ライフサイエンスコーパス: dehydration

1 ed insight into the radical mechanism of Hyp dehydration.

2 during tag assembly and can be stabilized by dehydration.

3 he photosynthetic apparatus during prolonged dehydration.

4 same path as loss of K(leaf) in response to dehydration.

5 and died rapidly from massive hemorrhage and dehydration.

6 hat are induced under conditions of cellular dehydration.

7 rganisms must ingest water to compensate for dehydration.

8 declined with rehydration time but not with dehydration.

9 conductance to SSWU (K(surf) ) declines with dehydration.

10 to leaf-microbe interactions and in limiting dehydration.

11 3.1; P = 0.002), probably due to diarrhea or dehydration.

12 sequence of failure of leaf function during dehydration.

13 mals, especially small insects vulnerable to dehydration.

14 otecting the ear from diseases infection and dehydration.

15 af water transport system during strong leaf dehydration.

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

17 ntial xylem embolism arose only under severe dehydration.

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

19 st, which transforms to denser eclogite upon dehydration.

20 former is favored during the final stages of dehydration.

21 ssociated with primary or secondary cellular dehydration.

22 tate of fluids generated during serpentinite dehydration.

23 dominantly inherited disorder of erythrocyte dehydration.

24 ed intramolecular Friedel-Crafts cyclizative dehydration.

25 e structure of alkanols in the E1 pathway of dehydration.

26 average of 6.5 days (2-20) and 4 with severe dehydration.

27 diameter, or 12- to 21-mum droplets prior to dehydration.

28 ntly higher (p < 0.05) than 3-deoxyglucosone dehydration.

29 to the nucleobase pai-system and subsequent dehydration.

30 up-regulation in gametophyte in response to dehydration.

31 ch the snake was kept when alive, leading to dehydration.

32 that help to mitigate the adverse effects of dehydration.

33 encapsulated versus free RNAs increase with dehydration.

34 impact of ozone treatment during winegrapes dehydration (10 and 20% weight loss) on the content of p

35 ade 3 to 4 toxicities included nausea (11%), dehydration (11%), electrolyte abnormality (19%), thromb

36 like cysteine protease (PLCP) 'Responsive to Dehydration 21A' (RD21A), which has been shown to functi

37 nthetic steps including 6-epimerization, 6,8-dehydration, 4-epimerization, and 6-transamination that

38 injury, which was associated variously with dehydration (45.4%), sepsis (41.1%), cardiogenic shock (

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

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

41 he photochemical apparatus occurs at extreme dehydration, after complete stomatal closure, and seems

42 Dehydration and aromatization of the obtained cycloadduc

43 arbon which can readily be produced from the dehydration and dimerization of isobutanol, produced fro

44 action on tertiary alcohols proceeds through dehydration and dimerization.

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

46 prevent acute kidney injury by avoidance of dehydration and excessive exercise.

47 quent and intense heat waves to cause lethal dehydration and hyperthermia is well documented, but the

48 ds in shaded microsites, the risks of lethal dehydration and hyperthermia will remain low during the

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

50 y dehydration, while FabA is primed for both dehydration and isomerization.

51 ystems, which would make ticks vulnerable to dehydration and microbial dysbiosis.

52 and hydrogenation, the consolidated alcohol dehydration and oligomerization (CADO) approach describe

53 ntified highlight the importance of avoiding dehydration and performing close clinical and laboratory

54 reactions e.g., oxidation, dehydrogenation, dehydration and polymerisation.

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

56 in carnallite salt through the carnallite's dehydration and purification.

57 condary-structure transitions in response to dehydration and slightly amplified tertiary-structure tr

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

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

60 s of F(v) /F(m) occurred after much stronger dehydration and were not recovered with leaf rehydration

61 ant human pathogens that result in diarrhea, dehydration, and deaths in many children around the worl

62 dity, as demonstrated by titrations, alcohol dehydration, and dehydra-decyclization of 2-methyltetrah

63 slows down food decay by retarding ripening, dehydration, and microbial invasion is reported.

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

65 wer content in HMF and furfural, the intense dehydration, and the extensive darkening of granulated p

66 Photosynthesis is particularly sensitive to dehydration, and the increased abundance of ELIPs may he

67 A-Induced 2 (HAI2), and are more tolerant to dehydration; and ABA strongly upregulates class 1 Glbs.

68 ic acid decarboxylation and furfuryl alcohol dehydration are activated as from about 140-160 degrees

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

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

71 s study was to examine the effect of osmotic dehydration as a method of pumpkin flesh 'Melon Yellow'

72 dentify the combination of insulinopenia and dehydration as a potential target to prevent euglycemic

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

74 lines, which allowed us to identify multiple dehydration associated genes two of which were sex-linke

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

76 on among samples, constitutive expression of dehydration-associated transcripts, the sequestration of

77 compared VCs constructed using the bench-top dehydration (BD), air-injection-flow (AI), pneumatic-air

78 ses of leaf rehydration capacity occurred at dehydration beyond 50% declines of g(s) , K(leaf) and tu

79 were similar to those generated using bench dehydration, but indicated 50% loss of conductivity at l

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

81 m dots were prepared utilizing the degree of dehydration/carbonization of citric acid (carbon skeleto

82 The emergence of the dehydration chemistry is expected to be exclusively the

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

84 in air as the terminal redox reagents (redox dehydration conditions).

85 are reluctant to react with aldehydes under dehydration conditions.

86 ight, identical to that observed during leaf dehydration, confirming that the optical method detects

87 Nts neurons that intercept either leptin or dehydration cues, and which conceivably could regulate f

88 in every catalytic cycle via intramolecular dehydration/cyclization.

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

90 h species are dehydrated and that saccharide dehydration depends on the nature of the cation.

91 tly, lattice transformations associated with dehydration/desolvation events were readily observed by

92 Grade >= 3 anemia, dehydration, diarrhea, and fatigue were greater in patie

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

94 results in light of the phase diagram, with dehydration-driven ionic strength increase being particu

95 olor across Ryugu's surface supports partial dehydration due to internal heating of the asteroid's pa

96 p. nebraskensis (CN8) bacteriophages against dehydration during storage.

97 to drive successive C-N and C-C bond-forming dehydration events via the serial action of a catalytic

98 Hydration-dehydration explains signaling by a dynamic allosteric m

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

100 ain fatty acids and hydrocarbons for an anti-dehydration function likely conserved in mice.

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

102 us platinum-etoposide group (cardiac arrest, dehydration, hepatotoxicity, interstitial lung disease,

103 In response to dehydration, humans experience thirst.

104 diranib arm had more grade 3 and 4 diarrhea, dehydration, hypertension, and weight loss.

105 w greater sensitivity to closure during leaf dehydration, i.e., a higher leaf water potential at whic

106 RD26 protein is stabilized by ABA and dehydration in a BIN2-dependent manner.

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

108 gen entry and cell wall properties affecting dehydration in leaves.

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

110 Under dehydration in plants, antagonistic activities of histon

111 The low free energy barrier to partial dehydration in the absence of conformational change indi

112 slab melting in the transition zone to slab dehydration in the lower mantle supports a lower-mantle

113 l mediated by higher ABA accumulation during dehydration in these species resulted in an increase in

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

115 r rates (per H(+) ) for methanol and ethanol dehydration increase with the fraction of H(+) sites sha

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

117 We assessed dehydration-induced losses of rehydration capacity and m

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

119 As theory and experiment have shown, protein dehydration is a major contributor to protein folding.

120 ( c) Dehydration is aversive, and median preoptic nucleus (Mn

121 aerial plant surfaces that protects against dehydration is considered a fundamental innovation in th

122 velocities, whereas the preceding history of dehydration is consistent with the locations of higher v

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

124 Osmotic dehydration is used as a pre-treatment before drying.

125 The detection of dehydration is well understood and involves signals of p

126 successive triflic anhydride mediated amide dehydration, ketimine addition, and Pictet-Spengler-like

127 Upon dehydration, leaves fold and the cells shrink which is r

128 50 and 400 degrees C, HCONH(2) decomposes by dehydration (major pathway) and decarbonylation (minor p

129 of nursing home residents, which may lead to dehydration, malnutrition, severe complications and hosp

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

131 Dehydration may be common amongst this population and ma

132 raulic conductance (K(leaf) ) in response to dehydration may be recovered through SSWU, and that the

133 Modeling reveals that bouts of dehydration may have a significant impact on population

134 and Cs forms and its structural response to dehydration measured: the unit cell volumes decrease by

135 discontinuity has been widely attributed to dehydration melting.

136 tic lofting, ice sublimation, phyllosilicate dehydration, meteoroid impacts, thermal stress fracturin

137 nvestigated the effect of pressurization and dehydration methods on the chemical composition of JPS,

138 Considering that both dehydration methods produced a jabuticaba powder rich in

139 o non-invasive sweat electrolyte sensors for dehydration monitoring in fitness applications.

140 =1), hypokalaemia (n=1), anorexia (n=1), and dehydration (n=1), and no grade 4 adverse events occurre

141 cediranib, and the most common symptoms were dehydration (n=2), vomiting (n=2), and proteinuria (n=2)

142 n eight (20%) patients; the most common were dehydration (n=4) and diarrhoea (n=2).

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

144 ubpopulation lacks LepRb and is activated by dehydration (Nts(Dehy) neurons).

145 Moreover, deamidation and dehydration occur not only during cyclization to pGlu, b

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

147 unds (TPC) and vitamin C compared to osmotic dehydration (OD).

148 Grape controlled dehydration of "Cesanese" and "Sangiovese" wine grapes,

149 Air-dehydration of 'Amadeus' petals prior to extraction in 5

150 dG(N(1)-H)(*) is produced by the formal dehydration of a hydroxyl radical adduct of dG as well a

151 The higher activity in BEA than in MFI for dehydration of a tertiary alkanol, 2-methyl-2-hexanol, i

152 The dehydration of alcohols is involved in many organic conv

153 us sp. OxB-1 was used as a biocatalyst for a dehydration of aldoximes as readily available starting m

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

155 aldehydes, obtained from the regioselective dehydration of biomass-derived sugars, to provide access

156 The dehydration of crotyl alcohol to 1,3-butadiene is facile

157 to efficiently catalyze the radical-mediated dehydration of CTP to ddhCTP.

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

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

160 etics studies of the Bronsted acid-catalyzed dehydration of fructose to hydroxymethylfurfural (HMF) s

161 Specifically, in the representative dehydration of fructose to produce 5-hydroxymethylfurfur

162 e proton and chloride anions and promote the dehydration of fructose.

163 ation of 2-furoic acid, and 2-methylfuran by dehydration of furfuryl alcohol under dry conditions.

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

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

166 se (HypD), was discovered that catalyzes the dehydration of Hyp to (S)-Delta(1)-pyrroline-5-carboxyli

167 conduits in stipes embolized before cellular dehydration of living tissues within the vascular cylind

168 mation using whole cells exemplified for the dehydration of n-octanaloxime to n-octanenitrile catalys

169 or, isolated TiO(2) sites play a role in the dehydration of off-gassing isopropyl alcohol.

170 th more rapid elimination rates than thermal dehydration of photohydrates, and regenerate parent ster

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

172 diated mechanism associated with the partial dehydration of PW and of the PNIPAM, which is related to

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

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

175 pores smaller than those of zeolite BEA for dehydration of secondary alkanols, 3-heptanol and 2-meth

176 e through an unusual glutamyl-tRNA-dependent dehydration of Ser and Thr.

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

178 Complete dehydration of silicates is expected before plate subduc

179 dration number for sucrose demonstrated that dehydration of sucrose occurs in presence of both studie

180 ed non-centrifugal sugar obtained by intense dehydration of sugarcane juice.

181 d theoretical investigation of the catalytic dehydration of tert-butyl alcohol (TBA) used to probe th

182 Cystic fibrosis is characterized by dehydration of the airway surface liquid layer with pers

183 hosphate anion during general acid-catalyzed dehydration of the carbinolamine intermediate.

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

185 n zero field splitting (ZFS) were induced by dehydration of the material, revealing that one of the F

186 We find that hydrophobic dehydration of the methyl group does not contribute to t

187 e type reaction mechanism is suggested, with dehydration of the MGO-dihydrate as a rate determining s

188 a draining of the interface inducing a local dehydration of the tissues, which become intrinsically a

189 Herein, dehydration of the ultramicroporous metal-organic framew

190 flow through the subducted crust, following dehydration of the underlying, serpentinised slab mantle

191 The current dehydration of these fracture zones coincides with the c

192 is end focused on 3-step processes featuring dehydration, oligomerization, and hydrogenation, the con

193 We quantified effects of leaf dehydration on K(surf) and effects of SSWU on recovery o

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

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

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

197 a (one [2%]), decreased appetite (one [2%]), dehydration (one [2%]), hyperkalaemia (one [2%]), acute

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

199 viscoelastic to elastic like properties upon dehydration or repeated loading.

200 of the skull as well as hazardous chemicals, dehydration, or embedding, limiting their scalability an

201 rge diagnoses (eg, sepsis, febrile seizures, dehydration, or other non-respiratory viral illness).

202 ood long-term stability against temperature, dehydration, organic solvents, and or aggressive pH, and

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

204 heterocyclic nucleus via a Grignard addition-dehydration procedure.

205 stems maintaining coacervates throughout the dehydration process are further evaluated to understand

206 own an innovative application of the osmotic dehydration process for the design of food with health-p

207 The dehydration process is a prerequisite to preserve saffro

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

209 lity (decreased storage moduli, G'); ( ii) a dehydration process of cations (i.e., from Na(+).2H(2)O

210 s from a noncanonical NRPS pathway featuring dehydration processes and catalysed by unusual condensat

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

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

213 oxidation products, as well as electrophilic dehydration products of the cholesterol hydroperoxides,

214 ing a deep understanding of the evolution of dehydration, proteolysis and lipolysis during the matura

215 NIR spectral bands characterising dehydration, proteolysis and lipolysis were individuated

216 ther hand, the pretreatment (raw, salting or dehydration) proved to have a low influence.

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

218 Alkanol dehydration rates catalyzed by hydronium ions are enhanc

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

220 nes Responsive to ABA (RAB18), Responsive to Dehydration (RD29A) and Highly ABA-Induced 2 (HAI2), and

221 utamate elimination by LanBs to effect a net dehydration reaction of Ser and Thr.

222 ese one-pot aza-Michael-addition/cyclization/dehydration reaction sequences.

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

224 Gly67 tripeptide, we modeled cyclization and dehydration reactions.

225 erns are a novel system for studying extreme dehydration recovery and embolism repair in the petioles

226 as a strong proton donor for electrochemical dehydration reductions.

227 n of lactate dehydrogenase (LDH) under heat, dehydration-rehydration and freeze-thaw treatments.

228 activity, other solute-induced stresses, and dehydration-rehydration cycles.

229 aracterized expression dynamics throughout a dehydration-rehydration time-course in six diverse genot

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

231 families were differentially expressed upon dehydration-rehydration.

232 nd timescales, influenced by the spontaneous dehydration/rehydration dynamics at the filter.

233 Here, we investigate dehydration/rehydration of complex coacervates, which ar

234 nstrate changes in pectin composition during dehydration/rehydration which is suggested to affect cel

235 re, we demonstrate that the majority of seed-dehydration-related genes showed similar expression patt

236 mplex therefore leading to the activation of dehydration-related responses and leaf folding.

237 ikely in response to increased selection for dehydration resistance on the hotter slope.

238 arly-diverging aeroterrestrial algae mount a dehydration response that is similar to that of land pla

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

240 The C-repeat binding factor (CBF)/dehydration-responsive element binding (DREB1) proteins

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

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

243 The unaged seeds of two independent maize DEHYDRATION-RESPONSIVE ELEMENT-BINDING2A mutant (zmdreb2

244 d zinc complexation facilitate magnesium ion dehydration, resulting in a dramatic decrease in inducti

245 sylated peptide by virtue of enumerating the dehydration scars imprinted on the O-glycosylated sites.

246 The dehydration sequence of saccharides was explained from t

247 ent integrate information from these "early" dehydration signals.

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

249 f atomization and heat treatment (during the dehydration step) on the molecular interactions within c

250 intermediate in its reaction to facilitate a dehydration step.

251 1 family, plays crucial roles in response to dehydration stress and abscisic acid (ABA) in Arabidopsi

252 Larval dehydration stress directly reduces production of storag

253 new function of a histone demethylase under dehydration stress in plants.

254 ntrols histone methylation homeostasis under dehydration stress remains unknown.

255 methylase activity of JMJ17 was required for dehydration stress response.

256 OST1 mRNA abundance, thereby modulating the dehydration stress response.

257 jmj17 loss-of-function mutants displayed dehydration stress tolerance and ABA hypersensitivity in

258 e H3K4me3 levels and activated a plethora of dehydration stress-responsive genes.

259 1 promotes survival of rice seedlings during dehydration stress.

260 d source as well as a buffer for thermal and dehydration stress.

261 Furthermore, their D values increase with dehydration, suggesting a positive H isotope fractionati

262 as since lost volatiles from its surface via dehydration, supporting its connection to the Pallas fam

263 y mercuric chloride eliminates XA21-mediated dehydration survival, suggesting that XA21 enables plant

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

265 or comparison of the effect of the different dehydration techniques and methods of extraction on the

266 ng the bilayer membrane rigidity against the dehydration tension and decreasing the leakage of loaded

267 a urine concentration defect in response to dehydration that was accompanied by reduced AQP-2 protei

268 Upon acid-promoted dehydration, the desired products were obtained with gen

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

270 On dehydration, the material loses its acidity.

271 Across species, tissue dehydration thresholds were intercorrelated, suggesting

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

273 The contribution of fructose dehydration through fructofuranosyl cation on the format

274 ross-polarization OCT (CP-OCT) during lesion dehydration to identify transparent surface zones indica

275 ese OH groups act as catalytic sites for TBA dehydration to isobutylene, and (3) TBA also reacts to b

276 The ability to survive dehydration to the point of desiccation is a key adaptiv

277 shown that LepI can catalyse stereoselective dehydration to yield a reactive (E)-quinone methide that

278 y conditions, the material is stable against dehydration to ~151 degrees C, and this results in a par

279 The ZFS increased dramatically upon dehydration (to -1.5 cm(-1)), owing to lower symmetry an

280 cit occurs along a continuum in plants, with dehydration tolerance (DhT) and desiccation tolerance (D

281 wo of which were sex-linked, suggesting that dehydration tolerance may be impacted by sex-specific ge

282 To investigate dehydration tolerance, we capitalized on a difference be

283 imorphisms, and the genomic underpinnings of dehydration tolerance.

284 y tract infection (training: 2, control: 0), dehydration (training: 0, control: 2), and dyspnea (trai

285 er-type pressure chamber to categorize plant dehydration under drought into three distinct phases and

286 We show that LLPS-HS promotes tau protein dehydration, undergoes maturation and directly leads to

287 ts revealed that ultrasound assisted osmotic dehydration (UOD) led to the loss of total phenolic comp

288 Dehydration upon folding can be characterized directly b

289 O(4).5H(2)O) and a water droplet followed by dehydration using a carbon dioxide laser.

290 investigate the behaviour of Mo during slab dehydration using two suites of exhumed fragments of sub

291 cies act as Bronsted bases, facilitating TBA dehydration via a carbocation intermediate in an E1 mech

292 systems to alert users to the potential for dehydration via skin sensations initiated by sweat-trigg

293 Dehydration (water loss >2.0% of body weight) has signif

294 and abscisic acid (ABA) concentration during dehydration were quantified, as well as pressure-volume

295 ps, the HCEC may decompensate to keep cornea dehydration which leads to corneal edema.

296 h that FabZ is preorganized to catalyze only dehydration, while FabA is primed for both dehydration a

297 Cutting and blanching followed by osmotic dehydration with assisted sonication eased sucrose penet

298 ontained higher L. casei viable counts after dehydration with FD compared to CD and VD methods.

299 udy was to investigate the effect of osmotic dehydration (with and without sonication) and the use of

300 tures and that many amides are unaffected by dehydration within the bilayer.