ライフサイエンスコーパス: copper

1 a suitable alternative for trace analysis of copper.

2 formation of multi-carbon products than pure copper.

3 r and polar insulating Cu2N terminating bulk copper.

4 per-deficiency markers are down-regulated by copper.

5 clades also exhibited distinct responses to copper.

6 S results obtained after exposing zinc oxide/copper (111) [ZnO/Cu(111)] surfaces to hydrogen (H2) and

7 ane tetraacetic acid (DOTA) and labeled with copper 64 ((64)Cu) or fluorescent dye.

8 son's disease is a genetic disorder in which copper accumulates in the liver, brain, and other tissue

9 copper-dependent growth in yeast and enhance copper accumulation in Ctr1(-/-) mouse embryonic fibrobl

10 Copper, acting on unknown precursors, was associated wit

11 isolated COX deficiency in these cells, and copper addition to the culture medium suppressed these b

12 fts in tryptase mRNA levels, suggesting that copper affects tryptase gene regulation.

13 rized by severe Cu and Al aggregation into a copper aluminate phase (CuAl2O4 spinel).

14 sight into the atypical interactions between copper and BACE1 and into its non-enzymatic activities.

15 nt enzyme activity) toxicity in acute (96 h) copper and cadmium exposures, using the shallow-water ec

16 y suggest different mechanisms of action for copper and cadmium, and highlight that mechanistic under

17 nc superoxide dismutase (Sod1) by delivering copper and facilitating the oxidation of the Sod1 intram

18 Among these, copper and iron zeolites are remarkably reactive, hydrox

19 We focused on copper and its transporter ATP7A because ATP7A null muta

20 stigated the influence of the amino terminal copper and nickel binding (ATCUN) motif on derivatives o

21 The reduced redox state of the active-site copper and not the subsequent formation of the activated

22 In a seminal example, Schonecker showed that copper and O2 promoted the hydroxylation of steroid-cont

23 lat two-dimensional nanocrystalline films of copper and other metals exhibiting small stacking fault

24 t method and fabricated structures made from copper and PDMS.

25 Copper and pH were important in modulating MeSH and EtSH

26 sp3s) capable of binding large quantities of copper and preventing toxicity.

27 spinal cord, where concomitant increases in copper and SOD1 activity are also evident.

28 Furthermore, the higher redox potential of copper and the enhanced weakening of the O-O bond from t

29 teractions with other trace elements such as copper and zinc, altered gut microbiota to more pathogen

30 of anaerobic digestion on the speciation of copper and zinc, two metals that generally occur at high

31 trace element dataset from the paired Cu-Au (copper) and Sn-W (tin) magmatic belts in Myanmar.

32 (3) performing a column separation to remove copper, and (4) determining the elements of interest by

33 ansition metals (e.g., iron, cobalt, nickel, copper, and nickel-cobalt alloy), accomplished by a faci

34 hese findings demonstrated that hierarchical copper- and zinc- buds dressing gamma-AlOOH mesostrands,

35 synthesis of the mixed-valent organometallic copper APNC, [Cu20(CCPh)12(OAc)6)] (1), via reduction of

36 s contain greater crustal contributions than copper arc rocks.

37 Copper arc zircons have juvenile epsilonHf (+7.6 to +11.

38 higher electron density in the d orbital of copper are central to its higher oxidase activity over i

39 oduced by femtosecond Laser Ablation of pure copper are presented.

40 d dynamics of ionic and atomic emission from copper as well as the surrounding atmosphere in order to

41 values of 96.66% and 98.91% for the iron and copper assays, respectively.

42 s were isolated that differ in the number of copper atoms bound to the BB unit.

43 majority of efforts has been to use oxidized copper-based materials.

44 was employed to transplant shp topology into copper-based MOFs by employing the copper paddlewheel [C

45 d controlling the oxidation and reduction of copper-based nanoparticles.

46 Through the design and synthesis of a new copper-based photoredox catalyst, bearing a tridentate c

47 Our copper-based sensor features a low-cost electrode materi

48 ay suggest alternate pathways are at work in copper-based water oxidation.

49 ts with Earth-abundant metals, with iron and copper being particularly attractive owing to their low

50 physically coupling the domains involved in copper binding and those involved in ATP hydrolysis.

51 In many bacteria, separate genes encode a copper binding chaperone and a copper efflux pump, but i

52 croscopy can define the subunit topology and copper binding of a manganese oxidizing complex, and des

53 ment, humic colloids lost up to 50% of their copper-binding capacity, expressed as a molar ratio to o

54 Within the plume, both iron- and copper-binding organic ligands showed a linear, conserva

55 BACE1 has been described as a copper-binding protein and its oligomeric state as being

56 Using a copper-binding tracker, results showed that labile coppe

57 hynylbenziodoxol-(on)e reagents and a simple copper bisoxazoline catalyst.

58 isseminate to other tissues, and combat host copper bombardment mechanisms that would otherwise mitig

59 process and indicate that the charge on the copper-bound carbon and delocalization of charge onto th

60 de, generated in situ from the coupling of a copper-carbene with a spirocyclic thietane.

61 ities into peptide oligomers via solid-phase copper-catalysed azide-alkyne cycloaddition (SP-CuAAC) c

62 cribe an iterative application of asymmetric copper catalysis towards the synthesis of six distinct o

63 1,3-dienes with a sulfur diimide reagent, a copper catalyst, and alkyl Grignard reagents.

64 In the presence of a chiral copper catalyst, substituted allylic iodides couple with

65 30 degrees C) through the use of light and a copper catalyst.

66 sure to air followed by immediate removal of copper catalyst; (2) adding excess reducing agents post-

67 hermore, we combined Staudinger ligation and copper catalyzed azide alkyne cycloaddition (CuAAC) reac

68 ssembly undergo covalent cross-linking using copper catalyzed click chemistry.

69 ncorporation via AUG codon reassignment, and copper-catalyzed azide-alkyne cycloaddition, we can over

70 Post-polymerization modification via copper-catalyzed azide-alkyne cyloaddition was enabled b

71 An efficient copper-catalyzed carbenoid insertion reaction of alpha-d

72 ched to this bio-orthogonal amino acid using copper-catalyzed click chemistry, either before or after

73 esis has also been improved using a reported copper-catalyzed coupling of arylbismuth(V) reagents tha

74 A copper-catalyzed cross-coupling of 2-alkyl-/2-arylazirid

75 l-3-yl)-1H-imidazol-3-ium bromides undergo a copper-catalyzed intramolecular direct C arylation under

76 sylbenzamides and related substrates undergo copper-catalyzed intramolecular sulfamidation at the ben

77 room temperature by a visible-light-mediated copper-catalyzed photoredox process.

78 The process underwent copper-catalyzed tandem C-N/C-C bond formation, producin

79 al reduction of oxygen to water using a haem-copper centre.

80 f phenols to catechols through the binuclear copper centres.

81 We show that the copper chaperone Atox1, which delivers copper to ATP7B,

82 Acyl-RAC further revealed that endogenous copper chaperone for SOD1 (CCS) is S-acylated in both hu

83 The copper chaperone for superoxide dismutase (Ccs1) activat

84 Copper-chlorophylls extracts exhibited similar green hue

85 Cytotoxicity of zinc- and copper-chlorophylls extracts was slightly different and

86 fully reduced mu4S(2-) bridged tetranuclear copper cluster to N2O via a single Cu atom to accomplish

87 troscopic measurements reveal differences in copper co-ordination upon the binding of xylan and gluca

88 using spark plasma infiltrating sintering of copper-coated graphene (Cu@Gr) composite powders.

89 Moreover, we identify the ditiocarb-copper complex as the metabolite of disulfiram that is r

90 A copper complex, [Cu(I)(tmpa)(MeCN)](+), effectively redu

91 duced on iron homeostasis by a wide range of copper concentrations in the growth media and by altered

92 The related copper-containing amine oxidase human vascular adhesion

93 oduce relatively more siderophores following copper contamination.

94 The observed differences in the copper content of the silver base of the different threa

95 the copper oxidation state and succession of copper coordinating ligands within the biomass.

96 the combustion of printed circuit boards and copper-core cables emitted large amounts of OM with Br-r

97 Human urinary copper (Cu) content is elevated during UTI caused by uro

98 .5 and 1 muM of arsenic (As), lead (Pb), and copper (Cu) from solution via adsorption.

99 ), phosphorus (P), zinc (Zn), iron (Fe), and copper (Cu) in the fruit pulp was similar with all three

100 Copper (Cu) is an essential cofactor for various enzymat

101 A deficiency of the micronutrient copper (Cu) leads to infertility and grain/seed yield re

102 1034 1034 References 1034 Copper (Cu) microRNAs are upregulated by Cu deficiency a

103 OUND & AIMS: Wilson disease is a disorder of copper (Cu) misbalance caused by mutations in ATP7B.

104 b) in surface water samples using a low-cost copper (Cu)-based electrochemical sensor.

105 The best characterized are the copper deficiency and toxicity disorders Menkes and Wils

106 athy has been recognised in association with copper deficiency but has not been well characterised.

107 onditions for copper detoxification, whereas copper deficiency results in a redistribution of CUA-1 t

108 the most common neurological complication of copper deficiency.

109 y copper transport protein, as well as other copper-deficiency markers are down-regulated by copper.

110 , physiological and pathological features of copper-deficient peripheral neuropathy.

111 LPMOs are copper-dependent enzymes (EC 1.14.99.53-56) that, with g

112 n human and mouse Ctr2 proteins that support copper-dependent growth in yeast and enhance copper accu

113 e, stochastic nucleation events of nanoscale copper deposits are visualized in real time for the firs

114 d breakdown spectroscopy allowed the precise copper determination (coefficient of variation = 3.1%, n

115 testine under copper overload conditions for copper detoxification, whereas copper deficiency results

116 by reversible dissociation of HBpin from the copper dihydridoborate species.

117 he possible implication of O-type species in copper-/dioxygen-dependent enzymes such as tyrosinase (T

118 sacrificial anode rods than does presence of copper dosed as soluble cupric ions.

119 enes encode a copper binding chaperone and a copper efflux pump, but in some the chaperone encoding g

120 bution of CUA-1 to basolateral membranes for copper efflux to peripheral tissues.

121 2 and enhance the expression of OsIRO2 under copper excess, which suggests a role of copper transport

122 plasm into the secretory pathway, as well as copper export across the plasma membrane.

123 pper homeostasis is maintained by intestinal copper exporter trafficking that is coordinated with ext

124 To overcome this temperature distribution, a copper flange was introduced to enhance the temperature

125 articles produced by the laser ablation of a copper foil is of a few attograms corresponding to a nan

126 , indicating that the cofactors (hemes b and copper for CcoN and cytochromes c for CcoO and CcoP) wer

127 terconnected framework of ultrathin metallic copper formed provides a high conductivity backbone and

128 n of a novel prosthetic group, followed by a copper-free click conjugation to a modified adnectin to

129 A silver- and copper-free rhodium-catalyzed C-H acetoxylation reaction

130 During galvanostatic deposition of copper from an acidic electrolyte, we find that the grow

131 t mitochondrial signaling to the etiology of copper handling disorders.

132 Various forms of oxidized copper have been demonstrated as electrocatalysts that s

133 A key regulator of copper homeostasis in mammalian cells is the copper-tran

134 r to the biosynthetic pathways and maintains copper homeostasis in the liver.

135 we identify a mechanism by which organismal copper homeostasis is maintained by intestinal copper ex

136 ded with caution, because adverse effects in copper homeostasis may occur.

137 es for the machinery that ultimately governs copper homeostasis, and further establish the importance

138 at have their own intrinsic requirements for copper homeostasis, have evolved mechanisms to acquire c

139 oxidase (COX) assembly and the regulation of copper homeostasis.

140 ccessed allylic hydroxylamine esters undergo copper hydride-catalyzed intramolecular hydroamination w

141 ive allylphenyl carbonates as chemoselective copper-hydride elimination is faster with an achiral Cu-

142 tivity between arylazides N3 Ar with a bulky copper(I) beta-diketiminate.

143 e role of dirhodium(ii) and the emergence of copper(i) catalysts are described, as are the different

144 tives utilizing diaryliodonium triflates and copper(I) chloride as a catalyst.

145 studies revealed that a DTBM-SEGPHOS-ligated copper(I) dihydridoborate complex is the resting state o

146 in the macrocycle cavity are able to chelate copper(I) endotopically.

147 ion of a parent gold hydride to a bent d(10) copper(I) fragment.

148 nal alkene is insertion of the alkene into a copper(I) hydride formed by reversible dissociation of H

149 dition of cyclam for complete removal of the copper(I) ions.

150 nds and alpha-diazocarboximides catalyzed by copper(I) or dirhodium(II) have been developed.

151 hondria of eukaryotic cells contain a labile copper(I) pool localized in the matrix where also the mi

152 m alpha-diazoesters using 5 mol% of a simple copper(I) salt as catalyst.

153 ]-cycloaddition was successfully achieved by copper(I) triflate/double-sidearmed bisoxazoline complex

154 stituted alkyne, has been established by the copper(I)-catalyzed cross-coupling of 1,1-dibromoenamide

155 ng/C(sp(3) )-C(sp(3) ) bond formation in the copper(I)-catalyzed reaction of cyclopropanols with diaz

156 y than one involving intermediates with only copper(I).

157 Copper(II) aryl species are proposed key intermediates i

158 A highly crystalline copper(II) benzenehexathiolate coordination polymer (Cu-

159 of UV irradiation and ppm concentrations of copper(II) bromide and Me6-TREN (TREN = tris(2-aminoethy

160 was converted into a hydrophobic complex of copper(II) diethyldithiocarbamate and subsequently extra

161 As proof of concept, copper(II) in aqueous samples was converted into a hydro

162 ying an electron deficient beta-diketiminato copper(II) nitrito complex [Cl2NNF6]Cu(kappa(2)-O2N).THF

163 hiols occurs from the reaction of RSNO and a copper(II) thiolate [Cu(II)]-SR intermediate formed upon

164 The potential of copper(II) to induce gas-phase fragmentation reactions i

165 In addition, copper(II) was also used to induce radical fragmentation

166 ive describes the development of a family of copper(II)-catalyzed alkene difunctionalization reaction

167 The fast degradation of copper in ambient conditions, however, largely overshado

168 Copper in steel causes metallurgical problems, but is pe

169 The unique high selectivity of copper in the electrochemical reduction of CO2 to hydroc

170 valuated with a complete characterization of copper in the global steel system and this is presented

171 to dithiocarbamic acid with CS2, followed by copper in the presence of ammonia to promote complex for

172 ings reveal a hitherto unrecognized role for copper in the regulation of mast cell gene expression an

173 ied for dispersive solid phase extraction of copper in water and cereal samples followed by FAAS.

174 Copper incubation experiments suggest that Clade IV popu

175 sor ion scan experiments, demonstrating that copper-induced fragmentation reactions can potentially i

176 (induced by hydroxyl and peroxyl radicals), copper-induced LDL-cholesterol peroxidation, as well as

177 opic, and cell-based data supporting a novel copper-induced mechanism for Sod1 activation.

178 -requiring enzyme in the cytoplasm, and this copper-induced mechanism of disulfide bond formation obv

179 ucture, stability, and reactivity of alkenyl copper intermediates, as well as insight into the source

180 e report the wicking performances for porous copper inverse opals having pore diameters from 300 to 1

181 high yield by reacting the metal precursors (copper iodide and indium acetate) in dodecanethiol (DDT)

182 e) functionalized perylenediimide (PDI-HIS), copper ion and graphene oxide (GO) and that could be uti

183 an inverse relationship between DOC and free copper ion concentration owing to complexation by predom

184 Although the copper ion transporter CopA has been known in Escherichi

185 c BACE1 TMS is accessible to metal ions, but copper ions did not trigger trimerization.

186 Exposure to Cu(OH)2 nanopesticide and copper ions induced alterations in the metabolite profil

187 Competition between binding of copper ions to a membrane-embedded synthetic transducer

188 Copper is an essential element for proper organismal dev

189 Copper is an essential yet potentially toxic trace eleme

190 Copper is essential for life but also potentially toxic.

191 Here, we show that copper is essential for spore germination in Schizosacch

192 -binding tracker, results showed that labile copper is preferentially localized to the spore body.

193 Copper is required for the activity of cytochrome c oxid

194 and copper or metal ion pairs namely, silver-copper (Janus bionanocage) and co-polymeric shell of the

195 terface of ultrasonically welded aluminum to copper joints using transmission electron microscopy, an

196 heir content of aluminium, arsenic, cadmium, copper, lead and mercury in the dry product and in the i

197 on of trace level concentrations of cadmium, copper, lead, and silver as model analytes has been demo

198 Median serum copper level was 0.11 mug/mL (range 0-0.58).

199 Thus, TTM reduces copper levels and MAPK signaling, thereby inhibiting BRA

200 ing that is coordinated with extraintestinal copper levels in Caenorhabditis elegans Specifically, we

201 d by a temporal decrease in COX activity and copper levels in the longer-lived Sco1stm/stm mice.

202 Contrary, copper levels, related to lower levels of free MeSH, and

203 sion tomography (PET) radioligands using the copper-mediated (18)F-fluorination of aryl boron reagent

204 Copper-mediated coupling between alkynes to generate a s

205 (2-bromophenyl)pyrrolyl-1,2,4-triazoles via copper-mediated intramolecular direct C-arylation of 1,2

206 ciated transcription factor are dependent on copper-mediated modulation of MAPK signaling.

207 A copper-mediated picolinamide directed regioselective cro

208 ects of the biogeochemical transformation of copper mobilized from malachite (Cu2 (CO3 )(OH)2 ) and b

209 (i) compared to chemical denitrosation with copper monochloride or triiodide, the UV-photolysis does

210 n enzymes is provided, with implications for copper monooxygenase mechanisms.

211 n boundaries at the surface of nearly planar copper nanocrystalline (111) films.

212 Copper nanoparticles (CuNPs) are attractive as a low-cos

213 towards glucose through synergetic effect of copper nanoparticles and nitrogen-doped graphene.

214 ynamic oxidation and reduction mechanisms of copper nanoparticles.

215 ic-intensity femtosecond lasers with aligned copper nanorod array targets.

216 For copper nanorod targets with a length of 5 mum, a maximum

217 Copper nanowire networks are considered a promising alte

218 report the fabrication of vertically aligned copper nanowires (v-CuNWs) using electrosynthesis on tem

219 at driven benzoin radicals to grow ultrathin copper nanowires with tunable diameters.

220 a novel green chemistry approach to assemble copper-nanowires/reduced-graphene-oxide hybrid coatings

221 noble and base metals (platinum, palladium, copper, nickel, and cobalt) were synthesized with averag

222 synthesis from a mixture of graphene oxide, copper nitrate and uric acid, followed by thermal anneal

223 ft to oxalate coordination of bioaccumulated copper occurred in the central older region of ammonium-

224 Wines were in contact with copper one week, centrifuged and stored at 50 degrees C

225 Copper-only SOD sequences similar to those seen in fungi

226 in large polypeptides we refer to as CSRPs (copper-only SOD-repeat proteins).

227 The eukaryotic copper-only SODs are particularly unique in that they la

228 trate contains metal ions such as silver and copper or metal ion pairs namely, silver-copper (Janus b

229 nelles (gut granules) in the intestine under copper overload conditions for copper detoxification, wh

230 Haem-copper oxidase (HCO) catalyses the natural reduction of

231 the colony and its microenvironment and the copper oxidation state and succession of copper coordina

232 Copper oxide clusters synthesized via atomic layer depos

233 gin of high-temperature superconductivity in copper oxides and the nature of the 'normal' state above

234 een subject to strong controversy in high-Tc copper oxides.

235 ion dose, as well as chemical signatures of copper, oxygen and sulfur.

236 characteristics and reactivity trends of the copper-oxygen cores discussed.

237 esents the local electronic structure of the copper-oxygen plane.

238 en limited to well-characterized examples of copper-oxygen species but seeks to provide a thorough pi

239 logy into copper-based MOFs by employing the copper paddlewheel [Cu2(O2C-)4] as the complementary squ

240 by ICPMS gave similar results than ELPI for copper particles ejected during the ablation shot by sho

241 nitrogen dioxide (NO2 ) gas sensor based on copper phthalocyanine (CuPc) thin film transistors (TFTs

242 This process reduced the copper, potassium, and phosphorus content, but had littl

243 Lastly, we showed that high levels of copper (previously shown to elevate CUP1 transcription)

244 Here, we describe site-selective, copper-promoted couplings of boronic acids with carbohyd

245 The copper-promoted glycosylation was also proven to be comp

246 in-streptavidin (Sav) technology, artificial copper proteins have been developed to stabilize a Cu(II

247 We discovered that copper released from corrosion of plumbing materials can

248 validate this mechanism for the emergence of copper resistance in budding yeast.

249 ble, inexpensive, and commercially available copper salt is used and no added ligand is required.

250 s suggest the reaction is catalyzed by trace copper salts and that a Z- to E-hydrazone isomerization

251 Copper salts find widespread use in Pd-catalyzed oxidati

252 on, we demonstrate that various solutions of copper salts, bases, and ancillary ligands can be utiliz

253 dependent and stable cyclic response in bulk copper samples that contain highly oriented nanoscale tw

254 Here we show that ultrasmall clusters of copper selenide exhibit a disordered cationic sub-lattic

255 aphene sheets were deposited on 1.00mm thick copper sheet at 850 degrees C using acetylene (C2H2) as

256 ate guidance and have an unusual open-access copper site, yet they can still react with superoxide at

257 Using a cohort of 8,014 male copper smelter workers who were hired between 1938 and 1

258 species is [Cu(phen)(SAc)] regardless of the copper source.

259 e influence of DOC from different sources on copper speciation in estuaries and concludes that DOC is

260 is not necessarily an accurate predictor of copper speciation.

261 eterologous expression in yeast complemented copper-specific defects observed upon deletion of PIC2 A

262 these results highlight the effects of rice copper status on iron homeostasis, which should be consi

263 ctions involves intermediates that contain a copper-substituted stereogenic carbon centre.

264 gold, palladium and nickel were generated on copper substrates to demonstrate the underlying CL dynam

265 lite nanoconstruct is designed by assembling copper sulfide (CuS) nanoparticles on the surface of [(8

266 varying from >10(22) cm(-3) to intrinsic) in copper sulfide nanocrystals by electrochemical methods.

267 Control over the doping density in copper sulfide nanocrystals is of great importance and d

268 the hole doping density and fluorescence of copper sulfide nanocrystals presented in this work and t

269 ition, morphology, and crystal structure for copper sulfide-based nanocrystals, but also provide a pa

270 he proportion of amorphous or nanostructured copper sulfides as well as amorphous or nanostructured z

271 xygen reductase that is a member of the heme-copper superfamily that utilizes ubiquinol-8 (Q8H2) as a

272 sence of a thin suboxide structure below the copper surface is essential to bind the CO2 in the physi

273 the initial steps of CO2 electroreduction on copper surfaces, the best current catalysts.

274 sured as compared to that with a thick plane copper target under the same laser conditions.

275 ensor features a low-cost electrode material-copper-that offers simple fabrication and competitive pe

276 t the copper chaperone Atox1, which delivers copper to ATP7B, and the group of the first three metal-

277 eostasis, have evolved mechanisms to acquire copper to successfully colonize the host, disseminate to

278 The human transporter ATP7B delivers copper to the biosynthetic pathways and maintains copper

279 t studies in bacterial organisms showed that copper toxicity is also strictly connected to iron-sulfu

280 regulatory mechanism in which Atox1-mediated copper transfer activates ATP7B by releasing inhibitory

281 The results show that copper transfer from Atox1 decreases domain interactions

282 sporting P-type ATPase ATP7A, which mediates copper transport from the cytoplasm into the secretory p

283 nder copper excess, which suggests a role of copper transport in iron signaling.

284 ntrations in the growth media and by altered copper transport in Oryza sativa plants.

285 d from Atp7a(LysMcre) mice exhibit decreased copper transport into phagosomal compartments and a redu

286 on of OsCOPT1, which encodes a high-affinity copper transport protein, as well as other copper-defici

287 sistent with a conserved role for SLC25A3 in copper transport, its heterologous expression in yeast c

288 tly demonstrated that SLC25A3 functions as a copper transporter.

289 ngs reveal unique and opposing functions for copper transporters of the host and pathogen during infe

290 Cu-ATPases are membrane copper transporters present in all kingdoms of life.

291 copper homeostasis in mammalian cells is the copper-transporting P-type ATPase ATP7A, which mediates

292 ATP7B is a copper-transporting P1B-type ATPase (Cu-ATPase) with an

293 s made of ultra low background electroformed copper (ULB EF-Cu) foil cut and folded into boats, (2) d

294 ctic reaction where sodium is exchanged with copper under mild conditions.

295 Additionally, the density of copper vacancies was extracted; this quantitatively show

296 nnealing temperature leads to a reduction in copper vacancies.

297 s-coupling of these radicals is catalyzed by copper via an out-of-cage mechanism in which [Cu(I)(carb

298 of either ammonium or nitrate determined how copper was distributed within the colony and its microen

299 DPM-1001 also chelates copper, which enhanced its potency as a PTP1B inhibitor.

300 ge body of evidence has reported the role of copper, zinc and iron, and oxidative stress in several n

301 peroxide dismutase (Ccs1) activates immature copper-zinc superoxide dismutase (Sod1) by delivering co