ライフサイエンスコーパス: storage

1 abundant in packed boxes at the end of cold storage.

2 ed as an attractive medium for archival data storage.

3 ar distribution of proteins involved in IMTG storage.

4 t when they have used up their elastic water storage.

5 itatory feedback, or synaptic plasticity for storage.

6 entially from the start, reaching 85% during storage.

7 al phenomena that enable new means of energy storage.

8 tion to LDs has been shown to assist in IMTG storage.

9 ms that contribute to sex differences in fat storage.

10 asingly critical field of environmental fuel storage.

11 content of procyanidins and flavanols after storage.

12 d, therefore, less softening after long-term storage.

13 s which can be enriched by post-harvest cold storage.

14 c charge carriers for electrochemical energy storage.

15 biosynthesis, in acerola during postharvest storage.

16 to examine transcriptomic changes with cold storage.

17 enabling stretchable electrochemical energy storage.

18 ate change mitigation results in increased C storage.

19 reference and frozen-thawed fish during its storage.

20 rts have distinct responses to cold ischemic storage.

21 n all samples decreased or disappeared after storage.

22 en sausage refrigerated for up to 42 days of storage.

23 he climate change benefit from increased SOC storage.

24 reating shrimps in GLE-S before refrigerated storage.

25 developmental stages and during postharvest storage.

26 iched nanoemulsion formulation during 50-day storage.

27 ions including cellular signaling and energy storage.

28 timately reach its full potential for energy storage.

29 antageous to chemical reaction and molecular storage.

30 otential approaching -30 mV until the end of storage.

31 going temperature changes during shipment or storage.

32 retinyl palmitate (RP) during simmering and storage.

33 t showed phase separation after two weeks of storage.

34 romising alternatives for large-scale energy storage.

35 s, including polymer folding and information storage.

36 g CFU/g on day 60 and/or 90 of refrigeration storage.

37 nt device components for digital information storage.

38 namic organelles with functions beyond lipid storage.

39 r runoff rate/amount, but increased moisture storage (+14%).

40 Ls (BNLs) didn't change significantly during storage (40 days).

41 e scenarios with different configurations of storage additions, new renewable capacity, and carbon pr

42 tchable and flexible electronics, and energy storage, among others.

43 ns in chemical sensing and electrical energy storage, among others.

44 importance of computation in data collection/storage and algorithm design.

45 Storage and computational costs mount sharply with data

46 PALs retain higher activity after prolonged storage and confer reusability for over 100 runs with le

47 tion that this will increase net ecosystem C storage and contribute to climate change mitigation.

48 aterial with tremendous potential for energy storage and conversion applications.

49 directly affects the electrochemical energy storage and conversion processes occurring at the electr

50 s devices and applications related to energy storage and conversion, environmental remediation, sensi

51 ROSALIND system can be freeze-dried for easy storage and distribution, and we apply it in the field t

52 yond classical metabolic functions in energy storage and energy expenditure, adipose tissue is also a

53 thesized samples was investigated for energy storage and generation applications, in which superior p

54 Current methods require careful samples storage and handling, skilled personnel, and expensive i

55 l role of the sulfated salicinoids in sulfur storage and homeostasis is discussed.

56 ocalization, supporting catalytic processes, storage and inheritance of specific molecules, and buffe

57 k significantly reduces oligodendrocyte iron storage and maturation.

58 The charge storage and membrane applications of graphene oxide (GO)

59 ide evidence for a shifting balance of lipid storage and metabolism due to FGF21-induced weight loss

60 forebrain demonstrated progressive lysosomal storage and microglial activation despite a lack of cere

61 e that these adaptations of LDs support IMTG storage and minimise accumulation of lipid metabolites t

62 ocardial lipids that exceed the capacity for storage and oxidation can be lipotoxic and induce non-is

63 e standard actions applied (machine-grading, storage and re-use of topsoil, hydroseeding of commercia

64 ding signaling robustness and cost-effective storage and recycling.

65 complex (HC) is central to long-term memory storage and retrieval as well as spatial navigation acro

66 ions to realizing the goals of viable energy storage and retrieval based on the N-H bonds of ammonia

67 en leveraged for applications related to the storage and separation of small molecules and the incorp

68 with increasing amounts of data; management, storage and sharing challenges arise.

69 e products are required for Drosophila sperm storage and sperm viability, and a spermathecal-derived

70 recognition, enzymatic function, information storage and structure and is thought to be a prerequisit

71 tuents playing essential functions in energy storage and the cellular signaling processes of cells.

72 annelrhodopsin-1 derivate ReaChR that energy storage and transfer into the protein depends on the pro

73 which must be compressed to enable efficient storage and transfer.

74 nsect OBPs are implicated in the perception, storage and transport of chemosensory signaling molecule

75 ted the hypothesis that increased soil water storage and transport resulting from cultivation may enh

76 old pulsatile machine perfusion (MP) for the storage and transportation of kidneys donated after circ

77 e solid microparticle is more convenient for storage and transportation, and have great potential for

78 h were transported to the adipose tissue for storage and triggered greater insulin secretion.

79 bjects provided plasma samples for long-term storage and were then monitored for cancer occurrence.

80 erties, such as charge amplification, energy storage, and differential capacitance, strongly depend o

81 ion of proteins involved in the acquisition, storage, and efflux of iron accordingly.

82 nduces ethanol production through low oxygen storage, and ethanol application on softening of Braebur

83 of 1 pg/mL ZIKV, desirable specificity, data storage, and geographic location surveillance were simul

84 ing food webs, macronutrient cycling, carbon storage, and human disease risk [10-12], so understandin

85 ly specialized for iron uptake, utilization, storage, and secretion.

86 ne-electrostatically localized proton energy storage; and 2) The geometric effect of a mitochondrial

87 In particular, hot spots of charge storage are identified.

88 the mechanisms underlying changes in soil C storage are not well understood, hampering long-term pre

89 he deep Pacific is a site of respired carbon storage associated with periods of decreased global atmo

90 Storage at 3 degrees C resulted in the lowest soluble so

91 th varied levels of tolerance to cold during storage at 6 and 13 degrees C.

92 ntly, they perform nearly an ideal DL charge storage at high charge-discharge rate (up to 30 000 mV s

93 In storage at room temperature, it presents a short shelf l

94 al stabilities were assessed under long-term storage at two temperatures.

95 After 42 days of refrigerated storage, autologous 51-chromium 24-hour posttransfusion

96 allows calculating the future catotelm peat storage based on today's acrotelm characteristics, and t

97 sts in electrochemical energy conversion and storage because of unique electronic and structural prop

98 hane-based bioenergy with carbon capture and storage (BECCS) system.

99 crops in conjunction with carbon capture and storage (BECCS).

100 ditions of gas formation or during reservoir storage, becoming indistinguishable from equilibrium in

101 mal function accelerated the accumulation of storage bodies in AF(+) cells and led to impaired microg

102 ox-active material for energy conversion and storage, but the chemical structures present in this het

103 n ACN vapor, enhancing the reversible charge storage by a factor of 78 compared to that in vacuum.

104 in contact could boost efficiency of energy storage by electron transfer and identifies size-mismatc

105 arious non-human animals demonstrate similar storage capacities, the evolution of manipulation abilit

106 elation between the pore volume and hydrogen storage capacity is examined and two empirical equations

107 More tree species can increase the carbon storage capacity of forests (here referred to as the mor

108 ons are rationalized to predict the hydrogen storage capacity of MOFs with different pore geometries.

109 Soil water storage capacity was also an important risk factor, corr

110 ngineering in PBAs as a means of controlling storage capacity, anisotropy and transport efficiency.

111 sequestration (SCS), and carbon capture and storage (CCS) integrated with cellulosic biofuel product

112 pportunities for low-cost carbon capture and storage (CCS) scenarios with process emissions from the

113 With carbon capture and storage (CCS), reductions in emission intensities ranged

114 ich are part dependent on carbon capture and storage (CCS).

115 velopment of molecular switching systems and storage-class memories.

116 ted proteins and as an intracellular calcium storage compartment, facilitating calcium-release-depend

117 rs and buffers were analyzed under different storage conditions (argon purging, pH variation) using C

118 f sugar component ratio, water fraction, and storage conditions on crystallisation and glass transiti

119 preserve canine fecal samples under various storage conditions simulating shipping in hot or cold cl

120 dicted) of GIP over control, irrespective of storage conditions.

121 pecimen types under a variety of temperature storage conditions.

122 pression and HMGB1 translocation during cold storage, data supported by in vitro studies where hepati

123 Organic C contents and storage decreased from upstream to downstream, likely du

124 fast-kinetics dual-ion-intercalation energy storage device is further assembled by combining the mod

125 bon nanostructures and carbon-derived energy storage devices is presented with particular emphasis on

126 The development of energy storage devices that can endure large and complex deform

127 m metal batteries are next generation energy storage devices with high energy density, but face chall

128 s is essential for magnetic sensors and data storage devices(5).

129 s govern the behavior of a variety of energy storage devices, including electrocatalytic reactions at

130 of electrode materials in energy-harvesting/storage devices, ranging from solar cells to rechargeabl

131 can lead to miniaturized non-volatile memory storage devices.

132 , and for improving the efficiency of energy storage devices.

133 omal recessive, neurodegenerative, lysosomal storage disease caused by mutations in CLN3, which encod

134 s and inflammatory bowel disease in glycogen storage disease type Ib (GSD-Ib).

135 G6Pase-alpha or G6PC) deficiency in glycogen storage disease type-Ia (GSD-Ia) leads to impaired hepat

136 essive and fatal neurodegenerative lysosomal storage disease, GM1 gangliosidosis.

137 cal onset of the neurodegenerative lysosomal storage disease, GM1 gangliosidosis.

138 n two animal models of neuropathic lysosomal storage diseases (LSDs), Gaucher's and Krabbe's diseases

139 se, muscular disorders, cancer, and glycogen storage diseases.

140 Gaucher disease is a lysosomal storage disorder caused by insufficient glucocerebrosida

141 While lysosomal storage disorders have been described for many years, it

142 del could be extrapolated to other lysosomal storage disorders in which immune response hinders ERT.

143 stic convergence between aging and lysosomal storage disorders.

144 gel network stability increased upon frozen storage due to protein denaturation.

145 onsidered next-generation devices for energy storage due to their advantages in safety and potentiall

146 level basis for retrospective evaluation and storage during ongoing behavior.

147 metabolites in tissues not suited for lipid storage (e.g., the liver, vasculature, heart, and pancre

148 iation to determine whether sugar and starch storage, energy reserves for trees under extreme conditi

149 tes in diverse applications including energy storage, flexible electronics, and bioelectronics.

150 mg/day dosing and may not require cold chain storage for global health and developed world long-actin

151 regulation of HSL biases cells towards lipid storage for subsequent utilization during invasion of pa

152 est degradation ratio of thymoquinone during storage for the BCSO was 96.78% while the lowest one was

153 ys additional roles, e.g. as a transport and storage form of nitrogen, released via endogenous recycl

154 American erosion, mass transfer and sediment storage from the late Pleistocene to the present day.

155 materials in the field of capacitive energy storage, from the viewpoint of materials science and cha

156 n lemon juice solution), freezing and frozen storage (FS) on single and total polyphenols (free and c

157 ium induced a significant increment of lipid storage in ccRCC cells that had a low 36-kDa AnxA3 expre

158 to lipid and protein oxidation over 250 days storage in chilled or ambient conditions.

159 e are largely explored; however, solid CH(4) storage in confined pores of MOFs in the form of hydrate

160 .7%) levels, was determined during real-time storage in dark conditions at room temperature for 22 mo

161 ing in inhibition of long-term carbon energy storage in diapausing females.

162 le (RV, n=4) after 0, 4, and 8 hours of cold storage in histidine-tryptophan-ketoglutarate preservati

163 required for dietary fat absorption and fat storage in humans(1).

164 The mechanisms coordinating lipid storage in LDs with cellular metabolism are unclear but

165 ry neuroinflammation from galactosylceramide storage in macrophages.

166 stresses of ~3-12 MPa, consistent with their storage in mush piles with thicknesses of a few hundred

167 ks and bottlenecks, and dysregulated glucose storage in patients with AH.

168 continued abnormalities in fat and/or lipid storage in PLWH treated with newer drugs (including inte

169 However, the spatial heterogeneity of carbon storage in seagrass sediments needs to be better underst

170 We interpret the increase in peptide storage in the fall and the shift to a more anti-Bd micr

171 ded to enable short-term and seasonal energy storage in the form of liquid fuels.

172 n will lead to greater or weaker long-term C storage in the future.

173 ses that set carbon supply, consumption, and storage in the oceans' interior.

174 ons in electrochemical energy conversion and storage, including electrocatalysis, supercapacitors, an

175 that can potentially enable renewable energy storage, including water, CO(2) and N(2) electrolysis.

176 ty and potentially compromises the reservoir storage integrity through pore fluid pressure build-up.

177 vel multielectron handling toward electrical storage is a worthwhile approach to solar energy harvest

178 t of diseases in which glucose metabolism or storage is altered, for instance, diabetes, cardiac dise

179 Energy storage is an integral part of modern society.

180 Large-scale energy storage is becoming increasingly critical to balancing r

181 Our study predicts that memory storage is dynamic, and sleep enables continual learning

182 climate mitigation induced by increased SOC storage is generally overestimated if associated N(2) O

183 We found that cold storage led to a global reduction in gene expression, in

184 duced coagulation activation, the ability of storage lesion-induced RBC-MVs to activate each zymogen

185 Storage lesion-induced, red cell-derived microvesicles (

186 te that cell lines manifesting high glycogen storage level showed increased tolerance to glucose defi

187 s the expression of metabolic genes to lipid storage levels.

188 ted progress of proteolysis occurring during storage, light negatively affected milk flavour especial

189 omic analyses revealed a marked reduction in storage lipids and an increase in membrane phospholipids

190 ay a critical role as depots for energy-rich storage lipids.

191 the CNS including accumulation of lysosomal storage material and glial activation, and has limited p

192 se (GCase), resulting in the accumulation of storage material in visceral organs and in some cases th

193 s chemical sensors, electrocatalysts, energy storage materials, and electronic devices.

194 of these magmatic systems where intermediate storage may occur has been a longstanding challenge.

195 e of the Li-layer size, the intrinsic charge storage mechanism (two-phase vs solid-solution) and loca

196 introduce DNA punch cards, a macromolecular storage mechanism in which data is written in the form o

197 ed from renewable energies can act as energy storage media, thus mitigating the effects of fossil fue

198 The potential of DNA as an information storage medium is rapidly growing due to advances in DNA

199 density, DNA is considered a promising data storage medium.

200 Our results suggest that storage method is important in microbiota studies and th

201 n sample integrity, which can be affected by storage methods.

202 7 degrees C) in both adherent and suspension storage models.

203 nted antennas, printed energy harvesting and storage modules, and printed displays, are discussed.

204 at low frequencies and ten-fold increase in storage modulus.

205 efficacy of normothermic MP over static cold storage, MP is likely here to stay for the foreseeable f

206 tween the hippocampus (HPC) and other memory storage networks.

207 tructures were for large surplus capture and storage of aquatic resources that were controlled and ma

208 in applications ranging from processing and storage of biopharmaceuticals to cryo-EM analysis of pro

209 eral amygdala is necessary for the long-term storage of conditioned-threat responses, whereas de novo

210 Proper storage of excessive dietary fat into subcutaneous adipo

211 ble sources have driven interest in chemical storage of intermittent solar and wind energy(1,2).

212 s established in 2015 to enable curation and storage of known BGCs.

213 However, controlling the storage of molecules in nanoparticles is challenging, be

214 y, data analyses require the computation and storage of multiple metrics for a wide range of ribosome

215 Specifically controlling the storage of multiple types of molecules allows us to opti

216 ity is continuously modified due to noise or storage of other patterns, similar to recent observation

217 e film should be further investigated during storage of perishable food products at temperatures abov

218 tional deficits and decreased expression and storage of S100A12.

219 ew results on the source, decomposition, and storage of SOC in estuarine wetlands with four vegetatio

220 Although temperature controls the storage of soil organic carbon at mid and high latitudes

221 The storage of solar energy in chemical bonds will depend on

222 rent relevant conditions or treatments: over storage of soy flours, over fractionation to yield soy p

223 ires multiple-step, intensive processing and storage of soy ingredients, which can increase the produ

224 ul weathering of limestone and the long-term storage of the captured CO(2).

225 out the nature and the site of formation and storage of this new extinction memory.

226 n of cerebellar structures in the persistent storage of visual information.

227 Capture and storage of volatile radionuclides that result from proce

228 o understanding the origin of boosted charge storage on heteroatom-doped carbons, none of the present

229 The effect of frozen storage on the chemical properties and ingredient functi

230 After prolonged storage or during the shipment of raisins, a crystalline

231 Lipid droplets (LDs) are neutral lipid storage organelles assembled at the endoplasmic reticulu

232 Lipid droplets (LDs) are energy storage organelles composed of neutral lipids, such as t

233 d widespread attention for grid-scale energy storage owing to the natural abundance of sodium.

234 omising candidate for next-generation energy storage owing to their excellent safety features.

235 required the continuous exploration of novel storage paradigms, materials, and devices with increasin

236 triggers HIF-dependent activation of a lipid storage pathway involving PPARgamma and the prometastati

237 Storage period explained most of the variance in ascorbi

238 different varieties, agricultural practices, storage periods and processing conditions, were used to

239 ration stress directly reduces production of storage proteins and key accessory gland components, a f

240 The suppression of storage proteins led to the elaboration of membrane stac

241 ynthesis and does not contain cytosolic iron-storage proteins.

242 s and stimulates the genes encoding for iron storage proteins.

243 bility (variety, agricultural practice, cold storage, puree mechanical refining level) and (ii) estab

244 trongly suggests that such amnesia is due to storage rather than retrieval impairments.

245 y ~3.6 km(3), accounting for 40% of total GW storage recovery during 2006-2018.

246 central South-to-North Water Diversion on GW storage recovery in Beijing within the context of climat

247 practices with a flatbed dryer and hermetic storage reduced the discoloration of rice grains by 3 to

248 upport complete oxidation of FA and glycogen storage regardless of Met supply.

249 n that affected the gene encoding the carbon storage regulator CsrA.

250 Three heat storage-release schemes were discovered involving differ

251 me and nighttime with no necessity of energy storage remains challenging.

252 However, the physical controls governing the storage, remobilization and pathways of transfer in fluv

253 ic, and beta-eleostearic acids after 30 days-storage, respectively) and protected the oil against vol

254 d croplands had 328 and 730 Mg C/ha less SIC storage, respectively, compared to their native vegetati

255 Our findings uncover a paradigm for a lipid storage response in which binding of MLX transcription f

256 tagonizes CRF-mediated hormone release, this storage/resurfacing mechanism may allow for a physiologi

257 wing different amount of sucrose loss during storage revealed genotype-specific main driver genes and

258 t tolerance and high carbohydrate-containing storage roots.

259 ith the current gold standard of static cold storage (SCS).

260 getation) and two ecosystem services (carbon storage, sediment retention) across four case studies (i

261 Thermal and storage stability as well as optimal pH and temperature

262 ntial to improve the sublingual delivery and storage stability of protein-based vaccines.

263 h an RSD of 1.1% (n = 12), as well as a good storage stability up to 3 weeks.

264 ion of multifunctional energy generation and storage systems that can be twisted and folded to multip

265 ive organics for potential grid-scale energy storage systems.

266 h often is called the "Holy Grail" of energy storage systems.

267 optical responses and applications in energy storage systems.

268 New storage technologies are needed to keep up with the glob

269 provide an economic stimulus to capture and storage technologies.

270 ed a state-of-the-art electrochemical energy storage technology for decades now, but their energy den

271 Storage temperature (- 20 vs. - 80 degrees C) did not si

272 Storage temperature affected stability of anthocyanins,

273 Storage temperature also explained most of the variance

274 acid, which declined rapidly independent of storage temperature.

275 sed in plasma separator tubes, storage-time, storage-temperature, and repeated freeze-thaw cycles on

276 nalysed after seven days under two different storage temperatures, 4 degrees C and 20 degrees C.

277 polyphenols was more strongly influenced by storage than by orchard location.

278 This polynomial method needs less computer storage than the interpolation method and can be readily

279 showed higher oxidative stability during the storage than unencapsulated oil (p < 0.05) with better r

280 are promising materials for onboard hydrogen storage thanks to the tunable pore size, pore volume, an

281 However, total ecosystem C storage that includes soil organic C (SOC) must be consi

282 didate for next-generation grid-scale energy storage, the implementation of the Na metal anode has be

283 In the context of electron storage, this "super-LUMO" serves as an empty reservoir,

284 igation strategies based on fostering carbon storage through increased tree diversity.

285 Storage time affected pH and acidity of the beans and MP

286 fected by the type of plasma separator tube, storage-time, and number of freeze-thaw cycles.

287 nticoagulant used in plasma separator tubes, storage-time, storage-temperature, and repeated freeze-t

288 concentrations in e-liquids over foreseeable storage times, safeguards against high concentrations of

289 phloem from photosynthetic source tissues to storage tissues.

290 erefore, shipping them after several days of storage to be used in a DMEK surgery cannot be recommend

291 ng from sustainability and energy harvesting/storage to tissue engineering and additive manufacturing

292 le metrics for future studies evaluating SOC storage under alternative management in changing climate

293 pomaces and extrudates retain crispiness in storage under moderate environmental relative humidity c

294 gh 25HC is a potent regulator of cholesterol storage, uptake, efflux and biosynthesis, how these meta

295 The strongest degradation of flavonols after storage was in apples grown in the most southern region

296 To design secure storage, we need to understand how the fluids are config

297 Pink and Granny Smith apple in ozonized cold storage, were investigated.

298 p. flour led them to better stability during storage with lower syneresis.

299 ice bran protected RP the best during forced storage, with a 35% recovery after 8 weeks.

300 d, reduces toxicity, and enables lyophilized storage without loss of activity.