ライフサイエンスコーパス: energy demand

1 tial to meet the rapid worldwide increase in energy demand.

2 ing a stimulus paradigm that increased local energy demand.

3 to offset projected increases in residential energy demand.

4 olism is expected to meet the quickly rising energy demand.

5 l fuel resources, fresh water resources, and energy demand.

6 ecause of their polarized structure and high energy demand.

7 re, in addition to efforts to reduce end-use energy demand.

8 a useful carbohydrate in times of increased energy demand.

9 st, incurs systolic benefits without raising energy demand.

10 for the treatment of disorders with altered energy demand.

11 neuronal dendrites and localize to sites of energy demand.

12 adapt to the metabolic challenges of altered energy demand.

13 tivity of the matrix and the concomitant low energy demand.

14 ns yield desirable products with a decreased energy demand.

15 d fuels the tricarboxylic acid cycle to meet energy demand.

16 cristae were widened, suggesting a sustained energy demand.

17 singly rely on coal to satisfy their growing energy demand.

18 The heart is a muscle with high energy demands.

19 help cells to produce more ATP to meet their energy demands.

20 pon endurance training to cope with enhanced energy demands.

21 can equally be used for different, competing energy demands.

22 o produce high quality effluent with minimal energy demands.

23 homes use solid fuel to meet their household energy demands.

24 technologies to meet ever-increasing global energy demands.

25 e to the cellular environment and changes in energy demands.

26 hich requires metabolic changes to match the energy demands.

27 HSCs use glycolytic metabolism to meet their energy demands.

28 r cells undergo glutaminolysis to meet their energy demands.

29 tion in other organs with temporally varying energy demands.

30 optical interconnect systems to meet strict energy demands.

31 best long-term solutions for meeting future energy demands.

32 digestible carbohydrate-C to fuel-heightened energy demands.

33 ental orchestrator of cellular adaptation to energy demands.

34 e benefit of photophosphorylation to augment energy demands.

35 growth factor-induced increases in cellular energy demands.

36 timately fusion require substantial cellular energy demands.

37 are distributed within cells to match local energy demands.

38 thus allowing energy supply to be matched by energy demands.

39 chondrial number and function in response to energy demands.

40 ive glucose metabolism to meet the increased energy demands.

41 ally meet water quality goals while reducing energy demands.

42 ptake active normally in neurons to maintain energy demands.

43 and can charge and discharge quickly for low energy demands.

44 and act as slow, steady suppliers for large energy demands.

45 ycolysis are adapted to the different axonal energy demands.

46 mphis utilized oxidative metabolism to meet energy demands.

47 t of North American plans for meeting future energy demands.

48 pumping function in the context of changing energy demands.

49 stem to meet the activity-driven increase in energy demands.

50 ems that are largely driven by the metabolic energy demanded.

51 t the HR and associated processes are highly energy demanding.

52 a significant contribution to N. norvegicus energy demand (0.21 to 10.7 times the energy required fo

53 echanisms to tightly couple fuel supply with energy demand across a wide range of physiologic and pat

54 conserve metabolic stores and participate in energy-demanding activities that are critical for fitnes

55 ms are unclear but may involve alteration in energy-demanding activities, such as protein synthesis.

56 energy-saving activities and less time to 2 energy-demanding activities.

57 al mitochondrial biogenesis to meet the high-energy demands after birth.

58 This paradoxical combination of increased energy demands along with decreased masticatory and dige

59 h heart rate is a key determinant of cardiac energy demand, AMPK functions in an organ-specific manne

60 onsiderably according to the balance between energy demand and availability.

61 growing tumors is associated with increased energy demand and diminished vascular supply, resulting

62 Parameters affecting operational energy demand and energy conversion are the most influen

63 tion probably exacerbates a mismatch between energy demand and energy production when myocardial oxyg

64 Global energy demand and environmental concerns have stimulated

65 Synapses are sites of high energy demand and extensive calcium fluctuations; accord

66 ies, resulting in considerably lower primary energy demand and GHG emissions.

67 olysis is stimulated by hormones that signal energy demand and is suppressed by the antilipolytic hor

68 loping world faces dual crises of escalating energy demand and lack of urban sanitation infrastructur

69 itochondrial dynamics to the balance between energy demand and nutrient supply, suggesting that chang

70 This program functions in tissues with high energy demand and oxidative capacity and is highly enric

71 nction of axonal mitochondria and imbalanced energy demand and supply are implicated in degeneration

72 ultiobjective optimization model of building energy demand and supply for the case of a Swiss municip

73 cific cell groups, perhaps those with a high-energy demand and the concomitant production of high lev

74 position of a mammalian cell we quantify the energy demand and the OxPhos burden of cell biosynthesis

75 ies for accommodating increases in metabolic energy demand and their biological limitations can serve

76 d thermal simulation to quantify operational energy demand and to account for differences in thermal

77 as well as trade-off analysis between rising energy demand and water use sustainability.

78 ort the pursuit of new therapies that reduce energy demand and/or augment energy transfer in heart fa

79 a-C(sp(3))-H bond activation relatively less energy demanding and opens the possibility for a competi

80 Growing global energy demands and climate change motivate the developme

81 as a node coordinating liver growth with its energy demands and emphasize the need of lipids for rege

82 astewater carbonaceous substrates can offset energy demands and enable net power generation; yet, the

83 ogy considered, but had significantly higher energy demands and environmental emissions.

84 As coordinators of energy demands and nutritional supplies, the PGC-1 famil

85 at forms in vivo near synapses to meet local energy demands and support synaptic function in Caenorha

86 mperature is thought to increase maintenance energy demands and thereby decrease available resources

87 ic transmission is expensive in terms of its energy demands and was recently shown to decrease the AT

88 tt-induced neurotoxicity because neurons are energy-demanding and particularly susceptible to energy

89 en consumption by substrate availability and energy demand, and ATP/ADP/P(i) was estimated as a funct

90 to quantify greenhouse gas emissions, fossil energy demand, and criteria air pollutant emissions for

91 tivity is important under conditions of high energy demand, and that specific cell types are uniquely

92 ntial indicator, the nonrenewable cumulative energy demand, and the Swiss ecological scarcity indicat

93 in response to changing nutrient sources or energy demands, and homologous SNF1-related kinase (SnRK

94 ntegrated assessment of multiple feedstocks, energy demands, and system costs is critical for making

95 idal alternatives exist, but high cost, high energy demands, and/or formation of disinfection byprodu

96 at may be linked to oxidative metabolism and energy demand appears to be the main determinant of mito

97 of a smart synthesis of methane hydrates in energy-demanding applications (for example, transportati

98 These data show that daily energy demands are extrinsically defined, with a link to

99 bolic costs, the biochemical bases of actual energy demands are rarely quantified.

100 tive phosphorylation to neuronal presynaptic energy demands are unclear.

101 Because neurons, which have a high energy demand, are particularly dependent on the mitocho

102 e more glucose than normal cells to meet the energy demand arising due to their uncontrolled prolifer

103 uel for the brain in situations of increased energy demand, as following a traumatic brain injury (TB

104 ons are metabolically active cells with high energy demands at locations distant from the cell body.

105 tivity create local and transient changes in energy demands at synapses.

106 e decline in TAN was not caused by increased energy demand, but by ATP release from the liver.

107 st neurons fire in bursts, imposing episodic energy demands, but how these demands are coordinated wi

108 al conversion is of great promise for future energy demands, but often limited by the kinetically slu

109 subjected to extensive Ca2+ fluxes and high energy demands, but the extent to which the synaptic mit

110 Here, we review the possible reductions in energy demand by state-of-the-art seawater desalination

111 h swimming cycle, thereby reducing metabolic energy demand by swimming muscles.

112 n increases its metabolism to meet increased energy demands by glycolysis after injury.

113 1 plays a key role in cellular adaptation to energy demands by translating physiological signals into

114 Other indicators, such as Cumulative Energy Demand (CED) and EcoIndicator99 H were calculated

115 parative life cycle assessment of cumulative energy demand (CED) and global warming potential (GWP) o

116 HG) emissions, water consumption, cumulative energy demand (CED), and energy payback time (EPBT).

117 e flux results suggested a trade-off between energy-demanding CO(2) fixation and biomass growth rate;

118 esources in areas distant from the origin of energy demand complicate the design of policy to ensure

119 ntensive subsector of health care, with high energy demands, consumable throughput, and waste volumes

120 As world energy demand continues to rise and fossil fuel resource

121 these specific anaplerotic steps can support energy demand despite HIFs degradation.

122 udy, we tested the hypothesis that increased energy demand during beta-AR stimulation plays an import

123 Increased energy demand during lymphocyte stimulation is coordinat

124 metabolic processes servicing the increased energy demand during persistent atrial fibrillation (AF)

125 These data suggest that increased energy demand during sustained beta-AR stimulation weake

126 and chemokinesis and provided adaptation to energy demand during tracking and engulfment.

127 ess, and can be enhanced by PCr buffering of energy demands during actin cytoskeletal rearrangements

128 sary for meeting the increased metabolic and energy demands during organ recovery after acute injury,

129 How cells meet the dynamic and localized energy demands during signal transmission is unknown.

130 Increasing energy demand, especially in the transportation sector,

131 particularly neurons, at risk of death when energy demands exceed cellular energy production.

132 to maintain circulating nutrient levels when energy demands exceed feeding opportunities.

133 , at risk of dysfunction and even death when energy demand exceeds cellular energy production.

134 nt, food supply, or physiologic status where energy demand exceeds supply.

135 changes for copper, we modeled and analyzed energy demand, expressed in fossil energy equivalents (F

136 which could satisfy up to 60% of the overall energy demand for biogas upgrading.

137 lows cells to sense and respond to increased energy demand for G2/M transition and, subsequently, to

138 hyperglycemia, conditions that greatly alter energy demand for gluconeogenesis, affected the ATP/ADP

139 the methane in a biogas stream can meet the energy demands for aeration and agitation, and recovery

140 ized in the case of food deprivation or high energy demands--for example, during certain developmenta

141 six impact categories, including cumulative energy demand, global warming (IPCC 2007), acidification

142 nic climate change and an increase in global energy demand have made the search for viable carbon-neu

143 ironmental concerns and an increasing global energy demand have spurred scientific research and polit

144 bally problematic emissions and material and energy demands, have not been examined in detail.

145 on, cancer cells have increased anabolic and energy demands; however, different cancer cell types exh

146 metabolic pathways in meeting the increased energy demands [i.e., ATP production (J(ATP))] of task-i

147 ious mismatch between substrate delivery and energy demands imposed by neural activity.

148 to replenish brain ATP during times of high energy demand in BD.

149 Cortical signaling requirements dominated energy demand in the awake state, whereas nonsignaling r

150 cose transport was not caused by a decreased energy demand in the neurons, because ouabain, which inh

151 rate (BMR) is the largest component of daily energy demand in Western societies.

152 chanism that matches substrate delivery with energy demands in brain.

153 ndicate that under energy stress conditions, energy demands in C. elegans synapses are met locally th

154 appears to impose an equivalent increase in energy demands in control and ischemic brain, but the ab

155 one volume, minimal weight, and also minimal energy demands in maintenance.

156 etabolism is essential for meeting increased energy demands in response to stressors, such as exposur

157 w provides an overview of ATP production and energy demands in the kidney and summarizes preclinical

158 his high rate of PI metabolism increased the energy demands in these cells.

159 ly allocate cellulosic biomass feedstocks to energy demands in transportation, electricity, and resid

160 dria play critical roles in meeting cellular energy demand, in cell death, and in reactive oxygen spe

161 mal aging, particularly in tissues with high energy demands including skeletal muscle.

162 ortex matures suggests that function-related energy demands increase during development, a process th

163 As energy demands increase, new, more direct, energy collec

164 in February voles in poorer sites had higher energy demands, indicating that DEE was forced upwards,

165 chanisms that translate perceived whole body energy demands into subsequent appetitive behavior are i

166 Indeed, T2 correlated with energy-demanding intracellular translocation of the inju

167 t inhibition of contraction, suggesting that energy demand is attenuated.

168 Total cumulative energy demand is comparable.

169 e glucose more effectively than lactate when energy demand is high.

170 Global energy demand is increasing as greenhouse gas driven cli

171 emic response (approximately 60%), (ii) this energy demand is met through oxidative metabolism, and (

172 Meeting the growing global energy demand is one of the important challenges of the

173 Matching blood flow to myocardial energy demand is vital for heart performance and recover

174 ce greenhouse gas (GHG) emissions and fossil energy demand, is increasingly seen as a threat to food

175 in hepatic metabolic adaptation to increased energy demands; it preserves tissue iron for vital activ

176 E because photoreceptor cells have very high energy demands, largely satisfied by oxidative metabolis

177 This inability to meet the increased energy demand leads to activation of cell death.

178 goals, and show how the target depends upon energy demand levels.

179 ty, typically necessitating the operation of energy-demanding low temperature fractional distillation

180 pollution caused by continuously increasing energy demands make hydrogen an attractive alternative e

181 that seen in PD, and suggests that increased energy demand may contribute to the mechanism by which L

182 e found in the abdomen, suggesting that here energy demand may relate to sperm formation and reproduc

183 ning global mine production data resulted in energy demand median values of around 50 MJ/kg Cu irresp

184 To survive, cells must fine-tune energy-demanding metabolic processes in response to nutr

185 on to nutrient availability and supports the energy-demanding metabolism of cancer cells.

186 rast to their role in cell types with higher energy demands, mitochondria in endothelial cells primar

187 oducts per household) and impact (cumulative energy demand (MJ) and greenhouse gas emissions (MT CO2

188 of BDNF, which is intimately associated with energy-demanding neuronal activity.

189 om the influent was 151 gN m(-2) d(-1) at an energy demand of 26.1 kJ gN(-1).

190 ed at a current density of 50 A m(-2) and an energy demand of 56.3 kJ gN(-1).

191 This study provides estimation tools for the energy demand of a representative set of food process un

192 rving the intricate balance between the high energy demand of active neurons and the supply of oxygen

193 eover, the model is utilized to quantify the energy demand of amino acid and enzyme de novo synthesis

194 The brain has the highest mitochondrial energy demand of any organ.

195 ial amelioration of the supposed increase in energy demand of demyelinated axons by remyelination.

196 ulating evidence suggests that the increased energy demand of impulse conduction along excitable demy

197 nction of ATP production to support the high energy demand of presynaptic terminals, their relative i

198 These results indicate that (i) the energy demand of task-induced brain activation is small

199 ntricular assist device (LVAD) decreases the energy demand of the failing human heart.

200 n and chemical catalysis, while reducing the energy demand of the overall process.

201 The energy demand of the temperature-vacuum-swing adsorption

202 urons through glycolysis to satisfy the high energy demand of these cells.

203 Nonrenewable cumulative energy demand of wooden buildings is 18% lower, compared

204 It is suggested that the heightened energy demands of activated neurons are met through incr

205 vements, and we modeled the consequences for energy demands of adult females in the Beaufort and Chuk

206 The higher energy demands of brain communication that hinges upon h

207 lect, here we propose a simple model for the energy demands of brain functional connectivity, which w

208 cose uptake and ATP accumulation to meet the energy demands of chemotaxis in activated T cells.

209 ted a comprehensive literature study for the energy demands of CO2 supply, and constructed a database

210 The energy demands of data centers (DCs) worldwide are rapid

211 To meet the high-energy demands of embryogenesis, mature oocytes are furn

212 gy will be better suited to satisfy the high-energy demands of growing urban areas.

213 exercise, is correlated with the increasing energy demands of high-intensity exercise.

214 es, this method will facilitate the study of energy demands of living systems with subcellular resolu

215 g glucose uptake and ATP production to match energy demands of migration.

216 To meet the energy demands of nerve conduction, small mitochondria a

217 the cortex that allows the brain to meet the energy demands of neuronal computations?

218 n maintenance of the synapse and meeting the energy demands of neurons.

219 mates, features that help to offset the high energy demands of our brains.

220 tion (with the formation of GlcN-6-P) or the energy demands of phosphorylation.

221 to assess how well-nourished women meet the energy demands of pregnancy and to identify factors that

222 d women use different strategies to meet the energy demands of pregnancy, including reductions in DIT

223 ortant ways in which pregnant women meet the energy demands of pregnancy.

224 These may reflect the metabolic energy demands of processes such as gliosis, neuronal ou

225 males accrue fitness benefits by timing peak energy demands of reproduction to coincide with maximum

226 gy stores are sufficient to support the high energy demands of reproduction, and may be a major deter

227 l was able to capture variations in reported energy demands of selected mining sites (FEE: 0.07 to 0.

228 inct metabolic programs to meet the changing energy demands of self-renewing HSCs.

229 The energy demands of the adult mammalian heart are met larg

230 rgy-generating capacity of the liver and the energy demands of the body mass, with liver regeneration

231 systems mount adaptive responses to meet the energy demands of the cell and to compensate for dysfunc

232 ntiating stem cells is required to cover the energy demands of the different organ-specific cell type

233 nd capacity for ATP production with changing energy demands of the heart.

234 store and release energy in response to the energy demands of the insect.

235 olism, occur in parallel with the increasing energy demands of the mother and the fetus, adaptation o

236 neuronal excitability, thereby reducing the energy demands of the neuron.

237 atteries have the potential to meet the high-energy demands of the next generation of batteries.

238 ributions of different geochemistries to the energy demands of these ecosystems, we draw together thr

239 ay be functional sites that serve local high-energy demands of unmyelinated fibers and signal transmi

240 We investigated whether increased energy demand on the remnant liver after PHx contributes

241 lcium sequestering and extrusion place heavy energy demands on a cell, we hypothesized that calbindin

242 r-limit of 5-30% of the current U.S. primary energy demand or 4-30% of the current U.S. liquid fuel d

243 llular energy homeostasis in periods of high-energy demand or energy supply fluctuations.

244 ylation in response to stimuli that increase energy demand or reduce its supply.

245 ls in the visual cortex during times of high energy demand (photic stimulation).

246 o fix atmospheric N2 to NH3 through the less energy-demanding photochemical process.

247 electron-transporting catalyst to carry out energy-demanding photochemical reactions.

248 oneogenesis from amino acids and lactate (an energy demanding process) but intact gluconeogenesis fro

249 Since eukaryotic gene expression is an energy demanding process, differences in the energy budg

250 T cell activation is an energy-demanding process fueled by increased glucose con

251 Nitrogen fixation is an energy-demanding process requiring tight control of meta

252 Adaptive thermogenesis is an energy-demanding process that is mediated by cold-activa

253 eparation of hydrocarbons is one of the most energy demanding processes.

254 mbryonic tissues develop to support the more energy-demanding processes of cell division and organoge

255 synthesis and H(2) oxidation, as well as the energy-demanding processes of N(2) fixation and CO(2) as

256 apacity, making them more vulnerable to high energy-demanding processes such as ischemia.

257 Based on future world energy demand projections, we estimate that if growth of

258 ission reductions and greater variability in energy demand projections.

259 to neurons during activation, (2) heightened energy demand rapidly activates glycolysis in neurons, a

260 on the OMM, depend on the cytoplasmic pH and energy demand rate.

261 ubstrate loss after MI and those that reduce energy demand rather than those that increase energy tra

262 memory, a cognitive function reliant on the energy-demanding recurrent excitation of neurons within

263 As body condition is a 'barometer' of energy demands relative to energy intake, we explored th

264 Lastly, the thermal energy demand required for the case of active temperatur

265 ily through a "pull mechanism" due to higher energy demand resulting from increased ion fluxes and th

266 By 2100 transport energy demand rises >1000% in Asia, while flattening in

267 hese beads, in the first visualization of an energy demand signaling gradient.

268 rial membrane potential varies, depending on energy demand, subcellular location, and morphology and

269 lpha-regulated pathways in tissues with high energy demand such as the heart, gene expression profili

270 ed in phenotypes involving tissues with high-energy demand, such as the brain and retina.

271 lectron transfer (SPLET) mechanisms are less energy demanding than the first ones indicating 2H(+)/2e

272 to cope with changes in nutrient supply and energy demand that naturally occur throughout the day.

273 Nutrient enrichment might offset some of the energy demands that warming can exert on organisms by st

274 es in regards to the nonrenewable cumulative energy demand, the ecological scarcity indicator, and li

275 Besides satisfying annual final energy demand, the model constraints comprise availabili

276 from adenylate kinase during states of high energy demand, the ornithine cycle enzyme argininosuccin

277 respiration increases to adapt for increased energy demands; the underlying mechanisms are still not

278 al ATP production is continually adjusted to energy demand through coordinated increases in oxidative

279 t cells to adapt to changing nutritional and energy demands through protein catabolism.

280 e a range of pathologies, commonly affecting energy-demanding tissues such as muscle and brain.

281 production, and are highly expressed in two energy-demanding tissues, heart and brain.

282 , we report that COX7AR is expressed in high energy-demanding tissues, such as brain, heart, liver, a

283 in swollen and dysfunctional mitochondria in energy-demanding tissues.

284 ke pathway provides a mechanism that couples energy demand to increased ATP production through the ca

285 The brain regulates blood flow to match energy demand to nutrient supply.

286 sorption of hexoses to support the increased energy demand to trigger plant defense reactions and to

287 bservations indicate that AMPK couples local energy demands to subcellular targeting of mitochondria

288 ploited by T. brucei to carefully coordinate energy demands to translational rates in response to env

289 o modeled ATP/NADPH demand, CEF responded to energy demand under high light but not low light.

290 flux is tightly correlated to the change of energy demand under varied brain activity levels, and th

291 is in white adipose tissue (WAT) to adapt to energy demands under stress, whereas superfluous lipolys

292 tions and represent a beneficial decrease in energy demands upon a neuron.

293 antly higher in every perturbation where the energy demand was either higher or uncompromised.

294 ditions, which enables the body to cope with energy demand when oxygen supply is insufficient.

295 igher temperatures increased community-level energy demand, which was presumably satisfied by higher

296 d firing of axons, with consequent increased energy demands, which may lead to neuroaxonal degenerati

297 To meet the growing energy demand while mitigating the environmental concern

298 Due to population growth, food and energy demands will soon surpass supply capabilities.

299 m that allows muscle to integrate autonomous energy demand with systemic energy storage and turnover.

300 within minutes as they cannot meet cellular energy demands with anaerobic metabolism.