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1                                              NaCl did not cause any changes in emulsion droplet size.
2                                              NaCl dose-dependently promoted lipid oxidation as measur
3                                              NaCl increased the wrinkles but CaCl2 softened the surfa
4 , 4.0 M in H2O, 107.2 Ah/L, and 3.0 M in 2.0 NaCl, 80.4 Ah/L) and N(1)-ferrocenylmethyl-N(1),N(1),N(2
5 y was observed in a 10% CM at pH 10, in 0.01 NaCl.
6 to a normal- or chronic high-salt intake (1% NaCl).
7 fruits were sonicated in water or brine (15% NaCl).
8 20ml of Tris-HNO3 (pH=8) containing: a) 0.1M NaCl and 2g of skimmed milk powder at 21 degrees C for 6
9 milk powder at 21 degrees C for 60min; b) 1M NaCl and 1g of skimmed milk powder at 21 degrees C for 6
10 cipitation, and acetone extraction (with 1mM NaCl), which resulted in an 86.3% yield, and 53.8 purifi
11 etathesis reactions MCl2 + Na2S2 --> MS2 + 2 NaCl (M = Fe, Co, Ni) using synchrotron powder X-ray dif
12 e activity at a concentration range of 0-20% NaCl.
13            Rats fed a normal-salt diet (0.3% NaCl) served as controls (n=13).
14 zed water and 100 mM NH4OH), more than 99.3% NaCl was removed from samples containing physiological N
15  were compared with others that contained 3% NaCl content (the amount typically used for surimi proce
16 ta2m (mbeta2m) requires the addition of 0.3M NaCl to cause fibrillation.
17 as leached off under high ionic strength (3M NaCl).
18 egrees C) of potato chips (0%, 1%, 3% and 5% NaCl) for 100min/d for five consecutive days in eight sy
19 h two common boiling practices viz., with 5% NaCl solution (BSW) and normal water (BNW) in a domestic
20                   For phase separation, 1.5g NaCl and 4g anhydrous MgSO4 were added.
21 esence of high concentrations of salts (0.5M NaCl) and biomacromolcules (1.0% DNA and 2.0% alginate),
22 vent and a 1.0 mL juice sample containing 8% NaCl under seven extraction cycles of air pumping by syr
23 sensitive rats were fed a high-salt diet (8% NaCl) from 7 weeks of age to induce HFpEF (n=38).
24         None of the patients reacted to 0.9% NaCl alone.
25 atin (5 mg/kg), and the fourth vehicle (0.9% NaCl and 5% glucose).
26  right iliac fossa and pelvis, or 20 mL 0.9% NaCl control.
27 ncreasing concentrations of rMal d 1 in 0.9% NaCl were sublingually administered to 72 birch pollen-a
28 omized to either 3 mg kg HA or placebo (0.9% NaCl), given preoperatively (day 0) and again on day 2.
29     The emulsion was then transferred into a NaCl solution of large volume to extract the organic sol
30 t D757R Slo2.1 channels were activated by a [NaCl]i of 70 mM.
31  30min) WPI solutions with either 20mM added NaCl (WPI+NaCl), 5mM N-ethylmaleimide (WPI+NEM) or 20mM
32 5mM N-ethylmaleimide (WPI+NEM) or 20mM added NaCl and 5mM NEM (WPI+NaCl+NEM).
33 /TCE organic phase can be achieved by adding NaCl and creating water-in-oil emulsions in the organic
34 ction times, and the influence of additives (NaCl and skimmed milk powder) in a total of 36 different
35 ly associated to the presence of adulterants NaCl, tripolyphosphate and carrageenan.
36 e of cytosolic calcium ([Ca(2+) ]cyt ) after NaCl treatment.
37 a, map3k1, spn and stat5b was enhanced after NaCl treatment, consistent with the findings in lupus CD
38             For all egg yolk samples and all NaCl-containing LDL samples, the sigmoidal changes in th
39 owever, grinding the reactants in air allows NaCl to form directly without annealing and displaces th
40 eady stability in alkaline (upto pH 8.5) and NaCl (up to 10(-1)M) solutions.
41 bon electrodes (10(2) cm geometric area) and NaCl solutions having concentrations between 50 and 350
42 ffers (phosphate buffer saline, Tris-HCl and NaCl) on the extraction efficiency of total protein was
43 nding mode is modulated by magnesium ion and NaCl concentration, but unlike EcoSSB, the mtSSB does no
44 n on other known carbohydrates, both KCl and NaCl act as salting-out agents towards trehalose, as see
45  well as binary mixtures of NaCl and MA, and NaCl and nonanoic acid (NA) determined by AFM using area
46 actice, a solution of mixed heavy metals and NaCl salts was directly deposited on a Nichrome filament
47 cs under different histone protein (NCP) and NaCl concentrations using single-pair Forster resonance
48 ense changes in extracellular osmolarity and NaCl.
49  emulsified in a polyvinyl alcohol (PVA) and NaCl solution of small volume to form embryonic microsph
50 on of SOA particles when added to an aqueous NaCl core phase, in addition to the shell of SOA.
51 ne three initial chemical systems of aqueous NaCl, aqueous glycerol, and squalane at approximately 75
52 e primary variables: background salinity (as NaCl), concentration of a competing species (here Fe), a
53                Though B1 structures, such as NaCl and HfC predominately slip on 110{110}, the ISF her
54 tween ionic rock salt alkali halides such as NaCl or KBr and polar insulating Cu2N terminating bulk c
55 tal superlattices that are produced, such as NaCl, AlB2, NaZn13, and MgZn2, are well in agreement wit
56 can be enhanced by a simple compound such as NaCl.
57                                   The AS/BC, NaCl/BC, and HA/BC particles had AAEs of 1.43 +/- 0.05,
58  D757R Slo2.1 channels were not activated by NaCl, but were activated by the fenamate niflumic acid,
59 e five basic tastes and is often elicited by NaCl.
60 e influenced by pH and to a lesser extent by NaCl.
61 that OA adsorption was largely unaffected by NaCl concentrations (10-1000 mM).
62 s induced by various stresses such as CdCl2, NaCl, NaHCO3, and H2O2 treatments.
63 hydrochloride (GdnHCl), and sodium chloride (NaCl) added.
64 omposed of single component sodium chloride (NaCl) and malonic acid (MA), as well as binary mixtures
65 were at 0.6, 1.2, and 2.4 M sodium chloride (NaCl), equivalent to salinity of seawater, brine at 50%
66  the use of an advantageous sodium chloride (NaCl)-based method for radiolabeling of chelator-modifie
67  [potassium chloride (KCl), sodium chloride (NaCl)], 2:1 electrolytes [magnesium chloride (MgCl2), ca
68  (ammonium sulfate, AS, and sodium chloride, NaCl) and BC with a weakly absorbing brown carbon surrog
69   In this study, high salt (sodium chloride, NaCl), under physiological conditions, was demonstrated
70 dentification of the integrated compensatory NaCl reabsorption mechanisms provides insight into thiaz
71 astants, including sugars, bitter compounds, NaCl, and sour.
72 f the idler pulses using the bulk compressor NaCl, and by indirectly controlling the higher-order idl
73 dilute NaCl solutions and avoid concentrated NaCl, we found no evidence for two separate populations
74 igh (0.513 M) or low (0.017 M) concentration NaCl solutions in channels separated by a filtration mem
75 measurements in aqueous solutions containing NaCl, KCl, CaCl2, and Tris buffer show that the magnitud
76 mol Na(+)/day) and high (300 mmol Na(+)/day) NaCl diets, administered 4 weeks apart.
77 ly induced in response to UV-B, dehydration, NaCl, methyl jasmonate, and abscisic acid treatments ind
78                   Specifically for desalting NaCl, this enhancement of unipolar cation conduction sav
79 ivity to angiotensin II (Ang II) and dietary NaCl, whilst SM-alpha2 overexpression lowers basal BP an
80    These findings indicate that high dietary NaCl intake enhances the expression and activity of ENaC
81 umans and highlight the influence of dietary NaCl on these interactions.
82 ere measured on an Ag electrode in different NaCl solutions, adjusting for the influence of ionic str
83                  Although mice prefer dilute NaCl solutions and avoid concentrated NaCl, we found no
84  Gene silencing of TET2 obviously diminished NaCl-induced Tfh cell polarization in vitro.
85 iodes (OLEDs) are demonstrated using a doped NaCl film with a phosphorescent emitter as the emissive
86                                       During NaCl depletion, only dKO mice developed marked intravasc
87 ime, more than 92% of inorganic salts (i.e., NaCl and Na2SO4) would permeate through the fibers, redu
88  Rhodamine-WT, and a background electrolyte, NaCl, were higher than those of the PES support without
89 yte/silica interface, for four electrolytes: NaCl, KCl, MgCl2, and CaCl2.
90 etain potassium by increasing electroneutral NaCl reabsorption, therefore reducing Na(+)/K(+) exchang
91 ed a novel thiazide-sensitive electroneutral NaCl transport mechanism resulting from the parallel ope
92 d that the presence of deoxycholate enhances NaCl rejection in these graphene-based membranes.
93 nergetically preferred over the experimental NaCl-type and ZnS-type ones.
94 -2Cl(-)-cotransporter (NKCC2) is crucial for NaCl reabsorption in kidney thick ascending limb (TAL) a
95 measured and compared with existing data for NaCl and (NH4)2SO4.
96 ion concentrations (CCC) were determined for NaCl, CaCl2, and MgCl2 electrolytes.
97 /barttin chloride channels are essential for NaCl re-absorption in Henle's loop and for potassium sec
98            The obtained detection limits for NaCl and Na were 175 and 69 ppm, respectively.
99 was both internally and externally mixed for NaCl/BC particles.
100 ed swelling, which exhibit 97% rejection for NaCl.
101 nctioning actin cytoskeleton is required for NaCl-induced peroxisome division.
102 by TET2, and spn was not the sole target for NaCl.
103 olysis of alpha-terpineol adsorbed on glass, NaCl, and kaolinite, and identified the same three major
104          The late addition of coarse-grained NaCl (crystal size: 0.4-1.4 mm) to pizza dough led to an
105 ed a decreasing trend of Na2SO4 > (NH)2SO4 > NaCl > NH4Cl > NH4NO3 for the studied organic compounds,
106                                   After 24-h NaCl treatment, almt9 knock-out mutants had reduced shoo
107                                         High NaCl intake increases renal synthesis of dopamine and do
108                                         High NaCl, deletion of CodY or Sae also resulted in higher ca
109                              Thus, on a high NaCl diet fenoldopam causes natriuresis by inhibiting re
110 residue at the beta-dimer interface and high NaCl concentrations destabilize the clamp, but neither f
111 ain mechanisms, activated by Ang II and high NaCl, regulate sympathetic drive and a novel neurohumora
112 rm is unwrapped, previously observed at high NaCl concentrations, is also explained by this salt-indu
113                                  On the high NaCl diet, fenoldopam-induced natriuresis was associated
114 the exposure to stress stimuli, such as high-NaCl concentration or LPS, exacerbated the mitochondrial
115 5 site size ((SSB)65) mode formed at higher [NaCl] (> 200mM), where ssDNA wraps completely around the
116 rk examines the effect of including hydrated NaCl and CaCl2 (up to 6% w/w) on the physicochemical pro
117 nfusion of either 0.9% (ISO) or 3.0% (HYPER) NaCl saline, 12 subjects were passively heated until cor
118 ay an increased discharge to both hypertonic NaCl (+7.5 mm) and mannitol (+15 mm).
119                          However, hypertonic NaCl stimulates a greater increase in discharge frequenc
120 : Systemic or central infusion of hypertonic NaCl and other osmolytes readily stimulate thirst and va
121 tracerebroventricular infusion of hypertonic NaCl evokes a greater increase in OVLT neuronal discharg
122 fusion or local OVLT injection of hypertonic NaCl increases lumbar sympathetic nerve activity, adrena
123 ed that intracarotid injection of hypertonic NaCl produced a concentration-dependent increase in OVLT
124  In contrast, central infusion of hypertonic NaCl produces a greater increase in arterial blood press
125 tor; however, central infusion of hypertonic NaCl produces a greater sympathoexcitatory and pressor r
126 of OVLT neurons are responsive to hypertonic NaCl or mannitol.
127 LT neurons respond differently to hypertonic NaCl versus osmolarity and subsequently regulate body fl
128 y sense or respond differently to hypertonic NaCl versus osmolarity.
129 d a greater discharge response to hypertonic NaCl vs mannitol.
130 NF-1beta mutant mIMCD3 cells with hypertonic NaCl inhibited the induction of osmoregulated genes, inc
131 uted kernels based on density differences in NaCl solutions was evaluated.
132 odes the ClC-Kb chloride channel involved in NaCl reabsorption in the renal tubule.
133                    AR dramatically increased NaCl-elicited responses in cells transfected with NHE1 s
134          Here, we have shown that increasing NaCl, either in vitro or in murine models via diet, mark
135        Collectively, these findings indicate NaCl and osmotic stimuli produce different responses acr
136 injecting solutions of non-meat ingredients (NaCl, phosphates, carrageenan, maltodextrin) in bovine m
137 cooperativity using pairs of spherical ions (NaCl > NaBr > NaI) correlates to experimental observatio
138                             The mechanism is NaCl-induced DNA demethylation via the recruitment of th
139 osheets in a variety of salt solutions (KCl, NaCl and CaCl2) at low salt concentrations (<10(-4) M) s
140 scharge coincides with salt removal (1.96 kg-NaCl kWh(-1)).
141 ntoms that contained 10-, 20-, and 30-mmol/L NaCl solution and 5% agarose gel as a reference.
142 5 to 75 degrees C), ionic salts (2.0 M LiCl, NaCl, and KCl), as well as in the presence of protein de
143 al and distal tubule transport, but on a low NaCl diet the increased RAAS activity prevents the D1-li
144 ditives improving the characteristics of low NaCl surimi gels.
145                              For zero or low NaCl electrolyte concentrations, interfacial repulsions
146                                   On the low NaCl diet, fenoldopam decreased renal distal tubule sodi
147 with the 35 site size ((SSB)35) mode at low [NaCl], whereas the 65 site size ((SSB)65) mode formed at
148 cular (icv) infusion (5 mul/10 min) of 1.0 m NaCl produced a significantly greater increase in lumbar
149 Second, OVLT microinjection (20 nl) of 1.0 m NaCl significantly raised lumbar SNA, adrenal SNA and AB
150  3.1 M in H2O, 83.1 Ah/L, and 2.0 M in 2.0 M NaCl, 53.5 Ah/L) were synthesized through structural dec
151             The cell was filled with 0.095 M NaCl electrolyte containing 10 mum polystyrene beads to
152 - and postsurgically acquired CTAs (to 0.1 M NaCl and 0.1 M sucrose, respectively) were assessed post
153 ) < [Pu]tot/M < 10(-8)) with illite in 0.1 M NaCl at pH between 3 and 10, Pu uptake was characterized
154 variety of peptides, which are stable in 1 M NaCl solution at a pH value of 3-4 during reaction.
155                          The addition of 1 M NaCl was found to further increase the stability of the
156 ) M KCl and 58.68 mV/dec (10(-6) to 10(-1) M NaCl) was observed.
157                                  In 10(-1) M NaCl, the clay was preaggregated into larger and more sp
158 ated that the dipping of CIGS films in 0.2 M NaCl solution for 20 minutes followed by selenization at
159                       1 m sorbitol and 0.2 m NaCl, which induce the HOG pathway, rescued growth of th
160  oocytes using micropipettes filled with 2 M NaCl.
161  and other proteins were washed off with 3 M NaCl, while retaining AChE bound to Hupresin.
162  to 48.3 bar and concentrations of up to 3 M NaCl.
163      With dispersed clay platelets (10(-3) M NaCl), secondary heteroaggregation driven by bridging na
164                            When fed with 4 M NaCl, the MDC achieve a current density of 300 A m(-3) (
165 sed bacteria were increased at 1.2 and 2.4 M NaCl.
166 e-mixed with 0.1, 10(-2), 10(-3), or 10(-4)M NaCl or Na2SO4, prior to ultrasonication.
167                Lastly, icv infusion of 0.5 m NaCl produced significantly greater increases in OVLT di
168 diameter) and then eluted with acidified 5 M NaCl solution directly into a sodium acetate-buffered so
169 rved, which were attributed to M.Cl(-) or [M.NaCl]Cl(-)complexes.
170 a prolonged period (120 h) while maintaining NaCl rejection near 85% and 96% for an anionic dye.
171 with different elicitors (sucrose, mannitol, NaCl, 1-aminocyclopropane-L-carboxylic acid, salicylic a
172  the apical surface regulates NKCC2-mediated NaCl absorption and blood pressure.
173 ing-point ternary molten salts CaCl2 -MgCl2 -NaCl, which still retains high CaSiO3 solubility, and a
174  phase separation with the addition of MgSO4:NaCl.
175 f 254 differentially expressed genes at 0 mM NaCl and 391 genes at 300 mM NaCl in P. indica-colonized
176 leaf samples were harvested at control (0 mM NaCl) and severe salt stress (300 mM NaCl) in P. indica-
177                At concentrations above 10 mM NaCl, pitting is initiated at the outer rim of the confi
178  rim of the confined zone, while below 10 mM NaCl, pitting is initiated inside the confined zone.
179  3-9.5 in a background electrolyte of 100 mM NaCl and 1 mM CaCl2 in equilibration with 400 ppmv CO2(g
180 ing all fullerene clusters, even at a 100 mM NaCl concentration.
181 ffects of O2 deficiency and salinity (100 mM NaCl) on radial O2 concentrations and cell-specific ion
182 temperature (25 degrees C), and salt (100 mM NaCl).
183 on lipid Nanodiscs at 20 degrees C in 100 mM NaCl, 50 mM Tris, at pH 7.4.
184       Exposure to a high salt stress (150 mM NaCl) triggered a rapid repression of overall aquaporin
185 osphate buffer solution, pH 7.4, with 150 mM NaCl), higher glucose oxidation current densities, 0.41
186 overy (FRR) during BW at 8 V AC using 155 mM NaCl.
187 to be approximately 200 mM, 35 mM, and 30 mM NaCl, respectively.
188 d genes at 0 mM NaCl and 391 genes at 300 mM NaCl in P. indica-colonized compared to non-inoculated s
189 l (0 mM NaCl) and severe salt stress (300 mM NaCl) in P. indica-colonized and non-inoculated barley p
190                 Under salt stress (50-400 mM NaCl), miRNVL5 expression was repressed, with concomitan
191 s injected into the carrier solution (0.5 mM NaCl) and subsequently transported to the detection cell
192 o wild-type Z. xanthoxylum grown under 50 mm NaCl.
193 ronments (20-50 degrees C, 2-10 pH, 0-500 mM NaCl, and 0-35 days storage at 25 degrees C) depended on
194 nd was estimated as 220, 150, 100, and 70 mM NaCl and 10, 12, 6, and 7.5 mM CaCl2 for nC60, nC70, nC7
195 ution to potassium homeostasis by modulating NaCl transport.
196 tically studied under a wide range of mono- (NaCl) and divalent (CaCl2) electrolytes and using time-r
197 extraction and disperser solvents (100 muL), NaCl at 2% of the sample volume and extraction time of 6
198                        In the Uvhog1 mutant, NaCl treatment failed to stimulate the accumulation of s
199 AORFBs were operated in noncorrosive neutral NaCl supporting electrolytes using a low-cost anion-exch
200 ocesses in real time in different pH-neutral NaCl solutions and applied surface potentials of nickel
201  10% in one single step or to replace 30% of NaCl by KCl without a noticeable loss of salty taste.
202 e use of PDMS/DVB fibre, 2mL of wine, 30% of NaCl, 40 degrees C for 30min.
203          To address the effect of absence of NaCl on myosin heavy chain polymerization during two-ste
204 ng conditions (e.g. pH2.5) in the absence of NaCl, mouse beta2m (mbeta2m) requires the addition of 0.
205                              The addition of NaCl (300-400 mM) only caused flocculation in nanodisper
206                                  Addition of NaCl did not safeguard the katB mutant from H2O2, sugges
207        Unique biochemical characteristics of NaCl activation were also observed.
208 of hygroscopic aerosol particles composed of NaCl, Na2SO4, (NH4)2SO4, and nonhygroscopic Al2O3 as the
209 when frying temperature and concentration of NaCl increased.
210 rature, frying duration and concentration of NaCl increased.
211 ely inhibited with the same concentration of NaCl.
212 .15% w/w) were examined at concentrations of NaCl (0, 0.01, 0.25, 0.3, 0.5mol/l) and at different pH
213 B media containing reduced concentrations of NaCl (100 mM or less), and also within suckling mice, a
214 ve in the presence of high concentrations of NaCl.
215 and/or of low quality due to high content of NaCl (coastal areas or areas where underground water is
216                                       CSP of NaCl, alkali molybdates and V2 O5 with small concentrati
217 he aptamer sequence eliminated the effect of NaCl on its affinities for cocaine and analogues, but no
218 ntation model, we investigated the effect of NaCl on the alloimmune response in vitro and in vivo.
219                  Antiplasticising effects of NaCl and CaCl2 on the non-phosphorylated tapioca starch
220 mount of lattice energy via the formation of NaCl, and the crystallization of the metal sulfide is a
221 esence of Ca(2+) and Mg(2+) as a function of NaCl concentration, pH, and temperature, and in solvents
222                          Epitaxial growth of NaCl on NaCl (001) is explored as a function of temperat
223 -) ion produced by the thermal ionization of NaCl is employed as the dopant or the ionizing reagent t
224 hannels were rapidly activated by leakage of NaCl solution into the cytoplasm.
225 nic acid (MA), as well as binary mixtures of NaCl and MA, and NaCl and nonanoic acid (NA) determined
226 rations of the target analytes and 150 mM of NaCl.
227 ch pastes were determined in the presence of NaCl and CaCl2 (0, 50, 100, 150 and 200mM).
228                               A reduction of NaCl by 25% with an addition of KCl achieved high accept
229             In this study, the regulation of NaCl-induced responses was investigated in cultured huma
230 pose a molecular mechanism for resorption of NaCl by MRCs during development, and conclude that disru
231  is purified water or an aqueous solution of NaCl with an initial conductivity of 10500 muS cm(-1).
232 ron spectrum of a simple aqueous solution of NaCl.
233        The effect of partial substitution of NaCl by KCl and the addition of flavor enhancers (l-argi
234 k studies the effects of the substitution of NaCl with KCl and CaCl2 on the physicochemical, mineral
235 e increase in aldosterone levels expected on NaCl depletion was attenuated in dKO mice, and single-kn
236                  Epitaxial growth of NaCl on NaCl (001) is explored as a function of temperature and
237 udies under different salt (50-150 mM KCl or NaCl) and ATP concentrations on different GQ constructs
238 d under high concentrations of either KCl or NaCl.
239 ronary (10 mL) sodium nitrite (1.8 mumol) or NaCl (placebo) before balloon inflation.
240 emoved from samples containing physiological NaCl concentrations.
241 its specificity for cocaine in physiological NaCl relative to an off-target ligand.
242 ecreases with the inclusion of physiological NaCl.
243 rmed to examine the Na at 589 nm to quantify NaCl.
244 s of the thick ascending limb (TAL) reabsorb NaCl via the apical Na(+)/K(+)/2Cl(-) co-transporter NKC
245  C, using inexpensive and nontoxic reagents (NaCl, diluted HCl, water).
246 ypertension of rats exposed to chronic salt (NaCl) intake from weaning until adult age.
247 f materials, even including pure table salt (NaCl).
248 mulsions in the presence of different salts (NaCl and CaCl2), ionic strengths, pHs, and temperatures
249                       The thiazide-sensitive NaCl cotransporter (NCC) is important for renal salt han
250 d reduced activity of the thiazide-sensitive NaCl cotransporter may support renal adaptation by activ
251 ne, synthetic formation brine, and synthetic NaCl+CaCl2 brine were collected at the pressures from 10
252 inant variation from time-course rather than NaCl intensity within 24 hours salt shock.
253           We however recently evidenced that NaCl, used in vaccine formulation, provokes AH particle
254              Light micrographs revealed that NaCl roughened the surface of PG starch particles while
255                     In summary, we show that NaCl negatively affects the regulatory balance of T cell
256 alondialdehyde formation was affected by the NaCl level, with the saltiest samples exhibiting lower c
257                             Furthermore, the NaCl and MA mixture was substrate-deposited both wet and
258                     On exposure to H2O2, the NaCl-treated Anabaena showed reduced formation of reacti
259                    Dopamine responses to the NaCl US following sodium depletion updated independent o
260 um-permeable channel that contributes to the NaCl-induced [Ca(2+) ]cyt signal.
261  550 nm with increasing wavelength while the NaCl/BC enhancement was essentially wavelength independe
262 ncentration was linearly correlated with the NaCl concentration.
263 d its expression decreased after exposure to NaCl or abscisic acid.
264 bidopsis leaves following 5-hour exposure to NaCl, no proliferation was detected in the salt-suscepti
265           Interestingly, addition of pN15 to NaCl-washed PSII membranes decreased PSII's oxygen-evolv
266 d in peroxisome proliferation in response to NaCl stress.
267 r the anion effect by measuring responses to NaCl and Na-gluconate (small and large anion sodium salt
268 ly increased the number of cell responses to NaCl, whereas no effect was observed with RE, ER, DD, or
269 ical reactions, such as high solubilities to NaCl and O2.
270     The cerk1 mutant was more susceptible to NaCl than was the wild type.
271 aneously by applying media changes (water to NaCl solutions), unspecific adsorption of bovine serum a
272                        High stability toward NaCl was also evident up to 3M.
273                                   Salt type (NaCl or CaCl2) did not affect the Cl LC50, Daphnia life
274  using solvent extraction, and solvent type, NaCl concentration, and ionic strength of the final solu
275 her reactive oxygen species production under NaCl and a larger density of reactive oxygen species-act
276  plants germinate worse than wild-type under NaCl stress and in response to abscisic acid (ABA).
277 lect distinct cellular mechanisms underlying NaCl- versus osmo-sensing.
278 is-localized in the DeltaFgvps27 mutant upon NaCl treatment.
279                                        Using NaCl and CH3NH3PbI3 as examples, we illustrate these une
280 n at 23 degrees C, 23 degrees C with 12% w/v NaCl and -10 degrees C with 12% w/v NaCl.
281  12% w/v NaCl and -10 degrees C with 12% w/v NaCl.
282 aline solutions (NaOH: 0.54 M, EtOH: 1.17 v, NaCl: 2.5%) to end the protein hydrolysis and to precipi
283 be toggled electrostatically through varying NaCl concentration in the bulk solution.
284 s were enhanced with addition of CaCl2 while NaCl exhibited an opposite trend for all of these factor
285 o combat the health problems associated with NaCl overconsumption by humans.
286 cterium Anabaena, pretreatment of cells with NaCl resulted in unusually enhanced tolerance to oxidati
287 enced a "stabilizing" effect of cooking with NaCl and CaCl2 on bean proteins.
288          Overall, BA contents decreased with NaCl level (2785.1mgkg(-1), 1148.1mgkg(-1) and 307.7mgkg
289 A) reduced lipid oxidation in emulsions with NaCl, with EDTA being more effective.
290 o a solution of 3 in 2:1 water/methanol with NaCl, the fluorescence intensity increased.
291                 Plant seedlings treated with NaCl at different concentrations showed higher allantoin
292 han the control cells (i.e. not treated with NaCl) exposed to H2O2.
293                              Treatments with NaCl favored the expression of genes involved in allanto
294 d polyethylene glycol, while treatments with NaCl resulted in AtRGGA down-regulation.
295 sis demonstrated that the heated WPI and WPI+NaCl solutions had higher levels of aggregated protein,
296 en proteins, than the heated WPI+NEM and WPI+NaCl+NEM solutions.
297 I solutions with either 20mM added NaCl (WPI+NaCl), 5mM N-ethylmaleimide (WPI+NEM) or 20mM added NaCl
298 WPI+NEM) or 20mM added NaCl and 5mM NEM (WPI+NaCl+NEM).
299 g-term evaporation experiment with a 15 wt % NaCl solution, the GO leaf demonstrated stable performan
300 e corrosion of J55 and N80 steel in 3.5 wt.% NaCl solution saturated with CO2 was evaluated using wei

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