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1 il colloids facilitated the release of AgNP (cotransport).
2 hore to drive chloride efflux via H(+)/Cl(-) cotransport.
3 these sites result in constitutively active cotransport.
4 nd decrease in bumetanide-sensitive chloride cotransport.
5 Similar constraints must apply to cotransport.
6 fects of bumetanide, an inhibitor of Na-K-Cl cotransport.
7 changes in the transporter protein accompany cotransport.
8 nd 8 of EAAC1, Asp-367 and Asp-454, in Na(+) cotransport.
9 transepithelial transport, e.g., Na+/glucose cotransport.
10 al pH and, thus, does not contribute to H(+) cotransport.
11 ay recruit them as a complex, enabling their cotransport.
12 E681OH AE1, thereby allowing Cl(-)/SO(4)(2-) cotransport.
13 t pH(i) increases triggered by Na(+)-glucose cotransport.
14 processes such as the Na+-K+-ATPase and ion cotransport.
15 ment and pH(i) increases after Na(+)-glucose cotransport.
16 horylation after initiation of Na(+)-glucose cotransport.
17 horylation after initiation of Na(+)-glucose cotransport.
18 ant presence of reticulocytes with high K-Cl cotransport.
19 , revealing the reversibility of Na(+)/sugar cotransport.
20 ransmitter uptake to the sodium and chloride cotransport.
21 approximate 1:1 coupling ratio for Na(+)-GSH cotransport.
22 o be nonelectrogenic, inseparable H(+)/Cl(-) cotransport.
23 p an ideal coordinator of ER tubule and mRNA cotransport.
24 mbrane potential, indicating substrate/Na(+) cotransport.
25 glucose is primarily absorbed by Na-glucose cotransport 1 (SGLT1) and coupled NaCl by the dual opera
29 omain transporters; PepT1 has proton/peptide cotransport activity and is selectively expressed in int
30 les exhibit apparently normal Na(+) /HCO3(-) cotransport activity but that Q913R is associated with a
32 Intracellular Ca(2+) activates Na(+),HCO3(-) cotransport activity in VSMCs in a calcineurin-dependent
34 close-to-normal per molecule Na(+) /HCO3(-) cotransport activity in Xenopus oocytes, suggesting that
35 raise intracellular [Ca(2+)], Na(+),HCO3(-) cotransport activity was inhibited 20-30% by calcineurin
37 ls and was due to a local decrease in K+-Cl- cotransport activity, effectively reducing the strength
41 asolateral membrane is achieved by Na+-HCO3- cotransport and also by a H+-ATPase and Na+/H+ exchanger
42 ves coordinate upregulation of PE-side NaKCl cotransport and an NPE-side DIDS-inhibitable mechanism(s
43 riety of mechanisms, including chloride/H(+) cotransport and chloride/nitrate, chloride/bicarbonate,
44 of bath bumetanide, an inhibitor of Na-K-2Cl cotransport and Cl(-) secretion, resulted in a significa
45 er content, particularly associated with KCl cotransport and Gardos channel activation, have revealed
47 cAMP-mediated stimulation of hepatic Na+/TC cotransport and Ntcp translocation requires activation o
48 P and cell swelling stimulate hepatic Na+/TC cotransport and Ntcp translocation via the phosphoinosit
49 es HCO3-dependent HOE694-insensitive Na-HCO3 cotransport and plays a critical role in pHi regulation
51 t review we summarize the evidence for water cotransport and propose how this occurs during the enzym
53 ry coupling of water transport to Na-glucose cotransport and the mechanism of action of a number of p
55 in (SN1) involves H+ exchange as well as Na+ cotransport and, under physiological conditions, mediate
58 of otherwise cell-impermeable discotics via cotransport as a function of supramolecular coassembly.
59 everal studies suggest that SCb proteins are cotransported as one or more macromolecular complexes, b
61 is, the pentose phosphate pathway (PPP), KCl cotransport, ATP release, Na(+)/K(+)-ATPase activity, an
66 f ferret erythrocytes stimulates Na+-K+-2Cl- cotransport by 111% (s.d., 46) compared to controls in a
67 e of the cavity conveys an advantage, as the cotransport by calix[6]arenes was observed to be more ef
70 anthraquinone unit, followed by either H+/e- cotransport by transmembrane diffusion of SP-AQH* or, fo
71 her the O(2) dependence of Na(+)/K(+)/2Cl(-) cotransport (catalyzed by Na(+)/K(+)/2Cl(-) cotransporte
73 lity in monolayers with active Na(+)-glucose cotransport, confirming a functional role for MLCK1.
74 activation after initiation of Na(+)-glucose cotransport, confirming the functional role of Akt2.
77 that early tubular growth and sodium-glucose cotransport enhance proximal tubule reabsorption and mak
79 form increasingly organized clusters during cotransport from basolateral to perinuclear endosomes.
82 BC1-mediated electrogenic sodium bicarbonate cotransport function were transfected with either pNBC1
87 ermease is an integral membrane protein that cotransports H(+) and lactose into the bacterial cytopla
90 acilitate transmembrane H(+) /Cl(-) symport (cotransport) have anti-cancer potential due to their abi
91 ugh sequential extraction of a peat soil) to cotransport hexavalent uranium (U) within water-saturate
92 of wild-type and mutant human sodium glucose cotransport (hSGLT1) proteins to identify the Na(+) bind
93 explained without proposing Cl(-)/SO(4)(2-) cotransport if the rate-limiting event for (35)SO(4)(2-)
94 both single and mixed reaction pathways for cotransport in a simple environment with a single substr
99 quantitative and qualitative effects on K-Cl cotransport in mouse red cells and activate mouse K-Cl.
103 In contrast, OsHKT2;2 mediated Na(+)-K(+) cotransport in plant cells such that extracellular K(+)
105 arathyroid hormone inhibits sodium-phosphate cotransport in proximal renal tubule cells through activ
106 Elucidation of the origin of elevated K-Cl cotransport in red cells with mutant hemoglobins has bee
108 can account simultaneously for hydrodynamic cotransport in the presence of changes in fluorescence q
110 SCb proteins that we previously showed were cotransported in our system: alpha-synuclein, synapsin-I
112 asin B, but not the sodium-dependent glucose cotransport inhibitor phloridzin, prevented overload-ind
116 sly, we suggested that the mechanism of H(+) cotransport involves protonation of the conserved glutam
130 med the ISO domain), is required for KCC2 to cotransport K(+) and Cl(-) out of the neuron under isoto
133 bservations suggest that O2 activates K+-Cl- cotransport (KCC) and deactivates Na+-K+-2Cl- cotranspor
142 ecretory glands is fueled by Na(+)/HCO(3)(-) cotransport mediated by basolateral solute carrier famil
143 activated transport, constitutive K(+)-Cl(-) cotransport mediated by KCC2 is completely independent o
146 ements of Na(+)-dependent OH(-) and/or HCO3- cotransport (NBC) activities in SMG acinar and duct cell
147 e native acid-extruding proteins, Na+ -HCO3- cotransport (NBC) and Na+ / H+ exchange (NHE), expressed
148 kedly reduced by inhibition of Na(+)/HCO3(-) cotransport (NBC) or Na(+)/Ca(2+) exchange (NCX), and ab
151 otransport (KCC) and deactivates Na+-K+-2Cl- cotransport (NKCC) in these cells via separate O2 sensor
153 rmational changes underlying Na(+)/galactose cotransport occur at or near the extracellular domain be
154 ple if those transporters were driven by the cotransport of 2 Na+ (rather than of 3 Na+ as for GLT-1)
155 was found to be driven, as for GLT-1, by the cotransport of 3 Na+ and 1 H+ and the counter-transport
156 ino acid transporters (EAATs), involving the cotransport of a proton and three Na(+) ions and the cou
158 uring cotransport of HANPs and GNPs, and the cotransport of both NPs is highly sensitive to solution
161 ich at least two Na+ ions are coupled to the cotransport of each aspartate molecule by GltPh, and whe
164 elution of smaller particles occurred during cotransport of HANPs and GNPs, and the cotransport of bo
165 cause of decreased NKAalpha mRNA, but due to cotransport of mislocalized rhodopsin and NKAalpha to ly
168 nd Na(+) binding sites, and the mechanism of cotransport of Na(+) ions, using molecular dynamics simu
169 ent with the hypothesis that the macroscopic cotransport of Na+ plus two HCO3- occurs as NBC transpor
171 es the thermodynamic and kinetic controls of cotransport of Pantoea agglomerans cells and Zn in quart
172 transport protein (PTP) catalyzes the proton cotransport of phosphate into the mitochondrial matrix.
176 ne 282 to a glutamate not only uncouples the cotransport of protons and peptides of the wild-type Pep
181 rs couple the uptake of one glutamate to the cotransport of three sodium ions and one proton and the
183 diffusion maps that reveal interactions and cotransport of two distinct molecular species labeled wi
186 , glucose and water transport, i.e. there is cotransport of water along with Na+ and sugar, that will
189 scale distribution system: consistent with a cotransport phenomenon, the two metals were detected in
190 pertinent aspects of ion channel theory and cotransport physiology to provide background for the cha
193 itis delta virus use the sodium/taurocholate cotransporting polypeptide (a bile acid transporter) as
194 BV entry receptor, human sodium-taurocholate cotransporting polypeptide (hNTCP), on macaque primary h
196 stably transfected with sodium taurocholate cotransporting polypeptide (HuH-NTCP cells) and in rat h
197 (OATP) 1B1 and sodium-dependent taurocholate cotransporting polypeptide (NTCP) allelic variants were
198 h the HBV entry receptor sodium taurocholate cotransporting polypeptide (NTCP) and impaired its bile
199 tes translocation of Na(+)-taurocholate (TC) cotransporting polypeptide (Ntcp) and multidrug resistan
200 ma membrane localization of Na+-taurocholate cotransporting polypeptide (NTCP) and multidrug resistan
203 ded inhibition of Na+ -dependent taurocholic cotransporting polypeptide (NTCP) expression and activit
204 ke by translocating sodium-taurocholate (TC) cotransporting polypeptide (Ntcp) from an endosomal comp
207 a(+) and the presence of sodium-taurocholate cotransporting polypeptide (NTCP) indicate a Na(+) -depe
210 le salt transporters Na(+)/taurocholate (TC) cotransporting polypeptide (Ntcp), and bile salt export
211 cterization of the shrew sodium taurocholate cotransporting polypeptide (Ntcp), CSHBV/MSHBV surface p
212 salt export pump (BSEP), Na(+)/taurocholate cotransporting polypeptide (NTCP), OATP1, OATP2, ABCG5,
214 cells reconstituted with sodium taurocholate cotransporting polypeptide (NTCP), the currently accepte
215 rt term regulation of the Na(+)-taurocholate cotransporting polypeptide (Ntcp), the major bile salt u
216 SLC10A1 codes for the sodium-taurocholate cotransporting polypeptide (NTCP), which is a hepatocell
218 ubsequently binds to the sodium taurocholate cotransporting polypeptide (NTCP, encoded by SLC10A1), t
221 specifically target the sodium-taurocholate cotransporting polypeptide (NTCP; SLC10A1) on the sinuso
222 h the human HBV receptor sodium taurocholate cotransporting polypeptide but could not be neutralized
223 2, OATP1A1, OATP1A4, and Na(+) -taurocholate-cotransporting polypeptide only in central hepatocytes o
226 ver, common BA importers (Na(+)/taurocholate cotransporting polypeptide, apical sodium-dependent bile
227 l membrane protein, Na(+)/taurocholate (TCA) cotransporting polypeptide, at the site of a pharmacolog
228 ly transfected with human Na(+)-taurocholate cotransporting polypeptide, BSEP, MDR3, and ABCG5/G8 and
229 ) 1a1, Oatp1a4, Oatp1b2, sodium taurocholate cotransporting polypeptide, multidrug resistance-associa
230 rs (e.g., ABCB4, ABCB11, sodium/taurocholate cotransporting polypeptide, organic solute transporter a
231 lateral membrane protein, Na(+)/taurocholate cotransporting polypeptide, with the 14-mer peptide tail
232 ile acid transporter and Na(+) -taurocholate cotransporting polypeptide, within the enterohepatic cir
233 X receptor and sodium-dependent taurocholate cotransporting polypeptide; new insights into the pathog
234 uptake, by inhibition of sodium-taurocholate cotransporting polypetide (NTCP; Slc10a1) with Myrcludex
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
238 sodium-dependent inorganic phosphate (P(i)) cotransport proteins 2a-2c, has facilitated the identifi
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 functional level, interference with this cotransport reduces the number of spine protrusions and
244 onsible for the electroneutral Na(+)/lactate cotransport reported in mammalian and amphibian kidneys.
245 s, ezrin phosphorylation after Na(+)-glucose cotransport requires p38 MAP kinase activity, but p38 MA
246 e data show that initiation of Na(+)-glucose cotransport resulted in rapid increases in both apical m
248 proximal renal tubule cell sodium-phosphate cotransport, stimulates several signal transduction path
252 proportional to the rate of Na+-glucose-H2O cotransport such that the amount of urea transport was a
253 arrier of Escherichia coli is a sugar-cation cotransport system that utilizes Na(+), Li(+), or H(+).
254 ponents: one is classical active Na+-glucose cotransport, the other is the diffusive apical GLUT2 pat
257 s clear up excess extracellular glutamate by cotransporting three Na(+) and one H(+) with the counter
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
262 e via AE2 is coupled to basolateral NaHCO(3) cotransport to support CFTR-mediated chloride and bicarb
263 S) within its primary amino acid sequence or cotransport to the nucleus with another karyophilic prot
264 the number of water molecules that might be cotransported to ECF per NAA molecule released is as yet
268 unique in mediating constitutive K(+)-Cl(-) cotransport under isotonic conditions; the other three K
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
272 nce of chloride, making it unlikely that KCl cotransport was an important pathway under these conditi
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
278 repancies in the alternating access model of cotransport, which cannot consistently explain substrate
283 phorylated after initiation of Na(+)-glucose cotransport with kinetics that paralleled activation of
284 ove the neurotransmitter from the synapse by cotransport with three sodium ions into the surrounding
285 se that the cadherin-beta-catenin complex is cotransported with AMPA receptors to synapses and dendri
286 ytic machinery, i.e., PS1 and BACE1, are not cotransported with APP in the sciatic nerves of mice.
287 itions under which salinity is favored to be cotransported with CO(2) into shallow aquifers will be i
289 We furthermore show that Na(+) and H(+) are cotransported with glutamate in the forward part of the
290 brane were they recruited into filopodia and cotransported with host motor myosin 10 toward the buddi
294 e find that tea3p fused to GFP or mCherry is cotransported with tea1p by microtubules to cell tips, b
296 tly depends on the presence of GSH, which is cotransported with the anthocyanins and is sensitive to
297 , a fraction of the NLS-minus E1 protein was cotransported with the E2 protein into the nucleus and s
300 lower pH (increased release of silver), and cotransported zeolites (reduced silver in solution).