ライフサイエンスコーパス: cesium

1 bined with tissue concentrations of (134+137)Cesium.

2 thin-film systems containing corannulene and cesium.

3 between the sym-triazine radical cation and cesium.

4 its remarkable ion-exchange selectivity for cesium.

5 m or the permeability of calcium relative to cesium.

6 g altered current kinetics and inhibition by cesium.

7 el blockers barium and amantadine but not by cesium.

8 NH4 subset Rh4Ru3 has a higher affinity for cesium.

9 activated GIRK currents that were blocked by cesium.

10 ective potassium channel blockers barium and cesium.

11 nteraction studies in atomic systems such as cesium.

12 ommendation can be made for or against using cesium-131 or HDR monotherapy.

13 The methodology, which has been applied to cesium-134 and cesium-137 deposits within 80-km of the n

14 significant fission product radionuclides of cesium ((135)Cs and (137)Cs) at concentrations found in

15 From these recordings, the level of cesium-137 ((137)Cs) contamination was determined for in

16 The largest concern on the cesium-137 ((137)Cs) deposition and its soil contaminati

17 Cesium-137 ((137)Cs) with a half-life of 30.1 y causes t

18 -Dawley rats were exposed to 10 Gy WBI using Cesium-137 as the radiation source.

19 gy, which has been applied to cesium-134 and cesium-137 deposits within 80-km of the nuclear site, pr

20 mg/kg diet) and radiation exposure (0.375 Gy cesium-137 every other day for 16 d) on markers of oxida

21 e light from a synchrotron X-ray source or a cesium-137 gamma-ray source.

22 e light from a synchrotron X-ray source or a cesium-137 gamma-ray source.

23 We first tested cytotoxicity of cesium-137 irradiation plus venetoclax in 14 B-NHL cell

24 efficiency of 3.9% measured with an intense cesium-137 source.

25 Cesium-137 was deposited mostly in Pacific and Atlantic

26 We also report americium-241, cesium-137, plutonium-238, and plutonium-239,240 activit

27 We report here that treatment of cesium-137-irradiated Ptch1+/- mice with immunosuppressi

28 utonium-238, americium-241, bismuth-207, and cesium-137.

29 Lithium, sodium, potassium, rubidium, and cesium 2-benzoyl-1,1,3,3-tetracyanopropenides were chara

30 Extracellular application of cesium (3-9 mM) or ZD 7288 (25-100 microM) blocked Ih an

31 Interestingly, in the case of cesium (a co-contaminant of plutonium), no difference wa

32 Intracellular perfusion of cesium acetate (CsAc) and the sodium/potassium channel b

33 Cesium acetate was employed as a cationizing agent.

34 The cesium adsorbed on the column was effectively eluted wit

35 Cesium adsorption onto Illite has been widely studied, b

36 iate that dominates in the cross-coupling of cesium alkenylsilanolates.

37 In addition, intracellular cesium also blocked the inward current, suggesting the i

38 ne (NBQX, 1 microM), but not by inclusion of cesium and N-(2, 6-dimethylphenylcarbamoylmethyl) trieth

39 This reflects intrinsic differences between cesium and plutonium sorption/desorption behavior (charg

40 ifying mixed cationic conductance blocked by cesium and potassium conductances blocked by 4-aminopyri

41 rystal structures of complexes of FTHFS with cesium and potassium ions were examined and monovalent c

42 m classic empirical IMS data of atomic ions, cesium and potassium, each showing its own distinct form

43 Thus, cesium and rubidium are ten-coordinate, whereas potassiu

44 of freeze-thaw cycles on the mobilization of cesium and strontium in association with colloids in int

45 ively, increased and decreased the dissolved cesium and strontium, but both treatments increased the

46 Two intact cores were contaminated with cesium and strontium.

47 but both treatments increased the colloidal cesium and strontium.

48 wn blockers of these ion channels (barium or cesium and ZD 7288, respectively).

49 um from a feed of dissolved lithium, cobalt, cesium, and boric acid.

50 of formamidinium (FA), methylammonium (MA), cesium, and rubidium lead halides which provide power co

51 ferential flow paths through which colloids, cesium, and strontium were mobilized.

52 diological dispersal devices (RDDs), cobalt, cesium, and strontium, were studied by DMS to demonstrat

53 10(5) for molybdenum; the chemical yields of cesium are more than 85% for samples of less than 10 g.

54 sham-irradiated or irradiated with (1)(3)(7)Cesium at a dose of 10Gy.

55 3.51 electron volts) lower than that of the cesium atom (which has the lowest gas-phase ionization e

56 A single cesium atom trapped within the mode of an optical cavity

57 rd quantum limit for sensing the motion of a cesium atom.

58 formed by collisional electron transfer from cesium atoms to protonated peptides HAL, AHL, and ALH at

59 The motion of individual cesium atoms trapped inside an optical resonator is reve

60 A cesium base not only promoted alkylation of primary amin

61 With the cesium-based diode-pumped alkali laser and remote plasma

62 Cesium-based perovskite nanocrystals (PNCs) possess allu

63 liquid metal in perovskite films leads to a cesium-based ternary perovskite solar cell with stabiliz

64 diamines, and polyamines was developed using cesium bases in order to prepare secondary amines effici

65 The use of cesium benzoate as a base and a common phosphine ligand

66 cyclic sulfate 12 and its ring opening with cesium benzoate followed by saponification of the benzoa

67 es are obtained for potassium, rubidium, and cesium; binding wells are shallow and the central barrie

68 Cesium bis(perfluoro-triphenylborane)amide, Cs[H2NB2(C6F

69 an ion-pair receptor for cesium chloride and cesium bromide in nitrobenzene solution.

70 /mol larger for cesium chloride than for the cesium bromide.

71 icating the formation of an ion-paired 1:1:1 cesium:calix[4]pyrrole:halide complex.

72 rticle also highlights the first use of mild cesium carbonate as a cesium source for the construction

73 nd method involves the use of aryl chloride, cesium carbonate base, n-butyl-di-1-adamantylphosphine l

74 Cesium carbonate catalyzed hydrolysis then generated the

75 Subsequent aromatization using cesium carbonate gave rise to isopropylidene-protected h

76 Treatment with primary amines and cesium carbonate in a two-step sequence gives rise to 3-

77 s in the presence of copper(II) chloride and cesium carbonate in acetonitrile solvent is reported.

78 able ketones, and nitro groups provided that cesium carbonate is employed as the base.

79 ridine (secondary amine) in combination with cesium carbonate is necessary for effective direct aryla

80 nylmethanephosphonate (1) in the presence of cesium carbonate undergoes efficient 1,4-addition to Mic

81 ing in aqueous solution of two cesium salts, cesium carbonate, and cesium nitrate.

82 which, in the presence of sodium hydride or cesium carbonate, underwent nucleophilic cyclization to

83 anol and glyoxal (trimeric form) mediated by cesium carbonate, which affords in crystalline form 3-ni

84 Cesium carbonate-mediated anomeric O-alkylation of vario

85 Cesium carbonate-mediated reaction of 2-hydroxybenzaldeh

86 l was reproducible and dominated by cesiated cesium carboxylates [RCOOCs + Cs]+.

87 hese consists of a contact ion pair with the cesium cation and chloride anion both being bound within

88 n the calix[4]pyrrole-halide complex and the cesium cation are nearly the same within experimental un

89 e NH protons of a calixpyrrole subunit and a cesium cation sandwiched between two cone shaped calix[4

90 was not observed in the absence of a cobound cesium cation; however, it was seen in this solvent mixt

91 used to achieve direct ion exchange of large cesium cations for the small sodium cations found in the

92 Exceptionally high affinity for cesium cations was achieved in aqueous solution using tw

93 For example, sodium and cesium cations were studied to represent metal ions, tet

94 nitrido ligand bridging two uranium and one cesium cations.

95 The cesium chloride (CsCl) density gradient profile of virus

96 Mucins were isolated by cesium chloride (CsCl) gradient centrifugation and size

97 nt density and can be purified by banding in cesium chloride (CsCl) gradients.

98 x[4]pyrrole acts as an ion-pair receptor for cesium chloride and cesium bromide in nitrobenzene solut

99 HOX proteins regulate transcription we used cesium chloride centrifugation-based chromatin purificat

100 Cesium chloride density gradient centrifugation demonstr

101 tion followed by additional separation using cesium chloride density gradient centrifugation.

102 Mucins were separated by cesium chloride density gradient centrifugation.

103 In this work, 311 cesium chloride double perovskites (Cs(2)BB'Cl(6)) were

104 detected in Et743-treated CEM cells by using cesium chloride gradient centrifugation followed by top1

105 s substantially more effective than standard cesium chloride gradient purification.

106 ithout relying on tedious and time-consuming cesium chloride gradient separations and extractions.

107 purified adenovirus preparations to repeated cesium chloride gradient separations.

108 egree of precision and good agreement with a cesium chloride gradient/SDS-PAGE quantitation method of

109 etermined by sedimentation through isopycnic cesium chloride gradients.

110 100S, have a buoyant density (1.28 g/ml) on cesium chloride similar to that of HCV capsids from othe

111 le was found to be about 7 kJ/mol larger for cesium chloride than for the cesium bromide.

112 was that HGV was consistently more stable in cesium chloride than HCV.

113 t density of formaldehyde-fixed ribosomes in cesium chloride was 1.41 g/cm(3).

114 formations: from B1 (sodium chloride) to B2 (cesium chloride) crystal structures above 0.36 TPa, and

115 radient centrifugation, isopycnic banding in cesium chloride, and saline density flotation centrifuga

116 .0:1.6 blend of tetrabutylammonium chloride, cesium chloride, and the ionic liquid 1-butyl-3-methylim

117 Ribonucleic acid was isolated using the cesium chloride-guanidine method and was reverse transcr

118 The cesium chloride-isolated spores were further purified us

119 ion in hydrogen fluoride and the addition of cesium chloride.

120 The analysis of both cesium concentration monitoring in the source reservoir

121 the rock sample, the slower the decrease of cesium concentration, and the thinner the penetration de

122 A sharp increase in the pH and cesium concentrations in the receiving phase is observed

123 beta-diketones in THF, 1-3, with lithium and cesium counterions.

124 5) with mixed cations of MA(+) , FA(+) , and cesium (Cs(+) ).

125 tage-clamp recordings (n = 90) indicate that cesium (Cs) (5 mM) blocked 77.2% of the I(h) current, an

126 nts that form when an ultracold ground-state cesium (Cs) atom becomes bound within the electronic clo

127 nic crystal system for interacting with cold cesium (Cs) atoms.

128 The effect of external potassium (K) and cesium (Cs) on the inwardly rectifying K channel ROMK2 (

129 , surpassing the current best evaluations of cesium (Cs) primary standards.

130 study HC relaxation dynamics in LHP NCs with cesium (Cs), methylammonium (MA, CH(3)NH(3)(+)), and for

131 d to exploiting all-inorganic PVSCs by using cesium (Cs)-based perovskite materials, such as alpha-Cs

132 version efficiency (PCE) of triple-A cation (cesium (Cs)/methylammonium (MA)/formaminidium (FA)) pero

133 We measured the effects of changing internal cesium (Cs+) and external sodium (Na+) concentrations on

134 eading to complete block of the channel when cesium (Cs+) is the current carrier.

135 eprotonation in cyclohexylamine catalyzed by cesium cyclohexylamide.

136 be impossible for the open-field radioactive cesium decontamination applications.

137 The effective diffusion coefficient (De) for cesium decreased from 18.5 x 10(-11) m(2) s(-1) at full-

138 itrobenzene was determined from plots of the cesium distribution ratios vs cesium salt and receptor c

139 2)(OH)(12)], Cs(2)1, was prepared by heating cesium dodecahydro-closo-dodecaborate(2-), Cs(2)[closo-B

140 Cesium does not appear to create any electronic effects

141 of the larger formamidinium with the smaller cesium, due to octahedral tilting.

142 4) revealing the roles of the CsF base (and "cesium effect") in the Pd(0)/PCy3-catalyzed intermolecul

143 The cesium enolate of 6-phenyl-alpha-tetralone (CsPAT) has a

144 y to equilibria and reactions of lithium and cesium enolates in THF.

145 Crack pattern analyses revealed that the cesium-exchanged material exhibited a significantly lowe

146 The results showed that cesium exhibited a clear trend related to the saturation

147 ng of thick corannulene layers on top of the cesium film leads to the formation of a stable film comp

148 show that Ar4000+ bombardment combined with cesium flooding enhances secondary ion signals by a fact

149 The use of cesium flooding for the imaging of cells was also invest

150 Hence, cesium flooding has also a vast potential for SIMS analy

151 ination of ion bombardment with simultaneous cesium flooding is valid not only for monatomic ion bomb

152 erformed with only the presence of catalytic cesium fluoride and a stoichiometric amount of a disilan

153 CF3) in the presence of catalytic amounts of cesium fluoride have been studied.

154 ibition was attenuated by loading cells with cesium fluoride.

155 ve to the [Formula: see text] line of atomic cesium for [Formula: see text] atoms trapped along the P

156 ng an optical frequency comb referenced to a cesium fountain primary frequency standard.

157 tinuously, and efficiently remove cobalt and cesium from a feed of dissolved lithium, cobalt, cesium,

158 This method enables to separate cesium from large size of samples for the determination

159 tory released to the environment relative to cesium from venting Units 1 and 3 to be approximately 0.

160 The body-centered cubic A15-structured cesium fulleride Cs3C60 is not superconducting at ambien

161 Reduction of M(CNXyl)(6)I by cesium graphite gave the respective Cs[M(CNXyl)(6)], whi

162 lowed during spike trains, and block by 1 mM cesium had no effect on firing frequency.

163 evelopment, microwave atomic clocks based on cesium have achieved fractional uncertainties below 1 pa

164 The silicon dioxide is converted to cesium hexafluosilicate by dissolution in hydrogen fluor

165 analysis is accomplished by decomposing the cesium hexafluosilicate with concentrated sulfuric acid

166 etter cesium platinide, Cs2 Pt, and the salt cesium hydride CsH according to Cs9 Pt4 H identical with

167 (I)Cl complexes 2(R) (R = (i)Pr, (t)Bu) with cesium hydroxide in THF leads to the corresponding monom

168 honidinium bromide catalyst 9 (10 mol %) and cesium hydroxide provided S-alkylation products 2 at -35

169 In the presence of cesium hydroxide, molecular sieves, and DMF, benzenesele

170 low the cross-coupling of both potassium and cesium hydroxides with (hetero)aryl halides to afford a

171 s well as a notable luminescent response for cesium(I) ions and urea.

172 pectrometry (SIMS), the beneficial effect of cesium implantation or flooding on the enhancement of ne

173 oscopic origins of the structural effects of cesium in styrene epoxidation on silver catalysts.

174 Low coverages of cesium induce a (1 x 2) missing-row reconstruction of th

175 d on the Ag(111) microfacets produced by the cesium-induced reconstruction, which leads to selectivit

176 ng, high-resolution multielement images of a cesium-infiltrated Opalinus clay rock were recorded usin

177 ntials was a tetrodotoxin-insensitive (TTX), cesium-insensitive, voltage-independent, cationic flux c

178 Using cesium iodide cluster signals, we show that the mass ran

179 Interpretation of SID spectra for cesium iodide clusters was greatly simplified with IM pr

180 flat-panel x-ray detector with a structured cesium iodide scintillator layer and an amorphous silico

181 monolithic glass substrate with a structured cesium iodide scintillator layer and an amorphous silico

182 ibution becomes homogenized upon addition of cesium iodide, either alone or with rubidium iodide, for

183 mance is assessed using both particle-phase (cesium iodide, glycine) and gas-phase (dimethylamine, di

184 ations as low as 10(2) ng m(-3)) composed of cesium iodide, levoglucosan, and levoglucosan within a c

185 ient, probably because of its chelation with cesium ion.

186 icient (Kd) for absorbing of the radioactive cesium ion.

187 reaching optimum conditions for the largest cesium ion.

188 electivity of this extraction process toward cesium ions and the use of a sacrificial cation exchange

189 In particular, cesium ions are found to induce pentameric assembly of D

190 resulting in either expulsion or trapping of cesium ions depending on the anion employed.

191 Solvent extraction of cesium ions from aqueous solution to hydrophobic ionic l

192 orms of 1 a, both forming pai-complexes with cesium ions in the solid state.

193 r zero levels of potassium, rubidium, and/or cesium ions.

194 ial for selectively trapping the radioactive cesium ions; its high tendency to form stable colloids i

195 rradiated (14 Gy total body irradiation in a cesium irradiator).

196 re subjected to 12 Gy gamma-irradiation in a cesium irradiator.

197 h 12 Gy of whole-body gamma-irradiation in a cesium irradiator.

198 lar behavior could have been expected, since cesium is known to diffuse in the same parts of the pore

199 G50W-X8 columns and sensitive measurement of cesium isotopes with triple quadrupole inductively coupl

200 D) appeared to be higher for iodine than for cesium isotopes.

201 , AMADs for (131)I were about half those for cesium isotopes.

202 the application of the inorganic perovskite cesium lead bromide (CsPbBr(3)) quantum dots (QDs) as hi

203 itaxial films of inorganic materials such as cesium lead bromide (CsPbBr(3)), lead(II) iodide (PbI(2)

204 The cesium lead bromide (CsPbBr3 ) created using a new poly(

205 d X-ray diffraction, performed on perovskite cesium lead bromide nanocrystals, maps the lattice respo

206 idual three-dimensional and zero-dimensional cesium lead bromide PNCs.

207 Cesium lead halide (CsPbX3) perovskite nanocrystals (NCs

208 All-inorganic cesium lead halide (CsPbX3, X = Br(-), I(-)) perovskites

209 ful synthesis of brightly emitting colloidal cesium lead halide (CsPbX3, X = Cl, Br, I) nanowires (NW

210 synthesis of quantum confined all inorganic cesium lead halide nanoplates in the perovskite crystal

211 he low-temperature, solution-phase growth of cesium lead halide nanowires exhibiting low-threshold la

212 fect formation and the origin of emission in cesium lead halide perovskite materials, which foster th

213 tical properties of presynthesized colloidal cesium lead halide perovskite nanocrystals (NCs), from g

214 Cesium lead halide perovskite quantum dots (QDs) have ga

215 s particularly pressing for the novel NCs of cesium lead halide perovskites (CsPbX(3); X = Cl, Br) ow

216 Blending phenylethylammonium chloride into cesium lead halide perovskites yields a mixture of two-d

217 y of their pure inorganic counterparts, like cesium lead halides (CsPbX3), lags far behind.

218 e materials are known for their instability, cesium lead halides offer a robust alternative without s

219 The emergence of cesium lead iodide (CsPbI(3) ) perovskite solar cells (P

220 Cesium lead iodide (CsPbI(3)) perovskite has shown great

221 nthesize single crystals of perovskite-phase cesium lead iodide (gamma-CsPbI(3)) that are kinetically

222 to passivate the surface of a formamidinium-cesium lead iodide perovskite (Cs(0.08) FA(0.92) PbI(3)

223 Herein, we report that cesium lead iodide perovskite quantum dots (CsPbI3 QDs)

224 -based ionic compound into the formamidinium-cesium lead-trihalide perovskite absorber.

225 timony, arsenic, barium, beryllium, cadmium, cesium, lead, mercury, platinum, thallium, tin, and uran

226 small crystals as well as larger rubidium or cesium leucite crystals.

227 either tetragonal rubidium leucite or cubic cesium leucite.

228 Improvements required to obtain a cesium-limited frequency measurement are described and a

229 Post (137)Cs removal, the cesium-loaded sRF column was eluted with 0.45 M HNO(3).

230 Using a cesium matter-wave interferometer near a spherical mass

231 in hexamethylphosphoramide with potassium or cesium metal.

232 esized by chemical reduction with sodium and cesium metals, and crystallized as the corresponding sal

233 ne metals including barium, cadmium, cobalt, cesium, molybdenum, lead, antimony, thallium, tungsten,

234 raphene oxide (GO) with Cs(2)CO(3) to afford Cesium-neutralized GO (GO-Cs), GO derivatives with appro

235 porcelain powder was mixed with rubidium or cesium nitrate and heat-treated.

236 n of two cesium salts, cesium carbonate, and cesium nitrate.

237 obilization of historic (pre-Fukushima) (137)cesium observed concurrently in these soils suggests tha

238 The adsorption of a small amount of cesium on Ag(110) redirects the partial oxidation produc

239 icant influence on the binding properties of cesium on soil.

240 There was no effect of either 10 mM K or cesium on the high open probability (P(o) = 0.97 +/- 0.0

241 rred as soon as ROMK was exposed to external cesium or 10 mM K.

242 medium-sized neuron and was blocked by 1 mm cesium or 15 microm ZD7288.

243 ed when methylammonium (MA) is replaced with cesium or formamidinium (FA).

244 ow concentrations, selected cations (such as cesium or rubidium ions) exhibit an effective reduction

245 polymers (BCP)) using either ultralow energy cesium or the more recently introduced C60(++) (under NO

246 e as a cesium source for the construction of cesium organometallic scaffolds.

247 s use the solid polymer, polyethylene oxide: cesium perchlorate (PEO:CsClO(4)), to induce degenerate

248 cation, positive reversal potential, limited cesium permeability, and sensitivity to SOCE channel blo

249 ons over sodium (PK/PNa = 2.68 +/- 0.21) and cesium (PK/PCs = 1.39 +/- 0.03) ions.

250 This cesium platinide hydride can formally be considered as a

251 lt of the "alloy" cesium-platinum, or better cesium platinide, Cs2 Pt, and the salt cesium hydride Cs

252 e considered as a double salt of the "alloy" cesium-platinum, or better cesium platinide, Cs2 Pt, and

253 the stable stoichiometries and structures of cesium polynitrides at high pressures.

254 re similar with pipette solutions containing cesium, potassium, or sodium.

255 idated this hypothesis through the prototype cesium-potassium system investigated experimentally by D

256 refer the CF(3) end of the molecule, whereas cesium prefers the Br end of the molecule.

257 ot achieve the same quality of images as the cesium primary ion source used to produce negative secon

258 Higher AMAD for cesium probably results from higher AMAD observed at the

259 cobalt (Ptrend = 0.59), 1.31 (0.90-1.91) for cesium (Ptrend = 0.29), 1.76 (1.24-2.50) for molybdenum

260 A new family of mixed anion cesium rare earth silicates exhibiting intense scintilla

261 and a (3 x 5) surface oxide structure on the cesium-reconstructed Ag(110) surface.

262 Highly radioactive cesium-rich microparticles (CsMPs) released from the Fuk

263 ring in the source reservoir and post-mortem cesium rock concentration profile of the samples was car

264 ng the van der Waals repulsive force between Cesium Rydberg atoms located inside different cavities i

265 m plots of the cesium distribution ratios vs cesium salt and receptor concentration, indicating the f

266 The addition of KClO(4) to these cesium salt complexes leads to a novel type of cation me

267 In this study, we have chosen the cesium salt of BiEDTA (CsBiEDTA) and have investigated t

268 The cesium salt of the icosahedral borane anion dodecahydrox

269 pe and position of the anion employed in the cesium salt, the enhanced strength of Tl...pi vs Cs...pi

270 ious N-heterocycles 1a-l using potassium and cesium salts in DMSO is described.

271 r(-), and NO(3)(-) but will bind these other cesium salts in the absence of fluoride, both in solutio

272 Specifically, the sodium and cesium salts of complexes of Bi/EDTA, Pb/EDTA, Cd/EDTA,

273 the hydroxide and carbonate anions as their cesium salts, as confirmed by (1) H NMR spectroscopic ti

274 y the structuring in aqueous solution of two cesium salts, cesium carbonate, and cesium nitrate.

275 eceptor forms stable complexes with the test cesium salts, CsCl and CsNO(3), in solution (10% methano

276 he liquid-liquid extraction-based removal of cesium salts, specifically CsOH and Cs2 CO3 , from highl

277 methyl-11H-benzo[b]fluorene, has a pK on the cesium scale of 23.39.

278 ur Li scale, pK(Li) = 22.09, compared to the cesium scale, pK(Cs) = 28.60.

279 as caused by the activation of a barium- and cesium-sensitive inwardly rectifying potassium channel.

280 Three new cesium silver(I) copper(I) cyanides with three-dimension

281 The structural transformations between cesium silver-copper cyanides under modest conditions, b

282 the first use of mild cesium carbonate as a cesium source for the construction of cesium organometal

283 mpared to the conventional duoplasmatron and cesium sources.

284 The cesium stabilizes the oxametallacycle intermediate and h

285 eproducibility exceeding that of the primary cesium standard.

286 ertainty within a factor of 3 of that of the cesium standard.

287 CPL activity ever measured was observed for cesium tetrakis(3-heptafluoro-butylryl-(+)-camphorato) E

288 Comparable performance is also achieved for cesium tin iodide solar cells with en loading, demonstra

289 rate the use of the lead-free, all-inorganic cesium tin-germanium triiodide (CsSn(0.5)Ge(0.5)I(3)) so

290 and in the presence of trimethylamine and of cesium, two competitive inhibitors.

291 KMS-1 displays significant cesium uptake both under strongly acidic (pH 0.7-2.6) or

292 hemical-transport code where the sorption of cesium was described by a multisite ion-exchange model.

293 Complexation of cesium was evidenced by (133)Cs NMR spectroscopy and by

294 Cesium was simply released by acid leaching using aqua r

295 The diffusion of cesium was studied in an unsaturated core of Callovo-Oxf

296 For diastolic blood pressure, urinary cesium was tentatively replicated; however, this factor

297 on, and the thinner the penetration depth of cesium was.

298 Child blood levels of copper and cesium were associated with higher BMI, and levels of or

299 tal samples by chromatographic separation of cesium with AMP-PAN and AG50W-X8 columns and sensitive m

300 nalysis indicated that the concentrations of cesium, zinc, and selenium were significantly reduced in