ライフサイエンスコーパス: Zn

1 Zn and/or polycyclic aromatic hydrocarbons (pyrene, phen

2 Zn(2+) has been shown to have a wide range of modulatory

3 Zn-DeAlBEA was found to be highly active for ethanol deh

4 Zn-HAB is shown to have microporosity with a band gap of

5 ysts employing Pd(ii), Cu(i), Ni(ii), Fe(0), Zn(ii), Ag(i), and Au(i/iii) metal based precursors.

6 as the presence of the redox inactive 3d(10) Zn(2+) is expected to perturb the long range in-plane CT

7 oxide (HEO) Co(0.2) Ni(0.2) Cu(0.2) Mg(0.2) Zn(0.2) O material with mesoporous structure is prepared

8 ent with alkyl metal reagents, such as Et(2) Zn and Bu(2) Mg.

9 h 3-center-2-electron sigma bonding in Ge(2) Zn or Ge(2) Cd triangles plays a vital role in the stabi

10 capsulated Zn(TFSI)(2) -TFEP forms a ZnF(2) -Zn(3) (PO(4) )(2) solid electrolyte interphase (SEI) pre

11 d hydrogen-bonded sql-net; and 2(H(2)NMe(2))[Zn(2)(cpb)] CTH-13, a similarly mixed yav-net.

12 H-10 and the two polymorphs of 2(H(2)NMe(2))[Zn(2)(cpb)].1.5dmac, Zn-MOF-888 and CTH-11, show kgd-net

13 hX (X = I and Br) in the presence of NiCl(2)/Zn as the precursors for the assumed Ni(0) complexant to

14 isostructural conductive MOFs with Mn(2+) , Zn(2+) , and Cd(2+) .

15 2+), Mn(2+), Fe(2+), Al(3+), Ni(2+), Cu(2+), Zn(2+), Co(2+), Pb(2+) and Ru(3+)) and aqueous compatibi

16 ing from [2 Fe:9 Zn:6 protomers] to [8 Fe:21 Zn:12 protomers], these protein cages represent some of

17 others of full-term (Fe = 0.733, Cu = 0.234, Zn = 2.91 and I = 0.255 mg L(-1)) infants.

18 an antiparallel dimer in the presence of 2-3 Zn(2+) ions.

19 This clathrate consists of a 3D Zn-Sb framework hosting K(+) ions inside polyhedral cage

20 antibacterial systems (Ti-Mg and Ti-Mg-3wt% Zn) that can selectively eradicate E. coli while not har

21 mothers of pre-term (Fe = 0.997, Cu = 0.506, Zn = 4.15 and I = 0.458 mg L(-1)) and mothers of full-te

22 morphs of 2(H(2)NMe(2))[Zn(2)(cpb)].1.5dmac, Zn-MOF-888 and CTH-11, show kgd-nets; [Cu(2)(cpb)(acetat

23 pitated Zn/Cu-bearing solids contained 33.6% Zn and 21.7% Cu, whereas the Fe content was less than 0.

24 The (66)Zn/(64)Zn ratio (expressed as delta(66)Zn value) shows an enric

25 e (66)Zn/(64)Zn ratio (expressed as delta(66)Zn value) shows an enrichment of the heavy isotope in ma

26 For both metals, delta((66)Zn) and delta((65)Cu) in solution exhibited complex but

27 The (66)Zn/(64)Zn ratio (expressed as delta(66)Zn value) shows a

28 With stoichiometries ranging from [2 Fe:9 Zn:6 protomers] to [8 Fe:21 Zn:12 protomers], these prot

29 A Zn(II)(histidine)(3)(H(2)O) centre can be incorporated a

30 omposed of 5-17 B-repeats, each containing a Zn(2+)-binding G5 and a spacer subdomain, is responsible

31 alkaline phosphatase superfamily, contains a Zn(2+) ion at its active center, and is structurally sim

32 MOF electrolyte protected Zn anode enables a Zn||Ti cell to achieve a high average Coulombic efficien

33 eature within its CDR3 loop, which harbors a Zn(2+)-binding site that substitutes for a loop-stabiliz

34 e of 0.0047 % per cycle over 600 cycles in a Zn||MnO(2) full cell with a low capacity ratio of Zn:MnO

35 ZnT8 is a Zn(2+)/H(+) antiporter that belongs to SLC30 family and

36 However, the application of a Zn anode is hindered by severe dendrite formation and si

37 owledge, we present the first structure of a Zn(II)-dependent aromatic dehalogenase that does not req

38 small intestine villi of mice subjected to a Zn-enriched diet was imaged using the 0.6 mum spot size,

39 cal metalloenzyme inhibitors of Zn(II)-ACE1, Zn(II)-HDAC, Fe(II)/(III)-5-LO or Cu(II)-tyrosinase from

40 includes genes encoding Zn import (adcABC), Zn sparing (rpsN.2), and Zn scavenging systems (adcAII,

41 Additionally, Zn(2+) was found to dramatically reduce the area per lip

42 n both OW and amended soils (i.e., amorphous Zn-phosphate and Zn sorbed on hydoxylapatite).

43 Zn import (adcABC), Zn sparing (rpsN.2), and Zn scavenging systems (adcAII, phtD, and phtY).

44 of pH, Na(+) , K(+) , Ca(2+) , Mg(2+) , and Zn(2+) ions.

45 his channel sensitive to 4-aminopyridine and Zn(2+).

46 ront passivation approaches: (i) both Cd and Zn impurities beneficially reduce the high native net do

47 lays a key role in the evaporation of Cu and Zn at temperatures above 700 degrees C, while at relativ

48 cycles on physicochemical parameters, Cu and Zn concentrations, and isotopic composition in solution

49 te the functions of free/metal-bound Cys and Zn sites in proteins.

50 formation of 1,3-butadine over Y-DeAlBEA and Zn-DeAlBEA does not occur via aldol condensation of acet

51 an is limited by the water decomposition and Zn dendrite growth.

52 e Zn anodes owing to water decomposition and Zn dendrite growth.

53 ing by combining soil column experiments and Zn speciation characterization in OWs and amended soils.

54 For Fe and Zn, 39 accessions, including 15 with multiple nutrients,

55 25 ng mL(-1) for Pb(II), Cu(II), Cd(II), and Zn(II) cations, respectively.

56 On the other hand, integrating Co, Mn, and Zn turns Li(2) S into a prelithiation agent, forming met

57 .3-1, 3-14 and 0.5-2 ppm for Fe, Cu, Mn, and Zn, respectively, and varied as a function of the origin

58 Moreover, Mo and Zn, likely incorporated into enzymes only after the Grea

59 te tensile strength 646.69 +/- 12.79 MPa and Zn-0.8Li-0.8Mn alloy with elongation 103.27 +/- 20%.

60 ntent of minerals (Ca, Fe, K, Mg, Mn, Na and Zn), dietary fiber (total, soluble and insoluble), tanni

61 Results showed, the mean values of Pb and Zn were higher in crop than Food and Agriculture Organiz

62 nded soils (i.e., amorphous Zn-phosphate and Zn sorbed on hydoxylapatite).

63 Here, we suppress water reduction and Zn dendrite growth in dilute aqueous electrolyte by addi

64 nerals (Ca, Cu, Fe, K, Mg, Mn, Na, P, Se and Zn) and trace metals (As, Cd, Pb, U and V).

65 determination of Al, Cr, Cu, Fe, Mn, Sr, and Zn.

66 heets of 9,10-dicarboxytriptycene struts and Zn(2)(CO(2))(4) secondary binding units.

67 , Mo, Na, Ni, P, Pb, Th, Tl, Sb, U, V, Y and Zn) in 73 commercial products marketed in Spain.

68 Aqueous Zn batteries are promising energy storage devices for la

69 Aqueous Zn batteries are promising energy-storage devices.

70 electrolyte that is immiscible with aqueous Zn(TFSI)(2) -H(2) O bulk electrolyte.

71 ined in the acid and further precipitated as Zn/Cu-bearing solids by adjusting the solution pH to 9.

72 he entry of certain non-iron metals, such as Zn, Mn, and Co.

73 scopy analyses were then conducted to assess Zn speciation in OW and OW-amended soils.

74 ious functional groups involved in bacterial Zn binding were identified by FT-IR spectroscopy and ele

75 a remarkably lowered binding energy between Zn(2+) and host O(2-) , which explains the favorable kin

76 e conformation of an unstructured bimetallic Zn(II) complex can be controlled by its inclusion in the

77 In this work, binary Zn alloys with alloying elements Mg, Ca, Sr, Li, Mn, Fe,

78 idues do not bind RNA or Ca(2+), but do bind Zn(2+), which promotes further association.

79 is more efficient for attracting and binding Zn(2+) via the essential histidines than the monomer or

80 In summary, biocompatible Zn-based BMs with strength close to pure Ti are promisin

81 The lack of bound Zn(2+) also made the CDR3 loop highly flexible, as obser

82 detected in TB and nodes, and was induced by Zn deficiency.

83 ological tasks but are strongly inhibited by Zn(2+) cations.

84 dification of Mg with alloying elements (Ca, Zn), the degradation rates of Mg alloys were controlled,

85 n binding to OM at low concentrations and Ca-Zn competition, that is, typical conditions that occur i

86 oxy-cytidine dinucleotide near the catalytic Zn(2+), yet not in the catalytic position, where the int

87 incorporation of manganese (Mn) ions into Cd(Zn)-chalcogenide QDs activates strong spin-exchange inte

88 esentative metal ions were examined: Pb, Cd, Zn, Ce (III), Ba, Ni, Fe(II), Fe(III), Cu(II), Cr, Mo, C

89 t heterometallic supertetrahedral clusters, [Zn(6) Ge(16) ](4-) and [Cd(6) Ge(16) ](4-) , were direct

90 precursor [HNEt(3) ](2) [M(pdms)(2) ] (M=Co, Zn) allow for multiple charge transfers (CTs) between th

91 r Zn(2+) was 20-100 muM, which covers common Zn(2+) safety standards.

92 ystem selectively bound the thiol-containing Zn(II)-ACE1 inhibitors captopril and omapatrilat, and th

93 dvantage of the ability of His to coordinate Zn(2+) to promote metal ion bridges, and we have found t

94 CPX-Zn complex was successfully synthesized and characterize

95 CPX and CPX-Zn nanosuspensions (NSs) were prepared using an evaporat

96 single intraductal injection of CPX NS, CPX-Zn NS or CPX-Zn NPs was administered.

97 ductal injection of CPX NS, CPX-Zn NS or CPX-Zn NPs was administered.

98 erum and 12 elements (Mg, S, Mn, Fe, Co, Cu, Zn Se, Br, Rb, Mo, and Cs) in less than 250 000 cells.

99 nts (Mg, P, S, K, Ca, V, Cr, Mn, Fe, Co, Cu, Zn, Se, Br, Rb, Sr, Mo, I, Cs, and Ba) in 10 muL of seru

100 lowing elements were chosen: Ti, Mn, Fe, Cu, Zn, Br, Rb, Sr.

101 , heavy metals including Cr, Mn, Co, Ni, Cu, Zn, As, and Cd in 55 Thai local rice (4 varieties) were

102 near-complete extractions of Mn, Co, Ni, Cu, Zn, Cd, and Pb ions from natural water samples prior to

103 sition metal ions M(II) (M = Mn, Co, Ni, Cu, Zn, Pd, and Cd) under mild conditions.

104 SOD, namely, the fully mature functional Cu,Zn state and the E,Zn-SOD state in which the Cu site is

105 guanosine (8-OHdG), superoxide dismutase (Cu-Zn SOD), and thiobarbituric acid reactive substances (TB

106 In addition to Cu-THQ, the CT in Cu/Zn-THQ after incorporating Zn(2+) guest metal was also e

107 reaction of a stable monomeric variant of Cu/Zn superoxide dismutase (mSOD1), an enzyme responsible f

108 ng of SOD5 strongly deviate from those of Cu/Zn-SODs in its animal hosts, making Cu-only SODs a possi

109 Here, we examine the trajectory that Cu/Zn superoxide dismutase (SOD1) dimers take over the unfo

110 elopment, which is associated with decreased Zn distribution to the panicles.

111 s high coulombic efficiency (ca. 97 %), deep Zn plating/stripping (10 mAh cm(-2) ), and long cycle li

112 bovine wound infection 'digital dermatitis', Zn/Cu-shellac adhered rapidly and robustly over pre-appl

113 C), a deadly disease associated with dietary Zn deficiency and inflammation.

114 ) O(5) -dissolution mechanisms for different Zn-salt aqueous electrolytes and their implications to t

115 sor was applied to wastewater with different Zn(2+) concentrations and the results showed that the de

116 ration and composition and related dissolved Zn speciation.

117 Two distinct Zn sites characteristic of the parent crystals transform

118 experiment, and phosphate was found to drive Zn speciation in both OW and amended soils (i.e., amorph

119 (0.19-1.53 ug/g dw); Fe (8.6-18.8 ug/g dw); Zn (20.8-41.5 ug/g dw); Ca (6.2-15.2 mg/g dw).

120 ully mature functional Cu,Zn state and the E,Zn-SOD state in which the Cu site is empty.

121 entified by FT-IR spectroscopy and elemental Zn in bio-chelated cell lysate complex was confirmed by

122 The MOF encapsulated Zn(TFSI)(2) -TFEP forms a ZnF(2) -Zn(3) (PO(4) )(2) soli

123 The AdcR regulon includes genes encoding Zn import (adcABC), Zn sparing (rpsN.2), and Zn scavengi

124 developed dissolution method allowed Ca, Fe, Zn, and Mg determination in milk samples with adequate a

125 ntrations of 16 elements (K, Na, Mg, Ca, Fe, Zn, Hg, Se, As, Cu, Cd, Mn, Ni, Cr, Pb and Co) were dete

126 Micro-nutrient profiling showed Ca, Fe, Zn, P, K and Mn in the range of 2400.00-3400.00, 40.28-4

127 heritability (> 0.81) were observed for Fe, Zn, Ca, P, Mo, and Mg.

128 ) and supplemented with either OM or IM (Fe, Zn, Mn, Cu, and Se).

129 ro- (Mg, P, S, K, Ca) and micronutrient (Fe, Zn, Mn, Cu) concentrations of leaves and edible parts of

130 N, P, Ca, Na, K, Mg) and micronutrients (Fe, Zn, Co, Mn, I) were sufficient to contribute to daily di

131 Low phloem mobile nutrients Ca, Mn, Fe, Zn, and Cu showed the largest differences in correlation

132 fied wheat diet containing increased NA, Fe, Zn and DMA (long-term exposure).

133 can be attributed to a number of very fine, Zn/Ca-containing nanoscale precipitates, along with ultr

134 ) nanoparticles as the cathode in a flexible Zn-air battery (ZAB).

135 mice, indicating the direct competition for Zn between CP and proteins encoded by the GAS AdcR regul

136 ate mechanical integrity can be expected for Zn alloys when considering bone fracture healing.

137 results showed that the detection range for Zn(2+) was 20-100 muM, which covers common Zn(2+) safety

138 5 and a spacer subdomain, is responsible for Zn(2+)-dependent assembly leading to accumulation of bac

139 ion coordination geometries (tetrahedral for Zn(2+), tetrahedral to octahedral conversion for Co(2+),

140 A gas-phase approach to form Zn coordination sites on metal-organic frameworks (MOFs)

141 on, the decomposition of solvated DMSO forms Zn(12)(SO(4))(3)Cl(3)(OH)(15).5H(2)O, ZnSO(3), and ZnS e

142 HsZnT8 forms a dimeric structure with four Zn(2+) binding sites within each subunit: a highly conse

143 to have square-pyramidal geometry with four Zn-N bonds in the equatorial plane and one Zn-OH(2) bond

144 ESCC-free, Zn-deficient miR-31(-/-) rat esophagus displayed no geno

145 Here, we separate aqueous electrolyte from Zn anode by coating a thin MOF layer on anode and fillin

146 Further, Zn enriched cell lysates were prepared by Ultrasonicatio

147 les for individual AdcR regulon genes in GAS Zn acquisition.

148 a representative glass, namely ZIF-62 glass (Zn(C(3)H(3)N(2))(1.75)(C(7)H(5)N(2))(0.25)), is measured

149 o a significant stabilization of 5 via Ru -> Zn donation.

150 highly active organometallic heterodinuclear Zn(II)/Mg(II) catalyst applied in a one-pot procedure to

151 nd filling the pores of MOF with hydrophobic Zn(TFSI)(2) -tris(2,2,2-trifluoroethyl)phosphate (TFEP)

152 +), and transition metal ions such as Cu(I), Zn(II), and Cd(II).

153 accumulated in the soil surface layer, (iii) Zn uptake by lettuce increased with repeated OW applicat

154 The N-(2-methoxyphenyl)iminodiacetate Zn(2+) ion sensor has a sensitivity of 1 umol L(-1) with

155 ared to other pancreatic cells; importantly, Zn(II)-mediated hydrolysis triggers cargo activation.

156 applications, and (iv) no radical change in Zn speciation was observed at the end of the 12-week exp

157 he coordination mode of the oleate ligand in Zn-oleate to be achieved (including information on Zn...

158 )-H(2)O, in which DMSO replaces the H(2)O in Zn(2+) solvation sheath due to a higher Gutmann donor nu

159 of the ternary Zn-Li alloy system results in Zn-0.8Li-0.4Mg alloy with the ultimate tensile strength

160 its the most effective strengthening role in Zn, followed by Mg.

161 7 times more active than the active sites in Zn-DeAlBEA.

162 e)](2+) analog containing the redox-inactive Zn(II) ion.

163 Importantly, when the complex also included Zn(2+), a significant increase in cell membrane GLUT1 wa

164 THQ, the CT in Cu/Zn-THQ after incorporating Zn(2+) guest metal was also examined to uncover the cont

165 This suggests that CP induces Zn deficiency in the host.

166 Greater than 99% of the initial Zn and Cu was retained in the acid and further precipita

167 We interpreted Zn and Cu diel cycles as a combination of a desorption o

168 ansformation of V(2) O(5) atomic layers into Zn(3) V(2) O(7) (OH)(2) .2 H(2) O (ZVO) nanoflake cluste

169 Adding elements Mg, Ca, Sr and Li into Zn can improve the cytocompatibility, osteogenesis, and

170 We also introduced Zn(2+) in the porphyrin core in an attempt to modulate i

171 rption capacities for the zinc subgroup ions Zn(II), Cd(II) and Hg(II).

172 r, their lifespan is limited by irreversible Zn anodes owing to water decomposition and Zn dendrite g

173 640 mV more positive than the isostructural [Zn(tpyPY2Me)](2+) analog containing the redox-inactive Z

174 (2) O (ZVO) nanoflake clusters, also a known Zn-ion and proton intercalatable material.

175 the combination of the two through the known Zn-cysteine finger redox trap effect.

176 id solution containing 23.5 g/L Fe, 4.45 g/L Zn and 2.81 g/L Cu, which was subjected to hydrothermal

177 Hierarchical marigold flower-like Zn layer decorated by n-type dichalcogenides interfacial

178 hat is, typical conditions that occur in low-Zn soils.

179 ent compounds (Me(2)NH(2))(2)[M(2)L(3)] (M = Zn, Mn; H(2)L = 2,5-dichloro-3,6-dihydroxo-1,4-benzoquin

180 GAS counterstrategies to combat CP-mediated Zn limitation and the in vivo relevance of CP-GAS intera

181 itivity of the mutant strains to CP-mediated Zn limitation suggests distinct roles for individual Adc

182 of a method for the determination of Ca, Mg, Zn, and Fe in liquid and powdered cow milk.

183 cally synthesized ((Fc(2)PDI)MCl(2), M = Mg, Zn, Fe, and Co) and characterized crystallographically,

184 nclude alkali (Li/Na/K) and multivalent (Mg, Zn)-based electrolytes for conventional "sealed" batteri

185 twork structure is unperturbed at micromolar Zn(2+) concentrations, but strong bundle formation is ob

186 in LC-PUFAs and micro-nutrients (Cu, Fe, Mn, Zn), including species considered as potentially edible

187 foods, we analysed selected minerals (Fe-Mn-Zn-Cu-Mg) in wild-harvested and commercially available t

188 s of deviations between measured and modeled Zn concentrations reveal specific limitations of the cur

189 le, in particular metals such as Ca, Al, Na, Zn, and Fe and halogens like Cl and F, occurring in conc

190 Consequently, the Zn@Nafion-Zn-X composite anode delivers high coulombic efficiency

191 hanesulfonyl)imide, this ketone formed a new Zn(4) L(4) tetrahedron 1 bearing twelve uncoordinated py

192 and the glucose, sucrose, Brix, Cd, Pb, Ni, Zn, and Cr values were found in the highland honeys; the

193 ere also moderate dietary sources of Se, Ni, Zn and Ca.

194 e production of crystals of MUV-101(Fe,Co,Ni,Zn) and MUV-102(Cu), heterometallic titanium MOFs isostr

195 this process are =Si-O-Y(OH)-O-Si= or =Si-O-Zn-O-Si-O= groups closely associated with adjacent silan

196 erence in reactivity reflects the ability of Zn to promote a rate-limiting C-H reductive elimination

197 magnesium-based alloy, with trace amounts of Zn, Ca, and Mn (~ 2% by wt.).

198 den and ESCC-associated metabolic changes of Zn-deficient wild-type rats.

199 with the low-cost, high-voltage chemistry of Zn/graphite batteries.

200 This interlayer, composed of Zn, ZnLi(x) alloy, Li(3) N, Li(2) O, and other species,

201 xposing the bilayer to muM concentrations of Zn(2+) but not Mg(2+), Cu(2+), Co(2+), or Mn(2+).

202 permeability, with a positive correlation of Zn(2+) (0-400 muM).

203 is technology, the elemental distribution of Zn in small intestine villi of mice subjected to a Zn-en

204 meters controlling the environmental fate of Zn following OW application on cultivated soils is scant

205 this study highlighted that (i) the fate of Zn in water-soil-plant compartments was similar, regardl

206 ligand pai-pai stacking, as incorporation of Zn(2+) in Cu-THQ significantly reduced photoconductivity

207 ntal or clinical metalloenzyme inhibitors of Zn(II)-ACE1, Zn(II)-HDAC, Fe(II)/(III)-5-LO or Cu(II)-ty

208 In the presence of 20 muM of Zn(2+), the activation currents of L366H:F370H channels

209 olytes by 0.45 V and enable the operation of Zn/graphite dual-ion cells at 2.80 V with a long cycle l

210 tion to non-toxic species in the presence of Zn(2+) ions.

211 nO(2) full cell with a low capacity ratio of Zn:MnO(2) at 2:1.

212 the method by mapping metal-binding sites of Zn(7-x)MT species using a bottom-up MS approach with res

213 Upregulation of Zn(II)-Cys6 transcription factors were uniquely induced

214 ate to be achieved (including information on Zn...O distances) and (ii) the mode of attachment of ole

215 r Zn-N bonds in the equatorial plane and one Zn-OH(2) bond in the axial plane.

216 The mechanism of interaction between SB-OP-Zn(2+) trio is investigated by spectrofluorometric, spec

217 ide-chains, with dissolved Li(+), Cu(2+), or Zn(2+) salts.

218 ovalently linked to porphyrins (free base or Zn), were prepared and characterized.

219 porphyrin prisms using MTPyP (M = Co(II) or Zn(II), TPyP = 4-tetrapyridylporphyrin) and functionaliz

220 of Cu(II)-, Fe(III)-, Ga(III)-, Ni(II)-, or Zn(II)-IMAC resins to reversibly bind experimental or cl

221 e prepared by Ultrasonication, as an organic Zn source.

222 In this work, porous Zn nanoparticles (P-Zn) were adopted as a model catalyst to investigate the

223 entially toxic elements (Cu, Cr, Mn, Fe, Pb, Zn, Ni) were analysed by atomic absorption spectrometer

224 The formation of a Pd-Zn alloy in situ was identified to be the critical facto

225 In this work, porous Zn nanoparticles (P-Zn) were adopted as a model catalyst

226 This led us to search for potential Zn(2+)-binding sites outside of the dimer interface.

227 xture of uncoordinated and coordinated (PPIX)Zn or all coordinated depending on the ratio of peptide/

228 d chromophore, zinc protoporphyrin IX, (PPIX)Zn.

229 The precipitated Zn/Cu-bearing solids contained 33.6% Zn and 21.7% Cu, wh

230 olid electrolyte interphase (SEI) preventing Zn dendrite and further suppressing water decomposition.

231 olid electrolyte interphase (SEI) preventing Zn dendrite and water decomposition.

232 cy depends upon the catalyst, and previously Zn(II)Mg(II) heterodinuclear catalysts showed good perfo

233 lowing for alternating access to the primary Zn(2+) site during the transport cycle.

234 nests of dealuminated BEA zeolite to produce Zn-DeAlBEA and Y-DeAlBEA.

235 Zn(TFSI)(2) -TFEP@MOF electrolyte protected Zn anode enables a Zn||Ti cell to achieve a high average

236 upported lipid bilayers (SLBs), forming a PS-Zn(2+) complex with an equilibrium dissociation constant

237 Ni-N(4) /GHSs/Fe-N(4) endows a rechargeable Zn-air battery with excellent energy efficiency and cycl

238 The aqueous rechargeable Zn-air batteries assembled with this carbon aerogel exhi

239 t TLSB could be desorbed with HCl to recover Zn(II) and Cd(II) and with HNO(3) to recover Hg(II) afte

240 ly and plays an essential role in regulating Zn(2+) accumulation in the insulin secretory granules of

241 e electrochemical reaction during repetitive Zn(2+) insertion and extraction, as demonstrated by in s

242 dicate that Aap from S. epidermidis requires Zn(2+) as a catalyst that drives amyloid fiber formation

243 The highly reversible Zn anode brings a high energy density of 210 Wh kg(-1) (

244 Each active-site Zn(II) ion resides in a distorted trigonal bipyramid geo

245 entation that coordinates to the active-site Zn(II) ions via a CN and that maximizes a pai-pai intera

246 then used for the synthesis of a metal soap (Zn-oleate) and the surface-functionalization of ZnO nano

247 zobacterial diversity; among these, the soil Zn contents decreased significantly across the rhizobact

248 tanding air cathode for flexible solid-state Zn-air batteries without the use of carbon paper/cloth a

249 ce of this inhibition.SIGNIFICANCE STATEMENT Zn(2+) is present along with glutamate in synaptic vesic

250 ivity of Pb(2+) with the extremely strained [Zn(2)Ga(2)O(7)](4-) framework along the c-axis.

251 Here we have systematically studied Zn(2+) inhibition of AMPARs by varying calcium permeabil

252 ous extraction conditions, and subsequently, Zn speciation was modeled using the generic non-ideal co

253 devices with ZnO layer result in substantial Zn diffusion, which can penetrate the full absorber thic

254 The "masked" terminal Zn sulfide, [K(2.2.2-cryptand)][(Me) LZn(S)] (2) ((Me) L

255 Further optimization of the ternary Zn-Li alloy system results in Zn-0.8Li-0.4Mg alloy with

256 Here we report that Zn(II) or Fe(II) ions can be used to weave ligand strand

257 Model predictions show that Zn in solution is mainly bound to dissolved humic acids.

258 Herein, we show that Zn(2+) binds to phosphatidylserine (PS) lipids in suppor

259 We also show that Zn(2+) inhibition is significant during rapid repetitive

260 ubunits, and activation levels and show that Zn(2+) inhibits AMPARs in an activity-dependent manner,

261 Here we show that Zn(2+) inhibits GluA2(Q) homomeric receptors in an activ

262 These results suggest that Zn speciation in OW is a key determinant controlling the

263 These measurements suggest that Zn(2+) caused lipid blebbing by decreasing the area per

264 The Zn(II)-IMAC system selectively bound the thiol-containin

265 The Zn(II)-targeting mechanism enriches the inactive cargo i

266 The Zn(TFSI)(2) -TFEP@MOF electrolyte protected Zn anode ena

267 , the histidine-dependent DNAzyme g1 and the Zn(2+)-ion-dependent DNAzyme g2.

268 action is over one billion years old but the Zn-fingernail appears only in VARP homologues in the lin

269 We performed mutagenesis to compromise the Zn(2+)-binding site and observed that this change severe

270 Consequently, the Zn@Nafion-Zn-X composite anode delivers high coulombic e

271 te in transmembrane domain (TMD) housing the Zn(2+) substrate; an interfacial site between TMD and C-

272 ies provide the structural insights into the Zn(2+)/H(+) exchange mechanism of HsZnT8.

273 d C-terminal domain (CTD) that modulates the Zn(2+) transport activity of HsZnT8; and two adjacent si

274 ss dendrite growth and side reactions of the Zn anode.

275 ile remedy for the limited cycle life of the Zn anode.

276 y, the local coordination environment of the Zn center was determined to have square-pyramidal geomet

277 the type of soil and OW, (ii) >97.6% of the Zn input from OW accumulated in the soil surface layer,

278 lsion with tunable lifetime depending on the Zn segment length.

279 residue, His(114), is hydrogen-bonded to the Zn(II)-bound water/hydroxide and likely functions as the

280 quencing, and metabolomics analyses in these Zn-deficient rats revealed the molecular basis of ESCC a

281 Subjecting the inner hydrogel layer to Zn(2+)-ions and/or the outer hydrogel layer to acidic pH

282 odel parameters, particularly with regard to Zn binding to OM at low concentrations and Ca-Zn competi

283 flies (Ephemeroptera, Baetis tricaudatus) to Zn.

284 gate to bind a terpyridine zinc complex (Tpy-Zn), forming a fluorescent [Tpy-Zn]-SPP complex (K(ass)

285 complex (Tpy-Zn), forming a fluorescent [Tpy-Zn]-SPP complex (K(ass) 106,000 M(-1) in EtOH-CHCl(3)) w

286 It also plays a role in transporting Zn to meristem cells in the TBs.

287 ectively, OsZIP4 is involved in transporting Zn to the phloem of diffuse vascular bundles in the node

288 are generated from 1,1-dichloroalkenes using Zn as a stoichiometric reductant.

289 While Zn(2+) inhibition of the NMDA subtype of the ionotropic

290 is needed to achieve the same effect as with Zn(2+), which suggests the importance of salt-protein in

291 FC biosensor have a linear relationship with Zn(2+) concentrations (0, 100, 200, 300, and 400 muM, re

292 ected cell volume expansion of CaBa(1-x)Pb(x)Zn(2)Ga(2)O(7) (0 <= x <= 1), which is a unique structur

293 evolution of the unit cell for CaBa(1-x)Pb(x)Zn(2)Ga(2)O(7) is due to the combination of the high ste

294 We show here that antibacterial zinc (Zn) and copper (Cu) species greatly enhance the barrier

295 Aqueous zinc (Zn) batteries (AZBs) are widely considered as a promisin

296 o the presence of contaminants such as zinc (Zn).

297 Isotopes of the trace element zinc (Zn) in bioapatite constitute a promising proxy to infer

298 mine (NA) is a natural chelator of Fe, zinc (Zn) and other metals in higher plants and NA-chelated Fe

299 hibits GAS growth in vitro by imposing zinc (Zn) limitation.

300 th P(zntA) promoter, which could sense zinc (Zn(2+)) for riboflavin and porin production.