ライフサイエンスコーパス: bicarbonate

1 ding is strongly enhanced by the presence of bicarbonate.

2 annel for small anions, such as chloride and bicarbonate.

3 eature of this system: ROS-GC is a sensor of bicarbonate.

4 bility and recovery of Ce in the presence of bicarbonate.

5 atalyzing the oxidation of formate to H2 and bicarbonate.

6 ate of decline of serum hematocrit and serum bicarbonate.

7 on of the carboxylate and subsequent loss of bicarbonate.

8 iobium-tantalum bearing minerals with sodium bicarbonate.

9 agnostic criteria to distinguish the role of bicarbonate.

10 m, and, following the final exposure, higher bicarbonate.

11 e- to 20-fold) compared to defects caused by bicarbonate.

12 ensitivity of ToxT to its positive effector, bicarbonate.

13 , and completely overcome by the addition of bicarbonate.

14 nism for the enhancement of ToxT activity by bicarbonate.

15 degradation in microcosms amended with 10 mM bicarbonate.

16 ated more pyruvate conversion to lactate and bicarbonate.

17 creased pancreatic and biliary fluid rich in bicarbonate.

18 rganic cofactor biotin for the activation of bicarbonate.

19 binding site for the physiological activator bicarbonate.

20 pidly the interconversion of aqueous CO2 and bicarbonate.

21 oteins, whereas sAC is uniquely activated by bicarbonate.

22 tural abundance, in inorganic carbonates and bicarbonates.

23 vate ratio but had no effect on the [1-(13)C]bicarbonate + (13)CO2:[1-(13)C]pyruvate ratio, an index

24 vestigational product administered in sodium bicarbonate 15 minutes after each meal.

25 74g.L(-1)), hydrogen peroxide (21.0g.L(-1)), bicarbonate (4.0g.L(-1)), carbonate (4.0g.L(-1)), chlori

26 s evidenced by significant changes in [(13)C]bicarbonate (-48%), [1-(13)C]acetylcarnitine (+113%), an

27 extracellular pH with 1 mm HEPES, removal of bicarbonate abolished feedback.

28 und that AE2 deficiency led to intracellular bicarbonate accumulation and increased expression and ac

29 by facilitating the exchange of chloride and bicarbonate across the plasma membrane of erythrocytes.

30 ion with 0.9% sodium chloride or 1.4% sodium bicarbonate administered with the same infusion protocol

31 Serum magnesium, bicarbonate, albumin, and phosphate levels were the main

32 rove the observed trend via reduced cellular bicarbonate allocation to calcification.

33 icrobial fuel cells (MFCs) by using ammonium bicarbonate (AmB) solutions in multiple RED cell pair st

34 There was no interaction between sodium bicarbonate and acetylcysteine with respect to the prima

35 ferent from those produced in the absence of bicarbonate and are most likely specific for simian SOD1

36 However, feeding the bacterium (13)C-bicarbonate and cellobiose followed by NMR analysis show

37 ed evidence on the association between serum bicarbonate and clinical outcomes.

38 trations of inorganic forms of carbon (i.e., bicarbonate and CO2) in order to improve the efficiency

39 carboxysomes play key roles in accumulating bicarbonate and CO2, but other regulatory elements of ca

40 de surface through rapid equilibrium between bicarbonate and dissolved CO2.

41 change of sulfate or oxalate for chloride or bicarbonate and electroneutral chloride:bicarbonate exch

42 he produced gas, a mixture of ethanolaminium bicarbonate and ethanolamine bisulphide is also produced

43 ttack of the carbamic acid, and formation of bicarbonate and MNPZ.

44 extracted from four agricultural soils by Na-bicarbonate and Na-pyrophosphate, by two complementary a

45 Intravenous sodium bicarbonate and oral acetylcysteine are widely used to p

46 trophic for its energy source and using both bicarbonate and organic matter as carbon sources.

47 Serum bicarbonate and pH decreased.

48 ed mode chromatography with aqueous ammonium bicarbonate and pyridine buffer solutions as mobile phas

49 s with the observed zero-order dependence in bicarbonate and simulated interfacial concentration grad

50 zed to receive tOPV with or without a sodium bicarbonate and sodium citrate buffer at age 6, 10, and

51 effective complexation of chloride, nitrate, bicarbonate and sulfate anions via hydrogen bonding.

52 ined as the difference between the converted bicarbonate and the initial carbonate concentration.

53 applied to soluble inorganic carbonates and bicarbonates and then extended to insoluble carbonates b

54 was 115 for [1-(13)C]pyruvate, 56 for (13)C-bicarbonate, and 53 for [1-(13)C]lactate.

55 in vitro by incubation of UreG with nickel, bicarbonate, and GTP.

56 use the equilibrium between carbon dioxide, bicarbonate, and protons to buffer their pH.

57 h a continuous flow of (13)C-enriched sodium bicarbonate, and the sodium persulfate oxidation reactio

58 growth in media containing glucose and CO(2)/bicarbonate, and there is a positive correlation between

59 A three-variable model of IL-8, bicarbonate, and tumor necrosis factor receptor-1 accura

60 least 4-fold lower after reaction with 10 mM bicarbonate ( approximately pH 8.3).

61 ined the (13)C/(12)C ratio of carbonates and bicarbonates ( approximately 50-100 mg) with a precision

62 o tricarboxylic acid cycle intermediates and bicarbonate are declining.

63 ntrations of ammonium phosphate and ammonium bicarbonate are used to extract bone proteins.

64 l solvent mixture, and tetra-n-butylammonium bicarbonate as a phase-transfer agent.

65 ts within the small intestine using bile and bicarbonate as chemical cues and responds by modulating

66 ion was carried out using water and ammonium bicarbonate as mobile phase in gradient mode.

67 ATP-dependent carboxylation of biotin, using bicarbonate as the CO(2) donor.

68 can hydrogenate CO2 to formate in water with bicarbonate as the only added reagent.

69 the digests were eluted with 200 mM ammonium bicarbonate at pH 8.2 for CZE-MS/MS analysis using 1 M a

70 be a unique type of PII protein that senses bicarbonate availability, consistent with its apparent g

71 kinetic properties might limit intracellular bicarbonate availability.

72 This chamber is immersed in a container of a bicarbonate-based physiological buffer that mimics the S

73 ery of oil bodies from rapeseed using sodium bicarbonate-based soaking and grinding media (pH 9.5) wa

74 In bicarbonate-bearing matrices, the fractionation depended

75 1) the presence of amines and water leads to bicarbonate being present and/or (2) the multiple types

76 P=0.003), sodium (beta=0.101; P=0.006), and bicarbonate (beta=0.094; P=0.009) were associated with h

77 g; P = .25), although daily changes of serum bicarbonate (between-group difference, -0.8 mEq/L; 95% C

78 ansporter, permeable to Na(+), H(+) (OH(-)), bicarbonate, borate, and NH4 (+).

79 In VSCTA-SAX, the use of ammonium bicarbonate buffer for elution improves resolution throu

80 of viral infection fibrils formed in sodium bicarbonate buffer remain stable over time, but semen-de

81 changed by using 40 mm HEPES in addition to bicarbonate buffer.

82 racellular fluid pH under OA by accumulating bicarbonate but exhibited a slight alkalosis in response

83 and SbtA, where BicA has a low affinity for bicarbonate but high flux rate, and SbtA has a high affi

84 The effect is not limited to carbonate/bicarbonate, but is extendable to a series of ions.

85 Carbonate/bicarbonate can also be sensitively detected.

86 e Regulator (CFTR) is the secretory chloride/bicarbonate channel in airways and intestine that is act

87 manner encodes an epithelial transporter of bicarbonate, chloride, and thiocyanate, named pendrin, t

88 esence of nitrate and significant amounts of bicarbonate (close to 2 mM), 5-fluorouracil was rapidly

89 K activity, and both were reduced by sodium bicarbonate co-transporter (P </= 0.0001) and carbonic a

90 on, they modulate the activity of the sodium-bicarbonate co-transporter, leading to a hyperpolarizati

91 hydrogen ion exporters, particularly sodium bicarbonate co-transporters and carbonic anhydrases, whi

92 n, sAC acts as a physiological sensor for pH/bicarbonate/CO2, and it has been implicated as a therape

93 iron, as iron chelation combined with sodium bicarbonate completely protected endothelial cells from

94 Initial bicarbonate concentration ( approximately 1 mM) was obta

95 uggesting that NBCe1 may operate over a wide bicarbonate concentration in these cells.

96 gallbladder containing dilute bile with high bicarbonate concentration.

97 r prevalence of vasopressor use, lower serum bicarbonate concentrations, and a higher prevalence of s

98 substantially above seawater values and that bicarbonate contributes a significant amount of the DIC

99 The electrogenic Na(+)/bicarbonate cotransporter (NBCe1) of the Slc4 gene famil

100 out of astrocytes by the electrogenic sodium bicarbonate cotransporter (NBCe1) played a crucial role

101 The electrogenic sodium bicarbonate cotransporter NBCe1 (SLC4A4) is a robust reg

102 SLC4A4 encodes the electrogenic sodium bicarbonate cotransporter NBCe1, a membrane protein that

103 c carbonic anhydrases, the basolateral Na(+) bicarbonate cotransporter Nbce1, and the basolateral ani

104 des the widely-expressed electrogenic sodium bicarbonate cotransporter NBCe1, results in the bicarbon

105 heterologously expressed electrogenic Na(+)/bicarbonate cotransporter NBCe1-A in an excised macropat

106 racterize Fe plaque using dithionite-citrate-bicarbonate (DCB) extraction and elemental analysis reve

107 ims of this work were to examine whether the bicarbonate-dependent peroxidase activity of hSOD1 (hSOD

108 The bicarbonate-dependent peroxidase activity of hSOD1 cause

109 Although bicarbonate-dependent SACY activity requires Ca(2+), bas

110 Concern has arisen regarding high-bicarbonate dialysate and dialysis-induced alkalemia, bu

111 estinal epithelium by promoting chloride and bicarbonate efflux into the lumen through activation of

112 We introduce a novel carbonate-bicarbonate eluent generation system in which CO2 is int

113 Demonstrably purer carbonate-bicarbonate eluent systems are possible compared to manu

114 ible compared to manually prepared carbonate-bicarbonate eluents and with considerable savings in tim

115 When applied to retinal photoreceptors, bicarbonate enhanced the circulating current, decreased

116 We propose that bicarbonate enhances the rate of CO production on Au by

117 racted with Na-pyrophosphate but not with Na-bicarbonate, except for one soil.

118 Anion exchanger-1 (AE1) mediates chloride-bicarbonate exchange across the plasma membranes of eryt

119 e or bicarbonate and electroneutral chloride:bicarbonate exchange.

120 (ENaC) and the pendrin/Na(+)-driven chloride/bicarbonate exchanger (pendrin/NDCBE) transport system w

121 Bile flow, bicarbonate excretion, and total bile acids were measure

122 In contrast, bicarbonate exerted an effect when applied to the inner

123 in ToxT binding affinity in the presence of bicarbonate explains the elevated level of virulence gen

124 Carbamates and bicarbonate fall within a small (13)C chemical shift ran

125 changes in HC membrane voltage also require bicarbonate flux across the HC membrane.

126 focused on use of N-acetylcysteine or sodium bicarbonate for the prevention of contrast-induced AKI a

127 Intracellular bicarbonate generated by luminal H(+) secretion is remov

128 llected main peak in pH 9 buffer or ammonium bicarbonate generated chromatograms that are highly simi

129 saline group and 53 patients (35.1%) in the bicarbonate group (absolute risk difference, -1.8%; 95%

130 Patients randomized to the bicarbonate group (n = 151) showed a higher urinary pH a

131 in 110 of 2511 patients (4.4%) in the sodium bicarbonate group as compared with 116 of 2482 (4.7%) in

132 99) were also similar between the saline and bicarbonate groups, respectively.

133 (VI) are in the following order: phosphate > bicarbonate > borate.

134 sulfate > hydrogen phosphate > thiocyanate > bicarbonate > chloride > formate approximately bromide >

135 change of hyperpolarized (13)C label between bicarbonate (H(13)CO3(-)) and carbon dioxide ((13)CO2),

136 oncrete (or those lacking adsorbed carbonate/bicarbonate) H2O2 activation for CWA decontamination is

137 ous acid production, and serum potassium and bicarbonate), hazard ratios of the composite outcome of

138 Chloride (Cl(-) ) and bicarbonate (HCO3 (-) ) are two major anions and their p

139 interconversion of carbon dioxide (CO2) and bicarbonate (HCO3 (-)).

140 Bicarbonate (HCO3(-)) is an abundant anion that regulate

141 te (RnNCOO(-)), carbamic acid (RnNCOOH), and bicarbonate (HCO3(-)) moieties.

142 Removal of bicarbonate (HCO3(-)) shifts the Em from approximately -

143 ifferent concentrations (1, 3, and 10 mM) of bicarbonate (HCO3(-)) under light and dark conditions.

144 rbon dioxide gas (CO2) or its hydrated form, bicarbonate (HCO3(-)), into target molecules.

145 ong these, only sAC is directly activated by bicarbonate (HCO3(-)); it thereby serves as a cellular s

146 together with elevated terrestrial export of bicarbonate (HCO3(-); 3.6 mueq L(-1) yr(-1)).

147 ese data are consistent with the presence of bicarbonate, HCO3(-), since it is commonly observed at a

148 e, chloride, iodide, cyanide, pyrophosphate, bicarbonate, hydrosulphide, peroxynitrite, hypochlorite

149 ne and sulfate and production of sulfide and bicarbonate, (ii) methane loss coupled to production of

150 tomic analysis of CB1190 cells grown with H2/bicarbonate implicated the Calvin-Benson-Bassham (CBB) c

151 t that disrupting pH homeostasis by blocking bicarbonate import might broadly relieve the common resi

152 hich is then exchanged for urea and ammonium bicarbonate in a centrifugal filter, before treating wit

153 H regulator sensitive for acid that secretes bicarbonate in exchange for chloride.

154 e-mediated process, particularly the role of bicarbonate in increasing CO2 reduction rates, is still

155 the transmembrane transport of chloride and bicarbonate in model phospholipid liposomes, induce acid

156 planation was confirmed by administration of bicarbonate in the drinking water, which elevated tumor

157 Therefore, the presence of bicarbonates in the environment stimulates the photodeco

158 Many bicarbonate-incorporating carboxylases rely on the organ

159 conversion of (13)C1-pyruvate to lactate and bicarbonate, indicating active glycolytic and OxPhos met

160 ident in all but slac1 and ost1 mutants, the bicarbonate-induced activation of S-type anion channels

161 Lack of MPK12 impaired bicarbonate-induced activation of S-type anion channels.

162 uscular blockade agents or nitric oxide use, bicarbonate infusion, cardiac arrest, PaCO2, and peak in

163 ents of colored and alkaline waters (NOM and bicarbonate) inhibited the catalytic effects of Fe(VI) d

164 osphate in the mitochondria from ammonia and bicarbonate, initiating nitrogen disposal.

165 Although bicarbonate injection enhanced local rates near the inje

166 und that in all three species, CFTR secreted bicarbonate into airway surface liquid.

167 ating machinery to transport Ca(2+), Pi, and bicarbonate into maturation-stage enamel.

168 eloblasts express Dra and Slc26a6 to secrete bicarbonate into the enamel space in exchange for Cl(-).

169 meloblasts suggests that these cells secrete bicarbonates into the forming enamel, but it is unknown

170 ngle components of pancreatic juice, such as bicarbonate ions and calcium carbonate crystals, induce

171 However, in the presence of bicarbonate ions, a significantly higher photoreduction

172 cal species such as hydroxide, carbonate and bicarbonate ions.

173 MR showed that the formation of carbonate or bicarbonate is excluded.

174 We show that bicarbonate is neither a general acid nor a reaction par

175 al concentration gradients, we conclude that bicarbonate is not a general acid cocatalyst.

176 In contrast, in cases where bicarbonate is present at a higher concentration, aqueou

177 Bicarbonate is taken up into the V. cholerae cell, where

178 Because ammonium bicarbonate is used, the samples can be evaporated rathe

179 H2O2 activation by surface-bound carbonates/bicarbonates (known H2O2 activators for CWA decontaminat

180 cilitating the measurement of anions such as bicarbonate, lactate, citrate and urate in a variety of

181 After adjusting for bicarbonate less than 20 mEq/L, lactate concentration, r

182 tion in multivariate analysis included serum bicarbonates less than 20 mM (odds ratio, 4.9 [95% CI, 1

183 ltinomial logistic regression model, a serum bicarbonate level less than 10 mEq/L (compared with >/=1

184 Both high and low serum bicarbonate levels associate with an increased risk of m

185 could identify patients with CKD and normal bicarbonate levels who might benefit from alkali before

186 Elevating intracellular bicarbonate levels within HCs prevented this loss of fee

187 Oxidation of D2:(244)Y, which is a bicarbonate ligand for the nonheme iron, induces the pro

188 Notably, neutralizing tumor acidity with bicarbonate monotherapy impaired the growth of some canc

189 gimes (1) N-acetylcysteine (NAC), (2) sodium bicarbonate (NaHCO3) infusion, (3) NAC in combination wi

190 line, statin, N-acetylcysteine (NAC), sodium bicarbonate (NaHCO3), NAC+NaHCO3, ascorbic acid, xanthin

191 remote basic site in the anion namely, OH of bicarbonate, NH of prolinate, and activated water in the

192 Ni(cyclam)(CO)](+), and a Ni(II) coordinated bicarbonate, [Ni(cyclam)(CO2OH)](+).

193 etylsalicylic acid, N-acetylcysteine, sodium bicarbonate, off-pump coronary revascularization, goal-d

194 A third species that is either bicarbonate or a second carbamate is evident from bimoda

195 cent studies indicate, however, that neither bicarbonate or borate is a substrate.

196 iography to receive intravenous 1.26% sodium bicarbonate or intravenous 0.9% sodium chloride and 5 da

197 radical, and did not occur in the absence of bicarbonate or with enzymes that lack the Trp(32) residu

198 , there was no benefit of intravenous sodium bicarbonate over intravenous sodium chloride or of oral

199 iated with the decision to administer sodium bicarbonate (p<0.0001).

200 rlier acid-base indicator of risk than serum bicarbonate, particularly in patients without acidosis.

201 evidence that pore dilatation increases the bicarbonate permeability (P HC O3/ Cl ) of anion channel

202 Pore dilatation increases the bicarbonate permeability (P HC O3/ Cl ) of CFTR, ANO1 an

203 Compared to bicarbonate, phosphate (1.0 mM) has a net stabilizing ef

204 w baseline chloride was associated with high bicarbonate, poor diuretic response, less hemoconcentrat

205 ed in medians (interquartile ranges) for the bicarbonate powder after 5, 10, 15, and 20 seconds, resp

206 ical diameter open for instrumentation using bicarbonate powder and glycine powder.

207 ts with exposed root surfaces, cleaning with bicarbonate powder cannot be recommended.

208 pture, chemical conversion, and storage as a bicarbonate, predominantly as NaHCO3.

209 Paratyphi A following sodium bicarbonate pretreatment at 1 of 2 dose levels (group 1:

210 the hypothesis that impeding the reuptake of bicarbonate produced extracellularly by CA9 could exacer

211 d L-lactate, showing that CanB is crucial in bicarbonate provision for pyruvate carboxylase-mediated

212 The elusive neutral bicarbonate radical and the carbonate radical anion form

213 This marks the bicarbonate radical as the strongest known carboxylic ac

214 thermodynamic and activation parameters for bicarbonate radical dissociation, obtained from DFT comp

215 ations at the CAM-B3LYP level applied to the bicarbonate radical itself.

216 w report experimental studies for a model of bicarbonate radical, namely, methyl carbonate (methoxyca

217 The acidity of bicarbonate radicals was also examined by DFT methods.

218 DFT computations with bicarbonate radicals, solvated with up to eight water mo

219 renal function, the benefit of using sodium bicarbonate rather than isotonic sodium chloride for pre

220 To test whether hydration with bicarbonate rather than isotonic sodium chloride reduces

221 e 60 minutes after occlusion, the lactate-to-bicarbonate ratio in the AAR recovered but was still ele

222 At reperfusion, the average lactate-to-bicarbonate ratio increased in the AAR relative to that

223 These changes associated with less bicarbonate reabsorption and higher lithium clearance in

224 n with 5 mM glucose stimulates NHE3-mediated bicarbonate reabsorption.

225 Via bicarbonate regulation, sAC acts as a physiological sens

226 t release the mucus, but further addition of bicarbonate rendered the CF mucus normal, suggesting tha

227 /- 0.2 muM and 22.5 +/- 0.3 mM carbonate and bicarbonate, respectively).

228 The expression of both is controlled by the bicarbonate-responsive transcriptional regulator, AtxA.

229 mycosis, but not aspergillosis, while sodium bicarbonate reversed this susceptibility.

230 y formed by precipitation with carbonates in bicarbonate-rich environments, and their migration may b

231 mulates the exocrine pancreatic secretion of bicarbonate-rich fluid from the acinar cells of the panc

232 consisting of ethanol and FeCl2, and sodium bicarbonate (SBC) as a bubble-generating agent.

233 ITPR3 is required for bicarbonate secretion by bile ducts, and its expression

234 nd containing less chloride (suggesting more bicarbonate secretion).

235 s cellular processes, including gastric acid/bicarbonate secretion, mucus secretion, and cell migrati

236 stinal (GI) tract CFTR promotes chloride and bicarbonate secretion, playing an essential role in ion

237 In addition to reducing biliary chloride and bicarbonate secretion, up-regulation of toll-like recept

238 ked reduction in pancreatic ductal fluid and bicarbonate secretion.

239 Anion exchanger 2 (AE2), the principal bicarbonate secretor in the human biliary tree, is down-

240 that many pH-sensing systems measure pH via bicarbonate-sensing soluble adenylyl cyclase.

241 bunit Cox5a, homologue of human COX4i1, in a bicarbonate-sensitive manner.

242 lts demonstrate a surprisingly high apparent bicarbonate sensitivity mediated by NBCe1 in cortical as

243 l cyclase (sAC), an evolutionarily conserved bicarbonate sensor.

244 Because proton and bicarbonate shift concomitantly, it remained unclear whe

245 Citrate, metabolized to bicarbonate, should decrease calcium excretion by reduci

246 The appearance of (13)C-bicarbonate signal after administration of hyperpolarize

247 g of the downstream metabolites showed (13)C-bicarbonate signal mainly confined to the left ventricul

248 rized [1-(13)C]pyruvate, the resulting (13)C-bicarbonate signal was found to be 24 +/- 6% lower in th

249 is a positive correlation between the CO(2)/bicarbonate signal, AtxA activity and homomultimerizatio

250 The magnitude of both lactate and bicarbonate signals were positively correlated with the

251 molarity of medium used; the use of a sodium bicarbonate solution (pH 9.5, 0.1M) in the grinding and

252 noculum of virulent S. Typhi administered in bicarbonate solution can be performed safely using an am

253 d-naive volunteers when ingested with sodium bicarbonate solution.

254 less than 200 mV of overpotential in aqueous bicarbonate solutions.

255 N-acetylcysteine, sodium bicarbonate, statins, and ascorbic acid have been studie

256 In mutant sperm lacking the bicarbonate-stimulated SACY activity, bPAC restored moti

257 In the presence of atmospherically derived bicarbonate the formation of the bis-carbonato inner-sph

258 mediated increase in c-di-GMP is quenched by bicarbonate, the intestinal pH buffer secreted by intest

259 vant is the selectivity between chloride and bicarbonate, the major inorganic anions in biological sy

260 be inefficient conversion of gaseous CO2 to bicarbonate, the required substrate of various carboxyla

261 Furthermore, combining bicarbonate therapy with anti-CTLA-4, anti-PD1, or adopt

262 Further, we demonstrate that bicarbonate, through equilibrium exchange with dissolved

263 s blood electrolyte concentration to convert bicarbonate to CO2 before entering the membrane lung, en

264 ontrolled proton sink allowed one to convert bicarbonate to the detectable carbonate species.

265 y, showing evidence of impaired provision of bicarbonate to the four enzymes that participate in key

266 lleague's likelihood of administering sodium bicarbonate to the same patient under the same circumsta

267 injured hemisphere, while the hyperpolarized bicarbonate-to-lactate ratio was 33 +/- 8% lower in the

268 polarization of HCs also involves changes in bicarbonate transport across the HC membrane.

269 regulated, vectorial, basolateral-to-apical bicarbonate transport in polarized HAT-7 cells.

270 was recapitulated by selectively inhibiting bicarbonate transport in vitro and ex vivo.

271 A bicarbonate transport inhibitor, 4,4'-diisothiocyano-2,2

272 for NADH dehydrogenase subunit D4)/cmpA (for bicarbonate transport system substrate-binding protein A

273 ased viscosity in situ due to the absence of bicarbonate transport, explaining defective MCT that occ

274 inding protein A)/sbtA (for sodium-dependent bicarbonate transporter A): Delta4 mutant of Synechocyst

275 ransporter family with homology to the human bicarbonate transporter Band 3.

276 SLC4A10 encodes a sodium bicarbonate transporter with a brain-restricted expressi

277 rough a Na(+)/H(+) exchanger (sNHE) and/or a bicarbonate transporter, which utilizes the inward drivi

278 poxia induced the expression of at least one bicarbonate transporter.

279 Transmembrane bicarbonate transporters and carboxysomes play key roles

280 requent inductions were of the sodium-driven bicarbonate transporters SLC4A4 and SLC4A9, which rely u

281 a small-molecule inhibitor of sodium-driven bicarbonate transporters, increased apoptosis in the cel

282 AE2 creates a "bicarbonate umbrella" that protects cholangiocytes from

283 cal and isotopic equilibrium between CO2 and bicarbonate under these conditions.

284 f disparate practices with respect to sodium bicarbonate use.

285 at was not statistically significant: sodium bicarbonate versus IV saline in patients receiving low-o

286 Bicarbonate was coinjected in half of the domain to mobi

287 ion, pH, ionic strength, and the presence of bicarbonate was considered.

288 Bicarbonate was effective when applied either to the out

289 Bicarbonate was found to increase the activation of ToxT

290 The conversion of pyruvate into lactate and bicarbonate was imaged by using dedicated MR sequences a

291 arbonate cotransporter NBCe1, results in the bicarbonate-wasting disease proximal renal tubular acido

292 beled mu-(16)O(bridging-oxo) 1A(+) and (18)O-bicarbonate/water shows (1) no exchange of (18)O into th

293 ction and biliary secretion of bilirubin and bicarbonate were significantly higher after HMP, compare

294 s work identified another intestinal signal, bicarbonate, which enhances the ability of ToxT to activ

295 Increasing the luminal concentration of bicarbonate, which mimics CF transmembrane conductance r

296 active uptake of CO2 (70% contribution) and bicarbonate, while at high CO2 , cells were restricted t

297 from GTP at faster rates in the presence of bicarbonate with an ED50 of 27 mM for ROS-GC1 and 39 mM

298 )C isotope ratio in inorganic carbonates and bicarbonates with applications in different fields, such

299 ning the cold precursors THP-PSMA and sodium bicarbonate, with no further manipulation.

300 ielded the greatest improvement in PaCO2 and bicarbonate, with significant differences relative to th