ライフサイエンスコーパス: Mg

1 Mg(2+) ions associate with SLV when it is part of the ju

2 Mg(2+), Zn(2+), Cu(2+), K(1+), EDTA and beta-mercaptoeth

3 mprised of approximately 4,100,000-5,200,000 Mg of sediment OC.

4 mean OC accumulation rate was 0.55 +/- 0.02 Mg OC ha(-1) yr(-1).

5 both increased by an average of 9.4 and 5.1 Mg C ha(-1) , respectively, which are equivalent to incr

6 Fe(3+), 1.11mmolL(-1) Ca(2+) and 3.4mmolL(-1)Mg(2+) (8.82%, 40% and 57% of their total concentrations

7 re, we study two interfaces- {112}beta1/{100}Mg and {111}beta1/{110}Mg- that are commensurate with be

8 n of energetically favorable {112}beta1/{100}Mg interfaces, and predict that beta1 grows along <110>M

9 aces- {112}beta1/{100}Mg and {111}beta1/{110}Mg- that are commensurate with beta1/hcp-Mg orientation

10 the migration of metastable {111}beta1/{110}Mg.

11 ut evolution and, in mammals, consists of 12 Mg(2+)-dependent 3'-end RNases with substrate specificit

12 most of the PFOS mass in the Arctic (63-180 Mg) and is projected to continue increasing to 2038.

13 additional abatement ranged from $61 to $187 Mg CO2e(-1) and was substantially greater than the socia

14 ct frequency comb spectroscopy of single (25)Mg ions confined in a Paul trap, at deep-UV wavelengths.

15 ) than those in nonriverine settings (44-271 Mg/ha).

16 to have the largest impact on yield (over 3 Mg/ha estimated yield losses).

17 S. county of 500000 people generating 320000 Mg of waste annually.

18 Tg, with an average density of 5.95 +/- 0.35 Mg C ha(-1).

19 ks increased significantly with logging (+38 Mg ha(-1) ) and the abundance of large trees (+2.4 Mg ha

20 -1) ) and the abundance of large trees (+2.4 Mg ha(-1) for every tree >60 cm dbh).

21 reater than the social cost of carbon of $50 Mg CO2e(-1).

22 n river deltas had larger OC stocks (175-504 Mg/ha) than those in nonriverine settings (44-271 Mg/ha)

23 included no or high stover removal (0 or 6.8 Mg DM ha(-1) yr(-1) , respectively) under no-till (NT) o

24 e grain: Mn, -28.3%; Fe, -26.7%; Zn, -21.9%; Mg, -22.7%; Mo, -40.4%; K, -22.4%; and Ca, -19.5%.

25 ownstream fjord in 2012, equivalent to 30.95 Mg of carbon.

26 in the surface 1 m averaged 165.41 (SE 6.96) Mg OC ha(-1) (range 14-963 Mg OC ha(-1)).

27 165.41 (SE 6.96) Mg OC ha(-1) (range 14-963 Mg OC ha(-1)).

28 We report a Mg alloy Mg-2.2Nd-0.1Zn-0.4Zr (wt.%, denoted as JDBM-2)

29 of KATP/Ca(2+) signaling control by low ADP.Mg(2+) rather than by high ATP levels; and a role for a

30 ignificant amount of calcite, and nearly all Mg-bands, after the final chamber forms.

31 We report a Mg alloy Mg-2.2Nd-0.1Zn-0.4Zr (wt.%, denoted as JDBM-2) showing g

32 ption of divalent cations such as Ca(2+) and Mg(2).

33 ia californica in the presence of Ca(2+) and Mg(2+) at a resolution of 3.5 A.

34 concentrations of Zn(2+), Fe(3+), Ca(2+) and Mg(2+) in a red wine (Raimat, Catalonia, Spain) have bee

35 ter revealed that the presence of Ca(2+) and Mg(2+) inhibited intramolecular charge-transfer within p

36 ace interactions between divalent Ca(2+) and Mg(2+) ions and the nanochannel walls reduced the native

37 nd function with a combination of Zn(2+) and Mg(2+), although including Mn(2+) increases the activity

38 was found to be richest in K(+), Ca(2+) and Mg(2+).

39 loop drives paracellular Na(+), Ca(2+), and Mg(2+) reabsorption via the tight junction (TJ).

40 nst major ions such Na(+), K(+), Ca(2+), and Mg(2+).

41 myosin VI motor domain in rigor (4.6 A) and Mg-ADP (5.5 A) states bound to F-actin.

42 of different counterions (Na:AOT, K:AOT, and Mg:AOT) that consequently also result in different sized

43 tilization temperature of 2300 degrees C and Mg as a chemical modifier.

44 N fertilizer, but they contained more Ca and Mg.

45 ficantly affected the total N, P, K, Ca, and Mg stored in living biomass of forests, and the Acrisols

46 Whether the nutrients (N, P, K, Ca, and Mg) stored in forest biomass and their partitioning patt

47 ols group displayed the lowest P, K, Ca, and Mg.

48 conditions, Mg(II)-2,12-dibromoporphyrin and Mg(II)-2-bromoporphyrin could be obtained in up to 11% a

49 ling procedure has been developed for Fe and Mg determination in cassava starch using flame atomic ab

50 alternative for the determination of Fe and Mg in cassava starch samples.

51 for example, glauconite-nontronite), Fe- and Mg-serpentine, Mg-Fe-Ca-carbonate and probable Fe-sulphi

52 by using the large collection of Mn(II) and Mg(II) binding sites available in the protein data bank

53 The N, K, and Mg stored in living biomass tended to be greater in incr

54 ally relevant mixture of proteins, on Mg and Mg alloy degradation.

55 Cu, Zn and Si and secondary lines for Mn and Mg were selected to carry out the measurements.

56 mounts of charge-balancing Li(+), Na(+), and Mg(2+) ions for MOFs.

57 The respective Li(+)-, Na(+)-, and Mg(2+)-loaded materials exhibit high ionic conductivity

58 accuracy of quantification of Ca, K, Na, and Mg concentration by APE was not significantly different

59 were allowed to separate and Ca, K, Na, and Mg were determined in aqueous phase by means of inductiv

60 20, 19, and 24 ng.mL(-1) for Ca, K, Na, and Mg, respectively).

61 ll battery chemistries (lower than Li/O2 and Mg/O2 but comparable to Li/S), and Mg metal allows rever

62 site formed in experiments with olivine, and Mg- and Ca-bearing siderite formed in experiments with f

63 es the conversion of phosphoenolpyruvate and Mg-ADP to pyruvate and Mg-ATP.

64 osphoenolpyruvate and Mg-ADP to pyruvate and Mg-ATP.

65 Li/O2 and Mg/O2 but comparable to Li/S), and Mg metal allows reversible operation (100% Coulombic eff

66 aqueous Fe(3+) with small amounts of aqueous Mg(2+).

67 Lipins 1, 2, and 3 are Mg(2+)-dependent phosphatidic acid phosphatases and cata

68 ggesting that CLCA1-TMEM16A interactions are Mg(2+)- and metal ion-dependent adhesion site-dependent.

69 f organic compounds and minerals is made, as Mg released from minerals gets trapped into organic comp

70 rsible insertion of multivalent ions such as Mg(2+) and Al(3+) into electrode materials remains an el

71 anced by removing low-valent cations such as Mg(2+).

72 The 2.2-A Rnl1*ATP*(Mg(2+))2 structure highlights a two-metal mechanism, whe

73 4 encodes a mitochondrial inner membrane ATP-Mg/Pi carrier.

74 Mitochondrial ATP-Mg/Pi carriers import adenine nucleotides into the mitoc

75 tutions, as well as R1150Q/R1150W, augmented Mg-nucleotide activation.

76 tration of twenty-seven elements (Li, Be, B, Mg, Al, P, K, Ca, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Sr, Mo

77 e method is demonstrated for ionophore-based Mg(2+)-, Ca(2+)-, and Na(+)-selective electrodes.

78 hat when introduced into a nanocomposite bcc Mg is far more ductile, 50% stronger, and retains its st

79 lity regulates DNA ligation in vivo, because Mg(2+) levels are higher in the mitochondria than in the

80 kalinity/salinity conditions especially bias Mg/Ca temperatures in the eastern Mediterranean (eMed).

81 that are not observed when the enzyme binds Mg(II).

82 one-metal mechanism in which a ligase-bound Mg(2+)(H2O)5 complex lowers the lysine pKa and engages t

83 ariation in the position of putatively bound Mg(2+).

84 erence from Na(+),K(+),NH(+4) and Ca(2+) but Mg(2+),Cu(2+) and ascorbic acid but had slight interfere

85 Although p-type activation of GaN by Mg underpins a mature commercial technology, the nature

86 pacts conformational switching of stem II by Mg(2+) or the U2 protein Cus2; however, when Mg(2+) and

87 ine patch in C2B domain and is stabilized by Mg(2+), which neutralizes the Ca(2+)-binding aspartic ac

88 LV shows a conformational shift triggered by Mg(2+) ion association.

89 Some light elements as He, C, Mg, Al are depleted, while Si and P are enhanced.

90 ountains (Central Europe), the average [Ca + Mg] concentrations increased (2.5 mueq L(-1) yr(-1)), to

91 The percent increase in [Ca + Mg] concentrations in nonacidic lakes (0.3-3.2% yr(-1))

92 esses increased N, P and K and decreased Ca, Mg, Fe, Mn, Zn and Cu contents.

93 roup) and mineral contents (N, P, Na, K, Ca, Mg and Fe) were stimulated by the irradiation doses comp

94 ids, and ascorbic acid) and minerals (K, Ca, Mg, Na, Fe, Li, Zn) were also higher in pressed honey.

95 ent on the bioaccessibility of major (K, Ca, Mg, P) and trace elements (As, Ba, Cu, Fe, Mn, Cd, Cr, H

96 and applied for the determination of K, Ca, Mg, S, P, Cu, Fe, Mn and Zn in 72 guarana seed samples f

97 types exhibited a net reduction in shoot Ca, Mg, P, Fe, and Cu, while Mn and Zn increased under salin

98 le magnesium pins (as-drawn pure Mg, as-cast Mg-Zn-Mn, and extruded Mg-Zn-Mn) in a bioreactor applyin

99 nstrate the essential roles of the catalytic Mg(2+) for the active state formation and stability.

100 chanism, whereby: a ligase-bound "catalytic" Mg(2+)(H2O)5 coordination complex lowers the pKa of the

101 Depending on the conditions, Mg(II)-2,12-dibromoporphyrin and Mg(II)-2-bromoporphyrin

102 Solutions containing Mg or Mn, where all three situations can prevail, are us

103 resulted from the systematically controlled Mg(2+) cations distribution and concentrations in octahe

104 cell wall and cytoplasmic membrane controls Mg(2+) transport into the fungal cell.

105 ly, also a significant proportion of coupled Mg and Si vacancies are present.

106 idate elements linking asparagus (Zn, P, Cr, Mg, B, K) and pistachio (Mn, P, Cr, Mg, Ti, B, K, Sc, S)

107 , P, Cr, Mg, B, K) and pistachio (Mn, P, Cr, Mg, Ti, B, K, Sc, S) to the production areas were identi

108 istent with a model in which PhoPQ-dependent Mg(2+) homeostasis protects Salmonella against nitrooxid

109 at expression of PhoQ is essential to detect Mg(2+) and reduce the expression of OprH, a previously u

110 In this study, developed Mg-based helical stent was inserted and expanded in vess

111 d to the characterization of three different Mg(2+) binding modes: 1) direct binding via N7 coordinat

112 4 different contexts, eight of which display Mg(2+) binding at the Hoogsteen edge of guanine.

113 amenable to host divalent metal ions, i.e., Mg(2+) and Ca(2+), in aqueous electrolytes, where the va

114 ) in selected reactions containing elemental Mg, Al, Mn and Sn particles.

115 The quantification of elements (Mg, Ca, Na and K) through LIBS was done using calibratio

116 13)) near TRPM6, which encodes an epithelial Mg(2+) channel, and rs35929 (P=2.1x10(-11)), a variant o

117 illion mega-grams carbon-dioxide-equivalent (Mg CO2e(-1)) compared to those without an ILUC factor, d

118 Linking the distinct Eu-Mg defect configurations with the shallow transient and

119 ir nonmetastatic counterparts, which exhibit Mg(2+)- and Ca(2+)-insensitive adhesion.

120 ntly reduced in the absence of extracellular Mg(2+), and mutation of residues within the conserved me

121 rawn pure Mg, as-cast Mg-Zn-Mn, and extruded Mg-Zn-Mn) in a bioreactor applying cyclical loading and

122 g(2+), whereas TJs dominated by cldn16 favor Mg(2+) over Na(+); (iii) cldn10b does not interact with

123 tion, beef is an important source of Cu, Fe, Mg, and Zn to the human diet.

124 The bioaccessibility of Ca, Cu, Fe, Mg, Zn, and crude protein was evaluated after submitting

125 ed elevated accumulation rates of Ca, K, Fe, Mg, P, and S, with P being up to 5 times greater in samp

126 linear range increased up to 110mgL(-1) for Mg, 200mgL(-1) for Si and 13mgL(-1) for Zn.

127 .8mgkg(-1) for Fe and 23.7-64.5mgkg(-1), for Mg.

128 c acid (EDTA) complexes at delta 2.70ppm for Mg(2+) and delta 2.56ppm for Ca(2+).

129 ] as the Al-concentration increased, and for Mg-Zn alloys, this direction changes from [Formula: see

130 Surprisingly, the affinity of LIG3 for Mg(2+) was ten times weaker than that of LIG1, suggestin

131 the crystals reach sizes of 0.1-0.5 mum for Mg(2+) and 1-2 mum for PSS.

132 In particular, for Mg-Al alloys, this direction changes from [Formula: see

133 iagenetic processes may affect foraminiferal Mg/Ca.

134 linity gradients (deduced from foraminiferal Mg/Ca and stable oxygen isotopes, delta(18)O) in combina

135 However, an increase of free [Mg(2+)]cyto to 1.5 mM could increase the period between

136 bserved that the crystal structures of free, Mg(2+)-bound, and beryllofluoridated CKI1RD (a stable an

137 or no cross sensitivity to other ions (e.g., Mg(2+), Ca(2+), K(+)) and its insensitivity to potential

138 e lattice location of Mg in doubly doped GaN(Mg):Eu.

139 ta1-Mg3Nd precipitates, that grow along <110>Mg in bulk hcp-Mg and on dislocation lines.

140 ces, and predict that beta1 grows along <110>Mg on dislocation lines due to the migration of metastab

141 On the other hand, Mg(2+) and [Formula: see text] ions can also reach to th

142 110}Mg- that are commensurate with beta1/hcp-Mg orientation relationship via first principles calcula

143 pitates, that grow along <110>Mg in bulk hcp-Mg and on dislocation lines.

144 mation of beta1-like precipitates in the hcp-Mg matrix will require well-bonded coherent interface al

145 ultifloral (Ca, Cr, Mo, Se), common heather (Mg, Na), bearberry (Ba, Fe, Pb) and sage (Ag) honeys.

146 nd that such Mg thin film is hexacoordinated Mg compounds by in-situ STXM and XAS.

147 nts, despite their similar stability at high Mg(2+) concentrations, are considerably less stable than

148 Here we show that high Mg/Ca-calcite forms at night in cultured specimens of th

149 are: 20% calcite, 6% aragonite, 60% high-Mg calcite, and 14% amorphous carbonate.

150 h A32 playing a structural role and hydrated Mg(2+) playing a catalytic role in cleavage.

151 long-range interactions mediated by hydrated Mg(2+) cations.

152 ological characteristics, we have identified Mg(2+)- and Ca(2+)-mediated differences in adhesion stre

153 he event, however the magnitude of change in Mg/Ca suggests this event was not as pronounced on the w

154 sic non-dendritic nature of Mg deposition in Mg ion batteries.

155 n that MAGT1 was involved in the disorder in Mg(2+) homeostasis after Epstein-Barr virus (EBV) infect

156 ssociation of two other hairpins (H5/H4b) in Mg(2+).

157 t is unbound, but there is no specificity in Mg(2+) binding for the SLI loop.

158 of the chlorophyll biosynthesis intermediate Mg-protoporphyrin IX monomethylester (Mg-proto MME), con

159 Free intracellular Mg(2+) can approach 5 mm, but at this level Mn(2+), Ni(2

160 cent experiments demonstrate that intrashell Mg variability in Orbulina universa, which forms a spher

161 hosphates (PIP2 and ATP) and magnesium ions (Mg(2+)).

162 e carrier species (H(+), Li(+), Na(+), K(+), Mg(2+)), temperature (-35 to 25 degrees C), and atmosphe

163 easily ionized elements (EIEs), i.e., Ca, K, Mg, and Na, as well as the foreign ions (Al, Cu, Fe, Mn,

164 The levels of the minerals: Ca, K, Mg, Na, P, and the trace elements: Cd, Cu, Fe, Mn, Ni, P

165 o, Ni, Se, Th and U), common heather (Co, K, Mg, Na, V), sage (Ag, Cd, Cu), and bearberry (Ba, Fe, Pb

166 concentrations of Ag, As, Ba, Cu, Co, Fe, K, Mg, Mn, Mo, Na, Ni, Se, Sb, U and Th (p<0.05, all) among

167 vered a gene-environment interaction linking Mg(2+) deficiency to insulin resistance and obesity.

168 any species display alternating high and low Mg-bands within their shell walls that cannot be explain

169 d in the presence of 0.15 M HClO4 and 0.15 M Mg(ClO4)2 due to the protonation or complexation with th

170 Magnesium (Mg(2+)) homeostasis is critical for metabolism.

171 Magnesium (Mg) alloys are promising materials for biodegradable imp

172 ilizers, but the calcium (Ca) and magnesium (Mg) was higher with ORG and 2xORG.

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

174 ator of basal intracellular free magnesium ([Mg(2+)]i) levels.

175 tion of malic enzyme by increases in matrix [Mg(2+)], [NAD(+)], and [ADP].

176 gest that the accumulation of the metabolite Mg(2+) from MgATP hydrolysis is required to make dantrol

177 (3) production of intermediate products (MgO/Mg(OH)2 and Ca/P) during degradation; and (4) intermedia

178 ory data for Earth's most abundant mineral, (Mg,Fe,Al)(Al,Fe,Si)O3 bridgmanite (also known as silicat

179 tation of hexafluoroisopropanol with a mixed Mg/Li amide, to give pentafluoroalcohols.

180 ve a potential near the DNA surface at 20 mM Mg(2+) that is much less substantial than at 20 mM K(+)

181 l multi-element determination of Cu, Zn, Mn, Mg and Si in beverages and food supplements with success

182 ediate Mg-protoporphyrin IX monomethylester (Mg-proto MME), consistent with the impairment of Mg-prot

183 , is suggestive of the existence of multiple Mg(2+) binding modes for this basepair.

184 e presence of several elements like C, O, N, Mg, Ca, Na and K in seeds.

185 ond of two magnesium(I) dimers, [((Ar)Nacnac)Mg-]2 (Ar = C6H2Me3-2,4,6 (Mes); C6H3Et2-2,6 (Dep)), yie

186 1,2-dimagnesioethane products, [{((Ar)Nacnac)Mg}2(mu-CH2CPh2)], is described.

187 uction of the alanate complex, ((Dep) Nacnac)Mg(mu-H)3 AlH(NEt3 ).

188 ature, namely the dianion in [{((Dep) Nacnac)Mg}2 (mu-H)]2 [H3 Al-AlH3 ] ((Dep) Nacnac=[(DepNCMe)2 CH

189 By contrast, the 1.55-A LigA*NAD(+)*Mg(2+) structure reveals a one-metal mechanism in which

190 organic complexes containing Si-O-C and Si-O-Mg bonds.

191 the ATP alpha phosphate; a second octahedral Mg(2+) coordination complex bridges the beta and gamma p

192 this construct, along with the abundance of Mg ions and DNA molecules present, provides many interac

193 and conducted a genome-wide meta-analysis of Mg(2+) homeostasis.

194 severely restricts practical applications of Mg.

195 lysis of the complex degradation behavior of Mg-based alloys in vivo.

196 ng attention owing to the unique benefits of Mg metal electrodes, namely high reversibility without d

197 as significantly compromised the benefits of Mg/S chemistry and hindered the development of Mg/S batt

198 increase the intracellular concentration of Mg(2+) thereby contributing to tumor progression and met

199 In the presence of blood concentrations of Mg(2+) , a PhoQ mutant bound more C3 and was more suscep

200 ance to RNS is linked to the coordination of Mg(2+) homeostasis through the PhoPQ-regulated MgtA tran

201 in turn affect the mechanical deformation of Mg.

202 signing experiments to assess degradation of Mg-based implants.

203 eta' precipitates caused rapid depletion of Mg and Zn solute atoms in the MPZ.

204 /S chemistry and hindered the development of Mg/S batteries.

205 endall voids due to the outward diffusion of Mg.

206 the effects of MAGT1-mediated disturbance of Mg(2+) homeostasis on chronic hepatitis B virus (HBV)-in

207 roto MME), consistent with the impairment of Mg-proto MME cyclase activity.

208 Our detailed investigation of Mg(2+)-bound G:C W:W Trans pairs occurring in high-resol

209 ctator ion' to probe the lattice location of Mg in doubly doped GaN(Mg):Eu.

210 FBS reduced the mass loss of Mg-Yttrium (MgY) alloy with an oxidized surface during i

211 reversibility issue and failure mechanism of Mg ion batteries.

212 t with the intrinsic non-dendritic nature of Mg deposition in Mg ion batteries.

213 In the presence of Mg(2+) , ATP cannot effectively activate RyR1 from Tric-

214 f divalent cations, thus, in the presence of Mg(2+) , ATP is inadequate as an activator.

215 ignificant amounts of ROS in the presence of Mg(2+) and NAD(+) and the absence of exogenous substrate

216 fier K(+) channel Kir6.2, in the presence of Mg(2+) and nucleotides.

217 The extraordinary creep-resistance of Mg-Nd-based alloys can be correlated to the formation of

218 We report the study of Mg cathodic electrochemical deposition on Ti and Au elec

219 e, but is not fully understood for olivine ((Mg, Fe)2SiO4) the most abundant mineral in this region.

220 re variability over the last 21 kyr based on Mg/Ca ratios in a sub-thermocline dwelling planktonic fo

221 and diffusion energies of atomic clusters on Mg surfaces determine the surface roughness and formatio

222 racellular solution pH, the pH-dependence on Mg isotope fractionation is thus due to differences in f

223 ar beam epitaxy (MBE) grown NiO(001) film on Mg(001) substrate as the defect free NiO prototype and N

224 iologically relevant mixture of proteins, on Mg and Mg alloy degradation.

225 e very first systematic fundamental study on Mg/S system is conducted by combining experimental metho

226 Interestingly, hosting one Mg(2+) ion requires the coordination from three PTCDA mo

227 ways diverge with the insertion of Fe(2+) or Mg(2+) into protoporphyrin by ferrochelatase or magnesiu

228 Cation binding, either Ca(2+) or Mg(2+), stabilized the secondary and tertiary structures

229 he membrane or activation of K(+), Ca(2+) or Mg(2+)-dependent enzymes then constitute a cellular resp

230 's second metal binding site for Mn(II) over Mg(II), suggesting that T7 DNA primase activity modulati

231 ) TJs dominated by cldn10b prefer Na(+) over Mg(2+), whereas TJs dominated by cldn16 favor Mg(2+) ove

232 ferred orientation (CPO) of post-perovskite (Mg,Fe)SiO3 (pPv) has been believed to be one potential s

233 Conversely, JNK2 blockade prevented Mg(2+)-insensitive preNMDAR signaling from regulating sp

234 We demonstrate that a PTCDA Mg-ion electrode delivers a reversible capacity of 125 m

235 g degradation processes on commercially pure Mg with metallic or oxidized surfaces and on MgY alloy w

236 biodegradable magnesium pins (as-drawn pure Mg, as-cast Mg-Zn-Mn, and extruded Mg-Zn-Mn) in a biorea

237 al of 17 variables) on SOC change rate (rC , Mg C ha(-1) yr(-1) ).

238 with lower polarity organometallic reagents (Mg(CH2 SiMe3 )2 and Al(TMP)iBu2 ), key intermediates in

239 relief and reestablishment of NMDA receptor Mg(2+) block.

240 confirmed the feasibility of a rechargeable Mg/S battery; however, only limited cycling stability wa

241 rt the development of the first rechargeable Mg/S battery with a MgTFSI2 /MgCl2 /DME electrolyte (DME

242 agnesium and its application in rechargeable Mg batteries has received increasing attention owing to

243 he best cycling stability among all reported Mg/S batteries by suppressing polysulfide dissolution.

244 est performing material previously reported, Mg-MOF-74.

245 and metabolic pathways and serves to reveal Mg cycling in ecosystems.

246 nstrate a new strategy to achieve reversible Mg(2+) and Al(3+) insertion in anatase TiO2, achieved th

247 le for global cooling and increased seawater Mg/Ca over the past 50 million years.

248 r the Phanerozoic, with minima when seawater Mg and SO4 are low.

249 auconite-nontronite), Fe- and Mg-serpentine, Mg-Fe-Ca-carbonate and probable Fe-sulphide that likely

250 any organism with cells that follow similar Mg uptake and metabolic pathways and serves to reveal Mg

251 inner-sphere coordination of the active-site Mg(2+) cation to N7 of G33 makes the ribozyme drasticall

252 Species-specific Mg/Ca thermometry indicates that P. calcariformata preci

253 fungus Knufia petricola fractionates stable Mg isotopes in a time- and pH-dependent manner.

254 ase reaction pathway circumvents solid-state Mg(2+) diffusion and ensures a large interfacial reactio

255 We found that such Mg thin film is hexacoordinated Mg compounds by in-situ

256 NMR studies revealed that Mg(2+) binding and beryllofluoridation alter the conform

257 Through a mass balance model we show that Mg uptake into the fungal cell is not associated with a

258 es weaker than that of LIG1, suggesting that Mg(2+) availability regulates DNA ligation in vivo, beca

259 Our data illustrate that [Mg(2+)]i plays a key role in control of HBV infection.

260 The Mg thin film was not dissolvable during the following di

261 The Mg(2+) and ClO4(-) ions appear charge-ordered, confining

262 The Mg/S couple is of particular interest owing to its high

263 The Mg:Ca ratio is also of interest due to the observed asso

264 were obtained using laser ablation, and the Mg/Ca of the most recently grown final chambers were use

265 ion segment, which additionally contains the Mg(2+) binding loop and a P + 1 loop that is important i

266 mechanistic study of sulfur reaction in the Mg cation environment has severely hindered our understa

267 Variations in the Mg, Ca, Sr, and SO4 concentrations of paleoseawater can

268 m of action of dantrolene is to increase the Mg(2+) affinity of the RyR (or "stabilize" the resting s

269 e insertion of 1,1-diphenylethylene into the Mg-Mg bond of two magnesium(I) dimers, [((Ar)Nacnac)Mg-]

270 ure commercial technology, the nature of the Mg acceptor in GaN is still controversial.

271 llow transient and deep ground states of the Mg acceptor in the Lany-Zunger model, we determine the e

272 In vitro cytotoxicity test of the Mg extract via human vascular endothelial cells (HUVECs)

273 recently raised doubts regarding some of the Mg(2+) assignments near the imino nitrogen of guanine, i

274 nt strain, suggesting a direct effect of the Mg(2+) on the modulation of expression of a bacterial co

275 tional impact of recruiting or releasing the Mg(2+) cofactor highlights two loop regions for which fr

276 arge voltage hysteresis is mainly due to the Mg anode overpotential.

277 yl-1,3-diaminopropane (dmpn) appended to the Mg(2+) sites lining the channels of Mg2(dobpdc) (dobpdc(

278 ggest substantial thermal stability of these Mg-metalorganics (CHOMg compounds).

279 This Mg isotope fractionation dependence on pH might also be

280 mentally characterized, the dynamics of this Mg(2+)-dependent loop-loop interaction have been elusive

281 s are localized on N atoms axially bonded to Mg acceptors.

282 sinidius PhoQ was found to be insensitive to Mg(2+) , Ca(2+) and pH.

283 duction under these conditions is related to Mg(2+)-dependent NADH generation by malic enzyme.

284 not typical due to low Ca and Sr relative to Mg and SO4 in modern seawater.

285 ty is the result of increased sensitivity to Mg(2+)- and Ca(2+)-mediated focal adhesion disassembly i

286 components, suggest that for G:C W:W Trans , Mg(2+) binding can fine tune the basepair geometries wit

287 probing a transition frequency in a trapped Mg+ ion using a single mode of a UV frequency comb.

288 ture, the RNA polymerase domain contains two Mg(II) ions.

289 During charging, a uniform Mg film was deposited on the electrode, which is consist

290 fungal cell is not associated with a unique Mg isotope fractionation factor.

291 Using Mg/Ca paleothermometry of the ostracode Krithe and sea-i

292 e wide bandgap MgZnO thin films with various Mg mole fractions were grown on c-sapphire substrate usi

293 Mg(2+) or the U2 protein Cus2; however, when Mg(2+) and Cus2 are used in combination, the impacts of

294 ts in muscle fibers and isolated RyRs, where Mg(2+) is present or absent, respectively, and define th

295 Whether Mg-heterogeneity is also diurnally paced in species with

296 y inhibited in the presence of Ca(2+), while Mg(2+) has no effect with 100 nm liposomes and modest ef

297 her replacement of extracellular Ca(2+) with Mg(2+) or the addition of SOCE inhibitors (BTP-2 and 2-A

298 on, direct protonation, or coordination with Mg(2+), accumulation of positive charge near N7 of guani

299 ery, in which the soluble iodine reacts with Mg(2+) to form a soluble intermediate and then an insolu

300 rs, {[Tism(Pr(i)Benz)]M}[HB(C6F5)3] (M = Zn, Mg), which are rare examples of these metals in trigonal