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1 xicology Program: a case study on hexavalent chromium.
2 elium due to the antiferromagnetic nature of chromium.
3 , undergoing oxidation/reduction rather than chromium.
4 tri- or tetramerization in combination with chromium.
5 Cr (III), which is a much less toxic form of chromium.
6 ntain metal ions including silver, iron, and chromium.
7 in (18.66-20.23%), and rare minerals such as chromium (0.67-2.54 mg/100 g) and manganese (1.07-2.34 m
8 ricarbonyl(1-chloro-2-deuteriomethylbenzene) chromium(0) was computed, showing that reasonable predic
9 days of refrigerated storage, autologous 51-chromium 24-hour posttransfusion RBC recovery (PTR) stud
10 ine concentrations, and results for GFR from chromium-51 ((51)Cr) EDTA excretion measurements ((51)Cr
12 r structures composed of iron, titanium, and chromium accounting for the magnetic properties of these
19 nic ligands in the biogeochemical cycling of chromium and has significant implications for chromium r
25 ains elevated pseudo-total concentrations of chromium and nickel, this soil is not a significant sour
26 ications; and steel alloying elements (e.g., chromium and niobium) as well as elements used in high-t
27 ieties while the levels of cadmium, arsenic, chromium and thallium were within permissible range.
29 r aerobic conditions, the levels of arsenic, chromium, and boron in leachate decreased up to 96%, 49%
30 ching of metals/metalloids (arsenic, copper, chromium, and boron) from treated wood in aged mature co
34 iors and certain parts of weapons is rich in chromium, and we demonstrate that chromium on the metals
35 gestion, we found that potassium, magnesium, chromium, and zinc in were bioaccessible in sugarcane sa
37 tu formed tricarbonyl(eta(6)-2-methylindenyl)chromium anion with a series of Pd and Pt metallacycles
40 uilibrium of a macroscopic ensemble of S = 3 chromium atoms pinned in a three dimensional optical lat
42 c oxidations, this oxidation is catalytic in chromium because oxygen, not the chromium reagent, is th
43 e genome assembly by integrating PacBio, 10x Chromium, BioNano DLS optical mapping, and Hi-C mapping
44 on center (CGC(Et)Ti) covalently linked to a chromium bis(thioether)amine ethylene trimerization cent
45 se, iron, copper and zinc) and heavy metals (chromium, cadmium, lead and nickel) were determined in v
46 on between non-heteroatom-stabilized alkynyl chromium carbene complexes prepared in situ and furfural
47 n the metal matrix with in-situ formation of chromium carbide (Cr7C3) at the CNT/copper (Cu) interfac
48 discovery of an easily accessible bimetallic chromium catalyst is reported for this transformation.
53 ng titanocene-catalyzed epoxide opening with chromium-catalyzed hydrogen activation and radical reduc
56 e established several systems based on zinc, chromium, cobalt, and aluminum catalysts for the ring-op
57 terpene-based cyclic anhydrides catalyzed by chromium, cobalt, and aluminum salen complexes is report
58 y occurring trace metals, including arsenic, chromium, cobalt, nickel, and lead, likely due to the mi
60 As one of the world's leading producers of chromium compounds, the U.S. is facing growing challenge
61 t weight with a mean of 15.9 +/- 3.5 ppm and chromium concentrations ranged from 2.0 to 73.6 ppm wet
63 washing to remove traces of e-liquid, lead, chromium, copper and nickel were all detected in the cig
64 al potentially toxic metals, including lead, chromium, copper, and nickel were detected in the e-liqu
65 luminum, antimony, arsenic, cadmium, cobalt, chromium, copper, iron, lead, manganese, nickel, seleniu
67 strogen, and 9 other metals-arsenic, cobalt, chromium, copper, mercury, molybdenum, lead, tin, and va
70 al chromate (Cr2O7(2-)) anions consisting of chromium Cr(VI) was used as a model environmental stress
72 ort for the first time the use of hexavalent chromium (Cr(VI)) as an electrocatalyst in electrochemic
75 after exposure to welding fumes, hexavalent chromium (Cr(VI)), and nickel, we analyzed 3,418 lung ca
76 damage response (DDR) induced by hexavalent chromium (Cr(VI)), but the molecular mechanism remains u
78 uding Lead (Pb), Mercury (Hg), Arsenic (As), Chromium (Cr) and Cadmium (Cd) are considered to be high
79 o be more sensitive to cell death induced by chromium (Cr) and nickel (Ni) exposure than an isogenic
83 manganese (Mn), lead (Pb), copper (Cu), and chromium (Cr) in hair, blood, urine, nails, and saliva f
89 icrobial activities on the transformation of chromium (Cr) remediation products has generally been ov
90 ese (Mn), iron (Fe), copper (Cu), zinc (Zn), chromium (Cr)) and heavy metals (cadmium (Cd), lead (Pb)
91 tion of naturally occurring As, cobalt (Co), chromium (Cr), and nickel (Ni) from wetland sediments ca
93 inly lead (Pb), aluminium (Al), nickel (Ni), chromium (Cr), cadmium (Cd), iron (Fe) and zinc (Zn) wer
94 , arsenic (As), lead (Pb), cadmium (Cd), and chromium (Cr), from primary anthropogenic sources in Chi
95 was studied with heavy metals (cadmium (Cd), chromium (Cr), lead (Pb), arsenic (As)) which was found
106 was applied to chromium speciation and total chromium determination in real samples and gave recoveri
112 s) comparing the surgical use of the erbium, chromium-doped: yttrium, scandium, gallium, and garnet (
113 with all DES compared with BMS, with cobalt-chromium EES, platinum chromium-EES, SES, and BES also h
114 with BMS, with cobalt-chromium EES, platinum chromium-EES, SES, and BES also having lower target-vess
116 monstrated that the second-generation cobalt-chromium everolimus-eluting stent (CoCr-EES) is superior
117 ing Absorb BVS (n=2164) or the Xience cobalt-chromium everolimus-eluting stent (CoCr-EES; n=1225).
120 discontinuation before 30 days after cobalt chromium everolimus-eluting stent implantation was stron
122 umerically excess stroke and PCI with cobalt-chromium everolimus-eluting stent with numerically incre
124 al studies have in fact reported that cobalt-chromium everolimus-eluting stents (CoCr-EES) coated wit
126 At a median follow-up of 3.8 years, cobalt-chromium everolimus-eluting stents (EES) were associated
128 ention (PCI) with fluoropolymer-based cobalt-chromium everolimus-eluting stents (PCI group, 948 patie
129 o either PCI with fluoropolymer-based cobalt-chromium everolimus-eluting stents (PCI group, 948 patie
130 ruption is safe in patients receiving cobalt chromium everolimus-eluting stents remains controversial
134 olution-growth of ZnO nanowires using a thin chromium film as a nucleation inhibitor and Au size-sele
137 II) solids of environmental relevance, i.e., chromium hydroxide Cr(OH)3(s), chromium oxide Cr2O3(s),
138 MFCs were examined at three types of shocks (chromium, hypochlorite and acetate) in a batch-mode cham
139 ) method for the determination of hexavalent chromium i.e. Cr(VI) in food samples is established with
141 uggest that the in situ generated low-valent chromium(I) species might be the active catalyst for the
142 molecular analog of SnO) and binary dimeric chromium(II) bis(mu2,kappa(2),kappa(2)) derivative [Cr2(
145 ern half based on nerol and acetoacetate and chromium(II)-mediated Reformatsky reactions as a powerfu
148 electronically conductive solid solution of chromium(iii) and aluminium oxides in the corundum struc
149 d emissive oxygen- and temperature-sensitive chromium(III) complex ([Cr(ddpd)(2)][BPh(4)](3), CrBPh(4
150 The optimized constant for the monomeric chromium(III) complex was in between those of the iron(I
151 siloxide complex in propionitrile leads to a chromium(III) complex with an end-on bound superoxide li
153 roughput methodology was employed to produce chromium(III) complexes suitable for the surface modific
154 the coordination chemistry and stability of chromium(III) complexes with natural organic matter (NOM
156 , contains two antiferromagnetically coupled chromium(III) metal ions and provides a classic example
158 didate, [Cr(OH)6](3-), which was formed from chromium(III) perchlorate and pH adjusted with ethylened
163 S results showed a predominance of monomeric chromium(III)-NOM complexes at low pH (<5), in which onl
167 lour change has been correctly attributed to chromium impurities and their absorption band in the yel
168 old of the central BC(5) ring coordinates to chromium in an eta(6) fashion while only the B=C unit bi
187 pproach involves deposition of an additional chromium layer (superlayer) onto a bonded system, where
188 iciencies for five metals (arsenic, cadmium, chromium, lead and nickel) were compared under varying c
190 oncentrations of Arsenic, Antimony, Cadmium, Chromium, Lead, Selenium and Vanadium were evaluated in
192 e highest to the lowest quartiles of toenail chromium levels was 0.80 (0.66-0.98; Plinear trend = 0.0
197 tals, termed M-Pt3Ni/C, where M is vanadium, chromium, manganese, iron, cobalt, molybdenum (Mo), tung
199 Gy/h) ionizing radiation (IR), heavy metals (chromium, mercury), elevated temperature (up to 50 degre
200 lements (aluminium, cadmium, cobalt, copper, chromium, mercury, manganese, molybdenum, nickel, lead a
202 ehavior to the metallic density wave seen in chromium metal than the insulating stripes typically fou
203 lost from the taper junction between Cobalt-Chromium-Molybdenum (CoCrMo) and Titanium (Ti) component
206 sm is attributed to atomic-scale disorder in chromium nanoparticles, leading to abundant unbalanced s
207 of some heavy metals such as cadmium, lead, chromium, nickel and cobalt in domestic cultivated and i
208 e evidence of normal physiological function (chromium, nickel, tungsten, and vanadium), and 12 with k
210 is rich in chromium, and we demonstrate that chromium on the metals is contamination from nearby lacq
213 eagents (based around toxic elements such as chromium or selenium) or expensive catalysts (such as pa
215 rive fundamental insights into mechanisms of chromium oxidation during combustion of solid fuels.
216 conductive CrOx bridges across a thin native chromium oxide barrier between the nanodots and an under
217 evance, i.e., chromium hydroxide Cr(OH)3(s), chromium oxide Cr2O3(s), and copper chromite Cu2Cr2O5(s)
218 e previously reported that the micronutrient chromium picolinate (CrP), with long-standing cardiovasc
221 pends on the long-term potential for reduced chromium precipitates to remain immobilized under oxidiz
223 n performance, highlighting the influence of chromium promoter on the enhancement in both activity an
227 Under oxidizing conditions, immobilized chromium reduced under predominantly denitrifying condit
231 nd chemical sequestration of N, Cl, and S by chromium result in quantitative conversion of compound-s
232 f platinum, gold, high-temperature iron- and chromium-rich spherules, and native iron particles rarel
234 w that ~13-21% of cell barcodes from the 10x Chromium scATAC-seq assay may have been derived from a d
235 nding metal complexes, as exemplified by the chromium series, and the effect of the metal appears to
236 metal halides, metal thio/selenophosphates, chromium silicon/germanium tellurides, and more, are int
237 ing gas is achieved using a high temperature chromium-silver reactor that retains carbon, oxygen and
240 r drug-eluting stents: the thin-strut cobalt-chromium sirolimus-eluting Orsiro stent and the stainles
241 ultrathin strut biodegradable polymer cobalt-chromium sirolimus-eluting Orsiro stent in an all-comers
242 h is explained in terms of the occurrence of chromium/sodium vacancy antisite during desodiation and
246 novel method was developed by SAE-DLLME for chromium speciation in water and rice samples using 2-th
247 results challenge the old vision of "naked" chromium species (i.e., low coordinated) as the active s
249 s compared with an everolimus-eluting cobalt-chromium stent, was within the prespecified margin for n
251 It was discovered that the sulfur in sodium chromium sulfide is electrochemically active, undergoing
254 ogy, largely represented by the 10x Genomics Chromium system, is able to measure the gene expression
255 Linked-Read technologies, such as the 10x Chromium system, use a microfluidic system and a special
258 ess in NaCrS2 where it is sulfur rather than chromium that works as the electrochemical active specie
262 ase features are analyzed for catalysts from chromium to gold for ionic hydrogenations, bifunctional
263 ed the ability to reduce the amount of toxic chromium to levels within the range of the EPA contamina
264 n of 3 pKa units for complexes of the metals chromium to nickel, molybdenum, ruthenium to palladium,
266 e differing redox behavior of molybdenum and chromium to provide constraints on seafloor redox evolut
267 is review paper has outlined the overview of chromium toxicity, conventional analytical techniques al
268 This belief was based on the detection of chromium traces on the surface of bronze weapons buried
269 two-dimensional (2D) magnetic semiconductor chromium tribromide (CrBr(3)), which was enabled by the
270 sensing using a novel Raman reporter, arene chromium tricarbonyl linked aminothiophenol (Cr(CO)3-ATP
271 Carlo simulations, we propose that monolayer chromium trichloride (CrCl(3)) can be a promising candid
275 ect microscopy to demonstrate that monolayer chromium triiodide (CrI3) is an Ising ferromagnet with o
276 nd-alignment between tungsten diselenide and chromium triiodide can be exploited to excite localized
277 hich NO is oxidized quantitatively to NO2 by chromium trioxide (CrO3), before conversion to NO2(-) an
282 uction for practical applications where both chromium (VI) cations and organic dyes are the main poll
283 id, which is able to effectively remove both chromium (VI) cations and organic pollutants simultaneou
285 olution pH, and is capable of decreasing the chromium(VI) concentration in water from 1 ppm to 10 ppb
292 framework can take up from 90 to 200 mg/g of chromium(VI), depending on the solution pH, and is capab
296 In the glass substrate, lead, cadmium, and chromium were present at concentrations up to about 1100
298 ude use of lasers, most recently the erbium, chromium:yttrium-scandium-gallium-garnet (Er,Cr:YSGG) la
300 bon (EC) and nine trace elements: potassium, chromium, zinc, iron, titanium, arsenic, calcium, mangan