ライフサイエンスコーパス: ion transport

1 n on Na/K-ATPase-mediated ATP hydrolysis and ion transport.

2 imultaneous lipid scrambling and nonspecific ion transport.

3 sion of mRNAs that regulate BP through renal ion transport.

4 These response speeds are limited by ion transport.

5 n signaling, lipid metabolism, and potassium ion transport.

6 ot a NOS2 inhibitor, also partially restored ion transport.

7 x confer unique constraints on mitochondrial ion transport.

8 in the process and the mechanism of required ion transport.

9 impacts the local defect chemistry and oxide ion transport.

10 late intestinal barrier function and colonic ion transport.

11 ancies in the depletion zone slow down oxide ion transport.

12 ontributes to the regulation of renal tubule ion transport.

13 ds on adequate airway hydration, governed by ion transport.

14 elevance to oxidative stress, apoptosis, and ion transport.

15 Li ions, while the Li-based SEI shuts off Na-ion transport.

16 y a regulatory role in mitochondrial calcium ion transport.

17 larity and redundant roles in metabolite and ion transport.

18 lving the use of calix[4]pyrrole systems for ion transport.

19 never been shown to directly influence water/ion transport.

20 solute carriers, which are also involved in ion transport.

21 tune the membrane charge density and control ion transport.

22 ranes using ligated nanoparticles to control ion transport.

23 ovement of TM10 during the occlusion step of ion transport.

24 rganelle morphology, membrane recycling, and ion transport.

25 dexamethasone dependent amiloride-sensitive ion transport.

26 mediating proton transfers and facilitating ion transport.

27 als movements of the protein associated with ion transport.

28 ified a regulatory function for PTEN in lens ion transport.

29 actions on renal hemodynamics and epithelial ion transport.

30 (MRCs) indicates that they mediate vectorial ion transport.

31 mathematical model of human nasal epithelial ion transport.

32 that TMEM165 expression is linked to Ca(2+) ion transport.

33 rarchical porous structure facilitates rapid ion transport.

34 cal processes with renewable sunlight-driven ion transport.

35 ins are important for regulation of cellular ion transport.

36 nctions of small transmembrane regulators of ion transport.

37 sting of Li2 CO3 -LiF, which enables fast Li-ion transport.

38 equal to the direct activation of neurogenic ion transport.

39 ish that must be corrected through branchial ion transport.

40 3(f/f) mice significantly reduced neurogenic ion transport.

41 es like photosynthesis, ATP biosynthesis and ion transport.

42 predominantly by active chloride and sodium ion transport.

43 e observation that nhTMEM16 does not mediate ion transport.

44 igh density of grain boundaries for enhanced ion-transport.

45 olactam analogues show a correlation between ion transport abilities in artificial liposomes and cyto

46 e materials is crucial as it may enable fast ion transport, abundant-surface-controlled energy storag

47 In the human lung CFTR loss causes abnormal ion transport across airway epithelial cells.

48 Gated ion transport across biological membranes is an intrinsi

49 on events at the micro- and nanoscale and of ion transport across biomimetic soft interfaces.

50 ical family of protein kinases that regulate ion transport across cell membranes.

51 eed to directly assess net water rather than ion transport across epithelial cell layers.

52 To model ion transport across protocell membranes in Hadean hydro

53 n the apical membrane, despite the fact that ion transport across respiratory epithelia involves both

54 Studies of ion transport across respiratory epithelial cells in viv

55 l of alveolar edema fluid depended on active ion transport across the alveolar epithelium.

56 respiration, and ATP production necessitate ion transport across the inner mitochondrial membrane.

57 each other to form a channel for facilitated ion transport across the membrane.

58 is rooted in half a century of research into ion transport across the plasma and vacuolar membranes o

59 on of calcium, sodium, hydrogen, or chloride ion transport across the plasma membrane.

60 omplex cellular functions that often require ion transport across their membranes.

61 isplayed lower thermal stability and reduced ion transport activity compared with the wild-type enzym

62 rotein kinases and phosphatases that control ion transport activity in response to environmental stim

63 We show that the reported lack of ion transport activity of nhTMEM16 is due to the lipid c

64 erin to the cell surface independent of NCX1 ion transport activity.

65 duced capacitive currents that reflect KR2's ion transport activity.

66 inated tripeptides illustrates the selective ion-transport activity.

67 In mice with colitis, ion transport almost completely disappeared.

68 to the inner rung electrodes to control the ion transport and accumulation inside the ion trapping r

69 eir introns may play roles in cell adhesion, ion transport and axon guidance, among other biological

70 up antigen production, and the regulation of ion transport and blood pressure.

71 urrent status of the field, a colloquium on "Ion Transport and Cancer" was held, covering the roles o

72 nic CLDN10 mutations affect TAL paracellular ion transport and cause a novel tight junction disease c

73 pression analysis revealed downregulation of ion transport and cell cycle genes, leading to altered c

74 ficantly up-regulated and down-regulation of ion transport and circadian genes.

75 process requires the intricate regulation of ion transport and controlled changes to the pH of the de

76 rous structure to facilitate the electron or ion transport and electrolyte diffusion, so as to ensure

77 lts support three-dimensional simulations of ion transport and electroosmotic transport through nanof

78 ises to advance the present understanding of ion transport and enables regulation of cell junctions c

79 t are required to maintain the high-capacity ion transport and endocytic functions of this nephron se

80 s, interacting proteins, cellular migration, ion transport and epithelial barrier function.

81 s (CaCCs) are key players in transepithelial ion transport and fluid secretion, smooth muscle constri

82 pathways can provide hierarchical pores for ion transport and form uniform coatings on each active p

83 simultaneously ensure efficient electron and ion transport and help withstand the mechanical stress d

84 erge from i) mechanical stretch with calcium ion transport and ii) fluid shear stress induced nitric

85 This defect alters chloride ion transport and impairs water transport across the cel

86 ion with polar groups allows manipulation of ion transport and ion-to-electron transduction.

87 regulators of melanin synthesis, melanosome ion transport and its contribution to pigmentation remai

88 ons, and our data suggest that renal organic ion transport and mitochondrial function are dysregulate

89 whose airways are characterized by abnormal ion transport and mucociliary clearance, but TGF-beta1 i

90 that P. aeruginosa also perturbs epithelial ion transport and osmosis, which may be important for th

91 Whole-GUV patch-clamping allows ion transport and other voltage-dependent processes to b

92 or the trafficking of proteins essential for ion transport and PD development.

93 polar Fe3 O4 cores facilitate fast electron/ion transport and promote continuous reactivation of the

94 lymer is designed specifically to facilitate ion transport and promote electrochemical doping.

95 Knowledge of the molecular ion transport and regulation mechanisms and the control

96 Recent discoveries of new ion transport and regulatory pathways in the distal neph

97 anopore is proposed to actively regulate its ion transport and selectivity.

98 ing is mediated by the complex regulation of ion transport and solute biosynthesis.

99 Fast ion transport and superior mechanical properties of soli

100 -1 release, modulation of intestinal mucosal ion transport and transit in wild-type (WT) and FFA2(-/-

101 urface modified ion selective membranes, (b) ion transport and water splitting in bipolar membranes a

102 ain of epithelia that regulates cell volume, ion transport, and acid-base balance; mice knocked out f

103 dule for efficient ion confinement, lossless ion transport, and ion mobility separations at different

104 layer capacitance, open structures for rapid ion transport, and redox-active moieties that enable far

105 in proteins is essential in catalysis, metal ion transport, and regulatory metallobiochemistry.

106 extra lithium storage sites, accelerated Li-ion transport, and sufficient buffering space for volume

107 ogical functions, including nutrient uptake, ion transport, and waste removal.

108 The ion channels that mediate electrogenic ion transport are regulated by extracellular purinergic

109 ith liquid electrolytes, while enabling fast ion transport, are essential to address chemical instabi

110 structural stability, and fast electron and ion transport, are explored for boosting LIBs in terms o

111 and resulting in cation dependent nanoscale ion transport as seen through conductance measurements a

112 he macrocycle is an interesting scaffold for ion-transport as it is able to discriminate between vari

113 hree-fold reduction in activation energy for ion transport at a sodium bromide interphase.

114 The blocking of ion transport at interfaces strongly limits the performa

115 play an important role in directing lithium ion transport at nanoscale.

116 tablished that electroconvection can enhance ion transport at polarized surfaces such as membranes an

117 arge gives rise to an additional barrier for ion transport at the grain boundary.

118 ities in the diameter dependence of interior ion transport because of structuring of the internal flu

119 Nevertheless, intrinsic ion transport behavior of OIPCs is not fully understood,

120 restricted power density due to the poor Li-ion transport between the electrodes via the electrolyte

121 d-alumina interface allows effective lithium ion transport between the lithium metal anode and garnet

122 y insulating solid layer that allows lithium ion transport but stops further electrolyte redox reacti

123 th respect to macromolecular degradation and ion transport, but consistent with a widespread loss of

124 The ion transport by a modified hopping mechanism was demons

125 antiport as the operational mechanism of the ion transport by bis(sulfonamides).

126 We have quantified water motion and ion transport by combining Quasi Elastic Neutron Scatter

127 Instead, our data suggest that ion transport by MSL1 leads to dissipation of mitochondr

128 disturbed pH regulation results from reduced ion transport by NCKX4 and NaPi-2b.

129 cal relationship between the number of Na(+) ions transported by NKA per molecule of glucose consumed

130 An alternative approach is described whereby ion transport can be revealed and quantified through dir

131 te pathways that up-regulate endocytosis and ion transport capacity.

132 s because of the favourable electron- and Li-ion-transporting capacity provided by the ordered rylene

133 and a missense mutation S427L in TM1 impairs ion transport, causing proximal renal tubular acidosis.

134 environmental factors, genetic manipulation, ion transport, cell-water separation, process design, sa

135 eletion heterozygotes found mis-localized ES ion transport cells only in the genetic background exhib

136 ent absence of an ED, mis-localization of ES ion transport cells relative to inner ear sensory organs

137 ecause of the difficulties of probing buried ion transport channels.

138 sents an exceptionally low energy barrier to ion transport, comparable to that of metallic magnesium.

139 by abnormal purine nucleotide regulation of ion transport, contribute to the pathogenesis of CB.

140 r sunlight involves thermally activated fast ion transport coupled with a lattice-expanding phase tra

141 ing factor to influenza infection-associated ion transport defects.

142 mbrane conductance regulator (CFTR) exhibits ion transport deficiencies reported in human CF airways,

143 h suggests small transmembrane regulators of ion transport emerged early in the vertebrate lineage.

144 ted genes involved in synaptic transmission, ion transport, epilepsy, behavioral abnormality, chemoki

145 ted to form the conductive pathway, mediates ion transport even in the absence of the C-domain.

146 Growth in plants depends on ion transport for osmotic solute uptake and secretory me

147 t must be neutralized, presumably by HCO3 (-)ions transported from ameloblasts into the developing en

148 expected to severely diminish or abolish the ion transport function of the protein.

149 Ion transport function was examined by measuring intrace

150 s accompanied by reduced KCC2 clustering and ion transport function.

151 ive RNA sequencing reveals the enrichment of ion-transport functions among genes with higher expressi

152 ylene oxide) crystallization detrimental for ion transport, giving a composite that exhibits high mod

153 Transmembrane ion transport has long been recognised to contribute to

154 mical agents to identify molecules targeting ion transport, has traditionally involved low-throughput

155 el structures and the acidic groups on water/ion transport have been studied before, the surface chem

156 etic relationships among these regulators of ion transport have led to inconsistencies in their class

157 , including the regulation of exocytosis and ion-transport; however, its precise mechanistic role is

158 This subset included genes related to ion transport, hypoxia-reoxygenation and cell cycle regu

159 t something different is at play by studying ion transport in a bicrystal of yttria (9% mol) stabiliz

160 Electrokinetic ion transport in a pH-regulated nanopore, taking into ac

161 provides the platform for comparing lithium ion transport in amorphous and crystalline polymer domai

162 Understanding and controlling the lithium ion transport in battery electrodes becomes crucial to t

163 ies of both the gating process and water and ion transport in C1C2, and will spark interest in furthe

164 re advanced and better-controlled studies of ion transport in CDI systems, which can potentially cata

165 on uridine-5'-triphosphate (UTP)-stimulated ion transport in differentiated, pseudostratified epithe

166 framework for investigating the function of ion transport in health and disease.

167 '-cyclic monophosphate-mediated electrogenic ion transport in infected colonic tissues, attributable

168 ir importance of proteolytic degradation and ion transport in maintaining normal cell function.

169 Fast-ion transport in many of these solids is supported by a

170 ntributes to the dysregulation of intestinal ion transport in mice with colitis.

171 We investigated enteric glial regulation of ion transport in mice with trinitrobenzene sulfonic acid

172 pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.

173 Regulation of ion transport in plants is essential for cell function.

174 Ion transport in plants is not only strictly regulated o

175 asis for experimental findings that reported ion transport in polyILs to be decoupled from polymer se

176 at we can directly probe local variations in ion transport in polymer devices by measuring subnanomet

177 PT cells in vivo acutely regulate ion transport in response to changes in glomerular filtr

178 by providing a basis for detailed studies of ion transport in roots.

179 EnPEn can robustly capture ion transport in sub-millimeter architectures with submi

180 in the literature detailing these aspects of ion transport in the inflamed gut.

181 ontributes to the regulation of electrogenic ion transport in the intestine through effects on neuron

182 The mechanisms governing ion transport in the wild-type and mutant Hv1 channels w

183 onal assays verified the vectorial nature of ion transport in this system.

184 on colonic barrier function and electrogenic ion transport in Ussing chambers.

185 Pase play fundamental roles in regulation of ion transport in vertebrates.

186 Evidence for UPEC genes involved in ion transport, including copper efflux, nickel and potas

187 In vivo rates of protein synthesis and ion transport increased approximately 50% under acidific

188 However, the mechanisms for ion transport inside electrified nanopores remain largel

189 t iron binding channels that facilitate iron ion transport into the core of the complex.

190 hat the surface diffusion barrier for sodium ion transport is a sensitive function of the chemistry o

191 To date, the mechanism by which this ion transport is achieved has remained obscure, in part

192 ASL pH gradient produced by defective apical ion transport is balanced out by paracellular shunting o

193 Ion transport is exceptionally well understood, whereas

194 A quantitative understanding of how ion transport is integrated and controlled is key to mee

195 These results indicate lithium-ion transport is not confined within a single nanorod an

196 Initially, fast lithium-ion transport is observed along the long axis with small

197 Transmembrane ion transport is performed by the catalytic alpha subuni

198 Hence, ABA-dependent gene transcription and ion transport is regulated by a variety of protein kinas

199 Oxygen ion transport is the key issue in redox processes.

200 ole of dispersed and aggregated particles on ion-transport is considered.

201 volution of oxides.Information on how oxygen ions transport is crucial to understanding field-induced

202 wo NiCo2O4 electrodes and separating them by ion transporting layer.

203 Disturbances in the control of ion transport lead to epithelial barrier dysfunction in

204 guishable, and offers a testbed for studying ion transport limits in dense nanostructured electrode a

205 n mammalian urine and has important roles in ion transport, maintenance of water and electrolyte bala

206 ide applications in, for example, biomimetic ion transport manipulation, molecular sieving, water tre

207 ce, suggesting that reversed transepithelial ion transport may promote lung edema by driving active a

208 Combining ion transport measurements across a single grain boundar

209 The major ion transport mechanisms and ion channels that are invol

210 ridine nucleotides [NAD(P)(H)] also regulate ion transport mechanisms.

211 s been constructed to explore the underlying ion transport mechanisms.

212 are highly attractive model systems to study ion-transport mechanisms and could potentially be of hig

213 This Review is focused on ion-transport mechanisms and fundamental properties of s

214 gnificant water transport and even uncoupled ion transport mediated by transporters has challenged th

215 nd product, and served as a good solid state ion transport medium for reflectometric nitrite determin

216 We identified significant changes in ion transport, metabolism related to energy generation a

217 orm that utilizes the molecular mechanics of ion transport, metabolism, and signaling of the guard ce

218 -responsive genes included oxidative stress, ion transport, mitochondrial damage, and DNA repair.

219 Consistent with the ion transport model introduced, we showed the possibilit

220 For pH < 4, the hydrogen ion transport number becomes substantial and its mode of

221 ane proteins play crucial role in signaling, ion transport, nutrient uptake, as well as in maintainin

222 allows direct visualization of heterogeneous ion transport of biological samples for the first time.

223 ng on guard cell dynamics, gas exchange, and ion transport of guard cells.

224 Ion transport of multi-ionic solutions through layered e

225 annels and are important for transepithelial ion transport, olfaction, phototransduction, smooth musc

226 ), revealed through the strong dependence of ion transport on ionic strength.

227 f typical ion exchange membranes (namely, co-ion transport, osmosis, and electro-osmosis) can detrime

228 diverse transport behaviours consistent with ion transport over a free-energy barrier arising from io

229 iency, such as resistance losses inherent to ion transport over macroscale distances, loss of charge

230 The limited Li-ion transport over the Li6PS5Cl-Li2S interface, orders o

231 ts are used to unambiguously characterize Li-ion transport over the solid electrolyte-electrode inter

232 m, but diverse biological functions, such as ion transport (P=7.1E-3) and tissue morphogenesis (P=1.0

233 de abundant electroactive zones and electron/ion transport paths, and the monolithic sandwich-type co

234 Multiple lithium-ion transport pathways and local phase changes upon lith

235 essible surface area, efficient electron and ion transport pathways as well as a high packing density

236 rrant junctions, and losses in transcellular ion transport pathways, likely leading to the MVID clini

237 s to gain insight into the properties of the ion-transporting pathways in acinar cells that might acc

238 an Hyperglycemic Hormone (CHH) and arthropod Ion Transport Peptide (ITP) superfamily for venom expres

239 In contrast, we found the expression of the ion transport peptide (ITP) to be consistent within the

240 nsity at the nanopore wall and the resulting ion transport phenomena, such as ion concentration polar

241 lue < 0.001) including, 9nucleotide binding; ion transport, phosphorous metabolic process, and the MA

242 ltures to show their functional relevance to ion transport physiology and pathophysiology.

243 rane, likely reflecting the effectiveness of ion transport porins.

244 vation of glial activity evoked electrogenic ion transport primarily through neural pathways and was

245 y the lipophilicity of a receptor during the ion-transport process.

246 and modeling of the electron-transfer gated ion transport processes in carbon nanopipets.

247 rovide a mechanism for a coupling of the two ion transport processes.

248 We demonstrate herein data on ion transport properties (D and t(+)) of concentrated Li

249 Understanding ion transport properties at various interfaces, especial

250 DAP triggers plasma membrane electrical and ion transport properties in an opposite way to those by

251 stability, but also influencing electron and ion transport properties in high-capacity oxide cathode

252 While the ensemble of ion transport proteins involved in cell volume regulatio

253 was used to measure expression levels of key ion transport proteins.

254 at introduces variation in the activities of ion-transport proteins between cells.

255 cking of various transmembrane receptors and ion-transport proteins.

256 Owing to the ubiquitous presence of ion transport-proteins and cell-cell heterogeneity in bi

257 ppropriate patterning, increases the overall ion transport rate by up to 80%.

258 Recent evidence suggests that the intrinsic ion transport rate, cell surface stability, and plasmale

259 ic mutagenesis experiments show that ClC-ec1 ion transport rates decrease as the size of the portal r

260 urprising fivefold enhancement of stochastic ion transport rates for single-walled carbon nanotube ce

261 , such as cytokinesis, pathogen defense, and ion transport regulation.

262 diffusional process is the bottleneck for Li-ion transport requires the ability to distinguish the va

263 tens the safety of batteries by piercing the ion-transporting separators between the cathode and anod

264 cellular allosteric site, independent of the ion transport sites, and an increase in turnover via an

265 Finally, the potential for ion transport studies was tested using the model ion cha

266 chment categories for gene ontology included ion transport, synaptic transmission and visual and sens

267 -derived enteroids are a model of intestinal ion transport that require validation by comparison with

268 the increased rates of protein synthesis and ion transport that were sustained in growing larvae coll

269 ar stress (FSS) modulate acute changes in PT ion transport thought to be mediated by microvillar bend

270 rect role for PTEN in the regulation of lens ion transport through an AKT-dependent modulation of Na+

271 transmembrane potentials, and mechanisms for ion transport through bilayers are discussed.

272 Water-mediated ion transport through functional nanoporous materials de

273 trolyte, is shown to both facilitate lithium-ion transport through its reconfigurable network of mobi

274 calix[4]pyrroles show excellent activity in ion transport through lipid-based lamellar membranes.

275 Better understanding in the dynamics of ion transport through nanopores or nanochannels is impor

276 a(+), and H(+) contributions to electrogenic ion transport through SLC4A11 stably expressed in Na(+)/

277 face of OLCs in OLC EDLCs without long-range ion transport through the bulk electrode.

278 iations caused by electrostatic screening of ion transport through the frit pores.

279 ol(-1) decrease in the activation energy for ion transport through the protein pore.

280 We report ion transport through ultimately narrow slits that are f

281 roximately 1 mus to discern the mechanism of ion transport throughout TWIK-1.

282 es from GFAP::hM3Dq mice evoked electrogenic ion transport to an extent equal to the direct activatio

283 ays and was sufficient to drive electrogenic ion transport to an extent equal to the direct activatio

284 l changes in polymer packing that may impede ion transport to different extents within the same macro

285 eotides may be required for integrating cell ion transport to energetics and for sensing oxygen level

286 y of physiological functions that range from ion transport to phospholipid scrambling and to regulati

287 cleotide binding domain 1 (NBD1) that allows ion transport to proceed in a regulated fashion.

288 ere we use a biophysical model for water and ion transport to quantify ion permeabilities of all path

289 ll metabolism, maintenance of DNA integrity, ion transport, transcription regulation, and allosteric

290 e has been no functional study investigating ion transport using human ES tissue.

291 x couple, and provides facile pathway for Na-ion transport via intra-/inter-layer defects of Mn5O8.

292 However, this ion transport was abolished in coi1-1 guard cells, sugge

293 Electrically evoked ion transport was measured in full-thickness segments of

294 receptor signaling, muscle contraction, and ion transport were already present in TGy.

295 ntly, the in vivo physiological increases in ion transport were not predicted from total enzyme activ

296 We report unexpected inter-nanorod lithium-ion transport, where the reaction fronts and kinetics ar

297 a significantly contribute to the neurogenic ion transport while glial activity does not appear to pl

298 equal to the direct activation of neurogenic ion transport with veratridine and glial driven response

299 first time-resolved visualization of lithium-ion transport within and between individual nanorods, wh

300 fion, with membranes that use light to drive ion transport would allow membranes in photoelectrochemi