ライフサイエンスコーパス: manganese

1 lated (EVP1001-1) or chelated (mangafodipir) manganese.

2 ion of ammonium in fertilizer helps mobilize manganese.

3 ect basolateral reuptake of freshly absorbed manganese.

4 availability of essential nutrients such as manganese.

5 king water including copper, zinc, iron, and manganese.

6 lated bi-phase synthesis towards large-scale manganese 1,4-benzenedicarboxylate (MnBDC) MOFs with a p

7 ls such as chromium (0.67-2.54 mg/100 g) and manganese (1.07-2.34 mg/100 g).

8 d complete a biogeochemical energy cycle for manganese(5,6) that may interface with other major globa

9 Manganese, a biologically active paramagnetic calcium an

10 efore hypothesized that increased intestinal manganese absorption could induce manganese hyperaccumul

11 To elucidate the role of ZIP14 in manganese absorption, here we used CaCo-2 Transwell cult

12 ivo studies in male C57BLJ mice suggest that manganese accumulates in dopamine neurons of the VTA and

13 It is unknown, however, how manganese accumulates in dopaminergic brain regions or h

14 Ferroportin disease mutations influence manganese accumulation and cytotoxicity.

15 channels prevented these effects as well as manganese accumulation in the mouse midbrain in vivo Our

16 t overexpression of pstSCAB does not disrupt manganese acquisition or result in overaccumulation of p

17 mbined with pyrazole and catalytic amount of manganese, active cobalt complex can be generated in sit

18 I, PET and MTC were similar, irrespective of manganese agent.

19 on the HO(t)Bu concentration, no observable manganese amide complex, and a high reaction constant in

20 Manganese and arsenic both threaten groundwater quality

21 the co-occurrence or physical separation of manganese and arsenic in groundwater systems under chang

22 Here we tested manganese and arsenic retention under conditions commonl

23 sed arsenic retention, while the presence of manganese and arsenic together increased both arsenic an

24 h fragmented and powder forms, precipitating manganese and calcium oxalates.

25 Elevated concentrations of manganese and dissolved organic carbon (DOC) in groundwa

26 Manganese and DOC concentrations are higher near rivers

27 ularly experience stress due to combined low manganese and iron availability.

28 ce protein signatures indicating late-season manganese and iron stress, consistent with concurrently

29 oth of which involve metal ions like copper, manganese and iron.

30 ter characteristics (high organics, iron and manganese) and lead and copper in point of use drinking

31 t analysis showed that cupper, iron, sodium, manganese, and lead in the soil had a relationship with

32 neonatal cord blood levels of lead, cadmium, manganese, and mercury after supplementation with vitami

33 ave been reported to be involved in calcium, manganese, and pH homeostases.

34 tion corrosion of lead by oxidized phases of manganese, and we used 16S rRNA sequencing to identify b

35 Lead and manganese are regulated in drinking water due to their n

36 These results implicate manganese as an important driver of Southern Ocean produ

37 hates into monophosphates in the presence of manganese at neutral to slightly acidic pH.

38 We investigated transport of lead and manganese at the tap in a full-scale distribution system

39 suggest an electronic structure wherein the manganese atom remains Mn(III) and the OIM ligand has be

40 field-based evidence suggests, however, that manganese availability may also play a role.

41 fresh insight into the failure mechanism of manganese-based cathode chemistries, which serves as bet

42 microscopy (SI-SECM) of two electrodeposited manganese-based electrocatalysts, amorphous MnO(x) and p

43 isualize its effectively defect-free, purely manganese-based ferromagnetic kagome lattice with atomic

44 The essential metal manganese becomes neurotoxic at elevated levels.

45 esisting manganese starvation imposed by the manganese binding immune effector calprotectin.

46 features of mycobacterial Pol1 POL include a manganese binding site in the vestigial 3' exonuclease s

47 ralized method for improving PLQYs in hybrid manganese bromides and is readily extended to designing

48 f these materials, we report five new hybrid manganese bromides with the general formula A(m)MnBr(4)

49 ntial metals, such as iron, copper, zinc and manganese, but also to toxic metals including lead, alum

50 al nutrients, including the transition metal manganese, by a process termed nutritional immunity.

51 inach photosystem-II particles devoid of the manganese-calcium cluster are tracked by visible-light a

52 on and concomitant dioxygen formation by the manganese-calcium cluster of oxygenic photosynthesis has

53 A sodium-manganese-carbonate (Mn-Na-CO(2)) thermochemical water-s

54 A non-noble and air-stable manganese catalyst (2 mol %) was used to perform this tr

55 introduce a highly active and chemoselective manganese catalyst for the hydrogenation of imines.

56 of nitriles using a homogeneous nonprecious manganese catalyst is presented.

57 trast, here, we report a molecularly defined manganese catalyst that allows for low-temperature/low-p

58 Using a small-molecule manganese catalyst, Mn(CF(3)PDP), at low loading (at a s

59 Herein, a manganese-catalyzed chemoselective hydroboration of carb

60 Ligand-free manganese-catalyzed homocoupling of arenes or aryl halid

61 formamide intermediates, which then undergo manganese-catalyzed hydrogenolysis, regenerating the pro

62 An efficient manganese-catalyzed N-alkylation of sulfonamides has bee

63 The first manganese-catalyzed oxidation of organosilanes to silano

64 Herein, we report on manganese-catalyzed regioselective Markovnikov addition

65 tical component of this host response is the manganese-chelating protein calprotectin.

66 property of Dps with addition of a dinuclear manganese cluster.

67 (Li (x)Co(1- x)O(2), LCO) and lithium nickel manganese cobalt oxide (Li (x)Ni (y)Mn (z)Co(1- y- z)O(2

68 ow-iron diet exhibited reduced mitochondrial manganese, cobalt, and zinc levels, but not reduced iron

69 Lithium-rich nickel-manganese-cobalt (LirNMC) layered material is a promisin

70 fibres, which, coupled with a lithium nickel-manganese-cobalt oxide cathode with a high nickel conten

71 II)(Cit)(2) and nicotianamine Zn(II)(NA) and manganese complex with asparagine Mn(II)(Asp)(2).

72 Then, the maneb concentration equivalent to manganese concentration was calculated.

73 Manganese concentration was determined by UV-Vis spectro

74 We found that manganese concentration-dependently increased the excita

75 il-aquifer connections in producing elevated manganese concentrations (>300 mug/L) in United States (

76 red soils, ~40% of the samples with elevated manganese concentrations have pH values < 6 and elevated

77 play an important role in producing elevated manganese concentrations in groundwater used for human c

78 Anthropogenic nitrogen may also affect manganese concentrations in groundwater.

79 otentially consume groundwater with elevated manganese concentrations, the highest densities of which

80 We also observed that welders exposed to manganese-containing fumes had plasma exosomes that cont

81 The manganese content was a discriminant marker of Liebana P

82 The manganese content, along with Rare Earth Elements (REE)

83 the distribution of Mehlich III extractable manganese, copper, zinc, boron, and iron in soils and (b

84 rsenic increased with time on dialysis while manganese decreased.

85 so necessary to maintain wild-type levels of manganese-dependent superoxide dismutase activity in the

86 cs and possibly facilitated early geological manganese deposits.

87 e of the uniaxial insulating antiferromagnet manganese difluoride and platinum.

88 pyrrole -PPy) and catalytic activities (from manganese dioxide -MnO(2)) were independent and compleme

89 Aqueous rechargeable zinc-manganese dioxide batteries show great promise for large

90 ture in Na(0.6)[Li(0.2)Mn(0.8)]O(2) inhibits manganese disorder and hence O(2) formation, suppressing

91 rmore, lithium-rich LiMn(2)O(4) with lithium/manganese disorder and surface reconstruction could effe

92 Meanwhile, fast manganese dissolution in turn triggers irreversible stru

93 ppress the irreversible phase transition and manganese dissolution.

94 understanding of the once-overlooked role of manganese-dissolution in electrolytes provides fresh ins

95 ecially those low in 12HBAs, induce cellular manganese efflux and that Slc30a10 induction by BA pools

96 SLC30A10 is a manganese efflux transporter critical for whole-body man

97 ations in SLC30A10, a cell surface-localized manganese efflux transporter in the brain and liver, ind

98 In addition, Slc30a10, encoding a manganese efflux transporter, was one of the genes most

99 By combining longitudinal manganese-enhanced magnetic resonance imaging (MEMRI) an

100 hown by histology, anterograde axon tracing, manganese-enhanced magnetic resonance imaging, and elect

101 We previously showed manganese-enhanced MRI (MEMRI) more accurately quantifie

102 ed with intensive but controlled cracking at manganese-enriched prior-austenite grain boundaries norm

103 ethod was developed for enrichment of maneb (manganese ethylene-bisdithiocarbamate) with a supramolec

104 ough transport into bile is a major route of manganese excretion, manganese levels in the brain, bloo

105 e efflux transporter critical for whole-body manganese excretion.

106 red that a deletion in mneA, which encodes a manganese exporter, restored ROS resistance of the toxR

107 Manganese exposure produces Parkinson's-like neurologic

108 assay centered on this small molecule, named manganese-extracting small molecule (MESM).

109 , we validated that this assay, termed here "manganese-extracting small molecule estimation route" (M

110 aline conditions favored dissolution of iron-manganese- (Fe-Mn-) oxyhydroxides (which adsorb (210)Pb)

111 Consequently, regulation of manganese flux at the blood-brain barrier (BBB) is criti

112 a pincer complex of the abundant earth metal manganese for an unprecedented acceptorless dehydrogenat

113 sing a model distribution system: increasing manganese from 4 to 215 mug L(-1) nearly doubled lead re

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

115 Hybrid manganese halides have attracted widespread attention be

116 The oxidation of manganese has long been theorized(1)-yet has not been de

117 ducing colourless Roman glass by addition of manganese have been uncovered, whereas the source of the

118 t BMVECs play a critical role in controlling manganese homeostasis in the brain.

119 Yet, the mechanisms by which brain manganese homeostasis is regulated are unclear.

120 ded as the main regulatory organ involved in manganese homeostasis, impaired hepatic manganese uptake

121 nknown role for BAs in intestinal control of manganese homeostasis.

122 e of intestinal ZIP14 in regulating systemic manganese homeostasis.

123 ction occurs through the formation of active manganese-hydride species via an insertion and bond meta

124 o proceed by a concerted process involving a manganese hydroperoxide species.

125 intestinal manganese absorption could induce manganese hyperaccumulation when ZIP14 is inactivated.

126 ource of protons in the protonation of vinyl-manganese(I) carbonyl intermediates.

127 Manganese(I) carbonyl-catalyzed C-H bond functionalizati

128 tal halide, ethylenebis-triphenylphosphonium manganese (II) bromide ((C(38)H(34)P(2))MnBr(4)), which

129 ides interfacial manganese species on anode, manganese(II) in bulk electrolyte also significantly des

130 Pairing lithium and manganese(II) to form lithium manganate [Li(2) Mn(CH(2)

131 on are catalyzed via their interactions with manganese(II).

132 electrochemical insertion of NO(3) (-) into manganese(II, III) oxide (Mn(3) O(4) ) as a cathode for

133 the antioxidants N-acetyl-cysteine (NAC) or manganese (III) tetrakis-(4-benzoic acid)porphyrin.

134 dyes 5,10,15,20-Tetraphenyl-21H,23H-porphine manganese(III) chloride (MnTPP), methyl red (MR), and br

135 thogens, Staphylococcus aureus possesses two manganese importers, MntH and MntABC.

136 ated that the intracellular concentration of manganese in both the toxR and ompU mutants was reduced.

137 rimary transporter responsible for obtaining manganese in culture in the presence of calprotectin.

138 The addition of manganese in culture medium restored ROS resistance in b

139 on-metal dissolution from cathode materials, manganese in particular, has been held responsible for s

140 alyzed by a pincer complex of earth-abundant manganese in the presence of a stoichiometric base, maki

141 These findings demonstrate the mechanism of manganese-induced dysfunction of dopamine neurons, and r

142 a potential therapeutic target to attenuate manganese-induced impairment of dopamine transmission.SI

143 uts, and only whole-body knockouts exhibited manganese-induced neurobehavioral defects.

144 eaved on discharge, reforming O(2-), but the manganese ions have migrated within the plane, changing

145 te type bound to photosystem II, with 50-100 manganese ions per photosystem.

146 Oxidation of dissolved manganese ions results in high-valent Mn(III,IV)-oxide n

147 ng the transcellular trafficking of divalent manganese ions within the microvascular capillary endoth

148 e site includes two octahedrally coordinated manganese ions.

149 sist of anionic complexes of a metal centre (manganese, iron or cobalt) sandwiched between two bulky

150 led transition metal chalcogenides (cadmium, manganese, iron, and nickel oxides and sulfides).

151 To the extent that manganese is a driver of lead release, controlling it du

152 dopamine transmission.SIGNIFICANCE STATEMENT Manganese is a trace element critical to many physiologi

153 Overexposure to manganese is an environmental risk factor for neurologic

154 in a calprotectin-deficient mouse, in which manganese is more readily available.

155 Manganese is one of the most abundant elements on Earth.

156 inhibitors at higher concentration, whereas manganese is only an activator and cobalt and nickel are

157 under basal physiological conditions, brain manganese is regulated by activity of SLC30A10 in the li

158 A mononuclear nonheme manganese(IV)-oxo complex binding the Ce(4+) ion, [(dpaq

159 not influence maternal cadmium, mercury, or manganese levels at delivery.

160 ure, pan-neuronal/glial knockouts had higher manganese levels in the basal ganglia and thalamus than

161 ile is a major route of manganese excretion, manganese levels in the brain, blood, and liver of liver

162 astrointestinal tract, had markedly elevated manganese levels in the brain, blood, and liver.

163 f such function of intestinal ZIP14 in vivo, manganese levels in the livers and brains of intestine-s

164 Iron and manganese levels in the source water and throughout the

165 Therefore, when manganese levels increase, activity of SLC30A10 in the b

166 Notably, however, brain manganese levels of endoderm-specific knockouts were low

167 Maternal cadmium, mercury, and manganese levels were nearly identical across groups.

168 ed to total protein levels, only calcium and manganese levels were significantly lower in the milk fr

169 risingly, unlike whole-body knockouts, brain manganese levels were unaltered in pan-neuronal/glial Sl

170 coccal growth when S. aureus is subjected to manganese limitations and exposed to oxidative stress.

171 transporter was also important for growth in manganese-limited environments when S. aureus was forced

172 ffects of water flow and dissolved Mn(II) on manganese-mediated redox reactions in saturated porous m

173 Arsenic, cadmium, copper, lead, manganese, mercury, selenium, and zinc concentrations we

174 itated by the high solubility of nitrogen in manganese metal, while its structural features are guide

175 Here we report that an Archean manganese mineral, rhodochrosite (MnCO(3)), can be photo

176 The oxidation states of manganese minerals in the geological record have been in

177 Divalent manganese (Mn(2+)) exposure can stimulate neurotoxicity

178 ing the potential role of the divalent metal manganese (Mn(2+)) in protein aggregation, we characteri

179 Manganese (Mn(2+)) is extruded from the cell by the zinc

180 water containing dissolved iron (Fe(II)) and manganese (Mn(II)).

181 ions in SLC39A8 result in undetectable serum manganese (Mn) and a Congenital Disorder of Glycosylatio

182 Here we show that reactive manganese (Mn) and iron (Fe) intermediates, rather than

183 n the bioavailability of the essential metal manganese (Mn) are seen in models of HD.

184 Higher soil manganese (Mn) availability, which apparently was a cons

185 mes and Odontotermes, showed remarkably high manganese (Mn) content (292-515 mg/100 gdw), roughly 50-

186 Chronic manganese (Mn) exposure causes the neurological disorder

187 Maintaining manganese (Mn) homeostasis is important for the virulenc

188 th conditions utilized, MntABC functioned in manganese (Mn) import.

189 The concentrations of P and manganese (Mn) in 0.45-mum-filtered extracts (10(-3) M C

190 hat Chlamydomonas reinhardtii can accumulate manganese (Mn) in proportion to extracellular supply, up

191 The incorporation of manganese (Mn) ions into Cd(Zn)-chalcogenide QDs activat

192 Manganese (Mn) is an essential micronutrient required fo

193 Manganese (Mn) is an essential nutrient metal required f

194 Manganese (Mn) is an essential trace element for plants

195 Available assays for measuring cellular manganese (Mn) levels require cell lysis, restricting lo

196 Pathogenic bacteria encounter host-imposed manganese (Mn) limitation during infection.

197 Here, we investigated the impact of manganese (Mn) on As removal, since the two often co-occ

198 Manganese (Mn) oxide minerals influence the availability

199 oxacin (NOR), with goethite (alpha-FeOOH) or manganese (Mn) oxide, and their impact on the subsequent

200 The sorption of thallium (Tl) onto manganese (Mn) oxides critically influences its environm

201 have been coated either with synthetic Fe or manganese (Mn) oxides for 30 days in a redoximorphic soi

202 Manganese (Mn) participates in a variety of distinct phy

203 an inverse relationship between nutritional manganese (Mn) status and IBD patients.

204 Manganese (Mn), an essential metal and nutrient, is toxi

205 Fpn has been implicated in the regulation of manganese (Mn), another essential nutrient required for

206 tating reduced metals, such as iron (Fe) and manganese (Mn), as plaques that form on the surface of t

207 We measured manganese (Mn), lead (Pb), copper (Cu), and chromium (Cr

208 Manganese (Mn)-induced neurotoxicity resembles Parkinson

209 of cobalt (Co), cadmium (Cd), lead (Pb), and manganese (Mn).

210 ile Se compounds in the presence of biogenic manganese [Mn(III, IV)] oxides and oxyhydroxides (hereaf

211 , suggesting river-derived DOC also supports manganese mobilization.

212 ons of 5 essential minerals (cobalt, copper, manganese, molybdenum, and zinc), 4 metals with some evi

213 rter in the brain and liver, induce familial manganese neurotoxicity.

214 dmium, cobalt, chromium, copper, iron, lead, manganese, nickel, selenium, tin, and zinc, were present

215 um precatalyst and 4 atm of H(2) in THF, the manganese nitride ((tBu)Salen)Mn=N underwent hydrogenati

216 Transformation of manganese nodule powder also occurred in a liquid medium

217 lus niger was able to colonize and penetrate manganese nodules embedded in solid medium and effect ex

218 Aspergillus niger to colonize and transform manganese nodules from the Clarion-Clipperton Zone in bo

219 ect interactions between geoactive fungi and manganese nodules.

220 ecomposition of a mixture of iron oleate and manganese oleate in a high-boiling solvent in the presen

221 We also studied the effect of manganese on lead release using a model distribution sys

222 Here we examine the influence of iron and manganese on protein expression and physiology in Phaeoc

223 of chlorophyll production upon additions of manganese or iron.

224 liary excretion is not the primary cause for manganese overload observed in individuals lacking funct

225 ulting mycelial pellets and transformed into manganese oxalate dihydrate (lindbergite) and calcium ox

226 skite CaMnO(3) , was used to investigate the manganese oxidation state relating to the oxygen evoluti

227 Knowledge of the manganese oxidation states of the oxygen-evolving Mn(4)C

228 andidate pathways for coupling extracellular manganese oxidation to aerobic energy conservation and a

229 oxide (LiCoO(2) ) and lithium nickel cobalt manganese oxide (LiNi(0.8) Co(0.1) Mn(0.1) O(2) , NCM 81

230 et in which hydrous ferric oxide and hydrous manganese oxide deposits had formed as a consequence of

231 Manganese oxide formation in cell-free filtrates occurre

232 ard to the colloidal stability of engineered manganese oxide nanoparticles (Mn(x)O(y) NPs).

233 Manganese oxide nanoparticles (NPs) are shown to catalyz

234 the ability of photosystems to form extended manganese oxide particles.

235 Manganese oxide was effective at both hydrolytic and oxi

236 sulted in the generation of small nodules of manganese oxide with which the cells associated.

237 beta-MnO(2)) to 1.18 +/- 0.01 W/m(2) (sodium manganese oxide).

238 his study investigated the use of iron-doped manganese oxide, synthesized via air oxidation under str

239 ter followed by down-sizing of protein-bound manganese-oxide nanoparticles to finally yield today's c

240 ose an evolutionary scenario, which involves manganese-oxide production by ancestral photosystems, la

241 However, this assumes that manganese oxides can be produced only in the presence of

242 e highest power densities were achieved with manganese oxides capable of intercalating sodium ions wh

243 Our results suggest that manganese oxides could have formed abiotically on the su

244 became prominent, light-driven formation of manganese oxides from dissolved Mn(2+) ions may have pla

245 Manganese oxides have been proposed as promising geomedi

246 Manganese oxides have been recently investigated as exce

247 We synthesized 12 manganese oxides having different crystal structures and

248 ago on the basis of the inferred presence of manganese oxides in Archaean sedimentary rocks.

249 photosynthetic microorganisms biomineralize manganese oxides in the absence of molecular oxygen and

250 his light-dependent process may also produce manganese oxides in the photic zones of modern anoxic wa

251 the selective synthesis of different yttrium manganese oxides through assisted metathesis reactions b

252 an accurate assessment of the reactivity of manganese oxides used as engineered geomedia for quinolo

253 d the crystal structures and morphologies of manganese oxides, which undergo redox reactions coupled

254 environmental processes involving insoluble manganese oxides, with practical relevance to chemoorgan

255 fluence the multistage oxidation pathways of manganese oxides.

256 ucosidase (BG), lignin peroxidase (LiP), and manganese peroxidase (MnP), but decreased laccase (LA) p

257 on phases are present in oxidized forms, but manganese persists as reduced and soluble Mn(II).

258 hese CO(2)-derived compounds, catalyzed by a manganese pincer complex, yields methanol in addition to

259 Manganese produces a Ca(2+) channel-mediated current, wh

260 zed RNA in vitro RNA polymerization required manganese rather than magnesium ions, was independent of

261 carbon, suggesting soil-derived DOC supports manganese reduction and mobilization in shallow groundwa

262 CpTiCl(2), prepared in situ by manganese reduction of CpTiCl(3), is an excellent new sy

263 o Our data provide a potential mechanism for manganese regulation of dopaminergic neurons.

264 retained all protein subunits after complete manganese removal and by oxygen detection via a custom b

265 w that the addition of bicarbonate increased manganese retention but decreased arsenic retention, whi

266 arsenic together increased both arsenic and manganese retention.

267 dation mechanism of high-energy lithium- and manganese-rich layered cathode materials.

268 e derivatives by employing an earth-abundant manganese salt and simple phosphine-free NNN-tridentate

269 ive for S. aureus growth under conditions of manganese scarcity.

270 aphylococcus aureus to calprotectin-mediated manganese sequestration.

271 Here, we report a simple manganese small-molecule catalyst Mn(CF(3)-PDP) system t

272 s and calculations that, besides interfacial manganese species on anode, manganese(II) in bulk electr

273 he two transporters when cells are resisting manganese starvation imposed by the manganese binding im

274 component system required for sensitivity to manganese starvation.

275 d offers a theoretical guidance for choosing manganese substituting elements in lithium-rich as well

276 Manganese superoxide dismutase (MnSOD) functions as a tu

277 The ubiquitous iron/manganese superoxide dismutase (SOD) family exemplifies

278 e surges in detached cells by regulating the manganese superoxide dismutase (SOD2).

279 Manganese supports numerous neuronal functions but in ex

280 ue cycloisomerization promoted at a tailored manganese surface.

281 with the addition of the catalytic amount of manganese, the active cobalt catalyst can be regenerated

282 luminal domain and transported intracellular manganese to the lumen.

283 y impaired basolateral-to-apical (secretory) manganese transport and strongly enhanced manganese tran

284 udies provided evidence that ZIP14 restricts manganese transport in the absorptive direction via dire

285 y) manganese transport and strongly enhanced manganese transport in the apical-to-basolateral (absorp

286 ive oxygen species through the regulation of manganese transport.

287 s encoding methionine transporter (metP) and manganese transporter (mtsA) are crucial for GBS surviva

288 (a domain of SACOL1062), and SACOL0688 (the manganese transporter MntC) for detection of chronic S.

289 zophrenia GWAS is a missense mutation in the manganese transporter SLC39A8, which is associated with

290 er 39 family member 14 (SLC39A14) gene) is a manganese transporter that is abundantly expressed in th

291 e uptake, and kinetic analyses revealed that manganese uptake depends on pH and bicarbonate and is up

292 d in manganese homeostasis, impaired hepatic manganese uptake for subsequent biliary excretion has be

293 the major transporter mediating basolateral manganese uptake in enterocytes.

294 ZIP8 and ZIP14 coincided with a decrease in manganese uptake, and kinetic analyses revealed that man

295 The concentration of soil manganese was greater under DP (131 mg kg(-1)) than unde

296 Manganese was increased in incident patients.

297 ate the role of SLC30A10 in regulating brain manganese, we compared the phenotypes of whole-body and

298 uch metals as vanadium, niobium, cerium, and manganese were found to facilitate the formation of 1,4-

299 Changes in vanadium and manganese were largest and appeared to have some effect

300 iderable amounts of selenium, calcium, iron, manganese, zinc, phosphorous, boron, cobalt, Vitamins A,