ライフサイエンスコーパス: NaCl

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