ライフサイエンスコーパス: Mg

1 Mg(2+) activation also decreased.

2 Mg(2+) is the most abundant divalent cation in metazoans

3 Mg-CUK-1L has a BET surface area of 2896 m(2) g(-1) and

4 Mg-doped GaN cubic epitaxial layers grown under optimize

5 Mg-nucleotide binding to SUR1 stimulates K(ATP).

6 al biomass accumulation rates of 3.6 +/- 1.1 Mg C ha(-1) year(-1) .

7 e pore-wall was modified with 0%, 6%, or 10% Mg-doped CSi slurry (CSi, CSi-Mg6, or CSi-Mg10) through

8 ock dry matter (15.6 +/- 1.4 vs 14.8 +/- 2.2 Mg ha(-1) yr(-1)) and slightly lower estimated ethanol e

9 (-1) across accession with an average of 2.2 Mg ha(-1).

10 SOC stocks by 1% over 0-30 cm (-2.5 +/- 4.2 Mg/ha) and 10% over 0-100 cm (-13.6 +/- 8.9 Mg/ha).

11 entropy oxide (HEO) Co(0.2) Ni(0.2) Cu(0.2) Mg(0.2) Zn(0.2) O material with mesoporous structure is

12 l metal reagents, such as Et(2) Zn and Bu(2) Mg.

13 diphosphate (V) dihydrate compound (NH(4))(2)Mg(H(2)P(2)O(7))(2)*2H(2)O using a wet chemical route.

14 ogical levels of pH, Na(+) , K(+) , Ca(2+) , Mg(2+) , and Zn(2+) ions.

15 ated through the separation of K(+), Ba(2+), Mg(2+), Na(+), Li(+), and Tris(+) in approximately 30 s,

16 , activity was decreased, except for Ca(2+), Mg(2+), and Ba(2+).

17 positive covariance of both cation (Ca(2+), Mg(2+), K(+), Na(+)) and suspended sediment yields with

18 he inner pore and a voltage-dependent Ca(2+)/Mg(2+) block.

19 ing model combined with intrinsic and Ca(2+)/Mg(2+)-dependent rectification to simulate I(SK) and inv

20 ndow (OPW) is extracted, in which the Mg(2+)/Mg(0) reduction can compete with electrolyte decompositi

21 pose in the double layer prior to the Mg(2+)/Mg(0) reduction, leading to electrochemically inactive r

22 xperimental therapy (TDF + pegIFN + REP 2139-Mg or REP 2165-Mg) or 24 weeks of control therapy (TDF +

23 rapy (TDF + pegIFN + REP 2139-Mg or REP 2165-Mg) or 24 weeks of control therapy (TDF + pegIFN) follow

24 orwide methane emissions are 19,000 +/- 2300 Mg for refineries, 136,700 +/- 25,900 Mg for landfills,

25 11) Omega resistor for the most abundant (24)Mg isotope and a 10(13) Omega resistor for the (26)Mg is

26 ermore, substitution of light magnesium ((24)Mg) by heavy, nuclear magnetic (25)Mg had no effect on O

27 resistors for the monitoring of both the (24)Mg and (26)Mg isotopes and up to twofold using a 10(11)

28 Large SIC losses (194-242 Mg C/ha) also occurred below 4.9 m deep under irrigated

29 ere, we used isotope effects (with (2)H, (25)Mg, and (18)O) to monitor O(2) activation and assess the

30 sium ((24)Mg) by heavy, nuclear magnetic (25)Mg had no effect on O(2) addition.

31 or the monitoring of both the (24)Mg and (26)Mg isotopes and up to twofold using a 10(11) Omega resis

32 rmediate and internal errors on the delta(26)Mg value were improved up to fourfold using 10(13) Omega

33 tope and a 10(13) Omega resistor for the (26)Mg isotope.

34 Potential sugar yield range from 0.5 to 5.3 Mg ha(-1) across accession with an average of 2.2 Mg ha(

35 (2+), but not monovalent metal ions, Cr(3+), Mg(2+), Y(3+), Sr(2+) or Ba(2+).

36 t the catchment was a large C sink (NLCB 334 Mg C km(-2) year(-1) ), and that savanna and wetland are

37 47 Mg C/ha for high marsh, and 1,064 +/- 38 Mg C/ha for tidal forest (high elevation/low salinity).

38 +/- 1,500 Mg for POTWs, and 11,100 +/- 3,400 Mg for composting.

39 land) pairs, and irrigated croplands had 402 Mg C/ha less than their rain-fed pairs (p < .0001).

40 417 +/- 70 Mg C/ha for low marsh, 551 +/- 47 Mg C/ha for high marsh, and 1,064 +/- 38 Mg C/ha for tid

41 /- 25,900 Mg for landfills, 11,900 +/- 1,500 Mg for POTWs, and 11,100 +/- 3,400 Mg for composting.

42 ks of 182-2,730 (mean +/- SD: 1,087 +/- 584) Mg C/ha, with the large variation driven by hydrogeomorp

43 20% increase in SOC at 0-30 cm (6.0 +/- 4.6 Mg/ha gain) and a total 10% increase over the 0-100 cm s

44 elevation and salinity gradients: 217 +/- 60 Mg C/ha for seagrass (low elevation/high salinity), 417

45 Moving to Mix (37.5 +/- 16.7 Mg C/ha) and Spe (36.8 +/- 19.8 Mg C/ha) provided only m

46 ss (low elevation/high salinity), 417 +/- 70 Mg C/ha for low marsh, 551 +/- 47 Mg C/ha for high marsh

47 -fed and irrigated croplands had 328 and 730 Mg C/ha less SIC storage, respectively, compared to thei

48 7.5 +/- 16.7 Mg C/ha) and Spe (36.8 +/- 19.8 Mg C/ha) provided only marginal gains in accuracy, but m

49 and conversion varied much more (-3.4 to 9.8 Mg CO(2) ha(-1) yr(-1)), indicating that the latter domi

50 1.95) and perovskite La(0.8) Sr(0.2) Ga(0.8) Mg(0.2) O(2.55) ) with a high concentration of oxygen va

51 ried moderately across cities (-2.1 to -0.87 Mg CO(2) ha(-1) yr(-1)), while emissions from the carbon

52 over the 0-100 cm soil profile (5.7 +/- 10.9 Mg/ha).

53 Mg/ha) and 10% over 0-100 cm (-13.6 +/- 8.9 Mg/ha).

54 - 2300 Mg for refineries, 136,700 +/- 25,900 Mg for landfills, 11,900 +/- 1,500 Mg for POTWs, and 11,

55 -A fold and the DxD motif that coordinates a Mg(2+) ion for binding the UDP-GlcNAc sugar donor.

56 nd an unusual mechanism for binding ATP in a Mg(2+)-independent manner, including a rare hydrophobic

57 Now, a Mg(II)Co(II) catalyst is reported that exhibits signific

58 Later this role was alluded to a Mg(2+) ion.

59 We also observe ADP-Mg(2+) bound in the nsp12 N-terminal nidovirus RdRp-asso

60 teral mobility of outer-spherically adsorbed Mg(2+).

61 strated benchmarked against NMC, NCA, and Al-Mg-codoped NMC (NMCAM) of identical Ni content (89 mol%)

62 rphology and distribution in magnesium alloy Mg-5.78Zn-0.44Zr subjected to a complex multi-step proce

63 deletion of the yifB gene, which encodes an Mg(2+)-chelatase protein belonging to the ATPases associ

64 d photoluminescence spectroscopy revealed an Mg ionization energy of about 100 meV, which agrees quit

65 e presence of two Mg(2+) ions (Mg(2+)(A) and Mg(2+)(B)).

66 dient of Al-base cation decoupling as Ca and Mg concentration approaches 1.4 mg L(-1) and 0.6 mg L(-1

67 bgrain boundaries and nanometer-scale Ca and Mg layers surrounding individual framboids.

68 elies on a chiral Ir-(P, olefin) complex and Mg(ClO(4) )(2) Lewis acid catalyst system to promote all

69 The dihydrogen and Mg(2+) in solution were detected by a gas chromatography

70 sized by a combination of Sb-flux method and Mg-vapor annealing, is reported.

71 81) were observed for Fe, Zn, Ca, P, Mo, and Mg.

72 ited highest antioxidant properties, TCC and Mg content.

73 d dissolution method allowed Ca, Fe, Zn, and Mg determination in milk samples with adequate analytica

74 econdary, rocksalt-type phase of MgSnN(2) at Mg-rich compositions and low temperatures.

75 he mechanism: epoxide coordination occurs at Mg(II), with reduced transition state entropy, while the

76 n-loop threonine residues and binding of ATP-Mg(2+).

77 sphorylated but is again stabilized with ATP-Mg(2+) bound.

78 orous 0.6-4.1 mum thick film, while the AZ31 Mg alloy produced a more compact 1.7-9.9 mum thick struv

79 eptor, 2) details of the competition between Mg(2+) and Na(+) cations for specific sites, 3) estimate

80 razilian Amazon stored 0.33 +/- 0.05 billion Mg of above-ground carbon but had offset just 9.37% of o

81 ngle site (Al) or across a metal-metal bond (Mg-Mg).

82 ostly a zero-order kinetic rate law for both Mg anode materials, and the rate constants (k) depended

83 Now, direct transformation of bulk Mg-Li alloys into Mg alkoxide NWs is demonstrated withou

84 a partially "hydrated" MgO layer followed by Mg(OH)(2), and magnesium hydroxy carbonates.

85 ective strengthening role in Zn, followed by Mg.

86 , protein, crude fiber, ash, folic acid, Ca, Mg, Fe, Mn, and Zn increased significantly in all sample

87 gar compounds, but several elements (Ba, Ca, Mg, Sr, Mn, Al, Co, Ni, Se) were marked as characteristi

88 0% of the soil samples (respectively for Ca, Mg and K), the plant-available pools measured by isotopi

89 ems, in particular when the resources of Ca, Mg and K are low.

90 ent of a method for the determination of Ca, Mg, Zn, and Fe in liquid and powdered cow milk.

91 exin and isovitexin) and minerals (K, P, Ca, Mg, Na and Fe) were predominant in WJP.

92 Potassium, Ca, Mg and Ni were low in laurel and rosemary; mint and thym

93 icles of eight elements (Na, Al, Ag, Sr, Ca, Mg, Fe, and Be) were injected into the conical torch, an

94 Weak binding of the catalytic Mg(2+) contributes to fidelity by sampling the correctly

95 ata indicating weak binding of the catalytic Mg(2+).

96 lowest compared with the highest circulating Mg category was 1.18 (1.06, 1.31) (I2 = 22%, P-heterogen

97 t and updated meta-analysis, low circulating Mg was associated with higher CAD risk than was higher M

98 Based on thermodynamic considerations, Mg(0) deposition should not be possible, which contrasts

99 Further, we provide evidence for a critical Mg(2+) in the active site that interacts with the scissi

100 erials and indicates that single-crystalline Mg(3) (Sb,Bi)(2) solid solutions can exhibit higher zT c

101 retical studies predict that single crystals Mg(3) (Sb,Bi)(2) can exhibit higher thermoelectric perfo

102 and compositional data of olivine crystals (Mg/Fe, Ni and P) from the tephra of the first months of

103 , we analysed selected minerals (Fe-Mn-Zn-Cu-Mg) in wild-harvested and commercially available termite

104 tion experiment, transformation of the cubic Mg(2)TiO(4) to the tetragonal structure was complete by

105 2 mm 9AC in the presence of high cytoplasmic Mg(2+) suppressed the effects of P(i) on [Ca(2+) ](SR) a

106 in individual hillock structures a decreased Mg cluster density is observed within hillock structures

107 SGR) gene encoding the chlorophyll-degrading Mg(++)-dechelatase were found to trigger higher and earl

108 rboxylases (MDDs) catalyze the ATP-dependent-Mg(2+)-decarboxylation of mevalonate-5-diphosphate (MVAP

109 nd terpyridine-magnesium complex dications, [Mg(Terpy)(2)](2+), are sequentially injected and mutuall

110 latform, we further demonstrate that dietary Mg(2+) supplementation significantly improves S. gordoni

111 and high ductility compared to other dilute Mg alloys.

112 ly demonstrate that the atomically dispersed Mg cofactors incorporated within graphene framework exhi

113 e of ionized impurity scattering in Te-doped Mg(3) Sb(2) single crystals proves that the thermally ac

114 thermoelectric properties of n-type Te-doped Mg(3) Sb(2) single crystals, synthesized by a combinatio

115 Among the minerals, the element Mg is important, which is essential for both plants and

116 Adding elements Mg, Ca, Sr and Li into Zn can improve the cytocompatibil

117 ork, binary Zn alloys with alloying elements Mg, Ca, Sr, Li, Mn, Fe, Cu, and Ag respectively, are scr

118 and Ba) in 10 muL of serum and 12 elements (Mg, S, Mn, Fe, Co, Cu, Zn Se, Br, Rb, Mo, and Cs) in les

119 ethod comprises the analysis of 20 elements (Mg, P, S, K, Ca, V, Cr, Mn, Fe, Co, Cu, Zn, Se, Br, Rb,

120 Metal ions, especially Mg(2+), neutralize these negatively charged nucleic acid

121 il organic C, total N and S, and extractable Mg, K, P in the 0-10 cm depth significantly increased in

122 Spectral lines of C, Ca, Fe, Mg, N and Na were selected as input variables for predic

123 lation of magnetite within a ferropericlase (Mg(0.60)Fe(0.40))O matrix suggests exsolution of the for

124 dation of two solvent-based electrolytes for Mg-metal batteries is investigated through a grand canon

125 ween polished and brown rice, especially for Mg, Mn, P, Fe and K, which were 2-4 times higher in brow

126 This novel role for Mg(2+) adds to the diversity of known catalytic RNA stra

127 In summary, our results support a role for Mg(2+) supplementation as a potential prebiotic to promo

128 that other metal cations can substitute for Mg(2+), raising questions about the role different metal

129 , we investigated carbonation of forsterite (Mg(2)SiO(4)) in humidified scCO(2) (50 degrees C and 90

130 ized variants of the metal-organic framework Mg(2) (dobpdc) are shown to adsorb CO(2) selectively via

131 change at a rate that is independent of free Mg(2+) concentration.

132 GaN, studied by comparative analysis of GaN:Mg films grown by MOCVD on high and low hillock density

133 By generating Mg(PTX) mice to genetically inhibit G(i) in microglia, w

134 f magnesium oxalate dihydrate (glushinskite, Mg(C(2) O(4) ).2H(2) O) occurring under growing colonies

135 g); and Russula sardonia (K > Na > Zn > Cu > Mg).

136 rder: Amanita pantherina (K > Na > Zn > Cu > Mg); Boletus edulis (edible) (K > Cu > Zn > Se > Na > Mg

137 tus edulis (edible) (K > Cu > Zn > Se > Na > Mg); Boletus mirabilis (edible) (K > Cu > Zn > Na > Mg);

138 letus mirabilis (edible) (K > Cu > Zn > Na > Mg); Lactarius deliciosus (edible) (K > Zn > Mg); and Ru

139 Mg); Lactarius deliciosus (edible) (K > Zn > Mg); and Russula sardonia (K > Na > Zn > Cu > Mg).

140 served self-compensation behavior in heavily Mg-doped GaN involving Mg-V(N) complexes.

141 ociated with higher CAD risk than was higher Mg.

142 dy establishes a better understanding of how Mg(2+)-ion interactions contribute to RNA structural pro

143 Importantly, a hydrated Mg(2+) ion remains innersphere-coordinated to N7 of G33

144 w structures shed light on a second hydrated Mg(2+) ion that approaches the scissile phosphate from i

145 emporal dynamics of intracellular Mg(2+) ((i)Mg(2+)) are integrated into cellular signaling, we imple

146 se findings reveal that lactate mobilizes (i)Mg(2+) and links the (m)Mg(2+) transport machinery with

147 ehensive screen to discover regulators of (i)Mg(2+) dynamics.

148 ends upon the catalyst, and previously Zn(II)Mg(II) heterodinuclear catalysts showed good performance

149 Ni, Fe(II), Fe(III), Cu(II), Cr, Mo, Co(II), Mg, Nd, Li, Ti, Ca, Cs, Ag, Tm, Er(III), La(III), Yb(III

150 active organometallic heterodinuclear Zn(II)/Mg(II) catalyst applied in a one-pot procedure together

151 Whether increasing Mg concentrations within healthy limits is a useful stra

152 Lactate initiates Mg(2+) release from the ER and subsequent uptake by the

153 ect transformation of bulk Mg-Li alloys into Mg alkoxide NWs is demonstrated without the use of catal

154 he spatio-temporal dynamics of intracellular Mg(2+) ((i)Mg(2+)) are integrated into cellular signalin

155 However, the intrinsic Mg defect chemistry makes it challenging to grow n-type

156 tified a sex-interaction whereby the inverse Mg-CAD association was much stronger among women than me

157 n behavior in heavily Mg-doped GaN involving Mg-V(N) complexes.

158 hosphate in the presence of two Mg(2+) ions (Mg(2+)(A) and Mg(2+)(B)).

159 onovalent and divalent cations (Na(+), K(+), Mg(2+)(,) and Ca(+2)).

160 13 other competing metal ions (Na(+), K(+), Mg(2+), Ca(2+), Mn(2+), Fe(2+), Al(3+), Ni(2+), Cu(2+),

161 ble soil phosphorus (P) and base cations (K, Mg) corresponded to declines in remotely sensed mean ann

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

163 ogically functional minerals (Ca, Cu, Fe, K, Mg, Mn, Na, P, Se and Zn) and trace metals (As, Cd, Pb,

164 ations of macroelements (C, N, P, Ca, Na, K, Mg) and micronutrients (Fe, Zn, Co, Mn, I) were sufficie

165 Ho, Er, Tm, Yb, Lu) and trace elements (Li, Mg, Mn, Ni, Co, Cu, Sr, Ba, Pb) via chemometric evaluati

166 Low Mg/Ca, and high U/Ca, Mo/Ca, and V/Ca potentially sugges

167 mediated degradation and are unstable in low Mg(2+) conditions; this greatly limits their utility in

168 matically synthesized ((Fc(2)PDI)MCl(2), M = Mg, Zn, Fe, and Co) and characterized crystallographical

169 , which facilitates mitochondrial Mg(2+) ((m)Mg(2+)) uptake in multiple cell types.

170 Intriguingly, suppression of (m)Mg(2+) surge alleviates inflammation-induced multi-organ

171 lactate mobilizes (i)Mg(2+) and links the (m)Mg(2+) transport machinery with major metabolic feedback

172 gate the relationships between plant macro- (Mg, P, S, K, Ca) and micronutrient (Fe, Zn, Mn, Cu) conc

173 obile phosphate (PO(4) (3-) ) and magnesium (Mg(2+) ), the latter reacting with excreted oxalate resu

174 ations that remodel the canonical magnesium (Mg(2+))-binding motif found in terpene cyclases.

175 Low serum magnesium (Mg) concentrations have been associated with higher coro

176 zing the first crystal structure of the MbtI-Mg(2+)-salicylate ternary complex.

177 catalytic activity of the main-group metals (Mg, Al and Ca) in oxygen reduction reaction is severely

178 ls (delta(30)Si >= -6.94 +/- 0.09 per mille, Mg/Si = ~0.001) whereas its silicate phases are isotopic

179 Si(EC-silicates) = -0.33 +/- 0.11 per mille, Mg/Si = ~1.01) and closer to BSE (delta(30)Si(BSE) = -0.

180 The ER-mitochondrial Mg(2+) dynamics is selectively stimulated by L-lactate.

181 (ER) stores, which facilitates mitochondrial Mg(2+) ((m)Mg(2+)) uptake in multiple cell types.

182 ns include alkali (Li/Na/K) and multivalent (Mg, Zn)-based electrolytes for conventional "sealed" bat

183 Concentrations of 16 elements (K, Na, Mg, Ca, Fe, Zn, Hg, Se, As, Cu, Cd, Mn, Ni, Cr, Pb and C

184 ayer to muM concentrations of Zn(2+) but not Mg(2+), Cu(2+), Co(2+), or Mn(2+).

185 te and glutathione) and uptake of nutrients (Mg, P, K, S, Ca, Fe, etc.

186 In the absence of Mg(2+), SUR1 increases the apparent affinity for nucleot

187 s to investigate the simultaneous binding of Mg(2+) and Na(+) cations to inactive and active crystal

188 presence of physiological concentrations of Mg(2+) Ca(2+) binding triggers an increase in protein mu

189 e the energetics and atomic-level details of Mg(2+)-RNA interactions that occur along an unfolding pa

190 dynamics to investigate the distribution of Mg(2+) and Na(+) in the mu-opioid receptor and their imp

191 re, not rainfall, as the principal driver of Mg variability.

192 Meanwhile, high oxygen-affinity elements of Mg and Ti well stabilize the surface oxygen of Li-rich m

193 his can be corroborated by the extraction of Mg in the infusion of hot water.

194 The favorable incorporation of Mg is attributed to Mg dopants incorporating substitutio

195 , we report that the reversible insertion of Mg-Cl superhalides in graphite delivers a record-high re

196 The insertion of Mg-Cl superhalides in graphite does not form staged grap

197 alation compounds; instead, the insertion of Mg-Cl superhalides makes the graphite partially turbostr

198 ructural and electrochemical modification of Mg with alloying elements (Ca, Zn), the degradation rate

199 The obtained isothermal bulk modulus of Mg(2)TiO(4) spinel is K(T0) = 148(3) GPa when K(T0)' = 6

200 wever, in different modes in the presence of Mg(2+) versus Mn(2+) ions.

201 -activity form, TK(high), in the presence of Mg(2+).

202 was accelerated when the degradation rate of Mg alloys increased.

203 rolled by tailoring the degradation rates of Mg alloys connected to Ti.

204 elements (Ca, Zn), the degradation rates of Mg alloys were controlled, and the H(2)O(2) release kine

205 emerged as an activator of rapid release of Mg(2+) from endoplasmic reticulum (ER) stores, which fac

206 We first examined the roles of Mg(2+) by kinetic analysis of single nucleotide incorpor

207 ity is a kinetic phenomenon and the roles of Mg(2+) ions in each step in the catalysis have not been

208 vironment and confirmed adequate sampling of Mg(2+) ion binding with a grand canonical Monte Carlo MD

209 inactive state, the putative binding site of Mg(2+) on the MOP receptor, as well as the molecular det

210 d light on 1) the preferred binding sites of Mg(2+) on the MOP receptor, 2) details of the competitio

211 management on the absorption and storage of Mg by commercial, ground, roasted Arabica coffee were in

212 nd utilised in the metathetical synthesis of Mg-Al and Ca-Al bonded derivatives.

213 The tendency of Mg-Ca and Al-Fe fouling was observed over the membrane s

214 We report herein the use of Mg(2+) -specific 10-23 or Zn(2+) -specific 8-17 RNA-clea

215 A large-pore version of Mg-CUK-1, a water-stable metal-organic framework (MOF) w

216 enabling the effect of temperature change on Mg partitioning to greatly exceed the effects of changes

217 isolation, an eta(3) -allyl configuration on Mg is energetically preferred over the eta(1) - (sigma-b

218 Ribozyme activity depends on Mg(+2) and monovalent cations but is resistant to protea

219 ucleoprotein complex that depends heavily on Mg(2+) for structure.

220 tions simultaneously in Co(60)Fe(20)B(20)/Pb(Mg(1/3)Nb(2/3))(0.7)Ti(0.3)O(3) heterostructures based o

221 e 24, 33, and 29 ng g(-1) for Ir, Ru, and Pd/Mg modifiers, respectively.

222 rium for nucleotide binding at physiological Mg(2+) concentrations.

223 Lightweight, recyclable, and plentiful Mg alloys are receiving increased attention due to an ex

224 trength and ductility not possible from pure Mg.

225 The pure Mg anode produced a porous 0.6-4.1 mum thick film, while

226 spacing (5.83 angstrom) enabling reversible Mg insertion.

227 ust be developed that show stable reversible Mg intercalation.

228 Chlorogenic acid was higher in S(Ca) and S(Mg) plants and chicoric acid levels were S(Mg) > S(Ca) >

229 S(Ca) and S(Mg) treatments raised ascorbate concentration and reduce

230 macrocation proportions (S(K), S(Ca), and S(Mg)) affected the corresponding minerals, P and Na conte

231 tion macrocation proportions (S(K), S(Ca), S(Mg)) on the bioactive content of hydroponically cultivat

232 The S(Mg)-treated red Salanova contained higher concentrations

233 S(Mg) plants and chicoric acid levels were S(Mg) > S(Ca) > S(K).

234 strategy based on utilization of sacrificial Mg alloys could broaden the current palette of antibacte

235 These results suggest that in these samples Mg is probably largely presented as different inorganic

236 5-Oxazolecarboxylic acid senses Mg(2+) ions, exhibiting a sensitivity of 0.10-0.44 mmol

237 Serum Mg was modeled as quintiles based on mean visit 1 (1987-

238 other CAD risk factors than was higher serum Mg (HR Q1 compared with Q5: 1.28; 95% CI: 1.11, 1.47; P-

239 Overall, low serum Mg was associated with higher CAD risk after adjustment

240 We aimed to test our hypothesis that serum Mg is inversely and independently associated with long-t

241 For this purpose, some Mg and P fractions were evaluated.

242 ermediate in the Mg-V-S compositional space, Mg(3)V(2)S(8), comprising [VS(4)](3-) tetrahedral units,

243 rameters (gamma(th)) of cubic and tetragonal Mg(2)TiO(4) phases are 1.01 and 0.63.

244 When its cofactor is Ca(2+) rather than Mg(2+), the reaction is fivefold faster, permitting mult

245 We demonstrate that Mg(2+) affects spxB transcription and SpxB abundance in

246 It was observed that Mg stored in the grain was concentrated in the inorganic

247 Kinetic analyses revealed that Mg dissolution to Mg(2+) followed mostly a zero-order ki

248 Here we show that Mg concentrations in a subaqueous speleothem from an Ita

249 We show that Mg.dNTP binding induces an enzyme conformational change

250 Kinetic analysis showed that Mg(2+) and Mn(2+) ions increase ribozyme efficiency by m

251 The Mg shows higher values during warm climate intervals and

252 The Mg(2+) or Zn(2+) in HeLa cells can be detected using bot

253 The Mg(2+)-dependent Mycobacterium tuberculosis salicylate s

254 he roles of the active site residues and the Mg(2+) ions in catalyzing the reaction.

255 eta(1) - (sigma-bonded) arrangement, but the Mg must be in a low coordination environment for it to b

256 steric modulation of the MOP receptor by the Mg(2+) cation.

257 ties (ARIC) Study article that evaluated the Mg-CAD association, based on 319 events occurring over 4

258 y barrier for the reaction with that for the Mg(2+)-assisted release of the product (i.e., pyrophosph

259 ith experiments and offers rationale for the Mg-battery failure in EC electrolyte and capacity fade i

260 of a previously unknown intermediate in the Mg-V-S compositional space, Mg(3)V(2)S(8), comprising [V

261 We also investigated the role of the Mg(2+) cofactor in catalysis, analyzing the first crysta

262 An increase of the Mg(2+) concentration from 0.25 to 10 mM increases nucleo

263 We simulated the Mg-doped GaN transport properties by density functional

264 We have studied the Mg doping of cubic GaN grown by plasma-assisted Molecula

265 y decompose in the double layer prior to the Mg(2+)/Mg(0) reduction, leading to electrochemically ina

266 orms a 2D coordination polymer, in which the Mg is surrounded by three allyl ligands.

267 indicate a push-pull mechanism in which the Mg(2+)-RNA interactions actually lead to destabilization

268 tial window (OPW) is extracted, in which the Mg(2+)/Mg(0) reduction can compete with electrolyte deco

269 with hydroxyl group intermediate, while the Mg atom coordinated to two nitrogen atoms has the near-o

270 ptimized antibacterial systems (Ti-Mg and Ti-Mg-3wt% Zn) that can selectively eradicate E. coli while

271 o design optimized antibacterial systems (Ti-Mg and Ti-Mg-3wt% Zn) that can selectively eradicate E.

272 vorable incorporation of Mg is attributed to Mg dopants incorporating substitutionally for Ga during

273 new experimental data show that L11 binds to Mg(2+)-dependent folded states, which we suggest lie alo

274 ordination mode for an allyl ligand bound to Mg.

275 tic analyses revealed that Mg dissolution to Mg(2+) followed mostly a zero-order kinetic rate law for

276 onal setting of the speleothem gives rise to Mg partition coefficients that are more temperature depe

277 Positioned substrates then can chelate two Mg(2+) ions for the two steps of the reaction.

278 des and pyrophosphate in the presence of two Mg(2+) ions (Mg(2+)(A) and Mg(2+)(B)).

279 hemistry makes it challenging to grow n-type Mg(3) (Sb,Bi)(2) single crystals.

280 with UDP:Mg(2+) and in complex with both UDP:Mg(2+) and a glycan acceptor, lacto-N-neotetraose.

281 ructures of human B3GNT2 in complex with UDP:Mg(2+) and in complex with both UDP:Mg(2+) and a glycan

282 Ultrasensitive Mg isotopic analysis was carried out for CSF from hydroc

283 ical method was developed for ultrasensitive Mg isotopic analysis of CSF microsamples via multicollec

284 hree different grain boundaries in unalloyed Mg using high-resolution electron backscatter diffractio

285 ral studies, we characterized its unexpected Mg(2+)-independent binding mode.

286 d structural transformations that occur upon Mg intercalation and deintercalation.

287 ution of Li-rich material is reported, using Mg(2) TiO(4) as a proof-of-concept material.

288 sponse to H(2) at levels relevant to in vivo Mg-implant biodegradation compared to the other indicato

289 sensor for noninvasive monitoring of in vivo Mg-implant biodegradation in research and clinical setti

290 xceed the effects of changes in source-water Mg/Ca.

291 ng, dehydrating the lipid headgroup, whereas Mg(2+) and Cu(2+) were bound without perturbing the hydr

292 mic details of potential mechanisms by which Mg(2+) leads to increased efficacy of opioid analgesics.

293 While Mg(2+) enables eEndoV to catalyze RNA cleavage, we show

294 he area per lipid in lipid monolayers, while Mg(2+) and Cu(2+) did not.

295 Instead, Si along with Mg isotope analyses carried out in the same aliquot of E

296 d type at 3.8 angstrom, both in complex with Mg(2+)-AMP-PNP.

297 s Chelate PA-1 resin or coprecipitation with Mg(OH)(2) and using either a Pb double spike or external

298 The enhancement of viability with Mg(2+)-based buffers led to the hypothesis that this enh

299 tion primarily dictated cell viability, with Mg(2+)-based buffers expanding the reversible electropor

300 sign a new magnesium sheet alloy-ZAXME11100 (Mg-1.0Zn-1.0Al-0.5Ca-0.4Mn-0.2Ce, wt.