ライフサイエンスコーパス: magnesium

1 eoside 5'-triphosphate insertion compared to magnesium.

2 rved during DNA synthesis in the presence of magnesium.

3 tors of crystallization, such as citrate and magnesium.

4 entrations in human serum in the presence of magnesium.

5 terize the dark side of deformation twins in magnesium.

6 ubstitution enables transport of calcium and magnesium.

7 01> tilt and twist grain boundaries (GBs) in Magnesium.

8 tly correlated with increased level of serum magnesium.

9 P levels to examine their relation to plasma magnesium.

10 on transport, comparable to that of metallic magnesium.

11 pinach (4g) was digested in vitro with added magnesium (0, 200, 400mg/L) and canola oil/coffee creame

12 enrichment in fine SSA for potassium (1.3), magnesium (1.4), and calcium (1.7), likely because of th

13 functionalized primary alcohol initiator and magnesium 2,6-di-tert-butyl phenoxide as a catalyst, was

14 Potassium ( approximately 5g/100g), magnesium (2g/100g) and calcium (0.6g/100g) are the majo

15 o stood out as potassium (378.69mg/100g) and magnesium (31.78mg/100g) contents, and yellow mombin as

16 women supplemented with calcium (1200 mg/d), magnesium (550 mg/d), and calcitriol (25 mug/d) given ei

17 vitamin A), vitamins C and E and the mineral magnesium (ACEMg) can be beneficial for reducing hearing

18 magnesioethane products are highly activated magnesium alkyls and show unprecedented, uncatalyzed rea

19 is commonly developed during the rolling of magnesium alloy and can even increase during annealing m

20 aled that the preferred growth directions of magnesium alloy dendrite change as the type and amount o

21 their high specific strength and stiffness, magnesium alloys are attractive for lightweight applicat

22 ation selection and morphology transition of magnesium alloys at the atomic level.

23 ltimicrometer-sized particles of aluminum or magnesium alloys into alkoxide nanowires of tunable dime

24 Unfortunately, the ductility of magnesium alloys is usually limited.

25 It was found that for most binary magnesium alloys, the preferred growth direction of the

26 ective towards designing formable and strong magnesium alloys.

27 This is done by first compressing a sodium-magnesium aluminosilicate glass at 1 GPa at Tg, followed

28 emerging electrolyte for Mg batteries is the magnesium aluminum chloride complex (MACC) which shows h

29 Magnesium Aluminum Chloride Complex was synthesized and

30 Herein, we have revealed that magnesium and calcium ions play a major role in modulati

31 otein Claudin-10, show enhanced paracellular magnesium and calcium permeability and reduced sodium pe

32 minor inorganic seawater components such as magnesium and calcium.

33 Plasma magnesium and hs-CRP were measured by inductively couple

34 The redox chemistry of magnesium and its application in rechargeable Mg batteri

35 sy to achieve, whereas reaction with lithium-magnesium and lithium-zinc amides affords C-2 or C-8 fun

36 ential treatment of 2,3-dichloropropene with magnesium and n-BuLi generated the equivalent of 1,3-dil

37 helix P2b and loop L1 is highly sensitive to magnesium and plays a key role in pre-organization.

38 models were developed; R(2)cal were 0.99 for magnesium and potassium and 0.97 for ash.

39 uantify concentrations of ash, potassium and magnesium and present the potential to classify differen

40 vestigated the association between intake of magnesium and risk of mortality due to liver diseases.

41 nd determine how solution conditions such as magnesium and sodium concentrations and temperature infl

42 velocities was observed in the systems with magnesium and spermidine ions compared to the system wit

43 nhibitory concentrations (EC50) for calcium, magnesium and zinc were 270+/-18, 253+/-75 and 420+/-322

44 rs, as well as the receptor's sensitivity to magnesium and zinc.

45 take combined with supplementation (calcium, magnesium, and calcitriol) was more effective than suppl

46 ity was observed for hexadeca-cationic zinc, magnesium, and metal-free phthalocyanines (Pcs) and tetr

47 Dietary intakes of vitamin B-6, magnesium, and zinc were below the Estimated Average Req

48 We found that magnesium- and ammonium-bearing minerals are ubiquitous

49 using the terms [antenatal or prenatal] and [magnesium] and [preterm or premature or neuroprotection

50 The transport of magnesium as oxide or silicate from the cooling core to

51 context of earlier findings indicating that magnesium at the product metal position blocks the rever

52 s derived from an earlier generation of high-magnesium basaltic rocks, suggesting that the arc-like s

53 rmed through partial melting of hydrated low-magnesium basaltic rocks; notably, these TTGs have 'arc-

54 East Pilbara Terrane, Western Australia, low-magnesium basalts of the Coucal Formation at the base of

55 rated through 150 years of work worldwide on magnesium-based inorganic cements, with a focus on both

56 d herein is a new microdevice, consisting of magnesium-based micromotors which can autonomously and t

57 Reactions of a magnesium-based pinacolatoboryl nucleophile with the ele

58 e predict and measure the gap opening on the magnesium-based surface band up to a critical temperatur

59 Magnesium batteries appear a viable alternative to overc

60 Rechargeable magnesium batteries have attracted considerable attentio

61 kg(-1)) than all other reported rechargeable magnesium batteries using intercalation cathodes.

62 ssing the kinetic limitation of rechargeable magnesium batteries.

63 The development of a competitive magnesium battery is plagued by the existing notion of p

64 e eventual development of an all-solid-state magnesium battery.

65 ch must be overcome in realizing a practical magnesium battery.

66 Here we show that the precipitation of magnesium-bearing minerals from the core could have serv

67 ise their intake of calcium, vitamin B12, or magnesium beyond the Recommended Dietary Allowance (RDA)

68 Magnesium biases the landscape toward a collapsed state

69 agnesium-enriched colonization niches causes magnesium binding to S. aureusteichoic acids and increas

70 ion results in the formation of a new carbon-magnesium bond and a new fluorine-magnesium bond and is

71 new carbon-magnesium bond and a new fluorine-magnesium bond and is analogous to Grignard formation in

72 The magnesium boryl is shown to act as an unambiguous nucleo

73 Here, we report a simple synthesis of a magnesium boryl through the heterolytic activation of th

74 ved two key steps: (1) the reaction of vinyl magnesium bromide with 2,2-dimethyl-6-t-butyl-dimethyl-s

75 can reverse trends of decreasing calcium and magnesium [Ca + Mg] leaching to surface waters in granit

76 ation (OA) as their skeleton is made of high-magnesium calcite, one of the most soluble forms of calc

77 urated fat, polyunsaturated fat, phosphorus, magnesium, calcium, and vitamin D) were performed.

78 Decreased magnesium-calcium ratios point toward a sustained increa

79 m(Pr(i)Benz)], has been employed to form the magnesium carbatrane compound, [Tism(Pr(i)Benz)]MgH, whi

80 The use of magnesium carbenoids allows carbon chains to be grown wi

81 h phase, a possible critical step needed for magnesium carbonate formation, was found.

82 Magnesium carbonate, phosphate, silicate-hydrate, and ox

83 for these transformations, both the zinc and magnesium catalytic systems are active at room temperatu

84 differential involvement of the two putative magnesium cations (Mg(2+)) at the active site, whereby o

85 chloride bond and slow diffusion of divalent magnesium cations in cathodes.

86 ip this scheme around, finding that, for the magnesium channel CorA, loss of ligand binding induces a

87 aracterization of its distant homologue CorA magnesium channel.

88 In chlorophyll biosynthesis, the magnesium chelatase enzyme complex catalyzes the inserti

89 2+) into protoporphyrin by ferrochelatase or magnesium chelatase, respectively.

90 Magnesium chloride (MgCl2) with the rhombohedral layered

91 , sodium chloride (NaCl)], 2:1 electrolytes [magnesium chloride (MgCl2), calcium chloride (CaCl2)], a

92 nated mainly due to the sluggish scission of magnesium-chloride bond and slow diffusion of divalent m

93 ium monochloride cations without scission of magnesium-chloride bond.

94 , 0.5 m/s; P = 0.90) but was improved in the magnesium compared with the placebo group by 1.0 m/s (95

95 ferentiated bodies have isotopically heavier magnesium compositions than chondritic meteorites.

96 catalytic hydrosilylation of CO2 involving a magnesium compound.

97 ation found between whitlockite fraction and magnesium concentration can be explained by the location

98 the NS5-SLA interaction is influenced by the magnesium concentration in a complex manner.

99 Colonization niches with different magnesium concentrations influence the bimodal system ac

100 Increasing magnesium concentrations negatively affected carotenoid

101 Cl2 but decreases with both lower and higher magnesium concentrations.

102 eby making the precipitation of calcium- and magnesium-containing minerals less favorable.

103 for at-line monitoring of ash, potassium and magnesium content of GF flours: tapioca, potato, maize,

104 Plasma magnesium decreased from NGT to prediabetes to T2D, and

105 with fatty liver disease are at high risk of magnesium deficiency.

106 haracterized previously) is an RNase H1-type magnesium-dependent endonuclease with stringent specific

107 Protein phosphatase magnesium-dependent-1A (PPM1A) dephosphorylates SMAD2/3,

108 achieved by treatment of an easily generated magnesium diboranate complex with 4-dimethylaminopyridin

109 wer source conditions, in conjunction with a magnesium diboride (MgB2) superconducting magnet.

110 nd investigate the effect of coating it with magnesium diboride layer on the vortex penetration field

111 owed that addition of bacteria enriched with magnesium did not change chemical parameters of the ice

112 Magnesium doping yielded p-type films with a carrier den

113 red to sodium chloride nodules surrounded by magnesium-enriched coatings.

114 For instance, magnesium-enriched colonization niches causes magnesium

115 rignard reagents prepared in situ by halogen/magnesium exchange with i-PrMgCl, or aryllithium reagent

116 nsumption, education, and urinary sodium and magnesium excretion, urinary potassium excretion was not

117 In addition, we reveal that magnesium exists in the SIR-nucleosome filament, with a

118 2+), or Co(2+) can be growth-inhibitory, and magnesium fluoride is toxic.

119 9b-RhoGAP in complex with GDP-bound RhoA and magnesium fluoride.

120 ream with addition of bacteria enriched with magnesium had higher adhesiveness.

121 Magnesium has attracted attention worldwide because it i

122 Loss of Trpm6 in mice also perturbs cellular magnesium homeostasis but additionally results in early

123 The terminal zinc and magnesium hydride compounds, [kappa(3)-Tism(Pr(i)Benz)]Z

124 mmunized with NS1 combined with aluminum and magnesium hydroxide, monophosphoryl lipid A + AddaVax, o

125 ks to be converted into lithium (t-BuLi) and magnesium (i-PrMgCl.LiCl) carbenoids in the presence of

126 -diphenylethylene into the Mg-Mg bond of two magnesium(I) dimers, [((Ar)Nacnac)Mg-]2 (Ar = C6H2Me3-2,

127 =2,6-diethylphenyl), has been prepared via a magnesium(I) reduction of the alanate complex, ((Dep) Na

128 tion can be explained by the location of the magnesium in calcified tissue.

129 ndings reveal a previously undefined role of magnesium in promoting CGRP-mediated osteogenic differen

130 The cooperation between SAM and magnesium in stabilizing important tertiary interactions

131 We manipulate concentrations of sodium and magnesium in the growth media, and we consider four diff

132 Viability of the bacteria enriched with magnesium in the obtained ice cream was lower in compari

133 The pseudoknot stabilization by magnesium, in combination with P1 stabilization by SAM,

134 Multivalent cations such as spermidine and magnesium induce attraction between packaged DNA sites t

135 s Calcrl or Ramp1 substantially reversed the magnesium-induced osteogenesis that we observed in this

136 Magnesium intake <2.3 mg/kg was related to increased ris

137 le of magnesium intake/kg, those with higher magnesium intake (>2.308 mg/kg) had decreased risk of HF

138 Although interactions between magnesium intake and alcohol use and hepatic steatosis a

139 ant (P > 0.05), inverse associations between magnesium intake and liver disease mortality were strong

140 We evaluated the association between total magnesium intake and mortality due to liver diseases in

141 tial mechanism by which an increased dietary magnesium intake beneficially affects cardiovascular hea

142 Daily magnesium intake derived from the questionnaire was divi

143 We hypothesize that magnesium intake relates to HF hospitalization in blacks

144 Overall magnesium intake was associated with a reduced risk of m

145 the analysis was repeated using quartiles of magnesium intake without accounting for body weight.

146 ssessed the association between quartiles of magnesium intake/kg and hospitalizations for HF adjustin

147 8, 2.309-3.147, 3.148-4.226, and >/=4.227 mg magnesium intake/kg).

148 d with participants in the first quartile of magnesium intake/kg, those with higher magnesium intake

149 y implantation of a pin containing ultrapure magnesium into the intact distal femur in rats.

150 rmediate and then an insoluble final product magnesium iodide.

151 As a result, the rechargeable magnesium/iodine battery shows a better rate capability

152 Here we report a rechargeable magnesium/iodine battery, in which the soluble iodine re

153 nique combination of an ADP molecule with no magnesium ion and a phosphate ion.

154 found that the binding mode is modulated by magnesium ion and NaCl concentration, but unlike EcoSSB,

155 f the F1-ATPase from C. thermarum, ATP and a magnesium ion are bound to the alpha-helices in the down

156 for the production of isochorismate, a high magnesium ion concentration suppresses the rate of relea

157 Our CEST and SAXS experiments, at different magnesium ion concentrations, quantitatively confirm our

158 e spectroscopy measurements that substantial magnesium ion mobility can indeed be achieved in close-p

159 oretical predictions also indicate that high magnesium ion mobility is possible in other chalcogenide

160 ons of polymerase beta, we find that a third magnesium ion positioned near the newly identified produ

161 Recently, a third active site magnesium ion was identified in some DNA polymerase prod

162 a key residue for catalysis coordinating the magnesium ion, moves closer, presumably switching nucleo

163 contacts to the water shell of an associated magnesium ion, which bridges fluoroquinolone-gyrase inte

164 e that is retained in the active site by the magnesium ion.

165 occurring polyphosphates (PIP2 and ATP) and magnesium ions (Mg(2+)).

166 itly identify target RNA motifs sensitive to magnesium ions and SAM.

167 anning counter-ion condensation and explicit magnesium ions are employed to calculate the folding fre

168 +) and Li(+) selectivity against calcium and magnesium ions in mixed solutions is improved by 4 and >

169 m our simulation results, demonstrating that magnesium ions induce collapse and pre-organization.

170 ulations, we calculate the effect of SAM and magnesium ions on the folding free energy landscape of t

171 We use this analysis to predict that magnesium ions remodel the landscape, shifting the equil

172 coordinate the viral RNA template, NTPs, and magnesium ions to facilitate nucleotide condensation1.

173 actococcus lactis JBB 500 were enriched with magnesium ions using Pulsed Electric Fields.

174 tion has long been considered to require two magnesium ions.

175 and a DNA-bound, fully cleaved complex with magnesium ions.

176 s and reference ones for calcium, potassium, magnesium, iron, manganese and zinc were 0.61, 0.79, 0.5

177 Availability of magnesium is a matter of concern due to its role in many

178 A major benefit of magnesium is the apparent lack of dendrite formation dur

179 We argue that possible magnesium isotope fractionation during condensation of t

180 11, to examine the association between serum magnesium level and NODAT.

181 ial interactions between serum and dialysate magnesium levels and risks associated with dialysate pot

182 -2) has been shown to regulate intracellular magnesium levels by forming a complex through an extende

183 (CNNM) family causes a rise in intracellular magnesium levels that promote oncogenic transformation.

184 iated with the host, including extracellular magnesium limitation, low pH, and the presence of cation

185 Hypomagnesemia (serum magnesium <0.74 mmol/L) also significantly associated wi

186 e concentration of calcium, potassium, iron, magnesium, manganese and zinc in artichoke samples.

187 silver and significantly greater amounts of magnesium, manganese, gold, and LREEs.

188 Our findings suggest higher intakes of magnesium may be associated with a reduced risk of morta

189 Magnesium may reduce carotenoid bioavailability by formi

190 ed dialkylated products was optimized with a magnesium/mercuric chloride reagent system and afforded

191 divalent, dendrite-free, and earth-abundant magnesium metal anode.

192 Magnesium metal is a superior anode which has double the

193 Magnesium (Mg(2+)) homeostasis is critical for metabolis

194 ese controls when experiencing low cytosolic magnesium (Mg(2+)), a divalent cation essential for ribo

195 Magnesium (Mg) alloys are promising materials for biodeg

196 In this work, we used magnesium (Mg) as a model to investigate the effect of a

197 three fertilizers, but the calcium (Ca) and magnesium (Mg) was higher with ORG and 2xORG.

198 itical regulator of basal intracellular free magnesium ([Mg(2+)]i) levels.

199 evels of intracellular concentration of free magnesium ([Mg2+]i), which was experimentally recorded i

200 The propulsion of drug-loaded magnesium micromotors in gastric media enables effective

201 ry is plagued by the existing notion of poor magnesium mobility in solids.

202 we report a battery chemistry that utilizes magnesium monochloride cations in expanded titanium disu

203 es the reversible intercalation of 1 and 1.7 magnesium monochloride cations per titanium at 25 and 60

204 show a battery that reversibly intercalates magnesium monochloride cations with excellent rate and c

205 ical study reveal fast diffusion kinetics of magnesium monochloride cations without scission of magne

206 ed amounts by 1.5-13% for copper, manganese, magnesium, niacin, phosphorus, potassium, folic acid, ri

207 metals (SaMMs), including copper, manganese, magnesium, nickel, tin, niobium, light rare earth elemen

208 HAPE and demonstrated a hysteretic effect of magnesium on 7SK folding dynamics including a 7SK GAUC m

209 The impact of magnesium on carotenoid bioaccessibility was modulated m

210 ion influenced potential negative effects of magnesium on carotenoid bioaccessibility.

211 itor bone mineral density, serum creatinine, magnesium, or vitamin B12.

212 etween dietary intake of calcium, potassium, magnesium, or vitamin D and fecundability, a greater con

213 f cGMP per mug protein with a preference for magnesium over manganese as a co-factor.

214 agonal zinc oxide (ZnO) films on cubic (001)-magnesium oxide (MgO) substrates using advanced scanning

215 ensembles of holmium (Ho) atoms supported on magnesium oxide (MgO).

216 ethanesulfonyl fluoride proceeds neatly with magnesium oxide as the base in an aqueous suspension to

217 ustic, bulk and surface vibrational modes in magnesium oxide nanocubes using an atom-wide electron be

218 on is demonstrated on a lithium titanate and magnesium oxide nanoparticle mixture.

219 from corner-shared magnesium oxyfluoride and magnesium oxide octahedra.

220 ssemblies of magnetic atoms (Fe and Co) on a magnesium oxide surface, we measure that the interaction

221 The cathodes based on magnesium oxide, cerium oxide and lanthanum oxide show e

222 ional structures built up from corner-shared magnesium oxyfluoride and magnesium oxide octahedra.

223 the structure of a mimetic of Martian water, magnesium perchlorate aqueous solution at its eutectic c

224 Here, the authors show that magnesium perchlorate has a major impact on water struct

225 scovery by the Phoenix Lander of calcium and magnesium perchlorates in Martian soil samples has fuele

226 The urinary excretion of potassium, calcium, magnesium, phosphate, sulfate, and other urinary markers

227 0 was correlated with higher levels of serum magnesium, phosphorus, and lower AKP level.

228 ally assess the degradation of biodegradable magnesium pins (as-drawn pure Mg, as-cast Mg-Zn-Mn, and

229 digested and afterward the elements calcium, magnesium, potassium, sodium, iron, zinc, phosphor, bari

230 calation hosts for multivalent-ion batteries.Magnesium rechargeable batteries potentially offer high-

231 Magnesium rechargeable batteries potentially offer high-

232 a and grain dynamics suggest the presence of magnesium-rich grains of silicate and oxide composition,

233 The fatty acid profile of the calcium and magnesium salts was stable after one year of storage in

234 the Magmaris sirolimus-eluting bioabsorbable magnesium scaffold and the Absorb bioresorbable vascular

235 the Magmaris sirolimus-eluting bioabsorbable magnesium scaffold was significantly less thrombogenic c

236 nt was explored as a new device opportunity (magnesium scaffold), which can be absorbed by the body w

237 0.1 mS cm(-1) at 298 K), specifically in the magnesium scandium selenide spinel.

238 these calcitic nanoparticles, being rich in magnesium, segregate during or just after transformation

239 ated relative of S. glossinidius, utilizes a magnesium sensing PhoP-PhoQ and an uncharacterized MarR-

240 ite mostly stabilizes the P1 and P3 helices, magnesium serves an important role in stabilizing a pseu

241 Here, newly developed highly biocompatible magnesium shallow doped gamma-Fe2 O3 (Mg0.13 -gammaFe2 O

242 ng implies that the isotopic compositions of magnesium, silicon and iron, and the relative abundances

243 Major rock-forming elements (magnesium, silicon, iron, and calcium) are present in co

244 pening the door for the realization of other magnesium solid ionic conductors and the eventual develo

245 Meanwhile, low magnesium status is linked to both chronic inflammation

246 s for growth on gluconate and under salt and magnesium stress.

247 0-500 mg IV thiamine every 8 hours, 64 mg/kg magnesium sulfate (approximately 4-5 g for most adult pa

248 Notably, pretreatment of pregnant dams with magnesium sulfate is sufficient to prevent the early inf

249 Continuous nebulization, addition of magnesium sulfate to SABA, and levosalbutamol compared t

250 rose, and shikimic acid) and inorganic gels (magnesium sulfate, MgSO4).

251 e transition from short-chain polysulfide to magnesium sulfide occurs at late stage.

252 Rechargeable magnesium/sulfur battery is of significant interest beca

253 Corticosteroids (such as betamethasone) and magnesium sulphate (MgSO4) are administered to women in

254 Antenatal magnesium sulphate given prior to preterm birth for feta

255 th (<37 weeks' gestation) were randomised to magnesium sulphate or control treatment and where neurol

256 nt reduction in the risk of death or CP with magnesium sulphate treatment compared with no treatment

257 Overall, there was no clear effect of magnesium sulphate treatment compared with no treatment

258 For cerebral palsy in survivors, magnesium sulphate treatment had a strong protective eff

259 preterm birth, the gestational age at which magnesium sulphate treatment was given, the total dose r

260 ment was given, the gestational age at which magnesium sulphate treatment was received, or the dose a

261 vere maternal outcome potentially related to magnesium sulphate treatment, no events were recorded fr

262 (MA) was to assess the effects of antenatal magnesium sulphate, compared with no magnesium treatment

263 the dose and timing of the administration of magnesium sulphate.

264 Our data indicate that a daily magnesium supplement of 350 mg for 24 wk in overweight a

265 ive was to evaluate the effects of long-term magnesium supplementation on arterial stiffness.

266 To our knowledge, the effect of magnesium supplementation on blood pressure (BP) in indi

267 before May 2017 that examined the effect of magnesium supplementation on BP in individuals with prec

268 .We sought to determine the pooled effect of magnesium supplementation on BP in participants with pre

269 Magnesium supplementation resulted in a mean reduction o

270 mm Hg in DBP.The pooled results suggest that magnesium supplementation significantly lowers BP in ind

271 d diastolic blood pressure (DBP) between the magnesium-supplementation group and the control group.El

272 weighted overall effects indicated that the magnesium-supplementation group had a significantly grea

273 ng more susceptible to inhibitory effects of magnesium than those digested with 8mM (p<0.001).

274 The dose of elemental magnesium that was used in the trials ranged from 365 to

275 AM, explains the requirement of both SAM and magnesium to form the fully collapsed metabolite-bound c

276 Interventions targeting serum magnesium to reduce the risk of NODAT should be evaluate

277 The magnesium transporter 1 (MAGT1) is a critical regulator

278 p present in the Bateman module of the CNNM3 magnesium transporter.

279 gm by uncovering that their association with magnesium transporters of the cyclin M (CNNM) family cau

280 tenatal magnesium sulphate, compared with no magnesium treatment, given to women at risk of preterm b

281 identified two loci associated with urinary magnesium (uMg), rs3824347 (P=4.4x10(-13)) near TRPM6, w

282 DTA-treated samples unless exogenous calcium/magnesium was added at the time of anti-IgE stimulation.

283 analyses, every 100 mg increase in intake of magnesium was associated with a 49% reduction in the ris

284 Among the mineral contents, Magnesium was found ranging from 855mug/g (Gham) to maxi

285 Thus, magnesium was found to potentially interfere with carote

286 However, serum magnesium was in the upper normal to hypermagnesemic ran

287 Plasma magnesium was independently and inversely associated wit

288 Consistently, plasma magnesium was inversely correlated with plasma hs-CRP in

289 centration for ascending quartiles of plasma magnesium were 1.29 (1.06-1.57), 1.16 (0.95-1.41), 1.00

290 Concentrations of ash, potassium and magnesium were determined with reference methods and LIB

291 oordinating molecules, over hard calcium and magnesium, which interact mainly ionically.

292 interest due to the observed association of magnesium whitlockite with malignancy.

293 procedure allowed determination of iron and magnesium with detection limits of 1.01 and 3.36mgkg(-1)

294 y aimed to assess the associations of plasma magnesium with prediabetes and type 2 diabetes (T2D) amo

295 We demonstrate a Magnesium Zinc Oxide (MZO) based high voltage thin film

296 We present a magnesium zinc oxide (MZO) nanostructure-modified quartz

297 ing concentrations (0-1000 mg/L) of calcium, magnesium, zinc and sodium (control) on the bioaccessibi

298 on, and reduced excretion of serum chloride, magnesium, zinc, and antidiuretic hormone.

299 metal ion chelators that bind iron, copper, magnesium, zinc, and other transition metals.

300 all methods, and variations in pH, calcium, magnesium, zinc, potassium, thymidine, and polysorbate 8