ライフサイエンスコーパス: zinc

1 rbapenem resistance, by removing active site zinc.

2 non-rechargeable batteries with anodes like zinc.

3 WPH-Ever for electrostatic interaction with zinc.

4 nsidered for treatment with antioxidants and zinc.

5 onal system for the community acquisition of zinc.

6 s upon adding small amounts of elements like zinc.

7 ion to appreciable content of phosphorus and zinc.

8 liquid phase sonication and then mixed with zinc acetate hexahydrate for the synthesis of graphene/z

9 narily conserved motif that we named the low zinc activation (LZA) element that was both necessary an

10 The essential micronutrient zinc acts as a HIZR-1 ligand, and activated HIZR-1 incre

11 Herein, knittable fiber-shaped zinc-air batteries with high volumetric energy density (

12 In application to quasi-solid-state zinc-air batteries, CoO0.87 S0.13 /GN as a freestanding

13 A rechargeable zinc-air battery assembled in a decoupled configuration

14 repare the key component of the fiber-shaped zinc-air battery, i.e., a bifunctional catalyst composed

15 rm-factor elevates the performance of nickel-zinc alkaline cells in three fields of use: (i) >90% the

16 with other trace elements such as copper and zinc, altered gut microbiota to more pathogenic bacteria

17 reaction with lithium-magnesium and lithium-zinc amides affords C-2 or C-8 functionalized derivative

18 Both zinc and copper pyrithione are also moderately selective

19 of evidence has reported the role of copper, zinc and iron, and oxidative stress in several neurodege

20 ular basis of cancer preventive functions of zinc and its association with Orai1-mediated cell prolif

21 atalysts for these transformations, both the zinc and magnesium catalytic systems are active at room

22 The terminal zinc and magnesium hydride compounds, [kappa(3)-Tism(Pr(

23 vity following iron amendment within the low zinc and moderately low iron Western North Atlantic.

24 Zinc and Ni were transported into the deeper CW layers t

25 We therefore examined the correlation of zinc and other divalent metals in human islets with rs13

26 ms by studying effects of larval exposure to zinc and warming before, during, and after metamorphosis

27 es (potassium, calcium, manganese, iron, and zinc), and discuss dose-appropriate guidelines for X-ray

28 d uptake of essential elements manganese and zinc, and higher uptake of the neurotoxin lead.

29 hromatography to separate free and complexed zinc, and identified appropriate cation exchange resins

30 ring peptic digestion was lower for WPH-Ever-zinc, and over 50% of zinc remained bound in both peptid

31 d the suitability of bacterially synthesized zinc- and cobalt-doped magnetite nanoparticles for biome

32 Cytotoxicity of zinc- and copper-chlorophylls extracts was slightly diff

33 st to the PhoA family of APases that utilize zinc as a cofactor, the recent discovery of iron as a co

34 The results identify zinc as the first inorganic molecule to function as a ph

35 dic ring nitrogen with the CA II active site zinc, as well as two hydrogen bonds between the oxazolid

36 Zinc assimilation efficiency (AE) varied from 28% for th

37 which lies in its phylogenetically conserved zinc-associated Cys-X-X-Cys motif near the catalytic dom

38 As such, the mechanisms of zinc binding and release among bacterial SBPs are of con

39 e suggest that the P73G mutation affects the zinc binding and/or the beta-annulus, making it more fra

40 The discovery of a new zinc binding chemotype from screening a nonbiased fragme

41 d primary benzenesulfonamides, the classical zinc binding group found in most CA II inhibitors.

42 By comparison, the zinc binding region of the P73G mutant, even under nativ

43 es (ZMCs) reactivate mutant p53 by restoring zinc binding to zinc-deficient p53 mutants.

44 WPH-Ever had lower amount of zinc-binding amino acids but showed higher zinc-chelatin

45 ) that has similarities to the cysteine-rich zinc-binding domain of DnaJ chaperones.

46 ed that the enzyme represents a new class of zinc-binding flavin-dependent halogenases and provides n

47 To question the precise role of the zinc-binding group (ZBG), we have carried out a study on

48 with peptoid-based cap groups and different zinc-binding groups.

49 tains a three-helix bundle in the middle and zinc-binding modules on each side.

50 r-CRL4 E3 ligase requires a highly conserved zinc-binding motif.

51 These differences include a novel zinc-binding site and regions unique to the mammalian IP

52 ed by a flexible loop near the high-affinity zinc-binding site.

53 The zinc binuclear cluster transcription factor CLR-1 is nec

54 icantly after steaming in all species, while zinc bioaccessibility increased in fish (tuna and plaice

55 How zinc bioavailability triggers activation of SczA is unkn

56 e crystal structure of the CdSe shell (cubic zinc-blende or hexagonal wurtzite) plays a key role in d

57 he bacterium Paracoccus denitrificans in the zinc-bound and apo-states.

58 ckly to promote the nucleophilic attack of a zinc-bound hydroxide ion onto the ceramide amide carbony

59 s demonstrated that hierarchical copper- and zinc- buds dressing gamma-AlOOH mesostrands, which are o

60 TAZ increased with increased dietary zinc, but plasma zinc concentrations and EZP size were u

61 een proposed to play a role in the export of zinc, but the transport mechanism of ZntB is poorly unde

62 ions were also positively related to aqueous zinc, but were 7-fold lower than larvae.

63 ion of vitamin A, vitamin B12, folate, iron, zinc, calcium, calories, and protein.

64 The PHP-exonuclease has a trinuclear zinc center, coordinated by nine conserved residues.

65 Hydroxamic acids are outstanding zinc chelating groups that can be used to design potent

66 f zinc-binding amino acids but showed higher zinc-chelating capacity than WPH-Pap.

67 ign and synthesis of potent but nonselective zinc-chelating MMP inhibitors (e.g., 10a and 10b).

68 lar zinc concentration by treatment with the zinc chelator N,N,N'-tetrakis-(2'-pyridylmethyl)ethylene

69 We previously discovered that small-molecule zinc chelators called zinc metallochaperones (ZMCs) reac

70 ose from untreated and steamed leaves, while zinc-chlorophylls extracts exhibited yellow-green color.

71 self-assembly of tris(2-pyridylmethyl)amine zinc complexes through imine condensation chemistry is r

72 ghtly more compact structure than the parent zinc compound NCp7-F2, which showed only one conformatio

73 Importantly, altering the intracellular zinc concentration by treatment with the zinc chelator N

74 ng wild-type and mutant SLC30A9 showed lower zinc concentration within mutant rather than wild-type S

75 ased with increased dietary zinc, but plasma zinc concentrations and EZP size were unchanged.

76 Erythrocyte and leukocyte zinc concentrations and zinc transporter expressions wer

77 zinc gradient (3-340 mug Zn/l) and measured zinc concentrations at different stages of metamorphosis

78 s on insect chemistry were large declines in zinc concentrations coupled with increased delta(15)N si

79 Adult zinc concentrations were also positively related to aque

80 that can disrupt the BoNT/A metalloprotease zinc-containing active site, thus impeding its proteolys

81 Moreover, we have shown that zinc coordination is also important for the assembly of

82 ed transcriptional activation in response to zinc deficiency in cells, suggesting a conserved pathway

83 r activation of transcription in response to zinc deficiency.

84 In zinc-deficient cells, RTC4 RNA with longer transcript le

85 In zinc-deficient cells, Zap1 binds to zinc responsive elem

86 hree C. elegans zipt genes were regulated in zinc-deficient conditions; these promoters contained an

87 vate mutant p53 by restoring zinc binding to zinc-deficient p53 mutants.

88 me time, zinc sequestration had no effect on zinc-dependent cellular protein functions.

89 etwork controlling phosphate accumulation in zinc-dependent manner.

90 Examination of reduced holomycin against zinc-dependent metalloenzymes revealed that it inhibits

91 A recent study shows that, in yeast, zinc depletion acts in a similar fashion.

92 RecQ paralogues; such a region consists of a zinc domain and a winged helix domain and plays an impor

93 However, a role for zinc during hepatic ER stress is largely unknown despite

94 Release of zinc during peptic digestion was lower for WPH-Ever-zinc

95 ncreases transcription of genes that promote zinc efflux and storage.

96 slet-specific zinc transporter ZnT8 mediates zinc enrichment in the insulin secretory granules of the

97 vented in S. pneumoniae by expression of the zinc exporter CzcD, whose expression is activated by the

98 Polydactyl zinc finger (ZF) proteins have prominent roles in gene r

99 finger protein-1 (Miz-1) is a poly-Cys2His2 zinc finger (ZF) transcriptional regulator of many cell

100 trate and further show that ZFP91 harbours a zinc finger (ZnF) motif, related to the IKZF1/3 ZnF, cri

101 entities (TUBEs) and the K29-selective Npl4 Zinc Finger 1 (NZF1) domain from the deubiquitinase TRAB

102 GLI family zinc finger 2 (GLI2) coordinates the Hh transcriptional

103 n thermogenic gene activation and identified zinc finger and BTB domain-containing 7b (Zbtb7b) as a p

104 Variation in the gene encoding zinc finger binding protein 804A (ZNF804A) is associated

105 d polyadenosine RNA-binding protein, ZC3H14 (Zinc finger CysCysCysHis domain-containing protein 14),

106 CCCTC-binding factor (CTCF) is an 11 zinc finger DNA-binding domain protein that regulates ge

107 and both its physical interaction to GR and zinc finger domain appear to be required for ZNF764 to r

108 quence specificity of the mutant recombinant zinc finger domain by performing biophysical measurement

109 residue within a novel viral integrase-like zinc finger domain.

110 transcription factors that contain conserved zinc finger domains involved in binding to target DNA se

111 the middle of the DH that is composed of the zinc finger domains of both hexamers.

112 To assess the effect of zinc finger E box-binding homeobox 1 transcription facto

113 Mechanistically, we find that the ZEB1 (zinc finger E-box binding homeobox 1) transcription fact

114 transcription factors SRY-box 10 (SOX10) and zinc finger E-box binding homeobox 2 (ZEB2).

115 iants affect a single conserved residue in a zinc finger motif crucial for DNA binding and are delete

116 Further analyses show that only three zinc finger motifs are essential for PAR recognition.

117 an cells revealed that intact PIN domain and Zinc finger motifs in human hUTP23 are essential for 18S

118 In addition, we used Zinc finger nucleases to generate isogenic SHANK3 knocko

119 strate how a missense mutation in the second zinc finger of Kruppel-like factor-1 (KLF1) leads to deg

120 the rapidly evolving Kruppel-associated box-zinc finger protein (KRAB-ZFP) family linked primarily t

121 The nuclear matrix protein Cip1-interacting zinc finger protein 1 (CIZ1) promotes DNA replication in

122 Among these, the GATA-3 repressor zinc finger protein 1 (Zfpm1) emerged as a potential med

123 NT The deletion of the Miz1 (Myc-interacting zinc finger protein 1) POZ (POxvirus and Zinc finger) do

124 lysis identifies allele-preferred binding of Zinc finger protein 148 (ZNF148) to rs36115365-C, furthe

125 al. investigate the interaction of CXXC-type zinc finger protein 5 (CXXC5) with Dishevelled as one su

126 We identify zinc finger protein 568 (ZFP568), a member of the rapidl

127 We studied the Zinc Finger Protein 598 (ZNF598) using PAR-CLIP and reve

128 tor for male-specific lethal [MSL] proteins) zinc finger protein binds these GA repeat motifs, increa

129 The zinc finger protein CTCF has been invoked in establishin

130 Here, we demonstrate that the zinc finger protein Zbtb20 is required for DNL.

131 d a distinct complex containing Mtr4 and the zinc finger protein ZFC3H1.

132 The zinc finger protein ZPR1 interacts with SMN.

133 We identify another zinc finger protein, Yin Yang 1 (YY1), at the base of lo

134 c-Myc-interacting zinc finger protein-1 (Miz-1) is a poly-Cys2His2 zinc fi

135 gi apparatus-specific Asp-His-His-Cys (DHHC) zinc finger protein.

136 gi apparatus-specific Asp-His-His-Cys (DHHC) zinc finger protein; (ii) a GODZ dominant-negative mutan

137 matically compared four different engineered zinc finger proteins (ZFP), four transcription activator

138 our known CRBN neo-substrates [Ikaros family zinc finger proteins 1 (IKZF1) and 3 (IKZF3), casein kin

139 ardiac reprogramming, we discovered that the zinc finger transcription factor 281 (ZNF281) potently s

140 Here, we identify the zinc finger transcription factor EGR1 as a negative regu

141 tion between Drosophila FOXO (dFOXO) and the zinc finger transcription factor Kruppel homolog 1 (Kr-h

142 gene 3 (Peg3), an imprinted gene encoding a zinc finger transcription factor postulated to function

143 Here we establish the zinc finger transcription factor Tshz1 as a marker of IT

144 EGR1 is an early growth response zinc finger transcription factor with broad actions, inc

145 report the functional characterization of a zinc finger transcription factor, OsGATA12, whose overex

146 mechanism through which STAT3 and the Ikaros zinc finger transcription factors Aiolos and Ikaros coop

147 eviously demonstrated that expression of the zinc finger transcriptional repressor Blimp1/PRDM1 is es

148 y, transcriptional targets recognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an e

149 des and RNA interference targeting mRNA, and zinc finger transcriptional repressors and CRISPR-Cas9 m

150 s and virally delivered RNA interference and zinc finger transcriptional repressors in advanced testi

151 ing zinc finger protein 1) POZ (POxvirus and Zinc finger) domain in Schwann cells causes a neuropathy

152 odule within KDM2A consisting of a CXXC type zinc finger, a PHD domain and a newly identified Heteroc

153 TAGGGAA-3') and encompasses a Myc-associated zinc finger-binding site that regulates KRAS transcripti

154 te immune cell interactions and a cluster of zinc finger-encoding genes associated with KMT2A rearran

155 en using small inhibitory RNAs revealed that zinc-finger antiviral protein (ZAP) inhibited virion pro

156 cription, whereas deletion of its C-terminal zinc-finger domain diminished this effect.

157 wn silencer for Thpok, and requires the last zinc-finger motif in Bcl11b protein, which by contrast i

158 developed a novel Bace1(-/-) rat line using zinc-finger nuclease technology and compared Bace1(-/-)

159 The C2H2 zinc-finger protein Pita binds to several BX-C boundarie

160 rated the target search process of the Egr-1 zinc-finger protein.

161 of decoys on the search process of the Egr-1 zinc-finger protein.

162 Kruppel-associated box zinc-finger proteins (KRAB-ZFPs) make up the largest fam

163 myelodysplastic syndrome 1 (MDS)/EVI encode zinc-finger proteins that have been recognized as import

164 PR-domain-containing proteins (PRDMs) are zinc-finger sequence-specific chromatin factors that hav

165 (NuRD) complex binding are required for the zinc-finger transcription factor CASZ1 to function as a

166 Kruppel-like factor 4 (KLF4, GKLF) is a zinc-finger transcription factor involved in a large var

167 The Zfp423/ZNF423 gene encodes a 30-zinc-finger transcription factor involved in key develop

168 osterix (osx; sp7) encodes a zinc-finger transcription factor that controls osteoblas

169 We show that Combgap (Cg), a zinc-finger transcription factor, antagonizes Eya-So fun

170 ctor (CTCF), containing a tandem array of 11 zinc fingers (ZFs), modulates the three-dimensional orga

171 g modules: full-length DNA binding proteins, zinc fingers (ZFs), transcription activator-like effecto

172 ormed by Zn(II) displacement from the parent zinc fingers (ZFs).

173 te that, in addition to binding DNA, PRDM9's zinc fingers also mediate its multimerization, and we sh

174 selective magnetic solid phase extraction of zinc followed by its determination by flame atomic absor

175 demonstrate that the three-dimensional (3D) zinc form-factor elevates the performance of nickel-zinc

176 Its crystal structure, determined as a novel zinc-free hexamer at 2.8 A, revealed a native insulin fo

177 g TORC1, leading to release and recycling of zinc from degraded proteins.

178 Bacteria can acquire the essential metal zinc from extremely zinc-limited environments by using A

179 nstrated amyloid properties, and addition of zinc further increased amyloid formation.

180 ion of antifungal agents (cinnamon bark oil, zinc gluconate and trans-ferulic acid) in oil-in-water e

181 The incorporation of zinc gluconate or trans-ferulic acid, independently of t

182 s) and their food (periphyton) to an aqueous zinc gradient (3-340 mug Zn/l) and measured zinc concent

183 We investigated low zinc homeostasis in Caenorhabditis elegans because the g

184 ption activator Zap1 plays a central role in zinc homeostasis in the budding yeast Saccharomyces cere

185 beginning to be defined in animals, but low zinc homeostasis is poorly characterized.

186 High zinc homeostasis mechanisms are beginning to be defined

187 he LZA element is a critical part of the low zinc homeostasis pathway.

188 cells, suggesting a conserved pathway of low zinc homeostasis.

189 Herein, we demonstrate that zinc homoenolates can react as carbonyl-electrophiles in

190 5,20-tetrakis(4-aminophenyl)porphyrin or its zinc(II) complex, 1H-4-imidazolecarbaldehyde, and either

191 plex, 1H-4-imidazolecarbaldehyde, and either zinc(II) or iron(II) salts, we were able to prepare O-sy

192 Zinc(II) phthalocyanine fused in peripheral positions oc

193 82, -96 and -183 in prostate cells decreased zinc import, which is a characteristic feature of PCa tu

194 ferential partitioning of isotopically heavy zinc in the complexed form, and the extent of fractionat

195 he selective extraction and determination of zinc in various samples including well water, drinking w

196 showed good agreement, except for sodium and zinc, in which analyses of 24h diet dairies overestimate

197 moderately volatile elements (such as lead, zinc, indium and alkali elements) relative to CI chondri

198 ns and reveal a possible molecular basis for zinc-induced cancer prevention and Orai1-SOCE signaling

199 intact cortical cytoskeleton is required for zinc-induced cis multimerization.

200 Zinc intoxication is prevented in S. pneumoniae by expre

201 led to the identification of a contaminating zinc ion as solely responsible for the observed effects.

202 e, a class III amidohydrolase, with a single zinc ion coordinated by His-6, His-8, His-179, and Glu-2

203 culations on cluster models suggest a single zinc ion may be sufficient to support phosphoethanolamin

204 ibitors, which interact with the active-site zinc ion of CSN5 through an unprecedented binding mode.

205 ontain hydroxamate moiety that chelates with zinc ion to become the cofactor of HDAC enzymes.

206 btain a maximum accumulation of selenium and zinc ions (simultaneously) in the biomass.

207 formed larger aggregations and released less zinc ions (Zn(2+)) at greater temperature and salinity,

208 stain electron microscopy demonstrated that zinc ions induce auto-association process of this TDP-43

209 emically dependant interplay between oceanic zinc, iron and phosphorus cycles.

210 isk allele C is associated with higher islet zinc levels and support prior evidence of cadmium's high

211 Despite its importance, high zinc levels can impair cellular processes, inhibiting gr

212 r reduced zinc transporter and intracellular zinc levels in benign prostate cells, PCa xenografts and

213 uire the essential metal zinc from extremely zinc-limited environments by using ATP-binding cassette

214 comparison of these structures revealed that zinc loss prompts significant structural rearrangements,

215 oped for the determination of lead, cadmium, zinc, manganese and iron in white and wild rice samples.

216 These data suggest that zinc may inhibit cell proliferation of esophageal cancer

217 on delocalization on electron transfer using zinc meso-tetraphenylporphyrin (ZnTPP) as a donor and a

218 ed that small-molecule zinc chelators called zinc metallochaperones (ZMCs) reactivate mutant p53 by r

219 Zinc metallopeptidase STE24 (ZMPSTE24) is a transmembran

220 Angiotensin-I converting enzyme (ACE) is a zinc metalloprotease consisting of two catalytic domains

221 ecanase-1 and -2 (ADAMTS-4 and ADAMTS-5) are zinc metalloproteases involved in the degradation of agg

222 MCR-1 periplasmic, catalytic domain to be a zinc metalloprotein with an alkaline phosphatase/sulphat

223 oth an acetato ligand and an amino ligand to zinc occurs in distinct confined environments, reminisce

224 Selective inhibitory effects of zinc on cell proliferation in esophageal squamous cell c

225 Aluminum-doped zinc oxide (AZO) was deposited by low-temperature atomic

226 nd molecular imprinting of nanocomposites of zinc oxide (ZnO) and polypyrrole (PPY) is structured and

227 This biosensor was based on thin films of Zinc Oxide (ZnO) deposited by atomic layer deposition (A

228 Zinc oxide (ZnO) is of widespread use for numerous appli

229 osed of alternating layers of aluminum-doped zinc oxide and zinc oxide.

230 issolution of a surface passivation layer of zinc oxide in CH3 COOH/H2 O and subsequent self-exchange

231 te hexahydrate for the synthesis of graphene/zinc oxide nanocomposite by solvothermal growth.

232 tform has been constructed based on graphene/zinc oxide nanocomposite produced via a facile and green

233 The as-synthesised graphene/zinc oxide nanocomposite was characterised with scanning

234 obilized onto a novel chitosan/coconut fibre/zinc oxide nanoparticles (CS/CF/nZnO) hybrid support to

235 umnar nanocomposites by sequential growth of zinc oxide nanowire carpets followed by layer-by-layer d

236 sed on multiwalled carbon nanotubes embedded zinc oxide nanowire for the ultrasensitive detection of

237 Zinc oxide nanowires electrodeposited epitaxially on a g

238 medium which enhances the LMR properties of zinc oxide thereby increasing the conductivity and hence

239 mbining these two effects in aluminium-doped zinc oxide via a two-colour laser field discloses new ma

240 radation phenomena affecting oil paints with zinc oxide, one of the most common white pigments of the

241 ting layers of aluminum-doped zinc oxide and zinc oxide.

242 s of the XPS results obtained after exposing zinc oxide/copper (111) [ZnO/Cu(111)] surfaces to hydrog

243 l for customized creation of nanoclusters of zinc peroxide.

244 morphous or nanostructured zinc sulfides and zinc phosphate as compared to raw waste.

245 co-assembly of L,L-diphenylalanine (FF) and zinc phthalocyanine complexes (ZnPc) in water.

246 irubin oxidase, and the anode is made from a zinc plate.

247 The essential element zinc plays critical roles in biology.

248 eptor molecular dyads were constructed using zinc porphyrin and free base porphyrin (Zn(i + 2)-Zn(i +

249 ry on triplet state delocalization in linear zinc porphyrin oligomers is explored by electron paramag

250 Twenty-four different zinc porphyrin-pyridine complexes were investigated in m

251 ained from the self-assembly of Fe(II) and a zinc-porphyrin-containing ligand.

252 of volatile elements and compounds, such as zinc, potassium, chlorine, and water, provide key eviden

253 with aldimines is efficiently catalyzed by a zinc-ProPhenol dinuclear complex under mild conditions t

254 study, we identify MT3-MMP, a membrane-bound zinc protease, to be necessary for the development of ex

255 the side chains of residues coordinating the zinc rearrange quickly to promote the nucleophilic attac

256 was lower for WPH-Ever-zinc, and over 50% of zinc remained bound in both peptide complexes after pept

257 In zinc-deficient cells, Zap1 binds to zinc responsive elements in target gene promoters and ac

258 The zinc-responsive transcription activator Zap1 plays a cen

259 escuing impaired fear extinction via dietary zinc restriction was associated with differential expres

260 al topologic similarity of the Zf-GRF to the zinc ribbon domains of TFIIS and RPB9.

261 a 6-wk controlled consumption study of a low-zinc, rice-based diet.

262 Zinc SBPs are characterized by a flexible loop near the

263 ted by the novel TetR-family transcriptional zinc-sensing regulator SczA.

264 At the same time, zinc sequestration had no effect on zinc-dependent cellu

265 Vpr-CRL4 E3 ligase function was achieved by zinc sequestration using N,N,N'-tetrakis-(2'-pyridylmeth

266 Here, we present intact structures for the zinc-specific SBP AztC from the bacterium Paracoccus den

267 is known to bind to Zn(II) and can induce a zinc starvation response in bacteria.

268 ams on whole-body and cellular indicators of zinc status.

269 ations, proved decisive for the formation of zinc stearate-like (ZnSt2) soaps.

270 fides as well as amorphous or nanostructured zinc sulfides and zinc phosphate as compared to raw wast

271 shearwaters were either made anosmic with 4% zinc sulphate solution, magnetically impaired by attachm

272 e dismutase (Ccs1) activates immature copper-zinc superoxide dismutase (Sod1) by delivering copper an

273 d nutrient supplement, deworming medication, zinc supplementation, a bed net, and malaria chemoprophy

274 ehydration solutions, continuous feeding and zinc supplementation.

275 nalyze the dissolution kinetics of the polar zinc-terminated (000-1) and nonpolar (10-10) crystal sur

276 d the impact of a modest increase in dietary zinc that was similar to that provided by biofortificati

277 ly raises the Lewis acidity of the catalytic zinc, thus increasing the activity at one active site at

278 nt defenses and suggested to protect against zinc toxicity.

279 on of any of these residues to Ala abrogated zinc transfer from AztD.

280 We propose ZIP14 mediates zinc transport into hepatocytes to inhibit protein-tyros

281 ivalent metal ion transporter best known for zinc transport.

282 verexpression of the miR-183 cluster reduced zinc transporter and intracellular zinc levels in benign

283 rocyte and leukocyte zinc concentrations and zinc transporter expressions were not altered.

284 narily conserved Zrt, Irt-like protein (ZIP) zinc transporter family members.

285 This granular zinc transporter is also a major self-antigen found in t

286 ganese transporter mutant but not a vacuolar zinc transporter mutant.

287 er ZIP14 (SLC39A14) is viewed primarily as a zinc transporter that is inducible via proinflammatory s

288 The islet-specific zinc transporter ZnT8 mediates zinc enrichment in the in

289 rs13266634 in the SLC30A8 gene encoding the zinc transporter ZnT8, is associated with an increased r

290 ic digestion on the speciation of copper and zinc, two metals that generally occur at high concentrat

291 Impaired hepatic zinc uptake in Zip14 KO mice during ER stress coincides

292 id regions that promotes autoaggregation and zinc uptake, and may serve as an additional system for t

293 -) (KO) mice, which exhibit impaired hepatic zinc uptake.

294 ly activated, and reduced holomycin chelates zinc with high affinity.

295 n exists in tolerance of excess copper (Cu), zinc (Zn) and cadmium (Cd).

296 technique to quantify the bioavailability of zinc (Zn) associated with natural particles using snails

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

298 interfering metals such as cadmium (Cd) and zinc (Zn), and stable response in natural water samples

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

300 and common terrestrial contaminants such as zinc (Zn).