ライフサイエンスコーパス: dehydration

1 nd assessed transcriptome changes during its dehydration.

2 tribute to wine aroma, particularly for fast dehydration.

3 ntial xylem embolism arose only under severe dehydration.

4 solution is recommended to treat and prevent dehydration.

5 ildren with mild gastroenteritis and minimal dehydration.

6 in the stem of an intact vine during 10 d of dehydration.

7 ethylene is formed directly through ethanol dehydration.

8 y and microstructural changes during osmotic dehydration.

9 conditions that are consequences of heat and dehydration.

10 dehydration, and 70 (14%) of 496 had severe dehydration.

11 lene, which is produced in situ from ethanol dehydration.

12 hydes yield aldol adducts without subsequent dehydration.

13 ilar to freezing, salt and drought can cause dehydration.

14 assess fluid intake adequacy or to diagnose dehydration.

15 af water transport system during strong leaf dehydration.

16 fever and are routinely given IV fluids for dehydration.

17 tes the sensation of thirst that accompanies dehydration.

18 likely due to artifacts in SEM introduced by dehydration.

19 ling of water either in the atmosphere or on dehydration.

20 ests were usefully diagnostic for water-loss dehydration.

21 st, which transforms to denser eclogite upon dehydration.

22 ing an unrivaled model system for polyketide dehydration.

23 o 60 months with gastroenteritis and minimal dehydration.

24 -cysteine via condensation, cyclization, and dehydration.

25 g electron microscopy, which requires sample dehydration.

26 he last step of the reaction to facilitate a dehydration.

27 d functional status of xylem conduits during dehydration.

28 potassium and sodium were lost during sample dehydration.

29 anemia characterized by primary erythrocyte dehydration.

30 vein thrombosis, bowel wall perforation, or dehydration.

31 ly equally between C3-dehydrogenation and C4-dehydration.

32 followed by transesterification and a final dehydration.

33 PSII remain stable throughout the course of dehydration.

34 tions tied to experiments of hydrous mineral dehydration.

35 former is favored during the final stages of dehydration.

36 ssociated with primary or secondary cellular dehydration.

37 h were presence of blood in stool and severe dehydration.

38 tate of fluids generated during serpentinite dehydration.

39 dominantly inherited disorder of erythrocyte dehydration.

40 main external indication of poor health was dehydration.

41 kles to develop raisin-like morphology after dehydration.

42 0.0185, CI -0.0313 to -0.0057, p=0.0046) and dehydration (-0.0831, -0.1477 to -0.0184, p=0.0118) asso

43 Hypotension (1615 [40%] patients) and dehydration (1536 [38%] patients) were the most common c

44 computed energy barriers at the cyclization-dehydration (17 kcal/mol) and oxidation (21 kcal/mol) st

45 n standard, 242 (49%) of 496 children had no dehydration, 184 (37%) of 496 had some dehydration, and

46 The most common causes of readmission were dehydration (42%), intraperitoneal infections (33%), and

47 oys [51.1%]; 441 (68.2%) without evidence of dehydration), 644 (99.5%) completed follow-up.

48 of changes occurring during the postharvest dehydration, a process undertaken to make some particula

49 attribute the steep rheological contrast to dehydration across the lithosphere-asthenosphere boundar

50 cell transcriptional profiling revealed that dehydration-activated MnPO neurons consist of a single e

51 Thus, the activity of dehydration-activated MnPO neurons establishes a scalabl

52 " to PRN ranibizumab seem to exhibit retinal dehydration after switching to aflibercept, whereas ther

53 ese findings point to an association between dehydration and adverse outcomes for children with HUS.

54 hese compounds are formed during roasting by dehydration and cyclization of their precursors, the chl

55 rmediate structure model, the LctM-catalyzed dehydration and cyclization reactions that occur in two

56 re that the enzyme PaaA catalyzes the double dehydration and decarboxylation of two glutamic acid res

57 phonate group, phosphono-peramivir (6a), the dehydration and deoxy derivatives (7a and 8a) as well as

58 isms of these risk factors and the impact of dehydration and electrolyte imbalance will improve healt

59 over a free-energy barrier arising from ion dehydration and electrostatic interactions.

60 roducts by its simultaneous stabilization by dehydration and extraction of bioactive compounds.

61 ely linked with each other and stimulated by dehydration and hyperosmolarity.

62 ; inactivation increased saline intake after dehydration and hypertonic saline injection.

63 bility barrier (EPB) prevents organisms from dehydration and infection.

64 m ethyl 3-hydroxypropanoate (ethyl 3-HP) via dehydration and nitrilation with ammonia over an inexpen

65 and was admitted to the hospital because of dehydration and persistent gastrointestinal symptoms.

66 benzene or other benzene derivatives through dehydration and polymerization reactions, and may posses

67 able from each other, suggesting significant dehydration and possible intermingling of the lipid head

68 A dehydration and re-watering experiment on potted P. muni

69 interaction and induce them via hydrolysis, dehydration and recrystallization to form coaxial (NiO,

70 Dehydration and rehydration affected mainly the gene exp

71 mination of water and carbon uses throughout dehydration and rehydration processes in adult trees wil

72 rongly associated with PLC variations during dehydration and rehydration processes, indicating that s

73 patens that were subject to ABA treatment in dehydration and rehydration stages.

74 During dehydration and rehydration, C. pumilum deactivates and

75 D4 gene also exhibited enhanced tolerance to dehydration and salt stresses, while the knockdown lines

76 lteration of gene expression occurring after dehydration and subsequent rehydration in comparison to

77 order to protect the body from infection and dehydration and to heal wounds.

78 ons within the 18-crown-6 leads to a partial dehydration and to the formation of alternating K(+) cat

79 losses must be tightly regulated to prevent dehydration and undesired metabolic changes.

80 urrection plant Craterostigma pumilum during dehydration and upon recovery from desiccation.

81 ng the common features of berries undergoing dehydration and/or commencing senescence.

82 ad no dehydration, 184 (37%) of 496 had some dehydration, and 70 (14%) of 496 had severe dehydration.

83 Readmissions are most commonly caused by dehydration, and are predicted by serious complications,

84 cause of intestinal inflammation, diarrhea, dehydration, and associated mortality in kittens.

85 ercalcemia with failure to thrive, vomiting, dehydration, and nephrocalcinosis.

86 All reaction steps including cyclization, dehydration, and oxidation are characterized at the unif

87 ional decline, visual or hearing impairment, dehydration, and sleep deprivation are effective for del

88 We show that cyclodehydration precedes dehydration, and that dehydration is catalyzed by two pr

89 rict structural changes during hydration and dehydration, and this in turn greatly reduces the extent

90 Early responses to dehydration are the closure of stomata and activation of

91 nisms by which these mutations result in RBC dehydration are unknown.

92 s indicated that the decline of Kleaf during dehydration arose first and foremost due to the vulnerab

93 in-boundary sliding) attending high-pressure dehydration as a likely seismogenic mechanism, unless a

94 ze change affects the energy barriers of ion dehydration as well as that of size-exclusion of anion p

95 al closure and xylem cavitation during plant dehydration, as well as the fate of embolized organs, ar

96 The Dehydration: Assessing Kids Accurately (DHAKA) score was

97 Few dehydration assessment measures provide accurate informa

98 etiology of diarrhea and the severe signs of dehydration associated with diarrhea.

99 Patients with EVD presented with evidence of dehydration associated with vomiting and severe diarrhea

100 mal, net Diels-Alder [4+2] cycloaddition and dehydration at 110 degrees C to access the target by dim

101 r, and 3% or more weight loss or significant dehydration at in-person follow-up.

102 cope with water deficit between resprouters (dehydration avoiders) and nonresprouters (dehydration to

103 uspicion of inadequate drinking or impending dehydration be considered.

104 e formation of a stable enolate resistant to dehydration but prone to thermal hydration.

105 d increased the odds of both some and severe dehydration by a factor of 1.4.

106 y barriers of size exclusion but that of ion dehydration by altering the electric permittivity of wat

107 P protects bacteria from osmotically induced dehydration by mediating the uptake of zwitterionic osmo

108 Dehydration, carbonyl cleavage, and redox reactions turn

109 o fold into alpha-helices already under mild dehydration conditions (97% relative humidity (RH), corr

110 including a lowered density during moderate dehydration, consistent with a lower level of PSII prote

111 s to reduced airway hydration, causing mucus dehydration, decreased mucociliary clearance, and recurr

112 Among these phosphonate compounds, the dehydration derivative 7a that has a relatively rigid cy

113 ng links this freshening to amorphous silica dehydration driven by rapid burial-induced temperature i

114 model to dehydration-embrittlement in which dehydration-driven stress transfer, rather than fluid ov

115 Dehydration due to diarrhoea is a leading cause of child

116 type to Bartter syndrome of salt wasting and dehydration due to reduced Na-K-2Cl-cotransporter activi

117 s a result of severe diarrhoea, vomiting and dehydration due to the actions of cholera toxin; more fe

118 hydrophilic ion is controlled by its partial dehydration during the formation of the adduct with a "w

119 Predominance of dehydration effect has been observed from calorimetry an

120 We propose an alternative model to dehydration-embrittlement in which dehydration-driven st

121 absorbance assay for FabA, the bifunctional dehydration/epimerization enzyme and key target in the F

122 'Early responsive to dehydration' (ERD) genes are a group of plant genes havi

123 ied geriatric events that included delirium, dehydration, falls and fractures, failure to thrive, and

124 Pyrexia (six patients [2%]) and dehydration (five patients [2%]) were the most common se

125 yme, LepI, that can catalyse stereoselective dehydration followed by three pericyclic transformations

126 and polar induction, and (iii) annealing and dehydration, followed by site-selective recrystallizatio

127 to 100% of Kleaf decline across the range of dehydration from mild water stress to beyond turgor loss

128 values do not provide accurate detection of dehydration from single measurements, directional change

129 urgery [grade 3]; recurrence of vomiting and dehydration [grade 3]; diarrhoea and fever associated wi

130 Fast dehydration grapes were richer in total free terpenes, a

131 e of the protein under conditions of gradual dehydration had not been investigated.

132 , oxygen capture, hydrogen transfer, and 1,4-dehydration, has been developed to facilitate aerobic ox

133 on the membrane structure and the headgroup dehydration have been extensively studied, the mechanism

134 rldwide, yet no clinical tools for assessing dehydration have been validated in resource-limited sett

135 to admissions for urinary tract infections, dehydration, heart failure, and bacterial pneumonia.

136 rein we demonstrate the programmable one-pot dehydration-hydration condensation of amino acids formin

137 ed hydrogel-elastomer hybrids including anti-dehydration hydrogel-elastomer hybrids, stretchable and

138 Water-loss dehydration (hypertonic, hyperosmotic, or intracellular

139 For example hydrous mineral dehydration in a subducting slab can produce fluid overp

140 ore is the first clinical tool for assessing dehydration in children with acute diarrhoea to be exter

141 tely (DHAKA) score was derived for assessing dehydration in children with diarrhoea in a low-income c

142 condary photoproducts are subject to thermal dehydration in dark conditions, leading to reversion to

143 lack the precision to detect common forms of dehydration in healthy individuals.

144 o leads to rapid resolution of diarrhoea and dehydration in neonatal calves, a clinical model of cryp

145 cally reduces oocyst shedding, diarrhea, and dehydration in neonatal calves.

146 have been widely advocated for screening for dehydration in older adults, we show, in the largest stu

147 have been widely advocated for screening for dehydration in older adults.

148 of urinary measures to screen for water-loss dehydration in older people.

149 and noninvasive tools for the assessment of dehydration in older people.

150 oughout petioles and vein orders during leaf dehydration in relation to conduit dimensions.

151 ihydrogen activation, "O"-atom transfer, and dehydration, in which metal-ligand cooperation plays a c

152 a response to abscisic acid that resulted in dehydration, increases in osmolytes and upregulation of

153 release proceeds through decarboxylation and dehydration independent of the thioesterase SphJ and yie

154 Dehydration induced limited changes in the anthocyanin p

155 Interestingly, GhWRKY59 is required for dehydration-induced expression of GhMAPK3K15, constituti

156 d with subduction zones can be attributed to dehydration-induced fluids and the formation of intercon

157 BINDING PROTEIN 2 (GhDREB2), which encodes a dehydration-inducible transcription factor regulating th

158 ildren with mild gastroenteritis and minimal dehydration, initial oral hydration with dilute apple ju

159 HMF is one of the primary dehydration intermediates of raw biomass and FDCA is of

160 Water-loss dehydration is associated with poor health outcomes such

161 lodehydration precedes dehydration, and that dehydration is catalyzed by two proteins in a tRNA(Glu)-

162 We demonstrate that complete dehydration is not required for these proteins to sample

163 te-depth earthquakes demonstrate that little dehydration is required to trigger embrittlement.

164 (hypertonic, hyperosmotic, or intracellular dehydration) is due to insufficient fluid intake and is

165 Dehydration leads to quality defects in cilantro such as

166 would help in decision-making on the optimal dehydration level of winegrapes and the best management

167 traluminal surface of the intestine displays dehydration-like phenotypes, Na(+) levels are increased

168 Dehydration may be a risk factor for unsuccessful lumbar

169 and hereditary spherocytosis, where cellular dehydration may be a significant contributor to disease

170 at is unprecedented for type I PKSs, a novel dehydration mechanism that could be exploited for polyke

171 mination of both canonical and non-canonical dehydration mechanisms reveals hidden catalytic activity

172 dia chinensis SVP2 confirm roles in ABA- and dehydration-mediated growth repression and reveal a cons

173 discontinuity has been widely attributed to dehydration melting.

174 eneath 60-100 km depth, marking the depth of dehydration metamorphism and eclogitization.

175 Simulations using this dehydration model are used to predict temperature, moist

176 rombosis (n = 1), transaminitis (n = 1), and dehydration (n = 1).

177 glu12 is highly induced in response to UV-B, dehydration, NaCl, methyl jasmonate, and abscisic acid t

178 tly, over what areas, and how rapidly lethal dehydration occurs; how EWL and die-off risk vary with b

179 Osmotic dehydration (OD) is a widely used preservation technique

180 The dehydration of alcohols is involved in many organic conv

181 ity-mass spectrometry (cryo-IM-MS) show that dehydration of alkyl diammonium cations induces a distin

182 olutes which stabilize RO by favoring burial/dehydration of amide oxygens and anionic phosphate oxyge

183 The dehydration of antigorite is believed to cause high-cond

184 nected networks of aqueous fluids during the dehydration of antigorite.

185 pores of zeolite HBEA catalyse aqueous phase dehydration of cyclohexanol at a rate significantly high

186 to a shift in mechanism; for both cases, the dehydration of cyclohexanol occurs via an E1 mechanism w

187 ion catalysis, exemplified by intramolecular dehydration of cyclohexanol, is markedly influenced by s

188 At a pressure of 1.1 gigapascals, dehydration of deforming samples containing only 5 vol%

189 , 56-60% RH) were investigated for efficient dehydration of dill (Anethum graveolens) greens with opt

190 l changes confirmed hypothesis about partial dehydration of gluten network after polysaccharides addi

191 We analyse the dehydration of gypsum to form bassanite and H2O which, l

192 ng energy barriers of size-exclusion and ion dehydration of HCO3 (-) permeation.

193 ere applied in acid-catalysed reactions, the dehydration of methanol to dimethyl ether and the total

194 at increased cation permeability may lead to dehydration of PIEZO1-mutant HX erythrocytes.

195 followed by dehydration or heterocyclization-dehydration of resulting products, removal of benzoyl pr

196 Dehydration of riper berries (20.5 degrees Brix) led to

197 fication reactions of lanthipeptides include dehydration of Ser and Thr residues to dehydroalanine an

198 utyrine (Dhb), two amino acids engendered by dehydration of serines and threonines, respectively.

199 Complete dehydration of silicates is expected before plate subduc

200 Dehydration of the attaching species, not the mineral su

201 In contrast to canonical DHs that catalyze dehydration of the beta-hydroxy groups of the nascent po

202 the dedicated dehydratase that catalyzes the dehydration of the C17 hydroxy group during iso-MGS bios

203 dicted an increase of 0.6% in the percentage dehydration of the child and increased the odds of both

204 also be prepared in good yields via the mild dehydration of the corresponding dicarbamic acids.

205 of protein conformers in the final stages of dehydration of the ESI process and within the instrument

206 e during polyketide biosynthesis through the dehydration of the nascent polyketide intermediate to pr

207 port of K(+) ions, a high flux rate, and the dehydration of U60 and K(+) ions.

208 eric dehydratase, Pac13, which catalyses the dehydration of uridine-5'-aldehyde.

209 CylM catalyzes seven dehydrations of Ser and Thr residues and three cyclizati

210 To date, the effects of dehydration on the electrical conductivity of antigorite

211 and p38 into Dhb and followed the impact of dehydration on the fate of the two MAPKs.

212 The impact of postharvest dehydration on the volatile composition of Malvasia mosc

213 der ambient and cryogenic conditions without dehydration or heavy metal staining.

214 beta-oxoesters or 1,3-diketones, followed by dehydration or heterocyclization-dehydration of resultin

215 place via ESIPT (or ESPT) that is coupled to dehydration or via a hitherto undisclosed pathway that i

216 ich are significantly changed by either 72 h dehydration, or 48 h starvation, compared to fed and euh

217 e rest died on Mount Sinjar from starvation, dehydration, or injuries during the ISIS siege.

218 Without chemical extraction and dehydration, our results provide multiscale structural d

219 t to the mechanism involving the cyclization-dehydration-oxidation sequence of the chromophore's matu

220 epressing meristem activity and ABA-mediated dehydration pathways.

221 Hyperemesis gravidarum (HG) leads to dehydration, poor nutritional intake, and weight loss.

222 the Elche" arils first underwent an osmotic dehydration pre-treatment (OD) with concentrated juices:

223 It was found that osmotic dehydration pretreatment substantially decreased the moi

224 Instead, the dehydration process is mediated by the A5OH adduct.

225 During the dehydration process, sampling was performed at 15%, 30%,

226 eserve grape quality during the post-harvest dehydration process.

227 tamylates Ser/Thr side chains as part of the dehydration process.

228 d evaporation of water in both hydration and dehydration processes for the OS, while the mixture show

229 solution suggesting an important role of the dehydration processes in BrC formation.

230 The gluten aggregation and dehydration processes were also reflected in the DSC res

231 arbon source that is readily obtainable as a dehydration product of lignocellulosic biomass and can s

232 zolinone derivatives and their corresponding dehydration products and at the same time exhibiting var

233 ack the evolution of structure upon stepwise dehydration provides direct insight into the intricate i

234 Upon further dehydration, PSII complexes are observed to arrange into

235 The effect of dehydration rate on the volatile composition of dehydrat

236 mainly proceeded via fructofuranosyl cation dehydration rather than 3-deoxglucosone, glucose contrib

237 Wacker process followed by an acid-mediated dehydration reaction has been developed.

238 was deforming, to test whether the lawsonite dehydration reaction induces unstable fault slip.

239 This dehydration reaction occurs more rapidly at higher tempe

240 The irreversible dehydration reaction of dihydroxyacetone (DHA) to methyl

241 pparently preventing BCA from catalyzing the dehydration reaction.

242 a key step facilitating the Diels-Alder and dehydration reactions in the acid sites of the zeolite.

243 t slip (that is, stick-slip) occurred during dehydration reactions in the lawsonite and acoustic emis

244 orphism and seismicity, particularly through dehydration reactions involving the mineral lawsonite.

245 m to form bassanite and H2O which, like most dehydration reactions, produces a solid volume reduction

246 e iterative chain elongation, reduction, and dehydration reactions.

247 osazine, react with other sugars and undergo dehydration reactions.

248 Gly67 tripeptide, we modeled cyclization and dehydration reactions.

249 people aged >/=65 y taking part in the DRIE (Dehydration Recognition In our Elders; living in long-te

250 as a strong proton donor for electrochemical dehydration reductions.

251 as developed to obtain a reference Hydration-Dehydration-Rehydration (H-D-R) transcriptome comprising

252 mponents of bacterial membrane vesicles by a dehydration-rehydration process generated giant cell-lik

253 Here we present and analyze the hydration-dehydration-rehydration transcriptomes in B. argenteum t

254 families were differentially expressed upon dehydration-rehydration.

255 During the dehydration/rehydration cycle c. 92 % of the total prote

256 f hours to days, with the photohydration and dehydration repeatable over several light/dark cycles.

257 nted abscisic acid (ABA) effect on the plant dehydration response.

258 .e., ERF (ethylene responsive factor), DREB (dehydration responsive element binding gene), RAV (relat

259 g proteins that recognize the C-repeat (CRT)/dehydration-responsive element (DRE) DNA regulatory elem

260 the constitutive expression of the C-REPEAT/DEHYDRATION-RESPONSIVE ELEMENT BINDING FACTOR (CBF) tran

261 r, GhWRKY59 directly binds to the W-boxes of DEHYDRATION-RESPONSIVE ELEMENT-BINDING PROTEIN 2 (GhDREB

262 the IDRs in three protein partners, DREB2A (dehydration-responsive element-binding protein 2A), ANAC

263 on, HSFA6b directly bound to the promoter of DEHYDRATION-RESPONSIVE ELEMENT-BINDING PROTEIN2A and enh

264 Dehydration resulted in both increased, but predominantl

265 ands the extent, frequency, and intensity of dehydration risk, and introduces new threats for larger

266 Studies of water deficit, dehydration, salt, and other osmotic stresses point towa

267 d that transcript levels were increased with dehydration, sodium chloride, low temperature, heat, abs

268 urses assessed children and classified their dehydration status using both the DHAKA score and the IM

269 Serial weights were obtained and dehydration status was established by percentage weight

270 upon attack of the hydrazine, followed by a dehydration step for gaining aromaticity.

271 that ethanol conversion involves endothermic dehydration step.

272 ion studies have shown a correlation between dehydration stress and the presence of dehydrins, the bi

273 Taken together, we report that dehydration stress could induce transcript 3' UTR extens

274 ng reduced transpiration during a subsequent dehydration stress.

275 bits 3' UTR extensions of their mRNAs during dehydration stress.

276 marked ultrastructural change, and enhanced dehydration susceptibility that resembles the phenotype

277 oes several purification protocols including dehydration, sweetening, and inert rejection.

278 In phase II, Ser/Thr dehydration (TclKL) and peptide macrocycle formation (Tc

279 ls and becomes supersaturated, causing rapid dehydration that removes all remaining soot via wet depo

280 During drought-induced dehydration, the leaf hydraulic conductance (Kleaf) decl

281 Upon cooling or dehydration, these membranes undergo a cooperative trans

282 lay a role in abiotic stresses, particularly dehydration through abscisic acid; however, their role t

283 tion to L-fuconate via a dehydrogenase, (ii) dehydration to 2-keto-3-deoxy-L-fuconate via dehydratase

284 ntact seeds was also determined during grape dehydration to evaluate how these changes affected the e

285 thermal rearrangement to cis-12-OH-TBOH and dehydration to regenerate its parent structure.

286 s (dehydration avoiders) and nonresprouters (dehydration tolerators); however, there is little resear

287 ts lost 4-5% of their body weight during the dehydration trials; volume loss was similar between tria

288 ral observations demonstrate that antigorite dehydration triggered dynamic shear failure of the olivi

289 grapevine genotypes subjected to postharvest dehydration under identical controlled conditions.

290 Dehydration was associated with later, longer, and repea

291 eaf xylem hydraulic conductance (Kx ) during dehydration was driven by embolism initiating in petiole

292 f brain damage, coma, convulsions, death and dehydration was high across many of the studies; however

293 Dehydration was the most frequent cause of acute kidney

294 ons associated with consequences of heat and dehydration were also strongly associated with high temp

295 Treatment and dehydration were performed at 10 degrees C.

296 des accurate single or serial assessments of dehydration when compared with gold-standard measures of

297 reduced by three mechanisms as follows: (i) dehydration, which increases protein concentration witho

298 the conformational change to the A-form upon dehydration will be used to explain the reason for the a

299 itriles, trapping with isopropylformate, and dehydration with phosphoryl chloride provides an efficie

300 addition, formylation, tautomerization, and dehydration, with CuCN catalyzing a key equilibration of