ライフサイエンスコーパス: manganese

1 ternal, high cord, or high maternal and cord manganese.

2 f the ZIP metal transporter family transport manganese.

3 y because of its ability to chelate zinc and manganese.

4 ial divalent transition metals like iron and manganese.

5 lso accumulated more copper and zinc but not manganese.

6 whereas fungi express LOX with iron or with manganese.

7 evidence shows that ZIP14 can also transport manganese.

8 antimicrobial activity by chelating zinc and manganese.

9 rresponding to a specific oxidation state of Manganese.

10 iques are limited by the biotoxicity of bulk-manganese.

11 l as potential synergism between arsenic and manganese.

12 lycerol, and full activity required divalent manganese.

13 ead, 0.6 (0.4-0.9) and 0.4 (0.3-0.6) mug/dL; manganese, 22.7 (18.8-29.3) and 41.7 (32.2-50.4) mug/L.

14 sion tomography (PET) radionuclides, such as manganese-52 ((52)Mn, T(1/2)=5.6days), allow the imaging

15 lligence and reductions in water arsenic and manganese: a two-year follow-up study in Bangladesh.

16 When acquired in excess, manganese accumulates in tissues of the CNS and is assoc

17 stinal tract, and a lack of ZIP14 results in manganese accumulation in critical tissues such as the b

18 This phenotype is likely related to excess manganese accumulation in the CNS.

19 ination creates the opportunity for atypical manganese accumulation in tissues, including the brain.

20 Manganese accumulation was fourfold to fivefold higher i

21 In agreement with excessive manganese accumulation was the impaired motor function o

22 of the Zip14 KO mice is indicative of major manganese accumulation.

23 btilis MntR metalloregulatory protein senses manganese, an essential element required for central met

24 However, transport of manganese and calcium into the thylakoid lumen remains p

25 We herein report that manganese and cobalt can bind to the same nonheme site a

26 articles from the solution-phase reaction of manganese and cobalt carbonyl complexes with trioctylpho

27 Slc30a10 knockouts also had elevated thyroid manganese and developed hypothyroidism.

28 ed by a pincer complex of the earth abundant manganese and forms hydrogen gas as the sole byproduct,

29 ial blood sampling was performed to quantify manganese and gadolinium plasma clearance by using induc

30 a = -0.001, P = 0.03, respectively), whereas manganese and intake of micronutrient supplements were p

31 or the determination of lead, cadmium, zinc, manganese and iron in white and wild rice samples.

32 gested to play a role in DNA interaction and manganese and iron storage.

33 broken into subsections based on the metal (manganese and iron) and porphyrinoid ligand (porphyrin,

34 The structure of LmFBPase, complexed with manganese and its catalytic product phosphate, shows the

35 Manganese and lead are also correlated with ASD severity

36 Associations between manganese and mental (MDI) and psychomotor (PDI) develop

37 agnesium, potassium, iron, copper, zinc, and manganese and phosphorous in various kinds of breads sam

38 catalyst only based on earth-abundant metals manganese and sodium is reported for the first time.

39 tion of calcium, potassium, iron, magnesium, manganese and zinc in artichoke samples.

40 nes for calcium, potassium, magnesium, iron, manganese and zinc were 0.61, 0.79, 0.53, 0.77, 0.54 and

41 es have reduced uptake of essential elements manganese and zinc, and higher uptake of the neurotoxin

42 oint effect of in utero exposure to arsenic, manganese, and lead on children's neurodevelopment.

43 y the joint effect of coexposure to arsenic, manganese, and lead on neurodevelopment using an adapted

44 t metals, including iron, cobalt, nickel and manganese, and represents a generic platform for the dis

45 key micronutrients (e.g., vitamin A, copper, manganese, and zinc) support iron's function in erythrop

46 m japonicum Mur and Escherichia coli Fur are manganese- and iron-responsive transcriptional regulator

47 ed chlorosis in irt1 plants, indicating that manganese antagonized Fe mainly at the level of transpor

48 protein with a preference for magnesium over manganese as a co-factor.

49 able to mimic the properties of enzymes with manganese as a cofactor in their composition, such as Mn

50 ycle, and a new variable for models that use manganese as a proxy to infer oxygenation events on earl

51 B. japonicum Mur responded to iron, but not manganese, as determined by in vivo promoter occupancy a

52 other-child pairs with low maternal and cord manganese, associations with neurodevelopment scores wer

53 o selectively prepare an extensive series of manganese-based electrode materials, manifesting the con

54 ascular contrast enhancement produced by the manganese-based magnetic resonance (MR) imaging contrast

55 Manganese-based ternary phosphides represent a promising

56 nding site alone, we show that both zinc and manganese binding are necessary for calprotectin's antih

57 Manganese binding to PSII was severely reduced in pam71

58 and three novel DEGs associated with stress, manganese binding, and gibberellin-regulated transcripti

59 new insights into the molecular mechanism of manganese biomineralization.

60 Earth-abundant manganese bipyridine (bpy) complexes are well-establishe

61 arsenic (UAs/Cr), blood As (BAs), and blood manganese (BMn) were assessed at both times.

62 d phenol) that is required for this class of manganese catalyst.

63 to access the doubly reduced states of these manganese catalysts by eliminating their ability to dime

64 Manganese-catalyzed C-H bond activation chemistry is eme

65 ge of alkyl halides, demonstrating the first manganese-catalyzed coupling with alkyl electrophiles.

66 This study represents the first example of a manganese-catalyzed environmentally benign, practical th

67 d use diverse, aprotic solvents in iron- and manganese-catalyzed hydrofunctionalizations.

68 commonly accepted, is the dominant dissolved manganese cation in LiPF6-based electrolyte solutions of

69 ) standards with that for samples containing manganese cations dissolved from active materials (LiMn2

70 of electronic and chemical properties for a manganese center in a cobalt oxide environment, and prov

71 apse and the orbital/spin-state of Mn(2+) in manganese chalcogenides and also provide deeper insights

72 c susceptibility of A. fumigatus to zinc and manganese chelation by neutrophil-derived calprotectin.

73 the Mn4CaO5-cluster agree with a specific bi-manganese cluster, likely a di-micro-oxo bridged pair of

74 ces between organisms in the vicinity of the manganese cluster.

75 second coordination shell residues with the manganese cluster.

76 A new (N-phosphinoamidinate)manganese complex is shown to be a useful pre-catalyst f

77 A new hydrogenation catalyst based on a manganese complex of a chiral P,N,N ligand has been foun

78 Some manganese complexes can catalyze both antioxidant and pr

79 High-valent iron and manganese complexes effect some of the most challenging

80 ynthesis of site-differentiated tetranuclear manganese complexes featuring three six-coordinate and o

81 or the first time specific molecular-defined manganese complexes that allow for the hydrogenation of

82 f the same substrates with H2O2 catalyzed by manganese complexes, supporting the hypothesis that both

83 study examines associations between prenatal manganese concentrations and placental transfer of manga

84 Elevated dissolved iron and manganese concentrations at the fringe of the methane pl

85 Maternal blood manganese concentrations were negatively associated with

86 Cord manganese concentrations were not associated with neurod

87 Along with manganese concentrations, isotope ratios of nitrogen and

88 ate oxidation of benzene with pure iron- and manganese-containing minerals, clays, and aquifer solids

89 antioxidants proteins such as mitochondrial manganese-containing superoxide dismutase and peroxiredo

90 However, elevated manganese content in E. coli did not confer activity on

91 The product manganese coordinates phosphate oxygens of the inserted

92 The manganese coordinating sphere is similar to iron ligands

93 even QTLs for tissue Phosphorus, Zinc, Iron, Manganese, Copper, Sulphur and Boron concentrations unde

94 no chemical example of this reactivity at a manganese cubane cluster has been reported.

95 ation, and a reactivity study of a synthetic manganese cubane cluster with a pendant manganese-oxo mo

96 a new biogeochemical link between carbon and manganese cycles.

97 Moreover, E. coli Fur activity was manganese-dependent in B. japonicum.

98 The mechanism of action of the manganese-dependent phosphotriesterase from Sphingobium

99 This manganese-dependent SodA activity allows the bacteria to

100 Manganese-dependent superoxide dismutase (MnSOD) express

101 Notably, zinc- and manganese-depleted portions of the biofilm repress the p

102 provide new insights into the mechanisms of manganese detoxification and manganese-induced thyroid d

103 SLC30A10 and SLC39A14 cooperatively mediate manganese detoxification, here we produced Slc39a14 sing

104 Importantly, a low-manganese diet produced lower tissue manganese levels in

105 Manganese dioxide (MnO2) is a common environmental oxida

106 f clinically suitable formulations of hybrid manganese dioxide (MnO2) nanoparticles (MDNP) using bioc

107 Pt catalysts with three-layered structure of manganese dioxide (MnO2), lanthanum oxide (La2O3), and P

108 Manganese dioxide cathodes are inexpensive and have high

109 trodes were modified by depositing amorphous manganese dioxide layers via cyclic voltammetry (CV) and

110 sults suggested that microwave absorption of manganese dioxides can be tailored with Co doping to exp

111 mputationally to the microwave absorption of manganese dioxides.

112 Manganese dissolution from positive electrodes significa

113 vely coupled plasma (ICP) can determine both manganese dissolution rates and relative Mn(3+) amounts,

114 temperature electron transport properties of manganese doped lead sulfide films.

115 se reduction is thus a new connection in the manganese-driven carbon cycle, and a new variable for mo

116 SLC30A10 and SLC39A14 are manganese efflux and influx transporters, respectively.

117 ed that SLC30A10 is a cell surface-localized manganese efflux transporter, and parkinsonism-causing m

118 ations in SLC30A10, a cell-surface-localized manganese efflux transporter, cause a heritable manganes

119 gh alanine substitution of Asp-248 abolished manganese efflux, that of Asn-43 and Asp-47 did not.

120 stinal tract of the KO mice, suggesting that manganese elimination is impaired with Zip14 ablation.

121 have discovered that ZIP14 is essential for manganese elimination via the gastrointestinal tract, an

122 Manganese-enhanced magnetic resonance imaging (MEMRI) wa

123 rations in disease progression in vivo using manganese-enhanced magnetic resonance imaging (MEMRI).

124 red auditory and limbic brain activity using manganese-enhanced MRI (MEMRI).

125 nsitive calcium dysregulation as measured by manganese-enhanced MRI and electrophysiology.

126 By contrast, manganese evoked weak Fe deficiency responses in wild-ty

127 C39A14 and SLC30A10 are required for hepatic manganese excretion.

128 Early postnatal manganese exposure causes lasting impairment of selectiv

129 Environmental manganese exposure has been associated with adverse neur

130 A change in log manganese from the 25th to the 75th percentile when arse

131 carbamates, pyrethroids, neonicotinoids, and manganese fungicides) and five individual organophosphat

132 ide groups (pyrethroids, neonicotinoids, and manganese fungicides).

133 significantly greater amounts of magnesium, manganese, gold, and LREEs.

134 Manganese has been used for indirect monitoring of calci

135 Manganese has long been employed as a T1-shortening agen

136 To examine a role for ZIP14 in manganese homeostasis, we used Zip14 knock-out (KO) male

137 The early formation of manganese (hydr)oxide nanoparticles at mineral-water int

138 r laboratory measurements of the growth of a manganese hydroxide membrane in a microfluidic channel,

139 -releasing molecule (photoCORM) derived from manganese(I) and 2-(quinolyl)benzothiazole (qbt) namely,

140 The use of low-cost manganese(II) bromide (MnBr2) and tetramethylethylenedia

141 tion near room temperature, during which the manganese(II) ions are oxidized to manganese(III) and tw

142 Manganese(II) removal was enhanced when the accumulation

143 Q), 1,4-naphthoquinone (1,4-NQ), copper(II), manganese(II), and iron (II and III).

144 xperiments included manganese(II)-phosphate, manganese(II)-carbonate, and manganese(III)-oxyhydroxide

145 hases produced in these experiments included manganese(II)-phosphate, manganese(II)-carbonate, and ma

146 l platform using electrospun semi-conducting Manganese (III) Oxide (Mn2O3) nanofibers for DNA Hybridi

147 manganese ions present in the superoxidized manganese (III/IV) catalase active site is determined by

148 which the manganese(II) ions are oxidized to manganese(III) and two of the three deprotonated radical

149 (II)-phosphate, manganese(II)-carbonate, and manganese(III)-oxyhydroxides.

150 Manganese(III)-peroxo can react through hydrogen-atom ab

151 The synthesis and characterization of a manganese(III)-peroxo complex with a pentadentate bispid

152 Both manganese(III)-peroxo complexes are characterized by UV-

153 udy on aldehyde deformylation by two side-on manganese(III)-peroxo complexes with bispidine ligands.

154 Fur or Mur, suggesting a regulatory pool of manganese in B. japonicum that is absent in E. coli.

155 edian levels [interquartile ranges (IQR)] of manganese in maternal and cord blood, respectively, were

156 Patients have elevated manganese in the blood and brain and develop neurotoxici

157 Soluble manganese in the intermediate +III oxidation state (Mn(3

158 Excessive accumulation of manganese in these patients results in rapidly progressi

159 The pathogen's ability to acquire manganese in turn promotes function of SodA and KatN, en

160 a pincer complex of an earth-abundant metal (manganese), in the absence of any additives, base, or hy

161 Kinetic analyses indicate that manganese increases the rate constant for deoxynucleosid

162 We then applied our method to evolve a manganese-independent alpha-L-threofuranosyl nucleic aci

163 dysfunction in the onset and progression of manganese-induced disease and identifies Slc30a10 knock-

164 To determine the mechanisms of manganese-induced hypothyroidism and understand how SLC3

165 e mechanisms of manganese detoxification and manganese-induced thyroid dysfunction.

166 of dissolution rates and oxidation states of manganese ions is essential for designing effective miti

167 hat the assigned oxidation states of the two manganese ions present in the site are the opposite of t

168 The oxidation state assignment of the manganese ions present in the superoxidized manganese (I

169 on of specific analytes (potassium, calcium, manganese, iron, and zinc), and discuss dose-appropriate

170 Although the levels of manganese, iron, copper, zinc and molybdenum in rice wer

171 Manganese is an essential metal that becomes toxic at el

172 ked neurodegeneration.SIGNIFICANCE STATEMENT Manganese is an essential micronutrient.

173 In particular, manganese is an important first-row metal involved in ke

174 Liver manganese is increased in patients lacking SLC30A10 but

175 UF and CPE comparably indicated that manganese is predominantly present in dissolved fraction

176 asured the sequence progression of microbial manganese(IV) oxide reduction mediated by chemical speci

177 Manganese(IV)-oxo complexes are often invoked as interme

178 In the Pabna district, which displayed high manganese levels [interquartile range (IQR): 4.8, 18 mug

179 /Slc39a14 double knockouts had lower thyroid manganese levels and normal thyroid function.

180 se metabolism disorder resulting in elevated manganese levels and parkinsonian-like movement deficits

181 n with disodium calcium edetate lowers blood manganese levels in patients and can lead to striking cl

182 lc30a10/Slc39a14 double knockouts had higher manganese levels in the blood and brain but not in the l

183 At 6 weeks, manganese levels in the brain, blood, and liver of the k

184 , a low-manganese diet produced lower tissue manganese levels in the knock-outs and rescued the pheno

185 rast, Slc30a10 single knockouts had elevated manganese levels in the liver as well as in the blood an

186 Serum copper, ceruloplasmin, and manganese levels were normal, but her urinary copper lev

187 n is an essential factor required to prevent manganese-linked neurodegeneration.SIGNIFICANCE STATEMEN

188 eeded labeled amounts by 1.5-13% for copper, manganese, magnesium, niacin, phosphorus, potassium, fol

189 and minor metals (SaMMs), including copper, manganese, magnesium, nickel, tin, niobium, light rare e

190 ganese efflux transporter, cause a heritable manganese metabolism disorder resulting in elevated mang

191 ssociated with the regulation of whole-blood manganese (Mn) and multiple physiological traits.

192 he essential transition metals iron (Fe) and manganese (Mn) are not readily available to invading pat

193 y role in obtaining sufficient quantities of manganese (Mn) but also in protecting against Mn toxicit

194 Although manganese (Mn) can enhance brain tissues for improving m

195 Exposure to excessive manganese (Mn) causes manganism, a progressive neurodege

196 onmental Protection Agency reported airborne manganese (Mn) concentrations in East Liverpool, Ohio, 3

197 Chronic manganese (Mn) exposure is associated with neuromotor an

198 lescents have associated early developmental manganese (Mn) exposure with inattention, impulsivity, h

199 Plants require trace levels of manganese (Mn) for survival, as it is an essential cofac

200 The essential micronutrient manganese (Mn) functions as redox-active cofactor in act

201 elop an effective approach for incorporating manganese (Mn) ions into nanocrystals of lead-halide per

202 l (Ni(2+)) ions, whereas, to a large extent, manganese (Mn) ions remain in their Mn(4+) state.

203 Manganese (Mn) is an essential micronutrient and require

204 Elevated, nontoxic doses of manganese (Mn) protect against Shiga toxin-1-induced cel

205 normal growth conditions and in response to manganese (Mn) treatment.

206 However, the mechanisms by which manganese (Mn), a common dietary supplement, alters infe

207 ation to the tonoplast, complementation of a manganese (Mn)-sensitive Saccharomyces cerevisiae yeast

208 ically varied low loadings of cobalt (CoOx), manganese (MnOx), and nickel oxides (NiOx) has been unde

209 gnetic resonance (MR) imaging contrast agent manganese-N-picolyl-N,N',N'-trans-1,2-cyclohexenediamine

210 ctive skeleton to anchor highly electrolytic manganese nanoparticles (Mn NPs), which were prepared by

211 orm may offer a different pathway to utilize manganese nanoparticles based CNTs composite for the det

212 the development of a novel three dimensional manganese nanostructures based carbon nanotubes (CNTs-Mn

213 ausative genes for the accumulation of zinc, manganese, nickel, calcium, and cadmium in sorghum seeds

214 The manganese-nitronyl-nitroxide two-dimensional coordinatio

215 na in the Peru Basin require the presence of manganese nodules as a substrate, and near total collaps

216 effect of the mixture of arsenic, lead, and manganese on cognitive score when cord blood metals conc

217 tudies found no evidence of redox cycling of manganese or cobalt in the enzymatic reactions and sugge

218 Excessive accumulation of manganese or of copper can lead to parkinsonism because

219 The bacterial manganese oxidase MnxG of the Mnx protein complex is uni

220 s generally decrease with decreasing average manganese oxidation state.

221 Manganese oxide (alpha-MnO2 ) has been considered a prom

222 by coating reduced graphene oxide (rGO) and manganese oxide (MnO2) composite on the carbon felt (CF)

223 We investigated the reaction of manganese oxide [MnOx(s)] with phenol, aniline, and tric

224 Gold nanoparticles supported on manganese oxide belong to the most active gold catalysts

225 ally compared the laccase-like reactivity of manganese oxide nanomaterials of different crystallinity

226 Low-dimensional cobalt oxide codoped manganese oxide nanoparticles (CMO NPs; dia.

227 nce of five compositionally distinct layered manganese oxide nanostructures.

228 Manganese oxide NS were synthesized via the exfoliation

229 This study examines the effects of manganese oxide octahedral molecular sieve chitosan micr

230 e report a class of Bi-birnessite (a layered manganese oxide polymorph mixed with bismuth oxide (Bi2O

231 se experiments suggest that Mn(II) catalyzes manganese oxide recrystallization and illustrate a new p

232 intercalated between two nanosheets (NS) of manganese oxide to form a bilayer structure.

233 Manganese-oxide minerals (MnOx) are widely distributed o

234 all significantly lower than those of binary manganese oxides (Mn3O4, Mn2O3, and MnO2), consistent wi

235 Manganese oxides are often highly reactive and easily re

236 Manganese oxides from anthropogenic sources can promote

237 Mn(II) exchanges with structural Mn(III) in manganese oxides in the absence of any mineral transform

238 ing the laccase-like reactivity of different manganese oxides nanomaterials, and provide a basis for

239 Mixed-valence manganese oxides present striking properties like the co

240 Manganese oxides with layer and tunnel structures occur

241 Nanostructured manganese oxides, e.g. MnO2, have shown laccase-like cat

242 ive study of gold nanoparticles on different manganese oxides, we developed a gold catalyst on MnO2 n

243 ws activity for Mn(2+)(aq) oxidation to form manganese oxides.

244 marily mediated by the reduction of iron and manganese oxides.

245 patterns gathered from natural and synthetic manganese oxides.

246 the subunit topology and copper binding of a manganese oxidizing complex, and describe early stage fo

247 tal measure for the spin state reactivity in manganese-oxo corrolazine complexes.

248 etic manganese cubane cluster with a pendant manganese-oxo moiety.

249 reactions promoted by an electron-deficient manganese pentafluorophenyl porphyrin catalyst, Mn(TPFPP

250 esis that the synergy of Fenton reaction and manganese peroxidase might play an important role in DR5

251 k, we report the synthesis of ternary cobalt manganese phosphide nanoparticles from the solution-phas

252 We conclude that Mnx exploits manganese polynuclear chemistry in order to facilitate a

253 The likely product stabilization role of the manganese product metal in pol mu is discussed.

254 by cord/maternal manganese ratio, cord/total manganese ratio (total=maternal+cord), and by joint clas

255 ntal transfer, approximated by cord/maternal manganese ratio, cord/total manganese ratio (total=mater

256 Cord/maternal and cord/total manganese ratios were positively associated with MDI [co

257 ygen-tolerant TCA cycle supporting anaerobic manganese reduction is thus a new connection in the mang

258 ion of ZIP14 and therefore would be prone to manganese-related neurological diseases.

259 o4-mediated polyphosphate synthesis mediates manganese resistance.

260 rpreting the processes occurring actively in manganese-rich environments and recorded in the geologic

261 -ever demonstration of stabilized Si/lithium-manganese-rich full cells, capable of retaining >90% ene

262 ments and recorded in the geologic record of manganese-rich strata.

263 Isocyanation of celestolide with a chiral manganese salen catalyst followed by trapping with anili

264 Using this approach, we fine-mapped manganese sensitivity to a single polymorphism in the tr

265 e Earth-abundant, first-row transition metal manganese serves as the catalyst.

266 The structure was solved by sulfur and manganese single wavelength anomalous dispersion to a re

267 , bromine, calcium, copper, iron, potassium, manganese, sodium, nickel, lead, sulfur, silicon, titani

268 e an evolutionary adaptation to the cellular manganese status.

269 spensable for transport of the physiological manganese substrate and similar divalents iron and cobal

270 ve oxygen species, in part, by deacetylating manganese superoxide dismutase (MnSOD) and mitochondrial

271 reased acetylation and decreased activity of manganese superoxide dismutase (MnSOD).

272 lternative oxidase, dynamin related protein, manganese superoxide dismutase and Lon protease, respect

273 h down-regulation of GR and up-regulation of manganese superoxide dismutase and reduced glutathione l

274 composed of 215 amino acids, and has an iron/manganese superoxide dismutase domain.

275 ns with 8Br-cGMP also activated catalase and manganese superoxide dismutase expression, indicating th

276 ochondrial adaptive or stress proteins (e.g. manganese superoxide dismutase, mitochondrial KATP chann

277 tant accumulated substantially more zinc and manganese than the wild type in the tissues surrounding

278 electricity and catalyzed by Earth-abundant manganese, this transformation proceeds under mild condi

279 ne methyl ester], that can partially inhibit manganese toxicity not only in the neuroblastoma cell li

280 s and rescued the phenotype, suggesting that manganese toxicity was the underlying cause.

281 ncoding either transporter induce hereditary manganese toxicity.

282 gests that arsenic might be a potentiator of manganese toxicity.

283 er, the C-terminal domain failed to transfer manganese transport capability to a related zinc transpo

284 d C-terminal domains together confer optimal manganese transport capability to SLC30A10 and suggest t

285 of patients with a novel autosomal recessive manganese transporter defect caused by mutations in SLC3

286 nstrate that SLC39A14 functions as a pivotal manganese transporter in vertebrates.

287 TaVIT2 also complemented a manganese transporter mutant but not a vacuolar zinc tra

288 demonstrate that ZIP14 is not essential for manganese uptake by the brain.

289 esence of copper/zinc efflux as well as iron/manganese uptake, and bacterial survival in amoebae.

290 aternal and cord blood at delivery, measured manganese using inductively coupled plasma mass spectrom

291 ial confounders, an IQR increase in maternal manganese was associated with -3.0 (95% CI: -5.3, -0.7)

292 Evidence of a nonlinear effect of manganese was found.

293 ow (above or below median) maternal and cord manganese, was evaluated as a predictor of neurodevelopm

294 25th to the 75th percentile when arsenic and manganese were at the median was associated with a decre

295 s between arsenic concentrations and lead or manganese were not statistically significant.

296 These organ-specific changes in manganese were recently recapitulated in knockout mice.

297 mechanisms that allow SLC30A10 to transport manganese, which are unclear, is essential to understand

298 gle knockouts is induced by elevated thyroid manganese, which blocks thyroxine production.

299 ue to the use of a multinucleated complex of manganese with mu-oxo units, which was able to mimic the

300 ese concentrations and placental transfer of manganese with neurodevelopment in 224 2-y-old children