ライフサイエンスコーパス: Mn

1 Mn is an essential micronutrient required for normal cel

2 Mn oxides are among the most ubiquitous minerals on Eart

3 Mn(II) supplementation improved growth when cop- was cul

4 lithium layered oxide, Li(Ni(0.91) Co(0.06) Mn(0.03) )O(2) (NCM9163), with minimal side effects.

5 Pairing with LiNi(0.8) Co(0.1) Mn(0.1) O(2) (NCM(811) ) further raises the energy densi

6 trolyte also enables a Li||LiNi(0.8) Co(0.1) Mn(0.1) O(2) (NMC811) full cell (2.5 mAh cm(-2) ) to ret

7 el cobalt manganese oxide (LiNi(0.8) Co(0.1) Mn(0.1) O(2) , NCM 811) cathodes exhibit 99.6-99.9% Coul

8 ethod were in the range of 0.0087 mg kg(-1) (Mn) to 1.6 mg kg(-1) (Ca).

9 this work, we investigate the Li(1.2)Ni(0.13)Mn(0.54)Co(0.13)O(2) particles morphologically, composit

10 detergent lysis-based assay, cellular Fura-2 Mn extraction assay, reduced the number of cells and mat

11 and commercially available LiNi(0.6) Co(0.2) Mn(0.2) O(2) (NCM(622) ) cathodes deliver ultrahigh ener

12 3) ) to create SPEs inside LiNi(0.6) Co(0.2) Mn(0.2) O(2) (NCM) || Li batteries that are able to over

13 h cathode material, O3-type Li(0.6) [Li(0.2) Mn(0.8) ]O(2) , is developed with the pristine state dis

14 nganese(II) to form lithium manganate [Li(2) Mn(CH(2) SiMe(3) )(4) ] enables the efficient direct Mn-

15 e product, (H(2) N(2) (CH(2) C=O(mu-S))(2) )[Mn(CO)(3) ](2) resulted from loss of M originally residi

16 generating anionic analogues to MN(2) S(2) .Mn(CO)(3) Br we introduced metallodithiolate ligands, MN

17 mA cm(-2)), a 1.0 mAh cm(-2) LiNi(0.6)Co(0.2)Mn(0.2)O(2) electrode maintains a substantial 74% of its

18 Experimental validation on Li(1.2)Ni(0.2)Mn(0.6)O(2) shows that sulfur deposition enhances stabil

19 tion pattern yielding the phase-pure P2-Na(2)Mn(2)FeO(6) quaternary oxide with high uniformity of met

20 ing metal ions (Na(+), K(+), Mg(2+), Ca(2+), Mn(2+), Fe(2+), Al(3+), Ni(2+), Cu(2+), Zn(2+), Co(2+),

21 ces in their bodies, such as Fe(3+), Cu(2+), Mn(2+), and organic radicals.

22 ch we examine in here in a Cantor-like Cr(20)Mn(6)Fe(34)Co(34)Ni(6) alloy, comprising both face-cente

23 e P2-type cathode-Na(0.85) Li(0.12) Ni(0.22) Mn(0.66) O(2) (P2-NLNMO) was developed.

24 honeycomb superstructure of Na(0.75)[Li(0.25)Mn(0.75)]O(2), present in almost all oxygen-redox compou

25 anionic redox reactions in LiNi(1/3) Co(1/3) Mn(1/3) O(2) .

26 the synthesis of ordered intermetallic Pt(3) Mn/rGO catalyst is provided as an example of a generally

27 Full cells with LiNi(1/3)Mn(1/3)Co(1/3)O(2) cathodes demonstrate >92% capacity re

28 overall oxidation state of either Mn(III)(3)Mn(IV) or Mn(III)Mn(IV)(3) for the S(2) state.

29 o work hardening behavior in a low SFE Fe(40)Mn(20)Cr(15)Co(20)Si(5) (at%) high entropy alloy, SFE ~

30 istical nature of the data collected for (54)Mn and the data while being presented here is not used f

31 all sources tested with the exception of (54)Mn.

32 has an S = 3 ground state with isotropic (55)Mn hyperfine coupling constants of -75, -88, -91, and 66

33 with a commercial cathode material LiNi(0.6)Mn(0.2)Co(0.2)O(2), full cells exhibit a gravimetric and

34 of >99 % for both the Li anode and LiNi(0.8) Mn(0.1) Co(0.1) O(2) (NMC811) cathodes.

35 We exemplify this on LiNi(0.8)Mn(0.1)Co(0.1)O(2) (NMC811)/graphite cells, which are ty

36 O(4) anode and Prussian blue analog Na(1.88) Mn[Fe(CN)(6) ](0.97) .1.35H(2) O cathode can be coupled

37 in superfamily previously characterized as a Mn(2+)-dependent deadenylation exoribonuclease.

38 rmore, we found evidence that MESM acts as a Mn-selective ionophore, and we observed that it has incr

39 ing a Co(3)O(4) nanocube core that carries a Mn(3)O(4) shell on each facet.

40 In contrast, mice fed a Mn-supplemented diet showed slightly increased tolerance

41 Here, we report the first example of a Mn(II) complex that can be activated by changing the pH

42 XAS and multifrequency EPR spectroscopy of a Mn(IV)(4)O(4) cuboidal complex as a spectroscopic model

43 Here we show that a Mn-catalyzed C-H oxidation directed by carboxylic acids

44 r REST protects dopaminergic neurons against Mn-induced toxicity and enhances expression of the dopam

45 ression and thereby protects neurons against Mn-induced toxicity and neurological disorders associate

46 ssociated protein 6 (Daxx) and attenuated an Mn-induced decrease in the antiapoptotic proteins Bcl-2

47 Kinetic analysis showed that Mg(2+) and Mn(2+) ions increase ribozyme efficiency by making trans

48 dicate that TMEM165 can transport Ca(2+) and Mn(2+), which are both required for proper protein glyco

49 ctivity, direct evidence for its Ca(2+)- and Mn(2+)-transporting activities is still lacking.

50 process occurs between octahedral Mn(3+) and Mn(4+) with no evidence of tetrahedral Mn(5+) or Mn(7+).

51 e-crystalline CdSe(ethylenediamine)(0.5) and Mn(2+)-doped nanosheets are synthesized via a solvotherm

52 , proline, pH, conductivity, Fe, Cu, Al, and Mn values were found in the chestnut honeys.

53 a, K, Rb and Cs), AE(2+) (AE=Ca, Sr, Ba) and Mn(2+) demonstrate that the dimensionality of the obtain

54 sed alloy, with trace amounts of Zn, Ca, and Mn (~ 2% by wt.).

55 d showed a consistent linkage between Co and Mn.

56 Recent advanced EPR and Mn K-edge X-ray spectroscopy studies converge upon the H

57 nding on the relative availability of Fe and Mn in a given soil environment.

58 n the fate of As during As(III), Fe(II), and Mn(II) co-oxidation.

59 At intermediate pH values, As(III) and Mn(II) also competed for the oxidants, but Mn(III) behav

60 At pH 8.5, As(III) and Mn(II) competed for Fe(IV), which led As(III) to persist

61 results indicate the amounts of Mn(III) and Mn(IV) species in MnO(x) and CaMnO(3) depend on potentia

62 trient profiling showed Ca, Fe, Zn, P, K and Mn in the range of 2400.00-3400.00, 40.28-47.60, 12.40-1

63 These studies show Li and Mn working together in a synergistic manner to facilitat

64 mia virus (GALV), with virion morphology and Mn(2+)-dependent virion-associated reverse transcriptase

65 ispersed transition metal (M: Fe, Co, or/and Mn) and nitrogen co-doped carbon (M-N-C) catalysts as th

66 When PIP and Mn(II) are simultaneously injected, competition between

67 eously injected, competition between PIP and Mn(II) for binding at the edge sites takes place during

68 as numerous cavitation nucleation sites and Mn(2+) for chemodynamic therapy (CDT), resulting in enha

69 ion by using a non-collinear antiferromagnet Mn(3)GaN, in which the triangular spin structure creates

70 Recently the noncollinear antiferromagnet Mn(3)Sn, a Weyl semimetal candidate, was reported to sho

71 I)(NA) and manganese complex with asparagine Mn(II)(Asp)(2).

72 ation route" (MESMER), can accurately assess Mn in mammalian cells.

73 The long-observed competition between Mn(2+) and Ca(2+) occurs at the second Mn site, and its

74 osis AtaC is monomeric in solution and binds Mn(2+) to specifically hydrolyze c-di-AMP to AMP via the

75 their abundance in natural systems, biogenic Mn oxides likely play an important role mediating Se bio

76 ormetic U-shaped relationship for biological Mn status and optimal brain health, with changes in the

77 Oxide-bound Mn(II) plays a crucial role in catalyzing oxidant decomp

78 lving the site of catalysis, a protein-bound Mn(4)CaO(x) complex, which passes through >=5 intermedia

79 oexcitation of a trinuclear u(3)-oxo-bridged Mn(III)-based SMM, whose magnetic anisotropy is closely

80 on of the carboxylic acid group to the bulky Mn complex ensures the rigidity needed for high enantios

81 d Mn(II) also competed for the oxidants, but Mn(III) behaved as a reactive intermediate that reacted

82 ession and Orai1-dependent SOCE (assessed by Mn(2+) influx).

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

84 ing ferrihydrite surfaces needed to catalyze Mn(II) oxidation by O(2) and by stabilizing Mn(II) via t

85 (K, Na, Mg, Ca, Fe, Zn, Hg, Se, As, Cu, Cd, Mn, Ni, Cr, Pb and Co) were determined in dorsal white a

86 or Mn exposures subsequently affect cellular Mn levels.

87 n of small molecules known to alter cellular Mn levels, we report here that one of these chemicals in

88 that MESMER can accurately quantify cellular Mn levels in two independent cells lines through an iono

89 lent substitution of Fe(III) for the central Mn(III) ion forms the target heterotrimetallic precursor

90 (Co, Pb, 85 degrees C), and insertions (Co, Mn, 85 degrees C).

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

92 les showed apparent coincident maxima of Co, Mn, and Fe, 2D images revealed mutually exclusive Co and

93 , Na, K, Mg) and micronutrients (Fe, Zn, Co, Mn, I) were sufficient to contribute to daily dietary mi

94 irmed that anaerobic respiration comobilizes Mn and P and that this leads to the release of colloidal

95 llumination as a function of the constituent Mn(2+) and Ca(2+) ions in genetically engineered membran

96 tions of potentially toxic elements (Cu, Cr, Mn, Fe, Pb, Zn, Ni) were analysed by atomic absorption s

97 In this study, heavy metals including Cr, Mn, Co, Ni, Cu, Zn, As, and Cd in 55 Thai local rice (4

98 more abundant transition metals like Ti, Cr, Mn, and Fe.

99 ysis of 20 elements (Mg, P, S, K, Ca, V, Cr, Mn, Fe, Co, Cu, Zn, Se, Br, Rb, Sr, Mo, I, Cs, and Ba) i

100 am epitaxy (MBE), a series of single crystal Mn(x) Fe(3-) (x) O(4) thin films with controlled stoichi

101 2-2.7, 0.3-1, 3-14 and 0.5-2 ppm for Fe, Cu, Mn, and Zn, respectively, and varied as a function of th

102 e LLOs are designed with linearly decreasing Mn and linearly increasing Ni and Co from the particle c

103 n each muscle cell are shared by a 1 degrees Mn bouton and at least one 2 degrees Mn bouton.

104 degrees Mn bouton and at least one 2 degrees Mn bouton.

105 Conversely, the secondary (2 degrees Mn) type facilitates and has low and variable Qc and Pr.

106 sition was not altered by changes in dietary Mn.

107 SiMe(3) )(4) ] enables the efficient direct Mn-I exchange of aryliodides, affording transient (aryl)

108 n on the effects of water flow and dissolved Mn(II) on manganese-mediated redox reactions in saturate

109 umns is altered by the presence of dissolved Mn(II), generated in situ as reduced ions or present in

110 ng this method, we achieve very high per-dot Mn contents (>30% of all cations) and thereby realize ex

111 Specifically, when treated with DSS, Mn-deficient mice showed increased morbidity, weight los

112 implies an overall oxidation state of either Mn(III)(3)Mn(IV) or Mn(III)Mn(IV)(3) for the S(2) state.

113 n over calcium compared with two established Mn ionophores, calcimycin (A23187) and ionomycin.

114 e and carbamic acid) with a well-established Mn electrocatalyst changes the product selectivity from

115 thereby realize exceptionally strong exciton-Mn exchange coupling with g-factors of ~600.

116 lele and demonstrate that these mice exhibit Mn deficiency in the colon associated with impaired inte

117 Here, we show that exogenous Mn can restore A. baumannii viability in the presence of

118 dependent on the high-affinity Nramp family Mn transporter, MumT, as a DeltamumT mutant is no more s

119 attices compounds, A(4)B(2)O(9) (A = Co, Fe, Mn; B = Nb, Ta), have been explored owing to the occurre

120 shrooms excluded As, Be, Ca, Cd, Co, Cr, Fe, Mn, Ni and Si, and accumulated elements in the following

121 for further determination of Al, Cr, Cu, Fe, Mn, Sr, and Zn.

122 ich in LC-PUFAs and micro-nutrients (Cu, Fe, Mn, Zn), including species considered as potentially edi

123 Fe-Mn- and sulfate-reduction and cation-exchange processes

124 s favored dissolution of iron-manganese- (Fe-Mn-) oxyhydroxides (which adsorb (210)Pb) and formation

125 sed foods, we analysed selected minerals (Fe-Mn-Zn-Cu-Mg) in wild-harvested and commercially availabl

126 We prepare the Fe-Mn-K catalyst by the so-called Organic Combustion Method

127 QTLs were located on chromosomes 3 and 7 for Mn containing six candidate genes.

128 all spherical structures highly enriched for Mn.

129 exceed current upper recommended intakes for Mn in both adults and children.

130 ion option to inform biomarker selection for Mn, Cu, and Cr.

131 cytotoxicity, and increased selectivity for Mn over calcium compared with two established Mn ionopho

132 ndidate gene that could be controlling grain Mn concentration.

133 s responsible for the concentration of grain Mn across 389 diverse rice cultivars grown in Arkansas a

134 In addition, the phenotypic data of grain Mn concentration were combined from three flooded-field

135 nd candidate genes associated with the grain Mn concentration.

136 es within the apo-protein exhibiting greater Mn(II) affinity than Fe(II) affinity.

137 n metal concentrations were as follows: hair Mn, 0.08 mug/g; hair Cu, 9.6 mug/g; hair Cr, 0.05 mug/g;

138 Heterobimetallic Mn/Fe proteins represent a new cofactor paradigm in bioi

139 ems include the difficulty in obtaining high Mn contents, considerable broadening of QD size dispersi

140 as a potential biological source of the high Mn concentrations.

141 tribution and bio-availability of these high Mn concentrations in termite alates is needed.

142 ontent; lastly, black pepper had the highest Mn and the lowest Pb contents.

143 structure has been assigned to a homovalent Mn(IV)(4) core with an S = 3 ground state.

144 between Fe(2+) and the ribosome and identify Mn(2+) as a factor capable of attenuating oxidant-induce

145 et (SCM) behavior is observed for a Mo(III) -Mn(II) chain that exhibits anisotropic magnetic exchange

146 n state of either Mn(III)(3)Mn(IV) or Mn(III)Mn(IV)(3) for the S(2) state.

147 oxidation of the previously reported Mn(III)Mn(IV)(3)O(4) cuboidal complex to the Mn(IV)(4)O(4) comp

148 K(a)(LAC-MeCN) values of hydrides of W(III), Mn(II), Fe(III), Ru(III), Co(II), and Ni(III).

149 Here the THz anomalous Hall conductivity in Mn(3)Sn thin films is investigated by polarization-resol

150 ; this gives rise to the observed overlap in Mn and O redox couples and reveals that the onset potent

151 that astrocytic YY1 plays a critical role in Mn-induced neurotoxicity in vivo, at least in part, by r

152 f the genes controlling natural variation in Mn in crop plants is limited.

153 lent transition metal ions tested, including Mn(2+), Fe(2+), Co(2+), Ni(2+), and Cu(2+) We also demon

154 tch variations in the amount of incorporated Mn.

155 ing superoxide dismutase (SOD1) and inducing Mn-containing SOD3 as a non-Cu alternative.

156 The presence of arsenate partially inhibited Mn(II) oxidation likely by blocking ferrihydrite surface

157 ic H(2) evolution rendering the intermediate Mn hydride more stable; subsequent CO(2) insertion appea

158 elationship between vitamin D and intestinal Mn efflux and indicate the importance of distal intestin

159 elements (As, Ba, Be, Bi, Cd, Co, Cr, Cu, K, Mn, Mo, Na, Ni, P, Pb, Th, Tl, Sb, U, V, Y and Zn) in 73

160 ther determination of Al, Ca, Cr, Cu, Fe, K, Mn, Mo and Ni in rice samples by ICP OES.

161 0 mug/L As(III), 5 mg/L Fe(II), and 0.5 mg/L Mn(II) in solutions containing relevant groundwater ions

162 lloys with alloying elements Mg, Ca, Sr, Li, Mn, Fe, Cu, and Ag respectively, are screened systemical

163 llographic studies has revealed the mixed Li/Mn constitution of the organometallic intermediates invo

164 en divalent transition metal ions M(II) (M = Mn, Co, Ni, Cu, Zn, Pd, and Cd) under mild conditions.

165 sulation of first-row transition metals (M = Mn, Fe, and Co) within a Keplerate cluster that was line

166 ORR) in the presence of L1(0)-CoMPt NPs (M = Mn, Fe, Ni, Cu, Ni).

167 ed graphene oxide (rGO) supported Pt(3) M (M=Mn, Cr, Fe, Co, etc.) intermetallic NPs (Pt(3) M/rGO-HF)

168 Manganese (Mn) is an essential micronutrient required for the norma

169 Manganese (Mn) is an essential nutrient metal required for a number

170 Manganese (Mn) is an essential trace element for plants and commonl

171 The concentrations of P and manganese (Mn) in 0.45-mum-filtered extracts (10(-3) M CaCl(2)) of

172 ced metals, such as iron (Fe) and manganese (Mn), as plaques that form on the surface of the roots.

173 Co), cadmium (Cd), lead (Pb), and manganese (Mn).

174 ble assays for measuring cellular manganese (Mn) levels require cell lysis, restricting longitudinal

175 Chronic manganese (Mn) exposure causes the neurological disorder manganism,

176 ntotermes, showed remarkably high manganese (Mn) content (292-515 mg/100 gdw), roughly 50-100 times t

177 ns utilized, MntABC functioned in manganese (Mn) import.

178 We measured manganese (Mn), lead (Pb), copper (Cu), and chromium (Cr) in hair,

179 relationship between nutritional manganese (Mn) status and IBD patients.

180 The incorporation of manganese (Mn) ions into Cd(Zn)-chalcogenide QDs activates strong s

181 re, we investigated the impact of manganese (Mn) on As removal, since the two often co-occur in groun

182 39A8 result in undetectable serum manganese (Mn) and a Congenital Disorder of Glycosylation (CDG) due

183 Higher soil manganese (Mn) availability, which apparently was a consequence of

184 sly been thought to occur via a single-metal Mn aryl species.

185 The content of minerals (Ca, Fe, K, Mg, Mn, Na and Zn), dietary fiber (total, soluble and insolu

186 ally functional minerals (Ca, Cu, Fe, K, Mg, Mn, Na, P, Se and Zn) and trace metals (As, Cd, Pb, U an

187 Er, Tm, Yb, Lu) and trace elements (Li, Mg, Mn, Ni, Co, Cu, Sr, Ba, Pb) via chemometric evaluation f

188 measurements and calculations on the monomer Mn(acac)(3), we conclude that the wavepacket motion in t

189 ted by two functionally distinct motoneuron (Mn) types.

190 However, mycogenic Mn oxides rapidly oxidized volatile Se products, recycli

191 rsor [Mn(II)(ptac)(3)-Na-Fe(III)(acac)(3)-Na-Mn(II)(ptac)(3)] (3) with an appropriate metal ratio of

192 )] (3) with an appropriate metal ratio of Na:Mn:Fe = 2:2:1.

193 of engineered manganese oxide nanoparticles (Mn(x)O(y) NPs).

194 e identified across experiments, whereas new Mn QTLs were identified that were not found in individua

195 ted single metal sites (M-N-C, M=Fe, Co, Ni, Mn) are the popular platinum group-metal (PGM)-free cata

196 M(1)/CN, M = Pt, Ir, Pd, Ru, Mo, Ga, Cu, Ni, Mn).

197 achieve 80-99% leaching efficiencies of Ni, Mn, Co, and Li from the LIB "black mass".

198 e Mn redox process occurs between octahedral Mn(3+) and Mn(4+) with no evidence of tetrahedral Mn(5+)

199 In the absence of Mn(II), we observed rapid As(III) oxidation and the form

200 magnetic ions occurs solely via addition of Mn-Se units without uncontrolled deposition of Cd-Se spe

201 Tunable amounts of Mn(2+)(0.5-8.0%) are introduced, resulting in lattice co

202 The results indicate the amounts of Mn(III) and Mn(IV) species in MnO(x) and CaMnO(3) depend

203 While high-valent oxygenated complexes of Mn, Fe, Co, and Cu are increasingly well-known, high-val

204 , resulting in an asymmetric contribution of Mn/Mn pathways.

205 s performed the near-complete extractions of Mn, Co, Ni, Cu, Zn, Cd, and Pb ions from natural water s

206 l-known, the overall biological functions of Mn are rather poorly understood.

207 ation in order to drive the incorporation of Mn(2+) into the high-valence Mn(4)CaO(5) cluster.

208 Higher adolescent levels of Mn, Pb, and Cr were associated with lower IQ scores, esp

209 rations (90th percentiles) of the mixture of Mn, Pb, and Cr (0.3 mug/g, 2.6 mug/dL, and 0.1 mug/g, re

210 V) infusion, mice were exposed to 330 mug of Mn (MnCl(2) 30 mg/kg, intranasal instillation, daily) fo

211 are efficiently ligated and the presence of Mn(2+) stimulates this coupled reaction in vitro.

212 available Co(II) catalyst in the presence of Mn(III) cooxidant and oxygen as a terminal oxidant and p

213 In the presence of Mn, the mechanism of As removal varied with pH.

214 II) polymers was enhanced by the presence of Mn.

215 d we observed that it has increased rates of Mn membrane transport, reduced cytotoxicity, and increas

216 By expanding our study to a series of Mn-based oxides, we reveal that the air-stability of P2-

217 acancy sites due to the continuous supply of Mn(II).

218 layer-to-tunnel structure transformation of Mn oxides, provided new insights for natural biotic and

219 might be a potential target for treatment of Mn toxicity and other neurological disorders associated

220 endant SMe is achieved by the employment of [Mn(III)((TMS)PS3)(DABCO)].

221 hat exhibits exponential growth dependent on Mn(II) oxidation to a co-culture of two microbial specie

222 ess of the underlying surface, Mn(IV)O(2) or Mn(III)OOH.

223 of Zn(2+) but not Mg(2+), Cu(2+), Co(2+), or Mn(2+).

224 +) with no evidence of tetrahedral Mn(5+) or Mn(7+).

225 t occurs only between like-cations (Fe/Fe or Mn/Mn).

226 crificial external oxidants such as Ag(I) or Mn(III) salts.

227 xidation state of either Mn(III)(3)Mn(IV) or Mn(III)Mn(IV)(3) for the S(2) state.

228 a betaproteobacterium that does not oxidize Mn(II) alone, and designate it Ramlibacter lithotrophicu

229 orms the target heterotrimetallic precursor [Mn(II)(ptac)(3)-Na-Fe(III)(acac)(3)-Na-Mn(II)(ptac)(3)]

230 lly, we applied MESMER to test whether prior Mn exposures subsequently affect cellular Mn levels.

231 re that one of these chemicals induces rapid Mn efflux.

232 ntly correlated to the abundance of reactive Mn(III) species.

233 dow and T(1) -MR imaging due to the released Mn(2+) , and inhibited orthotopic liver tumor growth via

234 llowing oxidation of the previously reported Mn(III)Mn(IV)(3)O(4) cuboidal complex to the Mn(IV)(4)O(

235 ) in 10 muL of serum and 12 elements (Mg, S, Mn, Fe, Co, Cu, Zn Se, Br, Rb, Mo, and Cs) in less than

236 In secondary analyses, saliva Mn, hair Cu, and saliva Cr were selected as the biomarke

237 tween Mn(2+) and Ca(2+) occurs at the second Mn site, and its occupation by competing Ca(2+) slows th

238 confirmed a specific reduction of only serum Mn, and plasma protein N-glycome profiling revealed redu

239 Here, we identified several Mn-related changes in human carriers of the common SLC39

240 s in soil pH and C : N, which increased soil Mn availability and altered microbial community structur

241 ut manganese persists as reduced and soluble Mn(II).

242 Mn(II) oxidation by O(2) and by stabilizing Mn(II) via ternary complex formation.

243 l system with mixed cation oxidation states (Mn(x) Fe(3-) (x) O(4) ).

244 synthesis of todorokite, a tunnel-structured Mn oxide, is extremely difficult while it is the dominan

245 MHz) due to axial distortion of substituted Mn(2+) (S = 5/2).

246 cycle, regardless of the underlying surface, Mn(IV)O(2) or Mn(III)OOH.

247 was programmed to not only bind a synthetic Mn-porphyrin but also maintain binding site access to fo

248 ) and Mn(4+) with no evidence of tetrahedral Mn(5+) or Mn(7+).

249 intenance of the intestinal barrier and that Mn deficiency exacerbates dextran sulfate sodium (DSS)-i

250 We conclude that Mn is necessary for proper maintenance of the intestinal

251 Furthermore, we demonstrate that Mn(2+) competes with Fe(2+) for rRNA-binding sites and t

252 Here, we provide evidence that Mn is critical for the maintenance of the intestinal bar

253 ur previous in vitro studies have shown that Mn repressed GLAST and GLT-1 via activation of transcrip

254 The Mn redox process occurs between octahedral Mn(3+) and Mn

255 The Mn(2+) content of maneb was extracted in the supramolecu

256 The Mn-O bond angles and lengths determined from density fun

257 l bipyramidal [Mo(CN)(7) ](4-) anion and the Mn(II) unit with a tridentate ligand results in a neutra

258 Increasing steric bulk around the Mn shuts down rapid homolytic H(2) evolution rendering t

259 a synergistic manner to facilitate both the Mn-I exchange and the C-C bond-forming steps.

260 synthetic O(2) evolution is catalyzed by the Mn(4)CaO(5) cluster of the water oxidation complex of th

261 of the alkyliodide ICH(2) SiMe(3) during the Mn-I exchange being essential to the aryl homocoupling p

262 On further examination, the Mn is located primarily in the abdomens of the Macroterm

263 For the Mn- and Fe-containing frameworks, a transition from ferr

264 Moreover, REST inhibited the Mn-induced proapoptotic proteins Bcl-2-associated X prot

265 dies on tetranuclear complexes mirroring the Mn oxidation states of the S(3) state remain rare.

266 n units in the open coordination site of the Mn center.

267 To gain better separation of the Mn centers and prevent energy transfer, a bulky singly p

268 y zinc ions gives quantitative yields of the Mn(2) product.

269 The photooxidative self-assembly of the Mn(4)CaO(5) cluster, termed photoactivation, utilizes th

270 ch quantifies the magnetic anisotropy of the Mn(III) centers.

271 Mn(III)Mn(IV)(3)O(4) cuboidal complex to the Mn(IV)(4)O(4) complex described here.

272 ty, which encompasses formate binding to the Mn, is considered.

273 roof of concept, the capacity to utilize the Mn-MOF for electrochemical CO(2) fixation and to spectro

274 contrast, CaMnO(3) perovskites in which the Mn(V) species formed at a less positive potential than t

275 Results show that this Mn(IV)(4)O(4) complex has an S = 3 ground state with iso

276 and the following elements were chosen: Ti, Mn, Fe, Cu, Zn, Br, Rb, Sr.

277 reaction, while at a later breakthrough time Mn(II) will occupy both edge and vacancy sites due to th

278 The structure of BON1 bound to Mn(2+) is also presented.

279 isite sensitivity of glycosyltransferases to Mn concentration.

280 ; M=Ni(II) , [V(IV) =O](2+) and Fe(III) ) to Mn(CO)(5) Br.

281 the WOC with W1 present as a water ligand to Mn(4), while the g = 4.8/4.9 form observed at high pH va

282 nto cellular biomass that was dependent upon Mn(II) oxidation.

283 ncorporation of Mn(2+) into the high-valence Mn(4)CaO(5) cluster.

284 solved manganese ions results in high-valent Mn(III,IV)-oxide nanoparticles of the birnessite type bo

285 rotein is capable of accessing a high-valent Mn(V)-oxo species which can transfer an O atom to a thio

286 erent modes in the presence of Mg(2+) versus Mn(2+) ions.

287 which is very likely mostly associated with Mn.

288 alterations in branching that improved with Mn supplementation, suggesting that the common variant e

289 abiotic nature of oxidative mechanisms, with Mn-mediated oxidation dominating within Mn-rich organic

290 family of isostructural conductive MOFs with Mn(2+) , Zn(2+) , and Cd(2+) .

291 with Mn-mediated oxidation dominating within Mn-rich organic soils and Fe-mediated oxidation dominati

292 dging sulfurs and carboxamide oxygens within Mn-mu-S-CH(2) -C-O, 5-membered rings.

293 cles throughout both fresh and degraded Li(x)Mn(2)O(4) electrodes.

294 near the surface and almost pure spinel Li(x)Mn(2)O(4) near the core.

295 l-containing cathode materials (e.g., LiNi(x)Mn(y)Co(z)O(2); NMCs), as they lose oxygen at lower oper

296 Herein, a high-Ni LiNi(1-) (x) (-) (y) Mn(x) Al(y) O(2) (NMA) cathode of desirable electrochemi

297 High-nickel LiNi(1-) (x) (-) (y) Mn(x) Co(y) O(2) (NMC) and LiNi(1-) (x) (-) (y) Co(x) Al

298 ntry of certain non-iron metals, such as Zn, Mn, and Co.

299 (Mg, P, S, K, Ca) and micronutrient (Fe, Zn, Mn, Cu) concentrations of leaves and edible parts of thr

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

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