ライフサイエンスコーパス: bicarbonate

1 stem to remove CO2 from blood in the form of bicarbonate.

2 y metabolized to [1-(13)C]lactate and [(13)C]bicarbonate.

3 ueous solutions of acetic acid, ammonia, and bicarbonate.

4 e of 0.96 mmol/L (0.45 to 1.47; p=0.0003) in bicarbonate.

5 consuming only water) before measurements of bicarbonate.

6 ated more pyruvate conversion to lactate and bicarbonate.

7 creased pancreatic and biliary fluid rich in bicarbonate.

8 iobium-tantalum bearing minerals with sodium bicarbonate.

9 agnostic criteria to distinguish the role of bicarbonate.

10 rganic cofactor biotin for the activation of bicarbonate.

11 binding site for the physiological activator bicarbonate.

12 pidly the interconversion of aqueous CO2 and bicarbonate.

13 oteins, whereas sAC is uniquely activated by bicarbonate.

14 ding is strongly enhanced by the presence of bicarbonate.

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

16 via a neuronal activity-dependent release of bicarbonate.

17 was completely dependent on the presence of bicarbonate.

18 tural abundance, in inorganic carbonates and bicarbonates.

19 ity interval exercise trial following either bicarbonate (0.40 g/kg) or placebo ingestion in a double

20 per 1.73 m(2)) and metabolic acidosis (serum bicarbonate 12-20 mmol/L), who had completed the 12-week

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

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

23 M-NanoSIMS) isotopic imaging to study (13) C-bicarbonate, (15) N-ammonium and (34) S-sulfate uptake.

24 albumin/creatinine (ACR) >=50 mg/g and serum bicarbonate 20-28 meq/L.

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 an anion channel that conducts chloride and bicarbonate across epithelial membranes.

30 justed odds ratio, 0.07; 95% CI, 0.06-0.08), bicarbonate (adjusted odds ratio, 2.0; 95% CI, 1.8-2.3),

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

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

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

34 ous electrolytes (ammonium acetate, ammonium bicarbonate, ammonium formate, and piperidine) was studi

35 hytoplankton associated fraction with (13) C-bicarbonate and (15) N-leucine as tracers.

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

37 reactivity of aqueous U and As mixtures with bicarbonate and Ca for acidic and neutral pH conditions.

38 7 was observed in reactors containing 10 mM bicarbonate and Ca, suggesting a kinetic reaction of aqu

39 Bicarbonate and calcium (Ca) can have major impacts on U

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

41 r 1 (AE1) is responsible for the exchange of bicarbonate and chloride across the erythrocyte plasma m

42 By taking up both bicarbonate and CO(2) as a carbon source for photosynthe

43 Future anthropogenic changes of bicarbonate and CO(2) concentrations may alter the speci

44 Concentrations of bicarbonate and CO(2) vary greatly with catchment geolog

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

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

47 Biophysical CCMs operate by concentrating bicarbonate and converting it into CO(2) in a compartmen

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

49 Bicarbonate and formate salts were hydrogenated to metha

50 aled that manganese uptake depends on pH and bicarbonate and is up-regulated by lipopolysaccharide, a

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

52 Serum bicarbonate and pH decreased.

53 Biliary bicarbonate and pH were significantly higher and biliary

54 y ion mass spectrometry combined with (13)C (bicarbonate and propionate) and (15)N-ammonia isotope la

55 CAs catalyze the conversion of CO(2) to bicarbonate and protons and are involved in various phys

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

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

58 Chloride, potassium, bicarbonate and sodium associated with 10, 58, 36 and 17

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

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

61 e of aqueous sample was buffered with sodium bicarbonate and treated with triethyloxonium tetrafluoro

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

63 otal bile production, biliary bilirubin, and bicarbonate), and significantly lowered levels of lactat

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

65 CPC), hydrogen peroxide (H(2) O(2) ), sodium bicarbonate, and antioxidants on periodontal/oral health

66 ntional TACE with extracellular pH-buffering bicarbonate, and five served as untreated controls.

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

68 ium, thiosulfate, sulfate, sulfite, sulfide, bicarbonate, and other macromolecule-stabilizing (kosmot

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

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

71 nts, with carbon monoxide (CO) and carbonate/bicarbonate as products.

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

73 h we name DabA and DabB, for DABs accumulate bicarbonate-assemble into a heterodimeric complex, which

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

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

76 kinetic properties might limit intracellular bicarbonate availability.

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

78 In bicarbonate-bearing matrices, the fractionation depended

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

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

81 tly higher ratios of [1-(13)C] lactate (Lac)/bicarbonate (Bicar) and [1-(13)C] Lac/total carbon (tC),

82 (kosmotropic), whereas ammonium formate and bicarbonate (both chaotropic) caused structural changes.

83 Protein analysis was done using ammonium bicarbonate buffer and size exclusion chromatography (SE

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

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

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

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

88 ociated with chloride, sodium, potassium and bicarbonate by running linear mixed models adjusting for

89 asopressin, amiodarone, lidocaine, atropine, bicarbonate, calcium, magnesium, and dextrose each year

90 des inhibit the function of the chloride and bicarbonate channel CFTR, causing intestinal cell stress

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

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

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

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

95 energy profiles of the metabolic substrates, bicarbonate, CO(2) and ribulose bisphosphate and the pro

96 CA) is a key constituent of the universal CA/bicarbonate/CO(2) buffer maintaining the pH of both bloo

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

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

99 Initial bicarbonate concentration ( approximately 1 mM) was obta

100 the long-term effects of veverimer on serum bicarbonate concentration and physical functioning.

101 unction in CKD, even if initiated when serum bicarbonate concentration is normal.

102 per 1.73 m(2)) and metabolic acidosis (serum bicarbonate concentration of 12-20 mmol/L).

103 e of 4 mmol/L or more from baseline in serum bicarbonate concentration or serum bicarbonate in the no

104 y ammonium excretion was 25% lower and serum bicarbonate concentration was 1.3 meq/L higher in HD-NaH

105 gallbladder containing dilute bile with high bicarbonate concentration.

106 plant species with this trait increases with bicarbonate concentration.

107 Bicarbonate concentrations in modern groundwater are pos

108 at week 52 (63% vs 38%, p=0.0015) and higher bicarbonate concentrations were observed with veverimer

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

110 (NBCe1 and NBCe2), the electroneutral sodium-bicarbonate cotransporter (NBCn1), and the sodium-depend

111 The SLC4A4 gene encodes electrogenic sodium bicarbonate cotransporter 1 (NBCe1).

112 O(3)(-) transport by the electrogenic sodium bicarbonate cotransporter 1, NBCe1.

113 S695T - and included the electrogenic sodium-bicarbonate cotransporter isoforms 1 and 2 (NBCe1 and NB

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

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

116 tions, indicating the in situ formation of a bicarbonate counterion (HCO(3)(-)).

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

118 of BCCP-BADC-BC subcomplexes catalyzing the bicarbonate-dependent hydrolysis of ATP, which is the fi

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

120 ires the activation of protein kinase A by a bicarbonate-dependent soluble adenylate cyclase.

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

122 Dialysis was then performed with a novel low bicarbonate dialysate.

123 Five bicarbonate dialysis experiments were performed.

124 Bicarbonate dialysis results in CO2 removal at rates com

125 emisorbed CO(2) species (e.g., alkylammonium bicarbonate, ditethered carbamic acid and silylpropylcar

126 ular pH (mean, 6.96 +/- 0.05; P = .02) using bicarbonate during TACE increased peri- and intratumoral

127 ese two reactions on the Au surface in 0.1 M bicarbonate electrolyte.

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

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

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

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

132 correlated to each other as set by the CO(2)/bicarbonate equilibrium.

133 r (NBCn1), and the sodium-dependent chloride-bicarbonate exchanger (NDCBE).

134 SLC26A7 encodes a chloride/bicarbonate exchanger expressed in the renal outer medul

135 tly regulates the intercalated cell chloride/bicarbonate exchanger pendrin is unclear, as are potassi

136 The chloride/bicarbonate exchanger SLC26A3 (downregulated in adenoma)

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

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

139 ed that PDK-deficient livers produce more HP-bicarbonate from HP-[1-(13)C]pyruvate than age-matched c

140 They generate bicarbonate from metabolic carbon dioxide and through ca

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

142 values were associated with low BDI: biliary bicarbonate greater than 18 mmol/L (P = 0.002), biliary

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

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

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

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

147 on veverimer than placebo had an increase in bicarbonate (>=4 mmol/L or normalisation) at week 52 (63

148 Bicarbonate has long been touted as a putative ergogenic

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

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

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

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

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

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

155 (80 Torr), +/- tromethamine (THAM) or sodium bicarbonate (HCO3) +/- AC probes in a micropuncture mode

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

157 Thirty bicarbonate hemodialysis (BHD) patients were randomized

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

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

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

161 tosynthesis in many aquatic plants relies on bicarbonate in addition to carbon dioxide (CO(2)) to com

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

163 rapid interconversion of carbon dioxide and bicarbonate in the cells, where carbon dioxide is produc

164 fluent gas streams and store it primarily as bicarbonate in the marine environment.

165 in serum bicarbonate concentration or serum bicarbonate in the normal range of 22-29 mmol/L, assesse

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

167 nd 1000 K indicate a higher concentration of bicarbonates in water than previously considered at cond

168 Many bicarbonate-incorporating carboxylases rely on the organ

169 ectroscopies (XAS) show that the addition of bicarbonate increased manganese retention but decreased

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

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

172 Importantly, bicarbonate ingestion prior to strenuous interval exerci

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

174 epithelia; its dysfunction causes the plasma bicarbonate insufficiency that underlies acidemia.

175 ever, the underlying mechanisms of action of bicarbonate intake on skeletal muscle metabolism have ye

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

177 Alongside the active transport of bicarbonate into the cell and localization of carbonic a

178 bonic anhydrase 4 catalyzes the formation of bicarbonate ions (HCO[Formula: see text]), for accumulat

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

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

181 th's carbon cycle, we focus on carbonate and bicarbonate ions.

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

183 orm of solid carbonate minerals or dissolved bicarbonate ions.

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

185 Despite lack of evidence, sodium bicarbonate is frequently used to correct pH; however, i

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

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

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

189 vate via PDH (pyruvate dehydrogenase, [(13)C]bicarbonate), lactate dehydrogenase ([1-(13)C]lactate),

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

191 We suggest that: 1) clinicians use a serum bicarbonate level <27 mmol/L to exclude the diagnosis of

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

193 ; PO(2), 89 mmHg; normal range, 75-100 mmHg; bicarbonate level, 17 mEq/L [17 mmol/L]; normal range 22

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

195 with epidermal growth factor (EGF) and that bicarbonate levels directly correlate with the extent of

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

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

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

199 ck size of seven) and stratified by baseline bicarbonate (<=18 mmol/L vs >18 mmol/L).

200 ith uranium (r = 0.72, p < 0.01), suggesting bicarbonate may mobilize uranium in this system.

201 s the capacity of CO(2) absorption through a bicarbonate mechanism.

202 e rat lenses cultured for 48 hours in TC-199 bicarbonate media through physical trauma, 10 mM ouabain

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

204 inary ammonium excretion and increased serum bicarbonate more than the lower dose but was associated

205 arterial pH generated by infusion of sodium bicarbonate (NaHCO(3) ), and completely abrogated by a c

206 Oral sodium bicarbonate (NaHCO(3)) may preserve kidney function in C

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

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

209 In depth investigation indicated that bicarbonate not only changed the Fe(VI)/SA complexation

210 patients required dose adjustment due to low bicarbonate or asthenia.

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

212 uncoupled chloride transport with negligible bicarbonate or sulfate permeability.

213 SS (Kcnj16-/-) rats chronically treated with bicarbonate or the carbonic anhydrase inhibitor hydrochl

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

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

216 and As mixtures, 10 mM Ca, and without added bicarbonate (pCO(2) = 3.5), aqueous U decreased to <0.25

217 tridges with solutions of tetraethylammonium bicarbonate, perchlorate or tosylate in polar aprotic so

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

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

220 Biliary bicarbonate, pH, and glucose during ex situ NMP of liver

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

222 ed with adsorbates acting as capping agents: bicarbonate, phosphate, and pyrophosphate.

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

224 Effect of no prehydration vs sodium bicarbonate prehydration prior to contrast-enhanced comp

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

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

227 Immunoblotting experiments confirmed that HP-bicarbonate production from HP-[1-(13)C]pyruvate paralle

228 ular experiments revealed that intracellular bicarbonate proportionally dictates total protein phosph

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

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

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

232 re produced by ambient drying using ammonium bicarbonate, rather than a conventional low surface tens

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

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

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

236 Via bicarbonate regulation, sAC acts as a physiological sens

237 Arterial pH increased after bicarbonate removal (7.13 +/- 0.04 vs 7.21 +/- 0.05; p <

238 stand the factors influencing blood pH after bicarbonate removal.

239 /- 0.2 muM and 22.5 +/- 0.3 mM carbonate and bicarbonate, respectively).

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

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

242 e device permitting detection of the eluting bicarbonate salt conductometrically in a background of n

243 increase with the concentration of ammonium bicarbonate salts from 360 to 530 m(2) g(-1), and that o

244 activity-dependent release of ATP triggering bicarbonate secretion by astrocytes via activation of me

245 This was consistent with a defect in bicarbonate secretion involving CFTR and SLC26A4 (pendri

246 estinal alkaline phosphatase (IAP) regulates bicarbonate secretion, detoxifies lipopolysaccharide (LP

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

248 s biliary proliferation, liver fibrosis, and bicarbonate secretion.

249 langiocytes, and loss of it impairs ductular bicarbonate secretion.

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

251 ative AEC CO(2) sensor and effector as it is bicarbonate sensitive and controls key mediators of AEC

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

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

254 In contrast, serum sodium and bicarbonate showed associations predominantly with amino

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

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

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

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

259 co-occurring oxo-anions (phosphate, sulfate, bicarbonate, silicate, and nitrate) were selected due to

260 Heating dissociates the ammonium bicarbonate, so generating CO(2) and NH(3) within the po

261 lusion of the base (in situ generated sodium bicarbonate/sodium biphosphate) is found to be energetic

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

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

264 ncludes transport of carbon dioxide, oxygen, bicarbonate, sucrose/glucose, bacteria, and autoinducer-

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

266 intestinal lumen, unlike current oral sodium bicarbonate therapy for metabolic acidosis that only neu

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

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

269 at least one third of all astrocytes release bicarbonate to buffer extracellular H(+) loads associate

270 PS was treated with acetic acid and sodium bicarbonate to improve pallatability.

271 Sodium bicarbonate to improve physical function in patients ove

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

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

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

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

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

277 ting in defective CFTR-mediated chloride and bicarbonate transport, with dysregulation of epithelial

278 xpression and function of the Sodium-Coupled Bicarbonate Transporter (NCBT) family of base loaders we

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

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

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

282 Transmembrane bicarbonate transporters and carboxysomes play key roles

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

284 rs associated with strenuous exercise and/or bicarbonate treatment responses, whereas structural eluc

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

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

287 Regionally, however, the frequency of bicarbonate use is reduced at sites where the CO(2) conc

288 requency of freshwater plants possessing the bicarbonate use trait.

289 aseline and at least one post-baseline serum bicarbonate value).

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

291 eGFR was 36+/-9 ml/min per 1.73 m(2), serum bicarbonate was 24+/-2 meq/L, and median (IQR) ACR was 1

292 For the first time, bicarbonate was found to significantly promote the oxida

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

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

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

296 gh concentrations of chloride, ammonium, and bicarbonate, which may hinder treatment processes.

297 carcinoma cell line A431, we discovered that bicarbonate, which reacts with H(2)O(2) to form the more

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

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

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