ライフサイエンスコーパス: Zn

1 Zn(2+)-binding sites are also recognized by other first-

2 Zn(II) was also a viable templating metal.

3 ) (Cu), 0.02mugL(-1) (Pb), and 0.10mugL(-1) (Zn).

4 porphyrin and free base porphyrin (Zn(i + 2)-Zn(i + 6)), and highly efficient energy transfer was dem

5 ivalent metal ions including Ca(2+), Cd(2+), Zn(2+), Ni(2+), Co(2+), and Sn(2+) are also studied, and

6 2+), Cu(2+), Pb(2+), Hg(2+), Mn(2+), Ni(2+), Zn(2+), Co(2+) and Cd(2+) at room temperature.

7 6.4 kW kg(-1) (based on the cathode and 200% Zn anode), making it a promising candidate for high-perf

8 Co, Cd and Cr; (2) Cu and Al; (3) Fe and (4) Zn.

9 Cu), from 32 to 42% (Pb) and from 38 to 58% (Zn).

10 urement of the diagnostic (68)Zn/(66)Zn, (64)Zn/(66)Zn, and (68)Zn/(64)Zn ratios, from which the thre

11 (68)Zn/(66)Zn, (64)Zn/(66)Zn, and (68)Zn/(64)Zn ratios, from which the three different isotopic forms

12 ar interior source with homogeneous delta(66)Zn approximately +1.4 per thousand.

13 ous measurement of the diagnostic (68)Zn/(66)Zn, (64)Zn/(66)Zn, and (68)Zn/(64)Zn ratios, from which

14 of the diagnostic (68)Zn/(66)Zn, (64)Zn/(66)Zn, and (68)Zn/(64)Zn ratios, from which the three diffe

15 nostic (68)Zn/(66)Zn, (64)Zn/(66)Zn, and (68)Zn/(64)Zn ratios, from which the three different isotopi

16 multaneous measurement of the diagnostic (68)Zn/(66)Zn, (64)Zn/(66)Zn, and (68)Zn/(64)Zn ratios, from

17 reases in the grain: Mn, -28.3%; Fe, -26.7%; Zn, -21.9%; Mg, -22.7%; Mo, -40.4%; K, -22.4%; and Ca, -

18 A Zn/AcOH-mediated reduction of the nitro functionality fo

19 asymmetries in the oxygen (O) 1s peak, and a Zn:O intensity close to 1:1.

20 entary alpha,gamma-cyclic peptides bearing a Zn porphyrin cap that is used for the selective recognit

21 Herein, we report a Zn-ProPhenol catalyzed aza-Darzens reaction using chlori

22 We report a Zn-ProPhenol catalyzed reaction between butenolides and

23 s a cap domain and a catalytic domain with a Zn(2+) bound at its active site.

24 MMP-13 and surround the catalytically active Zn(2+) ion without chelating to the metal.

25 ses Zn(2+) from intracellular vesicles after Zn(2+) overload.

26 ements and heavy metals (Cd, Cr, Cu, Co, Al, Zn, As, Pb and Fe) in 22 varieties of cooked rice using

27 In addition, we observed an alternative Zn-coordination conformation around the active center.

28 nce, with rapid synaptic entry of Ca(2+) and Zn(2+) contributing more in CA3, but with delayed and lo

29 ped CsPb1-xMxBr3 NCs (M= Sn(2+), Cd(2+), and Zn(2+); 0 < x </= 0.1), with preservation of the origina

30 ease and its permeation through Ca(2+)- (and Zn(2+))-permeable AMPA channels in CA3 and Zn(2+) mobili

31 nyl) ligand with a 60 degrees bite angle and Zn(II) ions.

32 d Zn(2+))-permeable AMPA channels in CA3 and Zn(2+) mobilization from MT-III predominating in CA1.

33 s were chosen for further analysis of Cd and Zn tolerance variation, which is evident at different pl

34 the exception of excessive amounts of Cu and Zn in one sample.

35 Cu and Zn ions are essential in most living beings.

36 Moreover, Cu- and Zn-AMSs enhanced maturation and cytokine release of bone

37 mpact than water stress on K, Ca, Cu, Fe and Zn levels.

38 servatives containing Al, Ca, Cu, Na, K, and Zn.

39 d G3 triangles by mixing organic ligands and Zn(II) , however, only generated a mixture of G1 and G2,

40 recipitates caused rapid depletion of Mg and Zn solute atoms in the MPZ.

41 ef is an important source of Cu, Fe, Mg, and Zn to the human diet.

42 In this paper, Cu, Fe, Mn and Zn contents in transgenic (T - MSOY7122RR) and non-trans

43 rmination of K, Ca, Mg, S, P, Cu, Fe, Mn and Zn in 72 guarana seed samples from Bahia state.

44 w approach to the analysis of Cu, Fe, Mn and Zn in flaxseed was developed based on infrared-assisted

45 in shoot Ca, Mg, P, Fe, and Cu, while Mn and Zn increased under salinity.

46 l, P, and transition metals (Fe, Cu, Mn, and Zn) were exchanged during incubation at 37 degrees C.

47 oscopy, micro X-ray fluorescence (muXRF) and Zn isotope measurements was applied to soil, plant organ

48 take at pH 4 corresponds with altered Ni and Zn adsorption mechanisms.

49 e and Mn mobilization, removal of Co, Ni and Zn and found evidence for the concurrent release and pre

50 e investigate the effect of Mn(II) on Ni and Zn binding to phyllomanganates of varying initial vacanc

51 The strong uptake of metals such as Ni and Zn by phyllomanganates results from adsorption on or inc

52 tration of metals such as Cu, Pb, Cd, Ni and Zn in two subspecies of Lactuca sativa L. and in the soi

53 issolved Mn(II) decreases macroscopic Ni and Zn uptake at pH 4 but not pH 7.

54 C. dubia was exposed to elevated Cu, Ni, and Zn concentrations, chemically fixed, dehydrated, stained

55 g the responses of the diatom to ZnO-NPs and Zn(2+) under various regimes of temperature and salinity

56 Inhibitor blends (Zn+orthophosphate and Zn+NOM+orthophosphate) had stronger inhibitory effects c

57 ionally defined speciation of Cd, Cu, Pb and Zn in apple beverages by anodic stripping chronopotentio

58 tection limits (DLs) achieved for Cu, Pb and Zn were 0.04mugL(-1) (Cu), 0.02mugL(-1) (Pb), and 0.10mu

59 The mean total concentrations of Cu, Pb and Zn were 69+/-20, 7.3+/-3.3, and 129+/-59mugL(-1) in appl

60 Fungi exposed to As, Cd, Cr Cu, Ni, Pb, and Zn showed that metal resistance depends on the microbial

61 ic Zn-cell wall complexes, respectively) and Zn-thiol species were observed in the roots, rhizomes an

62 e element (As, Ca, Cr, Cu, Fe, Mn, Ni, S and Zn) distributions in the root system Spartina alterniflo

63 The Cu, Se and Zn levels in all the meals were comparable to those in m

64 Mn, Cd, Cr, Hg, Mo, Ni, Pb, Se, Sb, Sn, and Zn) in three different pulse species: Vigna unguiculata

65 on of traditional RFBs, such as vanadium and Zn-Br2 RFBs, is limited due to a number of challenges re

66 /H2 O and subsequent self-exchange of Zn and Zn(2+) at the Zn/H2 O interface.

67 il)phthalonitrile in the presence of anhydro Zn(II) acetate and a strong organic base (DBU).

68 to symplastic Zn-organic acid and apoplasmic Zn-cell wall complexes, respectively) and Zn-thiol speci

69 Low-cost, environment-friendly aqueous Zn batteries have great potential for large-scale energy

70 be significant for essential metals such as Zn that are well regulated by metabolic processes.

71 ential candidate elements linking asparagus (Zn, P, Cr, Mg, B, K) and pistachio (Mn, P, Cr, Mg, Ti, B

72 ts reveal that the presence of the copper at Zn sites induces ferromagnetism at room temperature, con

73 otif previously demonstrated with free-base, Zn(II), and Ni(II) porphyrins.

74 s by the B1 enzymes NDM-1 and BcII in the bi-Zn(II) form, the mono-Zn(II) B2 Sfh-I and the mono-Zn(II

75 nd was used to coordinate with biocompatible Zn(2+) and encapsulate the photosensitizer chlorin e6 (C

76 Inhibitor blends (Zn+orthophosphate and Zn+NOM+orthophosphate) had stronge

77 cereal crops is critical for improving both Zn content and tolerance to low-Zn soils.

78 is a G-protein-coupled receptor activated by Zn(2+).

79 u(I) metallopeptide ions that were formed by Zn(II) displacement from the parent zinc fingers (ZFs).

80 the stabilization of the OH* intermediate by Zn atoms, while a pure Pt system forms highly stable COH

81 a modular structure that includes seven CCCH Zn fingers that bind to A-rich RNAs and fingers 5-7 are

82 ot reactions utilizing a Lewis acid BDI(CF3)-Zn-N(SiMe3)2 (1) catalyst.

83 sidues to generate enzymes that had a common Zn(2+) bimetallo core but little sequence similarity and

84 les using snails enriched with a less common Zn stable isotope.

85 we synthesized novel biologically compatible Zn(2+)/Ln(3+) metallacrowns (MCs) that possess attractiv

86 ld have high heavy metal contents (e.g., Cr, Zn, Ni, Sn, etc.) and the capacity to remove dissolved s

87 re analyzed and indicated the absence of Cr, Zn and Cu in the samples, except for Cu in strawberry ju

88 and 17 other elements (Na, K, V, Ni, Co, Cu, Zn, Ga, As, Se, Mo, Cd, Sn, Sb, Ba, W, and Pb), includin

89 rmation to the concentrations of Cd, Cr, Cu, Zn, Pb, Ni, Hg and Fe in wheat grains.

90 blood samples, Na, P, S, Cl, K, Ca, Fe, Cu, Zn, and Br elemental concentrations were determined.

91 titative determination of K, Ca, Mn, Fe, Cu, Zn, Br, Rb, Sr, Pb, As and Sn.

92 The main absorption lines for Cu, Zn and Si and secondary lines for Mn and Mg were selecte

93 Previously, we found that human Cu, Zn-superoxide dismutase (SOD1) is S-acylated (palmitoyla

94 Be, B, Mg, Al, P, K, Ca, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Sr, Mo, Cd, Sn, Sb, Ba, Hg, Pb, Bi, Th, and

95 equential multi-element determination of Cu, Zn, Mn, Mg and Si in beverages and food supplements with

96 estigated the history of heavy metal (V, Cu, Zn, Cd, Hg, Tl, Pb, U) pollution in Lake Baikal seals ov

97 Cu,Zn-SOD isolated from egg yolk had an optimum at pH 6.

98 Such bimetallic Cu,Zn-SODs are widespread, from the periplasm of bacteria t

99 its mitochondrial (Mn-SOD) and cystolic (Cu,Zn-SOD) isoform were measured.

100 in glaucoma patients (p = 0.048) however, Cu,Zn-SOD was not.

101 Biochemical characteristics of Cu,Zn-SOD derived from hen egg white and egg yolk were dete

102 We focused on Cu-Zn superoxide dismutase (SOD1), which protects cells fro

103 Cu/Zn superoxide dismutase (SOD1) reduction prolongs surviv

104 gregates of biomolecules, e.g., of enzyme Cu/Zn-superoxide dismutase, abnormal aggregation of which i

105 y suppressed by oligomers of mutant human Cu/Zn superoxide dismutase 1 (SOD1), which are associated w

106 ly shown that ALS-associated mutations in Cu/Zn superoxide dismutase 1 (SOD1) impair axonal transport

107 Ubiquitous expression of mutant Cu/Zn-superoxide dismutase (SOD1) selectively affects motor

108 revious studies have shown that levels of Cu/Zn superoxide dismutase (CSD) are down-regulated by miR3

109 nal death; under these conditions, cytosolic Zn(2+) rises persisted for 10-30 min after OGD, followed

110 utathione prevents TRPM7-dependent cytosolic Zn(2+) influx.

111 harmful because of the release of cytotoxic Zn(2+) ions during dissolution reactions.

112 oxygen species (ROS) trigger TRPM7-dependent Zn(2+) release from the vesicles, whereas reduced glutat

113 he alpha3 and L3 regions, which flank the di-Zn(II) active site, were selectively (19) F-labeled usin

114 Each Zn(2+) has two bis-coordinated histidine ligands, which

115 nergies and electron donor strengths, either Zn(II)Porphyrins or Zn(II)Phthalocyanines were linked to

116 Fe3 Pt/Ni3 FeN bifunctional catalyst enables Zn-air batteries to achieve a long-term cycling performa

117 lve the responses of two genetically encoded Zn(2+) sensors at a range of time points spanning severa

118 free Zn(2+) through influx of extracellular Zn(2+) ) were mostly independent of oxidative stress.

119 ive cell imaging revealed that extracellular Zn(2+) exerted rapid inhibitory effects on Orai1-mediate

120 ons of the following molar ratios: Zn:Cu, Fe:Zn, and Fe:Mn, pairs of elements that have been shown to

121 for Mg, 200mgL(-1) for Si and 13mgL(-1) for Zn.

122 Mn-transporting CDF with lower affinity for Zn.

123 m 18% of the recommended daily allowance for Zn, to 70% for Mn and Mo).

124 ure an equilibrium dissociation constant for Zn(2+) and human serum albumin (Kd = (5.62 +/- 0.93) x 1

125 chically functionalized hybrid electrode for Zn-air batteries is discussed that requires no carbon.

126 plexes and a five-coordinate environment for Zn(II) analogs.

127 e cooperative hydrolysis of GVL by framework Zn-OH and Bronsted acidic sites to butene and then to ar

128 A free Zn concentration of 1.76mumolL(-1) determined with DMT w

129 ces a marked redistribution of cellular free Zn(2+), increasing cytosolic free Zn(2+) and lowering fr

130 lular free Zn(2+), increasing cytosolic free Zn(2+) and lowering free Zn(2+) in the S(E)R.

131 metal stress (increase in intracellular free Zn(2+) through influx of extracellular Zn(2+) ) were mos

132 sing cytosolic free Zn(2+) and lowering free Zn(2+) in the S(E)R.

133 DMT was in excellent agreement with the free Zn concentration independently provided by the electroan

134 .g., Au, In, and Lu) to >1 mg day(-1) (e.g., Zn, Sc, Y, Nb, and Gd) and >1 g day(-1) (e.g., for P, Fe

135 ity found in oxide semiconductors like In-Ga-Zn-O (IGZO).

136 l filter materials in the order of Pb > Cu > Zn > Ni.

137 the reaction is observed [Cu(II) > Fe(II) > Zn(II)], which is mirrored in in vitro DNA-damaging outc

138 H2O2/Zn(2+) induced concentration-dependent increases in cyto

139 Pathological concentrations of H2O2/Zn(2+) induced substantial cell death that was inhibited

140 ronmental contaminants (Dioxins, PCBs, HBCD, Zn, Cu, Cd, Pb, As) were measured at significantly highe

141 r (70%) with canonical bidentate hydroxamate-Zn(2+) coordination geometry and a minor conformer (30%)

142 conformer (30%) with monodentate hydroxamate-Zn(2+) coordination geometry, reflecting a free energy d

143 ith varying Lewis acidity, including Ni(II), Zn(II), Al(III), Ti(IV) and Mo(VI), are anchored as meta

144 e structures of adsorbed GVL and immobilized Zn species in combination with EXAFS and NMR spectroscop

145 mise as efficient air electrode catalysts in Zn-air batteries.

146 RP-1 activation as an important mechanism in Zn(2+)-induced TRPM2 channel activation and, TRPM2-media

147 diastereoselectivity and regioselectivity in Zn-catalyzed allenylation reactions of N-protected l-alp

148 lactating mice and cultured MECs resulted in Zn(2+)-mediated degradation of phosphatase and tensin ho

149 Despite the similarity in Zn-coordinating donor groups, the fractionation factors

150 terms of content of protein (14% increase), Zn (45%), Ca (72%), and Fe (151%).

151 hibitory effects compared to each inhibitor (Zn, orthophosphate or NOM) alone, whereas Zn+NOM showed

152 Instead, Zn simulated the transcriptional response of typical Fe-

153 assess the consequences of the intracellular Zn(2+) accumulation, we used OGD exposures slightly shor

154 (II) and Co(II), or the noncognate metal ion Zn(II).

155 er aggregations and released less zinc ions (Zn(2+)) at greater temperature and salinity, toxicity of

156 but in this case the primary divalent ion is Zn(2+) rather than Ca(2).

157 t rs13266634 is associated with higher islet Zn concentration (C/C genotype: 16792 +/- 1607, n = 22,

158 a new diluted magnetic semiconductor, (Ba,K)(Zn,Mn)2As2 (BZA), with high Curie temperature was discov

159 The accumulation of labeled Zn by the earthworms showed a direct relationship with t

160 c acid) and minerals (K, Ca, Mg, Na, Fe, Li, Zn) were also higher in pressed honey.

161 rocess of allene dissolution, lithiation, Li-Zn transmetallation, and asymmetric propargylation provi

162 lt 14053 demonstrate that isotopically light Zn condensates also occur on some mare basalts after the

163 Increased expression in response to low Zn levels was observed for several of the wheat ZIPs and

164 proving both Zn content and tolerance to low-Zn soils.

165 following order: Mo(VI) < Ti(IV) < Al(III) < Zn(II) < Ni(II).

166 pairs, {[Tism(Pr(i)Benz)]M}[HB(C6F5)3] (M = Zn, Mg), which are rare examples of these metals in trig

167 M = Ru, Os)-(porphinato)metal(II) (PM'; M' = Zn, Pt, Pd) molecular architecture (M-(PM')n-M), wherein

168 Our results show that ZntB mediates Zn(2+) uptake, stimulated by a pH gradient across the me

169 (A = alkali metal, M = alkaline earth metal, Zn, Cd, or Pb) materials indicates that, on average, sma

170 The bioaccessibility of Ca, Cu, Fe, Mg, Zn, and crude protein was evaluated after submitting bee

171 magnesium pins (as-drawn pure Mg, as-cast Mg-Zn-Mn, and extruded Mg-Zn-Mn) in a bioreactor applying c

172 n pure Mg, as-cast Mg-Zn-Mn, and extruded Mg-Zn-Mn) in a bioreactor applying cyclical loading and sim

173 s the Al-concentration increased, and for Mg-Zn alloys, this direction changes from [Formula: see tex

174 and support a hypothesis that mitochondrial Zn(2+) accumulation in the early reperfusion period may

175 sed N, P and K and decreased Ca, Mg, Fe, Mn, Zn and Cu contents.

176 as well as the foreign ions (Al, Cu, Fe, Mn, Zn) to the solution on the in situ atomization and excit

177 For the first time, speciation of Fe, Mn, Zn, Ni, Cu and Pb was determined along the profiles of 8

178 We discuss a mechanism by which cellular Mn:Zn ratios dictate PhpP specific activity thereby regulat

179 M-1 and BcII in the bi-Zn(II) form, the mono-Zn(II) B2 Sfh-I and the mono-Zn(II) B3 GOB-18.

180 form, the mono-Zn(II) B2 Sfh-I and the mono-Zn(II) B3 GOB-18.

181 tructures reveal that an unusual monodentate Zn(2+) coordination mode is exploited by sterically bulk

182 yton) to an aqueous zinc gradient (3-340 mug Zn/l) and measured zinc concentrations at different stag

183 ic nanocrystals (PdM, M = V, Mn, Fe, Co, Ni, Zn, Sn, and potentially extendable to other metal combin

184 On selected sample positions minor (Ni, Zn, Ag, and Sb) and trace elements (C, P, Fe, and As) we

185 The toxicity of metal mixtures (Ni, Zn, Cu, Cd, and Pb) to Daphnia magna, Ceriodaphnia dubia

186 In Cd-Ni-Zn mixtures, the toxicity was less than additive or appr

187 ented at the vertices of the ferritin nodes (Zn(II), Ni(II), and Co(II)) and the synthetic dihydroxam

188 ith delayed and long-lasting accumulation of Zn(2+) within mitochondria occurring in CA1 but not CA3

189 ded via SiO2 condensation over aggregates of Zn-Fe oxide nanoparticles originating from the failure o

190 small proteins that can bind high amounts of Zn(ii) and Cu(i) ions in metal-cluster arrangements via

191 rate here the detection of isolated atoms of Zn and Fe on ferritin, using cryogenic annular dark-fiel

192 kout mutants grew poorly, but attenuation of Zn(II)2Cys6 expression yielded strains producing twice a

193 e resolution of individual atomic columns of Zn and organic linkers in the framework.

194 etal ions and function with a combination of Zn(2+) and Mg(2+), although including Mn(2+) increases t

195 isotope fractionation during complexation of Zn(2+) with the phytosiderophore 2'-deoxymugeneic acid (

196 ription factors, adding to the complexity of Zn homeostasis.

197 Free concentrations of Zn(2+), Fe(3+), Ca(2+) and Mg(2+) in a red wine (Raimat,

198 cale level of the nature and distribution of Zn soaps in the painting Alchemy by J.

199 ast, we find no difference in the effects of Zn(+2) on Abeta40 and Abeta42.

200 We measure the effects of Zn(2+) and curcumin on Abeta40, and compare these with t

201 microplastics, but there was no evidence of Zn accumulation, mortality, or weight change.

202 y, the process of formation and evolution of Zn soaps is not yet fully understood.

203 H3 COOH/H2 O and subsequent self-exchange of Zn and Zn(2+) at the Zn/H2 O interface.

204 mical properties may influence the extent of Zn bioavailability.

205 which the three different isotopic forms of Zn were quantified.

206 almitoyl acyltransferase enzymes, a group of Zn(2+)-finger DHHC-domain-containing proteins (ZDHHC).

207 In the presence of Zn or Mn, Cp2 ZrCl2 was found to dramatically accelerate

208 In the presence of Zn(+2), both of these fail to form proper fibrils, and t

209 Promoter analysis revealed the presence of Zn-deficiency-response elements (ZDREs) in a number of t

210 ligand l-lactic acid by varying the ratio of Zn(2+) to ligand from 0.5 to 0.85 mmol.

211 ligand geometry and catalytic reactivity of Zn(2).

212 s for the prediction of potential release of Zn(2+) into the environment.

213 n that exploits electrochemical sintering of Zn microparticles in aqueous solutions at room temperatu

214 ion-mediated laser printing and sintering of Zn nanoparticle is reported.

215 ifs, which are the predicted binding site of Zn(2+) in the Zn-deficiency response.

216 The relative binding strength of Zn sorption to the natural particles was inversely relat

217 e results provide a greater understanding of Zn-homeostatic mechanisms in wheat, demonstrating an exp

218 of 260 g moist soil containing 0.35 wt % of Zn-bearing microplastic (236-4505 mg kg(-1)) ingested th

219 ein, the critical role of structural H2 O on Zn(2+) intercalation into bilayer V2 O5 .nH2 O is demons

220 Clx or M(NO3)x (where M = Fe, Co, Ni, Cu, or Zn) to form uniform, amorphous films of metal oxides.

221 f 4-fold-symmetric porphyrins with Fe(II) or Zn(II) gave a new cubic M(II)8L6 cage framework with ele

222 loenediyne complexes [M = Cu(II), Fe(II), or Zn(II)] and their independently synthesized, cyclized an

223 donor strengths, either Zn(II)Porphyrins or Zn(II)Phthalocyanines were linked to different electron-

224 ly selective for MBLs when compared to other Zn(II) metalloenzymes.

225 ine site is thermodynamically preferred over Zn(II).

226 R325W transgenic line had lower pancreatic [Zn(2+)]i and proinsulin and higher insulin and glucose t

227 Because parasitic Zn(2+)- and NAD(+)-dependent HDACs play crucial roles in

228 The formation of Pb, Zn, and Cu carboxylates (soaps) has caused visible deter

229 tances (C, Cd, Cr, Cu, Fe, Hg, N, Ni, P, Pb, Zn) are developed to characterize this WM-system.

230 A soft porous Zn(II)-MOF (1) displays distinctive three-step hystereti

231 sing zinc porphyrin and free base porphyrin (Zn(i + 2)-Zn(i + 6)), and highly efficient energy transf

232 Highly selective, highly potent Zn(2+)-independent GPR39 agonists were found in subseque

233 in situ deposition of antibacterial prickly Zn-CuO nanoparticles and graphene oxide (GO) nanosheets

234 Calculations of the following molar ratios: Zn:Cu, Fe:Zn, and Fe:Mn, pairs of elements that have bee

235 A large prismatic rechargeable Zn-birnessite cell delivering approximately 140 Wh l(-1)

236 that ROS-mediated TRPM7 activation releases Zn(2+) from intracellular vesicles after Zn(2+) overload

237 revealed substantial differences in relevant Zn(2+) sources, with critical contributions of presynapt

238 in cages 3 and 4, incorporating respectively Zn(II) porphyrins and free-base porphyrins, is reported.

239 o reach the activity of ZnO/Cu with the same Zn coverage.

240 (Ag, Cd, Cu), and bearberry (Ba, Fe, Pb, Sb, Zn).

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

242 om helically aggregated dyes as sensitizers; Zn-porphyrins and triarylamines.

243 been detected in women that result in severe Zn(2+) deficiency in exclusively breastfed infants.

244 l approach is discovered to print and sinter Zn nanoparticle facilitated by evaporation-condensation

245 omprise SiO2 glass matrices and 10-nm-sized Zn-Fe-oxide nanoparticles associated with a wide range o

246 s, indicating that particle-bound, or sorbed Zn, was bioavailable from acid mine drainage wastes.

247 ild-type (WT) form of the beta-cell-specific Zn(2+) transporter, ZNT8, is linked to T2DM susceptibili

248 nder the reaction conditions so that surface Zn transforms into ZnO and allows ZnCu to reach the acti

249 and tetrahedral Zn (attributed to symplastic Zn-organic acid and apoplasmic Zn-cell wall complexes, r

250 dopamine transporter (DAT) has a tetrahedral Zn(2+)-binding site.

251 Octahedral and tetrahedral Zn (attributed to symplastic Zn-organic acid and apoplas

252 lcite (Omegacalcite = 13), demonstrated that Zn, orthophosphate, tripolyphosphate, and hexametaphosph

253 Further analysis indicate that Zn(2+) induced ROS production, PARP-1 stimulation, incre

254 typical Fe-regulated genes, indicating that Zn affects Fe homeostasis at the level of Fe sensing.

255 The Zn(2+)-dependent class IIb enzyme HDAC6 regulates microt

256 east mutant but only slightly alleviates the Zn sensitivity of the zrc1 cot1 yeast mutant.

257 ula: see text] or [Formula: see text] as the Zn-content varied.

258 equent self-exchange of Zn and Zn(2+) at the Zn/H2 O interface.

259 allosteric inhibition of DNA binding by the Zn efflux repressor CzrA (chromosomal zinc-regulated rep

260 reas the hydrated polar interface houses the Zn(2+)-binding histidines with binding geometries unusua

261 nd biochemistry approaches we identified the Zn-finger protein ZNF326, as a novel interaction partner

262 the predicted binding site of Zn(2+) in the Zn-deficiency response.

263 tent of fractionation was independent of the Zn:ligand ratio used, indicating isotopic equilibrium an

264 gand environment, leaving a free site on the Zn(2+) for water activation.

265 elating polar residues that bridged over the Zn(2+) binding site and reached into a solvent accessibl

266 e binding within the MMP-13 active site, the Zn(2+) chelating unit was replaced with nonchelating pol

267 Allosteric activation of DAT via the Zn(2+)-binding site may be of interest to restore transp

268 ing of donor-acceptor cyclopropanes with the Zn-AcOH reductive system was developed.

269 ce amounts of U are also associated with the Zn-Fe oxides.

270 Vancomycin is known to bind to Zn(II) and can induce a zinc starvation response in bact

271 e natural particles was inversely related to Zn bioavailability; a finding that would not have been p

272 nism in monocots and dicots in responding to Zn deficiency.

273 7mumolL(-1), amounting to 14.4% of the total Zn.

274 ship with the proportion of labeled to total Zn in the pore water, which increased with longer soil i

275 -9 and -13 supported an ability to transport Zn.

276 We hypothesized that ZIP7 and ZnT7 transport Zn(2+) in opposing directions across the S(E)R membrane

277 C6-trichostatin A complex, which reveals two Zn(2+)-binding conformers for the inhibitor: a major con

278 gest that UzcRS couples the perception of U, Zn and Cu with a novel extracytoplasmic stress response.

279 Unlike Zn/Pd- and Fe/Cu-mediated one-pot ketone syntheses, the

280 smooth dehydrogenation when generated using Zn(TMP)2 2 LiCl as a base in the presence of excess ZnCl

281 can be performed on biological systems using Zn K edge (1s) absorption to enhance internal structures

282 g knock-out animals (of MT-III and vesicular Zn(2+) transporter, ZnT3) and channel blockers revealed

283 poptosis-enabling mechanism is initiated via Zn(2+)-dependent dual phosphorylation of Kv2.1, increasi

284 TabZIPs may have specific roles in the wheat Zn-homeostatic network.

285 r (Zn, orthophosphate or NOM) alone, whereas Zn+NOM showed a lesser inhibitory effect than its indivi

286 he Ru(II) complexes, and then assembled with Zn(II) or Cd(II) to obtain high-generation metallo-trian

287 ithelium, and they were not colocalized with Zn granules found in the lysosome-containing vesicles or

288 d HCO mimics, respectively, as compared with Zn-bound mimics.

289 Herein, silver nanoparticles ensemble with Zn(II) complex of alpha-liopoic acid conjugated terpyrid

290 terials) were observed upon metallation with Zn(2).

291 Nd, Ni, Pr, Rb, Sm, Te, Ti, Tl, Tm, U, V, Y, Zn and Zr).

292 fering metals such as cadmium (Cd) and zinc (Zn), and stable response in natural water samples with m

293 ommon terrestrial contaminants such as zinc (Zn).

294 ts in tolerance of excess copper (Cu), zinc (Zn) and cadmium (Cd).

295 Enhanced zinc (Zn) uptake closely mimicked Fe deficiency by leading to

296 m picosecond-nanosecond motions impact zinc (Zn)-induced allosteric inhibition of DNA binding by the

297 anadium (V), cobalt (Co), nickel (Ni), zinc (Zn), and aluminum (Al) concentrations in atmospheric dep

298 que to quantify the bioavailability of zinc (Zn) associated with natural particles using snails enric

299 Understanding the molecular basis of zinc (Zn) uptake and transport in staple cereal crops is criti

300 level of nitrogen (N), phosphorus (P), zinc (Zn), iron (Fe), and copper (Cu) in the fruit pulp was si