ライフサイエンスコーパス: sodium ion

1 hydrogen bonding network that is mediated by sodium ion.

2 a small cation-friendly cavity occupied by a sodium ion.

3 two protons that are later exchanged for one sodium ion.

4 o solid-state electrochemical reactions with sodium ions.

5 nd had a more organised structure around the sodium ions.

6 accessible ligand-binding pocket that lacked sodium ions.

7 e, they are susceptible to interference from sodium ions.

8 r ~800 water molecules and for magnesium and sodium ions.

9 3 in the presence of potassium ions but not sodium ions.

10 yte battery, which involves the insertion of sodium ions.

11 the synapse, assisted by the co-transport of sodium ions.

12 rom singly charged precursor ions with bound sodium ions.

13 esting the disruption of hydrogen-bonding by sodium ions.

14 phate group, together with flanking zinc and sodium ions.

15 ysiology, including the balance of water and sodium ions.

16 us phase was correlated with the mobility of sodium ions.

17 nable allosteric inhibition by extracellular sodium ions.

18 of the pore domain and ensuing permeation of sodium ions.

19 e, with a high preference for potassium over sodium ions.

20 , 0.34% vs. 0.31%; silicon, 0.36% vs. 0.37%; sodium ion, 0.21% vs. 0.18%; and sulfate, 0.35% vs. 0.38

21 ltaenhC mutants showed a hypersensitivity to sodium ion, a phenotype associated with dysfunction of t

22 e carbonate source, but this also introduces sodium ions--a potential catalyst poison.

23 ree energy released by this reaction to pump sodium ions across the cell membrane.

24 ng oxidation of NADH with ubiquinone to pump sodium ions across the cytoplasmic membrane.

25 ree distinct GA dimeric species, detected as sodium ion adduct ions [2GA + 2Na](2+), and these are as

26 opropanol lead to a significant reduction in sodium ion adduction but are not as effective as acetoni

27 he effectiveness of this method for reducing sodium ion adduction is related to the low proton affini

28 This method of reducing sodium ion adduction to proteins is simple and requires

29 bF(6), can significantly lower the extent of sodium ion adduction to the molecular ions of proteins a

30 ction remains wide enough for the passage of sodium ions, aided by a continuous bridge of approximate

31 , mesitylenic acid, and solvent molecules on sodium ion all are critical in identifying the most favo

32 through a dual mechanism of intercalation of sodium ions along the x axis of the phosphorene layers f

33 ith cardiovascular hospitalizations, whereas sodium ion, aluminum, and magnesium, components abundant

34 gs differ from the conventional thought that sodium ions always lead to more severe fractures in the

35 d, the M3 receptor is bound by an allosteric sodium ion and confined mostly in the inactive state wit

36 A calcium ion, sodium ion and glycerol molecule were identified within

37 increased some of the allosteric effects of sodium ions and amiloride, whereas orthosteric ligand bi

38 nist and antagonist affinity, allosterism by sodium ions and amilorides, and receptor functionality w

39 small but significant decrease in hemolymph sodium ions and an increase in calcium ions after 24 h p

40 ynamics occur in the absence and presence of sodium ions and aspartate, but stall in sodium alone, pr

41 amate from synapses are driven by symport of sodium ions and counter-transport of a potassium ion.

42 In the presence of sodium ions and no potassium ions, LJM-3064 adopts an an

43 of one glutamate to the cotransport of three sodium ions and one proton and the countertransport of o

44 sists of cotransport of glutamate with three sodium ions and one proton, followed by countertransport

45 forms gated paracellular channels and allows sodium ions and other small positively charged ions to c

46 formation, the enzyme is able to capture two sodium ions and transport them to the external side of t

47 serve electroneutrality and osmotic balance, sodium ions and water also flow into the intestinal lume

48 ging rechargeable sodium-ion storage systems-sodium-ion and room-temperature sodium-sulfur (RT-NaS) b

49 , we show that this cation is a stably bound sodium ion, and although it is not a transported substra

50 on, elemental carbon, organic carbon matter, sodium ion, and ammonium.

51 otential role of structured water molecules, sodium ions, and lipids/cholesterol in GPCR stabilizatio

52 ed and reduced states, Na(+)-NQR binds three sodium ions, and that the affinity for sodium is the sam

53 A core domain of six helices harbours two sodium ions, and the remaining four helices pack in a ro

54 xcellent electrode material for lithium-ion, sodium-ion, and lithium-sulfur batteries.

55 One citrate molecule and one sodium ion are bound per protein, and their binding site

56 Sodium ions are actively pumped out of the lumen of the

57 Sodium ion batteries are being considered as an alternat

58 It is used as an anode in sodium ion batteries to deliver a high initial reversibl

59 as active electrode materials of lithium or sodium ion batteries, catalysts for water splitting, and

60 opper to survive harsh cycling conditions in sodium ion batteries.

61 NaMF3, the prospective cathode materials for sodium ion batteries.

62 and tested as a promising anode material for sodium ion batteries.

63 and development efforts on room-temperature sodium-ion batteries (NIBs) have been revitalized, as NI

64 a promising negative electrode candidate for sodium-ion batteries (NIBs) owing to its easy scalabilit

65 u of 0.1 V in PIBs, slightly higher than for sodium-ion batteries (SIBs) (0.01 V), and well above the

66 Organic sodium-ion batteries (SIBs) are potential alternatives o

67 Sodium-ion batteries (SIBs) are still confronted with se

68 Sodium-ion batteries (SIBs) have attracted increasing at

69 While sodium-ion batteries (SIBs) hold great promise for large

70 to develop high-energy-density cathodes for sodium-ion batteries (SIBs), low-cost, high capacity Na(

71 -performance negative-electrode material for sodium-ion batteries (SIBs).

72 ment of both anode and cathode materials for sodium-ion batteries (SIBs).

73 ncreasing interest in the development of new sodium-ion batteries and new analytical methods to non-i

74 formance when used in lithium-ion batteries, sodium-ion batteries and supercapacitors, respectively.

75 Sodium-ion batteries are a promising battery technology

76 Sodium-ion batteries are emerging as a highly promising

77 Sodium-ion batteries are emerging as candidates for larg

78 ategies for rational design of materials for sodium-ion batteries are presented to provide an overvie

79 All-solid-state sodium-ion batteries are promising candidates for large-

80 Presently, sodium-ion batteries based on Na(3)V(2)(PO(4))(2)F(3)/C

81 be a scalable, low-cost cathode material for sodium-ion batteries exhibiting high capacity, long cycl

82 The as-prepared sample used as an anode in sodium-ion batteries exhibits the best rate performance

83 ries, the application of these structures in sodium-ion batteries has attracted great attention in re

84 Sodium-ion batteries have captured widespread attention

85 ough recent reports on cathode materials for sodium-ion batteries have demonstrated performances comp

86 Sodium-ion batteries have recently attracted significant

87 Potential applications of sodium-ion batteries in grid-scale energy storage, porta

88 This allows sodium-ion batteries to have comparable voltages to lith

89 nd the manufacturing feasibility of low cost sodium-ion batteries with existing lithium-ion battery i

90 ural and chemical evolution of tin anodes in sodium-ion batteries with in situ synchrotron hard X-ray

91 ing electrochemical capacitors, lithium- and sodium-ion batteries, and lithium-sulfur batteries.

92 Sodium-ion batteries, as analogs of lithium-ion batterie

93 articular emphasis on lithium-ion batteries, sodium-ion batteries, catalysis of hydrogen evolution, o

94 mize the side reactions of red phosphorus in sodium-ion batteries, demonstrating stable electrochemic

95 re proposed to fabricate superior anodes for sodium-ion batteries, featuring high-rate capabilities a

96 lude electrodes in rechargeable lithium- and sodium-ion batteries, lithium-sulfur batteries, and supe

97 pplications including lithium-ion batteries, sodium-ion batteries, lithium-sulfur batteries, lithium-

98 owever, due to the difference in lithium and sodium-ion batteries, there are several issues that need

99 In the case of sodium-ion batteries, thermodynamically, the use of a so

100 chanism of high-capacity antimony anodes for sodium-ion batteries.

101 sing negative electrode material for aqueous sodium-ion batteries.

102 ould have impact in advancing development of sodium-ion batteries.

103 as a negative electrode material for aqueous sodium-ion batteries.

104 state-of-the-art carbon anode materials for sodium-ion batteries.

105 um-ion systems suggest untapped potential in sodium-ion batteries.

106 present a step forward in the development of sodium-ion batteries.

107 he growing area of new cathode materials for sodium-ion batteries.

108 material, as a viable positive electrode for sodium-ion batteries.

109 has been considered as a candidate anode for sodium-ion batteries.

110 -performance red-phosphorus-based anodes for sodium-ion batteries.

111 he synthesis of hollow structured anodes for sodium-ion batteries.

112 nO(2) materials have shown great promise for sodium-ion batteries.

113 ithium-ion, lithium-sulfur, lithium-air, and sodium-ion batteries.

114 lizing high-performance P2-type cathodes for sodium-ion batteries.

115 r sodium:transition-metal ratio for nonoxide sodium ion battery cathode materials are reported.

116 Such a design allows exceptional sodium ion battery performance in terms of high-power co

117 To improve lithium and sodium ion battery technology, it is imperative to under

118 n, we design a fully recyclable rechargeable sodium ion battery with bipolar electrode structure usin

119 pacity retention per cycle to be 99.88% as a sodium-ion battery (SIB) and 99.70% as a potassium-ion b

120 form of CTF-HUST-4 as an anode material in a sodium-ion battery achieving an excellent discharge capa

121 nSb) alloys are synthesized and applied as a sodium-ion battery anode.

122 highest capacity value reported for organic sodium-ion battery anodes until now.

123 molecular precursor for the next generation sodium-ion battery cathode material, Na(2)Mn(2)FeO(6), i

124 n, for the first time, we report a family of sodium-ion battery electrodes obtained by replacing step

125 Organic room-temperature sodium-ion battery electrodes with carboxylate and carbo

126 The sodium-ion battery is a promising battery technology owi

127 he cathode material used in a lithium-ion or sodium-ion battery is alkali-rich, this can increase the

128 ility, and cycle life, providing a practical sodium-ion battery powering an electric vehicle in frigi

129 The aqueous sodium-ion battery system is a safe and low-cost solutio

130 major scientific challenge for a competitive sodium-ion battery technology is to develop viable anode

131 a sustainable way has rekindled interest for sodium-ion battery technology, owing to the natural abun

132 tion enables the fabrication of a discharged sodium-ion battery with a non-sodium metal anode, and th

133 A symmetric sodium-ion battery with an aqueous electrolyte is demons

134 The advent of aqueous symmetric sodium-ion battery with high safety and low cost may pro

135 igh-rate capability and long cycle life in a sodium-ion battery.

136 At least two sodium ions bind before aspartate.

137 med to understand the mechanistic effects of sodium ion binding on dynamic activation of the M3 musca

138 Recently we identified a sodium ion binding pocket in a high-resolution structure

139 Because the sodium ion binding pocket is highly conserved in other c

140 ucted to have altered ion selectivities, the sodium ion binding site nearest the extracellular side i

141 e D2.50-protonated receptor does not exhibit sodium ion binding to the D2.50 allosteric site and samp

142 teric pockets is significantly weakened upon sodium ion binding.

143 e residue proposed to form part of the third sodium ion-binding site.

144 inactive state, and releases a proton when a sodium ion binds Asp163.

145 The central cluster harbors a putative sodium ion bound to the highly conserved aspartate resid

146 ve charge introduced at position 124 and the sodium ions bound at Na3' and Na1 underlies the protecti

147 Significantly, sodium ions can successfully move out and into without c

148 Addition of an allosteric sodium ion caused the receptor and ligand to adopt an in

149 validated the concept of full-titanium-based sodium ion cells through the assembly of symmetric cells

150 Full sodium-ion cells based on this phase as positive electro

151 ncreased expression of certain voltage-gated sodium ion channel (NaV) isoforms in peripheral sensory

152 The voltage-gated sodium ion channel (VGSC) belongs to the largest superfa

153 HN-associated VZV isolates induce changes in sodium ion channel currents known to be associated with

154 lular geometry, gap junctional coupling, and sodium ion channel distribution on propagation velocity

155 The effect of gap junctional coupling, sodium ion channel distribution, and extracellular condu

156 NaV1.7 is a voltage-gated sodium ion channel implicated by human genetic evidence

157 For example, the voltage-gated sodium ion channel Nav1.7 is expressed selectively in se

158 luates the delivery of dsRNA targeted to the sodium ion channel paralytic A (TcNav) gene in Tribolium

159 Single cell sodium ion channel recording was performed after 72 hr b

160 iscern the role of the cardiac voltage-gated sodium ion channel SCN5A in the etiology of dilated card

161 Voltage-gated sodium ion channel subtype 1.7 (Na(V)1.7) is a high inte

162 analogs that inhibit NaV1.7, a voltage-gated sodium ion channel that is a compelling target for impro

163 nctions as a potent agonist of voltage-gated sodium ion channels (NaVs).

164 e, and reversible inhibitor of voltage-gated sodium ion channels (NaVs).

165 on of Nav 1.6 and Nav 1.7 genes all encoding sodium ion channels the dysregulation of which is associ

166 by mutations in skeletal muscle chloride and sodium ion channels with considerable phenotypic overlap

167 mediated in part by the Nav 1.6 and Nav 1.7 sodium ion channels.

168 Aqueous sodium-ion charge storage devices combined with biocompa

169 djustment for gaseous copollutants, nitrate, sodium ion, chloride ion, magnesium, and nickel remained

170 s mutant, residual active outward pumping of sodium ions competes with passive inward transport of po

171 fferences in sodium ion mobility and in free sodium ion concentration, leading to differences in in-m

172 a dehydrated iron hexacyanoferrate with high sodium-ion concentration enables the fabrication of a di

173 demonstrate that sustained low extracellular sodium ion concentrations ([Na(+)]) directly stimulate o

174 ath by increasing intracellular chloride and sodium ion concentrations.

175 thesis and are found to irreversibly inhibit sodium ion conductance in recombinantly expressed wild-t

176 nts of the transition are open and closed to sodium ion conduction, respectively.

177 analysis, we find that the particles form a sodium-ion conductive film on the anode, which stabilize

178 Here, we introduce particularly high sodium ion conductivity into the zeolitic imidazolate fr

179 reased ionic conductivity in an archetypical sodium-ion conductor Na(3)PS(4) are not fully understood

180 establish the molecular basis for allosteric sodium ion control in opioid signalling, revealing that

181 Notably, norbuprenorphine interacted with sodium ion-coordinating residues W293(6.48) and N150(3.3

182 ed by the cardiac sodium channel [persistent sodium ion current (INa)].

183 in nature, is approximately 52% faster than sodium ion (DNa+ = 1.33, DCl- = 2.03[10(-9)m(2)s(-1)]).

184 into the cell, driven by the co-transport of sodium ions down their transmembrane concentration gradi

185 trides, (3) an electrostatically stabilizing sodium ion during nitride installation, (4) selecting th

186 co-deintercalation of the hydrated water and sodium-ion during the high potential charging process re

187 e by a rotary motor powered by a proton or a sodium ion electrochemical gradient.

188 ered birnessite (Na(0.27)MnO(2)) for aqueous sodium-ion electrochemical storage with a much-enhanced

189 tural chemistry and appreciable voltages for sodium-ion electrochemistry.

190 However, the performance of sodium-ion electrode materials has not been competitive

191 erization of the cocrystalline solid-organic sodium ion electrolyte NaClO4 (DMF)3 (DMF=dimethylformam

192 can lower the surface diffusion barrier for sodium ions, enabling stable electrodeposition.

193 odium gradient to facilitate the exchange of sodium ions for ionic calcium.

194 The release of one sodium ion from the crystallographically determined sodi

195 tion light-driven H(+)/Na(+) pumps, ejecting sodium ions from cells in the presence of sodium and pro

196 Here, an all-stretchable-component sodium-ion full battery based on graphene-modified poly(

197 A C/g-C(3) N(4) sodium-ion full cell (in which sodium rhodizonate dibasi

198 of hard carbon in a sodium metal cell and a sodium-ion full-cell configuration.

199 upled with an Sb-based anode, the fabricated sodium-ion full-cells also exhibit excellent rate and cy

200 n of reduced ferredoxin with generation of a sodium ion gradient.

201 ts human orthologues, the transporter uses a sodium-ion gradient for nucleoside transport.

202 For the first time, sodium ions have been imaged sitting inside the 7-member

203 rate, and Na1 and Na2 for two co-transported sodium ions) have been resolved, we still lack a mechani

204 aling the presence and fundamental role of a sodium ion in mediating allosteric control of receptor f

205 These new findings suggest that the sodium ion in the allosteric binding pocket not only imp

206 The bound anion and the nearby sodium ion in the Na1 site organize a connection between

207 titative assessment of the metabolic role of sodium ions in cellular processes and their malfunctions

208 ith a trained panel and in vivo retention of sodium ions in human volunteers.

209 was used to study the molecular mobility of sodium ions in model cheeses through measurements of the

210 ic, mucoadhesive thickener, the retention of sodium ions in the mouth is prolonged due to the mucoadh

211 for the first time the detailed locations of sodium ions in the selectivity filter of a sodium channe

212 ke potassium ions in potassium channels, the sodium ions in these channels appear to be hydrated and

213 olving large anharmonic displacements of the sodium ions inside multi-vacancy clusters.

214 in some prokaryotes, complex I may transport sodium ions instead, and three subunits in the membrane

215 Sodium ions interact with chemical moieties of the polys

216 The free energies of transferring a sodium ion into a prehydrated gate in functionally close

217 r from the synapse by cotransport with three sodium ions into the surrounding cells.

218 may also indicate the return pathway for the sodium ions involved in impulse formation.

219 reveals that the presence of binding-pocket sodium ions is necessary to stabilize the locked-occlude

220 Intra-axonal accumulation of sodium ions is one of the key mechanisms of delayed neur

221 vailable electrode materials, especially for sodium-ion layered oxides, motivating the exploration of

222 partate release invariably follows that of a sodium ion located near the HP2 gate entrance.

223 However, the sluggish kinetics of sodium ion makes it hard to achieve high-rate performanc

224 pid/protein ratios, 0% and 1% added NaCl) on sodium ion mobility ((23)Na NMR), in-mouth sodium releas

225 se composition, thus inducing differences in sodium ion mobility and in free sodium ion concentration

226 metal electrode, is attributed to increased sodium ion mobility in the dendrite.

227 phase, but no significant difference in the sodium ion mobility were obtained.

228 rmness and perceived hardness, and increased sodium ion mobility, in vivo sodium release and both sal

229 e cheeses, perceived hardness, and decreased sodium ion mobility, in vivo sodium release, saltiness a

230 We found that sodium ion (Na(+))-gated water-conduction nanochannels c

231 asma membranes in exchange for extracellular sodium ions (Na+).

232 GltPh coordinates L-aspartate as well as the sodium ion Na1.

233 lular electric fields and depletion of local sodium ion nanodomains.

234 We believe that the segregation of sodium ions next to the negatively charged sapphire subs

235 atter (OCM), elemental carbon (EC), silicon, sodium ion, nitrate, ammonium, and sulfate.

236 80A(7.45)) the negative allosteric effect of sodium ions on agonist binding.

237 oplasm-facing state and either apo, bound to sodium ions only, substrate, or blockers.

238 Addition of either sodium ions or the substrate 5-benzyl-l-hydantoin (L-BH)

239 monstrated to access similar capacities as a sodium-ion or potassium-ion cathode.

240 t utilize light energy to actively transport sodium ions out of the cell.

241 They exhibit strong selectivities for sodium ions over other cations, enabling the finely tune

242 ane with high selectivity for potassium over sodium; ion passage is blocked by specific chemical modi

243 and disrupt a continuous internal water and sodium ion pathway, preventing transitions to an active-

244 This phase can reversibly uptake 3 sodium ions per formula unit over the 1 to 4.8 V voltage

245 introduction of the R109Q mutation into the sodium ion pump of Dokdonia eikasta (KR2) results in pas

246 than in lithium analogues due to the larger sodium-ion radius.

247 Sodium is globally available, which makes a sodium-ion rechargeable battery preferable to a lithium-

248 uptake of neurotransmitter with one or more sodium ions, removing neurotransmitter from the synaptic

249 hich a thin polyelectrolyte film with mobile sodium ions replaces the liquid reservoir.

250 ges that may illuminate the pathway by which sodium ions return to the endoneurial space after they h

251 the ion movements or to the pathway taken by sodium ions returning to their original endoneurial loca

252 The pathway taken by sodium ions returning to their original location and the

253 tran, and altered apical side tight junction sodium ion selectivity, compared with wild-type mice.

254 Potentiometric sodium ion sensors were developed using a polyvinyl chlo

255 that single-particle mass spectra with weak sodium ion signals can be produced by the desorption of

256 ne)amiloride 2 (HMA) supposedly bind in this sodium ion site and can influence orthosteric ligand bin

257 The distinctive delta-OR sodium ion site architecture is centrally located in a p

258 The sodium ion site is an allosteric site conserved among ma

259 (3)H]ZM-241,385) from both the wild-type and sodium ion site W246A mutant hA2AAR.

260 A receptor (hA2AAR), in which the allosteric sodium ion site was elucidated, makes it an appropriate

261 receptor confirmed its likely binding to the sodium ion site.

262 Here, we show that external sodium ions stabilize the TRPV1 channel in a closed stat

263 he seven-transmembrane bundle core, with the sodium ion stabilizing a reduced agonist affinity state,

264 are evaluated as anode materials in aqueous sodium-ion storage devices.

265 ral disordering and structural water improve sodium-ion storage in a layered electrode and open up an

266 Emerging rechargeable sodium-ion storage systems-sodium-ion and room-temperatu

267 When used as anodes for sodium-ion storage, these 3D MXene films exhibit much im

268 The energy required to remove calcium and sodium ions subsequent to nerve excitation was estimated

269 fied new materials design rules for emerging sodium-ion systems that do not apply to lithium-ion syst

270 In contrast to monovalent lithium or sodium ions, the reversible insertion of multivalent ion

271 allosteric ENaC inhibition by extracellular sodium ions, thereby increasing the probability of chann

272 om-centric Pt sites are formed by binding to sodium ions through -O ligands, the ensemble being equal

273 s reveal that the GLIC channel is open for a sodium ion to transport, but presents a approximately 11

274 al stimulation, the channel opens and allows sodium ions to enter the cell, inducing a fast upstroke

275 ate of sufficient diameter to allow hydrated sodium ions to pass through.

276 Li-O(2) battery by using a cation additive, sodium ions, to the lithium electrolyte.

277 The sodium ion-translocating NADH:quinone oxidoreductase (Na

278 this site blocks the transmembrane-spanning sodium ion translocation pathway, providing a molecular

279 ria, a close model for the human enzyme, and sodium ion transport across the mitochondrial inner memb

280 An imbalance of chloride and sodium ion transport in several epithelia is a feature o

281 show that the surface diffusion barrier for sodium ion transport is a sensitive function of the chem

282 driven predominantly by active chloride and sodium ion transport.

283 te dense and homogeneous solid-liquid hybrid sodium-ion transportation channels through and along the

284 functional theory calculations suggest that sodium ions undergo occupancy-dependent stepwise inserti

285 es, which undergo redox reactions coupled to sodium ion uptake and release.

286 An allosteric sodium ion was found bound to a highly conserved D2.50 r

287 ence of binding-pocket leucine substrate and sodium ions, we have sampled plausible conformational st

288 ile range increases in OCM, EC, silicon, and sodium ion were associated with estimated increases in m

289 The mobility and release of sodium ions were assessed in model cheeses with three di

290 PBISEs for potassium and sodium ions were developed, and these ISEs present outst

291 Upon the binding of pVI to DNA, three sodium ions were displaced from the DNA.

292 rmation during dough mixing, compared to the sodium ion, were determined.

293 th manganese oxides capable of intercalating sodium ions when their potentials were prepoised prior t

294 Thus, a turn-on fluorescent probe for sodium ion, which does not respond to many other metal s

295 suggest specific localization sites for the sodium ions, which correspond with experimentally determ

296 D52A(2.50) directly affected the mobility of sodium ions, which readily migrated to another pocket fo

297 cations would strongly favor the passage of sodium ions while hindering translocation of chloride io

298 consumption during the diffusion process of sodium ions, while the carbon-coated structure can incre

299 h pHLIP and the bilayer; the coordination of sodium ions with the C-terminus of pHLIP led to localize

300 ges in helicity, whereas the coordination of sodium ions with the phosphate moiety of the phosphochol