コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
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
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
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
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
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
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
31 30min) WPI solutions with either 20mM added NaCl (WPI+NaCl), 5mM N-ethylmaleimide (WPI+NEM) or 20mM
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
37 a, map3k1, spn and stat5b was enhanced after NaCl treatment, consistent with the findings in lupus CD
39 owever, grinding the reactants in air allows NaCl to form directly without annealing and displaces th
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
49 emulsified in a polyvinyl alcohol (PVA) and NaCl solution of small volume to form embryonic microsph
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
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
58 D757R Slo2.1 channels were not activated by NaCl, but were activated by the fenamate niflumic acid,
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
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
77 ly induced in response to UV-B, dehydration, NaCl, methyl jasmonate, and abscisic acid treatments ind
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
82 ere measured on an Ag electrode in different NaCl solutions, adjusting for the influence of ionic str
85 iodes (OLEDs) are demonstrated using a doped NaCl film with a phosphorescent emitter as the emissive
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
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
94 -2Cl(-)-cotransporter (NKCC2) is crucial for NaCl reabsorption in kidney thick ascending limb (TAL) a
97 /barttin chloride channels are essential for NaCl re-absorption in Henle's loop and for potassium sec
103 olysis of alpha-terpineol adsorbed on glass, NaCl, and kaolinite, and identified the same three major
105 ed a decreasing trend of Na2SO4 > (NH)2SO4 > NaCl > NH4Cl > NH4NO3 for the studied organic compounds,
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
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
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
127 LT neurons respond differently to hypertonic NaCl versus osmolarity and subsequently regulate body fl
130 NF-1beta mutant mIMCD3 cells with hypertonic NaCl inhibited the induction of osmoregulated genes, inc
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
139 osheets in a variety of salt solutions (KCl, NaCl and CaCl2) at low salt concentrations (<10(-4) M) s
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
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
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.
158 ated that the dipping of CIGS films in 0.2 M NaCl solution for 20 minutes followed by selenization at
163 With dispersed clay platelets (10(-3) M NaCl), secondary heteroaggregation driven by bridging na
168 diameter) and then eluted with acidified 5 M NaCl solution directly into a sodium acetate-buffered so
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
173 ing-point ternary molten salts CaCl2 -MgCl2 -NaCl, which still retains high CaSiO3 solubility, and a
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-
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
181 ffects of O2 deficiency and salinity (100 mM NaCl) on radial O2 concentrations and cell-specific ion
185 osphate buffer solution, pH 7.4, with 150 mM NaCl), higher glucose oxidation current densities, 0.41
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
191 s injected into the carrier solution (0.5 mM NaCl) and subsequently transported to the detection cell
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
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
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.
204 ng conditions (e.g. pH2.5) in the absence of NaCl, mouse beta2m (mbeta2m) requires the addition of 0.
208 of hygroscopic aerosol particles composed of NaCl, Na2SO4, (NH4)2SO4, and nonhygroscopic Al2O3 as the
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
215 and/or of low quality due to high content of NaCl (coastal areas or areas where underground water is
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.
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
223 -) ion produced by the thermal ionization of NaCl is employed as the dopant or the ionizing reagent t
225 nic acid (MA), as well as binary mixtures of NaCl and MA, and NaCl and nonanoic acid (NA) determined
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).
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
237 udies under different salt (50-150 mM KCl or NaCl) and ATP concentrations on different GQ constructs
244 s of the thick ascending limb (TAL) reabsorb NaCl via the apical Na(+)/K(+)/2Cl(-) co-transporter NKC
248 mulsions in the presence of different salts (NaCl and CaCl2), ionic strengths, pHs, and temperatures
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
256 alondialdehyde formation was affected by the NaCl level, with the saltiest samples exhibiting lower c
261 550 nm with increasing wavelength while the NaCl/BC enhancement was essentially wavelength independe
264 bidopsis leaves following 5-hour exposure to NaCl, no proliferation was detected in the salt-suscepti
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
271 aneously by applying media changes (water to NaCl solutions), unspecific adsorption of bovine serum a
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
282 aline solutions (NaOH: 0.54 M, EtOH: 1.17 v, NaCl: 2.5%) to end the protein hydrolysis and to precipi
284 s were enhanced with addition of CaCl2 while NaCl exhibited an opposite trend for all of these factor
286 cterium Anabaena, pretreatment of cells with NaCl resulted in unusually enhanced tolerance to oxidati
295 sis demonstrated that the heated WPI and WPI+NaCl solutions had higher levels of aggregated protein,
297 I solutions with either 20mM added NaCl (WPI+NaCl), 5mM N-ethylmaleimide (WPI+NEM) or 20mM added NaCl
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
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。