ライフサイエンスコーパス: potassium

1 cated by elevated serum creatinine, BUN, and potassium.

2 significant changes in BP, weight, or serum potassium.

3 nts - particularly, nitrogen, phosphorus and potassium.

4 Voltage-gated potassium 11.1 (K(v)11.1) channels play a critical role

5 By using lipophilic bases such as potassium 2-ethyl hexanoate, the borylation reaction cou

6 GGN)13 repeat found within the 5' UTR of the potassium 2-pore domain leak channel Task3 mRNA.

7 e addition of extracellular sodium (+40 mM), potassium (+2 mM), or magnesium (+1 mM) reduces Th2:Th17

8 We report the synthesis of potassium acyltrifluoroborates (KATs) by a palladium-cat

9 A) acylboronates as well as alpha-methylated potassium acyltrifluoroborates in a one-pot manner.

10 A seven-membered N,N'-heterocyclic potassium alumanyl nucleophile is introduced and utilise

11 pproach can also be applied to the analogous potassium amide K{N(SiMe(3) )(2) }, leading to the forma

12 reaction for sodium, using aluminum nitrate, potassium and ammonium fluoride in an acid medium, with

13 Both potassium and calcium salts decomposed in temperatures h

14 Sorbic acid and its potassium and calcium salts used as food preservatives a

15 besides the previously reported link between potassium and osmolyte uptake, a connection between nitr

16 nd riboswitches, which are often involved in potassium and osmotic homeostasis.

17 oint mutations, we identify key residues for potassium and proton binding, which are conserved among

18 PBISEs for potassium and sodium ions were developed, and these ISEs

19 nt-available pools of calcium, magnesium and potassium and trace the soil phases that support these p

20 We report the detection of lithium, sodium, potassium, and calcium in the atmosphere of the white dw

21 that aids in the active transport of sodium, potassium, and chloride ions across cell membranes.

22 tment and stratification for albuminuria and potassium, and when modeling RAS inhibition as a time-de

23 A high-performance potassium anode achieved by confining potassium metal in

24 nt-available pools of calcium, magnesium and potassium are assumed to be stored in the soil as exchan

25 is being seriously challenged by sodium and potassium, as the alkali-metal mediation of organic reac

26 tant at neutral pH to probe the affinity for potassium at the selectivity filter.

27 We found the charge donated from the potassium atoms occupies antibonding pai orbitals of the

28 en exchanger-3) and Na(+)/K(+)ATPase (sodium-potassium-atpase) and phosphorylation of AT(2)R-cGMP dow

29 t time that K[Formula: see text] dynamics in potassium-based battery materials has been measured usin

30 The potassium binding affinity in the selectivity filter of

31 ansmembrane allosteric coupling controls the potassium binding affinity of the prototypical potassium

32 the open pH gate allosterically affects the potassium binding affinity of the selectivity filter.

33 idue (E120) in the pH sensor is sensitive to potassium binding, suggesting that this mutant also has

34 Large conductance Ca(2+)-activated potassium (BK) channels are S-acylated at two sites that

35 Large-conductance potassium (BK) channels are transmembrane (TM) proteins

36 Potassium bromate has significant effect on food biomole

37 is review explains in detail, the effects of potassium bromate on biomolecules, human health, environ

38 Potassium bromate, is an oxidizing agent and one of the

39 water by deuterium dilution, and total body potassium by whole-body gamma counting were combined to

40 Potassium, Ca, Mg and Ni were low in laurel and rosemary

41 r for measuring the concentration of sodium, potassium, calcium, chloride, and nitrite in urine, accu

42 yzing electrolytes in urine, such as sodium, potassium, calcium, chloride, and nitrite, has significa

43 vide a double and triple Nernstian slope for potassium-, calcium-, nitrate-, and carbonate-selective

44 nes, and alkenes using a JohnPhos ligand and potassium carbonate as a base in dimethylformamide at 10

45 ontaining over 50 wt% of sodium or 30 wt% of potassium carbonate, or at electrolysis temperatures les

46 investigated the role of the basic additive potassium carbonate, the use of which is crucial for eff

47 ur dioxide from the reaction medium, and the potassium cation plays a role in accelerating transmetal

48 aromatic system is stabilized by the nearby potassium cation.

49 ecific potassium nanosensor that can monitor potassium changes in the brain of freely moving mice und

50 ty mediated by decreased inwardly rectifying potassium channel (IRK) function.

51 Inward rectifier potassium channel (Kir) Kir2.2 has multiple interactions

52 odes the small conductance calcium-activated potassium channel 2 (SK2).

53 ular assemblies, including the ATP-sensitive potassium channel and the peptide-loading complex, but a

54 ion of the NKCC1 inhibitor bumetanide or the potassium channel antagonist Tetraethyl ammonium had no

55 These findings highlight the KCNQ-type potassium channel as a promising target for future drug

56 Decreased levels of functional K(v)11.1 potassium channel at the plasma membrane of cardiomyocyt

57 ardiac-specific germline deletion in mice of potassium channel beta subunit-encoding Kcne2 (Kcne2(CS-

58 y by chronic treatment with the FDA-approved potassium channel blocker 4-aminopyridine (4-AP) improve

59 KCl and the potassium channel blocker tolbutamide also stimulated pr

60 Applying specific potassium channel blockers diminished the hyperexcitabil

61 l action potential duration were reduced and potassium channel expression (Kv1.5) and current (I(Kur)

62 MthK, a two transmembrane calcium-activated potassium channel from thermophilic archaebacteria.

63 intrinsic excitability via the regulation of potassium channel function.

64 technology to increase the expression of the potassium channel gene Kcna1 (encoding Kv1.1) in mouse h

65 t with increased expression of voltage-gated potassium channel gene Kcna1 and decreased expression of

66 d expression of the 3.1 isoform of the KCNH2 potassium channel has been associated with cognitive dys

67 Knowing that downregulation of Kv1.2 potassium channel in the IN nerve terminals likely augme

68 euronal hyperexcitability, induced by M-type potassium channel inhibition, triggered intrinsic and sy

69 11.1 hERG (human ether-a-go-go related gene) potassium channel is a critical regulator of cardiomyocy

70 The function of the voltage-gated KCNQ1 potassium channel is regulated by co-assembly with KCNE

71 genes, an increase of the calcium-activated potassium channel Kcnn2 in the motor cortex correlated w

72 tassium binding affinity of the prototypical potassium channel KcsA in the context of C-type inactiva

73 The potassium channel Kir4.1 forms the Kir4.1/Kir5.1 heterot

74 The voltage-gated potassium channel Kv1.5 plays important roles in atrial

75 lular localization and cellular level of the potassium channel Kv3.1 in cells.

76 is and the role of an atrial specific 2-pore potassium channel TASK-1 as a therapeutic target for atr

77 The potassium channel THIK-1 is strongly expressed in the ce

78 rimental determination of the structure of a potassium channel VSD in the intermediate state has prev

79 l structure of the human KCNQ1 voltage-gated potassium channel VSD in the intermediate state.

80 action of a classical CaV-like channel and a potassium channel, BK (Slo1), whereas the second module

81 n associated with this trait we identify the potassium channel, Kcnh8, as a sword development gene.

82 reduced function of the inwardly rectifying potassium channel, Kir2.

83 red that TRESK, a calcium regulated two-pore potassium channel, plays a crucial role in this system.

84 on of the Ca(2+)-activated small conductance potassium channel, SK2, contributes to impairment of syn

85 rated that microglial Kv1.3, a voltage-gated potassium channel, was transcriptionally upregulated in

86 9 is also moderately active against the hERG potassium channel.

87 H) neurons through opening the ATP-sensitive potassium channel.

88 Two-pore-domain potassium channels (K(2P)) are the major determinants of

89 (4AP) is a specific blocker of voltage-gated potassium channels (K(V)1 family) clinically approved fo

90 Neuronal voltage-gated potassium channels (Kv) are critical regulators of elect

91 sensitivity to ATP, downregulation of Kir4.1 potassium channels and increased cytokine synthesis and

92 ts in the presynaptic terminals, where Kv1.2 potassium channels are downregulated.

93 Kv11.1 potassium channels are essential for heart repolarizatio

94 K2P potassium channels are known to be modulated by volatile

95 ecular gating mechanism in calcium-activated potassium channels by obtaining structures of the MthK c

96 In general, potassium channels have an intramembrane vestibule with

97 Potassium channels in parvalbumin-type models deactivate

98 we analyzed the expression of voltage-gated potassium channels in rodent and primate brains using qP

99 In neurons, inactivation of both sodium and potassium channels is crucial for the generation of acti

100 Kv3 voltage-gated potassium channels mediate action potential (AP) repolar

101 Slo2 potassium channels play important roles in neuronal func

102 n downstream recruitment of Ca(2+)-activated potassium channels to the plasma membrane.

103 Subsequently, sigma1 binds to Kv1.2 potassium channels, followed by accumulation of Kv1.2 in

104 tion is via blockade of axonal voltage gated potassium channels, thereby enhancing conduction in demy

105 However, in several voltage-gated potassium channels, using specific S4-S5(L)-mimicking pe

106 splicing defects in voltage-gated sodium and potassium channels, which alter their electrophysiologic

107 and AIS clustering of PSD93 and also of Kv1 potassium channels, which directly bind PSD93.

108 derivatives are able to block voltage-gated potassium channels.

109 d 2) reduced activation of voltage-dependent potassium channels.

110 ivity of the binding sites along the pore of potassium channels.

111 and more efficiently recruiting subthreshold potassium channels.

112 h the activation of associated calcium-gated potassium channels.

113 f the properties of voltage-gated sodium and potassium channels.

114 pening of small-conductance Ca(2+)-activated potassium channels.

115 tive humidity (ERH) of potassium sulfate and potassium chloride aerosol as well as the separation RH

116 ession ratios of the K(+)/Cl(-) transporters potassium-chloride cotransporter 2 (KCC2) and sodium-pot

117 a histidine point variation in the neuronal potassium-chloride cotransporter 2 (KCC2).

118 m-chloride cotransporter 2 (KCC2) and sodium-potassium-chloride transporter (NKCC1).

119 that the K-metal anode can be coupled with a potassium cobalt oxide cathode to achieve dendrite heali

120 SnF(2) alone and potassium combined with SnF(2) or hydroxyapatite were be

121 Acute desensitization of the potassium conductance induced by the somatostatin recept

122 re made, and the agonist-induced increase in potassium conductance was measured.

123 and activation of a large calcium-activated potassium conductance, G(BK) , that can be blocked by ag

124 he inactivation and deactivation of a second potassium conductance, G(K(LV)) .

125 d female rats, this action depends on M-like potassium conductance.

126 are the major determinants of the background potassium conductance.

127 es of photosynthesis) and, intriguingly, the potassium content of plant tissue, which is likely linke

128 orophyll content, as well as leaf sodium and potassium content under saline conditions, were most str

129 ocesses increased total phenolic content and potassium content, significantly.

130 control of ionic flux (calcium, sodium, and potassium) contributes to in utero developmental process

131 as a solvent-separated ion triplet with two potassium counterions.

132 of the rapidly activating delayed rectifier potassium current (I(Kr)) important for repolarization o

133 The M-current is a low voltage-activated potassium current generated by neuronal Kv7 channels.

134 esemble rapidly activating delayed rectifier potassium current in the human heart, are blocked by fen

135 nd TREK-2 provide the predominant background potassium current in the primary sensory neurons of the

136 ng by suppression of a low voltage-activated potassium current, M-current.

137 ng value, mediated by an inwardly rectifying potassium current, resulting in reduced neuronal excitab

138 A, neurons of the VTA by inducing an outward potassium current.

139 , enDUB treatment restored delayed rectifier potassium currents and normalized action potential durat

140 igher amplitudes and faster kinetics of fast potassium currents correlated with this hyperexcitabilit

141 ) was employed to block Kv3-mediated outward potassium currents in voltage- and current clamp experim

142 ation of ALD increased outward voltage-gated potassium currents significantly, and simultaneously upr

143 ype specific with the involvement of altered potassium currents that allow for a sustained, continued

144 A-type and delayed-rectifier (DR) potassium currents, two putative transcriptional targets

145 Further supporting the involvement of potassium currents, we observed an overexpression of KCN

146 increasing sodium currents and reducing fast potassium currents.

147 d by an increase in the amplitude of several potassium currents.

148 lve the use of highly toxic reagents such as potassium cyanide, the polymerization-based test uses si

149 Here, we show that potassium deficiency inhibits lateral root organogenesis

150 (SEI), covering the current understanding of potassium dendrites, and highlighting the deep-eutectic

151 report the crystal structure of the Reduced Potassium Dependency3/Histone Deacetylase1 (RPD3/HDA1) t

152 yeast Saccharomyces cerevisiae We found that potassium-dependent autophagy requires the core pathway

153 Feeding nephrotic mice with a low potassium diet prevented hyperkaliemia, gamma-ENaC cleav

154 The high electronic transport and fast potassium diffusion in this scaffold enable reduced loca

155 f the nonlinear optical crystalline material potassium dihydrogen phosphate and its 70% deuterated an

156 Recent interest in potassium-doped p-terphenyl has been fueled by reports o

157 tic fluctuation-induced superconductivity in potassium-doped p-terphenyl, which has a close analogy w

158 Here, we isolate a phase-pure crystal of potassium-doped p-terphenyl: [K(222)](2)[p-terphenyl(3)]

159 ear magnetic resonance (SSNMR) spectroscopy, potassium efflux assays, and Forster resonance energy tr

160 r cell and afferent membrane potentials; the potassium efflux from type I hair cells results from the

161 Moreover, blocking of potassium efflux improved the mitochondrial health in ad

162 riments showed that soticlestat can suppress potassium-evoked extracellular glutamate elevations in t

163 eased glomerular filtration rate and urinary potassium excretion associated with hyperkaliemia at day

164 ethanol) and two inner-sphere redox couples (potassium ferrocyanide and dopamine).

165 ults and with experiments carried out on the potassium ferrocyanide/ferricyanide redox couple.

166 These results show that Potassium fertilization as KCl is an important source of

167 The activation of potassium fluoride for nucleophilic fluorination of alky

168 ents by a combination of oxalyl chloride and potassium fluoride.

169 he traffic site while it was correlated with potassium for the domestic wood burning sample.

170 G-protein-gated inward rectifier potassium (GIRK) channels are regulated by G proteins an

171 ignaling pathway, driven by either sodium or potassium gradients.

172 f ((Mes)dmx)Cu(2)(mu(2)-N(C(6)H(4)OMe)) with potassium graphite initiates an intramolecular, benzylic

173 e [(eta(5) -C(5) (i) Pr(5) )(2) UI] (1) with potassium graphite produces the "second-generation" uran

174 action with the assistance of a redox probe (potassium hexacyanoferrate).

175 These results suggest that potassium homeostasis is a major determinant of the tubu

176 Potassium homeostasis is vital for all organisms, but is

177 rs our understanding of how bacteria control potassium homeostasis to maintain cell volume and osmoti

178 en uptake, exopolysaccharide production, and potassium homeostasis, each of which is critical for cel

179 portance of the KS-WNK1 isoform abundance on potassium homeostasis.

180 eved CO(2) electroreduction on copper in 7 M potassium hydroxide electrolyte (pH ~ 15) with an ethyle

181 Results showed that 60% potassium hydroxide solution with acetone in the ratio o

182 o activation steps using phosphoric acid and potassium hydroxide.

183 or air stimulus, arginine (2.22; 1.45-2.99), potassium + hydroxyapatite (2.44; 0.33-4.55), potassium

184 We identify the potassium importer KimA from Bacillus subtilis as a memb

185 d that the metals involved in the syntheses (potassium in the case of the trifluoromethyl reagent and

186 re described, a direct titration with dimsyl potassium in the presence of an indicator and a back-tit

187 re not capable of detecting small changes in potassium, in particular, in freely moving animals.

188 An optical potassium indicator is embedded in mesoporous silica nan

189 ypertension, such as high sodium intake, low potassium intake, obesity, alcohol consumption, physical

190 taurolidine, hydrogen peroxide, human serum, potassium iodide and doxorubicin/ oxaliplatin for both e

191 n by single mechanosensory neurons, with the potassium ion channel Kv3.3 emerging as one potential co

192 ic cages as the anionic parts and 18-crown-6/potassium ion complexes as the cationic parts.

193 alpha-subunit, largely abolished basolateral potassium ion conductance (to a degree similar to that o

194 ed nanosensor enables the spatial mapping of potassium ion release in the hippocampus of freely movin

195 However, investigation of potassium-ion (K[Formula: see text]) dynamics in materia

196 access similar capacities as a sodium-ion or potassium-ion cathode.

197 performed at higher temperatures reveal that potassium ions (K[Formula: see text]) become mobile abov

198 Substantial potassium ions are constantly released into the Corti fl

199 al switch, leading to a loss of affinity for potassium ions at the selectivity filter and therefore t

200 Recently, earth-abundant potassium ions have attracted considerable interest as f

201 Excess potassium ions in the Corti fluid are resorbed by suppor

202 ation buffer (extrinsic cobalt and intrinsic potassium ions), (iii) extrinsic bromine and intrinsic p

203 cations and allows the specific capturing of potassium ions.

204 coarse irregular SEI clumps at formation, 3D potassium islands with further SEI coarsening during pla

205 Potassium (K(+)) channels are highly conserved proteins

206 um (Ba(2+)) is a classic permeant blocker of potassium (K(+)) channels.

207 hannel (LCC) current (~33%), reduced outward potassium (K(+)) currents (~30%), and increased sodium/c

208 ntenance of adequate intracellular levels of potassium (K(+)).

209 ASK) channels-members of the two pore domain potassium (K(2P)) channel family-are found in neurons(1)

210 Both cells are equipped with ATP-regulated potassium (K(ATP) ) channels that are regulated by the i

211 ed whether activation of inwardly rectifying potassium (K(IR) ) channels underlies vasodilatation wit

212 In voltage-gated potassium (K(V)) channels, the voltage-sensing domain (V

213 ounds that open the two voltage-gated type 1 potassium (K(V)1) channels K(V)1.5 and Shaker, but not t

214 g season, then ecosystem productivity, plant potassium (K) and phosphorous (P), respectively.

215 r than that in the photosynthetic rate under potassium (K) deficiency stress.

216 The use of potassium (K) metal anodes could result in high-performa

217 Potassium (K) metal anodes suffer from a challenging pro

218 The internal efficiency (IE) of N and potassium (K) performed similarly in both climate region

219 Potassium (K) represents up to 10% of the plant's total

220 rameters: basal tone, contractions evoked by potassium (KCl 60 mM), acetylcholine (ACh 10 muM) or ser

221 Voltage-gated potassium (Kv) channels display several types of inactiv

222 Voltage-gated potassium (Kv) channels of the Kv4 subfamily associate w

223 ly silent (KvS) members of the voltage-gated potassium (Kv) subfamilies Kv5, Kv6, Kv8, and Kv9 select

224 n, we examined the role of the voltage-gated potassium Kv4.2 subunit, a molecular determinant of A-ty

225 Indeed, alterations of potassium levels can be related to neurological disorder

226 difference 0.01; 95% CI (0.25, -0.23)), but potassium levels were higher at the end of the study tha

227 t by blood pressure, vasopressor therapy, or potassium levels, but identified a possible mediation ef

228 blood pressure, kaliuresis, and lower serum potassium levels.

229 uding reduced viability, increased swelling, potassium loss, aberrant protein phosphorylation, and dy

230 re observed between the global radiation and potassium, magnesium and calcium contents (correlation c

231 wever, uncontrollable dendrite growth on the potassium metal anode has restrained their practical app

232 Potassium metal anodes are then critically reviewed, emp

233 Consequently, the as-developed potassium metal anodes exhibit a dendrite-free morpholog

234 otassium-sulfur batteries compared with bare potassium metal anodes.

235 Potassium metal batteries are considered as attractive a

236 This is the first report of successful potassium metal battery anode cycling with an aluminum-b

237 rmance potassium anode achieved by confining potassium metal into a titanium-deficient nitrogen-conta

238 ning during plating/stripping, possibly dead potassium metal on stripped surfaces, and rapid failure.

239 work can provide a new avenue for developing potassium metal-based batteries.

240 The dendrite-free sodium-potassium (Na-K) liquid alloy composed of two alkali met

241 e, we report a highly sensitive and specific potassium nanosensor that can monitor potassium changes

242 the placebo group, -1.2 +/- 6.8 mm Hg in the potassium nitrate group, and -0.5 +/- 6.6 mm Hg in the l

243 well as the effect of serum aldosterone and potassium on this response, we measured pendrin label in

244 identifying therapy-related changes in serum potassium or kidney function.

245 lithium induced attraction behavior, but not potassium or magnesium attraction thus clarifying the sp

246 e applied to boronic acid pinacol esters and potassium organotrifluoroborates using a slightly modifi

247 cross the membrane with high selectivity for potassium over sodium; ion passage is blocked by specifi

248 air cathode is the goal for superoxide-based potassium-oxygen (K-O(2) ) batteries, prior studies were

249 hich are shielded by an ultrathin layer of a potassium-permeable membrane, which prevents diffusion o

250 analytes were chosen for aggregating AgNPs, potassium phosphate for neutralizing the charges and a d

251 multiple nutrients (nitrogen, phosphorus and potassium plus nine essential macro- and micro-nutrients

252 The renal outer medullary potassium (ROMK) channel is essential for potassium tran

253 two-dimensional Fermi gas of spin-polarized potassium-rubidium (KRb) polar molecules, in which elast

254 rbonate exchanger pendrin is unclear, as are potassium's role in this response and the receptor's eff

255 icoid receptor blockade using canrenoic acid potassium salt (CAP).

256 The potassium salt presented a solid-solid phase transition

257 Ether-a-go-go (EAG) potassium selective channels are major regulators of neu

258 As a result, this potassium-sensitive hair cell conductance pairs with the

259 nsitive hair cell conductance pairs with the potassium-sensitive hyperpolarization-activated cyclic n

260 Potassium sensitivity of hair cell and afferent conducta

261 Thus, nitrogen and potassium share the ability to influence molecular suppl

262 carbon nanotubes (SWCNTs) can be doped with potassium, similar to graphite, leading to intercalation

263 We report on the use of (i) native intrinsic potassium single-wavelength anomalous dispersion methods

264 HCN) and small conductance calcium-activated potassium (SK) channels.

265 ffects to small-conductance Ca(2+)-activated potassium (SKs) channels.

266 otassium + hydroxyapatite (2.44; 0.33-4.55), potassium + SnF(2) (2.28; 0.87-3.69), CSP (1.98; 0.99-2.

267 veniently, positively charged species (i.e., potassium, sodium, and ammonium, among others) are repel

268 chieve simultaneous quantitative analysis of potassium, sodium, and calcium ions, demonstrated here i

269 E containing noncoding variants in the Hcn4 (potassium/sodium hyperpolarization-activated cyclic nucl

270 lel G4 in vitro exhibiting the stereotypical potassium specificity of G4s, remaining thermostable und

271 ntitative, high-throughput assay to identify potassium starvation as a new and potent inducer of auto

272 Electron microscopy of potassium-stimulated acute slices of the lumbar cord sho

273 However, the repletion of intracellular potassium stores could avoid HlyA induced macrophage cel

274 the efflorescence relative humidity (ERH) of potassium sulfate and potassium chloride aerosol as well

275 o a bimodal aerosol consisting of an Aitken (potassium sulfate) and accumulation mode (aged alpha-pin

276 electrolytes in establishing the reversible potassium sulfide K(2) S(n) phase sequence, the parasiti

277 This is the first review on potassium-sulfur (K-S) batteries (KSBs), which are emerg

278 tly improved electrochemical performances in potassium-sulfur batteries compared with bare potassium

279 ins with a critical discussion regarding the potassium-sulfur electrochemistry and on how it differs

280 adopt the one-electron redox process of O(2)/potassium superoxide (KO(2)).

281 nteractions could be tuned by exchanging the potassium surface ions for copper ions.

282 ts transport of ions such as copper, whereas potassium targets the organization of other cellular com

283 TWIK-related acid-sensitive potassium (TASK) channels-members of the two pore domain

284 ons of unactivated arenes in the presence of potassium tert-butoxide.

285 ed via a two-step sequence consisting of (i) potassium tert-butoxide/DMSO-catalyzed (E)-stereoselecti

286 recommend routine kidney function and serum potassium testing within 30 days of initiating ACE (angi

287 atients with outpatient serum creatinine and potassium tests in the 30 days after starting ACE inhibi

288 In this work the Stark active C=N stretch of potassium thiocyanate is used as a molecular probe of th

289 harmonic generation in a quadratic nonlinear potassium titanyl phosphate crystal.

290 ry potassium (ROMK) channel is essential for potassium transport in the kidney, and its dysfunction i

291 KUP transporters facilitate potassium uptake by the co-transport of protons.

292 ed in the plasma membrane and is involved in potassium uptake of differentiating xylem cells during v

293 tion, while unphosphorylated PtsN stimulates potassium uptake.

294 having abnormally high serum creatinine and potassium values in follow-up.

295 Gene expression of KCNA5 (potassium voltage-gated channel subfamily A member 5; en

296 and pendrin abundance per cell whether serum potassium was high or low.

297 Potassium was the most abundant element, except in the w

298 Furthermore, there was no evidence of potassium wasting (P=0.20) or renal dysfunction (P>0.11

299 neficial for air stimulus, and strontium and potassium were beneficial for tactile stimulus, with mod

300 erefore, selectively detecting extracellular potassium would allow the monitoring of disease.