ライフサイエンスコーパス: magnesium

1 by a denitriding reaction in the presence of magnesium.

2 rent Mg centers and the mononuclear dimethyl magnesium.

3 n/crystallization process in the presence of magnesium.

4 n RNA duplex and in the presence of chelated magnesium.

5 ial rescue of the reaction in the absence of magnesium.

6 solated quinoa starch is rich in Sulphur and Magnesium.

7 It is also strongly depleted in magnesium.

8 tly correlated with increased level of serum magnesium.

9 s localised corrosion in humid air than pure magnesium.

10 tage dependence, and complete competition by magnesium.

11 gen migration compared to those observed for magnesium (0.88 eV).

12 lular sodium (+40 mM), potassium (+2 mM), or magnesium (+1 mM) reduces Th2:Th17 ratio and augments Th

13 n number of additional albuterol treatments (magnesium: 1.49, placebo: 1.59; risk ratio, 0.94 [95% CI

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

15 Furthermore, substitution of light magnesium ((24)Mg) by heavy, nuclear magnetic (25)Mg had

16 urred in 17 of the 409 children who received magnesium (4%) and 5 of the 407 who received placebo (1%

17 ales), 816 completed the trial (409 received magnesium; 407, placebo).

18 otal of 178 of the 409 children who received magnesium (43.5%) were hospitalized vs 194 of the 407 wh

19 o act as refuge for extremely halophilic and magnesium-adapted stratified communities of microbes, ev

20 (adjusted odds ratio, 2.0; 95% CI, 1.7-2.3), magnesium (adjusted odds ratio, 2.2; 95% CI, 1.9-2.7; p

21 been developed by combining surface-modified magnesium alloy as the internal load-bearing skeleton an

22 and T6 yield strength (270 MPa) in this new magnesium alloy is comparable to that of common 6xxx ser

23 te (particle) morphology and distribution in magnesium alloy Mg-5.78Zn-0.44Zr subjected to a complex

24 ollable biodegradability of surface-modified magnesium alloy with the excellent biocompatibility and

25 Lightweight magnesium alloys are attractive as structural materials

26 results indicated that aluminium-containing magnesium alloys exhibited considerably less localised c

27 pure magnesium and two aluminium-containing magnesium alloys was characterised after 96 h at 95% RH

28 hetic diamond(10), even greater than that of magnesium alloys.

29 Serum 25(OH)D3, calcium, and magnesium, alone and their interactions, were not associ

30 In this study, a magnesium-aluminum layered double hydroxide coated on gr

31 ted 2-phenyl-2-oxazolines with mixed lithium-magnesium amides followed by reaction with different ele

32 Struvite (magnesium ammonium phosphate-MgNH(4) PO(4) .6H(2) O), wh

33 However, magnesium and calcium are important in vitamin D metabol

34 between the global radiation and potassium, magnesium and calcium contents (correlation coefficients

35 minor inorganic seawater components such as magnesium and calcium.

36 ysis localized endogenous elements including magnesium and copper, further differentiating the hypoxi

37 Increased sodium and magnesium and decreased albumin and lactate levels were

38 ly requirements for minerals, especially for magnesium and iron.

39 luding new constraints on the output flux of magnesium and isotopic fractionation during low-temperat

40 Magnesium and its alloys attract increasingly wide atten

41 A number of new magnesium and lithium silyl reagents were prepared and s

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

43 and substrate concentrations, covariation of magnesium and nucleoside triphosphates, and the effects

44 W stimulant suggested an interfering role of magnesium and phosphate salts with HVACP inactivation.

45 e-glutamate (PE)/PPE clusters, responsive to magnesium and phosphate, also showed a phthiocerol dimyc

46 st abundant were potassium, sodium, calcium, magnesium and phosphorus, respectively.

47 d ultramafic lithologies, rock types rich in magnesium and poor in phosphate that present special req

48 antify the plant-available pools of calcium, magnesium and potassium and trace the soil phases that s

49 The plant-available pools of calcium, magnesium and potassium are assumed to be stored in the

50 models to assess associations between serum magnesium and radiographic subarachnoid hemorrhage sever

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

52 AL1 expression is regulated by extracellular magnesium and that down-regulation of this transporter d

53 anced lightweight structural alloys based on magnesium and titanium rely critically on a control over

54 The surface film on pure magnesium and two aluminium-containing magnesium alloys

55 , lidocaine, atropine, bicarbonate, calcium, magnesium, and dextrose each year were calculated in pat

56 s were increased, whereas resting DeltaGATP, magnesium, and dynamic phosphocreatine to inorganic phos

57 features that make them unable to bind ATP, magnesium, and/or substrates.

58 Based on our structural analysis, a magnesium-assisted S(N)2-type mechanism would be involve

59 ed attraction behavior, but not potassium or magnesium attraction thus clarifying the specificity of

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

61 e present a new rare-earth and aluminum-free magnesium-based alloy, with trace amounts of Zn, Ca, and

62 Magnesium-based biodegradable metals (BMs) as bone impla

63 Magnesium-based bioresorbable scaffold (MgBRS) presents

64 m atom surrounded by three hydride and three magnesium-based ligands.

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

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

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

68 trast, we observed that the effect of fibre, magnesium, biotin and vitamin E on VFM was partially med

69 We report n-type magnesium bismuthide (Mg(3)Bi(2))-based materials with a

70 We observed that a magnesium-bound nucleotide first binds next to the tunne

71 m dication, thus coordinating the entry of a magnesium-bound nucleotide with shuttling of the second

72 of ketones with acetylenes followed by (ii) magnesium bromide etherate/DIPEA-soft enolization of the

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

74 The oceanic magnesium budget is important to our understanding of Ea

75 Here, we report the discovery of high-magnesium calcite [CaMg(CO(3))(2)] armor overlaying the

76 The discovery of biogenic high-magnesium calcite in the relatively well-studied leaf-cu

77 metallic anodes, such as sodium, potassium, magnesium, calcium, and aluminum.

78 citri were deficients in zinc, iron, copper, magnesium, calcium, and nitrogen.

79 36, 53 and 62% decrease in the rejection of magnesium, calcium, sodium, and chloride ions, respectiv

80 alkali metals or an alkali metal paired with magnesium, calcium, zinc, aluminum, or gallium.

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

82 calcium carbonate (calcite), and/or calcium magnesium carbonate (dolomite).

83 Biogenic magnesium carbonate mineral precipitation from the magne

84 onditions using synthetic, amorphous calcium magnesium carbonate nanoparticles.

85 ection infrared spectroscopy pinpointed that magnesium carbonate precipitation begins at 1.5 monolaye

86 Readily available magnesium catalysts achieve the selective hydroboration

87 anistic understanding is used to develop the magnesium-catalyzed hydrosilylation of the C-C sigma bon

88 A magnesium-catalyzed regiodivergent C-O bond cleavage pro

89 ducing agonist binding, whereas the divalent magnesium cation (Mg(2+)) has been shown to have the opp

90 The presence of free magnesium cations results in cleavage of the pyrophospha

91 The addition of calcium and magnesium causes a decrease in iron chelating capacity;

92 D1 utilises an active site, bi-metallic iron-magnesium centre that positions a hydroxide nucleophile

93 stent with findings demonstrating a role for magnesium channeling in T-cell responses to EBV.

94 endogenous genes that encode two subunits of magnesium chelatase, an enzyme necessary for chlorophyll

95 nthesis is catalyzed by a multimeric enzyme, magnesium chelatase, the subunit I of which is encoded b

96 an aqueous deep eutectic solvent comprising magnesium chloride and choline chloride.

97 ), sodium-chloride/sulfate (T4), and calcium/magnesium-chloride/sulfate (T5).

98 in vitro digestion, we found that potassium, magnesium, chromium, and zinc in were bioaccessible in s

99 e to K[A'] and greater than the homometallic magnesium complex [{MgA'(2) }(2) ].

100 subdomain and a non-catalytic water-bridged magnesium complex at the protein-DNA interface.

101 ated GSL anions, [GSL-H](-), and terpyridine-magnesium complex dications, [Mg(Terpy)(2)](2+), are seq

102 of the full length SAM-I riboswitch and its magnesium concentration dependence.

103 Total magnesium concentration in planar regions surrounding a

104 e ON population to vary non-monotonically as magnesium concentration increases.

105 he OFF state, but only up to an intermediate magnesium concentration level.

106 Higher magnesium concentration preferentially stabilizes the an

107 concentration regime near the physiological magnesium concentration ranges, striking a balance betwe

108 phosphomonoesters, phosphodiesters, pH, free magnesium concentration, and muscle dynamic recovery con

109 e destabilization of the OFF state at higher magnesium concentration.

110 H increased to 11-12, decreasing calcium and magnesium concentrations by >80%, and minimizing scaling

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

112 Increasing magnesium concentrations negatively affected carotenoid

113 Under varying magnesium concentrations, NIPAL1 knockdown decreased bot

114 temperatures, short chain alcohols, and high magnesium concentrations.

115 es and were associated with the thallium and magnesium content in the soil.

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

117 olate, beta-carotene, lutein and zeaxanthin, magnesium, copper, and alcohol.

118 in B6, beta-carotene, lutein and zeaxanthin, magnesium, copper, docosahexaenoic acid, omega-3 fatty a

119 Upon chemical propulsion, the magnesium core is depleted, resulting in a hollow struct

120 The oceanic magnesium cycle is largely controlled by continental wea

121 Uncertainties in the magnesium cycle propagate into other chemical budgets, a

122 he sources and sinks that define the oceanic magnesium cycle, including new constraints on the output

123 While intravenous magnesium decreases hospitalizations in refractory pedia

124 XMEN (X-linked immunodeficiency with magnesium defect, EBV infection, and neoplasia) is a com

125 n mutations in the MAGT1 gene cause X-linked magnesium deficiency with Epstein-Barr virus (EBV) infec

126 ine dinucleotide-, thiamine diphosphate- and magnesium-dependent enzyme that catalyses the first step

127 ofluorescence experiments confirmed NIPAL1's magnesium-dependent expression and that it specifically

128 Integrase catalyzes two successive magnesium-dependent polynucleotidyl transferase reaction

129 uced Phosphatase 1 (WIP1) is a member of the magnesium-dependent serine/threonine protein phosphatase

130 Mechanistically, magnesium depletion reduces intracellular ATP but up-reg

131 rovar Typhimurium in host tissues by causing magnesium deprivation.

132 Magnesium dialkylamides react with alcohol-derived 2-met

133 se dynamics are finely regulated by a second magnesium dication, thus coordinating the entry of a mag

134 ed in the gas phase with tris-phenanthroline magnesium dications by forming [FA - H + MgPhen](+) comp

135 inversion reaction with tris-phenanthroline magnesium dications.

136 rt on the successful synthesis of diammonium magnesium dihydrogendiphosphate (V) dihydrate compound (

137 on the enhanced incorporation efficiency of magnesium dopants into facets of hexagonal hillock struc

138 a chloro titanium triamidoamine complex with magnesium effects complete reductive cleavage of N(2) to

139 on-inspired multi-layer structure contains a magnesium engine core and inner chemoattractant and ther

140 , comprise two nanometric layers enriched in magnesium flanking a core rich in sodium, fluoride and c

141 A high quality factor magnesium fluoride whispering gallery mode resonator ena

142 detailed global map of the flux of dissolved magnesium from the ocean into deeper marine sediments (g

143 is flux accounts for 15-20% of the output of magnesium from the ocean, with a flux-weighted fractiona

144 um transporter 1 (MAGT1) critically mediates magnesium homeostasis in eukaryotes and is highly-conser

145 known as PTP4A1, PTP4A2, and PTP4A3) control magnesium homeostasis through an association with the CN

146 drated" MgO layer followed by Mg(OH)(2), and magnesium hydroxy carbonates.

147 his work highlights the utility of activated magnesium(I) adduct complexes as soluble organometallic

148 n that reduction of Ar(Pri(4))Pb(Br) using a magnesium(I) beta-diketiminate afforded a much improved

149 Aluminum(I) and magnesium(I) compounds are reported for the C-C sigma-bo

150 his study details syntheses of unsymmetrical magnesium(I)-adduct complexes, [((Ar)Nacnac)(D)Mg-Mg((Ar

151 ur study reveals the functional potential of magnesium in controlling transcription of its downstream

152 within NIPAL1 families suggested lower serum magnesium in NPC compared to unaffected members.

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

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

155 These data support the hypothesis that magnesium influences hemorrhage severity in patients wit

156 (NIPA-like domain containing 1), encoding a magnesium influx transporter, as an islet-enriched gene.

157 uncovered that stress resilience arises from magnesium influx, which prevents hyperpolarization.

158 ron spectroscopy reveal the reversibility of magnesium insertion/extraction and provide information o

159 An inverse association between magnesium intake (HRQ3 vs. Q1: 0.55; 95% CI: 0.32, 0.95

160 in D concentrations (>=50 nmol/L) and a high magnesium intake (median split) (HR: 0.53; 95% CI: 0.31,

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

162 of 25(OH)D3 in combination with an adequate magnesium intake is essential in lowering the risk of mo

163 tamin D deficient (<50 nmol/L) and had a low magnesium intake.

164 rmediate and then an insoluble final product magnesium iodide.

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

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

167 s extension is associated with a loss of the magnesium ion and a tilt in the position of the guanine

168 tegrated unit based on the design of printed magnesium ion aqueous asymmetric supercapacitors.

169 For magnesium ion batteries (MIBs) to be used commercially,

170 lt in clinical INSTI failure perturb optimal magnesium ion coordination in the enzyme active site.

171 ic strength and zinc complexation facilitate magnesium ion dehydration, resulting in a dramatic decre

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

173 an adenosine 5'-diphosphate molecule with no magnesium ion plus phosphate.

174 ructures reveal a previously uncharacterized magnesium ion residing at the core of the LpxD trimer.

175 ctivity that is dependent on the presence of magnesium ions and is linked to its function of regulati

176 While investigating the role of magnesium ions in crystallization pathways of amorphous

177 ributed by both domains coordinate two bound magnesium ions in the active site of B. pseudomallei OLD

178 Magnesium ions play a critical role in catalysis by many

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

180 Our results reveal that binding to magnesium ions underpins a fundamental weakness of the I

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

182 olymerization required manganese rather than magnesium ions, was independent of nucleotide primers, a

183 Magnesium is a cofactor for SpxB catalytic activity, and

184 vailable forms of phosphorus, potassium, and magnesium is also assessed.

185 This is intriguing because magnesium is the most abundant divalent cation in all li

186 Magnesium isotope ratios measured at a concentration lev

187 In recent years, magnesium isotopes (delta(26)Mg) have provided new const

188 Magnesium isotopic analysis of cerebrospinal fluid (CSF)

189 ion factor of ~0.9994 acting to increase the magnesium isotopic ratio in the ocean.

190 e tested the hypothesis that admission serum magnesium levels are associated with extent of hemorrhag

191 Here we show that modulating intracellular magnesium levels correlates with a rapid change of PRL e

192 A significant reduction in serum magnesium levels was observed among sporadic NPC cases c

193 ordinal and binary regression models, lower magnesium levels were associated with higher modified Fi

194 Circulating magnesium levels were measured in 13 individuals in 2 fa

195 and attenuate the translational response to magnesium levels.

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

197 ests that calcareous biominerals enriched in magnesium may be more common in metazoans than previousl

198 Magnesium mediated aptamer-expression platform domain cl

199 We report a new magnesium metal-organic framework (MOF) (CPM-107) with a

200 releasing mobile phosphate (PO(4) (3-) ) and magnesium (Mg(2+) ), the latter reacting with excreted o

201 In response to low levels of magnesium (Mg(2+) ), the PhoQP two component system indu

202 mmensal streptococcal H(2)O(2) production by magnesium (Mg(2+)) supplementation.

203 However, it was also claimed that MAGT1 is a magnesium (Mg(2+)) transporter.

204 ing modifications that remodel the canonical magnesium (Mg(2+))-binding motif found in terpene cyclas

205 the Syt1 C2 domains bind the membrane with a magnesium (Mg(2+))-mediated partial insertion of the ali

206 Magnesium (Mg) and its alloys have shown attractive bioc

207 Low serum magnesium (Mg) concentrations have been associated with

208 ciency; (2) potassium (K), calcium (Ca), and magnesium (Mg) efficiency for acid soils; and (3) iron (

209 (4)) solutions in contact with either a pure magnesium (Mg) or a Mg alloy as the anode and 316 stainl

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

211 N : potassium (K), N : calcium (Ca) and N : magnesium (Mg), and P : K, P : Ca and P : Mg, and natura

212 ing on calcium (Ca), copper (Cu), iron (Fe), magnesium (Mg), selenium (Se), iodine (I), zinc (Zn) and

213 Magnesium (Mg)-based micromotors are combined with live

214 e delivery platform is introduced, employing magnesium microparticles loaded within the microneedle p

215 t discuss the bioresorbable materials (e.g., magnesium, molybdenum, tungsten, silicon, germanium, sil

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

217 ound nucleotide with shuttling of the second magnesium necessary for the two-metal ion catalysis.

218 ate that using a sacrificial anode material (magnesium or aluminum), combined with a cheap, nontoxic,

219 ssociations between 25(OH)D3 concentrations, magnesium or calcium intake through diet and/or suppleme

220 The interaction between 25(OH)D3 and magnesium or calcium was assessed by investigating 1) jo

221 tarch) esterified with 3% OSA complexed with magnesium or calcium.

222 We aimed to investigate 25(OH)D3, magnesium, or calcium and their interaction among patien

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

224 of the media, and extensive precipitation of magnesium oxalate dihydrate (glushinskite, Mg(C(2) O(4)

225 creted oxalate resulting in precipitation of magnesium oxalate dihydrate which also accumulated withi

226 was associated with higher urinary citrate, magnesium, oxalate, phosphate, uric acid, volume, and pH

227 he ultraviolet (UV) reflective properties of magnesium oxide (MgO) and/or barium sulfate (BaSO(4)) we

228 Magnesium oxide (MgO) is an effective alternative to Cu

229 Magnesium oxide added to yellow sticky traps enhanced vi

230 Probing assays demonstrated that magnesium oxide alone or as a mixture with a phagostimul

231 yllids were evaluated on surfaces containing magnesium oxide or barium sulfate.

232 icles through chemical vapor deposition with magnesium-oxide particles as the catalyst and template.

233 0.11 for all biomarkers), whereas both serum magnesium (P<0.001) and uric acid levels (P=0.008) impro

234 The magnesium particles react with the interstitial fluid, l

235 ygen fertilizers (SOFs, calcium peroxide and magnesium peroxide) to reduce N(2)O production in minera

236 internal load-bearing skeleton and bioglass-magnesium phosphate bone cement as the osteoconductive m

237 patibility and osteoconductivity of bioglass-magnesium phosphate bone cement, thus providing support

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

239 Herein, magnesium-promoted NiO supported on mesoporous zirconia,

240 s well as decreased paracellular calcium and magnesium reabsorption.

241 resultant sulfonium salts with alkyllithium/magnesium reagents generates underexploited hypervalent

242 tic reactions of Sm(II) employing a terminal magnesium reductant and trimethylsilyl chloride in conce

243 Although the expression, distribution, and magnesium responsiveness of NIPAL1 in alpha-TC6 glucagon

244 Importing two temporary RISC cofactors from magnesium-rich hairpins and/or pseudoknots then kickstar

245 Hydrated, magnesium-rich minerals and subglacial brines exist on t

246 ecently found in melt inclusions in the most magnesium-rich olivine in 2.7-billion-year-old komatiite

247 ermodynamics of RISC cofactors and targeting magnesium-rich RNA secondary structures provide addition

248 ium carbonate mineral precipitation from the magnesium-rich tailings generated by many mining operati

249 a, such as stony corals, deposit metastable, magnesium-rich, amorphous calcium carbonate nanoparticle

250 achieved by bis-carbonylation at C-3 of the magnesium salt of 6-bromoindole with triphosgene to affo

251 We found that submicrometer-size magnesium samples exhibit high plasticity that is far gr

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

253 s: calcium, chromium, copper, iron, lithium, magnesium, selenium and zinc were supplemented in differ

254 These findings uncover a magnesium-sensitive mechanism controlling PRL expression

255 Thus, this new magnesium sheet alloy is highly attractive for sheet app

256 Here we design a new magnesium sheet alloy-ZAXME11100 (Mg-1.0Zn-1.0Al-0.5Ca-0

257 y-linked hexadecyl and phenyl functionalized magnesium silicates (MSil-C16 and MSil-Ph) were confirme

258 generation viscosifiers-organically modified magnesium silicates (MSils)-for reservoir drilling fluid

259 aily infant intakes of iron, zinc, selenium, magnesium, sodium, and B-vitamins (thiamin, riboflavin,

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

261 A complex with ATP and magnesium suggested a two-metal mechanism of lysine aden

262 3 nebulized albuterol treatments with either magnesium sulfate (n = 410) or 5.5% saline placebo (n =

263 There was no detectable association between magnesium sulfate availability and the rate of eclampsia

264 hical regions in 8 countries, in relation to magnesium sulfate availability.

265 ension (181 [1%] of 20 819) or intramuscular magnesium sulfate for pre-eclampsia (198 [1%]), of whom

266 e occurred after in-community treatment with magnesium sulfate or during transport to facility.

267 On average, magnesium sulfate was available in 74.7% of facilities (

268 l (PEG)/dextran (DEX)) and polymer/salt (PEG/Magnesium sulfate) for droplet generation in a flow-focu

269 tion of only monthly data on availability of magnesium sulfate, and is limited by the lack of demogra

270 pharmacologic interventions (aminophyllines, magnesium sulfate, anti-inflammatory agents, inhaled cor

271 t or had acute osmotic diarrhea induced with magnesium sulfate.

272 with severe preeclampsia/eclampsia received magnesium sulphate and 67% with antepartum haemorrhage w

273 Recent research has focused on intravenous magnesium sulphate and intrathecal antitoxin administrat

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

275 Upon addition of magnesium, the aptamer domain pre-organizes, populating

276 Magnesium titanate is technologically important due to i

277 tes more [Formula: see text] dislocations in magnesium to accommodate plasticity, leading to both hig

278 carbonate and in the presence and absence of magnesium to delineate the role of CaCO(3(S)) nucleation

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

280 The benefit of nebulized magnesium to prevent hospitalization is unknown.

281 evaluated vitamin D and mineral (iron, zinc, magnesium) transfer to the bolus aqueous phase during th

282 included genes postulated to be involved in magnesium transport (NIPAL1), EBV cell entry (ITGB6), mo

283 ostasis through an association with the CNNM magnesium transport regulators.

284 Magnesium transporter 1 (MAGT1) critically mediates magn

285 subunit STT3B or the oxidoreductase subunits magnesium transporter 1/tumor suppressor candidate 3) an

286 ore than 10 gene-rich regions, including the magnesium transporter cnnm2 and the translational repres

287 ncy caused by mutations in MAGT1, a putative magnesium transporter.

288 structure and is competitively inhibited by magnesium, two traits that are unlike natural ATPases.

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

290 etween thallium with lycopene and rutin with magnesium was found.

291 Mean magnesium was lower in patients with thick versus thin s

292 igating the interaction between 25(OH)D3 and magnesium, we observed the lowest risk of all-cause mort

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

294 he omega-3 (n-3) fatty acids, vitamin E, and magnesium were identified.

295 samples, concentrations of NOM, calcium, and magnesium were positively correlated with oil removal (

296 ead applications is the limited ductility of magnesium, which has been attributed to [Formula: see te

297 The findings do not support use of nebulized magnesium with albuterol among children with refractory

298 sthma in the emergency department, nebulized magnesium with albuterol, compared with placebo with alb

299 work, we present a biosensor consisting of a magnesium zinc oxide (MZO) dual gate thin-film transisto

300 quate Intake level) of vitamin A, vitamin K, magnesium, zinc, and copper was associated with reduced