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1 es in neuronal organization (dehydration and rehydration).
2 re differentially expressed upon dehydration-rehydration.
3 verged strongly from seed plant species upon rehydration.
4 ration at elevated temperatures, followed by rehydration.
5 o survive repeated cycles of desiccation and rehydration.
6  includes DNA breakage that is repaired upon rehydration.
7 3 transcripts and ABA, responses reversed by rehydration.
8 ne structure and fluidity during dehydration/rehydration.
9 ange in properties was fully reversible upon rehydration.
10  electrolyte imbalance by oral or parenteral rehydration.
11 dehydration, dehydroxylation, and subsequent rehydration.
12 f stressed plants also declined rapidly upon rehydration.
13 e of a membrane potential, is immediate upon rehydration.
14 ion, cytoplasmic osmoregulation, and/or seed rehydration.
15 lose strips after a cycle of dehydration and rehydration.
16 ked to the spatiotemporal sequence of tissue rehydration.
17 established by percentage weight change with rehydration.
18 d states, and much reduced aggregation after rehydration.
19 id and in protein aggregation measured after rehydration.
20 this treatment should favor aggregation upon rehydration.
21 e recovery of native protein molecules after rehydration.
22  growth patterns in the evening or upon soil rehydration.
23             This transition is reversible on rehydration.
24  13.7%) of children administered intravenous rehydration.
25 g lipid droplets during seed desiccation and rehydration.
26  tolerance and resumption of metabolism upon rehydration.
27  juice/preferred fluids received intravenous rehydration (2.5% vs 9.0%; difference, -6.5%; 99% CI, -1
28 psules and the corresponding emulsions after rehydration (7.7 and 9.9 mum respectively).
29 , together with a complementary study on the rehydration ability and sensorial attributes of samples,
30   The higher TPC, AOC, vitamin C content and rehydration ability were obtained from HD.
31 on the surface, which in turn exhibited good rehydration ability.
32                              Dehydration and rehydration affected mainly the gene expression for comp
33 ript level varying in response to drying and rehydration and all transcripts being stable in dried ti
34 psis model in which the mice were treated by rehydration and antibiotics, the production of colibacti
35 n addition to standard care with intravenous rehydration and antiemetic treatment or to standard care
36 any control of the reagent distribution upon rehydration and can be a source of error when pads do no
37 pidly stimulated (within < 15 min) following rehydration and coincides with the onset of ribosomal S6
38                                  Both in-gel rehydration and cup-loading methods were used for isoele
39 dergoes a 1,2-hydride shift competitive with rehydration and deprotonation.
40 r pollen to survive the hypoosmotic shock of rehydration and for full male fertility.
41 oenteritis in children can help promote oral rehydration and prevent medical visits for dehydration.
42 n of mobile ions within the glycocalyx and a rehydration and restoration of the layer to its equilibr
43 ing with both a fecal occult-blood test with rehydration and sigmoidoscopy fails to detect advanced c
44                      Treatment is limited to rehydration and supporting care suggesting an urgent nee
45           This precipitation is critical for rehydration and survival of the largest vertebrate group
46 nes was found to decrease by 10% upon drying/rehydration and the lateral diffusion coefficient decrea
47 d cells to water storage can be derived from rehydration and water-release curves on excised plant ma
48         Diarrhoea stopped during intravenous rehydration and when feeding a glucose-, galactose-, and
49  the spore core, including DPA excretion and rehydration, and also activates hydrolysis of the surrou
50 que adsorption, cation-exchange, dehydration-rehydration, and catalytic properties.
51 Acute therapy includes complete pain relief, rehydration, and encouragement of diuresis.
52 antly higher rates of initial and successive rehydration as well as smaller initial loss of soluble s
53                                  The peak in rehydration-associated transcript accumulation coincided
54 n PCN and may have contributed to inadequate rehydration behaviour.
55 lated above control levels during drying and rehydration but were barely detectable in desiccated tis
56                       During dehydration and rehydration, C. pumilum deactivates and activates partia
57  The samples dried by hot air shows a higher rehydration capacity than samples dried by combined meth
58 capacity (AOC), vitamin C content, color and rehydration capacity were followed.
59                                       Tissue rehydration caused a transitory change in delta(18)O(L),
60 reaks caused by the frequent desiccation and rehydration characteristic of bdelloid habitats.
61 ascorbic acid and carotenoids were retained, rehydration coefficients were higher and there were mini
62 hibited a substantial loss of viability upon rehydration compared with wild-type D. radiodurans.
63 lined in the morning and recovered upon soil rehydration considerably quicker than transpiration rate
64                               Immediately on rehydration, control cells without LEA proteins or treha
65  release of the enzyme from dried cells upon rehydration, counter the effects of oxidative stress imp
66                       During the dehydration/rehydration cycle c. 92 % of the total protein-coding tr
67 ge their shape and size in a dehydration and rehydration cycle.
68  lepidophylla was subjected to a five-stage, rehydration/dehydration cycle, then analyzed using non-b
69 r spore solute release or partial spore core rehydration during germination, (iii) indicate that mura
70 mposed by multiple cycles of desiccation and rehydration during UV-A or -B irradiation in situ.
71                   Antiemetics may facilitate rehydration efforts by limiting further fluid losses.
72                                    Following rehydration, embryos resume development via alterations
73 tin transcripts which can be translated upon rehydration enabling rapid initiation of cellular repair
74 ects the difference in dehydration/solvation/rehydration energies in the entry/exit steps of permeati
75                                   Subsequent rehydration, even after an extended period of time (e.g.
76                                   Imaging of rehydration experiments showed spatially variable recove
77 setron to children at greatest risk for oral rehydration failure.
78                                         Upon rehydration, Fe-containing superoxide disumutase (Fe-SOD
79 involved in the deoxy-dependent component of rehydration for dense, K(+)-depleted cells.
80              Rapid, large-volume intravenous rehydration for outpatients with dehydration did not sho
81 ment of diarrhoea-including an improved oral rehydration formulation, zinc supplementation, and rotav
82 vel method allows for consistent, controlled rehydration from patterned reagent storage depots direct
83  to obtain a reference Hydration-Dehydration-Rehydration (H-D-R) transcriptome comprising of 76,206 t
84      Secondary outcomes included intravenous rehydration, hospitalization, and frequency of diarrhea
85 ing within 7 days of enrollment: intravenous rehydration, hospitalization, subsequent unscheduled phy
86 ted with the H-D-R cycle and confirmed early rehydration (i.e. the R2 stage) as exhibiting the maximu
87 yte disturbances and regarding the method of rehydration (i.e., enteral versus parenteral) raise some
88 inantly form isomerized isoAsp residues upon rehydration (imbibition).
89 spital admissions and the use of intravenous rehydration in children with AGE in emergency-department
90 n occurring after dehydration and subsequent rehydration in comparison to cells kept constantly hydra
91         The ubiquitin response to drying and rehydration in evolutionarily diverse systems is charact
92 g mRNA levels in response to desiccation and rehydration in leaves of the desiccation tolerant grass
93 tiveness and advantages of rapid intravenous rehydration in the outpatient setting is discussed.
94 ncreases in modulus were rapidly reversed by rehydration in water.
95                No significant enhancement of rehydration is achieved when the microgrooves and microc
96 n between different stages of drying, on the rehydration kinetics of dry blueberries.
97                            Models describing rehydration kinetics were also studied.
98 he crystals, since the activation energy for rehydration may be extremely high.
99                                Rapid enteral rehydration may be used in the uncomplicated, mildly to
100 m amphiphilic gold nanocrystals using a film-rehydration method that can be completed within approxim
101 olipids and cholesterol using a dehydration/ rehydration method.
102  giant unilamellar vesicles using an agarose rehydration method.
103  with proteins that normally aggregate after rehydration, minimizing unfolding during freeze-drying w
104 aled package in a dry atmosphere, drying and rehydration must not change the transport characteristic
105      In a parallel set of experiments, acute rehydration of 48 h water-deprived rats significantly at
106 lter catalyses the dehydration, transfer and rehydration of a K+ ion in about ten nanoseconds.
107 id interactions are weakened and lead to the rehydration of amide groups.
108 a late dissociative transition state and the rehydration of B and the protein binding cavity in solut
109 hat catalyzes the stereospecific dehydration-rehydration of citrate to isocitrate in the Krebs cycle.
110 simulations have been performed to study the rehydration of compact and unfolded cytochrome c ions in
111                                         Upon rehydration of desiccated cells, there was a turnover of
112                                              Rehydration of desiccated leaves resulted in a decrease
113  differentially expressed transcripts during rehydration of desiccated moss (Tortula ruralis), was fu
114                                        Rapid rehydration of excised shoots was used as a means of dif
115 lating light SSRBCs, also contributes to the rehydration of high-density SSRBCs.
116        Two-dimensional separation, including rehydration of IEF strip and fluorescence detection was
117 rious species present during dehydration and rehydration of mesoporous silicas between -25 and 500 de
118 s and from photosynthetic activity following rehydration of nodules may mediate the rate of recovery
119 aper network immunoassay based on controlled rehydration of patterned, dried reagents.
120                           Conversely, during rehydration of rapidly dried tissue Tr288 transcript lev
121  due to an enzymatic step(s), and not simply rehydration of stored, active enzyme.
122                                  Conversely, rehydration of stressed leaves caused a rapid decrease i
123                                              Rehydration of the cis-homoaconitate produces (-)-threo-
124 ide of the heme pocket, perhaps accompanying rehydration of the deoxymyoglobin photoproduct or accomm
125 rprint was obtained, irrespective of time of rehydration of the DNA, using a primer (5'-GWCWATCGCC-3'
126 arranges during the first several minutes of rehydration of the film.
127 tructure of the cross-linked liposomes after rehydration of the freeze-dried powder of liposomes.
128 iral RNA is directly amplified following the rehydration of the immobilized samples, thus eliminating
129                                         Upon rehydration of the layered gel, we observed a preferred
130 nted samples, proper dehydration followed by rehydration of the proteoliposomes is essential.
131 ranscript was also evident during drying and rehydration of the roots of S. stapfianus, as well as in
132                  This allows for the partial rehydration of these moieties.
133 P707A2 mRNA levels were rapidly increased by rehydration of water-stressed leaves.
134 maged as 2-5mum long fragments that survived rehydration on natural and artificial surfaces (i.e. pla
135 ce of the recovery of membrane mobility upon rehydration on TDM fraction shows a functional form indi
136 tant roles in nitrogen remobilization during rehydration or in ROS scavenging.
137 s, skin tenting, dysentery, intravenous (IV) rehydration, or hospitalization.
138 ), during drought and through the subsequent rehydration period for a sample of eight canopy and unde
139  to 20 times between the peak of the de- and rehydration phases.
140 ll three cholera treatment centres and seven rehydration posts throughout Juba.
141  ondansetron use and 3 outcomes: intravenous rehydration (primary), hospitalization, and emergency de
142 ng membranes when undergoing dehydration and rehydration procedures, and the 1,2-dioleoyl-sn-glycero-
143  range of 40% to 90% was detected during the rehydration process after topical application of the HA.
144 bacterial membrane vesicles by a dehydration-rehydration process generated giant cell-like hybrid ves
145  the microchannels was removed by the drying/rehydration process, as compared to 11% for PC.
146 r and carbon uses throughout dehydration and rehydration processes in adult trees will contribute to
147 d with PLC variations during dehydration and rehydration processes, indicating that stored carbon con
148 e-cell (BS-WC) cholera vaccine is added to a rehydration program either preemptively or reactively.
149 ed their total polyphenol content and showed rehydration properties, which were even better than thos
150      In contrast, IMF had excellent flow and rehydration properties.
151              Effective interventions include rehydration, prostaglandin inhibitors, and vitamin B6.
152                          The highest initial rehydration rate and the smallest loss of soluble solids
153  rate was 74 microm/min, whereas the average rehydration rate was 12.4 microm/min.
154 creased during the study period, intravenous rehydration rates were unchanged.
155 ates, vitamin C, 2-furoylmethyl amino acids, rehydration ratio and leaching loss) have been determine
156                                          The rehydration ratio changed with varying both air velocity
157           While the shrinkage decreased, the rehydration ratio increased with increasing air temperat
158                                              Rehydration ratio was not affected by the power applied
159 ydrates, total polyphenols, protein profile, rehydration ratio, microstructure changes) of convective
160 ts perform the isomerization and dehydration/rehydration reactions.
161  Bronsted acidity drives the dehydration and rehydration reactions.
162 desiccation, TOF-SIMS imaging and subsequent rehydration reveals structural and morphological preserv
163 observed by 6 days of dehydration that, with rehydration, reversed back toward or beyond control leve
164 ), handwashing with soap (observation), oral rehydration salt solution preparation (demonstration), a
165 g evidence of an intervention effect on oral rehydration salt solution preparation and breastfeeding
166       Secondary outcomes were intake of oral rehydration salt solution, severity of vomiting, and ser
167 specific questions on fluids other than oral rehydration salts (ORS) should be eliminated to refocus
168 ation (9%); treatment of diarrhoea with oral rehydration salts and zinc, and careseeking for fever, m
169 , handwashing with soap, correct use of oral rehydration salts, and zinc administration.
170                                Although oral rehydration salts, the correct treatment for diarrhea, a
171                                   For in-gel rehydration, samples reduced with DTT were diluted with
172                                         Oral rehydration seems to be here to stay.
173 usly, we found that an amino acid-based oral rehydration solution (AA-ORS) improved gastrointestinal
174 water control (1337 +/- 330 g) after an oral rehydration solution (ORS) (1038 +/- 333 g, P < 0.001),
175  240) were aware of cholera (97.5%) and oral rehydration solution (ORS) (87.9%).
176 o a 90 mmol/L sodium-111 mmol/L glucose oral rehydration solution (ORS) enhances its effectiveness fo
177 on [so-called resistant starch (RS)] to oral rehydration solution (RS-ORS) improves the efficacy of O
178  for a respiratory complaint, and using oral rehydration solution for diarrhea.
179 n to recent efforts to develop improved oral rehydration solution formulations.
180                                  Use of oral rehydration solution has stagnated, despite being effect
181        This article reviews the role of oral rehydration solution in the treatment of acute diarrhea
182              Net sodium absorption from oral rehydration solution is increased by both glucose-sodium
183 nsport was the basis for development of oral rehydration solution, and was hailed as potentially the
184                Before widespread use of oral rehydration solution, treatment for diarrhoea was restri
185 esting of modifications to the standard oral rehydration solution.
186 stimulation of net sodium absorption by oral rehydration solution.
187                                         Oral rehydration solutions reduce diarrhea-associated mortali
188 ' physical examination, prescription of oral rehydration solutions, antibiotics and other medications
189 been primarily attributed to the use of oral rehydration solutions, continuous feeding and zinc suppl
190 nough" to ensure the appropriate use of oral rehydration solutions, zinc and antibiotics by healthcar
191 and might contribute to the efficacy of oral rehydration solutions.
192 cess as well as slow water absorption during rehydration, stabilize proteins, and scavenge reactive o
193  subject to ABA treatment in dehydration and rehydration stages.
194 ral lung damage and indicate that additional rehydration strategies may be required for effective tre
195 ccess disparities, including availability of rehydration supplies.
196 ecies without resin, we developed a modified rehydration technique that allows the separation of decl
197 nic saline or water deprivation with partial rehydration than did vehicle-treated rats.
198                                         Oral rehydration therapies are the mainstay of management of
199                                        Thus, rehydration therapies may slow the progression of CF lun
200 The features integral to the success of oral rehydration therapy are active glucose transport in the
201                                         Oral rehydration therapy followed institutional protocols.
202  alternative strategies in which appropriate rehydration therapy for cholera is introduced preemptive
203                                         Oral rehydration therapy for the management of dehydration in
204 esses globally, but the introduction of oral rehydration therapy has reduced mortality due to diarrhe
205                                         Oral rehydration therapy has reduced the number of deaths fro
206            Antiemetics as an adjunct to oral rehydration therapy have been proven well tolerated, eff
207 agement of cholera with oral and intravenous rehydration therapy have reduced the case fatality of ch
208 rs new approaches that might supplement oral rehydration therapy in controlling diarrheal diseases.
209 d by glucose, and this is the basis for oral rehydration therapy in patients with secretory diarrhoea
210 s protecting against cholera exist, and oral rehydration therapy is an effective treatment method, th
211                   Astrovirus, for which only rehydration therapy is required, should be considered as
212             In a situation with no available rehydration therapy suitable for the management of sever
213 ed on the treatment of dehydration with oral rehydration therapy, few studies have focused on the act
214 ammes in family planning, immunisation, oral rehydration therapy, maternal and child health, tubercul
215  understanding of the cellular basis of oral rehydration therapy.
216 t disrupt intermolecular interactions during rehydration, this treatment should favor aggregation upo
217 resent and analyze the hydration-dehydration-rehydration transcriptomes in B. argenteum to establish
218 sions of children with diarrhoea to the Oral Rehydration Unit of the Instituto de Salud del Nino in L
219 ly data on hospital admissions from the Oral Rehydration Unit, and meteorological data from the Peruv
220 ty of MLVs and OVA-encapsulating dehydration-rehydration vesicles (DRVs), but not of SUVs.
221                                         Post-rehydration viability decreased dramatically within the
222                                  Intravenous rehydration was administered to 43,413 of 232,706 childr
223 was reversed by charybdotoxin, implying that rehydration was delayed in some cells by the Ca(++)-acti
224           The calcium-mediated inhibition of rehydration was reversed by charybdotoxin, implying that
225 f liposomes after a cycle of dehydration and rehydration was studied using biotin-tagged, dye-loaded
226                                     To study rehydration, we subjected dense SSRBCs (rho > 1.107 g/cc
227 h possible nitrogen remobilization following rehydration, were markedly higher in S. lepidophylla.
228 unfolded in the dried solid aggregate during rehydration, whereas others refold.
229 f LDH, CRP, and PSA levels was achieved post-rehydration while more than 90% recovery was accomplishe
230 ehydration, and after subsequent intravenous rehydration with saline (EX-REH).

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