion activation.

139 H2O2 production using PS in an MPPC, and the energy requirement for H2O2 production was low ( approxi

140 lactic acidemia, was observed at the lowest energy requirement for instrumental activities of daily

141 concurrently by GTP hydrolysis but that the energy requirement for lipid mixing exceeds that for tet

142 central carbon catabolism to accommodate the energy requirement for nitrogenase activity is largely u

143 antitative assessment of energy value versus energy requirement for oxidation of PyOM should yield im

144 ks including hazardous byproducts and a high-energy requirement for regeneration; therefore, research

145 sults demonstrate for the first time a clear energy requirement for the uptake of a nuclease colicin

146 tion of ATP, excluding the possibility of an energy requirement for this pathway.

147 in weight and body composition is called the energy requirement for weight maintenance and can be det

148 ructose-sweetened beverages providing 25% of energy requirements for 10 weeks.

149 erfeeding was prescribed as 140% of baseline energy requirements for 56 d.

150 ung adults consumed 40% above their baseline energy requirements for 8 wk, and sleeping metabolic rat

151 as ineffective for reducing the pressure and energy requirements for a set permeate flux.

152 viduals may result in the underestimation of energy requirements for a significant percentage of girl

153 Free energy requirements for activation are defined with prot

154 on methanol was lower, possibly due to high energy requirements for C(1) assimilation.

155 eft ventricular ejection fraction or minimal energy requirements for defibrillation or pacing.

156 uture RO-PRO systems may reduce the specific energy requirements for desalination by approximately 1

157 Understanding the energy requirements for each configuration will allow op

158 f HN from different paramyxoviruses, varying energy requirements for fusion activation, F activation

159 ng the limits of energy barriers and minimal energy requirements for growth in reactions activated by

160 hods such as reverse osmosis have increasing energy requirements for higher concentrations of dissolv

161 patients with SLE was similar to the highest energy requirements for instrumental activities of daily

162 tracellular parasites, they have significant energy requirements for invasion and gliding motility th

163 hough previous investigators have focused on energy requirements for normal growth, little is known a

164 togenetic delivery characteristics determine energy requirements for optical stimulation and to ident

165 of these reductions varies as a function of energy requirements for production, process-related emis

166 The energy requirements for recycling copper from end-of-lif

167 h constitutes a stable arrangement with high energy requirements for substantial structure alteration

168 The energy requirements for terminating ischemically induced

169 Compton explanation alleviating the particle energy requirements for the emission observed at late ti

170 ture-dependent kinetic studies establish the energy requirements for the fundamental stepping cycle,

171 as made possible by substituting the thermal energy requirements for the growth with plasma decomposi

172 Thus lowering the energy requirements for the semiconductor synthesis step

173 the gB CTD regulates fusion by altering the energy requirements for the triggering of fusion mediate

174 The energy requirements for this expansion are formidable, a

175 ition in children with cystic fibrosis (CF), energy requirements for those children are often set abo

176 ctuates seasonally in response to changes in energy requirements, foraging patterns and resource avai

177 Individuals did underconsume relative to energy requirements from high-protein diets.

178 to water flux decline and increased pumping energy requirements from spacer blockage highlight the s

179 of synaptic vesicle release or whether these energy requirements go unmet in disease, primarily due t

180 tive value even when immediate physiological energy requirements have been met.

181 Methods to estimate energy requirements have not been devised for this patie

182 rvival and spring breeding, increased winter energy requirements have the potential to impact local s

183 just a few larvae can satisfy a crow's daily energy requirements, highlighting the substantial reward

184 glucose infusion at a level adequate to meet energy requirements, hyperinsulinemia induced by a hyper

185 asure total energy expenditure (TEE)-derived energy requirements in a biracial population of older ad

186 Black women had lower resting and nonresting energy requirements in both overweight and normal-weight

187 valuated 6 proposed formulas for calculating energy requirements in children with CF against a total

188 critical role of mitochondrial dynamics and energy requirements in neuronal development, the homozyg

189 and anthropometric characteristics determine energy requirements in SMAI.

190 gy buffer, which can bridge local short term energy requirements in the brain.

191 s to bioenergy would meet a large portion of energy requirements in the near future.

192 terminant of lower-than-normal TEE, and thus energy requirements, in women with RA.

193 strategies have been developed to reduce the energy requirements, including sequential reactions and

194 Skeletal muscle energy requirements increase at birth but little is know

195 Energy requirements increased from 4 MJ/d at 2 y to 11 M

196 In the normal-BMI group, energy requirements increased negligibly in the first tr

197 adjust energy intake in response to changing energy requirements is a defining feature of energy home

198 Positioning mitochondria at areas with high energy requirements is an essential solution to this pro

199 o adjust food intake in response to changing energy requirements is essential for survival.

200 s--ensuring that energy availability matches energy requirements--is essential for survival.

201 unique animal model because of an unrivaled energy requirement; its great drive to eat results in fe

202 ents and added to energy intake to calculate energy requirements. kg(-1) . d(-1) calculated from ener

203 to implementation, including economic cost, energy requirements, land use, and water use.

204 th have opposing effects on Wood Frog winter energy requirements, leading to geographically heterogen

205 Consistent with their higher energy requirements, males can consume significantly lar

206 However, energy requirements may have changed with new treatments

207 e-polarisation magnetic field as well as the energy requirements, mechanical forces and stresses duri

208 livestock are rarely fed at 100% maintenance energy requirements (MER) and the effect of sub-optimal

209 n occurs during mitosis to preserve the high energy requirements needed for the dynamic structural ch

210 processes and that such coupling imposes an energy requirement not apparent for any isolated process

211 0.001 mol h(-1) m(-2), respectively, and an energy requirement of 0.7 kWh kgCOD(-1) or 0.084 kWh m(-

212 The non-optimized filtration system had an energy requirement of 2.23 kWh/m(3) with an associated c

213 ve than neutral substituents in lowering the energy requirement of [1,3] shifts.

214 and analysis of filament shape indicated an energy requirement of approximately 13 kBT.

215 0% efficiency) could contribute to the total energy requirement of several countries, the highest bei

216 for the time lost to feeding and the greater energy requirement of spending more time in flight, by b

217 s was also performed to find out the minimum energy requirement of such a bilayer hydrogel-driven FO

218 vealed no correlation between the activation energy requirement of the different species and their mo

219 The energy requirements of 63 women [17 with a low body mass

220 electrode effects the electrical and pumping energy requirements of a FCDI system.

221 er, we determine the process performance and energy requirements of a gas recovery system (GRS) using

222 he goal was to develop equations to estimate energy requirements of ALS patients.

223 e artificial intelligence while reducing the energy requirements of computing platforms.

224 However, energy requirements of desalination plants account for h

225 This study was designed to estimate the energy requirements of healthy underweight, normal-weigh

226 atalog may reflect the dynamic role and high energy requirements of hGFs in extracellular matrix remo

227 Comparing energy requirements of HS-DAC and MEA-PCC, we find that

228 The total energy requirements of infants increased from 1.4 MJ/d a

229 tabolism was subserving the primary role for energy requirements of IPAH cells was provided by the ap

230 mate change is raising metabolic demands and energy requirements of marine ectotherms.

231 To support the high energy requirements of muscle contraction, myogenesis en

232 hese studies suggest that the morphology and energy requirements of neurons make them particularly su

233 The objective was to determine the energy requirements of nonobese men and women in the Com

234 nt insights into the molecular mechanism and energy requirements of NSF.

235 lin equations are recommended for estimating energy requirements of older adults.

236 The protein and energy requirements of patients with chronic renal failu

237 in clinical practice appear to underestimate energy requirements of patients with SBS, and revision i

238 Current DRIs for energy overestimate energy requirements of preschool-age children because of

239 peated transitions, possibly due to the high energy requirements of regulation.

240 However, do energy requirements of signaling and nonsignaling compon

241 Calculations of the energy requirements of small pelagic fish and jellyfish

242 enditure (TEE), and thus whether the dietary energy requirements of subjects with RA are higher or lo

243 However, little is known about the energy requirements of synaptic vesicle release or wheth

244 vents oedema, and metabolically supports the energy requirements of the brain.

245 During pregnancy, the energy requirements of the fetus impose changes in mater

246 tion products contribute less to the overall energy requirements of the host.

247 We resolve this paradox by considering the energy requirements of the last universal common ancesto

248 xosamine pathway that is in concert with the energy requirements of the organism.

249 cally generate sufficient ATP to satisfy the energy requirements of the rest of the cell in addition

250 The specific energy requirements of the TVS process based on the meas

251 ing approximately 70% of the daily estimated energy requirement, of which 60% was either glucose or g

252 y and policymakers to quantify manufacturing energy requirements on a product-output basis.

253 SSBs were provided at 25% of estimated energy requirement, or an equivalent volume of the aspar

254 cancer cells is limited by ATP and satisfies energy requirements other than ATP production.

255 ed to cDBS, and a corresponding reduction in energy requirements (p < 0.001).

256 16% +/- 16% of the subject's estimated total energy requirements (P = 0.880).

257 by comparing reported intakes with predicted energy requirements (pERs).

258 ation between TEE by using DLW and estimated energy requirements predicted from DRI equations (Pearso

259 Glucose infusion adequate to provide energy requirements resulted in a modest increase in blo

260 zation, length of axonal processes, and high-energy requirements (reviewed in [3]).

261 t and lactating women with asymptomatic HIV, energy requirements should approximate recommendations f

262 uring adolescence, pregnancy, and lactation, energy requirements should be based on TDEE plus the add

263 that corresponds to its bill morphology and energy requirements, supporting the hypothesis that feed

264 day, amounting to 58% +/- 39% of daily total energy requirements (TER).

265 energy intakes >/= 500 kcal below Estimated Energy Requirements than for vegetarians who did not res

266 n aid in metal recovery with lower costs and energy requirements than traditional metal-extraction ap

267 drate availability, and presumably a greater energy requirement, than G1 and G2.

268 the proportion of the standardized estimated energy requirement that was delivered as enteral nutriti

269 s and toxicity of reagents, generated waste, energy requirements, the number of procedural steps, min

270 MPES reduces the overall energy requirements thereby greatly expanding the range

271 ding EI was estimated as the sum of baseline energy requirements, thermic effect of food, and DeltaES

272 s supply the host with the majority of their energy requirements through the translocation of photosy

273 iets offered contained 125% of the estimated energy requirement to allow self-selection of food quant

274 of natural selection, which relate metabolic energy requirements to information gain under optimal co

275 The model is used to forecast electrical energy requirements to scale up the PV industry and dete

276 richia coli Lon exhibits a varying degree of energy requirement toward hydrolysis of different substr

277 The DRI-predicted energy requirements underestimated measured TEE by ~120

278 Defibrillation energy requirement values at 20%, 50%, and 80% were dete

279 In the hypothermia group, defibrillation energy requirement values at baseline did not significan

280 Similarly, the defibrillation energy requirement values in the control group did not c

281 The energy requirement was determined and correlated to the

282 Food equivalent to ~50% of energy requirements was delivered weekly to their homes.

283 d four different overfeeding diets with 200% energy requirements was measured in a metabolic chamber

284 he reduced selectivity and increased pumping energy requirements we observe in PRO will significantly

285 Thermal energy requirements were 2646 and 1357 kJ/kg, whereas el

286 Estimated energy requirements were calculated using Institute of M

287 ient study and 1 outpatient study), baseline energy requirements were determined by a doubly labeled

288 Predicted energy requirements were determined by using the Escott-

289 Energy requirements were determined for 217 healthy, wei

290 The lowest threshold energy requirements were found in Tip-->right ventricula

291 Values for defibrillation energy requirements were measured at baseline (normother

292 western part of the Great Lakes region where energy requirements were predicted to increase.

293 the metabolic index (MI) ratio (REE/expected energy requirements) were calculated.

294 nd chemical feedstocks with a relatively low energy requirement when compared to systems that source

295 117% +/- 12%, and 102% +/- 15% of estimated energy requirements when subjects consumed the fructose-

296 Individuals forage until their energy requirements, which are determined by their body

297 age comprised transcripts mainly involved in energy requirements while later stages were mostly assoc

298 (CR), the reduction of dietary intake below energy requirements while maintaining optimal nutrition,

299 the individual-level prediction of estimated energy requirements with the measured value of total ene

300 al empirically derived formulas to calculate energy requirements, yet the validity of these formulas