ライフサイエンスコーパス: sodium

1 tremia or the absolute decrease in the serum sodium.

2 purchases of junk foods, saturated fat, and sodium.

3 tic strains but it contains a high amount of sodium.

4 SSBs, and total calories, fiber, sugar, and sodium.

5 he lung, ENaC is responsible for movement of sodium.

6 yunsaturated fats, seafood omega-3 fats, and sodium.

7 most potent compound of the present series, sodium 1-amino-4-[4-(2,4-dimethylphenylthio)phenylamino]

8 sis, development, and in vivo application of sodium [1-(13)C]-glycerate ([(13)C]-Glyc) as a novel pro

9 Admixtures with excessive hypotonicity (sodium = 103 mEq/L), in contrast, decreased sRBC adhesio

10 Admixtures with intermediate tonicities (sodium = 111-122 mEq/L) resulted in optimal changes in s

11 Admixtures with higher tonicities (sodium = 141 mEq/L) affected sRBC biomechanics by decrea

12 00g) was the predominant element followed by sodium (170mg/100g) and phosphorus (130mg/100g).

13 Treatment with chemical chaperones, such as sodium 4-phenylbutyrate (PBA), reduces protein aggregati

14 Surprisingly, sodium accumulated in the colons of mice on an HSD, sugg

15 r a period of 180 days, when stored in 0.01M sodium acetate buffer pH 5.5 at 4 degrees C.

16 on the observations of different patterns of sodium acetate clusters that are characteristic for each

17 hat were of potential concern because of the sodium, added sugar, saturated fat, or trans fat content

18 ndards for energy, total and saturated fats, sodium, added sugars, protein, fiber, and calcium.

19 f a healthy diet, limiting intakes of excess sodium, added sugars, saturated fat, and trans fat has b

20 calibrant (CCS and K0) using singly charged sodium adducts of poly(ethylene oxide) monomethyl ether

21 duced by emulsification/internal gelation of sodium alginate dispersed within vegetable oils containi

22 for End-Stage Liver Disease including serum sodium and Child Pugh Scores.

23 Higher levels of sodium and lower levels of potassium intake are associat

24 the relationship of calibrated estimates of sodium and potassium excretion with cardiovascular outco

25 have improved the estimation of mean dietary sodium and potassium intakes.

26 r elements showed good agreement, except for sodium and zinc, in which analyses of 24h diet dairies o

27 alphafetoprotein at recurrence, donor serum sodium, and pretransplant recipient neutrophil-lymphocyt

28 to be spatially heterogeneous particles with sodium- and chloride-rich cores surrounded by organic en

29 ract (NTS(HSD2) neurons) were shown to drive sodium appetite.

30 lly, triethylammonium had the same effect as sodium as the counter-ion.

31 =1 mo, the ICCs ranged from 0.33 to 0.68 for sodium at various intervals between collections.

32 n of a highly conserved, alkaline-regulated, sodium ATPase was tolerant of genetic or chemical pertur

33 ion of o-alkynylaldehydes in the presence of sodium azide under mild reaction conditions is described

34 tion that was impaired by the SECA inhibitor sodium azide.

35 the clinical study were maintained on a high sodium balance, renin activity progressively declined wi

36 ul to have salt taste enhancers that are not sodium based.

37 Thus, sodium benzoate and sorbic acid have an inhibition effec

38 e of investigational product administered in sodium bicarbonate 15 minutes after each meal.

39 Intravenous sodium bicarbonate and oral acetylcysteine are widely us

40 thepsin K activity, and both were reduced by sodium bicarbonate co-transporter (P </= 0.0001) and car

41 for angiography to receive intravenous 1.26% sodium bicarbonate or intravenous 0.9% sodium chloride a

42 Paratyphi A following sodium bicarbonate pretreatment at 1 of 2 dose levels (g

43 stable renal function, the benefit of using sodium bicarbonate rather than isotonic sodium chloride

44 containing the cold precursors THP-PSMA and sodium bicarbonate, with no further manipulation.

45 converted to uracil through the addition of sodium bisulphite, allowing genome-wide quantification o

46 n to give materials that upon reduction with sodium borohydride and subsequent hydrolysis decarboxyla

47 on was determined by chemical reactions with sodium borohydride, hydrogen peroxide, alpha-methoxy-alp

48 nts: 1-butyl-3-methylimidazolium bromide and sodium borohydride.

49 articular, the histone deacetylase inhibitor sodium butyrate (SB) may indirectly (through reduced hyp

50 Following lytic reactivation by sodium butyrate, the levels of the approximately 23- to

51 Sodium butyrate-induced differentiation of HT29 and Caco

52 We previously reported that sodium butyrate-induced differentiation of HT29 colon ca

53 The electrogenic sodium/calcium exchanger (NCX) mediates bidirectional ca

54 cytosolic Ca(2+) oscillations induced by the sodium/calcium exchanger NCX1/3 working in its reverse m

55 cyanidin-3-O-glucoside (C3G), and 20nm-sized sodium caseinate nanoparticles (NaCas) at pH 7 and pH 2

56 Exchanging the sodium cation with tetraethylammonium or didodecyldimeth

57 The epithelial sodium channel (ENaC) has an important role in regulatin

58 a downregulates the expression of epithelial sodium channel (ENaC) subunits in enterocytes (ECs) to m

59 notyping and sequencing of the voltage gated sodium channel (VGSC) gene did not detect the common L10

60 owever, expression analysis of voltage-gated sodium channel alpha subunits revealed NaV 1.7 mRNA tran

61 Sodium channel and clathrin linker 1 (SCLT1) mutations w

62 nformational cycle in a single voltage-gated sodium channel and give insight into the structural basi

63 on between age at disease onset, response to sodium channel blockers and the functional properties of

64 r trigeminal neuralgia is treatment with the sodium channel blockers carbamazepine and oxcarbazepine,

65 ate onset epilepsies and lack of response to sodium channel blockers.

66 s transfected with siRNAs against epithelial sodium channel ENaCalpha or ENaCdelta compared to untran

67 n associated with mutations in voltage-gated sodium channel genes.

68 The Nav1.1 voltage-gated sodium channel is a critical contributor to excitability

69 xhibit high levels of selectivity over other sodium channel isoforms.

70 ABSTRACT: Voltage-gated sodium channel NaV 1.7 is required for acute and inflamm

71 SCN2A gene that disrupt the encoded neuronal sodium channel NaV1.2 are important risk factors for aut

72 in SCN2A, a gene encoding the voltage-gated sodium channel Nav1.2, have been associated with a spect

73 expression and function of the voltage-gated sodium channel Nav1.7 are increased in a preclinical mod

74 Specifically, voltage-gated sodium channel subtype NaV 1.7 is required for sensing a

75 in which the alpha-subunit of the epithelial sodium channel was conditionally deleted in taste buds (

76 clearly demonstrated that the voltage-gated sodium channel, Nav1.7, is critical to pain sensation in

77 uctural basis for state-dependent binding of sodium channel-blocking drugs.

78 vertebrates, target conserved voltage-gated sodium channels (NaV) of nerve and muscle, causing paral

79 Voltage-gated sodium channels (Navs) play crucial roles in excitable c

80 pagated by a single isoform of voltage gated sodium channels - SCN5A.

81 hwann cells, such as clustered voltage-gated sodium channels at the node of Ranvier and Shaker-type p

82 of the soma: the voltage-gated potassium and sodium channels Kv1.4 and Nav1.6 and the glycoprotein CD

83 lity, and that the first domain of all three sodium channels plays a role in determining the rate at

84 Calcium (Cav1 and Cav2) and sodium channels possess homologous CaM-binding motifs, k

85 native splicing also changes the activity of sodium channels, and while it is highly conserved, it is

86 selectively to the slow-inactivated state of sodium channels, in contrast to drugs like carbamazepine

87 separation as a compliment or alternative to sodium channels.

88 ntry through NMDA receptors or voltage-gated sodium channels.

89 resembling the properties of F1.Q54 neuronal sodium channels.

90 otoxin resistance through point mutations in sodium channels.

91 cerol, guanidine hydrochloride (GdnHCl), and sodium chloride (NaCl) added.

92 lent electrolytes [potassium chloride (KCl), sodium chloride (NaCl)], 2:1 electrolytes [magnesium chl

93 1.26% sodium bicarbonate or intravenous 0.9% sodium chloride and 5 days of oral acetylcysteine or ora

94 ater and DOCA provided with DOCA pellets and sodium chloride drinking water.

95 sing sodium bicarbonate rather than isotonic sodium chloride for preventing contrast-associated acute

96 dification of natural waters with millimolar sodium chloride level (freshwater, drinking water, and a

97 lets of oleic acid/sodium oleate mixtures in sodium chloride solution are analysed by simultaneous sy

98 unit alternated monthly between saline (0.9% sodium chloride) and balanced crystalloids (lactated Rin

99 identified eight loci associated with plasma sodium concentration at P<5.0 x 10(-6) Of these, rs9980

100 her a high-salt diet, as measured by urinary sodium concentration, is associated with faster conversi

101 ic membrane with creatininium, potassium and sodium confirms the strong selective interactions betwee

102 sodium content in humans, we determined skin sodium content at the level of the calf in 99 patients w

103 ently developed for the assessment of tissue sodium content in humans, we determined skin sodium cont

104 f toppings masked the effect of lowering the sodium content, allowing to increase the reduction level

105 Skin sodium content, but not total body overhydration, correl

106 lute carrier family 13 member 5 (SLC13A5), a sodium-coupled citrate transporter, plays a key role in

107 PA101 is a novel formulation of sodium cromoglicate delivered via a high-efficiency eFlo

108 a marked increase in both the peak and late sodium currents leading to prolongation of the action po

109 of the supernatant with phosphate buffer and sodium cyanide for derivatization in alkaline conditions

110 f absorbance in the test tube containing 10% sodium deoxycholate versus a blank control tube, after i

111 tide 1, and the BA transport systems, apical sodium-dependent bile acid transporter and Na(+) -tauroc

112 The sodium-dependent NADH dehydrogenase (Na(+)-NQR) is a key

113 the renal tubule by the action of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-I

114 Interestingly, in the absence of sodium-dependent Pi transport activity, the PiT1-PiT2 he

115 tegral membrane proteins responsible for the sodium-dependent reuptake of small-molecule neurotransmi

116 Following sodium depletion, and in the absence of either sucrose o

117 ly seek out salt when under a novel state of sodium deprivation, is a classic example of how homeosta

118 our chlorine solutions (sodium hypochlorite, sodium dichloroisocyanurate, high-test hypochlorite, and

119 Overall, chloride and its interaction with sodium did not add clinically relevant prognostic inform

120 Sodium diisopropylamide (NaDA)-mediated metalations of a

121 cellar liquid chromatography (MLC) employing sodium dodecyl sulfate (SDS) as surfactant, were determi

122 pane] radical initiator, of linoleic acid in sodium dodecyl sulfate micelles, have been determined in

123 Sodium dodecyl sulfate polyacrylamide gel electrophoresi

124 unodetection in leaf extract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresi

125 In this work, the stabilising effect of sodium dodecyl sulphate (SDS) micelles on pH-induced col

126 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophores

127 self-assembly of vinylic-C60-monoadduct with sodium dodecylsulfate micellar system, in the presence o

128 ad to hypertension, which appears to rely on sodium-driven neurogenic mechanisms.

129 onic regeneration in a mouse dextran sulfate sodium (DSS) colitis model, and we demonstrate that the

130 , SPF and GF mice were given dextran sulfate sodium (DSS) to induce colitis.

131 biotic cocktail (ATB) and/or dextran sulfate sodium (DSS).

132 crolimus (Tac), enteric-coated mycophenolate sodium (EC-MPS) and sirolimus (SRL) in oral dosage forms

133 Furthermore, sodium enhanced [(3)H]rauwolscine's interactions with th

134 ble N-[(2-benzoyloxy-1-tosyl)ethyl]urea with sodium enolates of beta-oxoesters or 1,3-diketones, foll

135 reshold electrical stimulation, postsynaptic sodium entry is almost entirely through AMPA receptors w

136 The objective was to evaluate replacement of sodium erythorbate with a natural antioxidant (oregano e

137 ed, including control (without antioxidant), sodium erythorbate, and three concentrations of oregano

138 e, alcohol consumption, smoking, and urinary sodium excretion levels measured at recruitment.

139 nt, each 1000-mg difference in usual 24-hour sodium excretion was directly associated with systolic (

140 ich is usually assessed by measuring urinary sodium excretion, has been inconsistently linked with le

141 ients with HF yields meaningful increases in sodium exit from the proximal tubule/loop of Henle.

142 ice were orally administered dextran sulfate sodium for 7 days and were compared with wild-type mice.

143 for the beneficial cardiovascular effect of sodium glucose co-transporter 2 inhibitors in T2DM.

144 Inhibiting glucose reabsorption by sodium glucose co-transporter proteins (SGLTs) in the ki

145 t-term trials, short-term treatment with the sodium-glucose co-transporter-2 (SGLT2) inhibitor empagl

146 Sodium-glucose co-transporters 2 (SGLT-2) inhibitors hav

147 acute administration of luseogliflozin, the sodium-glucose cotransporter 2 (SGLT2) inhibitor, on ren

148 Carbasugar sodium-glucose cotransporter 2 (SGLT2) inhibitors are hi

149 Lowering blood glucose using a sodium-glucose cotransporter 2 inhibitor (dapagliflozin)

150 Empagliflozin, a sodium-glucose cotransporter 2 inhibitor, reduced cardio

151 his study was to examine the effect of renal sodium-glucose cotransporter inhibition with empaglifloz

152 ectrical activity either by the electrogenic sodium-glucose cotransporter SGLT1, or by closure of ATP

153 Dapagliflozin is a sodium-glucose cotransporter-2 inhibitor approved for th

154 rachomatis respiratory chain could produce a sodium gradient that may sustain the energetic demands r

155 um transport controlled by the transmembrane sodium gradient.

156 Both chloride and sodium had a nonlinear association with the studied outc

157 compartment, have variable effects on renal sodium handling and the hypertensive response, accruing

158 immunity involvement in the kidney defect in sodium handling and the pathogenesis of salt-sensitive h

159 e immune system can play surprising roles in sodium homeostasis, such that the study of inflammatory

160 renal blood flow, higher abundance of renal sodium-hydrogen antiporter 3, and lower lithium clearanc

161 Activation of the sodium-hydrogen exchanger in the heart and vasculature (

162 We examined whether the scaffolding protein sodium-hydrogen exchanger regulatory factor 1 (NHERF1) i

163 Titration of indole with sodium hydroxide or ammonium hydroxide yields an increas

164 Sodium hypochlorite (dilute bleach) offers effective dis

165 reduction was even more efficient when using sodium hypochlorite solutions.

166 Damage to tonometer prisms can be caused by sodium hypochlorite, 70% isopropyl alcohol, 3% hydrogen

167 red the efficacy of four chlorine solutions (sodium hypochlorite, sodium dichloroisocyanurate, high-t

168 cient mice failed to resolve dextran sulfate sodium-induced colonic inflammation as a result of defec

169 chanistically, TCR stimulation induced rapid sodium influx in Napa(hyh/hyh) CD4 T cells, which reduce

170 To enhance selectivity and capacity via sodium insertion reactions, carbon aerogel electrodes we

171 s method to estimate the association between sodium intake and 38 metabolic pathways or groups.Six pa

172 (Dietary Patterns, Sodium Intake and Blood Pressure [DASH-Sodium]; NCT00000

173 ted surrogate markers [blood pressure within sodium intake and cardiovascular disease (CVD) context a

174 The combination of reduced sodium intake and the DASH diet lowered SBP throughout t

175 nsion was positively related to (calibrated) sodium intake and to the ratio of sodium to potassium.

176 or groups.Six pathways were associated with sodium intake at a Bonferroni-corrected threshold of 0.0

177 r understanding of the biological effects of sodium intake beyond blood pressure.The DASH-Sodium Tria

178 DDRs, SFFQ responses tended to underestimate sodium intake but overestimate intakes of energy, macron

179 Reducing sodium intake can decrease blood pressure and prevent hy

180 repared foods, a significant reduction of US sodium intake could occur.

181 al outcome changed up to 85% with the use of sodium intake estimations from short-term (1-year) and l

182 A decrease in sodium intake has been shown to lower blood pressure, bu

183 e association for the top-ranked metabolites.Sodium intake is associated with changes in circulating

184 Because excess sodium intake is associated with many health problems, i

185 High sodium intake is known to increase blood pressure and is

186 demiologic studies.We examined the effect of sodium intake on metabolites within the DASH (Dietary Ap

187 The optimal level of sodium intake remains controversial.

188 of all subjects switched between tertiles of sodium intake when the 1-, 5-, or 15-year average was us

189 bjects had a >0.8-g (>34-mmol) difference in sodium intake with long-term estimations.

190 in different estimations of an individual's sodium intake, whereas population averages remained simi

191 Sodium intake, which is usually assessed by measuring ur

192 between each log-transformed metabolite and sodium intake.

193 d and critical consideration of chloride and sodium interplay.

194 Anion transport by the human sodium-iodide symporter (hNIS) is an established target

195 novel PET radioligand for imaging the human sodium/iodide symporter (hNIS).

196 Sodium ion batteries are being considered as an alternat

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

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

199 Potentiometric sodium ion sensors were developed using a polyvinyl chlo

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

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

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

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

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

205 Conversely, activating the pump with the sodium ionophore monensin decreased burst frequency.

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

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

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

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

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

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

212 ncomycin plus piperacillin sodium/tazobactam sodium is associated with a higher risk of acute kidney

213 pound Na2IrO3 by a topotactic reaction where sodium is exchanged with copper under mild conditions.

214 s reduced to (64)Cu(I) with the existence of sodium L-ascorbate, DL-Dithiothreitol or cysteine.

215 A detailed comparison of sodium, lactate and cortisol from saliva is reported, de

216 with hard water had significantly increased sodium lauryl sulfate deposits.

217 Initial corrected sodium level of 145 mEq/L or greater (compared with 135-

218 nd BP when participants experienced changing sodium levels in water, switched from "conventional" pon

219 d rainwater harvesting] that aimed to reduce sodium levels, or experienced a combination of these cha

220 However, MAR did not consistently lower sodium levels.

221 (2 mug/d) or PLAC, each combined with a low-sodium (LS) or regular sodium (RS) diet.

222 Using (23)sodium-magnetic resonance imaging, a technique recently

223 Relative to a single baseline 24-hour sodium measurement, the use of subsequent 24-hour urine

224 A sodium metal anode protected by an ion-rich polymeric me

225 arbon batteries free from the unsafe lithium/sodium metals, and hence eliminates the long-standing sa

226 in determining eligibility for methotrexate sodium (MTX) therapy, monitor for the development of MTX

227 magnetic resonance imaging (MRI) phantom for sodium multi quantum (MQ) spectroscopy.

228 Seven SGLT isoforms (SGLT1 to 6 and sodium-myoinositol cotransporter-1, SMIT1) are known, al

229 electric field coupling, intercellular cleft sodium nanodomains, and LQT3-associated mutant channels,

230 This voltage-gated sodium (Nav) channel subtype also plays an important rol

231 erns, Sodium Intake and Blood Pressure [DASH-Sodium]; NCT00000608).

232 Treatment with PE (10(-5) m) or sodium nitroprusside (10(-5) m) induced a significant in

233 on in response to acetylcholine (P=0.01) and sodium nitroprusside (P=0.004).

234 Acoustically trapped droplets of oleic acid/sodium oleate mixtures in sodium chloride solution are a

235 gnesium and calcium permeability and reduced sodium permeability in the thick ascending limb (TAL), l

236 and phenotypic consequences of non-specific sodium permeation via calcium channels remain unknown.

237 strategies: (i) coordination of substituted sodium phenolates to form the substrate-bound O(MeAN)-RP

238 n of recombinant cKL downregulated the renal sodium-phosphate cotransporter Npt2a in alphaKL-null mic

239 arthropod predators encoding insect specific sodium, potassium and calcium channel blockers for their

240 vasoconstrictor that inhibits the membranous sodium-potassium ATPase pump across cell types and can c

241 fer between NADH and ubiquinone (UQ) to pump sodium, producing a gradient that sustains many essentia

242 Here we demonstrate that changes in sodium pump activity regulate locomotor networks in the

243 We describe a sodium pump-mediated afterhyperpolarization in spinal ne

244 evelop DR due to compensatory distal tubular sodium reabsorption, but whether this translates to huma

245 ostructural, textural, and sensory impact of sodium reduction and its partial replacement by potassiu

246 obiotic survival were observed; however, the sodium reduction and the addition of flavor enhancers di

247 The sodium reduction and the supplementation of Prato cheese

248 Bs)] and nutrients (e.g., total calories and sodium).Regardless of SNAP status, households had low me

249 .6%-75.7%) of the estimated diuretic-induced sodium release did not undergo distal reabsorption.

250 ly shifted the electrode potential window of sodium removal, reducing parasitic oxygen reduction and

251 trast, when participants were assessed under sodium-restricted conditions, physiological stimulation

252 or activator paricalcitol (PARI) and dietary sodium restriction on residual albuminuria in CKD.

253 However, whether T cells contribute to renal sodium retention and salt-sensitive hypertension is unkn

254 h combined with a low-sodium (LS) or regular sodium (RS) diet.

255 In proteomics, dodecyl sulfate (DS(-)) as sodium salt is commonly used in protein solubilization p

256 Within a total residence time of 9 min, the sodium salt of ciprofloxacin was prepared from simple bu

257 t disruption of the afferent taste signal to sodium salts disrupts the normal age-dependent "pruning"

258 can be activated by halide abstraction with sodium salts, with the resulting catalyst [kappa(5) -((1

259 ition label information (e.g., serving size, sodium, saturated fat, trans fat) for 1032 infant and to

260 1), higher Model for End-Stage Liver Disease Sodium scores ( P < .001), higher Child-Turcotte-Pugh sc

261 A series of sodium selective membranes with magnetic nano-inclusions

262 ) have been developed, and the corresponding sodium selective sensors were obtained for the first tim

263 tent with myrosinase activity below 3.5-mmol sodium selenate.

264 ickpea sprouts that were treated with a high sodium selenite content (2mg/100g seeds).

265 ying Health Canada benchmarks.If established sodium standards are applied to commercially processed a

266 Dextran sodium sulfate (DSS) and Citrobacter rodentium colitis (

267 alities after oral administration of dextran sodium sulfate (DSS).

268 ults were found when 0.5g mussel shell, 0.5g sodium sulfate and 5mL ethanol were used.

269 colon into the lymphatic system in a dextran sodium sulfate mediated model of inflammatory bowel dise

270 In response to dextran sodium sulfate, colonic infiltration of neutrophils and

271 Dextran sodium sulfate-induced colitis model was established in

272 rfering (si)RNA to C57BL/6 mice with dextran sodium sulfate-induced colitis.

273 tion of substituted alpha-methylstyrenes and sodium sulfinates (RSO2Na) in MeCN with good to excellen

274 aminosulfonylation of terminal alkynes with sodium sulfinates and TMSN3 is reported.

275 sulfonamides can be readily transformed into sodium sulfonates, sulfonate esters, and sulfonamides, a

276 sions stabilized with the surfactant dioctyl sodium sulfosuccinate (AOT).

277 porter (DAT) belongs to the neurotransmitter:sodium symporter (NSS) family of membrane proteins that

278 Neurotransmitter:sodium symporters (NSSs) are integral membrane proteins

279 pecific host factors like the receptor human sodium taurocholate cotransporting polypeptide (hNTCP).

280 lectrolyte containing gamma-cyclodextrin and sodium taurocholate micelles.

281 expression of the HBV entry receptor, human sodium-taurocholate cotransporting polypeptide (hNTCP),

282 mbination of IV vancomycin plus piperacillin sodium/tazobactam sodium is associated with a higher ris

283 th sulfur atoms in the carboxylate groups of sodium terephthalate which improves electron delocalizat

284 ns why KO(t)Bu is an active catalyst whereas sodium tert-butoxide and lithium tert-butoxide are not,

285 The primary aim of this study was to assess sodium thiosulfate for prevention of cisplatin-induced h

286 (117 [66%] of 177 participant cycles in the sodium thiosulfate group vs 145 [65%] of 223 in the cont

287 etry were randomly assigned (1:1) to receive sodium thiosulfate or observation (control group) in add

288 alibrated) sodium intake and to the ratio of sodium to potassium.

289 d estimates were a function of self-reported sodium-to-potassium ratio from a food frequency question

290 mated hazard ratio for a 20% increase in the sodium-to-potassium ratio was 1.13 (95% confidence inter

291 hydrotropic solution of highly concentrated sodium tosylate (NaOTs) can be used as a recyclable medi

292 nstrated by the corresponding alterations of sodium TQ/SQ MR signals.

293 Distal sodium transport is a final step in the regulation of bl

294 serve significant changes in other water- or sodium-transporting proteins in the gene-modified mice.

295 sodium intake beyond blood pressure.The DASH-Sodium Trial randomly assigned individuals to either the

296 etary Approaches to Stop Hypertension Trial)-Sodium Trial to further our understanding of the biologi

297 The utility of sodium triflate in facilitating this reaction is two-fol

298 Oligomeric micelles from sodium undecylenate (oSUD) were chemisorbed to magnetic

299 delocalization, electrical conductivity and sodium uptake capacity.

300 Azathioprine sodium use was observed more frequently in cases (odds r

301 h collected over the course of 1 y, ICCs for sodium were 0.32 in the NHS and 0.34 in the NHSII.

302 creatinine fall and fractional excretion of sodium were measured during perfusion.