ライフサイエンスコーパス: Se

1 Se content of G418-induced SELENOP was dependent on Se a

2 Se fortification was significant across different genoty

3 Se is essential for many species, including humans, but

4 Se-fortification decreased the antioxidant properties an

5 plicate measurements of 14 and 35microgL(-1) Se(IV), respectively.

6 hocytes and identified the photosensitizer 2-Se-Cl, which accumulates in stimulated T cells in propor

7 ronii tadpoles were exposed to dissolved (75)Se (as selenite) for 7 days and depurated until completi

8 esults of a two-dimensional solid-state (77) Se nuclear magnetic resonance (NMR) spectroscopic study

9 hains are characterized by their unique (77) Se NMR signatures and 2) the structure of amorphous Se c

10 Both (77)Se and (125)Te NMR chemical shifts of given chalcogenide

11 ChB-donor chalcogen atoms, heteronuclear (77)Se and (125)Te NMR were used to directly study how anion

12 Based on (77)Se NMR spectroscopy, a catalytic cycle for diselenide 8b

13 in the form of the buried volume and the (77)Se NMR chemical shift, in particular the sigmayy compone

14 The abrupt decline in delta(82/78)Se and Se/TOC values during the subsequent Shunga-France

15 c and Phanerozoic, when negative delta(82/78)Se values are observed in offshore environments, only a

16 We find that delta(82/78)Se values in offshore shales show a positive excursion f

17 west, shows evidence of negative delta(82/78)Se.

18 e precisely measured composition indicates a Se-rich FeSexTe1-x (0.6 < x < 0.8) as ascertained throug

19 Broccoli is a Se-hyperaccumulator plant, with Se-fertilization increas

20 e concentration and forms of Se accumulated, Se partitioning at the whole-plant and tissue levels, an

21 In addition, Se devices are air-stable, non-toxic, and extremely simp

22 Hyperaccumulation tends to negatively affect Se-sensitive ecological partners while facilitating Se-r

23 on microbiota were found to primarily affect Se bioaccessibility in the colon environment, with the p

24 umulation and tolerance in plants and algae, Se hyperaccumulation, and ecological and evolutionary as

25 signatures and 2) the structure of amorphous Se consists exclusively of infinity1Se chains.

26 roversy regarding the structure of amorphous Se relates to the relative fraction of Se atoms residing

27 ine allotropes of Se as well as of amorphous Se to unequivocally demonstrate that 1) the Se8 rings an

28 lms is approximately 25-300 nm red amorphous Se(0) aggregates of colloidal nanoparticles.

29 -structure spectroscopy showed red amorphous Se(0) with a first shell Se-Se interatomic distance of 2

30 nd steady-state kinetics with the SAM analog Se-adenosyl-l-selenomethionine (SeAM) as a cofactor surr

31 Selenium abundances and Se/TOC (total organic carbon) ratios similarly show a pe

32 rate in situ the same highly reactive Cd and Se precursors that were used in some of the original II-

33 otentially affecting species composition and Se cycling in seleniferous ecosystems.

34 rk, we investigate the Se concentrations and Se isotope systematics of groundwater and of U ore beari

35 developed for risk assessment of As, Cr, and Se in food, which is demonstrated here using three cooke

36 ultaneous speciation analysis of As, Cr, and Se in the bioaccessible fraction to determine the portio

37 ultaneous speciation analysis of As, Cr, and Se revealed that the simple act of cooking can convert a

38 ring potentially toxic elements (As, Cr, and Se) by inductively coupled plasma mass spectrometry (ICP

39 measured the internal nematode total Hg and Se concentrations for the highest concentrations of each

40 uggest that future assessments of the Hg and Se relationship should incorporate chemical compound int

41 and the concurrent reconfiguration of In and Se atoms across the layers.

42 existence of metal-Ti-atom incorporation and Se-anion defects, resulting in a high-spin-polarized cur

43 d was developed for inorganic Se [Se(IV) and Se(VI)] speciation analysis in Allium and Brassica veget

44 and Cr(VI)], and two Se species [Se(IV) and Se(VI)] were separated within 12 min.

45 to be significantly enriched in Ca, Na, and Se relative to desert soils.

46 optical emission spectrometry (ICP OES), and Se by graphite furnace atomic absorption spectrometry (G

47 ied as Playa-like, Desert-like, Ca-rich, and Se.

48 mass spectrometry (ICP-MS) to identify S and Se associations as proteins marker.

49 ibution in ReS2x Se2(1-x) alloy, where S and Se atoms are selectively occupied at different X sites i

50 broad range of trimeric and hexameric S- and Se-bridged inorganic macrocycles based on cyclophosphaza

51 The abrupt decline in delta(82/78)Se and Se/TOC values during the subsequent Shunga-Francevillian

52 Compared to SelenoPrecise and Se-ACE tablets, a yoghurt-based supplement exhibited a m

53 o determine the local structure of As(V) and Se(VI) complexes.

54 um phases such as basaluminite for As(V) and Se(VI) oxyanions, with adsorption capacities on the same

55 m(2) converts WSe2 into a mixture of WOx and Se-deficient WSe2.

56 iffered by stratum of high versus low Zn and Se.

57 elements (Na, K, V, Ni, Co, Cu, Zn, Ga, As, Se, Mo, Cd, Sn, Sb, Ba, W, and Pb), including air toxics

58 g, Al, P, K, Ca, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Sr, Mo, Cd, Sn, Sb, Ba, Hg, Pb, Bi, Th, and U) in gr

59 aring many other elements (e.g., Ni, Co, Au, Se, and platinum group elements) are significantly less

60 posure to atmosphere of rare earth-doped Bi2(Se, Te)3 thin films using x-ray absorption spectroscopy.

61 effectively substitute for Bi(3+) in the Bi2(Se, Te)3 matrix.

62 far unreported depletion of the bioavailable Se pool, a plausible driving mechanism of demonstrated n

63 le spatially separated in the top and bottom Se layers.

64 analysis, we identified pathways affected by Se status in rectal biopsies from 22 healthy adults, inc

65 e dithiocarbamate (APDC) complex followed by Se determination with electrothermal atomic absorption s

66 Specifically, S has been substituted by Se and Te in polythiophene, leading to polyseleophene an

67 2-benzisoselenazol-3(2H)-ones containing a C-Se-N bond.

68 r ligand (1,10-phenanthroline) facilitates C-Se bond formation during heating via a mechanism that li

69 ethylchalcogeno)-1,2,3-triazole (chalcogen = Se, Te) motif as a novel ChB donor for anion binding.

70 important but indirect factor in controlling Se as well as vanadium (V), cobalt (Co), nickel (Ni), zi

71 The Cu, Se and Zn levels in all the meals were comparable to tho

72 s obtained from other solution processed Cu2 Se thin films (<0.1 mW/(m K(2) )) and among the highest

73 flexible thermoelectric copper selenide (Cu2 Se) thin film, consisting of earth-abundant elements, is

74 The Cu2 Se thin film exhibits a power factor of 0.62 mW/(m K(2)

75 ledge, this is the first study demonstrating Se transference during metamorphic tissue remodelling.

76 in surface soil, rather than bedrock-derived Se (<0.1 mg/kg).

77 Fish treated with higher dietary Se doses (32.5 and 57.5 mug Se/g) exhibited impaired per

78 ople have been estimated to have low dietary Se intake.

79 uts could represent a good source of dietary Se and as an upgraded source of isoflavonoids.

80 he bioaccessibility of Se in three different Se-enriched food supplements and two different Se-enrich

81 -enriched food supplements and two different Se-enriched food crops, with reference to two pure Se st

82 corroborated experimentally using different Se fluxes, and supported theoretically using first-princ

83 ved on various substrates and with different Se content, x.

84 ssue levels, and the capacity to distinguish Se from sulfur.

85 show that selenate (Se(VI)) is the dominant Se species in Rosita groundwater, and while several up-g

86 eractions were only observed when the dosing Se solution concentration was 100-25,000 times greater t

87 f thorium, [K(18-crown-6)][Th(E)(NR2)3] (E = Se, 4; E = Te, 5), respectively.

88 tions for the highest concentrations of each Se compound.

89 troscopy indicated the presence of elemental Se (Se(0)).

90 ence of nano- or microparticles of elemental Se.

91 hile several up-gradient wells have elevated Se(VI), the majority of the ore zone and down-gradient w

92 suggest substantial promise for the emerging Se-rich Cu2 BaSnS4-x Sex family for high-efficiency and

93 s (2006-07, 2008-09 and 2009-10) to evaluate Se-enriched pasta through foliar fertilization at variou

94 d anti-cancer activities at levels exceeding Se nutritional requirements.

95 itive ecological partners while facilitating Se-resistant partners, potentially affecting species com

96 CCR contaminants, including SO4, Ca, Mn, Fe, Se, As, Mo, and V above background levels, were also ide

97 findings confirm the effectiveness of foliar Se fertilization to increase Se concentrations in durum

98 re observed in Ca and Mg, and the lowest for Se and Pb, by both infusion and decoction.

99 microm for GLS glass to about 15 microm for Se-added GLS glass defined by the 50% transmission point

100 through isoelectronic substitution of Te for Se have been prepared, and the crystal structure dilatio

101 vely, better resistance to interference from Se and Sb.

102 eneration of lithium selenocarboxylates from Se/LiEt3BH and acyl chlorides or carboxylic acids and th

103 food) or exceeded nutritional maximum (e.g. Se, 76% of wet food).

104 he interface, permitting the formation of Ga-Se bonds that help to passivate the underlying GaAs laye

105 GeSe displays a boat conformation for its Ge-Se six-membered ring ("six-ring"), while the previously

106 The Ge-Se interatomic distances extracted from XAS data show a

107 ant across different genotypes, with greater Se accumulation in landraces ('Timilia') and obsolete va

108 We utilized aqueous Hg/Se dosing molar ratios that were either above, below, or

109 ntrations in durum wheat grain, even at high Se rates (120gSeha(-1)).

110 acts as a tracer species, and a homogeneous Se-rich region is found nearing the TFMG/TE interface, w

111 Although concentrations of Co, Cr, Cu, I, Se and Zn where statistically higher in conventional mil

112 rtilization strategies to enrich broccoli in Se with minimal impairment of antioxidants properties.

113 ies to describe the impact of differences in Se status on colorectal expression patterns, revealing t

114 is is affected by physiologic differences in Se status.

115 olatilization of Se could play a key role in Se balance in other terrestrial environments worldwide.

116 gy; microorganisms play an important role in Se transformations in the environment.

117 The bioaccessibility of Se in Se-enriched food supplements and food crops was found to

118 By incorporating Se in the sulfide film, absorber layers with 1.55 eV ban

119 eness of foliar Se fertilization to increase Se concentrations in durum wheat grain, even at high Se

120 sulphur-containing compounds, but increased Se-methyl-selenocysteine content.

121 (VA-LLME) method was developed for inorganic Se [Se(IV) and Se(VI)] speciation analysis in Allium and

122 non-chromatographic separation of inorganic Se species in complex matrix samples such as garlic, oni

123 highly efficient (up to 89% of intracellular Se) and directly coupled to intracellular Se levels (R(2

124 ar Se) and directly coupled to intracellular Se levels (R(2) > 0.92) over an intracellular concentrat

125 nucleation point for the formation of large Se-Hg clusters, which can grow with age to over 5 mum in

126 d anticrossing interaction between localized Se states and the extended valence band states of the ho

127 respectively, together with highly localized Se(0) using the Se LIII edge.

128 hurt-based supplement exhibited a much lower Se bioaccessibility, possibly due to the presence of nan

129 these emissions via production of methylated Se compounds that volatilize into the atmosphere.

130 redict measured concentrations of methylated Se in natural waters.

131 th the exception of multifloral (Ca, Cr, Mo, Se), common heather (Mg, Na), bearberry (Ba, Fe, Pb) and

132 ieved by tuning the growth temperature or Mo:Se precursor ratio.

133 Through modelling Se biogeochemistry in China we found that deposition and

134 microM, which falls in the range of moderate Se nutritional status.

135 h higher dietary Se doses (32.5 and 57.5 mug Se/g) exhibited impaired performance in the latent learn

136 ionine (control, 2.3, 9.7, 32.5, or 57.7 mug Se/g dry weight) for 30 days.

137 netics of conversion, easy retrieval of nano-Se and the metabolic versatility of P. putida offer the

138 ion electron microscope (TEM) show that nano-Se particles synthesized by P. putida have a size range

139 ggers a slight elongation of the covalent Nb-Se bond, which weakens the covalent interaction and enha

140 arily in 4p orbitals of the four neighboring Se(2-) ligands, and Ag(+) is not oxidized.

141 it's deposition, resulting in negligible net Se input in soil.

142 o incorporate trace elements such as Co, Ni, Se, Au, and commonly As.

143 loral honey (Al, As, Be, Ca, Cr, Mn, Mo, Ni, Se, Th and U), common heather (Co, K, Mg, Na, V), sage (

144 , As, Ba, Cu, Co, Fe, K, Mg, Mn, Mo, Na, Ni, Se, Sb, U and Th (p<0.05, all) among honeys.

145 ne and down-gradient wells have little or no Se oxyanions.

146 shore environments, allowing nonquantitative Se reduction to drive the residual Se oxyanions isotopic

147 y-1,2-bisselenylvinylene (DESVS), with novel Se...O noncovalent conformational locks is designed and

148 us MSA inhibited angiogenesis at nutritional Se levels not only by down-regulating the expression of

149 ents to examine the energetics of O...S, O...Se, S...S, O...HC, and S...HC contacts and the associate

150 Subsequent addition of Se precursors to the partially etched nanorods in Zn ole

151 the chain and ring crystalline allotropes of Se as well as of amorphous Se to unequivocally demonstra

152 The minor amount of Se acts as a tracer species, and a homogeneous Se-rich r

153 The intimate association of Se(0) particles with protein and polysaccharide biofilm

154 onitoring post-mining natural attenuation of Se oxyanions at ISR sites.

155 the developmental stage at the beginning of Se-fortification, on antioxidant capacity, phenolics, gl

156 The bioaccessibility of Se in cereals ranged from 10% to 24%, that of pulses was

157 The bioaccessibility of Se in Se-enriched food supplements and food crops was fo

158 to examine in vitro the bioaccessibility of Se in three different Se-enriched food supplements and t

159 nificantly decreased the bioaccessibility of Se, SeMet and SeCys2.

160 ng estimation of saturation concentration of Se-methyl-selenocysteine in broccoli cv.

161 In the first step, small concentrations of Se and S were substituted simultaneously in the position

162 l variations, suggesting a seasonal cycle of Se volatilization and recondensation.

163 TexSe1-x alloy with respect to the degree of Se diffusion.

164 was developed for accurate determination of Se in the IL-enriched extracts and multivariate statisti

165 The diffusion of Se, which has the smallest atomic volume of all the elem

166 vacancies and subsequent P displacements of Se atoms around the vacancies in the resulting cobalt ph

167 Sub-micrometer XFI showed distributions of Se and endogenous metals, while Se K-edge X-ray absorpti

168 R-facility Figaro on the combined effects of Se deprivation and LDR gamma exposure in DNA repair knoc

169 here include beneficial and toxic effects of Se on plants, mechanisms of Se accumulation and toleranc

170 tions reveal that the synergistic effects of Se vacancies and subsequent P displacements of Se atoms

171 ens, but also gives rise to the evolution of Se-resistant specialists.

172 iquid (IL) was applied for the extraction of Se(IV)-ammonium pyrrolidine dithiocarbamate (APDC) compl

173 ies differ in the concentration and forms of Se accumulated, Se partitioning at the whole-plant and t

174 phous Se relates to the relative fraction of Se atoms residing in infinity1Se chains versus in Se8 ri

175 films is caused by a remarkable increase of Se content.

176 toxic effects of Se on plants, mechanisms of Se accumulation and tolerance in plants and algae, Se hy

177 Mechanisms of Se hyperaccumulation and its adaptive significance appea

178 ranted to explore the fate and metabolism of Se (and other metal and metalloids) during anuran develo

179 for predicting the stability and mobility of Se bioremediation products and understanding of Se bioge

180 e decreases could increase the prevalence of Se deficiency.

181 for the microbial dissimilatory reduction of Se(VI) to Se(IV) to Se(0).

182 e biosphere can be identified as a source of Se and of other trace elements in precipitation samples.

183 soil Se volatilization is similar to that of Se deposition, suggesting that Se volatilization offsets

184 bioremediation products and understanding of Se biogeochemical cycling.

185 This suggests that there was no upwelling of Se oxyanions from an oxic deep-ocean reservoir, which is

186 t that both deposition and volatilization of Se could play a key role in Se balance in other terrestr

187 igmayy component of the shielding tensor of [Se(NHC)] model compounds, respectively.

188 cheaper oils: rapeseed oil (R), sesame oil (Se) and sunflower oil (Su).

189 ent of G418-induced SELENOP was dependent on Se availability, and was completely suppressed by G418 u

190 action studies were conducted in the Cs/Sn/P/Se system.

191 (As, Ba, Cu, Fe, Mn, Cd, Cr, Hg, Mo, Ni, Pb, Se, Sb, Sn, and Zn) in three different pulse species: Vi

192 the trace elements: Cd, Cu, Fe, Mn, Ni, Pb, Se, Zn were determined in foods for 4-6, 7+ and 10+ mont

193 Plant Se accumulation affects ecological interactions with her

194 Plant Se accumulation and volatilization may be applied in cro

195 Elevated plant Se protects plants from generalist herbivores and pathog

196 subjects with suboptimal status (mean plasma Se = 0.86 muM).

197 11 controls with optimal status (mean plasma Se = 1.43 muM) and 11 subjects with suboptimal status (m

198 PM10 Se concentrations showed strong seasonal variations, sug

199 oribbon growth is narrowly defined by proper Se:Mo ratios, as corroborated experimentally using diffe

200 iched food crops, with reference to two pure Se standards, and changes in its speciation during intes

201 the abnormal changes in the chalcogen ratio (Se:Te) during the film growth and that the previously re

202 As liver regulates Se metabolism, we tested the aminoglycosides G418 and ge

203 ntitative Se reduction to drive the residual Se oxyanions isotopically heavy.

204 Tadpoles retained Se throughout metamorphosis, and partitioned the element

205 y to the environment and (Li2Fe)ChO (Ch = S, Se) melt congruently; the latter is advantageous for man

206 (Li2Fe)ChO (Ch = S, Se) possess cubic anti-perovskite crystal structures, wh

207 Both compounds (Li2Fe)ChO (Ch = S, Se) were tested as cathode materials against graphite an

208 the general composition (Li2Fe)ChO (Ch = S, Se, Te) are successfully synthesized.

209 Cs: the unary compounds Co6E8(PEt3)6 (E = S, Se, Te) and the binary compounds [Co6E8(PEt3)6][C60]2.

210 ds [Au4M4(mu3-E)4(IPr)4] (M = Ag, Au; E = S, Se, Te) has been synthesized from the combination of N-h

211 reatments for lead chalcogenide (PbE; E = S, Se, Te) QDs have lagged behind those of, for instance, I

212 iate [E....._ (S....._ )P(mu-NR)]2(2-) (E=S, Se) dianion, which can be reacted with electrophilic [Cl

213 M with W = Zr, Hf; H = Si, Ge, Sn; M = O, S, Se, Te) with identical band topology.

214 nctly different cosmochemical behavior of S, Se, Te and Sb within the proto-lunar disk, which is as o

215 tion was not accompanied by major loss of S, Se, Te, Sb from Moon-forming materials, consistent with

216 The high Z chalcohalides Hg3Q2I2 (Q = S, Se, and Te) can be regarded as of antiperovskite structu

217 transition-metal dichalcogenides VX2 (X = S, Se and Te) via first-principles calculations.

218 es, the lowest-lying excitons in WX2 (X = S, Se) are expected to be spin-forbidden and optically dark

219 egard, monolayer (ML) MX2 (M = Mo, W; X = S, Se) has drawn increasing attention due to its novel opto

220 dichalcogenides, MX2 (M=Mo, W, Tc, Re; X=S, Se, Te).

221 method has been used to produce Cu(In,Ga)(S,Se)2 (CIGS) solar cells.

222 In recent years, Cu2 ZnSn(S,Se)4 (CZTSSe) materials have enabled important progress

223 based on a tagging method that installs a S-Se bond in peptides that is cleavable upon 266 nm ultrav

224 from other hydride forming elements (As, Sb, Se) on Bi response by AAS using DBD and QTA atomizers wa

225 nce from other hydride-forming elements (Sb, Se, and Bi).

226 copy indicated the presence of elemental Se (Se(0)).

227 LLME) method was developed for inorganic Se [Se(IV) and Se(VI)] speciation analysis in Allium and Bra

228 cule, due to strong intramolecular secondary Se...N interactions, is completely planar.

229 Our results show that selenate (Se(VI)) is the dominant Se species in Rosita groundwater

230 Selenium (Se) exerts many effects beneficial to health.

231 Selenium (Se) is an essential element for the cell that has multip

232 ationship between mercury (Hg) and selenium (Se) toxicity is complex, with coexposure reported to red

233 activity we used arsenic (As) and selenium (Se).

234 Biogenic selenium (Se) emissions play a major role in the biogeochemical cy

235 in the supply of the trace element selenium (Se) as well as other essential trace elements to terrest

236 pinnata not only hyperaccumulates selenium (Se) to 0.5% of its dry weight, but also exhibits higher

237 References 1592 The importance of selenium (Se) for medicine, industry and the environment is increa

238 inic acid (MSA) is a metabolite of selenium (Se) in animal cells that exhibits anti-oxidative and ant

239 for the absolute quantification of selenium (Se) included in selenoprotein P (SEPP1), an important bi

240 1980-1999) global distributions of Selenium (Se), an essential trace element that is required for hum

241 s of volatile elements sulfur (S), selenium (Se), tellurium (Te), and antimony (Sb) in the silicate M

242 othesized that biosynthesis of the selenium (Se) transporter selenoprotein P (SELENOP) is particularl

243 cts of chronic dietary exposure to selenium (Se) on zebrafish cognition and also to elucidate possibl

244 roposed oxygen perturbations using selenium (Se) geochemistry, which is sensitive to redox transition

245 howed red amorphous Se(0) with a first shell Se-Se interatomic distance of 2.339 +/- 0.003 A.

246 innata showed higher rates of root and shoot Se accumulation and less competitive inhibition by sulfa

247 content will lead to overall decreased soil Se concentrations, particularly in agricultural areas; t

248 In Central China the rate of soil Se volatilization is similar to that of Se deposition, s

249 Contrary to small-scale studies, soil Se concentrations were dominated by climate-soil interac

250 es [Cr(III) and Cr(VI)], and two Se species [Se(IV) and Se(VI)] were separated within 12 min.

251 as a mechanism for altering tissue-specific Se burdens.

252 ate complexes, Th(ECH2SiMe3)(L3) (E = S, SS, Se, Te; 5-8).

253 pression patterns, revealing that suboptimal Se status could alter inflammatory signaling and cytoske

254 d cytoskeleton remodelling in the suboptimal Se status group.

255 h either selenite or selenate as substrates, Se methylation was highly efficient (up to 89% of intrac

256 y, phenolics, glucosinolates, sulphoraphane, Se-methyl selenocysteine and myrosinase in broccoli.

257 in reservoir sediments are likely to sustain Se toxicity for many years despite recent laws to limit

258 ductivity and Seebeck coefficient in Bi2 Te2 Se nanoplates, and bulk pellets made from them.

259 egression models gave r>0.77 confirming that Se dose and developmental stage largely determine the be

260 Importantly, our results demonstrate that Se biodistribution varies significantly throughout devel

261 It is hypothesised that Se deficiency, as it occurs in several parts of the worl

262 Furthermore, our results show that Se isotopes are excellent sensors for detecting and moni

263 Results suggest that Se-enriched chickpea sprouts could represent a good sour

264 ar to that of Se deposition, suggesting that Se volatilization offsets it's deposition, resulting in

265 The Se concentration decreased during milling (11%), while p

266 The Se content in the grain was increased by up to 35-fold t

267 In this work, we investigate the Se concentrations and Se isotope systematics of groundwa

268 iosynthesis can be severe, but depend on the Se status, and other parameters likely including age and

269 We show that the Se content of fish from lakes with the highest selenium

270 gether with highly localized Se(0) using the Se LIII edge.

271 When the Se/S concentration increases significantly, the system d

272 o investigate the mechanisms underlying this Se enrichment, we compared S. pinnata with the nonhypera

273 dry weight, but also exhibits higher tissue Se-to-sulfur (S) ratios than other species and its surro

274 of long-finned pilot whales are attached to Se-rich structures and possibly act as a nucleation poin

275 e importance of climate-soil interactions to Se distributions suggests that other trace elements with

276 ssimilatory reduction of Se(VI) to Se(IV) to Se(0).

277 crobial dissimilatory reduction of Se(VI) to Se(IV) to Se(0).

278 hane and glucosinolates' dependence on total Se supply was consistent with myrosinase activity below

279 ing three SeMNPV genes including a truncated Se-iap3 gene.

280 two Cr species [Cr(III) and Cr(VI)], and two Se species [Se(IV) and Se(VI)] were separated within 12

281 and was completely suppressed by G418 under Se-poor conditions.

282 e report that superconductivity emerges upon Se doping in CDW conductor ZrTe3 when the long range CDW

283 A previously proposed (V Se -V Cu ) divacancy model presents a widely accepted ex

284 the competitive bridging ability of S versus Se in these systems and the synthesis of the first air-s

285 The weak Se-N bond was not stable enough to survive the reaction

286 to elucidate possible mechanism(s) by which Se exerts its neurotoxicity.

287 ributions of Se and endogenous metals, while Se K-edge X-ray absorption spectroscopy indicated the pr

288 irment in zebrafish could be associated with Se-induced oxidative stress and altered dopaminergic neu

289 roccoli is a Se-hyperaccumulator plant, with Se-fertilization increasing its potential as a functiona

290 rs to sub-oxides and stepwise reactions with Se vapor to finally form MoSe2 .

291 f the B-B double bond enables reactions with Se(0) and Te(0) .

292 layer, we fully replace the top-layer S with Se atoms.

293 revention by influencing angiogenesis within Se nutritional levels.

294 the far-infrared conductivity of Pb1-x Sn x Se (x = 0.23-0.25) single crystals is dominated by the s

295 talline insulator, (001)-oriented Pb1-x Sn x Se in zero and high magnetic fields.

296 odynamically favored to occur when Pbx Sn1-x Se layers are interdigitated with TiSe2 monolayers.

297 depends on what is adjacent to the Pbx Sn1-x Se layers.

298 loy layers was discovered within [(Pbx Sn1-x Se)1+delta ]n (TiSe2 )1 heterostructures using electron

299 strategy to craft a set of CdSe/Cd(1-x)Zn(x)Se(1-y)S(y)/ZnS core/graded shell-shell QDs with suppres

300 s shift, the as-synthesized CdSe/Cd(1-x)Zn(x)Se(1-y)S(y)/ZnS QDs exhibited the suppressed re-absorpti

301 electrical contact resistivity, on a high-zT Se-doped AgSbTe2 substrate.