ライフサイエンスコーパス: cotransport

1 il colloids facilitated the release of AgNP (cotransport).

2 these sites result in constitutively active cotransport.

3 nd decrease in bumetanide-sensitive chloride cotransport.

4 Similar constraints must apply to cotransport.

5 fects of bumetanide, an inhibitor of Na-K-Cl cotransport.

6 changes in the transporter protein accompany cotransport.

7 nd 8 of EAAC1, Asp-367 and Asp-454, in Na(+) cotransport.

8 transepithelial transport, e.g., Na+/glucose cotransport.

9 al pH and, thus, does not contribute to H(+) cotransport.

10 ay recruit them as a complex, enabling their cotransport.

11 E681OH AE1, thereby allowing Cl(-)/SO(4)(2-) cotransport.

12 t pH(i) increases triggered by Na(+)-glucose cotransport.

13 processes such as the Na+-K+-ATPase and ion cotransport.

14 ment and pH(i) increases after Na(+)-glucose cotransport.

15 horylation after initiation of Na(+)-glucose cotransport.

16 horylation after initiation of Na(+)-glucose cotransport.

17 ant presence of reticulocytes with high K-Cl cotransport.

18 , revealing the reversibility of Na(+)/sugar cotransport.

19 ransmitter uptake to the sodium and chloride cotransport.

20 approximate 1:1 coupling ratio for Na(+)-GSH cotransport.

21 o be nonelectrogenic, inseparable H(+)/Cl(-) cotransport.

22 were without effect on glaucomatous TM cell cotransport.

23 p an ideal coordinator of ER tubule and mRNA cotransport.

24 mbrane potential, indicating substrate/Na(+) cotransport.

25 GlyT2 cotransports 3Na+/Cl-/glycine generating large rises of

26 omain transporters; PepT1 has proton/peptide cotransport activity and is selectively expressed in int

27 ately 3-4-fold greater than the H(+)/peptide cotransport activity as determined by measurements of H(

28 les exhibit apparently normal Na(+) /HCO3(-) cotransport activity but that Q913R is associated with a

29 could be associated with the decreased Na/Pi cotransport activity in potassium deficiency.

30 Intracellular Ca(2+) activates Na(+),HCO3(-) cotransport activity in VSMCs in a calcineurin-dependent

31 FK506 did not affect Na(+),HCO3(-) cotransport activity in VSMCs when cytosolic [Ca(2+)] wa

32 close-to-normal per molecule Na(+) /HCO3(-) cotransport activity in Xenopus oocytes, suggesting that

33 Na-K-Cl cotransport activity of glaucomatous TM cells was found

34 raise intracellular [Ca(2+)], Na(+),HCO3(-) cotransport activity was inhibited 20-30% by calcineurin

35 Na(+),HCO3(-) cotransport activity was investigated in VSMCs of mesent

36 anide (10(-5) M) was used to inhibit Na-K-Cl cotransport activity, and vasopressin (10(-7) M, 10(-8)

37 k cell monolayers were evaluated for Na-K-Cl cotransport activity, assessed as ouabain-insensitive, b

38 ls and was due to a local decrease in K+-Cl- cotransport activity, effectively reducing the strength

39 Despite this electroneutral cotransport activity, the transporter mediated a steady-

40 monophosphate was found to diminish Na-K-Cl cotransport activity, whereas these agents were without

41 n (10(-7) M, 10(-8) M) was used to stimulate cotransport activity.

42 tail of NKCC1, phosphorylate, and stimulate cotransport activity.

43 After initiation of Na(+)-glucose cotransport, Akt is activated with kinetics that paralle

44 ose transport showed an uncoupling of proton cotransport and a drastic reduction in Na(+)-coupled tra

45 asolateral membrane is achieved by Na+-HCO3- cotransport and also by a H+-ATPase and Na+/H+ exchanger

46 ves coordinate upregulation of PE-side NaKCl cotransport and an NPE-side DIDS-inhibitable mechanism(s

47 riety of mechanisms, including chloride/H(+) cotransport and chloride/nitrate, chloride/bicarbonate,

48 of bath bumetanide, an inhibitor of Na-K-2Cl cotransport and Cl(-) secretion, resulted in a significa

49 er content, particularly associated with KCl cotransport and Gardos channel activation, have revealed

50 ansport is comparable to that of Na+-glucose cotransport and indicates that the process is dependent

51 n the coordinate regulation of Na(+)-glucose cotransport and Na(+)-H(+) exchange.

52 cAMP-mediated stimulation of hepatic Na+/TC cotransport and Ntcp translocation requires activation o

53 P and cell swelling stimulate hepatic Na+/TC cotransport and Ntcp translocation via the phosphoinosit

54 es HCO3-dependent HOE694-insensitive Na-HCO3 cotransport and plays a critical role in pHi regulation

55 The voltage dependence of cotransport and presteady-state charge displacements (in

56 t review we summarize the evidence for water cotransport and propose how this occurs during the enzym

57 Here, we investigated the cotransport and retention of HANPs and GNPs in water-sat

58 ry coupling of water transport to Na-glucose cotransport and the mechanism of action of a number of p

59 ow that SV and AZ proteins exhibit extensive cotransport and undergo frequent pauses.

60 in (SN1) involves H+ exchange as well as Na+ cotransport and, under physiological conditions, mediate

61 ke, 2) an increase in the V(max) of Na(+)/TC cotransport, and 3) wortmannin-sensitive increases in TC

62 In axons, APP and BACE-1 were cotransported, and they also interacted during transit.

63 Variations in rates of drug cotransport are predicted to be due to differences in af

64 of otherwise cell-impermeable discotics via cotransport as a function of supramolecular coassembly.

65 everal studies suggest that SCb proteins are cotransported as one or more macromolecular complexes, b

66 localizing with extranuclear Wld(S), and was cotransported at least partially with mitochondria.

67 arizing GABA responses is caused by Na-K-2Cl cotransport because reduction of external Cl(-) or appli

68 Specific anion cotransport blockers, such as SITS, DIDS, furosemide, or

69 n nature, and they are not reversed by anion cotransport blockers.

70 r amiloride nor the inhibitor of Na+-K+-2Cl- cotransport bumetanide by itself was effective.

71 recovery from an acid load is not Na+-HCO3- cotransport, but amiloride-sensitive Na+-H+ exchange via

72 f ferret erythrocytes stimulates Na+-K+-2Cl- cotransport by 111% (s.d., 46) compared to controls in a

73 1 and SGLT1, Cl(-) modulates the kinetics of cotransport by altering Na(+) affinity, but does not con

74 Na(+)/glucose cotransport by SGLT1 is a tightly coupled process that i

75 anthraquinone unit, followed by either H+/e- cotransport by transmembrane diffusion of SP-AQH* or, fo

76 a positively charged amino acid replaces the cotransported cation.

77 lity in monolayers with active Na(+)-glucose cotransport, confirming a functional role for MLCK1.

78 activation after initiation of Na(+)-glucose cotransport, confirming the functional role of Akt2.

79 uggest that both the water channel and water cotransport could contribute to isotonic fluid transport

80 Simulated Na(+)-glucose cotransport demonstrates that active glucose accumulatio

81 s closely with development of Na(+)-nutrient cotransport-dependent tight junction regulation.

82 that early tubular growth and sodium-glucose cotransport enhance proximal tubule reabsorption and mak

83 Cation/glucose cotransport exhibits a coupling ratio of 2 Na+ (or 2 H+)

84 Because Na(+) currents and cotransport fluxes depend on the Na(+) concentration in

85 form increasingly organized clusters during cotransport from basolateral to perinuclear endosomes.

86 ulfonic acid, an inhibitor of sucrose-proton cotransport from the apoplast.

87 These findings indicate that Na-K-Cl cotransport function and regulation are altered in glauc

88 ytoplasmic domains of mouse KCC1 to its K-Cl cotransport function expressed in Xenopus oocytes.

89 to investigate the possibility that Na-K-Cl cotransport function may be altered in glaucomatous TM c

90 BC1-mediated electrogenic sodium bicarbonate cotransport function were transfected with either pNBC1

91 deficient in electrogenic sodium bicarbonate cotransport function, was transfected with kNBC1.

92 ical changes in oxygen tension can influence cotransport function.

93 acts as a proton donor for the anion/proton cotransport function.

94 m frog kidney, on stimulation of Na+-alanine cotransport GVD is activated, while GVI is unaffected.

95 ermease is an integral membrane protein that cotransports H(+) and lactose into the bacterial cytopla

96 Inhibition of erythroid K-Cl cotransport has emerged as an important adjunct strategy

97 f florfenicol to colloids and indicated that cotransport has little contribution.

98 ugh sequential extraction of a peat soil) to cotransport hexavalent uranium (U) within water-saturate

99 of wild-type and mutant human sodium glucose cotransport (hSGLT1) proteins to identify the Na(+) bind

100 explained without proposing Cl(-)/SO(4)(2-) cotransport if the rate-limiting event for (35)SO(4)(2-)

101 The V(max) for Na(+)/TC cotransport in basolateral liver plasma membrane was inc

102 tent with multiple novel roles for Na/HCO(3) cotransport in CNS physiology.

103 Na+-K+-2Cl- cotransport in ferret erythrocytes was measured as the b

104 e contention that HbS and HbC stimulate K-Cl cotransport in human red cells.

105 Initiation of Na(+)-glucose cotransport in intestinal absorptive epithelia causes NH

106 Initiation of Na(+)-glucose cotransport in intestinal epithelial cells leads to acti

107 quantitative and qualitative effects on K-Cl cotransport in mouse red cells and activate mouse K-Cl.

108 ulate the activity and/or regulation of K-Cl cotransport in mouse red cells.

109 of isotonic and swelling-induced K(+)-Cl(-) cotransport in neurons.

110 Elevation of K-Cl cotransport in patients with homozygous hemoglobin (Hb)

111 In contrast, OsHKT2;2 mediated Na(+)-K(+) cotransport in plant cells such that extracellular K(+)

112 electrogenic, amiloride-insensitive Na-HCO3 cotransport in proximal colon.

113 arathyroid hormone inhibits sodium-phosphate cotransport in proximal renal tubule cells through activ

114 Elucidation of the origin of elevated K-Cl cotransport in red cells with mutant hemoglobins has bee

115 Most K-Cl cotransport in the erythrocyte is attributed to potassiu

116 can account simultaneously for hydrodynamic cotransport in the presence of changes in fluorescence q

117 Activation of Na(+),HCO3(-) cotransport in vascular smooth muscle cells (VSMCs) cont

118 SCb proteins that we previously showed were cotransported in our system: alpha-synuclein, synapsin-I

119 remainder being sensitive to the Na+-K+-2Cl- cotransport inhibitor bumetanide.

120 asin B, but not the sodium-dependent glucose cotransport inhibitor phloridzin, prevented overload-ind

121 The sodium/phosphate cotransport inhibitor phosphonoformic acid blocked IL-8-

122 fter administration of the Na(+)/K(+)/2Cl(-) cotransport inhibitor, bumetanide.

123 A number of virulence proteins are cotransported into host cells concomitantly with the T-D

124 sly, we suggested that the mechanism of H(+) cotransport involves protonation of the conserved glutam

125 Alterations in glutamate and cotransported ion concentrations or in the membrane volt

126 contrast to the classical model of Cl- as a cotransported ion.

127 bitor, DL-TBOA in the presence of Na(+), the cotransported ion.

128 to a regulatory role rather than a coupled, cotransported-ion role.

129 dicted to result from stoichiometric flux of cotransported ions.

130 of the translocation pore for substrates and cotransported ions.

131 ch as the presence of GABA together with the cotransported ions.

132 Na(+)/glucose cotransport is abolished in the TMR6M-labeled mutant, bu

133 Swelling-activated K(+)-Cl(-) cotransport is abrogated by calyculin A, whereas isotoni

134 Airway epithelial Na-K-2Cl (NKCC1) cotransport is activated through hormonal stimulation an

135 Carrier-mediated water cotransport is currently a favored explanation for water

136 K-Cl cotransport is elevated in sickle erythrocytes, and the

137 The prevailing model of cotransport is the alternating access model, which sugge

138 omolecular complexes, but the basis for this cotransport is unknown.

139 med the ISO domain), is required for KCC2 to cotransport K(+) and Cl(-) out of the neuron under isoto

140 KCl cotransport (KCC) activation by cell swelling and pH was

141 KCl cotransport (KCC) activity contributes to pathologic deh

142 bservations suggest that O2 activates K+-Cl- cotransport (KCC) and deactivates Na+-K+-2Cl- cotranspor

143 potassium absorption is non-conductive, K-Cl cotransport (KCC) at the basolateral membrane may also b

144 K-Cl cotransport (KCC) is activated by nitric oxide donors an

145 Activation of Na(+)-nutrient cotransport leads to increased tight junction permeabili

146 treatment and suggest that blocking Na-K-Cl cotransport may reduce cerebral cell swelling.

147 An alternative cotransport mechanism is proposed where His-322 imidazol

148 ced conformational changes that underlie the cotransport mechanism.

149 e negative charge in the coordination of the cotransport mechanism.

150 (-) treatment, suggesting a Zn(2+)-HCO(3)(-) cotransport mechanism.

151 ecretory glands is fueled by Na(+)/HCO(3)(-) cotransport mediated by basolateral solute carrier famil

152 activated transport, constitutive K(+)-Cl(-) cotransport mediated by KCC2 is completely independent o

153 te dissociating first, followed by the three cotransported Na(+) ions.

154 NBCe1-A electrogenically cotransports Na(+) and HCO(3)(-) across the basolateral

155 ements of Na(+)-dependent OH(-) and/or HCO3- cotransport (NBC) activities in SMG acinar and duct cell

156 e native acid-extruding proteins, Na+ -HCO3- cotransport (NBC) and Na+ / H+ exchange (NHE), expressed

157 kedly reduced by inhibition of Na(+)/HCO3(-) cotransport (NBC) or Na(+)/Ca(2+) exchange (NCX), and ab

158 Na-HCO3 cotransport (NBC) regulates intracellular pH (pHi) and H

159 rried on Na+-H+ exchange (NHE) and Na+-HCO3- cotransport (NBC), and acid influxes carried on Cl--HCO3

160 (+) exchanger (NHE3) and the Na(+)-HCO(3)(-) cotransport (NBC3).

161 otransport (KCC) and deactivates Na+-K+-2Cl- cotransport (NKCC) in these cells via separate O2 sensor

162 Na(+)-K(+)-2Cl(-) cotransport (NKCC) mediates the movement of two Cl(-) io

163 rmational changes underlying Na(+)/galactose cotransport occur at or near the extracellular domain be

164 ple if those transporters were driven by the cotransport of 2 Na+ (rather than of 3 Na+ as for GLT-1)

165 was found to be driven, as for GLT-1, by the cotransport of 3 Na+ and 1 H+ and the counter-transport

166 ino acid transporters (EAATs), involving the cotransport of a proton and three Na(+) ions and the cou

167 ons, supporting the role of XRCC1 in nuclear cotransport of APLF.

168 uring cotransport of HANPs and GNPs, and the cotransport of both NPs is highly sensitive to solution

169 dendrite delivery, and live imaging reveals cotransport of both proteins.

170 The diuretic-sensitive cotransport of cations with chloride is mediated by the

171 ich at least two Na+ ions are coupled to the cotransport of each aspartate molecule by GltPh, and whe

172 Their transport cycle consists of cotransport of glutamate with three sodium ions and one

173 diated QO-SG transport that does not involve cotransport of glutathione.

174 elution of smaller particles occurred during cotransport of HANPs and GNPs, and the cotransport of bo

175 Our observations of the cotransport of multiple SCb proteins in single axons sug

176 terpretation that MX efflux by MRP1 involves cotransport of MX and glutathione.

177 nd Na(+) binding sites, and the mechanism of cotransport of Na(+) ions, using molecular dynamics simu

178 ent with the hypothesis that the macroscopic cotransport of Na+ plus two HCO3- occurs as NBC transpor

179 , couples the transport of amino acid to the cotransport of one Na(+) ion into the cell.

180 es the thermodynamic and kinetic controls of cotransport of Pantoea agglomerans cells and Zn in quart

181 transport protein (PTP) catalyzes the proton cotransport of phosphate into the mitochondrial matrix.

182 ne 282 to a glutamate not only uncouples the cotransport of protons and peptides of the wild-type Pep

183 Furthermore, cotransport of these three SCb proteins continued in act

184 tor complex either for separate transport or cotransport of these two cargos.

185 amino acid carrier (EAAC1) is coupled to the cotransport of three Na(+) ions and one proton.

186 tamate transporter (GlT) is catalyzed by the cotransport of three Na(+) ions.

187 rs couple the uptake of one glutamate to the cotransport of three sodium ions and one proton and the

188 ne glutamate transporter EAAC1 is coupled to cotransport of three sodium ions.

189 diffusion maps that reveal interactions and cotransport of two distinct molecular species labeled wi

190 phobic organic matter in the association and cotransport of U by HAs.

191 Dynamic cotransport of vesicles and synapsin particles is also s

192 , glucose and water transport, i.e. there is cotransport of water along with Na+ and sugar, that will

193 tilized to examine the effect of Na+-alanine cotransport on two previously identified volume- and Gd3

194 le to the modulation of either substrate/ion cotransport or the ligand-gated chloride current, the ma

195 s phosphate ligands or as part of the proton cotransport path.

196 UDC uptake by way of the Na(+) /taurocholate cotransporting peptide.

197 pertinent aspects of ion channel theory and cotransport physiology to provide background for the cha

198 Recent evidence suggests that Na-K-Cl cotransport plays a major role in blood-to-aqueous anion

199 may be important in controlling the fate of cotransported pollutants.

200 The Na+-taurocholate cotransport polypeptide (ntcp) is the primary transporte

201 itis delta virus use the sodium/taurocholate cotransporting polypeptide (a bile acid transporter) as

202 BV entry receptor, human sodium-taurocholate cotransporting polypeptide (hNTCP), on macaque primary h

203 like the receptor human sodium taurocholate cotransporting polypeptide (hNTCP).

204 stably transfected with sodium taurocholate cotransporting polypeptide (HuH-NTCP cells) and in rat h

205 (OATP) 1B1 and sodium-dependent taurocholate cotransporting polypeptide (NTCP) allelic variants were

206 h the HBV entry receptor sodium taurocholate cotransporting polypeptide (NTCP) and impaired its bile

207 tes translocation of Na(+)-taurocholate (TC) cotransporting polypeptide (Ntcp) and multidrug resistan

208 ma membrane localization of Na+-taurocholate cotransporting polypeptide (NTCP) and multidrug resistan

209 Identification of sodium taurocholate cotransporting polypeptide (NTCP) as an HBV receptor ena

210 The discovery of sodium taurocholate cotransporting polypeptide (NTCP) as the hepatitis B vir

211 ded inhibition of Na+ -dependent taurocholic cotransporting polypeptide (NTCP) expression and activit

212 ke by translocating sodium-taurocholate (TC) cotransporting polypeptide (Ntcp) from an endosomal comp

213 Sodium taurocholate cotransporting polypeptide (Ntcp) from the respective sp

214 Although sodium taurocholate cotransporting polypeptide (NTCP) has recently been repo

215 a(+) and the presence of sodium-taurocholate cotransporting polypeptide (NTCP) indicate a Na(+) -depe

216 The sodium taurocholate cotransporting polypeptide (Ntcp) is the major bile salt

217 The Na(+) -taurocholate cotransporting polypeptide (NTCP) mediates uptake of con

218 le salt transporters Na(+)/taurocholate (TC) cotransporting polypeptide (Ntcp), and bile salt export

219 salt export pump (BSEP), Na(+)/taurocholate cotransporting polypeptide (NTCP), OATP1, OATP2, ABCG5,

220 Moreover, the Na+-taurocholate cotransporting polypeptide (NTCP), responsible for bile

221 cells reconstituted with sodium taurocholate cotransporting polypeptide (NTCP), the currently accepte

222 rt term regulation of the Na(+)-taurocholate cotransporting polypeptide (Ntcp), the major bile salt u

223 SLC10A1 codes for the sodium-taurocholate cotransporting polypeptide (NTCP), which is a hepatocell

224 ubsequently binds to the sodium taurocholate cotransporting polypeptide (NTCP, encoded by SLC10A1), t

225 from portal circulation is Na+-taurocholate cotransporting polypeptide (NTCP, SLC10A1).

226 The Na(+) -taurocholate cotransporting polypeptide (NTCP/SLC10A1) is believed to

227 h the human HBV receptor sodium taurocholate cotransporting polypeptide but could not be neutralized

228 2, OATP1A1, OATP1A4, and Na(+) -taurocholate-cotransporting polypeptide only in central hepatocytes o

229 The Na(+)-taurocholate cotransporting polypeptide SLC10A1 (NTCP) plays a key ro

230 ly transfected with human Na(+)-taurocholate cotransporting polypeptide, BSEP, MDR3, and ABCG5/G8 and

231 ) 1a1, Oatp1a4, Oatp1b2, sodium taurocholate cotransporting polypeptide, multidrug resistance-associa

232 lateral membrane protein, Na(+)/taurocholate cotransporting polypeptide, with the 14-mer peptide tail

233 ile acid transporter and Na(+) -taurocholate cotransporting polypeptide, within the enterohepatic cir

234 X receptor and sodium-dependent taurocholate cotransporting polypeptide; new insights into the pathog

235 ich functions to facilitate the anion/proton cotransport process (a) by blocking the "redocking" of t

236 anism and biological role of these intricate cotransport processes in fungal models such as Saccharom

237 le acids, mediated by the Na(+)-taurocholate cotransporting protein (NTCP).

238 part of a diverse family of cation-chloride cotransport proteins that share a common predicted membr

239 reveal that EmrE can simultaneously bind and cotransport proton and drug.

240 However, it was also speculated that the cotransported proton is shared in a H(+)-binding network

241 y the results, which includes binding of the cotransported proton to E373 and binding of a modulatory

242 The resting cotransport rate was high but could be increased threefo

243 The Na+-K+-2Cl- cotransport rate was stimulated by treating erythrocytes

244 the functional level, interference with this cotransport reduces the number of spine protrusions and

245 K-Cl cotransport regulates cell volume and chloride equilibri

246 onsible for the electroneutral Na(+)/lactate cotransport reported in mammalian and amphibian kidneys.

247 s, ezrin phosphorylation after Na(+)-glucose cotransport requires p38 MAP kinase activity, but p38 MA

248 e data show that initiation of Na(+)-glucose cotransport resulted in rapid increases in both apical m

249 proximal renal tubule cell sodium-phosphate cotransport, stimulates several signal transduction path

250 In cells stored for 3 days or less, cotransport stimulation by arsenite could be described b

251 The HCO(3)(-) : Na(+) cotransport stoichiometry of the electrogenic sodium bic

252 Acetazolamide did not affect the cotransport stoichiometry or the ability of 8-Br-cAMP to

253 Surprisingly, the cotransported substrates Na(+) and aspartate induce oppo

254 proportional to the rate of Na+-glucose-H2O cotransport such that the amount of urea transport was a

255 arrier of Escherichia coli is a sugar-cation cotransport system that utilizes Na(+), Li(+), or H(+).

256 ponents: one is classical active Na+-glucose cotransport, the other is the diffusive apical GLUT2 pat

257 Although Na and Cl are putatively cotransported, they have opposite effects on the interna

258 ibits proximal renal tubule sodium-phosphate cotransport through a signaling complex dependent upon a

259 he form of NH(3), while the excess proton is cotransported through a highly conserved hydrogen-bonded

260 ecause secretory glycoproteins and Sfhex are cotransported through the same secretory pathway and bec

261 e via AE2 is coupled to basolateral NaHCO(3) cotransport to support CFTR-mediated chloride and bicarb

262 S) within its primary amino acid sequence or cotransport to the nucleus with another karyophilic prot

263 the number of water molecules that might be cotransported to ECF per NAA molecule released is as yet

264 Because multiple mRNAs are cotransported to the bud, it is likely that this process

265 All active maturation factors are cotransported to the cell surface when coexpressed with

266 y and sufficient for constitutive K(+)-Cl(-) cotransport under isotonic conditions.

267 unique in mediating constitutive K(+)-Cl(-) cotransport under isotonic conditions; the other three K

268 Inhibition of Na-K-Cl cotransport using Cl-free medium or bumetanide resulted

269 without bumetanide, an inhibitor of Na-K-2Cl cotransport, using ANCOVA with a 2 x 2 factorial study d

270 is that sphingomyelin and cholesterol may be cotransported via a Golgi-dependent pathway and that the

271 diverse levels of organization, while being cotransported via the polarized endocytic pathways.

272 nce of chloride, making it unlikely that KCl cotransport was an important pathway under these conditi

273 Electroneutral K+/Cl- cotransport was demonstrated in SiHa cells, in which K+

274 Although Na+-glucose cotransport was normal in the CF jejunum, absence of pas

275 2 cells, co-flux with paxillin; an analogous cotransport was seen for alpha6beta1-integrin and alpha-

276 with decreased bumetanide-sensitive chloride cotransport, whereas KCC2 immunoreactivity was increased

277 ocytes acidification activates Na(+)/HCO3(-) cotransport, which brings Na(+) inside the cell.

278 repancies in the alternating access model of cotransport, which cannot consistently explain substrate

279 a protein phosphatase inhibitor, stimulated cotransport with a lag of about 5 min.

280 We now show that LYAAT1 mediates H+ cotransport with a stoichiometry of 1 H+/1 amino acid, c

281 Block of NKCC cotransport with bumetanide reduced the EOG in epithelia

282 Inhibition of renal sodium-glucose cotransport with empagliflozin in subjects with IFG and

283 thermore, time-lapse microscopy revealed SMN cotransport with HuD in live motor neurons.

284 phorylated after initiation of Na(+)-glucose cotransport with kinetics that paralleled activation of

285 ove the neurotransmitter from the synapse by cotransport with three sodium ions into the surrounding

286 se that the cadherin-beta-catenin complex is cotransported with AMPA receptors to synapses and dendri

287 ytic machinery, i.e., PS1 and BACE1, are not cotransported with APP in the sciatic nerves of mice.

288 itions under which salinity is favored to be cotransported with CO(2) into shallow aquifers will be i

289 Unexpectedly, PrP(Sc) is cotransported with ferritin, a prominent component of th

290 We furthermore show that Na(+) and H(+) are cotransported with glutamate in the forward part of the

291 brane were they recruited into filopodia and cotransported with host motor myosin 10 toward the buddi

292 Viral particles are cotransported with KIF1A in axons of primary rat superio

293 wed that fluorescently tagged AnkG or Nav1.2 cotransported with KIF5 along axons.

294 d Smo mutants do not colocalize with nor are cotransported with Ptc1.

295 e find that tea3p fused to GFP or mCherry is cotransported with tea1p by microtubules to cell tips, b

296 ith Fe(2+) occurred with Co(2+), known to be cotransported with tetracycline.

297 tly depends on the presence of GSH, which is cotransported with the anthocyanins and is sensitive to

298 , a fraction of the NLS-minus E1 protein was cotransported with the E2 protein into the nucleus and s

299 transported to the rod outer segment without cotransporting with full-length rhodopsin.

300 lower pH (increased release of silver), and cotransported zeolites (reduced silver in solution).