ライフサイエンスコーパス: zinc

1 ese crowberry) is rich in calcium, iron, and zinc.

2 These particles did not contain oxidized zinc.

3 mized during 2013-2017 (1,185 folic acid and zinc, 1,185 placebo); they had a mean age of 33 years an

4 (cobalt, copper, manganese, molybdenum, and zinc), 4 metals with some evidence of normal physiologic

5 (0%) were low compared with deficiencies of zinc (60%) and vitamin A (34%).

6 isorder in ZIF glasses using ultrahigh-field zinc-67 solid-state nuclear magnetic resonance spectrosc

7 diting activity was sensitive to addition of zinc acetate or the zinc chelators 1,10-o-phenanthroline

8 uperiority analysis) within 30 minutes after zinc administration.

9 one rescues not only mutations that decrease zinc affinity, but also mutations that destabilize DBD w

10 genic p53 mutations and find that 80% impair zinc affinity, thermodynamic stability, or both.

11 ium-sulfur batteries, lithium-air batteries, zinc-air batteries, and aluminum-air batteries.

12 As the air electrode in zinc-air batteries, the SA-Fe-NHPC demonstrates a large

13 Levels of zinc, along with its mechanistically related metabolites

14 reover, we observed reduced plasma levels of zinc-alpha-2-glycoprotein, butyrylcholinesterase, and in

15 n response to changes in the availability of zinc, an essential micronutrient.

16 Zinc and copper are involved in neuronal differentiation

17 ll, these results indicate new functions for zinc and copper in the modulation of the cytoskeleton mo

18 tify essential trace elements (iron, copper, zinc and iodine) and establish their speciation in human

19 bread wheat genotypes characterized for the zinc and iron content, the most important micronutrients

20 availability of key heavy metal ions such as zinc and iron.

21 ch regulates concentrations of intracellular zinc and is increased in pancreatic cancer cells, in cel

22 Simultaneous spatial detection of zinc and its metabolites is not only a valuable tool for

23 The aim of this study is to extract zinc and manganese from foods and vegetables using an am

24 In this study, we analysed iron, zinc and phosphorus in cabbage, broccoli, pepper, spinac

25 veal the co-localization at the nanoscale of zinc and tubulin in dendrites with a molecular ratio of

26 Zinc and Yttrium single sites were introduced into the s

27 izes the known molecular mechanisms of iron, zinc, and B vitamin processing by human-associated bacte

28 t biochemical analytes, anthropometry, serum zinc, and body composition (via DXA).

29 the concentrations of vitamin C, vitamin E, zinc, and copper in both national and regional brands of

30 measured quantities of vitamin C, vitamin E, zinc, and copper were slightly higher than labeled but n

31 measures of serum ferritin (SF), vitamin A, zinc, and CRP measured using different assays with varia

32 endrites with a molecular ratio of about one zinc atom per tubulin-alphabeta dimer.

33 -incorporated InP MSCs that have chlorine or zinc atoms.

34 pendent on the lot, correlating with initial zinc availability (i.e., less MIC reduction with higher

35 le fertility commonly contain folic acid and zinc based on limited prior evidence for improving semen

36 ect, inhibitors bearing two pharmacophores-a zinc binding group and a Cys-reactive warhead-were desig

37 tions that destabilize DBD without impairing zinc binding.

38 tiple ribosomal (r-) proteins containing the zinc-binding CXXC motif are replaced by their motif-free

39 d a distinct architecture in which the beta' zinc-binding domain (ZBD) of RNAP stretches out from its

40 V, which has multiple domains: an N-terminal zinc-binding domain (ZBD), a 1B domain, and helicase cor

41 distal upstream DNA over the RNA polymerase zinc-binding domain, NusA rotates underneath one capping

42 zation of the E3 ligase complex, such as the zinc-binding motif and N- and C-terminal regions of the

43 Two predicted zinc-binding residues, Asp87 and His88, are required for

44 y, these studies reveal a previously unknown zinc-binding site on the surface of the ADAR1 deaminase

45 within the DNA-binding domain, distal to the zinc-binding site.

46 and Cu(2+) We also demonstrate that multiple zinc-binding sites on tau are involved in the LLPS-promo

47 When combined with a flexible triamine and zinc bis(trifluoromethanesulfonyl)imide, this ketone for

48 gradually evolved from polytwistane to more zinc-blende.

49 The Clp protease system destabilizes a zinc-bound form of Mpy recruitment factor (Mrf), which i

50 tive study on the intermediate states of the zinc-bound native CA II and non-native metal-substituted

51 The high intracellular zinc-chelating capacity of both compounds, deduced from

52 In addition, zinc chelation causes a decrease in the expression of cy

53 sensitive to addition of zinc acetate or the zinc chelators 1,10-o-phenanthroline and EDTA.

54 o provide a fast and simple method to detect zinc, citrate, and aspartate levels as a biomarker signa

55 Zinc, citrate, and aspartate were correlated with each o

56 is used as a surrogate to bind a terpyridine zinc complex (Tpy-Zn), forming a fluorescent [Tpy-Zn]-SP

57 tence, attributed to slower release from the zinc complex and the PLGA NPs, resulted in a 5-fold dose

58 Plasma or serum zinc concentration (PZC) is recommended to estimate zinc

59 at an approximately two-fold lower cellular zinc concentration than remodeling.

60 Zinc concentrations in cation-adjusted Mueller-Hinton br

61 per, lead, manganese, mercury, selenium, and zinc concentrations were measured by inductively coupled

62 i.e., less MIC reduction with higher initial zinc concentrations), while MICs for KPC-harboring isola

63 We concluded that histidine involved in zinc coordination at the active site reacted slower than

64 nd other antioxidants (vitamin C, vitamin E, zinc, copper) for 16 weeks.

65 5% CI: 21, 27 U/L; P < 0.001) and mean serum zinc decreased from baseline (0.75 mug/dL; 95% CI: 0.71,

66 PC alpha-defensin dysfunction is mediated by zinc deficiency and involved in the pathogenesis of AH.

67 and proliferation, yet the mechanisms of how zinc deficiency arrests these processes remain enigmatic

68 The role of zinc deficiency in alpha-defensin was evaluated in acute

69 12 PSC surveys, the estimated prevalence of zinc deficiency increased with increasing CRP deciles, a

70 Zinc deficiency induces quiescence and resupply stimulat

71 ey data, estimates of prevalence of iron and zinc deficiency were comparable but vitamin A deficiency

72 Zap1 controls their response to zinc deficiency.

73 d bidirectional control over the activity of zinc-dependent carbonic anhydrase in solution as an isol

74 ap B-repeat constructs assemble further into zinc-dependent functional amyloid fibers.

75 Dipeptidyl peptidase 3 (DPP3) is a zinc-dependent hydrolase involved in degrading oligopept

76 the caseinolytic protease (Clp) system in a zinc-dependent manner.

77 cture of the active site compared with other zinc-dependent nucleotide deaminases.

78 These results establish YbeY as a zinc-dependent single-strand specific endoribonuclease t

79 tion is a specific and conserved response to zinc depletion in both environmental and pathogenic myco

80 Monitoring cells before and after zinc deprivation we found the position of cells within t

81 aluated in acute and chronic mouse models of zinc deprivation.

82 ZnCl(3)(-) detection was validated by total zinc determination using laser ablation inductively coup

83 ssociations of silicon during pregnancy, and zinc during childhood, with MD.

84 Brain zinc dysregulation is linked to many neurological disord

85 the viral nucleocapsid protein NCp7, causing zinc ejection and preventing RNA encapsidation.

86 tion state and local electronic structure of zinc, electrons originating from the zinc oxide excitati

87 CCCH-type tandem zinc finger (TZF) domains are found in many RNA-binding

88 h heterozygous variants affecting the fourth zinc finger (ZF4) of Wilms' tumor 1 (WT1) (p.Ser478Thrfs

89 ted that the transcription factor GLI family zinc finger 1 (GLI1) mediates Sulf2 expression during HC

90 of the stem cell-expressed genes GLI family zinc finger 1 (Gli1) or achaete-scute homolog 1 (Ascl1).

91 ce transcription factors, VASCULAR PLANT ONE-ZINC FINGER 1 (OsVOZ1) and OsVOZ2, and promotes their de

92 ese results suggest an active role for GATA3 zinc finger 2 mutants in ER-alpha positive breast tumors

93 memory retrieval-associated increases in BLA zinc finger 268 (zif268) and activity regulated cytoskel

94 g three distinct targeted mutations of A20's zinc finger 7 (ZF7) ubiquitin-binding motif uniformly de

95 The ZZ-type zinc finger and EF-hand domain protein 1 (ZZEF1) is a mu

96 The MDMX acidic domain and zinc finger are necessary and sufficient for binding and

97 ovel RNA-binding protein interactors ZC3H14 (zinc finger CCCH-type containing 14) and THOC1 (THO comp

98 etase Long Chain Family Member 5 (ACSL5) and Zinc Finger DHHC-Type Containing 6 (ZDHHC6), was charact

99 Here, we identified zinc finger DHHC-type containing 7 (DHHC7) protein as an

100 catalytic SET domain and an intervening MYND zinc finger domain, as well as an extended C-terminal do

101 the highly conserved C-terminal DNA-binding zinc finger domains.

102 vivo and in vitro through their conserved C-zinc finger domains.

103 Zinc finger E-box binding homeobox 1 (Zeb1) has been dem

104 s with CRISPR/Cas9-mediated depletion of the zinc finger E-box binding homeobox 1 (ZEB1) in claudin-l

105 Located on chromosome 5A, B1 is a C2H2 zinc finger encoding gene with ethylene-responsive eleme

106 tanding of how a single mutation in the KLF1 zinc finger exerts effects on erythroid physiology in CD

107 n synthesis were detected at lower rates and zinc finger family transcripts were of poorer quality.

108 Very few other members of the zinc finger FYVE domain-containing family (zfyve) have d

109 in Kruppel-associated box domain-containing zinc finger genes on chromosome 19, both of which are as

110 The Cys2His2 zinc finger is the most common DNA-binding domain expand

111 Disruption of the zinc finger motifs in GATA-1, such as produced by germli

112 arsenic interacts with the N- and C-terminal zinc finger motifs of GATA-1, causing zinc loss and inhi

113 onserved cysteine-rich motifs reminiscent of zinc finger motifs.

114 go, first with meganucleases and followed by zinc finger nucleases, transcriptional activator-like ef

115 The structure of the second zinc finger of SALL4 in complex with pomalidomide, cereb

116 rol genes that include homologs of mammalian Zinc finger of the cerebellum and Purkinje cell protein

117 The Kruppel-associated box zinc finger protein (KRAB-ZFP) family diversified in mam

118 these effects and identify a cluster of KRAB zinc finger protein (KZFP) genes that modifies VM-IAPs i

119 SET1 methyltransferase activity is the CxxC zinc finger protein 1 (Cfp1).

120 CIP1-interacting zinc finger protein 1 (CIZ1) is a nuclear matrix associa

121 ut ZNF274, a Kruppel-associated box-A-domain zinc finger protein capable of recruiting epigenetic mac

122 that ARS2 (arsenite-resistance protein 2), a zinc finger protein that is essential for early mammalia

123 for awn inhibition in wheat, encodes a C2H2 zinc finger protein with EAR motifs which putatively fun

124 In addition, we identify the KRAB zinc finger protein, ZNF446, and its associated triparti

125 pproaches on two large, independent Cys2His2 zinc finger protein-DNA interaction datasets. We demonst

126 tion factor-binding motif for ZNF263, a C2H2 zinc finger protein.

127 -genome activation, implying that other KRAB-zinc finger proteins (KZNFs) recruit KAP1 prior to blast

128 To accomplish this task, we designed zinc finger proteins (ZFPs) targeting within -300 bps of

129 family of ubiquitously expressed human C2H2 zinc finger proteins comprised of ZFX, ZFY and ZNF711.

130 well as genes coding for aminotransferases, zinc finger proteins, and several uncharacterized protei

131 yltransferase Ehmt1 and stabilization of the zinc finger TF Zic2 at enhancers and promoters.

132 slocates to the nucleus and interacts with a zinc finger transcription factor (FgZC1), also required

133 The Arabidopsis thaliana zinc finger transcription factor (ZF-TF), S-nitrosothiol

134 er unmask a mutual requirement for Hivep3, a zinc finger transcription factor and adapter protein.

135 al erythropoiesis is highly regulated by the zinc finger transcription factor GATA-1.

136 otrophin signalling system; a high number of zinc finger transcription factors; and novel factors tha

137 ing only two predicted genes, including C2H2 zinc finger transcriptional repressor TraesCS5A02G542800

138 show that combined biallelic Cebpa and Gata2 zinc finger-1 (ZnF1) mutations cooperatively induce bili

139 ZNF281 binds XRCC4 through its zinc-finger domain and facilitates its recruitment to da

140 Previous studies have suggested that the zinc-finger epithelial-mesenchymal transition transcript

141 ls coexpressed MYC and MIZ1 (MYC-interacting zinc-finger protein 1 [ZBTB17]).

142 Here, we identify a novel role for the zinc-finger protein ZNF281 in participating in the order

143 ology approach, we identify a new network of zinc-finger proteins that are expressed in one class of

144 introduce three epigenome-editing platforms: zinc-finger proteins, transcriptional activator-like eff

145 Odd-paired (Opa), a zinc-finger transcription factor expressed at cellulariz

146 Here, we show that the zinc-finger transcription factor GLI1, a terminal effect

147 opment, POPOVICH (POP), which encodes a C2H2 zinc-finger transcription factor.

148 The SUPERMAN (SUP) gene encodes a C2H2 zinc-finger transcriptional repressor that regulates the

149 Gag or Gag mutants carrying deletions in NC zinc fingers (ZFs) or a nonmyristoylated version of Gag.

150 The CPSF30 subunit contains five CCCH zinc fingers (ZFs), with ZF2-ZF3 being required for the

151 this geometry are enriched in genomes where zinc fingers are prevalent and specificity transitions w

152 The GATA3 zinc fingers efficiently bind their target 5'-GAT-3' seq

153 sis likely through replacing zinc within the zinc fingers of the critical transcription factor GATA-1

154 a DNA-binding residue in the first of three zinc fingers.

155 n further depletion of zinc, presumably in a zinc-free form.

156 t muscle zinc homeostasis or muscle-specific zinc functions.

157 e of DNA fragmentation in the folic acid and zinc group and 27.2% in the placebo group; mean differen

158 ment groups (404 [34%] in the folic acid and zinc group and 416 [35%] in the placebo group; risk diff

159 Lower doses of zinc had noninferior efficacy for the treatment of diarr

160 on to understanding the relationship between zinc homeostasis and the pathogenic process in AD and re

161 zinc, however, little is known about muscle zinc homeostasis or muscle-specific zinc functions.

162 ion (Hut) system as being linked to nutrient zinc homeostasis, but whether the Hut system is importan

163 Mre11/Rad50 complex transiently opens at the zinc hook of Rad50.

164 l muscle represents the largest pool of body zinc, however, little is known about muscle zinc homeost

165 o 5800 h(-1), outperforming that of reported zinc hydride catalysts.

166 Three new dimeric bis-guanidinate zinc(II) alkyl, halide, and hydride complexes [LZnEt](2)

167 In this work, ten different zinc(II) Pcs with carboxylate functions or quaternary ni

168 The water-soluble thioglycosylated zinc(II) porphyrins having two meso-N-butylcarbazole gro

169 lysosomes of water-soluble thioglycosylated zinc(II) porphyrins in A549 cells.

170 efficiency of water-soluble thioglycosylated zinc(II) porphyrins were considerably higher than nonmet

171 metal separately by cysteine and hydrolyzed zinc(II), and synergistically by the combination of the

172 d copper-chelating salicylaldoxime, known as zinc imidazole salicylaldoxime supramolecule.

173 ess was based on the utilization of magnetic zinc-imidazole frameworks (ZIF-4), as a highly efficient

174 sed DNA damage levels, suggesting a role for zinc in maintaining genome integrity.

175 The role of zinc in neurobiology is rapidly expanding.

176 ly a valuable tool for analyzing the role of zinc in prostate metabolism but might also provide a fas

177 er, pharmacologically sustained elevation of zinc in WT eggs prior to activation resulted in abnormal

178 distribution of oleic acid-grafted-chitosan-zinc-insulin complexes into the hydrophobic core of PLA-

179 n was significantly improved by formation of zinc-insulin hexamers, further stabilized by electrostat

180 amics, membrane dynamics, RNA processing and zinc ion binding.

181 iber and hydrogel doped with the fluorescent zinc ion probe molecule meso-2,6-Dichlorophenyltripyrrin

182 An optical diffuser is incorporated into the zinc ion sensor based on optical fiber and hydrogel dope

183 Solid-state zinc ion sensor is developed with high enough resolution

184 structures, electrochemical performance, and zinc ion storage mechanisms.

185 other members of this enzyme class, a second zinc ion was present in the beta-CASP domain that leads

186 P: a group that interacts with the catalytic zinc ion, functionality that enhances affinity to the su

187 te acts as a counterion for the Lewis acidic zinc ion, which provides the activation of the aldehyde.

188 In situ metal-templating by zinc ions gives quantitative yields of the Mn(2) product

189 ed recently; however, both proteins have two zinc ions instead of two iron ions in the catalytic cent

190 in MeCN by using either the proper ratio of zinc ions or acid.

191 mbined with our previous results on divalent zinc ions, we propose a model that links the microscopic

192 t metals in drinking water including copper, zinc, iron, and manganese.

193 Zinc is a biologically essential element and involved in

194 ty of YbeY is enhanced when the occupancy of zinc is increased.

195 ation with a high-affinity modulator such as zinc is most likely to account for the error, and we sug

196 structures, and auditory brainstem, synaptic zinc is released from presynaptic terminals to modulate

197 Zinc is widely recognized as essential for growth and pr

198 Our findings showed that greater hair zinc levels were associated with lower brain activity du

199 reduced mitochondrial manganese, cobalt, and zinc levels, but not reduced iron.

200 icate for each lot of conventional caMHB and zinc-limited media by broth microdilution.

201 Zinc-limited media were prepared by the addition of EDTA

202 ion of EDTA to caMHB as a means of achieving zinc-limited media.

203 s of >=30 mug/ml was sufficient to provide a zinc-limited medium, resulting in MICs that reflect in v

204 rminal zinc finger motifs of GATA-1, causing zinc loss and inhibition of DNA and protein binding acti

205 y, we evaluated vitamin D and mineral (iron, zinc, magnesium) transfer to the bolus aqueous phase dur

206 ocopherol (mean: +8.7%; 95% CI: 3.6, 13.7%), zinc (mean: +2.3%; 95% CI: 0.5, 4.2%), thyroglobulin (me

207 OH)D (mean: +14.7%; 95% CI: 4.8, 25.6%), and zinc (mean: +5.8%; 95% CI: 1.0, 10.8%).

208 nt diastereo- and enantiocontrol followed by zinc-mediated Barbier allylation to set the third chiral

209 A ball-milling-enabled zinc-mediated Barbier-type allylation reaction is report

210 inc signaling (Z-LTP), evidenced by enhanced zinc-mediated inhibition of EPSCs.

211 Therefore, the developed zinc-mediated template synthesis strategy for boosting t

212 aft experiments demonstrate that a synthetic zinc metallochaperone rescues not only mutations that de

213 The results suggest that zinc metallochaperones have the capability to treat 120,

214 how rapid antibiotic-mediated evolution of a zinc metalloenzyme obligatorily occurs in the context of

215 are degraded by dihydropyrimidinase (DHP), a zinc metalloenzyme that is upregulated in solid tumors b

216 esses activate the inner membrane-associated zinc metallopeptidase OMA1 that cleaves L-OPA1, causing

217 ciated degradation ubiquitin ligase Hrd1 and zinc metalloprotease Ste24, promote degradation of chara

218 ctivation and presents the first evidence of zinc modulation during egg activation in a non-mammalian

219 s indicate that ZIP9 is essential for proper zinc modulation during zebrafish egg activation and pres

220 odorant responses induced by the endogenous zinc nanoparticles appears to be similar to the amplific

221 Naturally occurring zinc nanoparticles were detected in olfactory and nasal

222 to the amplification produced by engineered zinc nanoparticles.

223 not have the effects observed in the case of zinc nanoparticles.

224 ncentration (PZC) is recommended to estimate zinc nutritional status; however, concentrations may dec

225 t and ultraflexible amorphous indium-gallium-zinc oxide (a-IGZO) thin-film transistors (TFTs) and int

226 que, including semiconducting indium-gallium-zinc oxide (IGZO) and copper oxide, as well as conductin

227 nvestigated a sensor structure formed with a Zinc Oxide (ZnO) coating, deposited by Atomic Layer Depo

228 Zinc oxide (ZnO) is a stable, direct bandgap semiconduct

229 Here, we report an associative zinc oxide band-gap excitation and copper plasmonic exci

230 ease in resistance has been found in case of zinc oxide derived MEMS devices.

231 ture of zinc, electrons originating from the zinc oxide excitation and copper plasmonic excitation se

232 ly promote methanol-production at the copper-zinc oxide interfacial perimeter of copper/zinc oxide/al

233 he chitosan films with varying quantities of zinc oxide nanoparticles loaded gallic-acid (ZnO@gal) co

234 Chitosan (Ch) and zinc oxide nanoparticles loaded gallic-acid films, (Ch-Z

235 surface-micromachined cantilever arrays and zinc oxide surface-microfabricated interdigitated circui

236 transparent conducting oxide (aluminum doped zinc oxide) and pure VO(2) using pulsed laser deposition

237 g a fluorescent mouthguard consisting of the zinc oxide-poly(dimethylsiloxane) (ZnO-PDMS) nanocomposi

238 We present a tyrosinase-conjugated zinc oxide-reduced graphene oxide (Tyr/ZnO-rGO) nanocomp

239 r-zinc oxide interfacial perimeter of copper/zinc oxide/alumina (CZA) catalyst.

240 A series of PNP zinc pincer complexes capable of bond activation via aro

241 Utilizing this zinc pincer system, base-free catalytic hydrogenation of

242 ate the radiation spectra of superdense iron-zinc plasma mixtures at mass densities of rho = 250 to 2

243 hich two oligopyridine ligands bind inside a zinc porphyrin nanoring in a stacked arrangement.

244 hich is stabilized upon further depletion of zinc, presumably in a zinc-free form.

245 udomonas aeruginosa harbors three paralogous zinc proteases annotated as AmpD, AmpDh2, and AmpDh3, wh

246 s of the bound, light-activated chromophore, zinc protoporphyrin IX, (PPIX)Zn.

247 artificial protein specifically accumulated zinc protoporphyrin IX, a rare cofactor that is not used

248 a significantly depressed activation-induced zinc release compared to WT eggs.

249 atiometric extracellular zinc sensor probing zinc release, supported that Z-LTD is expressed, at leas

250 least in part, via reductions in presynaptic zinc release.

251 It has recently been proposed that zinc released by mammalian eggs at fertilization may blo

252 Zap1 caused a shift from SLT HNT1 RNA in zinc-replete cells to LLT HNT1 RNA in deficient cells.

253 Under zinc-replete conditions, the Fur-family metalloregulator

254 Finally, we demonstrate zinc-responsive binding of Mpy to ribosomes in Mycobacte

255 system utilizes water cooled chromium doped zinc selenide (Cr(2+):ZnSe) as the gain medium and is pu

256 Microorganisms use zinc-sensing regulators to alter gene expression in resp

257 ing studies with a ratiometric extracellular zinc sensor probing zinc release, supported that Z-LTD i

258 requency stimulation induced LTP of synaptic zinc signaling (Z-LTP), evidenced by enhanced zinc-media

259 As such, synaptic zinc signaling modulates sensory processing and enhances

260 bidirectional, long-term changes in synaptic zinc signaling.

261 experience-dependent plasticity of synaptic zinc signaling.SIGNIFICANCE STATEMENT In the neocortex,

262 Finally, we demonstrate that extracellular zinc similarly disrupts early embryonic development in e

263 Zinc starvation in mycobacteria leads to remodeling of r

264 rom unbinding of the regulator, which, under zinc-starvation conditions, exists in its metal-deficien

265 oduced long leader transcripts (LLTs) in one zinc status condition and short leader transcripts (SLTs

266 , we show that the divalent transition metal zinc strongly promotes this process, shifting the equili

267 adsorption and desorption capacities for the zinc subgroup ions Zn(II), Cd(II) and Hg(II).

268 TLSB nanocomposite dosage, concentration of zinc subgroup ions, solution pH, adsorption temperature

269 Copper/zinc superoxide dismutase (SOD) is a homodimeric metallo

270 agmentation was observed with folic acid and zinc supplementation (mean of 29.7% for percentage of DN

271 rtility treatment, the use of folic acid and zinc supplementation by male partners, compared with pla

272 ymptoms were more common with folic acid and zinc supplementation compared with placebo (abdominal di

273 ETTING, AND PARTICIPANTS: The Folic Acid and Zinc Supplementation Trial was a multicenter randomized

274 vo results for a digital solid-state cadmium-zinc-telluride SPECT/CT system with in vitro sampling.

275 ECT/CT using a novel general-purpose cadmium-zinc-telluride-based SPECT/CT system.

276 r different binding times to a solution of a zinc tetraphenylporphyrin (ZnTPP) derivative terminated

277 nded analogue of tetrathiafulvalene (exTTF), zinc tetraphenylporphyrin (ZnTPP), and tetracyanoanthraq

278 Replenishment of zinc to cells harboring hibernating ribosomes restores M

279 tem, glutamatergic nerve terminals corelease zinc to modulate excitatory neurotransmission and sensor

280 p14 (Slc39a14) was the most highly expressed zinc transporter in skeletal muscle of mice in response

281 The zinc transporter ZIP9 (SLC39A9) was recently characteriz

282 l ion transporters, such as copper, iron and zinc transporters were upregulated and transferase-encod

283 d depletion of anti-oxidant elements such as zinc, underpin the high incidence of CIN in domestic cat

284 stemic inflammation enhanced Zip14-dependent zinc uptake by muscle, increased expression of Atrogin1

285 rator sites, repressing the transcription of zinc uptake transporters.

286 In summary, zinc variability was observed among commercial lots of c

287 Zinc was associated with a decreased risk (OR = 0.50, 95

288 In WT eggs, zinc was detected in cortically-localized vesicles which

289 (2.5) levels of lead, arsenic, chromium, and zinc were significantly enriched at some locations by fa

290 G was reduced by ~20-fold in the presence of zinc, whereas DVT binding was almost completely lost.

291 Zinc, which does not promote high-affinity DNA binding,

292 nts with lead white (2PbCO(3).Pb(OH)(2)) and zinc white (ZnO) pigments, which are frequently found in

293 bromine fluorescein) lake mixed with lead or zinc white at lower concentrations than elemental X-ray

294 bits erythropoiesis likely through replacing zinc within the zinc fingers of the critical transcripti

295 nes with P(zntA) promoter, which could sense zinc (Zn(2+)) for riboflavin and porin production.

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

297 otianamine (NA) is a natural chelator of Fe, zinc (Zn) and other metals in higher plants and NA-chela

298 Aqueous zinc (Zn) batteries (AZBs) are widely considered as a pr

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

300 CP inhibits GAS growth in vitro by imposing zinc (Zn) limitation.